Skip to the content
 
  • Payment Plans
  • Login for Professionals
  • English
    • Deutsch
    • Français
    • Italiano
    • English
  • Healthy Travelling
  • Countries
  • News
  • Special travellers
  • Health risks
  • Vaccinations
  • Ask a specialist

MENU

  • LogIn
  • English
    • Deutsch
    • Français
    • Italiano
    • English
  • Healthy Travelling
  • Countries
  • News
  • Special travellers
  • Health risks
  • Vaccinations
  • Ask a specialist
 

Health Advice for Travellers
Swiss Expert Committee for Travel Medicine

 

Health Advice for Travellers
Swiss Expert Committee for Travel Medicine

 

Health Advice for Travellers
Swiss Expert Committee for Travel Medicine

Rwanda

Latest News

Clade Ib mpox virus (MPXV) (emerging clade): Available evidence suggests exclusive human-to-human contact transmission for this virus clade. Within the last 6 weeks, outbreaks continue to be reported in DRC (2’706 clade Ia/b), Uganda (914), Burundi (121), Kenya (66), Rwanda (1), Zambia (16), Congo (12, clade Ia, Ib, and IIa/b), Tanzania (15), Malawi (33), Ethiopia (18), and South Sudan. Travel-associated cases have been reported in several countries, including recently in China and Australia. For more information, see LINK.

 

Clade Ia MPXV is endemic in the following countries: DRC, Central African Republic, Republic of Congo, Cameroun, Sudan. Travel-related cases have been reported in China and Ireland. Epidemiological data and phylogenetic analyses still suggest that many outbreaks of clade Ia MPXV result from zoonotic spillover with secondary human-to-human transmission. However, there is emerging evidence of increasing sustained human-to-human transmission of one lineage of clade Ia MPXV from 2024, mainly through sexual contact, in Kinshasa.

 

Clade IIa MPXV is endemic in West Africa with rare zoonotic spillover to humans. Since 2024, increased number of cases in adults and children reported from Côte d’Ivoire, Ghana, Guinea, and Liberia in different locations, including their capital cities. Genomic sequencing analyses suggest the occurrence of repeated zoonotic spillover events followed by limited secondary human-to-human transmission.

 

Clade IIb MPXV (emerging clade): Available evidence suggests exclusive human-to-human contact transmission for this virus clade. Clade IIb sub-lineage B.1 (global epidemic in 2022) is still circulating worldwide at low level. Clade IIb sub-lineages A.x are circulating in Africa and the WHO Eastern Mediterranean Region. Within the last 6 weeks, outbreaks of clade IIb sub-lineages A.2 with community transmission have been reported from West Africa with Sierra Leone particularly affected (2’698 cases). In addition, cases have been reported from Liberia (100), Ghana (80 cases), Nigeria (17), Togo (18), Côte d’Ivoire (9), Guinea (1).

 

Weekly trends in Africa, see also LINK.

Mpox affected countries in Africa (source dashboard WHO):

 

 

mpox_page-0001.jpg

Follow local media and local health authority advice. Prevention measures should be followed during a stay in countries where mpox is endemic/epidemic (see also Factsheet Mpox).

 

General precautions (most important preventive measure!)

  • Worldwide:
    • Avoid close, skin-to-skin contact with people who have or may have mpox or people who have a rash (e.g., pimples, blisters, scabs).
    • Wash your hands often with soap + water or an alcohol-based hand sanitizer containing at least 60% alcohol.
    • Avoid touching potentially contaminated personal items such as bedding/clothing, towels or sharing eating utensils/cups, food or drink with a person who has, or may have mpox.
    • Avoid sex with sick persons; use of condoms for up to 12 weeks if your sexual partner have had mpox.
    • Follow advice of local authorities.


  • When travelling to endemic / epidemic areas in Africa, in addition to above mentioned general precautions:
    • Avoid contact with animals in areas where mpox regularly occurs.
    • Avoid eating or preparing meat from wild animals (bushmeat) or using products (creams, lotions, powders) derived from wild animals.

 

Vaccination

Recommendation of the Swiss Expert for Travel Medicine as of 23 June 2025:

1. Staying or travelling in African countries with mpox clade I and clade II outbreaks (see news):
Vaccination against mpox should only be considered for individuals at high risk and for whom proper implementation of the above general precautions is not possible (risk evaluation / consultation of a specialist in travel medicine is recommended!). High-risk situations are considered such as:

  • Health care and humanitarian work, including research or laboratory work
  • Working with animals
  • Commercial sex or multiple sexual partners

 

2. Staying in countries with mpox clade IIb sublineage B.1 (outside of Africa) in case of:

  • Increased risk (e.g. laboratory workers handling mpox virus, men who have sex with men, trans-persons with multiple sexual partners), see Swiss recommendations: see LINK.

 

The available vaccine against mpox (e.g. Jynneos®) is also effective against clade I. This vaccine is considered safe and highly effective in preventing severe mpox disease.

 

In case of symptoms:

  • Seek medical attention immediately.

 

If you are diagnosed with mpox:

  • Please stay at home (isolate yourself) until your mpox rash has healed and a new layer of skin has formed. Staying away from other people and not sharing things you have touched with others will help prevent the spread of mpox. People with mpox should regularly clean and disinfect the spaces they use to limit household contamination.
  • Wash your hands often with soap / water or an alcohol-based hand sanitizer containing at least 60% alcohol.
  • You should not have sex while while you have lesions or symptoms. Use condoms for 12 weeks after infection. This is a precaution to reduce the risk of spreading the virus to a partner.
  • For more information on what do if you are sick, see CDC LINK.

 

For clinicians:

  • Consider mpox as a possible diagnosis in patients with epidemiologic characteristics and lesions or other clinical signs and symptoms consistent with mpox. This includes persons who have been in DRC or, due to the demonstrated risks of regional spread, any of its neighboring countries in the previous 21 days.
  • Further information on clinical management and infection control for mpox (see WHO living guideline) and CDC LINK.
WHO Dashboard, accessed 23.6.2025

Within three weeks, mpox cases have increased by +4’758 to cumulative 14’078 confirmed cases (all clades), including 55 deaths. The following countries have reported new cases of clade I between 03 to 24 Nov 2024:

  • Democratic Republic of the Congo: +3’503 cases | cumulative 10’846 cases = clade Ia and I b
  • Burundi: +357  cases | cumulative 2’083 cases of clade Ib
  • Uganda: +290 cases | cumulative 649 cases of clade Ib
  • Central African Republic: +15 cases | cumulative 79 cases of clade Ia
  • Rwanda: +11 cases | cumulative 37 cases of clade Ib
  • Kenya: +5 cases | cumulative 19 cases of clade Ib

 

No new clade I cases have been reported within 3 weeks from Congo (22 clade Ia cases), Zimbabwe (2 clade Ib cases), and Zambia (1 clade Ib case).


A significant number of suspected mpox cases, that are clinically compatible with mpox remain untested due to limited diagnostic capacity in some African countries and thus never get confirmed.


For updates, details, suspected cases, epidemic curves, see WHO LINK).

afri.png

Follow local media and local health authority advice. Prevention measures should be followed during a stay in countries where mpox is endemic/epidemic (see also Factsheet Mpox).

 

General precautions

  • Worldwide:
    • Avoid close, skin-to-skin contact with people who have or may have mpox or people who have a rash (e.g., pimples, blisters, scabs).
    • Wash your hands often with soap + water or an alcohol-based hand sanitizer containing at least 60% alcohol.
    • Avoid touching potentially contaminated personal items such as bedding/clothing, towels or sharing eating utensils/cups, food or drink with a person who has, or may have mpox.
    • Avoid sex with sick persons; use of condoms for up to 12 weeks if you sexual partner have had mpox.
    • Follow advice of local authorities.

 

  • When travelling to endemic / epidemic areas in Africa, in addition to above mentioned general precautions:
    • Avoid contact with animals in areas where mpox regularly occurs.
    • Avoid eating or preparing meat from wild animals (bushmeat) or using products (creams, lotions, powders) derived from wild animals.

 

Vaccination

A vaccination against mpox is available (Jynneos®, manufactured by Bavarian Nordic). The Swiss Expert for Travel Medicine recommends vaccination against mpox in following situations, as of  3 October 2024 (the recommendation will be updated regularly depending on the development of the outbreak):

 

1.     People staying or travelling to Province Equateur and / or Eastern D.R. Congo (South/North Kivu) and / or Burundi in case of:

  • Clinical, research or laboratory work
  • Working with animals
    (a broader indication is still under discussion)

 

2.     People staying outside of Province Equateur and / or Eastern D.R. Congo (South/North Kivu) and / or Burundi (worldwide) in case of:

  • Increased risk (e.g. laboratory workers handling mpox virus, men who have sex with men, trans-persons with multiple sexual partners), see Swiss recommendations: see Link.

 

At the present time, it is assumed that the available vaccine against mpox (e.g. Jynneos®) is also effective against clade I. This vaccine is considered safe and highly effective in preventing severe mpox disease.

 

In case of symptoms

  • Seek medical attention immediately

 

If you are diagnosed with mpox:

  • Please stay at home (isolate yourself) until your mpox rash has healed and a new layer of skin has formed. Staying away from other people and not sharing things you have touched with others will help prevent the spread of mpox. People with mpox should regularly clean and disinfect the spaces they use to limit household contamination.
  • Wash your hands often with soap / water or an alcohol-based hand sanitizer containing at least 60% alcohol.
  • You should not have sex while symptomatic and while you have lesions or symptoms. Use condoms for 12 weeks after infection. This is a precaution to reduce the risk of spreading the virus to a partner.
  • For more information on what do if you are sick, see CDC LINK.

 

For clinicians:

  • Consider mpox as a possible diagnosis in patients with epidemiologic characteristics and lesions or other clinical signs and symptoms consistent with mpox. This includes persons who have been in DRC or, due to the demonstrated risks of regional spread, any of its neighboring countries in the previous 21 days.

Further information on evaluation and diagnosis: see CDC LINK.

WHO Dashboard, accessed 27.11.2024

On 27 September 2024, Rwanda reported its first Marburg virus disease outbreak (MVD), see also previous EpiNews.

 

  • The highest number of new confirmed cases were reported in the first two epidemiological weeks of the outbreak with 26 cases reported in epidemiological week 39 (23 to 29 September 2024) and 23 cases in week 40 (30 September to 6 October). This was followed by a sharp decline in weeks 41 and 42, with 12 and one case reported respectively.
  • As of 29 October 2024, 65 cases of MVD have been reported, including 15 deaths (23%); 3 patients are in isolation. So far, 47 patients have recovered. For updates, see LINK.
  • Most of the people infected are health workers, particularly those who work in intensive care units.
  • Contact tracing is ongoing, with 1’146 contacts under follow-up as of 20 October 2024.
  • Based on available updates from the outbreak investigation, the index case was a male between 20 and 30 years old with a history of exposure to bats in a cave.

2222.png

Marburg virus disease (MVD) is a rare but severe hemorrhagic fever, caused by Marburg virus (MARV). Although MVD is uncommon, MARV has the potential to cause outbreaks with significant case fatality rates (up to 88%). All recorded MVD outbreaks have originated in Africa.

 

Transmission: Fruit bats are the natural reservoir of MARV. The majority of MVD outbreaks have been connected to human entry into bat-infested mines and caves. Humans can also get infected by direct contact with an infected animal (e.g., non-human primate).

Person-to-person transmission occurs by direct contact (through broken skin or mucous membranes) with infected blood, secretions, and body fluids or by indirect contact with contaminated surfaces and materials like clothing, bedding and medical equipment. MVD is not an airborne disease, and a person is not  contagious before symptoms appear. As a result, if proper infection prevention and control precautions are strictly followed, the risk of infection is regarded as minimal.


Incubation period: usually five to ten days (range 2-21 days).


Symptoms: The onset of MVD is usually abrupt, with non-specific, flu-like symptoms such as a high fever, severe headache, chills and malaise. Rapid worsening occurs within 2–5 days for more than half of patients, marked by gastrointestinal symptoms such as anorexia, abdominal discomfort, severe nausea, vomiting, and diarrhea. In severe cases, a rash may develop, along with bleeding from various body areas. 

Treatment: There are several experimental drugs and vaccines for Marburg, but none has been licensed to date.

Further information, see ECDC Factsheet Marburg Virus, CDC.

Follow media and official reports! Follow all the recommendations of the local health authorities!

 

Travellers should be made aware of the ongoing outbreak. The risk for travellers to Rwanda is assessed as low, but it is high for family members and caregivers who have contact with sick people.

 

Preventive measures:

  • Wash your hands regularly and carefully using soap and water (or alcohol gel if soap is unavailable).
  • Avoid contact with sick people who have symptoms, such as fever, muscle pain, and rash.
  • Avoid contact with blood and other body fluids.
  • Avoid visiting healthcare facilities in the MVD-affected areas for no urgent medical care or non-medical reasons.
  • Avoid contact with dead bodies or items that have been in contact with dead bodies, participating in funeral or burial rituals, or attending a funeral or burial. 
  • Avoid handling, cooking, or eating bush/wild meat (meat of wild/feral mammals killed for food).
  • Wash and peel fruit and vegetables before consumption.
  • Avoid visiting mines or bat caves and contact with all wild animals, alive or dead, particularly bats.
  • If you decide to visit mines or caves inhabited by fruit bat colonies, wear gloves and other appropriate protective clothing, including masks and eye protection.
  • Practice safer sex.

 

Upon return from Rwanda:

  • Watch your health for symptoms of Marburg while in the outbreak area and for 21 days after leaving the outbreak area (no quarantine is required if there are no symptoms).

 

In case of symptoms:

If you develop fever and nonspecific symptoms such as chills, headache, muscle pain or abdominal pain:

  • you should separate yourself from others (isolate) immediately and
  • directly contact the in-country hotline by phone or contact a tropical institute or university hospital infectious disease unit.
  • alert the healthcare providers of your recent travel to an area with a Marburg outbreak.

 

For clinicians:

  • Consider Marburg as a possible diagnosis in patients with epidemiologic risks factors, especially in people with possible exposure of Marburg cases in Rwanda.
  • Further information on evaluation and diagnosis: see LINK and ECDC risk assessment.

111.png

RBC Rwanda, accessed 30.10.2024 | Travel advisory, Rwanda, 4.10.2024 | US Department of Health and Human Services, 7.10.2024

According to WHO, between 2 to 29 September 2024 (week 36 to 39), 17 countries shared their meningitis epidemiological data.

 

Epidemic:

  • Benin: Zoe region (Abdomey health district, crossed epidemic threshold on weeks 33 and 34), remaining in epidemic phase on week 36

 

Alert:

  • Benin: Alibori region, Atacora region, Bargou region, Collines region
  • Mali: Bamako region

 

For previous epidemics and alerts, see EpiNews or news at www.healthytravel.ch.

Vaccination with a quadrivalent meningococcal conjugate vaccine (Menveo® or Nimenrix®) is recommended:

  • During epidemics or alerts, vaccination is recommended for stays > 7 days or in the case of close contact with the population.

 

If no alert or epidemic is reported, vaccination is recommended for travel to the ‘meningitis belt’ during the dry season (typically occurring from December to June) across sub-Saharan Africa if

  • Travelling for >30 days or
  • For shorter stays, depending on the individual risk (e.g. close personal contacts, work in health care facilities, stay in heavily occupied accommodation, risk of epidemics).
WHO meningitis bulletin, week 36-39

On 27 September 2024, Rwanda reported its first Marburg virus disease outbreak (see EpiNews as of 3 Oct 2024). Updates as of 18.10.2024:

  • As of 16 October 2024, 62 cases of MVD have been reported, including 15 deaths (case fatality rate: 24%); 9 patients are in isolation. So far, 38 patients have recovered. For updates, see LINK. Cases are reported from eight of the 30 districts. Health care workers continue to be disproportionately affected.
  • Treatment trial: WHO announced the commencement of a randomized, controlled trial to test remdesivir and a monoclonal antibody designed specifically against MARV (derived from antibodies from a MVD survivor). Link to study with NHP model. Gilead donates remdesivir for emergency use to Rwanda.
  • Vaccination: On 6 October 2024, vaccinations (provided by Sabin Vaccine Institute) for healthcare workers and high risk contacts started as part of a Phase 2 rapid response open-label study; as of 16.10.2024 a total of 856 doses have been administered. Link to phase 1 study of the cAd3-vector based vaccine (single-dose i.m.). Link to the Marburg virus vaccine consortium, MARVAC. Link to GAVI, Marburg-page.
  • Rwanda continues implementing a number of control measures including: entry and exit screening at the airport, see EpiNews of 10.10.2024,
  • Link to history of Marburg Outbreaks via CDC webpage, see LINK.
  • CDC has put Rwanda on alert level 3 (Reconsider nonessential travel to the Republic of Rwanda).
  • As of 14 October 2024, the US Department of Health and Human Services started public health entry screening for those entering the country after having been to Rwanda the past 21 days, see LINK.

12.png

Marburg virus disease (MVD) is a rare but severe hemorrhagic fever, caused by Marburg virus (MARV). Although MVD is uncommon, MARV has the potential to cause outbreaks with significant case fatality rates (up to 88%). All recorded MVD outbreaks have originated in Africa.

 

Transmission: Fruit bats are the natural reservoir of MARV. The majority of MVD outbreaks have been connected to human entry into bat-infested mines and caves. Humans can also get infected by direct contact with an infected animal (e.g., non-human primate).

Person-to-person transmission occurs by direct contact (through broken skin or mucous membranes) with infected blood, secretions, and body fluids or by indirect contact with contaminated surfaces and materials like clothing, bedding and medical equipment. MVD is not an airborne disease, and a person is not  contagious before symptoms appear. As a result, if proper infection prevention and control precautions are strictly followed, the risk of infection is regarded as minimal.

 

Incubation period: usually five to ten days (range 2-21 days).

 

Symptoms: The onset of MVD is usually abrupt, with non-specific, flu-like symptoms such as a high fever, severe headache, chills and malaise. Rapid worsening occurs within 2–5 days for more than half of patients, marked by gastrointestinal symptoms such as anorexia, abdominal discomfort, severe nausea, vomiting, and diarrhea. In severe cases, a rash may develop, along with bleeding from various body areas. 

 

Treatment: There are several experimental drugs and vaccines for Marburg, but none has been licensed to date.

 

Further information, see ECDC Factsheet Marburg Virus, CDC

WHO assesses the risk of this outbreak as very high at the national level, high at the regional level, and low at the global level.

 

ECDC assess the overall risk for EU/EEA citizens visiting or living in Rwanda as low. This is because the likelihood of exposure to MVD – considering the low number of cases reported and the mode of transmission – and the impact are both assessed as low. For details, see LINK.

Follow media and official reports! Follow all the recommendations of the local health authorities!

 

Travellers should be made aware of the ongoing outbreak. The risk for travellers to Rwanda is assessed as low, but it is high for family members and caregivers who have contact with sick people.

 

Preventive measures:

 

  • Wash your hands regularly and carefully using soap and water (or alcohol gel if soap is unavailable).
  • Avoid contact with sick people who have symptoms, such as fever, muscle pain, and rash.
  • Avoid contact with blood and other body fluids.
  • Avoid visiting healthcare facilities in the MVD-affected areas for nonurgent medical care or non-medical reasons.
  • Avoid contact with dead bodies or items that have been in contact with dead bodies, participating in funeral or burial rituals, or attending a funeral or burial. 
  • Avoid handling, cooking, or eating bush/wild meat (meat of wild/feral mammals killed for food).
  • Wash and peel fruit and vegetables before consumption.
  • Avoid visiting mines or bat caves and contact with all wild animals, alive or dead, particularly bats.
  • If you decide to visit mines or caves inhabited by fruit bat colonies, wear gloves and other appropriate protective clothing, including masks and eye protection.
  • Practice safer sex.

 

Upon return from Rwanda:

  • Watch your health for symptoms of Marburg while in the outbreak area and for 21 days after leaving the outbreak area (no quarantine is required if there are no symptoms).

 

In case of symptoms

If you develop fever and nonspecific symptoms such as chills, headache, muscle pain or abdominal pain:

  • you should separate yourself from others (isolate) immediately and
  • directly contact the in-country hotline by phone or contact a tropical institute or university hospital infectious disease unit.
  • alert the healthcare providers of your recent travel to an area with a Marburg outbreak.

 

For clinicians:

  • Consider Marburg as a possible diagnosis in patients with epidemiologic risks factors, especially in people with possible exposure of Marburg cases in Rwanda.
  • Further information on evaluation and diagnosis: see LINK and ECDC risk assessment.

111.png

RBC Rwanda, accessed 18.10.2024 | Travel advisory, Rwanda, 4.10.2024 | US Department of Health and Human Services, 7.10.2024

In 2024, as of 06 October 2024, 16 countries have reported 7’524 confirmed cases (+770 new confirmed cases within 1 week), including 32 deaths. The three countries with the majority of the cases in 2024 (all clades) are Democratic Republic of the Congo (6’169), Burundi, (n = 987), and Nigeria, (n = 84).

 

(Note: A significant number of suspected mpox cases that are clinically compatible with mpox remain untested due to limited diagnostic capacity in some African countries and therefore never got confirmed.)


In 2024, 15 countries have reported both 31’527 suspected and laboratory tested cases (+5’160 within 1 week, all clades), including 998 suspected and confirmed deaths (+2 within 1 week).

 

According to WHO, in 2024 as of 29 Sept 2024 the cumulative confirmed mpox cases (+ cases since last update 29 Sep 2024) were reported in the below mentioned countries (for updates, details, suspected cases, epidemic curves, see WHO LINK):

 

Clade Ia and b:

  • D.R. Congo: according to WHO: 5’610 (+559 cases since 29 Sept 2024; note OV: in the week before the reported number was not conclusive)

 

Clade Ib

  • Burundi: 987 confirmed cases (+134 cases since 29 Sept 2024, stable increase of confirmed cases) (plus hundreds of suspected cases)
  • Uganda: 69 cases (+47 cases since 29 Sept 2024)
  • Kenya: 12 cases (+4 since 29 Sept 2024)
  • Rwanda: 6 cases (+0 cases since 29 Sept 2024)
  • Outside Africa: Sweden (1 case, imported from Burundi), Thailand (1 case, imported from DRC), India (1 imported case)

 

Clade Ia:

  • Republic of the Congo: 21 confirmed cases (+0)
  • Central African Republic: 57 confirmed cases (+2)
  • Cameroon: 6 cases (+0), including unknown number of cases with clade IIa and IIb

 

Clade II (a and/or b):

  • Côte d’Ivoire: 67 cases (+15)
  • Cameroon: 6 cases including unknown number of cases with clade 1a
  • Ghana: 1 case
  • Guinea: 1 case (+0)
  • Morocco: 3 case (+1)
  • Nigeria: 84 cases (+6)
  • South Africa: 25 cases (+0)

 

In addition, mpox cases have been reported in Africa in 2024 without specification of the clade:

  • Gabon: 2 cases (+0)
  • Liberia: 14 cases (+1)

Epicurve for Ib clade cases as 6 October 2024:

unnamed-chunk-69-.png

Follow local media and local health authority advice. The following prevention measures should be followed during a stay in countries where mpox is endemic/epidemic (see also Factsheet Mpox).

 

General precautions

  • Worldwide:
    • Avoid close, skin-to-skin contact with people who have or may have mpox or people who have a rash (e.g., pimples, blisters, scabs).
    • Wash your hands often with soap + water or an alcohol-based hand sanitizer containing at least 60% alcohol.
    • Avoid touching potentially contaminated personal items such as bedding/clothing, towels or sharing eating utensils/cups, food or drink with a person who has, or may have mpox.
    • Avoid sex with sick persons; use of condoms for up to 12 weeks if you sexual partner have had mpox.
    • Follow advice of local authorities.

  • When travelling to endemic / epidemic areas in Africa, in addition to above mentioned general precautions:
    • Avoid contact with and animals in areas where mpox regularly occurs.
    • Avoid eating or preparing meat from wild animals (bushmeat) or using products (creams, lotions, powders) derived from wild animals. 

     

 

Vaccination
A vaccination against mpox is available (Jynneos®, manufactured by Bavarian Nordic). The Swiss Expert for Travel Medicine recommends vaccination against mpox in following situations, as of  3 October 2024 (the recommendation will be updated regularly depending on the development of the outbreak):

 

1. People staying or travelling to Province Equateur and / or Eastern D.R. Congo (South/North Kivu) and / or Burundi in case of:

  • Clinical, research or laboratory work
  • Working with animals
    (a broader indication is still under discussion)

 

2. People staying outside of Province Equateur and / or Eastern D.R. Congo (South/North Kivu) and / or Burundi (worldwide) in case of:

  • Increased risk (e.g. laboratory workers handling mpox virus, men who have sex with men, trans-persons with multiple sexual partners), see Swiss recommendations: see Link.

 

At the present time, it is assumed that the available vaccine against mpox (e.g. Jynneos®) is also effective against clade I. This vaccine is considered safe and highly effective in preventing severe mpox disease.

 

In case of symptoms

  • Seek medical attention immediately

 

If you are diagnosed with mpox:

  • Please stay at home (isolate yourself) until your mpox rash has healed and a new layer of skin has formed. Staying away from other people and not sharing things you have touched with others will help prevent the spread of mpox.
  • People with mpox should regularly clean and disinfect the spaces they use to limit household contamination.
    Wash your hands often with soap /water or an alcohol-based hand sanitizer containing at least 60% alcohol.
  • You should not have sex while symptomatic and while you have lesions or symptoms. Use condoms for 12 weeks after infection. This is a precaution to reduce the risk of spreading the virus to a partner.
  • For more information on what do if you are sick, see CDC LINK.

 

For clinicians:

  • Consider mpox as a possible diagnosis in patients with epidemiologic characteristics and lesions or other clinical signs and symptoms consistent with mpox. This includes persons who have been in DRC or, due to the demonstrated risks of regional spread, any of its neighboring countries in the previous 21 days.
  • Further information on evaluation and diagnosis: see CDC LINK.
WHO Mpox Dashboard, accessed 10.10.2024

On 27 September 2024, Rwanda reported its first Marburg virus disease outbreak (see EpiNews as of 3 Oct 2024). 

 

  • As of 10 October 2024, 58 cases of MVD have been reported, including 13 deaths (case fatality rate: 22%); 30 patients are in isolation. So far, 12 patients have recovered. For updates, see LINK.
  • The cases are reported from eight of the 30 districts in the country. Among the confirmed cases, over 80% are health care workers from two health facilities in Kigali. Contact tracing is underway and follow-up of more than 300 contacts is ongoing.
  • On 6 October 2024, vaccinations for healthcare workers and high risk contacts started as part of a Phase 2 rapid response open-label study; vaccines have been provided by Sabin Vaccine Institute.
  • Rwanda has been implementing a number of control measures including: entry and exit screening at the airport, measures in education settings and conferences, ban on patient visits to hospitals, strengthening infection prevention and control protocols in hospitals, and measures to limit contact with dead bodies.
  • CDC has put Rwanda on alert level 3 (Reconsider nonessential travel to the Republic of Rwanda).
  • On 7 October 2024, the US Department of Health and Human Services announced that on the week of 14 October 2024 US CDC will start public health entry screening for those entering the country after having been to Rwanda the past 21 days, see LINK.

marburg.png

Marburg virus disease (MVD) is a rare but severe hemorrhagic fever, caused by Marburg virus (MARV). Although MVD is uncommon, MARV has the potential to cause outbreaks with significant case fatality rates (up to 88%). All recorded MVD outbreaks have originated in Africa.

 

Transmission: Fruit bats are the natural reservoir of MARV. The majority of MVD outbreaks have been connected to human entry into bat-infested mines and caves. Humans can also get infected by direct contact with an infected animal (e.g., non-human primate).

Person-to-person transmission occurs by direct contact (through broken skin or mucous membranes) with infected blood, secretions, and body fluids or by indirect contact with contaminated surfaces and materials like clothing, bedding and medical equipment. MVD is not an airborne disease, and a person is not  contagious before symptoms appear. As a result, if proper infection prevention and control precautions are strictly followed, the risk of infection is regarded as minimal.

 

Incubation period: usually five to ten days (range 2-21 days).

 

Symptoms: The onset of MVD is usually abrupt, with non-specific, flu-like symptoms such as a high fever, severe headache, chills and malaise. Rapid worsening occurs within 2–5 days for more than half of patients, marked by gastrointestinal symptoms such as anorexia, abdominal discomfort, severe nausea, vomiting, and diarrhea. In severe cases, a rash may develop, along with bleeding from various body areas. 

 

Treatment: There are several experimental drugs and vaccines for Marburg, but none has been licensed to date.

 

Further information, see ECDC Factsheet Marburg Virus, CDC.

WHO assesses the risk of this outbreak as very high at the national level, high at the regional level, and low at the global level.

 

ECDC assess the overall risk for EU/EEA citizens visiting or living in Rwanda as low. This is because the likelihood of exposure to MVD – considering the low number of cases reported and the mode of transmission – and the impact are both assessed as low. For details, see LINK.

Follow media and official reports! Follow all the recommendations of the local health authorities!

Travellers should be made aware of the ongoing outbreak. The risk for travellers to Rwanda is assessed as low, but it is high for family members and caregivers who have contact with sick people.

 

Preventive measures:

  • Wash your hands regularly and carefully using soap and water (or alcohol gel if soap is unavailable).
  • Avoid contact with sick people who have symptoms, such as fever, muscle pain, and rash.
  • Avoid contact with blood and other body fluids.
  • Avoid visiting healthcare facilities in the MVD-affected areas for nonurgent medical care or non-medical reasons.
  • Avoid contact with dead bodies or items that have been in contact with dead bodies, participating in funeral or burial rituals, or attending a funeral or burial. 
  • Avoid handling, cooking, or eating bush/wild meat (meat of wild/feral mammals killed for food).
  • Wash and peel fruit and vegetables before consumption.
  • Avoid visiting mines or bat caves and contact with all wild animals, alive or dead, particularly bats.
  • If you decide to visit mines or caves inhabited by fruit bat colonies, wear gloves and other appropriate protective clothing, including masks and eye protection.
  • Practice safer sex.

 

Upon return from Rwanda:

  • Watch your health for symptoms of Marburg while in the outbreak area and for 21 days after leaving the outbreak area (no quarantine is required if there are no symptoms).

 

In case of symptoms
If you develop fever and nonspecific symptoms such as chills, headache, muscle pain or abdominal pain:

  • you should separate yourself from others (isolate) immediately and
  • directly contact the in-country hotline by phone or contact a tropical institute or university hospital infectious disease unit.
  • alert the healthcare providers of your recent travel to an area with a Marburg outbreak.

 

For clinicians:

  • Consider Marburg as a possible diagnosis in patients with epidemiologic risks factors, especially in people with possible exposure of Marburg cases in Rwanda.
  • Further information on evaluation and diagnosis: see LINK and ECDC risk assessment.

pic.png

RBC Rwanda, accessed 10.10.2024 | Travel advisory, Rwanda, 4.10.2024 | US Department of Health and Human Services, 7.10.2024

According to WHO, between 29 to 1 September 2024 (week 31 to 35), 19 countries shared their meningitis epidemiological data.

 

Epidemic:

  • Benin: Zoe region (Abdomey health district, crossed epidemic threshold on weeks 33 and 34)
  • D.R. Congo: Province Sud-Ubangui and province Sankuru

Alert:

  • Benin: Bargou region, Collines region
  • D.R. Congo: Haut – Lomami province, Ituri province, Lomami province, Maindombe province
  • Ghana: Savannah region
  • Mali: Bamako region

For previous epidemics and alerts, see EpiNews or news at www.healthytravel.ch.

 

Vaccination with a quadrivalent meningococcal conjugate vaccine (Menveo® or Nimenrix®) is recommended:

 

  • During epidemics or alerts, vaccination is recommended for stays > 7 days or in the case of close contact with the population.

 

If no alert or epidemic is reported, vaccination is recommended for travel to the ‘meningitis belt’ during the dry season (typically occurring from December to June) across sub-Saharan Africa if

  • Travelling for >30 days or
  • For shorter stays, depending on the individual risk (e.g. close personal contacts, work in health care facilities, stay in heavily occupied accommodation, risk of epidemics).
WHO meningitis bulletin, week 31-35

On 27 September 2024, the Rwanda Ministry of Health announced the confirmation of Marburg virus disease in patients in health facilities in the country. As of 3 October, 36 cases of MVD have been reported, including 11 deaths (Case fatality rate: 31%). The cases are reported from seven of the 30 districts in the country (Gasabo, Gatsibo, Kamonyi, Kicukiro, Nyagatare, Nyarugenge and Rubavu districts). Among the confirmed cases, over 70% are health care workers from two health facilities in Kigali. Contact tracing is underway with 410 contacts under follow-up. The source of the infection is still under investigation.

 

One contact travelled to Belgium from Rwanda. WHO was made aware of this by the public health authorities in Belgium. They shared detailed information on the contact's situation, that they remained healthy, completed the 21-day monitoring period, did not present with any symptoms, and are not a risk to public health.

 

This is the first time MVD has been reported in Rwanda. The Government of Rwanda is coordinating the response with support from WHO and partners. The Ministry of Health of Rwanda announced several control measures including a ban on patient visits to hospitals, strengthening protocols in hospitals, and measures to limit contact with dead bodies.
Rwanda will start cinical trials of experimental vaccines and treatments for MVD in the next few weeks.

 

Marburg virus disease (MVD) is a rare but severe hemorrhagic fever, caused by Marburg virus (MARV). Although MVD is uncommon, MARV has the potential to cause outbreaks with significant case fatality rates (up to 88%). All recorded MVD outbreaks have originated in Africa.


Transmission: Fruit bats are the natural reservoir of MARV. The majority of MVD outbreaks have been connected to human entry into bat-infested mines and caves. Human can also get infected by direct contact with an infected animal (e.g., non-human primate).


Person-to-person transmission occur by direct contact (through broken skin or mucous membranes) with infected blood, secretions, and body fluids or by indirect contact with contaminated surfaces and materials like clothing, bedding and medical equipment MVD is not an airborne disease, and a person is not  contagious before symptoms appear. As a result, if proper infection prevention and control precautions are strictly followed, the risk of infection is regarded as minimal.

 

Incubation period: usually five to ten days (range 2-21 days)

 

Symptoms: The onset of MVD is usually abrupt, with non-specific, flu-like symptoms such as a high fever, severe headache, chills and malaise. Rapid worsening occurs within 2–5 days for more than half of patients, marked by gastrointestinal symptoms such as anorexia, abdominal discomfort, severe nausea, vomiting, and diarrhea. In severe cases, a rash may develop, along with bleeding from various body areas. 

Treatment: There are several experimental drugs and vaccines for Marburg, but none has been licensed to date.

Further information, see ECDC Factsheet Marburg Virus. CDC.

WHO assesses the risk of this outbreak as very high at the national level, high at the regional level, and low at the global level.

 

Follow media and official reports. The risk for travellers is usually very low, but it is high for family members and caregivers who have contact with sick people.

 

Preventive measures:

  • Wash your hands regularly and carefully using soap and water (or alcohol gel if soap is unavailable).
  • Avoid contact with sick people who have symptoms, such as fever, muscle pain, and rash.
  • Avoid contact with blood and other body fluids
  • Avoid visiting healthcare facilities in the MVD-affected areas for nonurgent medical care or non-medical reasons.
  • Avoid contact with dead bodies or items that have been in contact with dead bodies, participating in funeral or burial rituals, or attending a funeral or burial. 
  • Avoid handling, cooking, or eating bush/wild meat (meat of wild/feral mammals killed for food).
  • Wash and peel fruit and vegetables before consumption.
  • Avoid visiting mines or bat caves and contact with all wild animals; alive or dead, particularly bats.
  • If you decide to visit mines or caves inhabited by fruit bat colonies, wear gloves and other appropriate protective clothing, including masks.
  • Practice safer sex.

 

Upon return from Rwanda:

  • Watch your health for symptoms of Marburg while in the outbreak area and for 21 days after leaving the outbreak area (no quarantine is required if there are no symptoms).

 

In case of symptoms

 

If you develop fever and nonspecific symptoms such as chills, headache, muscle pain or abdominal pain:

  • you should separate yourself from others (isolate) immediately and
  • directly contact the in-country hotline by phone or contact a tropical institute or university hospital infectious disease unit.
  • alert the healthcare providers of your recent travel to an area with a Marburg outbreak.

 

For clinicians:

  • Consider Marburg as a possible diagnosis in patients with epidemiologic risks factors, especially in people with possible exposure of Marburg cases in Rwanda.

 

Further information on evaluation and diagnosis: see LINK.

WHO DON, 30.9.2024| Via ProMED 1.10.2024 | WHO 28.9.2024 | Reuters 3.10.2024

In 2024, as of 01 September 2024, 15 countries have reported 3’891 confirmed cases, including 32 deaths. The three countries with the majority of the cases in 2024 are The Democratic Republic of the Congo, (n = 3’361), Burundi, (n = 328), and Nigeria (n = 48).

 

Note: a significant number of suspected cases, that are clinically compatible with mpox are not tested due to limited diagnostic capacity and never get confirmed. WHO efforts on integrating these data is currently ongoing and will be included in future updates. Not all countries have robust surveillance systems for mpox, so case counts are likely to be underestimates.


According to WHO, in 2024 as of 1 Sept 2024, mpox due to monkeypox virus clade I were reported in (for updates, details, epidemic curves, see WHO LINK):

 

Clade Ia and b:

  • D.R. Congo: According to WHO: 3’361 cases. Increasing trend in number of cases.

According to Africa CDC, update 31 Aug 2024: Since the last update (23 August 2024 ), the MoH reported 1’838 confirmed, 1’095 suspected and 35 deaths (CFR: 2.2%) of mpox from 16 provinces. This is a 137% increase in the number of new cases reported compared to the last update. Cumulatively, 4’799 confirmed, 17’801 suspected and 610 deaths (CFR: 3.4%) of mpox have been reported from all 26 provinces in DRC. Children <15 years accounted for 66% of cases and 82% of deaths. Of the confirmed cases, 73% were males. Clade Ia and Ib was isolated from the confirmed cases.

 

Clade Ib

  • Burundi: 328 confirmed cases (plus more than 700 cases suspected cases), including more than 190 hospitalized patients. Increasing trend in cases (+8 % within one week).
    The majority of case are from North Bujumbura, Kayanza and South Bujumbura district. A total of 29 districts out of 49 districts) have reported at least one positive mpox case.
  • Rwanda: 4 cases
  • Uganda: 10 cases
  • Kenya: 4 cases
  • Outside Africa: Sweden (1 case, imported from Burundi), Thailand (1 case, imported from DRC)

 

Clade Ia:

  • D.R. Congo: 23 cases
  • Republic of the Congo: 49 confirmed cases
  • Central African Republic: 45 confirmed cases
  • Cameroon: 5 cases including unknown number of cases with clade IIa and IIb

Mpox due to monkeypox virus clade II (a and b) reported in 2024 (for updates, details, epidemic curves, see WHO LINK):

  • Côte d’Ivoire: 28 cases
  • Nigeria: 48 cases
  • South Africa: 24 cases
  • Marocco: 1 case
  • Cameroon: 5 cases including unknown number of cases with clade 1a

In addition, mpox cases have been reported in Africa without specification of the clade in 2024:

  • Gabon: 2 cases
  • Guinea: 1 case
  • Liberia: 7 cases

 

Clades globally detected (1 Jan 2022 to 01 Sept 2024), Link                        Outbreak status (active transmission = red), Link

News_Mpox_240830.jpg

WHO conducted the latest global mpox risk assessment in August 2024. Based on the available information, the risk was assessed as:

  • In eastern Democratic Republic of the Congo and neighbouring countries, the overall risk is assessed as high.
  • In areas of the Democratic Republic of the Congo where mpox is endemic, mpox risk is assessed as high.
  • In Nigeria and other countries of West, Central and East Africa where mpox is endemic, mpox risk is assessed as moderate.

 

WHO risk assesment, see LINK.

 

Follow local media and local health authority advice. The following prevention measures should be followed during a stay in countries where mpox is endemic/epidemic (see also Factsheet mpox).

General precautions

  • Worldwide:
    • Avoid close, skin-to-skin contact with people who have or may have mpox or people who have a rash (e.g., pimples, blisters, scabs).
    • Wash your hands often with soap + water or an alcohol-based hand sanitizer containing at least 60% alcohol.
    • Avoid touching potentially contaminated personal items such as bedding/clothing, towels or sharing eating utensils/cups, food or drink with a person who has, or may have mpox.
    • Avoid sex with sick persons; use of condoms for up to 12 weeks if you sexual partner have had mpox.
    • Follow advice of local authorities.
  • When travelling to endemic / epidemic areas in Africa, in addition to above mentioned general precautions:
    • Avoid contact with and animals in areas where mpox regularly occurs.
    • Avoid eating or preparing meat from wild animals (bushmeat) or using products (creams, lotions, powders) derived from wild animals.

Vaccination


A vaccination against mpox is available (Jynneos®, manufactured by Bavarian Nordic). The Swiss Expert for Travel Medicine recommends vaccination against mpox in following situations, status 30 August 2024 (the recommendation will be updated regularly depending on the development of the outbreak):

1. People staying or travelling to Eastern D.R. Congo and Burundi in case of:

  • Clinical, research or laboratory work
  • Working with animals

(of note: broader indication is under discussion)

2. People staying outside of Eastern D.R. Congo and Burundi (worldwide) in case of

  • Increase risk (e.g. laboratory workers handling mpox virus, men who have sex with men or trans-persons with multiple sexual partners), see Swiss recommendations: see Link.

At the present time, it is assumed that the available vaccine against mpox (e.g. Jynneos®) is also effective against the new clade I. This vaccine is considered safe and highly effective in preventing severe mpox disease.


In case of symptoms

  • Seek medical attention immediately

If you are diagnosed with mpox:

  • Please stay at home (isolate yourself) until your mpox rash has healed and a new layer of skin has formed. Staying away from other people and not sharing things you have touched with others will help prevent the spread of mpox. People with mpox should regularly clean and disinfect the spaces they use to limit household contamination.
  • Wash your hands often with soap /water or an alcohol-based hand sanitizer containing at least 60% alcohol.
  • You should not have sex while symptomatic and while you have lesions or symptoms. Use condoms for 12 weeks after infection. This is a precaution to reduce the risk of spreading the virus to a partner.
  • For more information on what do if you are sick, see CDC LINK.

For clinicians:

  • Consider mpox as a possible diagnosis in patients with epidemiologic characteristics and lesions or other clinical signs and symptoms consistent with mpox. This includes persons who have been in DRC or, due to the demonstrated risks of regional spread, any of its neighboring countries in the previous 21 days.
  • Further information on evaluation and diagnosis: see CDC LINK.
WHO mpox Dashboard, accessed 5.9.2024
  • Following the report of an imported Monkeypox virus (MPXV) clade Ib case in Sweden on 15 August 2024 in a returning traveler from Burundi, Thailand reported a confirmed imported case due to MPXV clade Ib on 22 August 2024. The case is a European man, with travel history to the Democratic Republic of Congo.
  • On August 22, 2024, Gabon reported a suspected case of mpox clade Ib in a person with a travel history to Uganda (LINK).

Epidemiological situation: Mpox outbreaks are caused by different clades, clades 1 and 2, see EpiNews as of 16 August 2024. Historically, clade 1 has been associated with a higher percentage of people with mpox developing severe illness or dying, compared to clade 2 (responsible for the global spread in 2022). D.R. Congo (DRC) has been the most affected country, with a large increase of mpox cases due to MPXV clade I being reported since November 2023. In April 2024, sequencing of mpox cases from Kamituga in South Kivu province in eastern DRC, within the context of an observational study, identified a subtype of clade I, clade Ib. Both MPXV clade Ia and clade Ib have been circulating in DRC, while clade Ia has been detected in Congo and Central African Republic.

 

Geographical spread of the new MPXV clade Ib variant occurs via transport routes through sexual contact (e.g. sex workers), and then local transmission is observed in households and other settings (which are becoming increasingly important).


In recent weeks, confirmed mpox cases due to MPXV clade Ib have been reported by countries neighbouring DRC, such as:

  • Burundi (highest number of cases outside DRC): As of 17 August 2024, there had been 545 alerts of mpox cases since the outbreak declaration, of which 474 suspected cases (86.9%) had been investigated and validated. Of 358 suspected cases tested, 142 (39.7%) tested positive for MPXV. Genomic sequencing analysis has confirmed clade Ib MPXV. About 37.5 cases % are among children <10 years old.
  • Kenya. 1 case confirmed, for details see LINK. As of 13 August, a total of 14 suspected cases had been identified, one case had tested positive for MPXV Clade Ib, 12 suspected cases had tested negative, and the test result for one case was pending.
  • Rwanda: 2 confirmed cases in July and 2 confirmed cases in August.
  • Uganda: 2 confirmed cases

 

On 14 August 2024, WHO declared the current clade I monkeypox virus outbreak a public health emergency of international concern (PHEIC).

 

The type of exposure reported by cases in DRC includes sexual contact, non-sexual direct contact, household contact and healthcare facility contacts. The cases reported in Rwanda had travel history to DRC and Burundi, investigation showed that the cases reported by Uganda took place outside the country, while the case reported in Kenya was detected at a point of entry. For clade Ib (reported in Eastern DRC, Burundi, Rwanda, Uganda and Kenya), close physical contact (sexual contact) has been documented as the predominant mode of transmission, while for clade Ia (in endemic areas of DRC, Congo and CAR) multiple modes of transmission have been documented including zoonotic transmission.


The local transmission (non-sexual) is alarming and will likely not only happening in Burundi but in all new African affected countries, still with new location affected through sexual network. 

 

For details of the cases, epidemiology, public health response and WHO advice, see WHO LINK.

Follow local media and local health authority advice. The following prevention measures should be followed during a stay in countries where mpox is endemic/epidemic:

General precautions:

  • Refrain from sexual or other close contact with people who are sick with signs and symptoms of mpox, including those with skin lesions or genital lesions.
  • Avoid contact with wild animals (alive or dead) in areas where mpox regularly occurs.
  • Avoid contact with contaminated materials used by people who are sick (such as clothing, bedding, or materials used in healthcare settings) or that came into contact with wild animals.
  • Avoid eating or preparing meat from wild animals (bushmeat) or using products (creams, lotions, powders) derived from wild animals.
  • Avoid sex with sick persons and use of condoms for up to 12 weeks after the convalescence of the sexual partner.

 

A vaccination against mpox is available (Jynneos®, manufacture Bavarian Nordic). There is an increased demand worldwide with risk of vaccine shortage. The Swiss Expert for Travel Medicine recommends vaccination against mpox in following situations, status 30 August 2024 (the recommendation will be updated regularly depending on the development of the outbreak):

 

People staying or travelling to Eastern D.R. Congo and Burundi in case of:

  • Clinical or research or laboratory work
  • Working with animals
  • (of note: broader indication is under discussion)

People staying outside of Eastern D.R. Congo and Burundi (worldwide) in case of

  • Increase risk (e.g. laboratory workers handling mpox virus, men who have sex with men or trans-persons with multiple sexual partners), see Swiss recommendations: see Link.

At the present time, it is assumed that the available vaccine (Jynneos®) is also effective against the new clade I. This vaccine is considered safe and highly effective in preventing severe mpox disease.

 

In case of symptoms:

  • Seek medical attention immediately


If you are diagnosed with mpox:

  • Please stay at home (isolate yourself) until your mpox rash has healed and a new layer of skin has formed. Staying away from other people and not sharing things you have touched with others will help prevent the spread of mpox. People with mpox should regularly clean and disinfect the spaces they use to limit household contamination.
  • Wash your hands often with soap and water or an alcohol-based hand sanitiser containing at least 60% alcohol.
  • Youshould not have sex while symptomatic and while you have lesions or symptoms. Use condoms for 12 weeks after infection. This is a precaution to reduce the risk of spreading the virus to a partner.
  • For more information: see Factsheet Mpox.

 

For clinicians:

  • Consider mpox as a possible diagnosis in patients with epidemiologic characteristics and lesions or other clinical signs and symptoms consistent with mpox. This includes persons who have been in DRC or, due to the demonstrated risks of regional spread, any of its neighboring countries (ROC, CAR, Rwanda, Burundi, Uganda, Zambia, Angola, Tanzania, and South Sudan) in the previous 21 days.
  • Further information on Evaluation and Diagnosis: see CDC LINK.
For more details, see LINK

Picture3.png

ECDC CDTR 23.8.2024

WHO Director-General Dr Tedros has determined that the upsurge of mpox (formerly monkeypox) in the Democratic Republic of the Congo (DRC) and a growing number of countries in Africa constitutes a public health emergency of international concern (PHEIC) under the International Health Regulations (2005) (IHR). The PHEIC will help to take further coordinated international action to support countries in combating disease outbreaks.

This PHEIC determination is the second in two years relating to mpox. Mpox was first detected in humans in 1970, in the DRC. The viral disease is caused by the Monkeypox virus (MPXV), which is present in the wildlife (in certain small mammals) and the disease is considered endemic in countries in central and west Africa. In July 2022, the multi-country outbreak of mpox was declared a PHEIC after an outbreak occurred in Europe and spread rapidly via sexual contact across a range of countries where the virus had not been seen before. That PHEIC was declared over in May 2023 after there had been a sustained decline in global cases.

Since November 2023, the Democratic Republic of the Congo (DRC) has seen a significant increase in mpox cases and the emergence of a new mpox clade I. The country has reported over 16’000 new cases and more than 500 deaths in 2024.  Mpox outbreaks are caused by different clades, clades 1 and 2. Historically, clade 1 has been associated with a higher percentage of people with mpox developing severe illness or dying, compared to clade 2. The clades are now subdivided into clade 1a, 1b and clade 2a, 2b.

  • Clade 1a is the clade endemic in DRC and other central and East African countries (e.g. the Central African Republic and the Republic of Congo) for decades, it affects mostly children and is spreading through multiple mode of transmission (including animal-to human transmission, close nonsexual contact, sexual contact).
  • Clade 1b, identified since September 2023, is currently causing the outbreak in eastern DRC and neighboring countries (Burundi, Rwanda, Kenya, and Uganda; and more recently in a returning traveler from Burundi to Sweden), it affects mostly adults of both sex and is spreading predominantly through intimal contact (sexual networks). Nonsexual transmission is also happening to a lesser extent. At present, there is no evidence that it is more transmissible or more severe than the clade 1a.
  • Clade 2a is endemic in various countries of West Africa for decades with low incidence and is spreading through multiple modes of transmission like clade 1a.
  • Clade 2b is the clade at the origin of the 2022/2023 global outbreak (116 countries), it affects mostly men (>96%) and is spreading primarily through sexual contact (particularly men having sex with men). It is still ongoing and could affect people with risk factors in all countries around the world, including African countries.


Details to Mpox, see LINKs of Swiss FOPH, Robert Koch-Institute Germany, ECDC, CDC.

 

Countries where mpox virus clade I and/or clade II have been detected:

Screenshot 2024-08-17 203116.png

Follow local media and local health authority advice.

The following prevention measures should be followed during a stay in countries where mpox is endemic/epidemic:

General precautions:

  • Refrain from sexual or other close contact with people who are sick with signs and symptoms of mpox, including those with skin lesions or genital lesions.
  • Avoid contact with wild animals (alive or dead) in areas where mpox regularly occurs.
  • Avoiding contact with contaminated materials used by people who are sick (such as clothing, bedding, or materials used in healthcare settings) or that came into contact with wild animals.
  • Avoid eating or preparing meat from wild animals (bushmeat) or using products (creams, lotions, powders) derived from wild animals.
  • Avoid sex with sick persons and use of condoms for up to 12 weeks after the convalescence of the sexual partner.

 

A vaccination against mpox is available (Jynneos®, manufacture Bavarian Nordic). There is an increased demand worldwide with risk of vaccine shortage. The Swiss Expert for Travel Medicine recommends vaccination against mpox in following situations, status 16 August 2024 (the recommendation will be updated regularly depending on the development of the outbreak):

1. People staying or travelling to Eastern D.R. Congo and Burundi in case of:

  • Clinical or research or laboratory work
  • Working with animals

2. People staying outside of Eastern D.R. Congo and Burundi (worldwide) in case of:

  • Increase risk (e.g. laboratory workers handling mpox virus, men who have sex with men or trans-persons with multiple sexual partners), see Swiss recommendations: see Link.

At the present time, it is assumed that the available vaccine (Jynneos®) is also effective against the new clade I. This vaccine is considered safe and highly effective in preventing severe Mpox disease.

 

In case of symptoms:

  • Please stay at home (isolate) until your mpox rash has healed and a new layer of skin has formed. Staying away from other people and not sharing things you have touched with others will help prevent the spread of mpox. People with mpox should clean and disinfect the spaces they occupy regularly to limit household contamination.
  • Wash hands often with soap and water or an alcohol-based hand sanitiser containing at least 60% alcohol.
  • You should not have sex while symptomatic and while lesions are present. Use condoms for 12 weeks after infection. This is a precaution to reduce the risk of spreading the virus to a partner.
  • Further information on what do if you are sick, see CDC LINK.

For clinicians:

  • Consider mpox as a possible diagnosis in patients with epidemiologic characteristics and lesions or other clinical signs and symptoms consistent with mpox. This includes persons who have been in DRC or, due to the demonstrated risks of regional spread, any of its neighboring countries (ROC, CAR, Rwanda, Burundi, Uganda, Zambia, Angola, Tanzania, and South Sudan) in the previous 21 days.
  • Further information on Evaluation and Diagnosis: see CDC LINK.

The European Center for Disease Control (ECDC) has issued a risk assessment on 16 August 2024 with specific advice, for details see LINK.

Details, see Link

Screenshot 2024-08-17 205928.png

WHO, 14.8.2024 | CDC 15.8.2024 and Health Alert 7.8.2024 | ECDC | ECDC Risk Assessment, 16.8.2024

In 2021, nine countries in the WHO African Region (Cameroon, Chad, Central African Republic (CAR), Côte d'Ivoire, Democratic Republic of Congo (DRC), Ghana, Niger, Nigeria, and Republic of Congo) reported human yellow fever cases that were confirmed in the laboratory. The number of cases in these outbreaks is increasing compared to previous years. Yellow fever cases classified as probable have also been reported in Benin, Burkina Faso, Gabon, Mali, Togo, and Uganda.

Some of the affected countries are classified as fragile, conflict-affected, or vulnerable, where population immunity to yellow fever is low.

 

Consequences for travelers

Yellow fever vaccination is strongly recommended when traveling to yellow fever endemic areas, see country pages www.healthytravel.ch/countries/ or 'Reisemedizinischen Tabellen' of the FOPH: LINK.

 

References

WHO DON, 23.12.2021

Masernausbrüche werden aus mindestens 14 Ländern Afrikas berichtet mit einigen Hundert bis mehreren Tausend Fällen seit Jahresbeginn 2021.

Masern sind eine hoch ansteckende Viruserkrankung, die über die Atemwege übertragen wird. Sie ist in der ganzen Welt verbreitet. Mit einem Impfstoff lässt sich die Krankheit sehr wirksam verhindern.

 

Folgen für Reisende

Eine Reise bietet eine ideale Gelegenheit, den Schutz vor Masern zu kontrollieren (2x geimpft oder durchgemachte Masern) und wenn nötig den Impfschutz zu aktualisieren.

 

Referenzen

WHO | Regional Office for Africa, Woche 38, 13.-19.9.2021

General Information

  • Although the public health emergency of international concern for COVID-19 was declared over on 5 May 2023, COVID-19 remains a health threat
  • Adhere to the recommendations and regulations of your host country
  • Check entry requirements of destination country: see regulary updated COVID-19 Travel Regulations Map of IATA (LINK).

Vaccinations for all travellers

 
Risk Area
Factsheet
Flyer
SOP
MAP
Bookmark
See map
 
 
 

 
WHO recommendation
  • For medical reasons: vaccination is not recommended.
 

 
Country requirement at entry

For administrative reasons, there is the following entry regulation of the country:

  • Vaccination is required if arriving within 6 days after leaving or transiting countries with risk of yellow fever transmission.

Exempt from this entry requirement:

  • Children younger than 1 year of age.
  • Passengers transiting Rwanda if not leaving the transit area.
 

  • Yellow fever is a life-threatening viral infection. A highly effective vaccine is available. 
  • Vaccination is strongly recommended for all travellers to regions where yellow fever occurs, even if it is not a mandatory entry requirement of the country.
  • A booster single booster dose is recommended for immuncompetent persons after 10 years.
  • The yellow fever vaccination must be administered by an authorized doctor or center at least ten days before your arrival in the destination country with record in the yellow vaccination booklet ('International Certificate for Vaccination').
  • For travellers who are pregnant, breastfeeding, or who have a condition that leads to immunosuppression, please consult a travel health advisor.

EKRM_Factsheet_Layperson_EN_Yellow-fever.pdf

EKRM_Factsheet_Layperson_EN_Mosquito-and-tick-bite-protection.pdf

  • For medical reasons: vaccination is not recommended.

For administrative reasons, there is the following entry regulation of the country:

  • Vaccination is required if arriving within 6 days after leaving or transiting countries with risk of yellow fever transmission.

Exempt from this entry requirement:

  • Children younger than 1 year of age.
  • Passengers transiting Rwanda if not leaving the transit area.

ETCM Map: Yellow fever vaccination recommendation in Africa

 

Yellow_fever_vaccination_map_AFRICA.jpg

CDC Map: Yellow fever vaccine recommendations for the Americas since 2025. 

 

 

  • Yellow fever occurs in sub-Saharan Africa and South America and is transmitted by mosquitoes.
  • Disease may be severe in unvaccinated travelers and death may occur in over 50%.
  • A highly effective vaccine is available.
  • Due to potentially severe side effects the vaccine is used with caution in immunocompromised or elderly individuals, as well as in pregnant women.
Yellow fever is an acute viral infection transmitted through the bite of mosquitoes. The disease occurs in sub-Saharan Africa and South America. It is a potentially lethal disease. However, the vaccination offers very high protection.
Yellow fever is endemic in countries of sub-Saharan Africa and South America, and in Panama. Transmission occurs all over the year but may peak in the rainy season. Although the same species of mosquitoes are present, yellow fever has not been found in Asia.
The yellow fever virus is transmitted to people primarily through the bite of infected daily active Aedes mosquitoes, or Haemagogus species mosquitoes, which are day and night active. Mosquitoes acquire the virus by feeding on infected primates (human or non-human) and then can transmit the virus to other primates (human or non-human). Yellow fever transmission and epidemics are facilitated by the interface of jungle, savannah and urban areas. Humans working in the jungle can acquire the virus and become ill. The virus then can be brought to urban settings by infected individuals and may be transmitted to other people.
Most people infected with yellow fever virus have mild or no symptoms and recover completely. Some people will develop yellow fever illness with onset of symptoms typically 3 to 6 days after infection. Symptoms are unspecific and flu-like (fever, chills, head and body pain). After a brief remission, about 10-20% will develop more severe disease. Severe disease is characterized by high fever, yellow skin and eyes, bleeding, shock and organ failure. About 30 to 60% of patients with severe disease die.
There is no specific medication. Treatment is only supportive and consists of providing fluid and lowering fever. Aspirin and other nonsteroidal anti-inflammatory drugs, for example ibuprofen or naproxen, should be avoided due to the risk of enhanced bleeding.

As against all mosquito-borne diseases, prevention from mosquito bites is during day and night (see “Insect and tick bite protection” factsheet). The available vaccine is highly efficacious and provides a long-term protection. It is recommended for people aged 9 months or older who are travelling to yellow fever endemic areas. In addition, providing proof of vaccination may be mandatory for entry into certain countries.

The vaccine is a live-attenuated form of the virus. In immunocompetent persons, protection starts about 10 days after the first vaccination. Reactions to yellow fever vaccine are generally mild and include headache, muscle aches, and low-grade fevers.  Side effects can be treated with paracetamol but aspirin and other nonsteroidal anti-inflammatory drugs, for example ibuprofen or naproxen, should be avoided.  On extremely rare occasions, people may develop severe, sometimes life-threatening reactions to the yellow fever vaccine – which is why this vaccine is used with caution in immunocompromised individuals, pregnant women and the elderly for safety reasons. Talk to your travel health advisor if you belong to this group.

In 2016, WHO changed from yellow fever booster doses every 10 years to a single dose, which is considered to confer life-long protection. However, this decision was based on limited data and mainly from endemic populations, potentially exposed to natural boosters (through contact with infected mosquitoes), which does not apply to travellers from non-endemic regions. As several experts have raised concerns about the WHO single dose strategy, the Swiss Expert Committee for Travel Medicine recommends a single booster dose ≥10 years (max. 2 doses per life-time) in immunocompetent persons after primo-vaccination before considering life-long immunity.
Yellow Fever Map - Centers for Disease Control and Prevention: https://www.cdc.gov/yellowfever/maps/index.html 
Yellow Fever Info - Centers for Disease Control and Prevention: https://www.cdc.gov/yellowfever/index.html 
Yellow Fever Info - European Centre for Disease Prevention and Control: https://www.ecdc.europa.eu/en/yellow-fever/facts 
Countrywide
 
 
Hepatitis A - Map
 

 
Recommendation
  • Hepatitis A vaccination is recommended for all travellers going to tropical or subtropical countries.
 

  • Hepatitis A is a liver infection caused by a virus.
  • The virus is easily transmitted through contaminated food or water, but can also be transmitted through sexual contact.       
  • There is a safe and very effective vaccine that offers lifelong protection.
  • The hepatitis A vaccination is recommended for all travellers to tropical or subtropical countries and for risk groups.

HEPATITIS A__ECTM_Factsheet_Layperson_EN.pdf

CDC Map: Estimated age of midpoint of population immunity (AMPI) to hepatitis A, by country
  • Hepatitis A is a liver infection caused by a virus.
  • The virus is easily transmitted by contaminated food or water but can also be transmitted through sexual contact.
  • A safe and very effective vaccine is available that affords long-lasting protection.
  • Hepatitis A vaccination is recommended for all travelers going to tropical or subtropical countries, and for risk groups.
Hepatitis A is caused by a highly contagious virus that affects the liver. It is also known as infectious jaundice or traveller's hepatitis. Hepatitis A is one of the most common infectious diseases that can be contracted when travelling if you have not been vaccinated against it.

Hepatitis A occurs worldwide, but the risk of infection is higher in countries with poor hygiene conditions. There is an increased risk in most tropical and subtropical countries as well as in some countries in Eastern Europe and around the Mediterranean. Outbreaks in northern European countries can also occur when unvaccinated children become infected during family visits to tropical and subtropical countries and transmit the virus in their care facilities on their return.

In recent years, there has also been an increase in cases in North America and Europe, including Switzerland, particularly among men who have sex with men (MSM).

 

Transmission mainly occurs through contaminated (faecal) drinking water or food. Other transmission routes are close personal contact, especially sexual contact (anal-oral sex) or inadequate hand hygiene.
Around 2-4 weeks after infection, symptoms such as fever, tiredness, nausea, loss of appetite and diarrhoea may occur. Yellow skin and eyes (jaundice) may follow within a few days. Most symptoms disappear after a few weeks to months, although fatigue can persist for months. In young children, there are usually few or no symptoms, but in older people, the disease can be severe and protracted. Once the infection has been cured, immunity is lifelong.
There is no specific treatment. Recovery from an acute hepatitis A infection can take several weeks to months. Vaccination up to 7 days after contact with the virus can prevent the outbreak or mitigate the course of the disease.

There is a safe and very effective vaccine that consists of two injections at least 6 months apart. It offers lifelong protection after the second dose. The hepatitis A vaccination can also be administered in combination with the hepatitis B vaccination (3 doses required if given to persons 16 years and older).

Vaccination against hepatitis A is recommended for all travellers to risk areas and for people with an increased personal risk, such as people with chronic liver disease, men who have sex with men and people with an increased occupational risk, such as in the health service or in contact with waste water.

 

  • Federal Office of Public Health (FOPH). Hepatitis A
  • Hepatitis Switzerland
     
See map
 
 
 
 

 
Recommendation

In addition to the basic immunisation against polio, a booster vaccination is recommended for

  • immunocompetent travellers <65 years: every 20 years
  • immunocompetent travellers ≥65 years: every 10 years
  • travellers with immunodeficiency: every 10 years
 

  • Polio is a vaccine-preventable viral disease of the nervous system that is acquired mainly through the consumption of food or water contaminated by feces.
  • The infection with the poliovirus can affect children and adults and may lead to permanent limb or respiratory muscle paralysis and death.
  • An effective, well-tolerated vaccine is available! Check if booster doses are recommended (on top of completed basic vaccination schedule).

EKRM_Factsheet_Layperson_EN_Polio.pdf

In addition to the basic immunisation against polio, a booster vaccination is recommended for

  • immunocompetent travellers <65 years: every 20 years
  • immunocompetent travellers ≥65 years: every 10 years
  • travellers with immunodeficiency: every 10 years

EKRM_Factsheet_Layperson_EN_Polio.pdf

  • Polio is a vaccine-preventable viral disease of the nervous system that is acquired mainly through the consumption of food or water contaminated by feces.
  • The infection with the polio virus can affect children and adults and may lead to permanent limb or respiratory muscle paralysis and death.
  • An effective, well- tolerated vaccine is available! Check if booster doses are recommended for the travel destination (on top of completed basic vaccination schedule).
Poliomyelitis, or polio, is a highly infectious viral disease that affects the nervous system and can cause total limb paralysis within a very short time period. People of all ages can be infected through consumption of contaminated food or water. Humans are the only known reservoir of the polio virus.  Infection may be mild or even without symptoms. If symptoms of muscular or nervous system complications appear, sequelae (long-term complications) almost always occur. There is no medication to cure polio but the vaccine against polio is highly efficacious.
Polio due to wild types of viruses has been eradicated from most countries. In Afghanistan and Pakistan, however, new infections still occur. In some countries, polio viruses derived from live, oral vaccines are circulating and cause outbreaks of polio disease, especially in countries where vaccination coverage against polio is low in the population.
Polio virus is mainly transmitted through the consumption of food or water contaminated by feces. The virus can also be acquired through secretions or saliva of an infected person. In the tropics, transmission occurs year round, whereas in temperate zones, a peak can be seen in summer.
Symptoms most commonly appear 3 to 21 days following exposure. Initial symptoms may include fever, fatigue, headache, vomiting, and diarrhea. Those with mild cases may recover within a week. More serious cases result in stiffness of the neck and pain in the limbs. 1 in 200 infections leads to irreversible limb or respiratory muscle paralysis.
There is no cure for polio. Treatment targets symptom alleviation only.

Regular hand washing after using the bathroom and before eating or preparing food. Avoidance of undercooked or raw food that is potentially contaminated with fecal material.

The most important prevention is vaccination. A very effective and well-tolerated vaccine against polio is available (inactivated (killed) polio vaccine (IPV)), which is part of the basic vaccination schedule during childhood. Combination vaccines (e.g. with diphtheria and tetanus) are also available. After basic vaccination, a booster dose is recommended every 10 years for travel to certain countries (see country page recommendations). WHO recommends a yearly vaccination for residents or long-stay visitors (minimum 4 weeks) in a country with ongoing polio infections or circulating vaccine-derived polio viruses. This recommendation not only targets individual protection, but aims to prevent the international spread of the virus.

Check the risk for polio in the region of travel, and ensure vaccination if recommended (see country page recommendations).
  • WHO: https://www.who.int/news-room/fact-sheets/detail/poliomyelitis
  • FOPH Switzerland: Swiss vaccination plan: https://www.bag.admin.ch/bag/de/home/gesund-leben/gesundheitsfoerderung-und-praevention/impfungen-prophylaxe/schweizerischer-impfplan.html
Worldwide
  
 
 
 
 

 
Recommendation

All travellers should have completed a basic immunisation and boosters according to the Swiss vaccination schedule, LINK.

 

 

Worldwide
 
 
 
 

 
Recommendation

All travellers should have completed a basic immunisation and boosters according to the Swiss vaccination schedule, LINK.

 

General information on measles, mumps and rubella (MMR)

Please consult the following FOPH links:

  • Measles
  • Mumps
  • Rubella

MMR_ECTM_Factsheet_layperson_EN.pdf

Worldwide
 
 
 
 

 
Recommendation

Travellers should be immune to chickenpox. Persons between 13 months and 39 years of age who have not had chickenpox and who have not received 2 doses of chickenpox vaccine should receive a booster vaccination (2 doses with minimum interval of 4 weeks), see Swiss vaccination schedule, LINK.

 

Please consult the following link of the FOPH:

 

General information about chickenpox (varicella) and shingles (herpes zoster)

  • Link to the document 

CHICKENPOX_SHINGLES_ECTM_Factsheet_Layperson_EN.pdf

Vaccinations for some travellers

 
Risk Area
Factsheet
Flyer
SOP
MAP
Bookmark
Worldwide
 
 
 
  • Hepatitis B is a liver infection caused by a virus.
  • The virus is transmitted through sexual contact, but can also be transmitted through blood (products), e.g. when sharing syringes, tattoo needles, etc.
  • There is a safe and very effective vaccine that offers long-lasting protection.
  • The hepatitis B vaccination is recommended for all infants and adolescents up to the age of 16 and for risk groups regardless of age.

    HEPATITIS-B_ECTM_Factsheet_Layperson_EN.pdf

    • Hepatitis B is a liver infection caused by a virus.
    • The virus is transmitted through sexual contact, but can also be transmitted through blood (products), e.g. when sharing syringes, tattoo needles, etc.
    • There is a safe and very effective vaccine that offers long-lasting protection.
    • The hepatitis B vaccination is recommended for all infants and adolescents up to the age of 16 and for risk groups regardless of age. 
    Hepatitis B is caused by a highly contagious virus that affects the liver. The course of the disease varies greatly, with up to a third of those infected showing no symptoms.
    Hepatitis B is found all over the world, but mainly in Asia, the Middle East, Africa and parts of America. In Switzerland, around 0.5 - 0.7 per cent of the population are chronically infected with the hepatitis B virus. Men who have sex with men (MSM) and the age group of the 30 to 59 year olds are most frequently affected, accounting for around two thirds of all acute cases.
    Transmission occurs mainly through contact with bodily fluids of infected persons, especially genital secretions and blood. Accordingly, infection occurs primarily during sexual intercourse (genital, anal, oral) and when sharing syringes. In countries where the virus is more widespread and hygiene conditions are poorer, it can also be transmitted through the use of non-sterile instruments by doctors / dentists or tattooists, as well as through blood transfusions or infusions. Furthermore, infected mothers can transmit the disease to their child during birth.
    One third of newly infected adults show no symptoms. The classic picture of hepatitis B presents itself 1.5 to 6 months after infection with fatigue, loss of appetite, nausea, vomiting, abdominal pain and fever. Jaundice (yellow skin and eyes) may also occur. The disease usually heals completely on its own, especially in adults. Around 5-10% of adults with the disease, but 90% of infants, develop chronic hepatitis B. This can lead to liver remodelling (liver cirrhosis) with functional impairment or liver cancer.
    In the first phases of the infection, treatment aims at relieving the symptoms, as the disease usually heals on its own. Chronic hepatitis B can be controlled with antiviral medication, but often without achieving a complete cure. It is important to prevent the infection of close contacts (family members, sexual contacts).
    There are safe and effective vaccines that offer lifelong protection after two to three doses. Vaccination is recommended for infants as part of the combined vaccination programme at 2, 4 and 12 months of age. For adolescents up to and including the age of 15 years, 2 vaccinations are recommended at intervals of 4-6 months. Adolescents aged 16 and over and adults require 3 vaccinations. Persons who would benefit from this vaccine are  people at increased risk, such as healthcare workers; MSM; people with other liver disease and drug users. There is also a combination vaccine with hepatitis A.
    • Federal Office of Public Health (FOPH). Hepatitis B:
      https://www.bag.admin.ch/bag/en/home/krankheiten/krankheiten-im-ueberblick/hepatitis-b.html
    • Hepatitis Switzerland: https://en.hepatitis-schweiz.ch/all-about-hepatitis/hepatitis-b/
    Countrywide
     
     
     
    • Rabies is mainly transmitted by dogs (and bats), but any mammal can be infectious.
    • The disease is invariably fatal at the time when symptoms occur.
    • Rabies is best prevented by a pre-travel vaccination and appropriate behavior towards mammals (avoiding contacts).
    • Pre-travel vaccination (see section prevention) is also recommended because vaccines and immunoglobulins are often not available in many travel countries.  
    • Attention: a bite or a scratch wound as well as a contact with mammal saliva on an open wound is always an emergency! Find out about the necessary actions below!

    RABIES_ECTM_Factsheet_Layperson_EN.pdf

    This fact sheet contains important information about rabies. For optimal travel preparation, we recommend that you read this information carefully and take the fact sheet on your trip!
    • Rabies is mainly transmitted by dogs (and bats), but any mammal can be infectious.
    • The disease is invariably fatal at the time when symptoms occur.
    • Rabies is best prevented by a pre-travel vaccination and appropriate behavior towards mammals (avoiding contacts).
    • Pre-travel vaccination (see section prevention) is also recommended because vaccines and immunoglobulins are often not available in many travel countries.  
    • Attention: a bite or a scratch wound as well as a contact with mammal saliva on an open wound is always an emergency! Find out about the necessary actions below!
    Rabies disease is invariably fatal, transmitted through the saliva or other body fluids of infected mammals.
    Dogs are responsible for more than 95 % of human cases. Bats, cats, (rarely) monkeys, and any other mammals can transmit rabies! The highest risk areas are Asia, Africa and some Latin American countries (e.g. Bolivia). Rabies may occur anywhere in the world except in countries where successful eradication has been achieved.
    Saliva from infected animals enters the human body through injured skin, either via bites and scratches or by licking already wounded skin. Once it has entered the body through the skin lesion, the rabies virus migrates along nerve pathways towards the brain. In most cases, this migration takes several weeks to months and proceeds without accompanying symptoms.
    Symptoms usually only appear when the virus has reached the brain. In most cases, this is the case after 2-12 weeks
    (range: 4 days - several years!) and manifests itself as encephalitis (inflammation of the brain), which in 99.99% of cases is fatal within a few weeks. As soon as symptoms of encephalitis appear, a fatal course can no longer be prevented.

    No treatment against rabies disease exists!

     

    Post-exposure measures: clean the wound immediately with plenty of water and soap for 10-15 minutes, then disinfect the wound (e.g. Betadine®, Merfen®), and immediately (i.e. during the trip!) get emergency post-exposure vaccination against rabies: for those having received full pre-exposure rabies vaccination before travel, two additional vaccine shots (any available brand) at an interval of 3 days suffice and should be administered as soon as possible on site (i.e. also while travelling). If full pre-exposure vaccination has not been given, in addition to vaccination, passive immunization is required with immunoglobulins within the shortest delay on site.

    Of note, immunoglobins (and sometimes vaccines) are often unavailable in low-resource settings, causing stress and uncertainty. Tetanus booster vaccination may be also warranted.

    Petting any mammals while travelling is not a good idea, even if they are cute! Do not feed them! Refrain from touching wild or unfamiliar or dead animals. 

    Vaccination against rabies (preexposure vaccination) is highly recommended for:

    • Repeated travels or long-term stay in endemic countries.
    • Short journeys with high individual risk, especially for travellers on ‘two wheels’ or treks in remote areas, toddlers and children.
    • Persons, working with animals, or cave explorers (bats!).

    The shortened vaccination schedule can be proposed to most travellers: 2 doses given at least 7 days apart before departure. A single lifetime booster dose (3rd dose) is recommended after one year or later when further travelling to rabies endemic countries is undertaken. If you have an immune deficiency, please consult your doctor, as different vaccination intervals apply to you.

    • In case of trips planned, schedule a visit at the travel clinic 4 weeks before departure at the latest. But if it's really urgent, an appointment 10 days before departure will suffice.
    • After exposure (bite, scratch injury): seek medical attention immediately (meaning even during travel!) to get wound treatment and postexposure vaccinations against rabies! This is also necessary even for those with a completed series of basic vaccinations before travel!
    • This information leaflet should be printed and kept handy during the trip!
    • FOPH Switzerland: LINK
    Countrywide
      
     
     
     
    • Typhoid fever is a serious disease that is caused by bacteria and transmitted through contaminated food or water.
    • The risk is very low for travellers who have access to safe food and drinks.
    • The best protection against typhoid fever is to follow optimal basic hygiene.
    • A vaccination against typhoid is available that is recommended in following circumstances
      • Visit to an area with poor hygienic conditions (e.g. travelling to rural areas)
      • Short stay (>1 week) in a high-risk (hyper-endemic) country (see country page)
      • Long-term stays (> 4 weeks) in an endemic country
      • Presence of individual risk factors or pre-existing health conditions. In that case, please talk to your health advisor.
    • Typhoid fever, also called enteric fever, is caused by the bacteria Salmonella Typhi and Salmonella Paratyphi.
    • Infected persons shed the bacteria in their feces. In countries with low sanitation standards, the bacteria can then enter the drinking water system and lead to infections in other people.
    • Frequent sources of infection are contaminated food and beverages.
    • The main preventive measure therefore is “cook it, peel it, boil it or forget it” – meaning: avoid drinking uncooked water or water from unsealed bottles; avoid cooled/frozen products (e.g. ice cubes in drinks, ice cream) unless from a known safe source; avoid uncooked vegetables, peel and clean fruit and vegetables yourself and only with known safe drinking water.
    • A vaccine is available and recommended: a) for travelers to the Indian subcontinent or to West Africa, b) for travelers visiting friends and relatives or for long-term travelers also to other sub-/tropical areas.
    Typhoid fever is a bacterial disease that affects the whole body and mainly presents with high fever, often accompanied by drowsiness (“typhos” in Greek stands for delirium) and severe headaches. If the infection is treated with appropriate antibiotics, mortality is very low. If left untreated however, complications may follow, which can lead to significant mortality. Typhoid fever must be clearly distinguished from salmonellosis, caused by a large range of non-typhoidal salmonella species that mainly cause benign diarrheal symptoms worldwide.
    The highest occurrence of typhoid fever is on the Indian subcontinent (Afghanistan, Pakistan, Nepal, Bhutan, India and Bangladesh). This is also the region with a steady increase in antibiotic resistance. The disease also occurs in the whole sub-/tropical region, but with lower frequency. It used to occur also in Europe and North America, but the disease has disappeared thanks to improved water and sanitation standards.
    Typhoid fever is transmitted via the fecal-oral route: bacteria are shed in the feces of infected persons and – if insufficient hand hygiene is practiced – infected persons may contaminate the food and drinking water supply of their families. In regions with low sanitation standards, contaminated feces may also contaminate the public drinking water supply.
    The incubation period – time between infection and first symptoms – can vary between 3 days to 3 weeks. The principle symptom of typhoid fever is high-grade fever (39° - 41° C) accompanied by strong headache and drowsiness. In the initial phase of the disease, patients often complain of constipation. In later stages, this may turn into diarrhea. In later stages of the disease - and in the absence of correct treatment - complications such as septicemia, intestinal hemorrhage or perforation can follow, which may lead to considerable mortality.
    Appropriate antibiotic treatment cures typhoid fever. Treatment should be adapted according to the resistance profile of the bacteria. On the Indian subcontinent, some strains may be multi-resistant, necessitating broad-spectrum intravenous antibiotic treatment. In severe typhoid fever with reduced consciousness (delirium) or coma, treatment with corticosteroids may need to be added.

    “Cook it, boil it, peel it or forget it” – this simple slogan would be sufficient to prevent typhoid fever nearly entirely. However, only few travelers fully adhere to this advice. Nevertheless, the value of food and water hygiene cannot be stressed enough: avoid buying water bottles without proper sealing, avoid drinking tap water from unknown sources, avoid eating cooled / frozen foods (i.e. ice cubes in water or ice cream) and avoid eating raw fruits and vegetables that you yourself have not peeled and washed with clean drinking water.

    Two types of vaccines are available:

    • Oral (live) vaccine consisting of three capsules to be taken on alternate days on empty stomach. These capsules require refrigeration before use. Protection from this vaccine is approximately 70% and starts 10 days after the third dose. After 1 to 3 years, the vaccine needs to be taken again before a new travel into at-risk areas. This vaccine cannot be given to patients with a severe chronic gastrointestinal disease (such as Crohn’s disease or ulcerative colitis) or with severe immunosuppression.
    • The single-dose vaccine is an inactivated vaccine and is injected intramuscularly. Protection also reaches around 70% and starts 14 days after the injection. This vaccine can be given to patients who should not take the oral vaccine. However, it is not registered in Switzerland, but most doctors with specialization in tropical and travel medicine and all travel health centres have the vaccine on stock. Duration of protection is around 3 years.
    Vaccination against typhoid fever is advised for long-term travelers and for travelers visiting areas where the risk of transmission is particularly high and/or the disease more difficult to treat due to severe antibiotic resistance.
    Federal Office of Public Health Switzerland: https://www.bag.admin.ch/bag/de/home/krankheiten/krankheiten-im-ueberblick/typhus-abdominalis-paratyphus.html 
    Worldwide
     
     
     

     
    Recommendation

    Vaccination recommendation according to the Swiss Federal Office of Public Health (BAG), see LINK.

    Entry requirement per country, see IATA LINK.

     

    • Covid-19 is a disease that affects the whole body, but mainly shows with respiratory symptoms such as cough and difficulty in breathing. It is caused by the SARS-CoV-2 virus.
    • The infection is mainly spread through respiratory droplets and possibly aerosols when infected persons cough, sneeze, speak or sing without wearing a mask.
    • The infection can be prevented very effectively by vaccination and an increasing number of vaccines are now approved and available for protection.
    • Vaccination is recommended according to the Swiss recommendations of the Federal Office of Public Health (FOPH), see LINK.
    • Furthermore, prevention relies heavily on people wearing face masks, on hand hygiene and on physical distancing (min. 1.5 m) if masks are not worn and people are not vaccinated.

    COVID19_ECTM_Factsheet_Layperson_EN.pdf

    For information, see LINK of the Federal Office of Public Health (FOPH)
    Countrywide
      
     
     
     
    • Influenza is common all over the world including sub-tropical and tropical countries.
    • Vaccination offers the best protection. 
    • Vaccination against flu is recommended for all travellers who belong to an “at risk” group such as pregnant travellers, travellers with comorbidities, elderly people (>65 years), or who plan a a high-risk trip (e.g. cruise-ship, pilgrimage).
    • The influenza vaccine does not offer protection against avian flu.

    INFLUENZA_ECTM_Factsheet_EN.pdf

    General informations about seasonal flu (influenza)

    Please consult the following FOPH links:

    • Seasonal flu (influenza)
     

    Malaria

     
    Risk Area
    Factsheet
    Flyer
    Infosheet
    MAP
    Bookmark
     
     
    Malaria - Worldmap
     

     
    High risk
    • Regions: entire country.

    Prevention: Mosquito bite prevention and chemoprophylaxis.
    Discuss with your travel health advisor which prophylactic medication is suitable for you. The travel health advisor will prescribe the appropriate medication and dosage.

     

    • Malaria is a life-threatening parasitic infection, which is transmitted by mosquitoes at night.
    • Great care should be given to preventive mosquito protection from dusk to dawn in all malaria risk areas.
    • In high-risk areas, taking regular prophylactic medication is strongly advised.
    • For stays in low risk areas: discuss with a travel health advisor whether carrying stand-by emergency self-treatment against malaria is recommended.
    • If you belong to a special risk group (pregnant women, small children, senior citizens, persons with pre-existing conditions and/or with immune deficiency): seek medical advice before the trip as malaria can quickly become very severe.
    • If you have a fever >37.5°C on measuring under your arm or in your ear (a functioning thermometer is indispensable!) during or after the trip, see a doctor / hospital immediately and have a blood test done for malaria! This applies regardless of whether you used prophylactic medication or not!
    • For personal safety, we strongly recommend getting informed in detail about malaria and reading the following information.

      EKRM_Factsheet_Layperson_EN_Malaria.pdf

      EKRM_Factsheet_Layperson_EN_Mosquito-and-tick-bite-protection.pdf

      • Regions: entire country.

      Prevention: Mosquito bite prevention and chemoprophylaxis.
      Discuss with your travel health advisor which prophylactic medication is suitable for you. The travel health advisor will prescribe the appropriate medication and dosage.

      2025-07-02_ADAPTED_World_Malaria_Map_2025_(c)_EN.jpg

      For personal safety, we strongly recommend getting informed in detail about malaria and taking this factsheet with you on your trip.
      • Malaria is a life-threatening parasitic infection, which is transmitted by mosquitoes at night.
      • Great care should be given to preventive mosquito protection from dusk to dawn in all malaria risk areas.
      • In high-risk areas, the intake of prophylactic medication is strongly advised.
      • For stays in low risk areas: discuss with a travel health advisor whether carrying an emergency self-treatment against malaria is necessary.
      • If you belong to a special risk group (pregnant women, small children, senior citizens, persons with pre-existing conditions and/or with immune deficiency): seek medical advice before the trip as malaria can quickly become very severe.
      • If you have a fever >37.5°C on axillary or tympanic measurement (a functioning thermometer is indispensable!) during or after the trip, see a doctor / hospital immediately and have a blood test done for malaria! This applies regardless of whether you have used prophylactic medication or not!
      Malaria is a life-threatening acute febrile illness caused by parasites called Plasmodia, which are transmitted by mosquitoes at night (between dusk and dawn). Rapid diagnosis and treatment are crucial to prevent complications and death, and to cure the disease. To prevent malaria, diligent mosquito-bite protection is important, as well as taking additional prophylactic (preventive) medication when staying in high-risk areas. Risk groups such as pregnant women, small children, elderly persons or travellers with complex chronic conditions should seek specialized advice.
      Malaria occurs widely in tropical and subtropical areas of Africa, Asia, South and Central America (see also malaria map).
      Plasmodia are transmitted to humans by Anopheles mosquitoes, which only bite between dusk and dawn. They sometimes go unnoticed, because they are small and make almost no noise.
      After visiting a malaria endemic area, the symptoms usually appear seven days to one month after infection, but sometimes after several months or more than a year. Symptoms begin with fever and may appear very similar to flu. Other symptoms may include headache, muscle pain, nausea, and sometimes diarrhea or cough. The diagnosis can only be confirmed with a blood test.

      Fever during or after a stay in a malaria-endemic area is an emergency! Prompt diagnosis and treatment are required as the health of people with malaria can deteriorate very quickly. That means: if you have fever >37.5° (use a thermometer!) you need to test for malaria within a maximum time-frame of 24 hours, regardless of whether or not you have used prophylactic medication (malaria chemoprophylaxis). Try to reach a doctor or hospital where you can reliably receive such a test. If the first test is negative, it should be repeated on the following day if the fever persists.

      Malaria can be treated effectively, but without treatment, this disease can quickly cause complications and become fatal. People who have had malaria in the past are not protected from being infected again.

      Prevention of malaria requires a combination of approaches:

      1. Diligent mosquito-bite protection at dusk and at night until dawn is of key importance. Use it for all regions where malaria is present, including areas where the risk is minimal. Bite protection is also effective against other insect-borne diseases that often occur in the same region. It consists of the following measures:
        • Clothing: Wear long-sleeved clothes and long trousers. For additional protection, impregnate the clothes beforehand with insecticides containing the active ingredient permethrin (e.g. Nobite® Textile).
        • Mosquito repellents: Apply a mosquito repellent to uncovered skin.
        • Sleeping room: Sleep in an air-conditioned room or under an impregnated mosquito net. Cautiously use ‘knockdown’ sprays indoors or burn mosquito coils strictly outside, e.g. under a table in the evening.
        • Chemoprophylaxis: Depending on the region and season, it may be necessary to take a prophylactic medication. This is recommended for all destinations with a high risk of malaria (marked as red on our maps). It needs to be taken with food before, during, and after your stay. Discuss with your travel health advisor to ascertain if you need to take chemoprophylaxis for your trip. The appropriate medication and the right dosage will be prescribed.
      2. Taking standby emergency self-treatment (SBET, drugs used to self-treat malaria) with you is recommended for special risk situations (stay in regions with low malaria risk and if there is no or uncertain medical care available). Following such a course of SBET, please consult a doctor as soon as possible. Talk to your travel health advisor to determine whether carrying SBET is necessary, especially if you plan a trip where reliable medical infrastructure is not assured.
      3. For some risk groups, malaria can quickly develop to a dangerous disease. If you are pregnant, if you are travelling with small children, or if you are a senior citizen and / or if you have other illnesses /pre-existing conditions and / or you are immunocompromised, you should seek advice from a specialist in travel medicine to determine whether chemoprophylaxis is recommended for your trip – even if the area is marked as low risk malaria zone.

      For travellers, there is currently no malaria vaccination available.

      • Take a functioning clinical thermometer with you!
      • Malaria symptoms develop at the earliest 7 days after entering the malaria area. A fever > 37.5° always means suspicion of malaria!
      • In case you have fever during or even months after a stay in a malaria area:
        • Immediately consult a health care facility to rule out malaria through a blood test.
        • This should be done within a maximum of 24 hours and applies regardless of whether you have used prophylactic medication or not!
        • The blood tests should be repeated if the result is negative or doubtful and fever persists or recurs.
      • For persons having visited a malaria area with low risk and for whom SBET was prescribed:
        • If you have fever: immediately try to get tested for malaria.
        • If this is not possible, and fever persists for longer than 24 hours or recurs: start taking the standby emergency-self-treatment as it was prescribed by your travel health advisor.
        • Even if you have started your self-treatment against malaria: seek medical advice as quickly as possible to get the cause of your fever diagnosed.

      Other health risks

       
      Risk Area
      Factsheet
      Flyer
      Infosheet
      MAP
      Bookmark
       
      • Dengue fever is the world's most common insect-borne infectious disease.
      • Great attention should be paid to mosquito protection during the day!
      • The disease can cause high fever, muscle and joint pain, and skin rashes. In rare cases, bleeding may occur.
      • There is no specific treatment. Vaccination is recommended only for people with evidence of previous dengue infection.
      • For personal safety, we strongly recommend that you inform yourself in detail about dengue.

      EKRM_Factsheet_Layperson_EN_Dengue.pdf

      EKRM_Factsheet_Layperson_EN_Mosquito-and-tick-bite-protection.pdf

      ECTM_Dengue_Vaccination_Statement_EN_Publication_Sept_2024.pdf

      CDC Map: Distribution of dengue

      • Dengue fever is the world's most common insect-borne infectious disease.
      • Great attention should be paid to mosquito protection during the day!
      • The disease can cause high fever, muscle and joint pain, and skin rashes. In rare cases, bleeding may occur. There is no specific treatment. Vaccination is recommended only for people with evidence of previous dengue infection.
      • For personal safety, we strongly recommend that you inform yourself in detail about dengue.

      Dengue fever is the most common insect-borne infectious disease worldwide. There are 4 known serotypes of dengue virus, so it is possible to be infected with dengue more than once. Approximately 1 in 4 infected individuals develop symptoms of dengue, resulting in high fever, muscle and joint pain, and skin rash. In rare cases, most often after a second infection, life-threatening bleeding and shock (severe drop of blood pressure) may occur.

      Dengue fever occurs in all tropical and subtropical regions between latitudes 35°N and 35°S (see also CDC map: https://www.cdc.gov/dengue/areaswithrisk/around-the-world.html).
      Dengue virus is transmitted mainly by day- and dusk-active mosquitoes, namely Stegomyia (Aedes) aegypti and Stegomyia (Aedes) albopictus. These mosquitoes breed in small water puddles, as they are often found around residential buildings or at industrial zones / waste dumps of human settlements. The main transmission season is the rainy season.

      In 3 out of 4 cases, an infection with the virus remains asymptomatic. After a short incubation period (5-8 days), 1 out of 4 infected people present an abrupt onset of fever, headache, joint, limb and muscle pain, as well as nausea and vomiting. Eye movement pain is also typical. A rash usually appears on the 3rd or 4th day of illness. After 4 to 7 days, the fever finally subsides but fatigue may persist for several days or weeks.

      In rare cases, severe dengue can occur. Particularly susceptible are local children and seniors as well as people who have experienced a prior dengue infection. Tourists extremely rarely present with severe dengue. In the first days, the disease resembles the course of classic dengue fever, but on the 4th/5th day, and usually after the fever has subsided, the condition worsens. Blood pressure drops, and patients complain of shortness of breath, abdominal discomfort, nosebleeds, and mild skin or mucosal hemorrhages. In the most severe cases, life-threatening shock may occur.

      There is no specific treatment for dengue virus infection. Treatment is limited to mitigation and monitoring of symptoms: fever reduction, relief of eye, back, muscle and joint pain, and monitoring of blood clotting and blood volume. Patients with severe symptoms must be hospitalised.

      For treatment of fever or pain, paracetamol or acetaminophen are recommended (e.g. Acetalgin® Dafalgan®). Drugs containing the active ingredient acetylsalicylic acid (e.g. Aspirin®, Alcacyl®, Aspégic®) must be avoided.

      Effective mosquito protection during the day and especially during twilight hours (i.e. sunset) is the best preventive measure:

      1. Clothing: Wear well-covered, long-sleeved clothing and long pants and treat clothing with insecticide beforehand (see factsheet “prevention of arthropod bites”).
      2. Mosquito repellent: Apply a mosquito repellent to uncovered skin several times a day (see factsheet “prevention of arthropod bites”).
      3. Environmental hygiene: Do not leave containers with standing water (coasters for flower pots, etc.) in your environment to avoid mosquito breeding sites.

      For further information, please refer to the factsheet on "Mosquito and tick bite protection".

      Note on the dengue vaccine Qdenga®:

      • Based on the data available, many European countries, as well as the Swiss Expert Committee for Travel Medicine (ECTM), currently recommend vaccination with Qdenga® only for travelers who have evidence of a previous dengue infection and who will be exposed in a region with significant dengue transmission. This is a precautionary decision, since the current data also include the possibility that people who are vaccinated with Qdenga® before a first dengue infection may experience a more severe course of the disease. A consultation with a specialist in tropical and travel medicine is recommended.


      Consistent mosquito protection during the day (see above) is still considered the most important preventive measure against dengue!

      Of note

      • Do not take any products containing the active ingredient acetylsalicylic acid (e.g. Aspirin®, Alcacyl®, Aspégic®) if you have symptoms, as they increase the risk of bleeding in the event of a dengue infection!
      • However, do not stop taking medications containing acetylsalicylic acid if it is already part of your regular treatment for an underlying condition.
      • Do not take any products containing the active ingredient acetylsalicylic acid (e.g. Aspirin®, Alcacyl®, Aspégic®) if you have symptoms, as they increase the risk of bleeding in the event of a dengue infection!
      • However, do not stop taking medications containing acetylsalicylic acid if it is already part of your regular treatment for an underlying condition.
      Dengue Map (Center for Disease Control and Prevention – CDC): https://www.cdc.gov/dengue/areaswithrisk/around-the-world.html 
      Countrywide
       
       
      • Chikungunya fever is a viral infection that is transmitted by mosquitoes. 
      • The disease typically manifests itself with fever and severe joint pain in the hands and feet, which can last for weeks to months in some patients.
      • Chikungunya fever can be prevented by protecting yourself from mosquito bites.

       

      Chikungunya_ECTM_Factsheet_Layperson_EN.pdf

      EKRM_Factsheet_Layperson_EN_Mosquito-and-tick-bite-protection.pdf

      Map: Distribution for Chikungunya

      • Chikungunya fever is a viral infection that is transmitted by mosquitoes. 
      • The disease typically manifests itself with fever and severe joint pain in the hands and feet, which can last for weeks to months in some patients.
      • Chikungunya fever can be prevented by protecting yourself from mosquito bites.
      Chikungunya fever is caused by the chikungunya virus, which was first described in Tanzania in 1952. The name probably comes from a local African language and means 'the bent walker', which refers to the posture of affected people who lean on walking sticks due to severe joint pain.
      Indian subcontinent, Southeast Asia and the Pacific islands, Central and South America, the Caribbean islands, sub-Saharan Africa, Arabian Peninsula. Cases in Europe and North America are mainly imported from endemic countries. However, there are also isolated local transmissions (Italy, France, USA).
      The chikungunya virus is transmitted by Aedes mosquitoes, which are mainly active during the day.

      The infection may cause some or all of the following symptoms: sudden onset of high fever, headache, muscle and joint pain, joint swelling, rash. The rash usually appears after the onset of the fever and usually affects the trunk and extremities. The joint pain and swelling usually occur symmetrically on both sides and mainly affect the hands and feet - but larger joints such as the knees or shoulders can also be affected. The intense joint pain can be very debilitating for those affected.

      Around 5 - 10 % of those infected have persistent severe joint and limb pain even after the fever has subsided, which in some cases lasts for several months or, although rarely, even years.

       

      The diagnosis can be confirmed by blood tests: A PCR test in the first week of symptoms or a serological test (measurement of antibodies) from the second week of the disease.
      There is no treatment for the virus itself, only symptomatic treatment of the joint pain (anti-inflammatory medication).

      Preventive measures against mosquito bites during the day: Apply mosquito repellent to uncovered skin; wear long clothing; treat clothing with insecticide. For more information, see the information sheet "Protection against insect and tick bites". Another very important protective factor is so-called 'environmental hygiene': breeding sites for mosquitoes in the immediate vicinity of human dwellings should be avoided by removing all forms of containers with water (e.g. flowerpot saucers, uncovered water containers, etc.).

       

      Vaccination: Two Chikungunya vaccines are currently approved in the US and EU (IXCHIQ® and VIMKUNYA®), but not yet in Switzerland. The Swiss Expert Committee for Travel Medicine is currently reviewing the recommendation for travellers.

       

      • BAG Switzerland EN
      • WHO - Chikungunya information sheet EN
      • Centre for Disease Control and Prevention (CDC) EN
      • European Centre for Disease Prevention and Control (ECDC) EN
        Countrywide
         
         
        • Zika is a usually mild viral disease transmitted by mosquitoes that bite during the day.
        • Infection during pregnancy (any time) can cause fetal malformation.
        • In areas with increased risk of Zika transmission, pregnant women or those planning a pregnancy should take extra precautions: please see the information below.

          ZIKA_ECTM_Factsheet_Layperson_EN.pdf

          EKRM_Factsheet_Layperson_EN_Mosquito-and-tick-bite-protection.pdf

          CDC LINK: Countries and Territories at risk for Zika

          WHO Map: LINK

          • The fact sheet contains important information on zika and prevention measures.
          • If you or your partner is pregnant or if you are planning a family, we strongly recommend that you inform yourself in detail about zika.
          • Zika is a usually mild viral disease transmitted by mosquitoes that bite during the day.
          • Infection during pregnancy (any time) can cause fetal malformation.
          • In areas with increased risk of Zika transmission, pregnant women or those planning a pregnancy should take extra precautions: please see the information below.
          Zika virus infection is a viral disease transmitted during the day by Aedes mosquitoes. About one in five people develop symptoms such as fever, rash, conjunctivitis, muscle pain and sometimes headaches. The disease is generally mild and resolves on its own. Immunological and neurological complications are rare. Infection during pregnancy can have serious consequences for the unborn child. Pregnant women are strongly advised not to travel to countries with an increased risk (current epidemic).

           

          The Zika virus was first found in 1947 in monkeys in Uganda’s Zika forest. Until May 2015, the virus circulation was mainly limited to Africa and South-East Asia. Then an epidemic spread to the Americas, starting in Brazil, and then to South and Central America, and the Caribbean. Since then, the disease has spread to most tropical and subtropical regions. While the risk of infection risk is currently low, epidemics may reappear and require specific travel advices (see below).

           

          Zika virus is transmitted by the bites of infected mosquitoes (Aedes spp. including ‘tiger mosquito’), which bite during the day, especially at dawn and dusk. These mosquitoes are also common in tropical and subtropical cities. The virus can be transmitted from person to person, during pregnancy  (from infected mother to her fetus), unprotected sex with an infected person (with or without symptoms) or blood transfusion.
          About 80% of infected people have no symptoms. When symptoms do appear, usually within 2 weeks of a mosquito bite, they are generally mild and include moderate fever, rash (often itchy), conjunctivitis, joint pain, headache, muscle pain, and digestive disorders. Most patients recover spontaneously in 5-7 days. Although rare, neurological (Guillain-Barré syndrome) and immunological complications may occur. Zika infection during pregnancy, at any stage, can lead to fetal malformations.

           

          Zika symptoms can resemble those of malaria, which requires urgent treatment, or other mosquito-borne diseases such as dengue. Therefore: If you have a fever, consult a doctor for an accurate diagnosis! Treatment for Zika targets reduction of fever and joint pain (with paracetamol). Avoid aspirin and anti-inflammatory drugs (e.g. ibuprofen) as long as dengue fever is not excluded. There is no vaccine available.

           

          If pregnant and experiencing fever during or after returning from a Zika virus transmission area, blood and/or urine tests are recommended. If Zika infection is confirmed, medical management should be coordinated with a gynecologist and specialists in infectious or travel medicine.

           

           

          • Travelling in pregnancy poses an increased risk for the mother and the baby for mosquito-transmitted diseases. Please refer to the pregnancy factsheet.
          • Always protect yourself from mosquito bites during the day and early evening, see factsheet mosquito-bite prevention.
          • If traveling in an area with increased risk of Zika transmission (see areas in Zika Health Travel Notice):
            • If you are pregnant: women at any stage of pregnancy should reconsider their travel plans. If travel is essential, consult a travel medicine specialist before departure.
            • If your partner is pregnant: use condoms throughout pregnancy to prevent possible sexual transmission of Zika.
            • If you or your partner is planning to become pregnant:
              • Use condoms throughout your trip and for at least two months after returning home to prevent possible sexual transmission of Zika without symptoms.
              • You should wait at least 2 months after returning from an area with an increased risk of Zika transmission before getting pregnant.

           

          • Zika virus infection during pregnancy (any trimester) can cause fetal malformation.
          • For most up-to-date information on Zika epidemics (= increased risk of transmission), please see ‘Zika Travel Health Notices’ of the US Center of Disease and Prevention (CDC): https://www.cdc.gov/zika/geo/index.html
          • US Center of Disease Control and Prevention: Zika virus: https://www.cdc.gov/zika/index.html
          • European Center for Disease Control and Prevenion: Zika virus disease
          Worldwide
           
           
           
          • Sexually transmitted infections (STIs) are a group of viral, bacterial and parasitic infections; while many are treatable, some can lead to complications, serious illness or chronic infection.
          • STIs are increasing worldwide.
          • Read the following fact sheet for more information.

          EKRM_Factsheet_Layperson_DE_STI.pdf

          EKRM_Factsheet_Layperson_DE_HIV-AIDS.pdf

          • Geschlechtskrankheiten sind ein weltweit verbreitetes Gesundheitsproblem und können durch Prävention, regelmässiges Testen und Behandlung in den Griff bekommen werden.
          • Das Wissen um Risiken sowie Safer-Sex-Praktiken inklusive Kondomgebrauch sind wichtig. Falls Sie mehr dazu erfahren wollen, wie Sie sich während der Reise optimal schützen können, besprechen Sie dies mit einer Fachperson.
          • Hatten Sie eine Risikosituation, ist es wichtig mit einer Fachperson so rasch wie möglich Rücksprache zu halten, um zu erörtern, ob eine HIV-Post-Expositions-Prophylaxe (PEP) durchgeführt werden soll, um eine Ansteckung mit HIV zu verhindern.
          • Im Nachgang einer Risikosituation ist es wichtig sich auf Geschlechtskrankheiten testen zu lassen. Auch dann, wenn Sie keine Symptome haben.
          Reisende, die Gelegenheitssex haben, sind einem erhöhten Risiko ausgesetzt, sich mit sexuell übertragbaren Infektionen, sogenannten Sexually Transmitted Infections (STIs), einschliesslich HIV, anzustecken. Ein Auslandaufenthalt, wobei man auch neue Menschen kennen lernt, kann damit verbunden sein, sich anders zu verhalten und mehr Risiken einzugehen, als man dies zu Hause tun würde. Es ist wichtig daran zu denken, dass ungeschützter Sex und mehrere neue Sexualpartner ein Risiko für Geschlechtskrankheiten darstellen. Geschlechtskrankheiten können unter Umständen schwere Komplikationen verursachen und zudem auf weitere Partner*innen übertragen werden, sofern diese nicht rechtzeitig bemerkt und behandelt werden. Sind Sie nicht sicher, ob es sich um eine Risikosituation handelt, dann hilft der 'Risk-Check' von Love Live weiter.
          Geschlechtskrankheiten sind Infektionen, die durch sexuellen Kontakt (vaginaler, analer oder oraler Sex) übertragen werden. Sie werden durch mehr als 30 verschiedene Bakterien, Viren oder Parasiten verursacht, die in oder auf Ihrem Körper vorkommen. Es ist auch möglich, dass gleichzeitig mehr als eine STI gleichzeitig übertragen wird. Einige bedeutendsten STIs sind HIV (Informationsblatt HIV-AIDS), Hepatitis B, das humane Papillomavirus (HPV), Herpes simplex (HSV), Syphilis, Chlamydien und Gonorrhö.
          Geschlechtskrankheiten treten weltweit auf und können jeden und jede treffen, unabhängig von Alter, Geschlecht oder auch der sexuellen Orientierung. STIs kommen in vielen Ländern mit schwächerem Gesundheitssystem häufiger vor.
          Geschlechtskrankheiten werden in der Regel durch ungeschützten vaginalen, oralen oder analen Geschlechtsverkehr übertragen. Sie können aber auch durch andere intime Kontakte weitergegeben werden, wie z. B. Herpes und HPV, die durch Hautkontakt/Küssen übertragen werden. Andere können auch auf nicht sexuellem Wege übertragen werden, z.B. über Blut. Viele Geschlechtskrankheiten - darunter Syphilis, Hepatitis B, HIV, Chlamydien, Tripper, Herpes und HPV - können auch während der Schwangerschaft und bei der Geburt von der Mutter auf das Kind übertragen werden.
          • Brennen oder Juckreiz im Genitalbereich
          • Schmerzhaftes oder häufiges Wasserlösen oder auch Schmerzen im Unterleib
          • Ungewöhnlicher Ausfluss aus dem Penis oder der Vagina
          • Wunden, Rötungen, Bläschen im Mund/Lippen oder Genitalbereich sowie Warzen im Intimbereich
          • Manchmal auch Fieber (eher selten)

          Wichtig: Eine STI kann auch ohne oder mit nur leichten Symptomen auftreten. Auch wenn Sie sich dessen nicht bewusst sind, können Sie andere anstecken. Deshalb ist es wichtig sich testen zu lassen.

          Geschlechtskrankheiten können bei einer körperlichen Untersuchung oder durch die Untersuchung von Urin, einer Wunde, eines Bläschens oder eines Abstrichs aus der Vagina, dem Penis oder dem Anus diagnostiziert werden. Bluttests können bei der Diagnose helfen. Auch wenn Sie keine Symptome haben, sollten Sie mit ihrer Ärztin, ihrem Arzt sprechen, wenn Sie im Ausland ungeschützten Geschlechtsverkehr hatten. Denn eine frühzeitige Erkennung und Behandlung ist wichtig, um eine Errergerübertragung und Komplikationen durch unbehandelte STIs zu verhindern.
          Viele Geschlechtskrankheiten sind heilbar, andere wie z.B. HIV jedoch nicht und bedeuten, dass lebenslang Medikamente eingenommen werden müssen, damit es nicht zu Komplikationen kommt. Beispielsweise können mit Antibiotika bakteriell verursachte STIs geheilt werden. Eine frühzeitige Behandlung verringert zudem das Risiko von Komplikationen. Denn unbehandelt können einige STIs langfristig unter Umständen zu Gesundheitsproblemen führen, wie z.B. zu Unfruchtbarkeit, Geburtskomplikationen und einigen Arten von Krebs. Wenn eine schwangere Frau eine STI hat, kann dies zu Gesundheitsproblemen beim Baby führen. Auch Sexualpartner sollten gleichzeitig behandelt werden, um eine erneute Infektion zu verhindern (Ping-Pong-Übertragung).
          • Beachten Sie die Safer Sex Regeln von Love Live. Dazu gehört auch bei jedem Anal- oder Vaginalverkehr Kondome zu verwenden.
          • Denken Sie daran, dass es bei Oralverkehr auch zu Übertragungen von STIs kommen kann.  
          • Lassen Sie sich impfen! Es gibt Impfstoffe zum Schutz vor HPV, Hepatitis A und Hepatitis B.
          • Hatten Sie eine Risikosituation, ist es wichtig mit einer Fachperson so rasch wie möglich Rücksprache zu halten, um zu erörtern, ob eine HIV-Post-Expositions-Prophylaxe (PEP) durchgeführt werden soll, um eine HIV-Infektion zu verhindern. Am wirksamsten ist eine HIV-PEP innerhalb weniger Stunden danach.
          • Es gibt auch weitere Präventionsmassnahmen für spezielle Situationen (Präexpositionsprophylaxe HIV-PrEP). Sprechen Sie mit einer damit erfahrenen Fachperson vor Abreise darüber.
          • Denken Sie daran, dass Alkohol oder Drogen zu erhöhtem Risikoverhalten führen.
          • Denken Sie daran, dass Sie eine weitere Person/bekannter Partner*in bei ungeschütztem Sex anstecken können, sofern bei Ihnen eine unbehandelte STI vorliegt.
          • Menschen mit einer neu diagnostizierten STI sind angehalten ihre früheren Sexualpartner*innen zu informieren, damit auch sie behandelt werden können.

          Durch Bakterien oder Parasiten hervorgerufen
          Alle diese Krankheiten können geheilt werden. Wichtig ist dabei, frühzeitig zu testen und umgehend zu therapieren, um Komplikationen und v.a. weitere Übertragungen zu vermeiden.

          • Syphilis
            Auch bekannt als Lues. Sie wird durch das Bakterium Treponema pallidum verursacht. Das erste Anzeichen ist eine schmerzlose Wunde an den Genitalien, im Mund, auf der Haut oder im Rektum, die hochgradig ansteckend ist und nach 3 bis 6 Wochen spontan abklingt. Da diese schmerzlos ist, nehmen nicht alle Patienten*innen diese Läsion wahr. Oft heilt diese Infektion jedoch nicht von selbst aus. In der zweiten Phase können Hautausschlag, Halsschmerzen und Muskelschmerzen auftreten. Unbehandelt kann die Krankheit im Verborgenen (latent) bleiben, ohne dass Symptome auftreten. Etwa ein Drittel der Infizierten mit unbehandelter Syphilis entwickelt im Verlauf Komplikationen. Diese Spätform wird als  sogenannt tertiäre Syphilis bezeichnet . In diesem Stadium kann die Krankheit alle Organe befallen: am häufigsten das Gehirn, die Nerven und die Augen. Die Infektion kann während der Schwangerschaft auf den Fötus und bei der Geburt auf das Kind übertragen werden.

          • Chlamydia trachomatis
            Chlamydien können ungewöhnlichen Ausfluss aus dem Penis oder der Vagina, Unbehagen beim Wasserlösen und Unterleibsschmerzen verursachen. Oft treten keine Symptome auf. Unbehandelt können sie zu Unfruchtbarkeit führen und die Krankheit kann auf Sexualpartner*innen übertragen werden. Die Bakterien können auch während der Schwangerschaft auf den Fötus, oder während der Geburt auf das Kind übertragen werden und Augeninfektionen oder Lungenentzündungen verursachen.

          • Gonorrhoe
            Auch bekannt als Tripper. Zu den häufigsten Symptomen gehören Ausfluss aus der Vagina oder dem Penis und schmerzhaftes Wasserlassen. Symptome müssen aber nicht immer auftreten. Sowohl bei Männern als auch bei Frauen kann Gonorrhoe auch den Mund, den Rachen, die Augen und den Anus infizieren und sich auf das Blut und die Gelenke ausbreiten, wo sie in eine schwere Krankheit übergehen kann. Bleibt sie unbehandelt, kann sie eine Beckenentzündung verursachen, die zu chronischen Beckenschmerzen und Unfruchtbarkeit führen kann. Die Krankheit kann während der Schwangerschaft auf den Fötus übertragen werden.

          • Weitere bakterielle STIs: Mykoplasmen und Ureaplasmen. Diese können ebenfalls behandelt werden.

          • Trichomoniasis
            Sie wird durch einen Parasiten verursacht, der mit einer einzigen Dosis eines Antibiotikums behandelt werden kann. Trichomoniasis kann bei Frauen einen übel riechenden Scheidenausfluss, Juckreiz im Genitalbereich und schmerzhaftes Wasserlassen verursachen. Bei Männern treten in der Regel weniger oder keine Symptome auf. Zu den Komplikationen gehört das Risiko einer vorzeitigen Entbindung bei schwangeren Frauen. Um eine Reinfektion zu verhindern, sollten beide Sexualpartner behandelt werden.

          Durch Viren hervorgerufen

          • HIV/AIDS - siehe Informationsblatt HIV-AIDS

          • Herpes simplex Virus
            Im Lippen-Mundbereich, auch bekannt als Fieberbläschen, ist nicht heilbar. Herpes kann aber mit Medikamenten bei akuten Beschwerden kontrolliert werden. Die Symptome sind in der Regel schmerzhafte, wässrige Hautbläschen und finden sich an oder um die Genitalien, den Anus oder den Mund. Nach der Erstinfektion ruht das Virus im Körper und die Symptome können über Jahre hinweg wieder auftreten. Schwangere Frauen können die Infektion an ihre Neugeborenen weitergeben, was zu einer bedrohlichen Infektion führen kann.

          • Virale Hepatitis (siehe auch Hepatitis Schweiz)
            • Hepatitis A (HAV)
              Hepatitis A ist eine durch Impfung vermeidbare Leberinfektion, die durch das Hepatitis-A-Virus verursacht wird. Das Hepatitis-A-Virus findet sich im Stuhl und im Blut infizierter Personen. Hepatitis A kann durch verunreinigtes Wasser und Lebensmittel sowie bei anal-oralen sexuellen Aktivitäten übertragen werden. Die Patienten*innen leiden an einer akuten und oft schweren Erkrankung, erholen sich aber allermeist spontan.
            • Hepatitis B (HBV)
              Das Hepatitis-B-Virus wird durch sexuelle Kontakte sowie durch den Kontakt mit anderen Körperflüssigkeiten, wie z.B. Blut, übertragen. Zur Übertragung kann es z.B. auch bei medizinischen Eingriffen oder Brennen eines Tatoos unter nicht optimalen hygienischen Bedingungen kommen. Hepatitis B kann eine schwere Leberinfektion verursachen, die sowohl zu einer sofortigen Erkrankung, als auch zu einer lebenslang andauernden Infektion führen kann mit möglicher Folge einer dauerhaften Lebervernarbung (Zirrhose) und Krebs. Schwangere Frauen mit Hepatitis B können das Virus während der Geburt auf ihr Kind übertragen. Zu Beginn der Infektion haben Sie möglicherweise keine Symptome.  Das Virus kann auf Sexualpartner*innen übertragen werden. Hepatitis B kann mit antiviralen Medikamenten behandelt werden, ist aber nur selten heilbar. Eine Impfung kann eine Hepatitis-B-Infektion verhindern.
            • Hepatitis C (HCV)
              In den meisten Fällen wird Hepatitis C durch den Kontakt mit infiziertem Blut übertragen. Seltener kann es durch analen Sexualkontakt oder von der Mutter auf das Kind während der Schwangerschaft und Geburt übertragen werden. Die meisten Infizierten sind sich ihrer Infektion nicht bewusst, weil sie keine Symptome entwickeln, aber diese chronische Infektion kann zu Leberzirrhose und Krebs führen. Hepatitis C kann behandelt werden, eine Impfung gibt es nicht.

          • Humanes Papillomavirus (HPV)
            HPV ist die häufigste Geschlechtskrankheit. Es gibt eine Vielzahl verschiedener HPV-Typen, und einige von ihnen können Genital-, Anal- und Mundwarzen sowie Gebärmutterhals-, Penis- oder Rachenkrebs verursachen. Die Symptome können auch noch Jahre nach dem Sex mit einer infizierten Person auftreten. Zwei verfügbare Impfstoffe schützen gegen die wichtigsten HPV-Typen, die Gebärmutterhals-, Penis- oder Analkrebs verursachen.

          • Zika - siehe Informationsblatt Zika
            In den meisten Fällen wird es vor allem durch Stechmücken übertragen. Es kann aber auch sexuell übertragen werden. Eine Ansteckung mit Zika während der Schwangerschaft kann bei dem sich entwickelnden Fötus Geburtsfehler wie Mikrozephalie (kleiner Kopf mit neurologischen Ausfällen) verursachen. Die einzige Möglichkeit, eine sexuelle Übertragung des Virus während der Schwangerschaft zu verhindern, besteht darin, Vorsichtsmassnahmen (Kondome) zu treffen oder Sex (mindestens 2 Monate nach der Rückkehr) mit jemandem zu vermeiden, der kürzlich in ein Risikogebiet gereist ist, auch wenn der Reisende keine Symptome hat.
          • Love Life: www.lovelife.ch 
          • Sexuelle Gesundheit Schweiz: www.sexuelle-gesundheit.ch 
          • Hepatitis Schweiz: https://hepatitis-schweiz.ch/formen/was-ist-hepatitis 
          • World Health Organization (WHO). Factsheets. Sexually transmitted infections (STIs). 14 June 2019: www.who.int/news-room/fact-sheets/detail/sexually-transmitted-infections-(stis) 
          • Centers for Disease Control and Prevention (CDC). Factsheet: Information for Teens and Young Adults: Staying Healthy and Preventing STDs (2017): www.cdc.gov/std/life-stages-populations/stdfact-teens.htm 
          • Centers for Disease Control and Prevention (CDC). How You Can Prevent Sexually Transmitted Diseases: www.cdc.gov/std/prevention/ 
          • Centers for Disease Control and Prevention (CDC) Sexual Transmission and Prevention. Zika Virus: www.cdc.gov/zika/prevention/protect-yourself-during-sex.html 
          • Centers for Disease Control and Prevention (CDC) Zika and Pregnancy; Pregnant Women and Zika (March 2021): www.cdc.gov/pregnancy/zika/protect-yourself.html 
          Countrywide
           
           
          • Schistosomes are parasitic worms that infect humans while bathing or walking in fresh water ponds, lakes, or slow-flowing rivers.
          • Avoid bathing, washing, or walking in fresh water in areas endemic for schistosomiasis, also called bilharzia.
          • Consult a general practitioner or a specialist in travel and tropical medicine after suspected skin contact with fresh water during a trip.
          • Specific diagnostic tests and an effective treatment are available, which can prevent long-term complications.

          EKRM_Factsheet_Layperson_EN_Schistosomiasis.pdf

          WHO Map: Schistosomiasis, countries or areas at risk, 2014
          • Schistosomes are parasitic worms that infect humans while bathing or walking in fresh water ponds, lakes, or slow-flowing rivers.
          • Avoid bathing, washing, or walking in fresh water in areas endemic for schistosomiasis, also called bilharzia.
          • Consult a general practitioner or a specialist in travel and tropical medicine after suspected skin contact with fresh water during a trip.
          • Specific diagnostic tests and an effective treatment are available, which can prevent long-term complications.
          Schistosomes are parasitic worms that infect humans while bathing or walking in fresh water ponds, lakes, or slow-flowing rivers. The larvae of the worm penetrate the skin and migrate in the body until they settle as adults in the veins surrounding the intestines or the genital and urinary tracts, depending on the parasite type. Chronic complications are due to the worms’ eggs, which trigger inflammation and fibrosis (scar tissue) in affected organs.
          Schistosomiasis occurs in Sub-Saharan Africa and the Arabian Peninsula, Asia (China, the Philippines, South-East Asia), north-eastern South America, and some Caribbean islands.
          The larvae of schistosomes are shed by fresh water snails and penetrate the skin of humans when they bath or swim in the water. The worms develop in various organs of the human body, producing eggs that later migrate through the walls of the intestines and the urinary bladder where they trigger an inflammation and can impair the function of the respective organ systems over the course of months or years. The eggs are deposited in fresh water bodies when humans defecate or urinate into them. Larvae hatch from these eggs and infect water snails, thus completing the parasitic cycle.
          Many infections do not cause any signs or symptoms. These depend on the stage of infection: soon after the larvae penetrate the human skin in fresh water, an itching rash may appear (‘swimmer’s itch’). An immunological reaction after 4-8 weeks sometimes occurs with fever and feeling sick, the so-called ‘Katayama fever’. Chronic symptoms such as bloody urine, pain in passing urine, (bloody) diarrhea, and abdominal pain eventually occur after months or years. If those symptoms occur and treatment is not given, damage to the urinary and gastrointestinal tract can lead to dysfunction of the organs.
          Consult a tropical disease specialist for diagnosis and management. Specific drugs are effective and prescribed when eggs are detected in the urine or stool, or when the blood test shows antibodies against the worms (see below).
          Avoid bathing, washing, or walking in fresh water ponds or slow-flowing rivers in endemic areas. Correctly treated swimming pools and sea water are safe! There is not enough evidence for post-exposure treatment.
          If any suspicious fresh water contacts occurs during a trip, a tropical medicine specialist or general practitioner should be consulted for a blood test, approximately 2 months after exposure.
          Areas above 2500 meters
           
           
           
          • Altitude sickness can be life-threatening and may be experienced by any traveler.
          • The danger begins at around 2500m and rises with increasing altitude.
          • People differ in their susceptibility to altitude sickness; this is not related to their physical fitness.
          • Severe altitude sickness with fluid accumulation in the brain or lungs can rapidly result in death.
          • If you are planning a stay in high altitudes, we strongly recommend you to consult your doctor for detailed recommendations and instructions.

          20230227_Factsheet_Layperson_EN_Altitude-sickness.pdf

          • Eine Höhenkrankheit kann lebensgefährlich sein und bei jedem Reisenden auftreten.
          • Die Gefahr beginnt bei ca. 2500m und nimmt mit zunehmender Höhe zu.
          • Wenn Sie einen Höhenaufenthalt planen, lesen sie bitte dieses Merkblatt aufmerksam durch!
          • Je nach Reiseart und / oder Vorerkrankungen wird die Beratung durch eine Fachperson dringend angeraten.
          Reisen in die Anden, den Himalaya oder Ostafrika (z.B. Kilimanjaro) können in ungewohnte Höhen führen. In vielen Reiseangeboten werden für diese Höhentreks nur wenige Tage vorgesehen, was eine ungewöhnliche Anforderung und zum Teil eine Überforderung für den Organismus bedeutet. Reisen in grosse Höhen sind nicht risikolos, auch nicht für gesund befundene Personen. Personen, die schon zu Hause an Atem- oder Herzbeschwerden leiden, sollten sich bei ihrem Hausarzt beraten lassen.
          Die Gefahr einer akuten Bergkrankheit besteht bei allen Personen. Das Risiko eine akute Bergkrankheit zu erleiden, ist weitestgehend unabhängig von Alter und Trainingszustand und wird in erster Linie von der Aufstiegsgeschwindigkeit und der Schlafhöhe bestimmt. Die Gefahr beginnt ungefähr bei 2500m und nimmt mit zunehmender Höhe zu. Die akute Höhenkrankheit äussert sind durch Kopfschmerzen, Übelkeit, Appetitverlust und Schlafstörungen.
          Nehmen die obigen Symptome zu, z.B. keine Reaktion der Kopfschmerzen mehr auf Kopfwehtabletten, und werden zusätzlich von Schwindel, Erbrechen, Teilnahmslosigkeit, Gangunsicherheit und ev. Atemnot begleitet, dann soll schnellstmöglich abgestiegen werden bzw. der Erkrankte in tiefere Lagen abtransportiert werden. Beim Nichtabsteigen besteht die Gefahr, dass es zu lebensbedrohlichen Zuständen wie Höhenhirnödem und/oder Höhenlungenödem kommt.
          1. Langsamer Aufstieg. Aufstiegsregeln: oberhalb von 2500m sollte die Schlafhöhe um nicht mehr als 300-500m pro Tag gesteigert werden und pro 1000m Schlafhöhengewinn sollte ein zusätzlicher Ruhetag eingelegt werden.
          2. Treten Beschwerden auf, die auf eine Bergkrankheit hinweisen (siehe oben), muss der Anstieg pausiert werden und er darf erst wieder bei Beschwerdefreiheit fortgesetzt werden. Bei Zunahme der Beschwerden muss abgestiegen werden bzw. Patient:innen in tiefere Lagen abtransportiert werden. Bei Ignorieren zunehmender Beschwerden können sich die lebensbedrohlichen Formen der Höhenkrankheit, das Höhenhirnödem und/oder das Höhenlungenödem entwickeln.
          3. Ist das Einhalten der oben genannten Aufstiegsregeln situativ oder geländebedingt nicht möglich, kann die Einnahme von Acetazolamid (DIAMOX®) das Risiko eine akute Höhenkrankheit zu entwickeln, vermindern. Die Verschreibung des Medikaments bedingt eine ärztliche Indikationsstellung sowie eine Aufklärung über allfällige Nebenwirkungen!
          • Kopfschmerzen: Paracetamol (z.B. PANADOL®, DAFALGAN®). Keine Schlafmittel verwenden!
          • Höhenhirnödem: sofortiger Abstieg. Falls verfügbar: Sauerstoffgabe, medikamentöse Notfalltherapie.
          • Höhenlungenödem (Atemnot auch in Ruhe, rasselndes Atemgeräusch, Reizhusten) Sofortiger Abstieg. Falls verfügbar: Sauerstoffgabe, medikamentöse Notfalltherapie.
            
           
           
           

          There is a risk of arthropod-borne diseases other than malaria, dengue, chikungunya or zika in sub-/tropical regions, and some areas of Southern Europe. These include the following diseases [and their vectors]:

          • in Europe
            • Borreliosis, FSME (= tick-borne encephalitis), rickettsiosis [ticks]
            • Leishmaniasis [sand flies]
            • West-Nile fever [mosquitoes]
          • in Africa
            • Rickettsiosis, in particular African tick bite fever [ticks]
            • Leishmaniasis [sand flies]
            • African trypanosomiasis = sleeping sickness [tsetse flies]
            • West-Nile fever [mosquitoes]
          • in Asia 
            • Scrub typhus [mites]
            • Rickettsiosis [fleas or ticks]
            • Leishmaniasis [sand flies]
            • West-Nile fever [mosquitoes]
            • Crimea-Congo-hemorrhagic fever [ticks]
          • in North and Latin America  
            • Rickettsioses and in particular Rocky Mountain spotted fever [ticks]
            • Leishmaniasis and Carrion's disease [sand flies]
            • American trypanosomiasis = Chagas disease [triatomine bugs]
            • West Nile fever [mosquitoes]
          Under construction
          Countrywide
           
           
           
          • Human African trypanosomiasis, or sleeping sickness, is transmitted by the bite of tsetse flies in some countries of sub-Saharan Africa.
          • Now a rare disease, it should be suspected if fever and local redness (chancre) appear within weeks after a tsetse bite.
          • Diagnosis and treatment require advice by a specialist in tropical medicine.

          African_Trypanosomiasis_ECTM_Factsheet_Layperson_EN.pdf

          EKRM_Factsheet_Layperson_EN_Mosquito-and-tick-bite-protection.pdf

          • Human African trypanosomiasis, or sleeping sickness, is transmitted by the bite of tsetse flies in some countries of sub-Saharan Africa.
          • Now a rare disease, it should be suspected if fever and local redness (chancre) appear within weeks after a tsetse bite.
          • Diagnosis and treatment require advice by a specialist in tropical medicine.
          The clinical presentation of Human African Trypanosomiasis (HAT) mainly depends on the parasite species and the stage of the disease. T.b. rhodesiense HAT is usually an acute life-threatening disease whereas T.b. gambiense HAT is characterised by a chronic progressive course. The disease occurs in two stages, the first (or haemo-lymphatic) stage and the second (or meningo-encephalitic) stage with invasion of the central nervous system (CNS) by the trypanosomes.
          T.b.gambiense HAT:  less than 1’000 cases reported yearly. West- and Central Africa, with the majority of cases reported in the Democratic Republic of Congo; T.b. rhodesiense HAT: less than 100 cases reported yearly. East Africa, with the majority of cases reported in Malawi. Sporadic cases have been reported among travelers in Eastern and Southern Africa.
          Bite of an infected tsetse fly (see picture).

          T.b. rhodesiense HAT has a short incubation period in travelers (less than 3 weeks). It is generally an acute, life-threatening disease with fever, headache, nausea/vomiting and a trypanosomal chancre (see picture) at the tsetse bite site. In travelers, sleeping disorders or neuro-psychiatric deficits are only rarely present.

           

          T.b. gambiense HAT is only exceptionally reported in travelers. It affects local rural population in endemic areas. The disease evolves over months or years. First stage is characterized by fever, itching, headache and lymph nodes. Once the parasite invades the CNS (second stage), various neurologic or psychiatric symptoms, including sleep disturbance, can occur.

          Detection of the trypanosomes in blood, for example during a search for malaria, lymph nodes or cerebrospinal fluid by microscopy. Screening by serology only for T.b. gambiense HAT.

          HAT can be cured in both first and second stages. Specific treatment requires advice by a specialist in tropical medicine.

           

          In case of a suspicious skin lesion, immediately consult a doctor as a rapid therapy as well as a supportive therapy must be initiated as soon as possible.

          • Protection against the bite of tsetse flies (see Factsheet “Mosquito and tick bite prevention measures”), in particular well-covering, light-coloured clothing impregnated with permethrin.
          • Avoid wearing blue or black dress that attract tsetse flies.
          • No drug prophylaxis advised.
          • WHO Factsheet on human African trypanosomiasis: https://www.who.int/news-room/fact-sheets/detail/trypanosomiasis-human-african-(sleeping-sickness)
           
           
          • Marburg virus disease is a rare but severe hemorrhagic fever.
          • The disease spreads through contact with infected animals or people.
          • Symptoms can be similar to other tropical diseases
          • There is no licensed treatment or vaccine for Marburg disease, and
          • Please have a look to the factsheet below.

          EKRM_Factsheet_Layperson_EN_MARBURG.pdf

          CDC Map: History of Marburg Outbreaks Marburg, Link CDC
          • Marburg virus disease is a rare but severe hemorrhagic fever.
          • The disease spreads through contact with infected animals or people.
          • Symptoms can be similar to other tropical diseases
          • There is no licensed treatment or vaccine for Marburg disease, and
          • Prevention measures are important to follow, see below.
          Marburg virus disease (MVD) is a rare but severe hemorrhagic fever, caused by Marburg virus (MARV). Although MVD is uncommon, it has the potential to cause epidemics with significant case fatality rates (50 to 88%).
          All recorded MVD outbreaks have originated in Africa. Fruit bats are the natural reservoirs for Marburg virus. Caves or mines colonized with bats are an important source of infection.
          The majority of MVD outbreaks have been connected to human entry into bat-infested mines and caves. Transmission occurs by direct contact (through broken skin or mucous membranes) with blood, secretions, and body fluids of an infected animal or human or by indirect contact with contaminated surfaces and materials like clothing, bedding and medical equipment (for instance in healthcare settings). MVD is not an airborne disease, and a person is not contagious before symptoms appear. As a result, if proper infection prevention and control precautions are strictly followed, the risk of infection is regarded as minimal.

          The incubation period (time between infection and onset of symptoms) ranges from a 2 to 21 days (usually 5 to 10 days). The onset of MVD is usually abrupt, with initially non-specific, flu-like symptoms such as a high fever, severe headache, chills and malaise. Rapid worsening occurs within 2–5 days for more than half of patients, marked by gastrointestinal symptoms such as anorexia, abdominal discomfort, severe nausea, vomiting, and diarrhoea. As the disease advances, clinical manifestations can become more severe and include liver failure, delirium, shock, bleeding (hemorrhaging), multi-organ dysfunction and death.

           

          In case of symptoms

          If think that you have had an exposure at risk and develop fever with nonspecific symptoms such as chills, headache, muscle pain, malaise or abdominal pain:

          • you should separate yourself from others (isolate) immediately and
          • immediately seek medical advice by contacting the in-country hotline by phone or contact a tropical institute or university hospital infectious disease unit.
          • alert the healthcare providers of your recent travel to an area with a Marburg outbreak.
          Currently, there are no licensed treatments for Marburg disease. Treatment is limited to supportive care (rest, hydration, managing oxygen status and blood pressure, treatment of secondary infections). Without supportive care, high proportion of infected people die.

          The risk for travellers is  very low if the below precautions are followed, but it is high for family members and caregivers who have contact with sick people.

           

          General precautions during travel to affected areas:

          • Wash your hands regularly and carefully using soap and water (or alcohol gel if soap is unavailable).
          • Avoid contact with sick people who have symptoms, such as fever, muscle pain, and rash.
          • Avoid contact with blood and other body fluids
          • Avoid visiting healthcare facilities in the MVD-affected areas for nonurgent medical care or non-medical reasons.
          • Avoid contact with dead bodies or items that have been in contact with dead bodies, participating in funeral or burial rituals, or attending a funeral or burial. 
          • Avoid handling, cooking, or eating bush/wild meat (meat of wild/feral mammals killed for food).
          • Wash and peel fruit and vegetables before consumption.
          • Avoid visiting mines or bat caves and contact with all wild animals; alive or dead, particularly bats.
          • If you decide to visit mines or caves inhabited by fruit bat colonies, wear gloves and other appropriate protective clothing, including masks and eye protection.
          • Practice safer sex.
          • Swiss Federal Office of Public Health: LINK
          • European Center for Disease Control and Prevention (ECDC): Marburg virus disease
          • US Center for Disease Control and Prevention (CDC): About Marburg Disease
          • World Health Organization: Marburg Virus Disease
          Woldwide
           
           
          • Mpox is a viral disease that typically causes a rash, swollen lymph nodes and fever.
          • An emerging variant is spreading rapidly in eastern D.R. Congo and neighbouring countries, leading the WHO to declare a new Public Health Emergency International (PHEIC) in August 2024.
          • Close physical contact (sexual or non-sexual) is the main route of transmission.
          • The disease is usually mild. Children, pregnant women and people with weakened immune systems are most at risk of complications.
          • Take general precautions (see factsheet) to prevent the disease.
          • There is a vaccination against Mpox, but it is currently only available for people at high risk.

          EKRM_Factsheet_Layperson_MPOX_EN.pdf

          WHO Map: 2025 Monkeypox Outbreak Global Map
          • Mpox is a viral disease that typically causes a rash, swollen lymph nodes and fever.
          • An emerging variant is spreading rapidly in eastern D.R. Congo and neighboring countries prompting a new WHO declaration of a public health emergency of international concern (PHEIC), as of August 14th 2024.
          • Close physical contact (sexual or non-sexual) is the main mode of transmission.
          • The disease generally follows a mild course. Children, pregnant women, and people with weak immune systems are the most at risk of complications.
          • Vaccination against mpox is available, but limited to groups at high risk of exposure. 
          Mpox (formerly monkeypox) is a disease caused by the Monkeypox virus, a virus from the same family as the virus that causes smallpox. It is a viral zoonotic disease, which means it can spread from animals to humans. It can also spread between people.

          Mpox has been commonly found in West and Central Africa for many years where the suspected reservoir - small mammals - is endemic. There are two types of Monkeypox virus called ‘clades’ that cause the disease mpox - clade I in Central Africa and clade II in West Africa. Since the end of smallpox vaccination campaigns in the early 1980’s, cases of mpox have increased, slowly at first and significantly in the last 5-10 years, especially in the Democratic Republic of Congo (DRC).

           

          In 2022, a new emerging subclade of clade II was responsible for a global epidemic that spread mainly through sexual contact among men who have sex with men. It resulted in the first public health emergency of international concern (PHEIC) declared by the WHO until 2023. Although the clade II epidemic is now under control, this virus variant continues to circulate worldwide.


          In 2024, the continued spread of mpox clade I in endemic regions of Central Africa, particularly in the DRC, and the emergence of a new subclade Ib in Eastern DRC and neighboring countries have raised global concern and prompted the WHO to declare a PHEIC for the second time in two years. The current geographical spread of the mpox clade Ib variant occurs via commercial routes through sexual contact (e.g. sex workers), followed by local transmission in households and other settings (which is becoming increasingly important).

          Animal to human transmission
          Mpox can spread from animal to human when they come into direct contact with an infected animal (rodents or primates).

           

          Human to human transmission
          Mpox can be spread from person to person through close physical contact (sexual and non-sexual contact) with someone who has symptoms of mpox. Skin and mucous membrane lesions, body fluids, and scabs are particularly infectious. A person can also become infected by touching or handling clothing, bedding, towels, or objects such as eating utensils/dishes that have been contaminated by contact with a person with symptoms. Household members, family caretakers, and sexual partners of a confirmed case of mpox are at higher risk for infection as are health care workers who treat a case without adequate personal protection.

          The incubation period (time between infection and onset of symptoms) ranges from a few days up to 3 weeks. Mpox causes a rash / skin eruption that can be painful associated with swollen lymph nodes and fever. Fever may start already before the rash phase. Other symptoms include muscle aches, back pain, and fatigue. The rash may be localized or generalized, with few or hundreds of skin lesions. It mainly affects the face, the trunk and the palms of hand and soles of the feet. It can also be present in genital areas and on mucous membranes such as in the mouth and throat. Symptoms usually last 2 to 4 weeks and the person remains contagious until all lesions have healed (once the cabs have fallen off).

          Complications include secondary bacterial infections, infections of the lung and brain and involvement of other organs, still birth and others. Children, pregnant women, and people with weak immune systems are at higher risk to develop a severe form of mpox.

          The majority of person with mpox recovers spontaneously and do not need specific antiviral treatment. Care management consists of relieving pain and other symptoms and preventing complications (e.g., superinfection). Several antiviral treatments are studied in various countries and may be used in trials or in clinical situations according to the recommendations of national medical societies.

           

          In case of symptoms: 

          • Seek medical attention immediately
          • If you are diagnosed with mpox
            • Please stay at home (isolate yourself) until your mpox rash has healed and a new layer of skin has formed. Staying away from other people and not sharing things you have touched with others will help prevent the spread of mpox. People with mpox should regularly clean and disinfect the spaces they use to limit household contamination.
            • Wash your hands often with soap and water or an alcohol-based hand sanitiser containing at least 60% alcohol.
            • You should not have sex while symptomatic and while you have lesions or symptoms. Use condoms for 12 weeks after infection. This is a precaution to reduce the risk of spreading the virus to a partner.
            • For more information on what do if you are sick, see CDC LINK.

          General precautions:

          • Worldwide:
            • avoid close, skin-to-skin contact with people who have or may have mpox or people who have a rash (e.g., pimples, blisters, scabs).
            • Wash your hands often with soap and water or an alcohol-based hand sanitiser containing at least 60% alcohol.
            • Avoid touching potentially contaminated personal items such as cups, bedding/clothing, towels or sharing eating utensils/cups, food or drink with a person who has, or may have mpox.
            • Avoid sex with sick persons; use of condoms for up to 12 weeks if you sexual partner have had mpox.
            • Follow advice of local authorities.
          • When travelling to endemic / epidemic areas in Africa, in addition to above mentioned general precautions: 
            • Avoid contact with and animals in areas where mpox regularly occurs.
            • Avoid eating or preparing meat from wild animals (bushmeat) or using products (creams, lotions, powders) derived from wild animals.

          Vaccination:

          There are several vaccines against mpox (e.g. Jynneos®, manufacture Bavarian Nordic). The Bavarian Nordic vaccine was originally developed to fight against smallpox, but offers a cross-protection against mpox. In Switzerland, the Jynneos® vaccine has been licensed by Swissmedic since 2024. Groups at risk (e.g., men who have sex with men or transgender people with multiple sex partners) are eligible for vaccination since 2022 and this recommendation remains unchanged (see FOPH recommendations). In light of the epidemiological situation in Africa in 2024, the Swiss Expert Committee for Travel Medicine recommends vaccination against mpox for professionals who are / will be in contact with suspect mpox patients or animals in endemic/epidemic regions or who work in a laboratory with the virus (for updates, see news).

          The risk to the general population and travelers (tourists) is considered extremely low if the above-mentioned general precautions are followed and vaccination is not recommended.

          • Seek medical attention immediately.
          • Mpox is not a sexual transmitted disease in the strict sense, physical contact with a person with symptoms of mpox (rash at any stage) is sufficient to transmit the disease. Condoms do not protect you from getting mpox!
          • Swiss Federal Office of Public Health (FOPH)                                                            
          • World Health Organisation: WHO FAQ
          • European Center of Disease Control and Prevention (ECDC)
          • US Center of Disease Control and Prevention (CDC)
           
            
           
           
           
          • There are other important travel related health risks such as diarrhoea, road traffic accidents, air pollution and more.
          • For more information, see the section "Healthy Travelling".

          Get in touch with us

          • Sekretariat Schweizerische Fachgesellschaft für Tropen- und Reisemedizin,
            Socinstrasse 55, Postfach, 4002 Basel

          • info@healthytravel.ch
          • Ask a specialist
          • News
          • Contact
          • Payment Plans
          • Sponsors
          • Legal notice

          Copyright © 2025. All Rights Reserved

          0

          Bookmarks