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CDC Health Information for International Travel 2008

Chapter 2
Pre- and Post-travel General Health Recommendations

The Post-Travel Period

Description

Many illnesses resulting from a particular exposure during travel may manifest clinically during travel, while others become clinically apparent after travelers have returned home (1-4). Some diseases present immediately after the traveler returns, while others may become evident weeks, months, or even years later (2). Therefore, obtaining a travel history is crucial when evaluating any ill patient and it is particularly important to obtain an exact itinerary and details of pre-travel preparation, whether chemoprophylaxis was taken, and what exposures the traveler encountered during the trip.

Risk for Travelers

The likelihood of a travel-related illness developing relates to the person’s specific travel destination, duration of travel, level of accommodation, underlying medical condition, immunization history, adherence to indicated chemoprophylactic regimens, and especially his or her history of exposure to potential infectious agents during travel (2-3). Eliciting a detailed history of the specific locales visited, the timing of travel relative to the onset of symptoms, and specific risk behaviors is essential in determining potential exposure to infectious pathogens and the likely incubation period (2,5-7,10,19). Particular groups of travelers are considered at higher risk of developing illness after returning to their place of residence (19). Adventure travelers and persons visiting friends and relatives overseas are at greater risk for becoming ill, in part because of increased exposure to pathogens (1-2,10). Travelers visiting friends and relatives are often also less likely to seek pretravel advice, obtain vaccinations or take antimalarial prophylaxis.

Clinical Presentation

Most travelers infected abroad become ill within 12 weeks after returning to the United States. However, some diseases, such as malaria, may not cause symptoms for as long as 6-12 months or more after exposure (see Table 2-3). If travelers become ill after they return home, even many months after travel, they should be advised to tell their physician where they have traveled. In particular, fever in a traveler returned from a malarious area should be considered a medical emergency. The possibility of malaria as a cause of the fever should be evaluated urgently by appropriate laboratory tests and qualified personnel, and testing should be repeated if the initial result is negative. In this regard, primary care physicians, general medicine practitioners, pediatricians, emergency medicine physicians and every health-care worker dealing with a febrile returned traveler from a malaria- endemic area should take the steps to ensure the patient has serial blood smears evaluated and consider hospitalization if there is any need for observation.

In evaluating patients seeking medical care, it is essential to obtain a detailed history of exposures such as insect bites, swimming in freshwater, animal bites, eating raw meat, seafood, or unpasteurized dairy products, and sexual contacts. Answers to these questions may provide important clues for diagnosis of a particular illness or syndrome in returned travelers (1-4). In addition, when suspecting an infectious disease, calculating an approximate incubation period is a useful step in ruling out possible etiologies (2). For example, fever beginning 3 weeks or longer after return greatly reduces the probability of dengue, rickettsial infections, and viral hemorrhagic fevers in the differential diagnosis. This important step helps focus the differential diagnosis on probable causative agents and eliminates unlikely considerations. As indicated by exposure history, time course of illness, and associated signs and symptoms, initial investigations for febrile travelers may include prompt evaluation of peripheral blood for Plasmodium species; a complete blood cell count with differential; liver enzymes; urinalysis; culture of blood, stool, and urine; and chest radiography. More specific diagnostic assays may be useful initially for diseases such as leptospirosis (serology) and acute HIV infection (RNA viral load). However, sometimes acute- and convalescent-phase serologies are required to confirm a particular diagnosis such as many rickettsial infections (2-4).

Since most primary-care physicians have little expertise in tropical diseases, a newly returned, ill international traveler should be evaluated by an infectious disease or tropical medicine practitioner. For assistance in finding a provider who practices clinical tropical medicine, one may access the American Society of Tropical Medicine website for a listing by state at http://www.astmh.org or the International Society of Travel Medicine at http://www.istm.org.

It may be prudent for asymptomatic international travelers who have been abroad for many months or longer, particularly in developing countries, to be screened for certain diseases. The decision to screen for particular pathogens will depend on the travel and exposure history. For example, travelers who have engaged in casual unprotected sex or have received an injection, a body piercing, or a tattoo may be screened for HIV, hepatitis C and other sexually transmitted diseases, and, if not immune, hepatitis B. Sometimes, testing for hepatitis C RNA viral load or HIV RNA viral load is recommended for travelers with high-risk factors presenting with a febrile illness. In addition, performing a tuberculin skin test to identify conversion in those travelers who were previously tuberculin negative is recommended, particularly after a prolonged stay in a developing country. Travelers who have been exposed to freshwater in areas endemic for schistosomiasis should be screened for this infection by serology and stool and/or urine tests (20). Eosinophilia in a returned traveler suggests the possibility of a helminth infection, of which the most important is strongyloidiasis. If left untreated, this infection may last for the lifetime of the host, and in an immuno-compromised person it has the potential to disseminate.

TABLE 2-3. Incubation period of febrile syndromes in returned travelers

INCUBATION
PERIOD
SYNDROMESETIOLOGIES
< 2 weeksFever with initial nonspecific signs and symptomsMalaria, Chikungunya, dengue, scrub typhus, spotted group rickettsiae, acute HIV, acute hepatitis C, Campylobacter, salmonellosis, shigellosis, East African trypanosomiasis, leptospirosis, relapsing fever, influenza, yellow fever
Fever and coagulopathy Meningococcemia, leptospirosis and other bacterial pathogens associated with coagulopathy, malaria, viral hemorrhagic fevers, enteroviruses
Fever and central
nervous system
involvement
Malaria, typhoid fever, rickettsial typhus (epidemic caused by Rickettsia prowazecki), meningococcal meningitis, rabies, arboviral encephalitis, East African trypanosomiasis, encephalitis or meningitis, angiostrongyliasis, rabies
Fever and pulmonary involvement Influenza, pneumonia due to typical pathogens,
Legionella pneumonia, acute histoplasmosis,
acute coccidioidomycosis,
Q fever, SARS
Fever and skin rash Viral exanthems (rubella, measles,varicella,
mumps, herpes simplex-6, enteroviruses)
Chikungunya, dengue, spotted or typhus
group rickettsiosis, typhoid fever, parvovirus
B19
2 to 6 weeksVarious syndromes
(fever with pulmonary,
dermatologic,
central nervous
system, or involvement
of other
sites)
Malaria, tuberculosis, hepatitis A, hepatitis
B, hepatitis C, hepatitis E, visceral leishmaniasis,
acute schistosomiasis, amebic
liver abscess, leptospirosis, African trypanosomiasis,
viral hemorrhagic fevers,
Q fever, acute American trypanosomiasis,
viral causes of mononucleosis syndromes
> 6 weeksVarious syndromes
(fever with pulmonary,
dermatologic,
central nervous
system, or involvement
of other
sites)
Malaria, tuberculosis, hepatitis B, hepatitis
E, visceral leishmaniasis, filariasis, onchocerciasis,
schistosomiasis, amebic liver abscess,
chronic mycoses, African trypanosomiasis,
rabies, typhoid fever

References

  1. Steffen R, Rickenbach M, Wilhelm U, Helminger A, Schar M. Health problems after travel to developing countries. J Infect Dis. 1987;156:84-91.
  2. Ryan ET, Wilson ME, Kain KC. Illness after international travel. N Engl J Med. 2002;347:505-16.
  3. Freedman DO, Weld LH, Kozarsky PE, Fisk T, Robins R, von Sonnenburg F, et al; GeoSentinel Surveillance Network. Spectrum of disease and relation to place of exposure among ill returned travelers. N Engl J Med. 2006;354:119-30.
  4. Wilson ME, Chen LH. Dermatologic infectious diseases in international travelers. Curr Infect Dis Rep. 2004;6:54-62.
  5. O’Brien D, Tobin S, Brown GV, Torresi J. Fever in returned travelers: review of hospital admissions for a 2-year period. Clin Infect Dis. 2001;33:603-9.
  6. Doherty JF, Grant AD, Bryceson AD. Fever as the presenting complaint of travellers returning from the tropics. QJM. 1995;88:277-81.
  7. CDC. Fatal yellow fever in a traveler returning from Amazonas, Brazil, 2002. MMWR Morbid Mortal Wkly Rep. 2002;51:324-5.
  8. Jelinek T, Bisoffi Z, Bonazzi L, van Thiel P, Bronner U, de Frey A, et al. Cluster of African trypanosomiasis in travelers to Tanzanian national parks. Emerg Infect Dis. 2002;8:634-5.  
  9. Isaacson M. Viral hemorrhagic fever hazards for travelers in Africa. Clin Infect Dis. 2001;33:1707-12.
  10. CDC. Update: outbreak of acute febrile illness among athletes participating in Eco-Challenge-Sabah 2000—Borneo, Malaysia, 2000. MMWR Morbid Mortal Wkly Rep. 2001;50:21-24.
  11. Matteelli A, Carosi G. Sexually transmitted diseases in travelers. Clin Infect Dis. 2001;32:1063-7.
  12. Mutsch MM, Spicher VM, Gut C, Steffen R. Hepatitis A virus infections in travelers, 1988-2004. Clin Infect Dis. 2006;42:490-7.
  13. Jensenius M, Fournier PE, Raoult D. Rickettsioses and the international traveler. Clin Infect Dis. 2004;39:1493-9.
  14. Basnyat B, Maskey AP, Zimmerman MD, Murdoch DR. Enteric (typhoid) fever in travelers. Clin Infect Dis. 2005;41:1467-72.
  15. Freedman DO, Leder K. Influenza: changing approaches to prevention and treatment in travelers. J Travel Med. 2005;12:36-44.
  16. Mutsch M, Tavernini M, Marx A, Gregory V, Lyn YP, Hay AJ, et al. Influenza virus infection in travelers to tropical and subtropical countries. Clin Infect Dis. 2005;40:1282-7.
  17. Leder K, Sundararajan V, Weld L, Pandey P, Brown G, Torresi J; GeoSentinel Surveillance Group. Respiratory tract infections in travelers: a review of the GeoSentinel surveillance network. Clin Infect Dis. 2003;36:399-406.
  18. Connor BA. Sequelae of traveler’s diarrhea: focus on postinfectious irritable bowel syndrome. Clin Infect Dis. 2005;41 Suppl 8:S577-86.
  19. Angell SY, Cetron MS. Health disparities among travelers visiting friends and relatives abroad. Ann Intern Med. 2005;142:67-72.
  20. Schwartz E, Kozarsky P, Wilson M, Cetron M. Schistosome infection among river rafters on Omo River, Ethiopia. J Travel Med. 2005; 12:3-8.
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  • Page last updated: June 15, 2007
  • Content source:
    Division of Global Migration and Quarantine
    National Center for Preparedness, Detection, and Control of Infectious Diseases
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