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Brief Summary

GUIDELINE TITLE

The practice of travel medicine: guidelines by the Infectious Diseases Society of America.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

Note from the National Guideline Clearinghouse (NGC): This guideline references a drug(s) for which important revised regulatory and/or warning information has been released.

  • July 08, 2008, Fluoroquinolones (ciprofloxacin, norfloxacin, ofloxacin, levofloxacin, moxifloxacin, gemifloxacin): A BOXED WARNING and Medication Guide are to be added to the prescribing information to strengthen existing warnings about the increased risk of developing tendinitis and tendon rupture in patients taking fluoroquinolones for systemic use.
  • February 28, 2008, Heparin Sodium Injection: The U.S. Food and Drug Administration (FDA) informed the public that Baxter Healthcare Corporation has voluntarily recalled all of their multi-dose and single-use vials of heparin sodium for injection and their heparin lock flush solutions. Alternate heparin manufacturers are expected to be able to increase heparin production sufficiently to supply the U.S. market. There have been reports of serious adverse events including allergic or hypersensitivity-type reactions, with symptoms of oral swelling, nausea, vomiting, sweating, shortness of breath, and cases of severe hypotension.

BRIEF SUMMARY CONTENT

 ** REGULATORY ALERT **
 RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Definitions of the levels of evidence (I-III) and grades of recommendation (A-E) are provided at the end of the "Major Recommendations" field.

Setting

  • Most travel medicine care should be carried out in a specialized travel clinic by persons who have training in the field, particularly for travelers who have complex itineraries or special health needs (C-III). Primary care physicians and non-specialists should be able to advise travelers who are in good health and visiting low-risk destinations with standard planned activities

Knowledge Base

Competency in Travel Medicine

  • Appropriate knowledge and aptitude for practicing travel medicine may be demonstrated by achieving a certificate of knowledge in field (see supporting text in the original guideline document). Maintaining competency includes ongoing education and performing pre-travel consultations on a frequent and regular basis. (B III)

Pre-travel Risk Assessment

  • The key element of the pre-travel visit is a health risk assessment of the trip (A-II). This balances the health of the traveller: age, underlying health conditions, medications, and immunization history, with the details of the planned trip: season of travel, itinerary, duration, and planned activities.

Spectrum of Travel Medicine Advice

  • Topics of health education and advice that should be covered for all travelers are vaccine preventable illness, avoidance of insects, malaria chemoprophylaxis (for itineraries that include a malaria risk), prevention and self-treatment of travelers' diarrhea, responsible personal behavior, sexually transmitted infections and safety, travel medical insurance, and access to medical care during travel (A-II). Other topics should be covered as indicated by the risk assessment. Consistent and clear advice that is provided in both verbal and written form will help increase traveler compliance with preventive measures (A-II). The interaction between traveler and health care provider should be collaborative and affords the opportunity to enhance preventive health knowledge.

Records and Procedures

  • Permanent records should be maintained for the pre-travel visit: traveler demographics and health history, travel health risk assessment, immunizations, recommendations, and prescriptions given (A-III).
  • Standard procedures for immunization should be followed: informed consent, vaccine storage, administration, record-keeping, and reporting of adverse events (A-III).

Immunization

  • The pre-travel visit should be used to update vaccines routinely recommended according to U.S. schedules and based on the traveler's age and underlying health status (A-I). These vaccines include tetanus, pertussis, diphtheria, Haemophilus influenzae type b, measles, mumps, rubella, varicella, Streptococcus pneumoniae, and influenza. Vaccines against hepatitis A and B, poliomyelitis, and Neisseria meningitidis may be recommended for travel as well as for routine health care.
  • Vaccination against yellow fever is usually indicated for travelers to countries in the endemic zone for yellow fever (areas in Africa and South America where conditions are conducive for yellow fever transmission) (A-III). In addition, under International Health Regulations, some countries that lie in or outside of the endemic zone may require yellow fever vaccination as a condition for entry. Recent recognition of serious adverse events associated with yellow fever vaccination requires that a careful risk-benefit assessment be performed before administration of the vaccine.
  • Hepatitis A vaccine should be considered for all travelers (A-III). Booster doses following the primary two-dose series are not currently recommended (A-II).
  • Vaccines against Japanese encephalitis, rabies, tick-borne encephalitis and typhoid fever should be administered based on a risk assessment (A-III). Quadrivalent (A/C/Y/W-135) meningococcal vaccine should be administered to travelers at risk. It is required by Saudi Arabia for religious pilgrims to Mecca for the Hajj or Umrah.

Travelers' Diarrhea

  • Travelers' diarrhea is the most common disease of travelers. Management of travelers' diarrhea includes education and advice about prevention: food and liquid hygiene (A-III), and provision for prompt self-treatment in the event of illness (A-I). The elements of self-treatment include hydration, loperamide for control of symptoms if necessary (when there is no fever >38.5 degrees C or gross blood in the stool), and a short course (single dose to three days) of a fluoroquinolone antibiotic (A-I). Antibiotic resistance of enteric pathogens, particularly for Campylobacter, in the destination country needs to be considered. For these destinations, as well as for other travelers, azithromycin may be indicated (B-II). Combination treatment with loperamide and an antibiotic may be considered for travelers with moderately severe diarrhea (B-III). Antibiotic prophylaxis is not recommended for most travelers (A-III).

Malaria

  • Malaria is one of the most severe infectious diseases of travelers. Nearly all cases in travelers are preventable. Prevention and best management of malaria include awareness of risk, avoidance of mosquito bites, compliance with chemoprophylaxis, and prompt diagnosis in the event of a febrile illness either during or on return from travel (A-I). When seeking medical care after return from travel, travelers should be instructed to inform their health provider of their travel history.
  • Travelers at risk for malaria should practice the following measures to prevent mosquito bites: protective clothing to cover exposed skin, application of repellents, and sleeping in areas protected by netting (preferably impregnated with a residual insecticide such as permethrin) and screens (A-I). Currently, repellents that contain 20% to 50% DEET are considered to provide sufficient protection (B-II).
  • The choice of chemoprophylaxis should be made following a careful assessment of malaria risk during the trip and whether the traveler has contraindications to a particular antimalarial.
  • The malaria risk assessment includes the itinerary, the species of malaria at the destination (and whether the most severe form of malaria, Plasmodium falciparum, is present and if it is resistant to chloroquine or other antimalarials), the season of travel, activities, duration, and access to medical care. Consultation with the latest resource information is necessary.

Personal Safety and Environmental Health

  • All travelers should be aware of personal safety during travel and exercise responsible behavior (A-III). Road and pedestrian safety, risk of blood borne infections, avoidance of animal bites, awareness of the risk of assault, sexually transmitted infections, and moderation in alcohol use should be discussed.
  • Travelers should understand the effects that air, sea, and land travel, sun, altitude, and heat and cold may have upon their health. In order to prevent deep venous thrombosis (DVT) long-haul travelers with journeys of 6 to 8 hours and longer should avoid constrictive clothing around their waist and lower extremities, exercise their calf muscles, and maintain hydration (A-III). Travelers with increased risk factors for DVT may consider wearing below the knee support stockings (B-II) or receiving low molecular weight heparin (B-I).
  • Ascent to altitudes above 3,000 m is often associated with various forms of high altitude illness. Staged ascent is an effective way to decrease the risk of altitude illness. Travelers who need to ascend rapidly may take acetazolamide for prevention (B-I).

Post-Travel Care

  • Health professionals who advise travelers should be able to recognize major syndromes in returned travelers (e.g., fever, diarrhea, respiratory illness, and rash) and either provide care for the traveler or promptly refer them for appropriate evaluation and treatment (A-III).

Definitions:

Quality of Evidence

  1. Evidence from >1 properly randomized, controlled trial
  2. Evidence from >1 well-designed clinical trial, without randomization; from cohort or case-controlled analytic studies (preferably from >1 center); from multiple time-series; or from dramatic results of uncontrolled experiments
  3. Evidence from opinions of respected authorities, based on clinical experience, descriptive studies, or reports of expert committees

Strength of Recommendation

  1. Good evidence to support a recommendation for use
  2. Moderate evidence to support a recommendation for use
  3. Poor evidence to support a recommendation for use
  4. Moderate evidence to support a recommendation against use
  5. Good evidence to support a recommendation against use

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is identified and graded for selected recommendations (see "Major Recommendations" field).

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2006

GUIDELINE DEVELOPER(S)

Infectious Diseases Society of America - Medical Specialty Society

SOURCE(S) OF FUNDING

Infectious Diseases Society of America (IDSA)

GUIDELINE COMMITTEE

Infectious Diseases Society of America (IDSA) Standards and Practice Guidelines Committee

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Authors: David R. Hill, MD, DTM&H (Chair); Charles D. Ericsson, Professor of Medicine, Head, Clinical Infectious Diseases, University of Texas Medical School at Houston, Department of Internal Medicine; Richard D. Pearson, Professor of Medicine and Pathology, Division of Infectious Diseases and International Health, University of Virginia School of Medicine; Jay S. Keystone, Professor of Medicine, University of Toronto, Staff Physician, Center for Travel and Tropical Medicine, Toronto General Hospital; David O. Freedman, Professor of Medicine and Epidemiology, Division of Geographic Medicine, University of Alabama at Birmingham; Phyllis E. Kozarsky, Professor of Medicine/Infectious Diseases, Chief, Travel and Tropical Medicine, Emory University School of Medicine, Expert Consultant, Division of Global Migration and Quarantine, Centers for Disease Control and Prevention, Atlanta The Emory Clinic; Herbert L. DuPont, Chief of Internal Medicine, St. Luke's Hospital, Director, Center for Infectious Diseases, University of Texas – Houston School of Public Health, Vice Chairman, Department of Medicine, Baylor College of Medicine; Frank J. Bia, Professor of Medicine and Laboratory Medicine, Co-Director – International Health Program, Yale School of Medicine; Philip R. Fischer, Professor of Pediatrics, Mayo Clinic, College of Medicine, Chair, Division of General Pediatric and Adolescent Medicine, Medical Director, Mayo Eugenio Litta Children's Hospital, Mayo Clinic; Edward T. Ryan, Director, Travelers' Advice and Immunization Center, Director, Tropical and Geographic Medicine Center, Associate Professor, Harvard Medical School, Tropical & Geographic Medicine Center, Division of Infectious Diseases, Massachusetts General Hospital

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Conflicts of Interest Declarations

David R. Hill: No declared conflicts of interest

Charles D. Ericsson:

  • Received honoraria for speaking engagements and grants for research from Pfizer
  • Served as consultant to, received research grants from, and received honoraria for speaking engagements from the manufacturers of rifaximin, Alfa Wasserman and Salix
  • Received honoraria for speaking engagements from Elan and Merck

Richard D. Pearson: No declared conflicts of interest

Jay S. Keystone:

  • Served as a paid consultant to GlaxoSmithKline, Sanofi-Pasteur, and Roche Pharmaceuticals
  • Received honoraria for speaking engagements for GlaxoSmithKline and Roche Pharmaceuticals

David O. Freedman:

  • Received honoraria for participation on advisory boards of GlaxoSmithKline, Sanofi Pasteur and Salix Pharmaceutical Company
  • Serves as a paid consultant for Shoreland, Inc, publishers of Travax and Travax Encompass

Phyllis E. Kozarsky:

  • Served as a paid consultant to Berna Products, Inc.
  • Received honoraria for speaking engagements for GlaxoSmithKline
  • Received honoraria for participation on the Advisory Board of Sanofi Pasteur

Herbert L. DuPont:

  • Received honoraria for sponsored talks and has received research grants from the manufacturers of rifaximin, Salix Pharmaceutical Company

Frank J Bia:

  • Served as a paid consultant to Pfizer, Sanofi Pasteur and GlaxoSmithKline.
  • Editor of Travel Medicine Advisor, Thomson American Health Consultants, Inc.

Philip R. Fischer: No declared conflicts of interest

Edward T Ryan: No declared conflicts of interest

GUIDELINE STATUS

This is the current release of the guideline.

GUIDELINE AVAILABILITY

Electronic copies: Available from the Infectious Diseases Society of America (IDSA) Web site.

Print copies: Available from Dr. David R. Hill, National Travel Health Network and Centre, Hospital for Tropical Diseases, Mortimer Market Centre, Capper St., London WC1E 6AU, England (david.hill@uclh.org)

AVAILABILITY OF COMPANION DOCUMENTS

The following is available:

  • Kish MA. Guide to development of practice guidelines. Clin Infect Dis 2001 Mar 15;32(6):851-4.

Electronic copies: Available from the Clinical Infectious Diseases Journal Web site.

Print copies: Available from Infectious Diseases Society of America, 1300 Wilson Boulevard, Suite 300, Arlington, VA 22209.

A PDA version of the original guideline document is available from www.idsaguidelinesforhandhelds.org.

PATIENT RESOURCES

None available

NGC STATUS

This summary was completed by ECRI on October 25, 2006. The information was verified by the guideline developer on December 5, 2007. This summary was updated by ECRI Institute on June 22, 2007 following the U.S. Food and Drug Administration (FDA) advisory on heparin sodium injection. This summary was updated by ECRI Institute on March 14, 2008 following the updated FDA advisory on heparin sodium injection. This summary was updated by ECRI Institute on July 28, 2008 following the U.S. Food and Drug Administration advisory on fluoroquinolone antimicrobial drugs.

COPYRIGHT STATEMENT

NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions.

DISCLAIMER

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