Doxycycline Malaria Prophylaxis Impact on Risk of Travelers' Diarrhea among International Travelers
- PMID: 32815505
- PMCID: PMC7646764
- DOI: 10.4269/ajtmh.20-0241
Doxycycline Malaria Prophylaxis Impact on Risk of Travelers' Diarrhea among International Travelers
Abstract
International travelers are frequently at risk for travelers' diarrhea (TD) and malaria. Doxycycline was one of the earliest antibiotics shown to have efficacy in TD prevention. With increasing resistance and recommendations against antibiotic chemoprophylaxis, doxycycline fell out of use. We evaluated TD incidence and risk factors in a prospective cohort of travelers, specifically in regard to malaria prophylaxis. Travelers' diarrhea was defined as ≥ 3 loose stools in 24 hours or two loose stools in 24 hours associated with other gastrointestinal symptoms. The Poisson regression model with robust error variance was used to estimate the RR of TD. Three thousand two hundred twenty-seven trips were enrolled: 62.1% of participants were male, with a median age of 39 years (interquartile range [IQR] 27,59) and a median travel duration of 19 days (IQR 12,49); 17.4% developed TD; 32% traveled to Africa, 40% to Asia, and 27% to the Caribbean and Latin America; and 20% took doxycycline for malaria chemoprophylaxis, 50% took other antimalarials, and 30% took none. Decreased RR of TD was associated with doxycycline (RR 0.62 [0.47-0.82], P < 0.01) and military travel (RR 0.57 [0.47-0.70], P < 0.01). Increased risk of TD was associated with female gender (RR 1.28 [1.09-1.50], P < 0.01), hotel accommodations (RR 1.30 [1.10-1.53], P < 0.01), travel to tropical South America (RR 1.34 [1.09-1.64], P < 0.01), and duration of travel (RR 1.00 [1.00-1.01], P < 0.01). The use of doxycycline for malaria prophylaxis is associated with lower TD risk, suggesting increasing bacterial enteropathogen susceptibility similar to previous observations. Doxycycline selection for antimalarial chemoprophylaxis may provide additional traveler benefit in infection prevention.
Conflict of interest statement
Copyright statement: Some authors are service members of the U.S. Government. This work was prepared as part of their official duties. Title 17 U.S.C. §105 provides that “Copyright protection under this title is not available for any work of the United States Government.” Title 17 U.S.C. §101 defines a U.S. Government work as a work prepared by a military service member or employee of the U.S. Government as part of that person’s official duties.
Disclaimer: The contents of this publication are the sole responsibility of the author(s) and do not necessarily reflect the views, opinions, or policies of Uniformed Services University of the Health Sciences (USUHS), the Department of Defense (DoD), the Department of the Army, the Department of the Navy, or the Department of the Air Force, or Brooke Army Medical Center, the U.S. Army Medical Department, the U.S. Army Office of the Surgeon General, Landstuhl Regional Medical Center, Walter Reed National Military Medical Center, Madigan Army Medical Center, Naval Medical Center Portsmouth, or the Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. The views expressed in this article are those of the author(s) and do not reflect the official policy or position of the Department of the Army, the Department of Defense, or the U.S. government. Mention of trade names, commercial products, or organizations does not imply endorsement by the U.S. government.
Disclosure: The investigators have adhered to the policies for the protection of human subjects as prescribed in 45 CFR 46.
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