Acute hepatitis A in international travellers: a GeoSentinel analysis, 2008–2020

Author:

Balogun Oluwafemi12,Brown Ashley3,Angelo Kristina M3,Hochberg Natasha S45,Barnett Elizabeth D6,Nicolini Laura Ambra7,Asgeirsson Hilmir8,Grobusch Martin P9,Leder Karin10,Salvador Fernando11,Chen Lin12,Odolini Silvia13,Díaz-Menéndez Marta14ORCID,Gobbi Federico15,Connor Bradley A16,Libman Michael17ORCID,Hamer Davidson H418

Affiliation:

1. Bureau of Infectious Disease and Laboratory Services, Massachusetts Department of Public Health, Boston, MA, USA

2. Department of Medicine, Massachusetts General Hospital and Harvard Medical School

3. Travelers’ Health Branch, Division of Global Migration and Quarantine, Centers for Disease Control and Prevention, Atlanta, GA, USA

4. Section of Infectious Diseases, Department of Medicine, Boston University School of Medicine, Boston, MA, USA

5. Department of Epidemiology, Boston University School of Public Health, Boston, MA, USA

6. Section of Pediatric Infectious Diseases, Department of Pediatrics, Boston Medical Center and Boston University School of Medicine, Boston, MA, USA

7. Department of Infectious Diseases, Ospedale Policlinico San Martino-IRCCS

8. Department of Infectious Diseases, Karolinska University Hospital and Karolinska Institutet

9. Department of Infectious Diseases, Division of Internal Medicine, Amsterdam University Medical Centers, University of Amsterdam, Meibergdreef 9, PO Box 22660, Amsterdam, The Netherlands 1100DD

10. Victorian Infectious Diseases Service (VIDS), Royal Melbourne Hospital, Melbourne, Australia Infectious Disease Epidemiology Unit, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia

11. Department of Infectious Diseases, Vall d'Hebron University Hospital, PROSICS Barcelona, Spain

12. Mount Auburn Hospital, Cambridge, MA, and Harvard Medical School, Boston, 02115, MA, USA

13. University Division of Infectious and Tropical Diseases, University of Brescia and Spedali Civili General Hospital, Brescia, Italy

14. National Referral Unit for Imported Tropical Diseases, Tropical & Travel medicine Unit, Infectious Diseases Department, La Paz- Carlos III University Hospital-IdiPAZ, Paseo de la Castellana, 261 28046 Madrid, Spain

15. Department of Infectious-Tropical Diseases and Microbiology (DITM), IRCCS Sacro Cuore Don Calabria Hospital, Negrar di Valpolicella, Verona, Italy

16. Weill Cornell Medical College and the New York Center for Travel and Tropical Medicine

17. J.D. MacLean Centre for Tropical Diseases, McGill University Health Centre, 1001 Decarie Blvd, Montreal, H4A 3J1, Canada

18. Department of Global Health, Boston University School of Public Health, Boston, MA, USA

Abstract

Abstract Background Non-immune international travellers are at risk of acquiring hepatitis A. Although hepatitis A vaccination is recommended for unvaccinated travellers to high or intermediate hepatitis A virus endemicity, compliance with this recommendation is not universal. The main objective was to describe the demographic and travel characteristics of international travellers infected with hepatitis A during travel. Methods Available data on travellers with confirmed (positive molecular test) or probable (symptomatic individuals with a single positive IgM test) hepatitis A diagnosed during and after travel from January 2008 to December 2020 were obtained from the GeoSentinel Surveillance Network database. We analysed demographic and travel characteristics of infected travellers. Results Among 254 travellers with hepatitis A (185 confirmed and 69 probable), the median age was 28 years (interquartile range: 19–40), 150 (59%) were male, and among 54 travellers with information available, 53 (98%) were unvaccinated. The most common reasons for travel included tourism (n = 120; 47%) and visiting friends or relatives (VFR; n = 72; 28%). About two-thirds of VFR travellers with hepatitis A (n = 50; 69%) were younger than 20 years old. Hepatitis A was acquired most frequently in South-Central Asia (n = 63; 25%) and sub-Saharan Africa (n = 61; 24%), but 16 travellers (6%) acquired hepatitis A in regions with low endemicity including Western Europe (n = 7; 3%), the Caribbean (n = 6; 2%) and North America (n = 3; 1%). Median duration from illness onset to GeoSentinel site presentation was ~7 days (interquartile range : 4–14 days). Among 88 travellers with information available, 59% were hospitalized. Conclusions Despite availability of highly effective vaccines, travellers still acquire hepatitis A, even when traveling to low-endemicity destinations. Providing pre-departure hepatitis A vaccine to susceptible travellers is crucial to reducing travel-associated hepatitis A and should be offered to all travellers as part of the pre-travel consultation, regardless of destination.

Funder

Public Health Agency of Canada

ISTM

Centers for Disease Control and Prevention

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Reference30 articles.

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