Abstract

Chagas disease (CD) in the United States is severely underdiagnosed, due to an absence of systematic screening as part of routine healthcare. We screened 189 relatives of 86 existing patients and found a CD prevalence of 7.4%. Screening close relatives of previously diagnosed individuals can effectively identify new CD cases.

Highlights

  • Chagas disease (CD), caused by the protozoan Trypanosoma cruzi, affects >6 million people globally, including over 300 000 in the United States [1, 2]

  • Congenital transmission of CD has been well documented, other epidemiological research on relatives of index cases diagnosed with CD has been limited

  • This may reflect the impact of regional programs focused on halting congenital transmission, and the fact that treatment recommendations have been largely restricted to children until recently

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Summary

Introduction

Chagas disease (CD), caused by the protozoan Trypanosoma cruzi, affects >6 million people globally, including over 300 000 in the United States [1, 2]. Treatment with antitrypanosomal drugs improves morbidity and mortality from CD and eliminates the potential for congenital transmission [4, 5] Such treatment must be administered while patients are still in the asymptomatic, indeterminate phase of the disease, when they are likely to be unaware of the infection, underscoring the importance of systematic screening programs. Congenital transmission affects the distribution of CD within families; in addition, relatives, including siblings and spouses, are likely to share exposures and risk factors [7], resulting in an elevated risk of CD In this investigation, we assess the prevalence of CD among spouses, siblings, parents, and children of T. cruzi-infected individuals in Los Angeles, California

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