Abstract

Background—Patients with Chagas cardiomyopathy (CC) have high mortality, and CC is a common indication for heart transplantation (HTx) in endemic countries. Chagas disease reactivation (CDR) is common after transplantation and is likely to cause adverse outcomes unless detected and treated appropriately. This study reviews our experiences with HTx among patients with CC, and the use of benznidazole (BZ) before transplantation. Methods—During the 18-year period from 1996 through 2014, 70 of 353 patients who underwent HTx (19.8%) had CC, and 53 patients met the inclusion criteria. The effectiveness of prophylactic treatment with BZ (dose of 5 mg/kg/day, two times per day, for at least four weeks and for a maximum of eight weeks) was determined based on the observed reduction in the incidence of CDR during the post-HTx period. Results—Prophylactic therapy was administered to 18/53 patients (34.0%). During the follow-up period, the incidence rate of CDR in our study was 34.0% (18/53). Based on logistic regression analysis, only prophylaxis (OR = 0.12; CI 0.02–0.76; p = 0.025) was considered to protect against CDR. Conclusion—Our study suggests that the use of BZ may reduce the incidence of CDR in patients undergoing HTx and warrants further investigation in a prospective, randomized trial.

Highlights

  • Chagas disease (CD) is a major cause of end-stage cardiomyopathy in Mexico, South America, especially in Brazil, and Central America, with 7.7 million people currently estimated to be infected in 18 countries [1]

  • Patients with chagasic cardiomyopathy (CC) have higher mortality than patients with other etiologies of cardiomyopathy [4]; Chagas cardiomyopathy (CC) is a common indication for heart transplantation (HTx) in endemic countries where this therapy is available

  • From 1996 through 2014, 353 heart transplantations were performed at Dante Pazzanese Institute of Cardiology

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Summary

Introduction

Chagas disease (CD) is a major cause of end-stage cardiomyopathy in Mexico, South America, especially in Brazil, and Central America, with 7.7 million people currently estimated to be infected in 18 countries [1]. The exodus from these rural communities in the late 20th century has resulted in a marked urbanization and globalization of CD. Patients with Chagas cardiomyopathy (CC) have high mortality, and CC is a common indication for heart transplantation (HTx) in endemic countries. Chagas disease reactivation (CDR) is common after transplantation and is likely to cause adverse outcomes unless detected and treated appropriately. Conclusion—Our study suggests that the use of BZ may reduce the incidence of CDR in patients undergoing HTx and warrants further investigation in a prospective, randomized trial

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