» Articles » PMID: 16702588

Long-term Cardiac Outcomes of Treating Chronic Chagas Disease with Benznidazole Versus No Treatment: a Nonrandomized Trial

Overview
Journal Ann Intern Med
Specialty General Medicine
Date 2006 May 17
PMID 16702588
Citations 226
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Benznidazole is effective for treating acute-stage Chagas disease, but its effectiveness for treating indeterminate and chronic stages remains uncertain.

Objective: To compare long-term outcomes of patients with nonacute Chagas disease treated with benznidazole versus outcomes of those who did not receive treatment.

Design: Clinical trial with unblinded, nonrandom assignment of patients to intervention or control groups.

Setting: Chagas disease center in Buenos Aires, Argentina.

Patients: 566 patients 30 to 50 years of age with 3 positive results on serologic tests and without heart failure.

Measurements: The primary outcome was disease progression, defined as a change to a more advanced Kuschnir group or death. Secondary outcomes included new abnormalities on electrocardiography and serologic reactivity.

Intervention: Oral benznidazole, 5 mg/kg of body weight per day for 30 days (283 patients), or no treatment (283 patients).

Results: Fewer treated patients had progression of disease (12 of 283 [4%] vs. 40 of 283 [14%]; adjusted hazard ratio, 0.24 [95% CI, 0.10 to 0.59]; P = 0.002) or developed abnormalities on electrocardiography (15 of 283 [5%] vs. 45 of 283 [16%]; adjusted hazard ratio, 0.27 [CI, 0.13 to 0.57]; P = 0.001) compared with untreated patients. Left ventricular ejection fraction (hazard ratio, 0.97 [CI, 0.94 to 0.99]; P < 0.002) and left ventricular diastolic diameter (hazard ratio, 2.45 [CI, 1.53 to 3.95]; P < 0.001) were also associated with disease progression. Conversion to negative results on serologic testing was more frequent in treated patients than in untreated patients (32 of 218 [15%] vs. 12 of 212 [6%]; adjusted hazard ratio, 2.1 [CI, 1.06 to 4.06]; P = 0.034).

Limitations: Nonrandom, unblinded treatment assignment was used, and follow-up data were missing for 20% of patients. Loss to follow-up was more common among patients who were less sick. Two uncontrolled interim analyses were conducted.

Conclusions: Compared with no treatment, benznidazole treatment was associated with reduced progression of Chagas disease and increased negative seroconversion for patients presenting with nonacute disease and no heart failure. These observations indicate that a randomized, controlled trial should now be conducted.

Citing Articles

Pharmacokinetics of two pharmaceutical presentations of benznidazole in adult Trypanosoma cruzi infected population.

Hernandez Y, Marson M, Fernandez M, Sued O, Frola C, Perez Lloret S Mem Inst Oswaldo Cruz. 2025; 120:e240177.

PMID: 40052995 PMC: 11884746. DOI: 10.1590/0074-02760240177.


Exploring Marine Natural Compounds: Innovative Therapeutic Candidates Against Chagas Disease Through Virtual Screening and Molecular Dynamics.

Maya-Ramirez C, Saih A, Mendez Tenorio A, Wong Baeza C, Nogueda Torres B, Santiago Hernandez J Life (Basel). 2025; 15(2).

PMID: 40003601 PMC: 11856606. DOI: 10.3390/life15020192.


Diagnosis and management of chagasic cardiomyopathy patients in several institutions in Argentina.

Chuit R, Antonietti L, Aguero R, Varela G, Mordini O, Alemandri E Front Parasitol. 2025; 2():1195646.

PMID: 39816819 PMC: 11731915. DOI: 10.3389/fpara.2023.1195646.


Impact of antiparasitic therapy on cardiovascular outcomes in chronic Chagas disease. A systematic review and meta-analysis.

Rassi Jr A, Grimshaw A, Sarwal A, Sah R, Shah S, Higuita N EClinicalMedicine. 2025; 79():102972.

PMID: 39810938 PMC: 11732499. DOI: 10.1016/j.eclinm.2024.102972.


The carbonic anhydrase enzymes as new targets for the management of neglected tropical diseases.

Renzi G, Ladu F, Carta F, Supuran C Arch Pharm (Weinheim). 2024; 358(1):e2400626.

PMID: 39520343 PMC: 11726158. DOI: 10.1002/ardp.202400626.