loading page

Adverse events associated with benznidazole treatment for Chagas disease in children and adults
  • +6
  • Cintia Cruz,
  • Andres Rabinovich,
  • Guillermo Moscatelli,
  • Nicolas Gonzalez ,
  • Samanta Moroni ,
  • Griselda Ballering ,
  • Facundo Garcia-Bournissen,
  • Hector Freilij,
  • Jaime Altcheh
Cintia Cruz
Mahidol University

Corresponding Author:cintiavcruz@gmail.com

Author Profile
Andres Rabinovich
Ricardo Gutierrez Children's Hospital
Author Profile
Guillermo Moscatelli
Ricardo Gutierrez Children's Hospital
Author Profile
Nicolas Gonzalez
Ricardo Gutierrez Children's Hospital
Author Profile
Samanta Moroni
Ricardo Gutierrez Children's Hospital
Author Profile
Griselda Ballering
Ricardo Gutierrez Children's Hospital
Author Profile
Facundo Garcia-Bournissen
London Health Sciences Centre
Author Profile
Hector Freilij
Ricardo Gutierrez Children's Hospital
Author Profile
Jaime Altcheh
El Hospital de Niños Ricardo Gutierrez
Author Profile

Abstract

AIM: Chagas disease (ChD) is a neglected disease affecting approximately 7 million individuals in Latin America. Benznidazole (BZ) is the most commonly used treatment. Therefore, understanding the adverse effects of BZ is crucial for devising targeted monitoring and interventions to enhance patient management. METHODS: A retrospective cohort study of patients with ChD treated with BZ to identify and characterize BZ adverse drug reactions (ADRs). RESULTS: 518 patients were enrolled: 449 children (median age: 4yrs, range 1mo-17.75yrs) and 69 adults (median age: 25yrs, range 18-59). A 75% of pediatric patients received a median dose of BZ of 6.6 mg/kg/day (IQR25–75 = 5.7-7.3) for at least 60 days. Adult patients received a median BZ dose of 5.6 mg/kg/day (IQR25–75 = 5.2-6.1) for a median duration of 31 days (IQR25–75 = 30-60). Overall, 152/518 (29.34%) patients developed BZ-related ADRs, with an incidence of 116/449 (25.83%) in children and 36/69 (52.17%) in adults (OR = 0.32, CI95 = 0.19 to 0.54, p < 0.001). The study identified 240 ADRs, primarily mild to moderate, but severe ADRs occurred in 1.11% of children and 1.45% of adults. The skin was the most affected system in both groups. A 10.23% of patients abandoned treatment (53/518). Adults discontinued treatment more frequently than children (OR = 3.36 CI95 = 1.7 to 6.4, p < 0.001). CONCLUSION: Our study supports the safety of BZ for ChD in children and adults. Avoiding BZ treatment due to safety concerns does not seem to be supported by the evidence.
Submitted to British Journal of Clinical Pharmacology
22 Mar 2024Review(s) Completed, Editorial Evaluation Pending
21 Jun 20241st Revision Received
24 Jun 2024Review(s) Completed, Editorial Evaluation Pending
03 Jul 2024Editorial Decision: Revise Minor
16 Jul 20242nd Revision Received
17 Jul 2024Submission Checks Completed
17 Jul 2024Assigned to Editor
17 Jul 2024Review(s) Completed, Editorial Evaluation Pending
19 Jul 2024Editorial Decision: Accept