Risk factors for treatment interruption and severe adverse effects to benznidazole in adult patients with Chagas disease
Open Access
- 26 September 2017
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 12 (9) , e0185033
Abstract
Etiological treatment of Chagas disease in chronic asymptomatic patients is still in debate and the adverse effects of traditional drugs are one of the main concerns in clinical practice. This study evaluated retrospectively the safety profile of benznidazole (BZN) and identified predictive factors for definite treatment interruption and development of severe reactions in adult patients treated with BZN in Colombia. Retrospective follow-up study conducted by review of medical records of adults with chronic Chagas disease treated with BZN in Colombia. A parametric survival analysis based on a generalized gamma distribution was used for assessing risk factors for treatment interruption. A multinomial logistic regression model was used to estimate the probability of severe adverse drug reactions (ADRs). Statistical associations were expressed as time ratios (TR) and adjusted odds ratios (aOR) respectively. In total 224 adults patients treated with BZN were included; 172 (76.8%) completed the standard therapy (60 days of treatment), 205 (91.5%) presented ADRs and 52 cases (23.2%) required treatment interruption. The predominant symptoms were: rash (37.9%), itching (33.7%), epigastric pain (26.4%), abdominal bloating (24.2%) and nausea (22.1%). ADRs were mild (57.4%), moderate (35.5%) and severe (7.3%). Time to treatment interruption was significantly shorter when using doses of BZN ≥ 6 mg/kg/day (TR 0.55; 95% CI 0.39–0.76), presenting severe ADRs (TR 0.12; 95% CI: 0.07–0.19) and eosinophilia (TR 0.68; 95% CI: 0.49–0.94). Female sex (aOR 3.98; 95% CI 1.56–10.16), dose of BZN ≥ 6 mg/kg/day (aOR 1.41; 95% CI 1.17–1.70) and presence of > 3 ADRs (aOR 6.47; 95% CI 1.24–34.34) were considered as risk factors for developing severe ADRs. Dose, severity of ADRs, eosinophilia and female sex were the main predictors for treatment interruption or severe ADRs. The potential implications of these findings are discussed.Keywords
This publication has 32 references indexed in Scilit:
- Safety of benznidazole use in the treatment of chronic Chagas' diseaseJournal of Antimicrobial Chemotherapy, 2012
- Adverse Events After the Use of Benznidazole in Infants and Children With Chagas DiseasePediatrics, 2011
- Tolerance and Safety of Nifurtimox in Patients with Chronic Chagas DiseaseClinical Infectious Diseases, 2010
- Tolerance of Benznidazole in Treatment of Chagas' Disease in AdultsAntimicrobial Agents and Chemotherapy, 2010
- Reações adversas em pacientes com doença de Chagas tratados com benzonidazol, no Estado do CearáRevista da Sociedade Brasileira de Medicina Tropical, 2010
- Chagas diseaseThe Lancet, 2010
- Parametric survival analysis and taxonomy of hazard functions for the generalized gamma distributionStatistics in Medicine, 2007
- Chemotherapy of trypanosomiases and leishmaniasisTrends in Parasitology, 2005
- How Important Are Gender Differences in Pharmacokinetics?Clinical Pharmacokinetics, 2002
- Sistema de Farmacovigilância do Ceará: um ano de experiênciaCadernos de Saude Publica, 1999