Abstract
BackgroundChagas disease treatment is limited by drug availability, adverse side effect profiles of available medications, and poor adherence.MethodsAdult Chagas disease patients initiating 60-days of benznidazole were randomized to weekly or twice-weekly evaluations of medication adherence and screening for adverse drug events (ADEs). Mid-week evaluations employed phone-based evaluations. Adherence was measured by self-report, pill counts with intentional over-distribution, and Medication Event Monitoring Systems (MEMS). Prospective data were compared to historical controls treated with benznidazole at the same hospital.Results162 prospective patients were compared to 172 historical patients. Pill counts correlated well with MEMS data (R = 0.498 for 7-day intervals, R = 0.872 for intervals >7 days). Treatment completion rates were higher among prospective than historical patients (82.1% vs. 65.1%), primarily due to lower abandonment rates. Rates of ADEs were lower among prospective than historical patients (56.8% vs. 66.9%). Twice-weekly evaluations increased identification of mild ADEs, prompting higher suspension rates than weekly evaluations. While twice-weekly evaluations identified ADEs earlier, they did not reduce incidence of moderate or severe ADEs. Many dermatologic ADEs were moderately severe upon presentation (35.6%), were not reduced by use of antihistamines, occurred among adult patients of all ages, and occurred throughout treatment, rather than the first few weeks alone.ConclusionsIntensive management improved completion and identified more ADEs, but did not reduce moderate or severe ADEs. Risk of dermatologic ADEs cannot be reduced by selecting younger adults or monitoring only during the first few weeks of treatment. Pill counts and phone-based encounters are reliable tools for treatment programming in rural Bolivia.
Highlights
Over 100 years after its discovery, there are still few effective treatment options for Chagas disease
This study demonstrated associations between increased follow-up and improved treatment completion, reduced adverse drug events (ADEs), earlier documentation of ADEs, and pretreatment factors associated with benznidazole toxicity
162 patients were randomized to weekly (n = 87) or twice-weekly evaluations (n = 75, Figure 1)
Summary
Over 100 years after its discovery, there are still few effective treatment options for Chagas disease. Chagas disease is caused by a vector-borne parasite, Trypanosoma cruzi, and is responsible for an estimated 430,000 DALYs lost and a cost of $1.2 billion in lost productivity each year [1]. Expanded vector control since 2000 has dramatically reduced infestation rates, opening the door for antiparasitic treatment. Current evidence supports treatment of adults without advanced cardiac disease or significant comorbidity using either benznidazole or nifurtimox [6,7]. Benznidazole is better-tolerated, but between intermittent shortages and drug rashes including Stevens-Johnson Syndrome, many rural Bolivians fail to complete treatment. Chagas disease treatment is limited by drug availability, adverse side effect profiles of available medications, and poor adherence
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