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Trypanocidal drugs for chronic asymptomatic Trypanosoma cruzi infectionVillar JC, Villar LA, Marin-Neto JA, Ebrahim S, Yusuf S
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SummaryStudies testing anti-parasitic drugs for people infected, but still free of Chagas' disease, are scarce and fail to provide evidence about them as preventive medications.Trypanosoma cruzi, a parasite causing Chagas' disease, infects about 18 million people living across Latin America. About 30% of them develop a major heart disease in their 30s or 40s, after decades of silent infection. No treatment is considered useful for preventing the disease among those infected, but still healthy. Drugs aimed to destroy the parasites may have this potential. Reviewers found only five published trials including 756 participants testing such agents. Although the anti-parasitic activity of most of these compounds was documented, no study addressed the efficacy of the drugs in terms of signs or symptoms of the disease.
This is a Cochrane review abstract and plain language summary, prepared and maintained by The Cochrane Collaboration, currently published in The Cochrane Database of Systematic Reviews 2010 Issue 1, Copyright © 2010 The Cochrane Collaboration. Published by John Wiley and Sons, Ltd.. The full text of the review is available in The Cochrane Library (ISSN 1464-780X).
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January 21. 2002 AbstractBackgroundPrior guidelines stated that trypanocidal therapy should not be used for treating chronic asymptomatic Trypanosoma cruzi infections. However, the recent availability of clinical trials reporting high rates of parasitologic cure in children with early chronic T. cruzi infection have produced changes of these recommendations in some countries. Because of the uncertainty regarding best treatment for this stage of T. cruzi infections, the literature was reviewed systematically for a synthesis of the available evidence. ObjectivesTo assess the effects of trypanocidal therapy for chronic asymptomatic T. cruzi infection Search strategyWe searched The Cochrane Controlled Trials Register (Issue 1, 2000), MEDLINE (start-Nov 1999), EMBASE (start - Feb 2000), LILACS (start - Feb 2000) and the Tropical Diseases Research Division of WHO database (Start - Feb 2000) . Reference lists of articles were searched for relevant material. Selection criteriaPublished RCTs of trypanocidal therapy for people with chronic, asymptomatic T. cruzi infections Data collection and analysisTwo reviewers independently screened papers for inclusion criteria, quality assessment and data extraction. Forms were used to collect data. Reviewers resolved differences by discussion then a third reviewer if necessary. Main resultsOf 43 papers assessed for inclusion, five RCTs (total population=756) met the inclusion criteria. The quality of the trials was rated as low (n=3) or intermediate (n=2). Two RCTs tested benznidazole in school children and three tested different agents in adults. The Odds Ratios and their 95%CI (Fixed models) were: Incidence of ECG abnormalities: 0.41 (0.09, 1.85); Negative seroconversion (AT ELISA): 10.91 (6.07, 19.58); Negative xenodiagnosis during the follow up: 5.37 (3.34, 8.64); Standardised mean reduction of antibody titres: 0.54 (0.31, 0.84). Nitroimidazolic derivatives substantially and significantly modified parasite-related outcomes compared to placebo. Other agents showed borderline or not significant effect. Authors' conclusionsDespite major public health importance, trypanocidal·therapy for chronic asymptomatic T. cruzi infection has been tested in few, small size RCTs which were designed to assess parasitic-related, but not clinical outcomes. Therefore, the potential of trypanocidal therapy to prevent Chagas' disease among asymptomatic, chronically infected subjects is promising, but remains to be evaluated. Trypanocidal therapy, particularly nitroimidazolic derivatives given to children or adults with positive xenodiagnosis improve parasite-related outcomes. The large contrast between the burden of Chagas disease and the existing evidence on its prevention points the need to test these or newer agents in more and larger RCTs that include clinical endpoints. |