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首页> 外文期刊>Antimicrobial agents and chemotherapy. >New Scheme of Intermittent Benznidazole Administration in Patients Chronically Infected with Trypanosoma cruzi: a Pilot Short-Term Follow-Up Study with Adult Patients
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New Scheme of Intermittent Benznidazole Administration in Patients Chronically Infected with Trypanosoma cruzi: a Pilot Short-Term Follow-Up Study with Adult Patients

机译:慢性感染克鲁斯锥虫的患者间歇性苯达唑治疗的新方案:成年患者的短期短期随访研究

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摘要

There is a clinical need to test new schemes of benznidazole administration that are expected to be at least as effective as the current therapeutic scheme but safer. This study assessed a new scheme of benznidazole administration in chronic Chagas disease patients. A pilot study with intermittent doses of benznidazole at 5 mg/kg/day in two daily doses every 5 days for a total of 60 days was designed. The main criterion of response was the comparison of quantitative PCR (qPCR) findings prior to and 1 week after the end of treatment. The safety profile was assessed by the rate of suspensions and severity of adverse effects. Twenty patients were analyzed for safety, while qPCR was tested for 17 of them. The average age was 43 +/- 7.9 years; 55% were female. Sixty-five percent of treated subjects showed detectable qPCR results prior to treatment of 1.45 (0.63 to 2.81) and 2.1 (1.18 to 2.78) parasitic equivalents per milliliter of blood (par. eq/ml) for kinetoplastic DNA (kDNA) qPCR and nuclear repetitive sequence satellite DNA (SatDNA) qPCR, respectively. One patient showed detectable PCR at the end of treatment (1/17), corresponding to 6% treatment failure, compared with 11/17 (65%) patients pretreatment (P = 0.01). Adverse effects were present in 10/20 (50%) patients, but in only one case was treatment suspended. Eight patients showed mild adverse effects, whereas moderate reactions with increased liver enzymes were observed in two patients. The main accomplishment of this pilot study is the promising low rate of treatment suspension. Intermittent administration of benznidazole emerges a new potential therapeutic scheme, the efficacy of which should be confirmed by long-term assessment posttreatment.
机译:临床上需要测试新的苯并硝唑方案,这些方案预期至少与目前的治疗方案一样有效,但更安全。这项研究评估了慢性恰加斯病患者使用苯尼达唑的新方案。设计了一项初步研究,以5毫克/千克/天的剂量间歇给药,每5天服用两次,每天两次,共60天。反应的主要标准是治疗结束前和治疗结束后1周的定量PCR(qPCR)结果的比较。通过悬浮液的速率和不良反应的严重程度评估安全性。分析了20例患者的安全性,其中17例进行了qPCR测试。平均年龄为43 +/- 7.9岁; 55%是女性。 65%的受治疗受试者显示出可检测到的qPCR结果,然后针对动能DNA(kDNA)qPCR和核仁治疗每毫升血液中的1.45(0.63至2.81)和2.1(1.18至2.78)寄生当量(par。eq / ml)。重复序列卫星DNA(SatDNA)qPCR。一名患者在治疗结束时(1/17)显示可检测到的PCR,相当于治疗失败的6%,而治疗前为11/17(65%)患者(P = 0.01)。 10/20(50%)患者存在不良反应,但只有一种情况被暂停治疗。 8名患者显示出轻度的不良反应,而2名患者中观察到肝酶升高的中度反应。这项初步研究的主要成就是有希望的低治疗暂停率。苯甲硝唑的间歇给药出现了一种新的潜在治疗方案,其疗效应通过长期评估后治疗予以证实。

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