[评估马达加斯加无并发症疟疾患者的磺胺多辛- pyrimsamthamine (Fansidar, Paludar)疗效:提出简化研究方案的初步研究]。

L Randrianasolo, A Randriamanantena, A Ratsimbasoa, J D Rakotoson, J Randriambelosoa, A Raveloson, N Rakotondrajaona, L Tuseo, M Randrianarivelojosia
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引用次数: 0

摘要

为了缓解经验丰富的医疗团队数量不足的问题,这些医疗团队受邀并接受监测对诊断为非复杂疟疾的患者所开药物的有效性,并确保监测马达加斯加目前使用的抗疟疾药物对恶性疟原虫的易感性,有必要与他们仔细讨论制定一项可行的研究方案。我们在两个农村地区开展了初步研究,采用基于观察性研究原则的简化方案,评估了磺胺多辛-乙胺嘧啶(SP)治疗无并发症恶性疟原虫疟疾的疗效。第0天给予单剂量SP与扑热息痛。接受药物治疗的人在第14天和第28天接受了医疗队一名成员的另外两次干预。随访19例,年龄3 ~ 63岁。该组合对19人的疗效进行了观察。我们的研究结果表明,恶性疟原虫菌株对SP敏感。由于SP将用于马达加斯加孕妇的间歇性预防治疗,延缓SP耐药寄生虫发生的一种方法是:(a)避免对非孕妇大量使用SP,以及(b)监测恶性疟原虫对SP的易感,作为使用世卫组织标准方案的试点研究的一部分(这对大多数外围卫生设施来说并不容易——在第0、1、2、3、7、14、21和28天进行临床检查和寄生虫学控制的后续程序)。并且通常采用简化的方案,例如本研究中说明的分析性观察研究。讨论了观察性研究的局限性和优点。
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[Assessment of sulfadoxine-pyriméthamine (Fansidar, Paludar) efficacy in patients with uncomplicated malaria in Madagascar: preliminary study to propose a simplified study protocol].

To alleviate the insufficient number of experienced medical teams invited to and accepting to monitor the effectiveness of drugs prescribed to patients with a diagnosis of uncomplicated malaria and to insure the surveillance of the susceptibility of P. falciparum to current antimalarials used in Madagascar, there is a need to draw a feasible study protocol carefully discussed with them. We carried out a preliminary study in two rural areas and assessed the efficacy of sulfadoxine-pyrimethamine (SP) for curing uncomplicated P. falciparum malaria, with a simplified protocol based on the principle of observational study. A single dose of SP was given on day 0 with paracetamol. The persons to whom the drugs were administered accepted two other interventions of one member of the medical teams on day 14 and day 28. Nineteen patients, 3-63 years old, fulfilled the follow-up. The efficacy of this combination was noted for the 19 persons. Our results show that P. falciparum strains are susceptible to SP. Since SP will be used in intermittent preventive treatment in pregnant women in Madagascar, one way to delay the occurrence of SP resistant parasites will be (a) to avoid massive use of SP for the non pregnant persons and (b) to monitor susceptibility of P. falciparum to SP as part of pilot studies using standard WHO protocol (which is not really easy for most of the peripheral health facilities--with the follow-up procedures with clinical examination and parasitological control at Days 0, 1, 2, 3, 7, 14, 21 and 28), and routinely with simplified protocol such as the analytical observational study illustrated in this present study. Limit and advantage of observational study are discussed.

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