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Effectiveness of two antifolate prophylactic strategies against malaria in HIV-positive pregnant women in Bangui, Central African Republic: study protocol for a randomized controlled trial (MACOMBA)

机译:中非共和国班吉的两种抗叶酸预防策略在HIV阳性孕妇中预防疟疾的有效性:一项随机对照试验(MACOMBA)的研究方案

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Background Co-infection with malaria parasite and HIV is an emerging public health problem in tropical areas, particularly in pregnant women, and management of the concurrent effects of these two infections is challenging. Co-trimoxazole is a sulfamide preparation used to prevent opportunistic infections in HIV-infected patients, and many studies have reported that it has significant activity against malaria. As the efficacy of intermittent preventive treatment (IPT) with sulfadoxine-pyrimethamine (SP) against malaria is decreasing, co-trimoxazole might be an alternative for preventing malaria among HIV-infected populations. The aim of this study is to compare the effectiveness of SP-IPT, which is recommended for the prevention of malaria during pregnancy in the Central African Republic, with that of a daily dose of co-trimoxazole against P. falciparum infections among HIV-infected pregnant women in Bangui, the capital of the Central African Republic. Methods/Design The MACOMBA study (MAternity and COntrol of Malaria-HIV co-infection in BAngui) is a multicentre open-label randomized clinical trial conducted at four maternity hospitals in Bangui. All HIV-infected pregnant women presenting for an antenatal clinic visit between the weeks 16 and 28 of amenorrhoea, with a CD4 count of more than 350 cells/mm3, will be eligible. All the women will provide written consent before being enrolled in the study and will then be randomly allocated to either SP-IPT (25 mg of sulfadoxine and 1.25 mg of pyrimethamine) or daily co-trimoxazole doses (960 mg per dose). The primary end-point is the placental malaria parasitaemia rate at delivery. Other main outcome measures include the number of malaria episodes during pregnancy, safety, and treatment compliance. Furthermore, the frequency of molecular resistance markers dhfr and dhps will be measured. Discussion In this trial, we seek to confirm whether co-trimoxazole is operationally suitable to replace SP-IPT in order to prevent malaria among pregnant women infected with HIV in the Central African Republic. Trial registration ClinicalTrials.gov Identifier: NCT01746199 .
机译:背景技术在热带地区,尤其是在孕妇中,疟疾寄生虫和HIV的共同感染是一个正在出现的公共卫生问题,这两种感染的同时影响的管理面临挑战。复方新诺明是一种磺胺制剂,用于预防HIV感染患者中的机会感染,许多研究报告说它具有显着的抗疟疾活性。随着磺胺多辛-乙胺嘧啶(SP)的间歇性预防性治疗(IPT)对抗疟疾的效力下降,co-trimoxazole可能是预防HIV感染人群中疟疾的替代方法。这项研究的目的是比较SP-IPT的有效性,建议将其用于预防中非共和国怀孕期间的疟疾,将其与每日三剂量的复方新诺明对抗艾滋病毒感染的恶性疟原虫感染进行比较。中非共和国首都班吉的孕妇。方法/设计MACOMBA研究(班吉的孕妇和疟疾-艾滋病毒共同感染控制)是在班吉的四家孕妇医院进行的多中心开放标签随机临床试验。所有在闭经前16至28周之间接受产前门诊就诊且CD4计数超过350细胞/ mm 3 的HIV感染孕妇均符合资格。所有妇女在参加研究前均需提供书面同意,然后随机分配至SP-IPT(25 mg磺胺多辛和1.25 mg乙胺嘧啶)或每日三甲唑剂量(960 mg /剂)。主要终点是分娩时胎盘疟疾寄生虫血症的发生率。其他主要结果指标包括怀孕期间疟疾发作的次数,安全性和治疗依从性。此外,将测量分子抗性标记dhfr和dhps的频率。讨论在本试验中,我们试图确认在特定的情况下,复方新诺明在操作上是否适合替代SP-IPT,以预防中非共和国感染艾滋病毒的孕妇中的疟疾。试用注册ClinicalTrials.gov标识符:NCT01746199。

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