Clinical and parasitological efficacy of artesunate and sulfadoxine-pyrimethamine (AS+SP) for the treatment of uncomplicated falciparum malaria in different transmission settings in India.

IF 0.8 4区 医学 Q4 INFECTIOUS DISEASES
Ritesh Ranjha, Rajendra Baharia, Vani H Chalageri, Bina Srivastava, Naseem Ahmed, Supriya Sharma, Prashant Kumar Mallick, Anupkumar R Anvikar, Praveen Kumar Bharti
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引用次数: 0

Abstract

Background objectives: In 2010, artesunate and sulfadoxine-pyrimethamine (AS+SP) were adopted as the first-line artemisinin based combination therapy for treatment of uncomplicated Plasmodium falciparum malaria in India. Continuous therapeutic efficacy monitoring of firstline anti-malarial drugs is required to update the treatment policy for malaria control and elimination. This study aimed to assess the therapeutic efficacy of artesunate and sulfadoxine-pyrimethamine (AS+SP) at three sites with different diseases transmission intensity.

Methods: A 28-day, single-arm, prospective study was conducted to evaluate the clinical and parasitological response to AS+SP. Patients received a six-dose regimen of AS+SP over three days and were monitored for 28 days through clinical and laboratory assessments. Participant recruitment and outcome classification was done as per the WHO guidelines for the surveillance of anti-malarial drug efficacy.

Results: A total of 170 participants were enrolled and 147 of them completed the follow-up. Adequate clinical and parasitological response (ACPR) was observed in 100% of the study participants who completed the follow-up. 100% fever clearance as well as parasite clearance was observed on day 3.

Interpretation conclusion: This study demonstrated high therapeutic efficacy and a good safety profile for artesunate and sulfadoxine-pyrimethamine at different transmission intensities. This suggests the continuation of the current artemisinin based combination therapy for the treatment of P. falciparum malaria in India.

青蒿琥酯和磺胺多辛-乙胺嘧啶(AS+SP)在印度不同传播环境中治疗无并发症恶性疟疾的临床和寄生虫学疗效
背景目的:2010年,印度采用青蒿琥酯联合磺胺多辛-乙胺嘧啶(AS+SP)作为治疗无并发症恶性疟原虫疟疾的一线青蒿素联合疗法。需要持续监测一线抗疟药物的疗效,以更新控制和消除疟疾的治疗政策。本研究旨在评价青蒿琥酯和磺胺多辛-乙胺嘧啶(AS+SP)在3个不同疾病传播强度部位的治疗效果。方法:进行一项为期28天的单臂前瞻性研究,评估AS+SP的临床和寄生虫学反应。患者接受为期3天的6次AS+SP治疗方案,并通过临床和实验室评估监测28天。根据世卫组织抗疟疾药物疗效监测指南进行了参与者招募和结果分类。结果:共纳入170例受试者,其中147例完成随访。在完成随访的研究参与者中,100%观察到足够的临床和寄生虫学反应(ACPR)。在第3天观察到100%的退热和寄生虫清除。解释结论:本研究显示青蒿琥酯和磺胺多辛-乙胺嘧啶在不同传播强度下具有较高的治疗效果和良好的安全性。这表明印度应继续采用目前以青蒿素为基础的联合疗法治疗恶性疟原虫疟疾。
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来源期刊
Journal of Vector Borne Diseases
Journal of Vector Borne Diseases INFECTIOUS DISEASES-PARASITOLOGY
CiteScore
0.90
自引率
0.00%
发文量
89
审稿时长
>12 weeks
期刊介绍: National Institute of Malaria Research on behalf of Indian Council of Medical Research (ICMR) publishes the Journal of Vector Borne Diseases. This Journal was earlier published as the Indian Journal of Malariology, a peer reviewed and open access biomedical journal in the field of vector borne diseases. The Journal publishes review articles, original research articles, short research communications, case reports of prime importance, letters to the editor in the field of vector borne diseases and their control.
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