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加纳 10 个哨点地区青蒿琥酯-阿莫地喹和青蒿琥酯-甲氟喹联合疗法治疗无并发症疟疾的疗效:2015-2017 年。

Therapeutic efficacy of artesunate-amodiaquine and artemether-lumefantrine combinations for uncomplicated malaria in 10 sentinel sites across Ghana: 2015-2017.

机构信息

Epidemiology Department, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, P. O. Box LG581, Legon, Accra, Ghana.

Centre for Tropical Clinical Pharmacology and Therapeutics, University of Ghana Medical School, P. O. Box GP4236, Accra, Ghana.

出版信息

Malar J. 2019 Jun 24;18(1):206. doi: 10.1186/s12936-019-2848-1.

Abstract

BACKGROUND

Routine surveillance on the therapeutic efficacy of artemisinin-based combination therapy (ACT) has been ongoing in Ghana since 2005. The sixth round of surveillance was conducted between 2015 and 2017 to determine the therapeutic efficacy of artesunate-amodiaquine (AS-AQ) and artemether-lumefantrine (AL) in 10 sentinel sites across the country.

METHODS

The study was a one-arm, prospective, evaluation of the clinical, parasitological, and haematological responses to directly observed treatment with AS-AQ and AL among children 6 months to 9 years old with uncomplicated falciparum malaria. The WHO 2009 protocol on surveillance of anti-malaria drug efficacy was used for the study with primary outcomes as prevalence of day 3 parasitaemia and clinical and parasitological cure rates on day 28. Secondary outcomes assessed included patterns of fever and parasite clearance as well as changes in haemoglobin concentration.

RESULTS

Day 3 parasitaemia was absent in all sites following treatment with AS-AQ whilst only one person (0.2%) was parasitaemic on day 3 following treatment with AL. Day 28 PCR-corrected cure rates following treatment with AS-AQ ranged between 96.7% (95% CI 88.5-99.6) and 100%, yielding a national rate of 99.2% (95% CI 97.7-99.7). Day 28 PCR-corrected cure rates following treatment with AL ranged between 91.3% (95% CI 79.2-97.6) and 100%, yielding a national rate of 96% (95% CI 93.5-97.6). Prevalence of fever declined by 88.4 and 80.4% after first day of treatment with AS-AQ and AL, respectively, whilst prevalence of parasitaemia on day 2 was 2.1% for AS-AQ and 1.5% for AL. Gametocytaemia was maintained at low levels (< 5%) during the 3 days of treatment. Post-treatment mean haemoglobin concentration was significantly higher than pre-treatment concentration following treatment with either AS-AQ or AL.

CONCLUSIONS

The therapeutic efficacy of AS-AQ and AL is over 90% in sentinel sites across Ghana. The two anti-malarial drugs therefore remain efficacious in the treatment of uncomplicated malaria in the country and continue to achieve rapid fever and parasite clearance as well as low gametocyte carriage rates and improved post-treatment mean haemoglobin concentration.

摘要

背景

自 2005 年以来,加纳一直在进行基于青蒿素的联合疗法(ACT)治疗效果的常规监测。第六轮监测于 2015 年至 2017 年进行,旨在确定青蒿琥酯-阿莫地喹(AS-AQ)和青蒿素-哌喹(AL)在全国 10 个哨点治疗无并发症恶性疟原虫疟疾的疗效。

方法

该研究是一项在加纳全国范围内进行的前瞻性、直接观察治疗的临床、寄生虫学和血液学反应的评估,纳入了 6 个月至 9 岁患有无并发症恶性疟的儿童。采用世界卫生组织(WHO)2009 年抗疟药疗效监测方案进行研究,主要结局是第 3 天的寄生虫血症患病率和第 28 天的临床和寄生虫学治愈率。次要结局评估包括发热和寄生虫清除模式以及血红蛋白浓度变化。

结果

在使用 AS-AQ 治疗后,所有地点的第 3 天寄生虫血症均为阴性,而在使用 AL 治疗后,仅有 1 人(0.2%)第 3 天寄生虫血症阳性。AS-AQ 治疗后第 28 天 PCR 校正治愈率在 96.7%(95%CI 88.5-99.6)至 100%之间,全国治愈率为 99.2%(95%CI 97.7-99.7)。AL 治疗后第 28 天 PCR 校正治愈率在 91.3%(95%CI 79.2-97.6)至 100%之间,全国治愈率为 96%(95%CI 93.5-97.6)。使用 AS-AQ 和 AL 治疗的第 1 天,发热的患病率分别下降了 88.4%和 80.4%,而第 2 天寄生虫血症的患病率分别为 AS-AQ 的 2.1%和 AL 的 1.5%。配子体血症在治疗的 3 天内保持在较低水平(<5%)。使用 AS-AQ 或 AL 治疗后,平均血红蛋白浓度均显著高于治疗前。

结论

AS-AQ 和 AL 在加纳各地的哨点中疗效超过 90%。因此,这两种抗疟药物在该国治疗无并发症疟疾仍然有效,并且继续实现快速退热和寄生虫清除以及较低的配子体携带率和改善治疗后平均血红蛋白浓度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25a6/6591907/fb0ac98dd7bb/12936_2019_2848_Fig1_HTML.jpg

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