Pharmacokinetics of piperaquine and its association with intermittent malaria preventive therapy outcomes during pregnancy.

IF 2.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Eulambius M Mlugu, Omary M S Minzi, Mats Johansson, Appolinary A R Kamuhabwa, Eleni Aklillu
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引用次数: 0

Abstract

Background: Dihydroartemisinin-piperaquine (DHP) recently showed superior effectiveness over sulfadoxine-pyrimethamine for malaria intermittent preventive treatment in pregnancy (IPTp). We investigated day 7 piperaquine pharmacokinetics and its therapeutic efficacy in preventing malaria during pregnancy.

Methods: Malaria-free (mRDT) pregnant women (n = 400) who received monthly IPTp-DHP were enrolled and followed till delivery. Day 7 Plasma piperaquine concentrations were determined after each IPTp dose using UPLC/MS/MS. IPTp outcomes (symptomatic malaria and parasitemia during pregnancy, placental malaria, and maternal malaria at delivery) were monitored. Linear mixed model and Cox regression were used to assess predictors of day 7 piperaquine concentration and treatment outcome, respectively.

Results: The incidences of symptomatic malaria and parasitemia during pregnancy per 100 person-year at risk were 2 and 33, respectively. The prevalence of histopathologically confirmed placental malaria and maternal malaria at delivery were 3% and 9.8%, respectively. Repeated monthly IPTp-DHP resulted in significantly increased day 7 plasma piperaquine concentration (p < 0.001). Following the 1st, 2nd, and 3rd monthly IPTp-DHP doses, the proportions of women with day 7 piperaquine concentration below the therapeutic threshold (< 30 ng/mL) were 6.1%, 4.1% and 3.6%, respectively. Factors such as maternal age, body weight and trimester were not significant predictors of day 7 piperaquine concentration. However, having a low day 7 piperaquine plasma concentration (< 30 ng/mL) was significantly associated with a higher risk of parasitemia during pregnancy (p = 0.004).

Conclusion: Lower day 7 piperaquine plasma concentration is a risk factor for parasitemia during pregnancy. Single plasma sampling at day 7 can be used to monitor piperaquine effectiveness during IPTp-DHP.

Trial registration: Registered 09/12/2016, PACTR201612001901313.

哌喹的药代动力学及其与孕期间歇性疟疾预防治疗效果的关系。
背景:双氢青蒿素-哌喹(DHP)最近在妊娠期疟疾间歇预防性治疗(IPTp)中显示出优于磺胺乙胺嘧啶的疗效。我们研究了哌喹第 7 天的药代动力学及其对预防孕期疟疾的疗效:方法:我们招募了无疟疾(mRDT)、每月接受 IPTp-DHP 治疗的孕妇(n = 400),并对其进行随访直至分娩。使用 UPLC/MS/MS 测定每次服用 IPTp 后第 7 天的血浆哌喹浓度。对 IPTp 的结果(孕期无症状疟疾和寄生虫血症、胎盘疟疾和分娩时产妇疟疾)进行了监测。线性混合模型和 Cox 回归分别用于评估第 7 天哌喹浓度和治疗结果的预测因素:每 100 个风险年中,孕期无症状疟疾和寄生虫血症的发病率分别为 2 和 33。经组织病理学证实的胎盘疟疾发病率和分娩时产妇疟疾发病率分别为 3% 和 9.8%。每月重复使用 IPTp-DHP 可显著提高第 7 天血浆中的哌啶浓度(p 结论:哌啶浓度越高,第 7 天血浆中的哌啶浓度越低:第 7 天较低的哌喹血浆浓度是导致孕期寄生虫血症的一个风险因素。第7天的单次血浆采样可用于监测IPTp-DHP期间哌喹的有效性:注册日期:2016年12月9日,PACTR201612001901313。
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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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