Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Antimicrob Agents Chemother. 2021 Feb 17;65(3). doi: 10.1128/AAC.01150-20.
Dihydroartemisinin-piperaquine (DP) is a long-acting artemisinin combination treatment that provides effective chemoprevention and has been proposed as an alternative antimalarial drug for intermittent preventive therapy in pregnancy (IPTp). Several pharmacokinetic studies have shown that dose adjustment may not be needed for the treatment of malaria in pregnancy with DP. However, there are limited data on the optimal dosing for IPTp. This study aimed to evaluate the population pharmacokinetics of piperaquine given as IPTp in pregnant women. Pregnant women were enrolled in clinical trials conducted in Kenya and Indonesia and treated with standard 3-day courses of DP, administered in 4- to 8-week intervals from the second trimester until delivery. Pharmacokinetic blood samples were collected for piperaquine drug measurements before each treatment round, at the time of breakthrough symptomatic malaria, and at delivery. Piperaquine population pharmacokinetic properties were investigated using nonlinear mixed-effects modeling with a prior approach. In total, data from 366 Kenyan and 101 Indonesian women were analyzed. The pharmacokinetic properties of piperaquine were adequately described using a flexible transit absorption ( = 5) followed by a three-compartment disposition model. Gestational age did not affect the pharmacokinetic parameters of piperaquine. After three rounds of monthly IPTp, 9.45% (95% confidence interval [CI], 1.8 to 26.5%) of pregnant women had trough piperaquine concentrations below the suggested target concentration (10.3 ng/ml). Translational simulations suggest that providing the full treatment course of DP at monthly intervals provides sufficient protection to prevent malaria infection. Monthly administration of DP has the potential to offer optimal prevention of malaria during pregnancy. (This study has been registered at ClinicalTrials.gov under identifier NCT01669941 and in the ISRCTN under number ISRCTN34010937.).
双氢青蒿素-哌喹(DP)是一种长效青蒿素复方疗法,具有有效的化学预防作用,并被提议作为妊娠期间间歇性预防治疗(IPTp)的替代抗疟药物。几项药代动力学研究表明,DP 治疗妊娠疟疾可能不需要调整剂量。然而,关于 IPTp 的最佳剂量的数据有限。本研究旨在评估哌喹作为 IPTp 在孕妇中的群体药代动力学。在肯尼亚和印度尼西亚进行的临床试验中招募了孕妇,并给予标准的 3 天 DP 疗程,从妊娠中期开始,每 4-8 周给药一次,直到分娩。在每次治疗前、突破性症状性疟疾发作时和分娩时采集哌喹药物的药代动力学血样。使用非线性混合效应模型和先验方法研究哌喹的群体药代动力学特性。总共分析了来自 366 名肯尼亚妇女和 101 名印度尼西亚妇女的数据。使用灵活的转运吸收( = 5)随后是三房室处置模型可以充分描述哌喹的药代动力学特性。胎龄不影响哌喹的药代动力学参数。在每月进行 3 轮 IPTp 后,9.45%(95%置信区间 [CI],1.8 至 26.5%)的孕妇的哌喹谷浓度低于建议的目标浓度(10.3 ng/ml)。翻译模拟表明,每月间隔给予 DP 的完整疗程可提供足够的保护以预防疟疾感染。每月给予 DP 有可能在妊娠期间提供最佳的疟疾预防。(本研究已在 ClinicalTrials.gov 上以标识符 NCT01669941 注册,并在 ISRCTN 下以编号 ISRCTN34010937 注册。)。