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用于治疗母婴配对中单纯性疟疾的抗疟药物的药代动力学:一项观察性药代动力学研究。

-Pharmacokinetics of antimalarial drugs used to treat uncomplicated malaria in breastfeeding mother-infant pairs: An observational pharmacokinetic study.

作者信息

Nakijoba Ritah, Nakayiwa Kawuma Aida, Ojara Francis Williams, Tabwenda Jovia C, Kyeyune Jacqueline, Turyahabwe Christine, Asiimwe Simon Peter, Magoola Johnson, Banda Clifford George, Castelnuovo Barbara, Buzibye Allan, Waitt Catriona

机构信息

Infectious Diseases Institute, Makerere University College of Health Sciences, Kampala, 256, Uganda.

Department of Pharmacology and Therapeutics, Gulu University, Gulu, 256, Uganda.

出版信息

Wellcome Open Res. 2023 Aug 10;8:12. doi: 10.12688/wellcomeopenres.18512.1. eCollection 2023.

Abstract

Data surrounding the exposure of the breastfed infant to drugs and any associated risks are sparse. Drugs usually are transferred to milk in small quantities, and many have been used without obviously noticeable infant toxicity for many years - this lack of a 'safety signal' has further reduced the interest in studying mother-to-infant transfer of the drugs. In sub-Saharan Africa, pregnant women are at risk of   infection, and one in four women have evidence of placental infection at the time of delivery. Artemisinin-based combination therapies (ACTs), primarily artemether-lumefantrine (AL), are the current first-line treatment for uncomplicated malaria, with the same dosing recommendations in breastfeeding women as those in the adult population. Dihydroartemisinin-piperaquine (DP) is routinely used as an alternative to AL in Uganda. However, lactation pharmacokinetics (PK) of ACTs are unknown. Pharmacokinetic characterization of anti-malarial transfer to breast milk and breastfed infants is crucial in understanding the potential consequences to the infant, in terms of therapeutic- and prophylactic effects as well as potential toxicity.   This observational study will enroll 30 mother-infant pairs, and aims to characterize the breastmilk transfer of antimalarial medications (AL and DP) to infants when these ACTs are administered to mothers as part of treatment for uncomplicated malaria. In addition, we will assess the mental health of the breastfeeding mothers enrolled as well as the well-being of their children. PK samples of maternal blood, breastmilk and breastfeeding infant's blood will be obtained at specific times points. Pharmacokinetic data will be analyzed using a population pharmacokinetic approach. We anticipate that findings from this research will guide to develop a PK model describing lumefantrine and piperaquine disposition and will provide a framework to foster other lactation pharmacokinetic studies in different disease areas.

摘要

关于母乳喂养婴儿接触药物及其任何相关风险的数据非常稀少。药物通常少量转移到乳汁中,许多药物多年来一直被使用,并未对婴儿产生明显的毒性——这种缺乏“安全信号”的情况进一步降低了对研究药物母婴转移的兴趣。在撒哈拉以南非洲,孕妇有感染风险,四分之一的妇女在分娩时有胎盘感染的迹象。以青蒿素为基础的联合疗法(ACTs),主要是蒿甲醚-本芴醇(AL),是目前治疗非复杂性疟疾的一线疗法,对哺乳期妇女的给药建议与成人相同。双氢青蒿素-哌喹(DP)在乌干达通常用作AL的替代品。然而,ACTs的泌乳药代动力学(PK)尚不清楚。抗疟疾药物向母乳和母乳喂养婴儿的药代动力学特征对于了解对婴儿的潜在影响至关重要,包括治疗和预防效果以及潜在毒性。 这项观察性研究将招募30对母婴,旨在描述在将这些ACTs作为非复杂性疟疾治疗的一部分给予母亲时,抗疟疾药物(AL和DP)向婴儿的母乳转移情况。此外,我们将评估参与研究的母乳喂养母亲的心理健康及其子女的健康状况。将在特定时间点采集母亲血液、母乳和母乳喂养婴儿血液的PK样本。药代动力学数据将采用群体药代动力学方法进行分析。我们预计这项研究的结果将指导建立一个描述本芴醇和哌喹处置的PK模型,并将提供一个框架,以促进不同疾病领域的其他泌乳药代动力学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54c8/10593497/ee958380dd2f/wellcomeopenres-8-22003-g0000.jpg

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