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吸入型抗病毒药物的临床药代动力学系统评价

A Systematic Review of Clinical Pharmacokinetics of Inhaled Antiviral.

机构信息

Department of Clinical Pharmacy, King Fahad Medical City, Riyadh 12211, Saudi Arabia.

Maternity and Children Hospital, Dammam 32274, Saudi Arabia.

出版信息

Medicina (Kaunas). 2023 Mar 23;59(4):642. doi: 10.3390/medicina59040642.

Abstract

: The study of clinical pharmacokinetics of inhaled antivirals is particularly important as it helps one to understand the therapeutic efficacy of these drugs and how best to use them in the treatment of respiratory viral infections such as influenza and the current COVID-19 pandemic. The article presents a systematic review of the available pharmacokinetic data of inhaled antivirals in humans, which could be beneficial for clinicians in adjusting doses for diseased populations. : This systematic review followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines. A comprehensive literature search was conducted using multiple databases, and studies were screened by two independent reviewers to assess their eligibility. Data were extracted from the eligible studies and assessed for quality using appropriate tools. : This systematic review evaluated the pharmacokinetic parameters of inhaled antiviral drugs. The review analyzed 17 studies, which included Zanamivir, Laninamivir, and Ribavirin with 901 participants, and found that the non-compartmental approach was used in most studies for the pharmacokinetic analysis. The outcomes of most studies were to assess clinical pharmacokinetic parameters such as the Cmax, AUC, and t1/2 of inhaled antivirals. : Overall, the studies found that the inhaled antiviral drugs were well tolerated and exhibited favorable pharmacokinetic profiles. The review provides valuable information on the use of these drugs for the treatment of influenza and other viral respiratory infections.

摘要

: 研究吸入性抗病毒药物的临床药代动力学非常重要,因为它有助于人们了解这些药物的治疗效果,以及如何在治疗流感和当前 COVID-19 大流行等呼吸道病毒感染方面最佳使用这些药物。本文对吸入性抗病毒药物在人体中的药代动力学数据进行了系统评价,这对于临床医生调整疾病人群的剂量可能是有益的。: 这项系统评价遵循了 2020 年系统评价和荟萃分析的首选报告项目 (PRISMA) 指南。使用多个数据库进行了全面的文献检索,并由两名独立评审员筛选研究以评估其合格性。从合格的研究中提取数据,并使用适当的工具评估其质量。: 这项系统评价评估了吸入性抗病毒药物的药代动力学参数。该综述分析了 17 项研究,其中包括扎那米韦、拉尼米韦和利巴韦林,共有 901 名参与者,发现大多数研究都使用非房室模型法进行药代动力学分析。大多数研究的结果是评估吸入性抗病毒药物的临床药代动力学参数,如 Cmax、AUC 和 t1/2。: 总体而言,研究发现吸入性抗病毒药物耐受性良好,表现出良好的药代动力学特征。该综述提供了有关这些药物治疗流感和其他病毒性呼吸道感染的使用的有价值的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f81/10145512/114d52733dc7/medicina-59-00642-g001.jpg

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