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高效抗逆转录病毒治疗突破替代抗逆转录病毒药物给药方式综述:粉碎及肠内管给药情况的实际考量

A HAART-Breaking Review of Alternative Antiretroviral Administration: Practical Considerations with Crushing and Enteral Tube Scenarios.

作者信息

Huesgen Emily, DeSear Kathryn E, Egelund Eric F, Smith Renata, Max Blake, Janelle Jennifer

机构信息

Department of Pharmacotherapy and Translational Research, College of Pharmacy, University of Florida, Gainesville, Florida.

Department of Pharmacy Practice, University of Illinois at Chicago, Chicago, Illinois.

出版信息

Pharmacotherapy. 2016 Nov;36(11):1145-1165. doi: 10.1002/phar.1835. Epub 2016 Oct 20.

DOI:10.1002/phar.1835
PMID:27636237
Abstract

Selection of an appropriate antiretroviral regimen for the patient infected with human immunodeficiency virus can be challenging, as various considerations must be taken into account including viral resistance mutations, patient comorbidities, drug interactions, and the potential for drug-related adverse effects and toxicities. Treatment is further complicated when a clinical scenario arises requiring an alteration in the dosage form. Factors ranging from dysphagia to administration through an enteral feeding tube can affect decisions regarding antiretroviral dosage forms. Limited pharmacokinetic data exist regarding the alteration of antiretroviral medications from their original form. Bioavailability may vary substantially between dosage forms, which can lead to unpredictable drug concentrations. Supratherapeutic or subtherapeutic antiretroviral drug concentrations can result in increased toxicity, virologic failure, or the emergence of drug resistance. We performed a systematic literature search to review the available antiretroviral literature on the modification of solid dosage forms as well as alternative routes of administration of oral antiretroviral agents and their application to clinical practice.

摘要

为感染人类免疫缺陷病毒的患者选择合适的抗逆转录病毒治疗方案具有挑战性,因为必须考虑多种因素,包括病毒耐药性突变、患者合并症、药物相互作用以及药物相关不良反应和毒性的可能性。当出现需要改变剂型的临床情况时,治疗会更加复杂。从吞咽困难到通过肠内喂养管给药等各种因素都会影响抗逆转录病毒剂型的决策。关于抗逆转录病毒药物从其原始剂型改变后的药代动力学数据有限。不同剂型之间的生物利用度可能有很大差异,这可能导致不可预测的药物浓度。超治疗或亚治疗性抗逆转录病毒药物浓度可能会导致毒性增加、病毒学失败或耐药性的出现。我们进行了系统的文献检索,以回顾有关固体剂型改变以及口服抗逆转录病毒药物替代给药途径及其在临床实践中的应用的现有抗逆转录病毒文献。

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