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药品标签外使用:伦理、实践和未来方向。

Off-label medicine use: Ethics, practice and future directions.

机构信息

BPharm (Hons), PhD, MPS, Professor and Director, Centre for Medicine Use and Safety, Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Vic.

BSc (Hons), Centre for Evidence-Based Medicine, Nuffield Department of Primary Care Health Sciences, University of Oxford, Radcliffe Observatory Quarter, Woodstock Road, UK.

出版信息

Aust J Gen Pract. 2021 May;50(5):329-331. doi: 10.31128/AJGP-08-20-5591.

Abstract

BACKGROUND

Medicine use is considered off-label when used for an indication, at a dose, via a route of administration or in a patient group not included in the approved product information. Off-label use varies according to therapeutic class and patient group, and often occurs in those who are vulnerable.

OBJECTIVE

The aim of this article is to discuss ethical, practice and policy considerations associated with off-label medicine use.

DISCUSSION

A number of professional organisations have issued guidance in relation to off-label medicine use. Prescribers should inform patients and document consent when prescribing off-label, including an open discussion about known and unknown benefits and risks. It is important that the prescriber documents the reason for off-label use in the patient's record and ensures that patients are aware of the intended duration and relevant monitoring. Australia's new national health priority of Quality Use of Medicine and Medicine Safety should stimulate all stakeholders including consumers to work together to address off-label medicine use.

摘要

背景

当药物用于批准的产品信息中未包含的适应证、剂量、给药途径或患者群体时,即被视为超适应证用药。超适应证用药因治疗类别和患者群体而异,通常发生在易受影响的人群中。

目的

本文旨在讨论与超适应证用药相关的伦理、实践和政策问题。

讨论

许多专业组织已经发布了与超适应证用药相关的指南。当开具超适应证处方时,处方者应告知患者并记录其同意,包括对已知和未知益处和风险的公开讨论。处方者在患者记录中记录超适应证用药的原因并确保患者了解预期持续时间和相关监测非常重要。澳大利亚新的国家卫生重点——合理用药和药物安全,应激励包括消费者在内的所有利益相关者共同努力解决超适应证用药问题。

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