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A practical guide to monitoring for adverse drug reactions during antihypertensive drug therapy.

机译:在降压药物治疗期间监测药物不良反应的实用指南。

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摘要

Monitoring of patients taking antihypertensive treatment can identify potential adverse drug reactions (ADRs). However, published guidelines give divergent or incomplete recommendations on monitoring for ADRs. Using a predetermined strategy, we undertook a systematic review to identify hypertension guidelines published from January 2001 to October 2011 with recommendations for monitoring for ADRs. We screened 88 abstracts and 187 web-based guidelines, and identified 19 published guidelines on monitoring the biochemical effects of antihypertensive drug therapy. We then produced a set of practical clinical guidelines, synthesized from those recommendations. Our recommendations are designed to provide efficient monitoring. They reduce the number of tests to a minimum consistent with safe practice and align monitoring schedules, so that creatinine, potassium and sodium concentrations are measured at the same times in all cases. The instructions for biochemical monitoring in current guidelines differ greatly, both in the extent of advice and in the detail provided. The current lack of consistent and workable instructions poses serious difficulties for practitioners. The recommendations distilled from this systematic review should help practitioners when they monitor therapy with antihypertensive drugs.
机译:监测接受降压治疗的患者可以确定潜在的药物不良反应(ADR)。但是,已发布的指南对ADR的监控提出了不同或不完整的建议。使用预定策略,我们进行了系统的审查,以确定2001年1月至2011年10月发布的高血压指南,以及监测ADR的建议。我们筛选了88篇摘要和187篇基于网络的指南,并确定了19篇关于监测降压药物治疗的生化作用的已发表指南。然后,我们根据这些建议制定了一套实用的临床指南。我们的建议旨在提供有效的监控。他们将检测次数减少到最低程度,以符合安全惯例并调整监测时间表,从而在所有情况下都同时测量肌酐,钾和钠的浓度。当前指南中有关生化监测的说明在建议的范围和所提供的详细信息上都大相径庭。当前缺乏一致和可行的指示给从业者带来了严重的困难。从本系统综述中提炼的建议应可帮助从业人员监控降压药的治疗。

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