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重症监护环境中的药物不良反应:一项系统综述。

Adverse Drug Reactions in Critical Care Settings: A Systematic Review.

作者信息

Lisha Joshua, Annalakshmi Velu, Maria Jose, Padmini Devi

机构信息

Department of Pharmacology, Gulf Medical University, Ajman. United Arab Emirates.

Department of Pharmacology, St. John's Medical College, St John's National Academy of Health Sciences, Bangalore, Karnataka. India.

出版信息

Curr Drug Saf. 2017;12(3):147-161. doi: 10.2174/1574886312666170710192409.

DOI:10.2174/1574886312666170710192409
PMID:28699492
Abstract

BACKGROUND

The prevalence of adverse drug reactions is reported to be high in critical care units. We conducted a systematic review to study the prevalence, drugs implicated, preventability, predictability, severity and determinants of adverse drug reactions in critical care settings.

METHODS

We searched MEDLINE, EMBASE, PROQUEST and OVID (January 1995 to June 2015) using pre-specified appropriate medical subject heading terms. Of 1552 studies, 34 studies were included for data extraction and synthesis.

RESULTS

Overall, the prevalence of adverse drug reactions was 0.3% to 17% in paediatric intensive care units and 4.5% to 34.1% in adult intensive care units. The highest prevalence reported among critical care settings was 117.4 per 1000 patient days. The most common drug classes implicated were antimicrobials in the medical intensive care units, cardiovascular drugs and anticoagulants in the coronary care units, and analgesics and sedatives in the surgical care units. The prevalence of fatal and severe adverse drug reactions ranged from 0.9 to 19% and 5.7 to 28.6% respectively. The predictable and preventable adverse drug reactions ranged from 74.3 to 90.2% and 8.6 to 62.8% respectively. Only 8 studies reported patient outcomes. About 5.6% to 25.5% of patients died.

CONCLUSION

There is wide variation in prevalence, characteristics and drug classes implicated in the occurrence of adverse drug reactions by type of intensive care unit. Findings of this study would help health care professionals to optimise pharmacotherapy in critical care settings.

摘要

背景

据报道,重症监护病房中药物不良反应的发生率很高。我们进行了一项系统综述,以研究重症监护环境中药物不良反应的发生率、涉及的药物、可预防性、可预测性、严重程度及决定因素。

方法

我们使用预先指定的适当医学主题词,检索了MEDLINE、EMBASE、PROQUEST和OVID数据库(1995年1月至2015年6月)。在1552项研究中,有34项研究被纳入数据提取和综合分析。

结果

总体而言,儿科重症监护病房中药物不良反应的发生率为0.3%至17%,成人重症监护病房中为4.5%至34.1%。在重症监护环境中报告的最高发生率为每1000患者日117.4例。涉及的最常见药物类别在医疗重症监护病房中是抗菌药物,在冠心病监护病房中是心血管药物和抗凝剂,在外科监护病房中是镇痛药和镇静剂。致命和严重药物不良反应的发生率分别为0.9%至19%和5.7%至28.6%。可预测和可预防的药物不良反应发生率分别为74.3%至90.2%和8.6%至62.8%。只有8项研究报告了患者结局。约5.6%至25.5%的患者死亡。

结论

不同类型的重症监护病房中,药物不良反应的发生率、特征及涉及的药物类别存在很大差异。本研究结果将有助于医护人员在重症监护环境中优化药物治疗。

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