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药物警戒对沙特阿拉伯教学医院内科住院患者药物不良反应报告的影响。

Impact of pharmacovigilance on adverse drug reactions reporting in hospitalized internal medicine patients at Saudi Arabian teaching hospital.

作者信息

Khan Lateef M, Al-Harthi Sameer E, Saadah Omar I, Al-Amoudi Ahmed B, Sulaiman Mansour I, Ibrahim Ibrahim M

机构信息

Department of Pharmacology, College of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.

出版信息

Saudi Med J. 2012 Aug;33(8):863-8.

Abstract

OBJECTIVES

To determine the incidence, diversity of adverse drug reactions (ADRs), and impact of pharmacovigilance on reporting it.

METHODS

This prospective and retrospective study was carried out in the Department of Medicine, King Abdulaziz University Hospital, Jeddah, Kingdom of Saudi Arabia between January to December 2011 in 600 patients of ADR. Data regarding age and gender distribution of the patients, incidence rate, drugs, body systems/organs involved in ADR, time of occurrence of adverse drug reactions, total number of drugs administered, and impact of pharmacovigilance on finding the incidence rate of ADR were recorded. Comparison of the 2 data was carried out to determine the impact of pharmacovigilance.

RESULTS

Incidence rate of ADRs in retrospective study was 3.1% and 5.5% in the prospective study. The highest incidence of ADR (retrospective 15% and prospective 14.5%) was observed in both groups in patients receiving more than 10 drugs. The frequency of ADR in relation to age in both groups was highest in patients of age >60 years; it was 52.7% in retrospective study and 54.5% in prospective study. Antibiotics were the more frequently involved in ADR, (48.5% in prospective study and 36.9% in retrospective study). The system most commonly involved in ADR was gastrointestinal tract 47.4% in retrospective study and 57.6% in prospective study. None of the ADR proved to be fatal.

CONCLUSION

Low incidence of hospitalized ADR in our study (5.5%) is due to lack of awareness in healthcare professionals in reporting ADR. Undoubtedly, pharmacovigilance brought more patients with ADR to record.

摘要

目的

确定药物不良反应(ADR)的发生率、多样性以及药物警戒对其报告的影响。

方法

这项前瞻性和回顾性研究于2011年1月至12月在沙特阿拉伯王国吉达阿卜杜勒阿齐兹国王大学医院内科进行,涉及600例药物不良反应患者。记录了患者的年龄和性别分布、发生率、药物、涉及药物不良反应的身体系统/器官、药物不良反应发生时间、给药药物总数以及药物警戒对发现药物不良反应发生率的影响。对两组数据进行比较以确定药物警戒的影响。

结果

回顾性研究中药物不良反应的发生率为3.1%,前瞻性研究中为5.5%。在接受超过10种药物的患者中,两组观察到的药物不良反应发生率最高(回顾性为15%,前瞻性为14.5%)。两组中与年龄相关的药物不良反应发生率在年龄>60岁的患者中最高;回顾性研究中为52.7%,前瞻性研究中为54.5%。抗生素更常涉及药物不良反应(前瞻性研究中为48.5%,回顾性研究中为36.9%)。药物不良反应最常涉及的系统是胃肠道,回顾性研究中为47.4%,前瞻性研究中为57.6%。没有药物不良反应被证明是致命的。

结论

我们研究中住院患者药物不良反应发生率较低(5.5%)是由于医护人员在报告药物不良反应方面缺乏意识。毫无疑问,药物警戒使更多药物不良反应患者得以记录。

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