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[医院中的药物不良事件:使用触发工具的试点研究]

[Adverse drug events in hospital: pilot study with trigger tool].

作者信息

Rozenfeld Suely, Giordani Fabiola, Coelho Sonia

出版信息

Rev Saude Publica. 2013 Dec;47(6):1102-11. doi: 10.1590/s0034-8910.2013047004735.

Abstract

OBJECTIVE

To estimate the frequency of and to characterize the adverse drug events at a terciary care hospital.

METHODS

A retrospective review was carried out of 128 medical records from a hospital in Rio de Janeiro in 2007, representing 2,092 patients. The instrument used was a list of triggers, such as antidotes, abnormal laboratory analysis results and sudden suspension of treatment, among others. A simple random sample of patients aged 15 and over was extracted. Oncologic and obstetric patients were excluded as were those hospitalized for less than 48 hours or in the emergency room. Social and demographic characteristics and those of the disease of patients who underwent adverse events were compared with those of patients who did not in order to test for differences between the groups.

RESULTS

Around 70.0% of the medical records assessed showed at least one trigger. Adverse drug events triggers had an overall positive predictive value of 14.4%. The incidence of adverse drug events was 26.6 per 100 patients and 15.6% patients suffered one or more event. The median length of stay for patients suffering an adverse drug event was 35.2 days as against 10.7 days for those who did not (p < 0.01). The pharmacological classes most commonly associated with an adverse drug event were related to the cardiovascular system, nervous system and alimentary tract and metabolism. The most common active substances associated with an adverse drug event were tramadol, dypirone, glibenclamide and furosemide. Over 80.0% of events provoked or contributed to temporary harm to the patient and required intervention and 6.0% may have contributed to the death of the patient. It was estimated that in the hospital, 131 events involving drowsiness or fainting 33 involving falls, and 33 episodes of hemorrhage related to adverse drug effects occur annually.

CONCLUSIONS

Almost one-sixth of in-patients (16,0%) suffered an adverse drug event. The instrument used may prove useful as a technique for monitoring and evaluating patient care results. Psycothropic therapy should be critically appraised given the frequency of associated events, such as excessive sedation, lethargy, and hypotension.

摘要

目的

评估一家三级护理医院中药物不良事件的发生率并对其进行特征描述。

方法

对2007年里约热内卢一家医院的128份病历进行回顾性研究,这些病历涵盖2092名患者。所使用的工具是一份触发因素清单,如解毒剂、异常实验室分析结果和治疗突然中断等。抽取了15岁及以上患者的简单随机样本。肿瘤和产科患者以及住院时间少于48小时或在急诊室的患者被排除在外。将发生不良事件患者的社会和人口统计学特征以及疾病特征与未发生不良事件的患者进行比较,以检验两组之间的差异。

结果

约70.0%的评估病历显示至少有一个触发因素。药物不良事件触发因素的总体阳性预测值为14.4%。药物不良事件的发生率为每100名患者26.6例,15.6%的患者发生了一次或多次事件。发生药物不良事件患者的中位住院时间为35.2天,而未发生不良事件患者的中位住院时间为10.7天(p < 0.01)。与药物不良事件最常相关的药理学类别与心血管系统、神经系统、消化道和代谢有关。与药物不良事件最常相关的活性物质是曲马多、安乃近、格列本脲和呋塞米。超过80.0%的事件引发或促成了对患者的暂时伤害并需要干预,6.0%的事件可能导致了患者死亡。据估计,该医院每年发生131例与嗜睡或昏厥有关的事件、33例与跌倒有关的事件以及33例与药物不良反应有关的出血事件。

结论

近六分之一的住院患者(16.0%)发生了药物不良事件。所使用的工具可能被证明是一种监测和评估患者护理结果的有用技术。鉴于相关事件(如过度镇静、嗜睡和低血压)的发生频率,应对精神药物治疗进行严格评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e9/4206103/adc0ca0624f4/rsp-47-06-1102-g01.jpg

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