首页> 外文期刊>Acta Pharmacologica Sinica >Risk factors of adverse drug reaction from non-steroidal anti-inflammatory drugs in Shanghai patients with arthropathy
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Risk factors of adverse drug reaction from non-steroidal anti-inflammatory drugs in Shanghai patients with arthropathy

机译:上海关节炎患者非甾体类抗炎药引起药物不良反应的危险因素

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AIM: The study was to screen the possible risk factors of adverse drag reaction (ADR) induced by non-steroidal anti-inflammatory drugs (NSAIDs) in Shanghai patients with arthropathy. METHODS: The subjects were randomly selected from a database of outpatients with arthropathy from 9 main hospitals in Shanghai. A door to door retrospective epidemiological survey was used to collect demographic information about the patients, both individual and familial. This included data on their medical histories, lifestyle and dietary habits, history of smoking and alcohol consumption, history of drug therapy, quality of life (QOL) prior to NSAIDs intake, history of NSAIDs therapy and its ADR events, etc. Descriptive statistical methods and univariate analysis were also used to identify possible risk factors for ADRs induced by NSAIDs. RESULTS: Of the 1002 patients surveyed, the average length of NSAIDs intake was 2 years. ADR incidence from different NSAIDs was high, in a range from 46.7%-66.2%. In general, the candidate risk factors for ADRs were different for each NSAID. Each of the candidate risk factors were defined and studied in order to evaluate its role in the determination of ADRs from NSAIDs. "Family history of ADRs caused by NSAIDs" was found to be a significant risk factor for the four commonly used NSAIDs: meloxicam, diclofenac, nimesulide, and nabumetone. CONCLUSION: A retrospective epidemiological survey was useful in detecting the risk factors for ADRs caused by NSAIDs. The study found that different NSAIDs might have different risk factors and that there is no single risk factor universally applicable to all NSAIDs.
机译:目的:本研究旨在筛查非甾体类抗炎药(NSAIDs)在上海关节炎患者中引起的不良药物不良反应(ADR)的可能危险因素。方法:从上海9家主要医院的关节病门诊患者数据库中随机选择受试者。进行了门到门的回顾性流行病学调查,以收集有关个体和家族患者的人口统计信息。其中包括有关他们的病史,生活方式和饮食习惯,吸烟和饮酒史,药物治疗史,服用NSAID之前的生活质量(QOL),NSAID治疗史及其ADR事件等数据。描述性统计方法还使用单变量分析来确定由NSAID引起的ADR的可能危险因素。结果:在接受调查的1002名患者中,非甾体抗炎药的平均摄入时间为2年。来自不同NSAID的ADR发生率很高,范围为46.7%-66.2%。通常,每个NSAID的ADR候选危险因素均不同。定义并研究了每种候选风险因素,以评估其在确定NSAID中ADR中的作用。发现“由非甾体抗炎药引起的ADR家族史”是四种常用非甾体抗炎药的重要危险因素:美洛昔康,双氯芬酸,尼美舒利和萘丁美酮。结论:回顾性流行病学调查有助于检测由非甾体抗炎药引起的不良反应的危险因素。研究发现,不同的非甾体抗炎药可能具有不同的危险因素,并且没有一种普遍适用于所有非甾体抗炎药的危险因素。

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