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首页> 外文期刊>Pharmacoepidemiology and drug safety >Increased risk of hospitalization for acute hepatitis in patients with previous exposure to NSAIDs.
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Increased risk of hospitalization for acute hepatitis in patients with previous exposure to NSAIDs.

机译:急性肝炎住院风险增加,患者以前接触NSAIDs。

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BACKGROUND: Epidemiological studies related to hospitalization due to the hepatotoxicity of traditional non-steroidal anti-inflammatory drugs (NSAIDs) are infrequent, and case reports of hepatotoxicity of nimesulide, celecoxib, and rofecoxib seem to be increasing. The reimbursement database of National Health Insurance (NHI) in Taiwan provided an opportunity for post-marketing surveillance. We conducted this study to determine the association between the use of hepatoxic NSAIDs and increased hospitalizations related to acute hepatitis. METHODS: We included hospitalized subjects with a major diagnosis of acute or sub-acute necrosis of liver or toxic hepatitis and excluded viral and other causes of hepatobiliary diseases from the NHI database from 1 April 2001 to 31 December 2004. We applied two kinds of models to analyze by uni-directional and bi-directional case-crossover designs during the 28 days exposure periods and performed conditional logistic regression models. RESULTS: There were 4519 cases of hospitalization relating to acute hepatitis, and the odds ratios of celecoxib, nimesulide, dicofenac, ibuprofen, and other hepatoxic NSAIDs were significantly increased. Compared with the adjusted odds ratios of other hepatoxic NSAIDs (OR = 2.13, 95%CI = 2.00, 2.28), celecoxib (OR =1.92, 95%CI = 1.38, 2.69) was similar during the 28 days by our uni-directional case-crossover design. CONCLUSIONS: Our results provide evidence for an increased risk of hospitalization with acute hepatitis among hepatoxic NSAIDs including celecoxib users. Further mechanistic research is warranted in order to document celecoxib's hepatotoxicity.
机译:背景技术由于传统非甾体抗炎药(NSAIDs)的肝毒性与住院有关的流行病学研究是不常见的,尼夏德,Celecoxib和Rofecoxib的肝毒性的病例报告似乎正在增加。台湾国家健康保险(NHI)的报销数据库为营销后监督提供了机会。我们进行了该研究,以确定肝毒性NSAID的使用和增加与急性肝炎有关的住院治疗之间的关联。方法:在2001年4月1日至2004年12月1日,我们包括肝脏或患有肝脏或患者肝炎的急性或亚急性坏死的急性或亚急性坏死的主要诊断,并排除了来自NHI数据库的病毒和其他原因。我们应用了两种模型在28天曝光期间通过单向和双向壳体交叉设计进行分析,并进行条件逻辑回归模型。结果:急性肝炎有4519例住院病例,塞克西布,尼夏德,双芬太芬,布洛芬和其他肝毒性NSAID的几率比例显着增加。与其他肝毒性NSAID的调整后的差距相比(或= 2.13,95%CI = 2.00,2.28),在我们的单向案件的28天中,塞克莫昔布(或= 1.92,95%CI = 1.38,2.69)相似-Crossover设计。结论:我们的结果提供了肝毒性NSAID在包括Celecoxib用户在内的肝毒性NSAID之间与急性肝炎的风险增加的证据。有必要进行进一步的机制研究,以便于塞克西布的肝毒性。

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