首页> 外文期刊>Pharmacoepidemiology and drug safety >Risk of upper gastrointestinal complications in a cohort of users of nimesulide and other nonsteroidal anti-inflammatory drugs in Friuli Venezia Giulia, Italy.
【24h】

Risk of upper gastrointestinal complications in a cohort of users of nimesulide and other nonsteroidal anti-inflammatory drugs in Friuli Venezia Giulia, Italy.

机译:尼夏德和其他非甾体抗炎药中群体群体中胃肠道并发症的风险在意大利。

获取原文
获取原文并翻译 | 示例
           

摘要

Information on the risk of upper gastrointestinal complications (UGIC) in users of nimesulide, the most used nonsteroidal anti-inflammatory drug (NSAID) in Italy, is scarce. In the context of the European regulatory review on nimesulide, we estimated and compared the risk associated with nimesulide and other individual NSAIDs with the risk in nonusers.We used 2001-2008 data from regional health databases in Friuli Venezia Giulia (FVG), Italy, to conduct a cohort and nested case-control study of users of NSAIDs. Cases were identified by specific and nonspecific hospital discharge diagnoses in primary and secondary position and validated through hospital records. Ten controls per case were selected using density-based sampling from the cohort. Conditional logistic regression was used to estimate adjusted relative risks (RRs) and 95% confidence intervals (CIs).The cohort included 588,827 NSAIDs users and 3031 UGIC cases. Nonspecific codes contributed to 23% of cases and secondary codes to 5%. Among current users, IR per 1000 person-years decreased from 4.45 cases in 2001 to 2.21 cases in 2008. The RR (95%CI) for current use of NSAIDs was 3.28 (2.86, 3.76). RR was <2 for rofecoxib, celecoxib, and nimesulide; 2 to <5 for naproxen, ibuprofen, diclofenac, etoricoxib, and meloxicam; and ≥ 5 for ketoprofen, piroxicam, and ketorolac.IRs of UGIC in FVG decreased about 50% between 2001 and 2008. Nimesulide was in the low-medium range of RR. A complete ascertainment of UGIC cases in databases may require validation of nonspecific codes, secondary codes, and additional codes such as peritonitis and acute posthemorrhagic anemia.
机译:有关尼夏德(Nimesulide)的上胃肠道并发症(UGIC)风险的信息,即意大利最常用的非甾体抗炎药(NSAID)是稀缺的。在欧洲对尼夏德的监管审查的背景下,我们估计并比较了与Nimesulide和其他个人NSAID相关的风险与非用户的风险相比。我们使用2001-2008来自Friuli Venezia Giulia(FVG),意大利的区域健康数据库的数据,对NSAIDS用户进行队列和嵌套案例控制研究。通过特定的和非特异性医院放电诊断鉴定初级和次要地位并通过医院记录进行验证。使用来自群组的基于密度的取样来选择每种情况的十个控制。条件逻辑回归用于估计调整后的相对风险(RRS)和95%的置信区间(CIS)。队列包括588,827个NSAIDS用户和3031个UGIC病例。非特异性代码有助于23%的病例和二级代码至5%。当前用户之间,每1000人的IR从2001年的4.45例减少到2008年的2.21例。目前使用NSAID的RR(95%CI)为3.28(2.86,3.76)。 rr为rofecoxib,celecoxib和nimesulide的<2。 2至<5用于萘普生,布洛芬,双氯芬酸,肉毒糖苷和美洛昔康; ≥5对于酮洛芬,皮索里康和酮洛拉克的FVG中的ketorolacs。2001年至2008年之间的UGIC在50%之间降低了约50%。尼美介质在低介质范围的RR中。数据库中的UGIC病例完全确定可能需要验证非特异性代码,二次代码和额外代码,例如腹膜炎和急性假血管性贫血。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号