服用选择性 COX-2 抑制剂的患者发生上消化道出血的风险因素:一项全国范围内基于人群的队列研究。
Risk Factors for Upper Gastrointestinal Bleeding in Patients Taking Selective COX-2 Inhibitors: A Nationwide Population-Based Cohort Study.
机构信息
Department of Medicine, National Yang-Ming University, School of Medicine, Taipei, Taiwan.
Division of Gastroenterology, Department of Medicine.
出版信息
Pain Med. 2018 Feb 1;19(2):225-231. doi: 10.1093/pm/pnx097.
OBJECTIVE
Cyclooxygenase-2 inhibitors (coxibs) are associated with less upper gastrointestinal bleeding (UGIB) than traditional nonsteroidal anti-inflammatory drugs (tNSAIDs). However, they also increase the risk of UGIB in high-risk patients. We aimed to identify the risk factors of UGIB in coxibs users.
DESIGN
Retrospective cohort study.
SETTING
2000-2010 National Health Insurance Research Database of Taiwan.
SUBJECTS
Patients taking coxibs as the study group and patients not taking any coxibs as controls.
METHODS
After age, gender, and comorbidity matching by propensity score, 12,145 coxibs users and 12,145 matched controls were extracted for analysis. The primary end point was the occurrence of UGIB. Cox multivariate proportional hazard regression models were used to determine the risk factors for UGIB among all the enrollees and coxibs users.
RESULTS
During a mean follow-up of three years, coxibs users had significantly higher incidence of UGIB than matched controls (P < 0.001, log-rank test). Cox regression analysis showed that coxibs increased risk of UGIB in all participants (hazard ratio = 1.37, 95% confidence interval = 1.19-1.55, P < 0.001). Independent risk factors for UGIB among coxibs users were age, male gender, diabetes, chronic renal disease, cirrhosis, history of peptic ulcer disease, PU bleeding (PUB), Helicobacter pylori (H. pylori) infection, and concomitant use of tNSAIDs, acetylsalicylic acid, or thienopyridines.
CONCLUSIONS
Among coxibs users, H. pylori infection and history of PUB were especially important risk factors for UGIB. Further studies are needed to determine whether proton pump inhibitors might play a protective role in these at-risk patients.
目的
环氧化酶-2 抑制剂(COXIBs)与传统非甾体抗炎药(tNSAIDs)相比,上消化道出血(UGIB)的风险较低。然而,它们也会增加高危患者发生 UGIB 的风险。我们旨在确定 COXIBs 使用者发生 UGIB 的危险因素。
设计
回顾性队列研究。
设置
台湾 2000-2010 年国家健康保险研究数据库。
受试者
服用 COXIBs 的患者为研究组,未服用任何 COXIBs 的患者为对照组。
方法
通过倾向评分进行年龄、性别和合并症匹配后,共提取 12145 例 COXIBs 使用者和 12145 例匹配对照者进行分析。主要终点是 UGIB 的发生。采用 Cox 多变量比例风险回归模型确定所有入组者和 COXIBs 使用者发生 UGIB 的危险因素。
结果
在平均 3 年的随访期间,COXIBs 使用者的 UGIB 发生率明显高于匹配对照组(P<0.001,对数秩检验)。Cox 回归分析显示,COXIBs 增加了所有参与者发生 UGIB 的风险(危险比=1.37,95%置信区间=1.19-1.55,P<0.001)。COXIBs 使用者发生 UGIB 的独立危险因素包括年龄、男性、糖尿病、慢性肾脏病、肝硬化、消化性溃疡病史、PU 出血(PUB)、幽门螺杆菌(H. pylori)感染以及同时使用 tNSAIDs、乙酰水杨酸或噻吩吡啶类药物。
结论
在 COXIBs 使用者中,H. pylori 感染和 PUB 病史是 UGIB 的重要危险因素。需要进一步研究质子泵抑制剂是否对这些高危患者具有保护作用。