首页> 美国卫生研究院文献>Journal of Clinical Biochemistry and Nutrition >Dual antiplatelet therapy does not affect the incidence of low-dose aspirin-induced small intestinal mucosal injury in patients after percutaneous coronary intervention for coronary stenosis: a multicenter cross-sectional study
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Dual antiplatelet therapy does not affect the incidence of low-dose aspirin-induced small intestinal mucosal injury in patients after percutaneous coronary intervention for coronary stenosis: a multicenter cross-sectional study

机译:双重抗血小板治疗不影响经皮冠状动脉介入治疗冠状动脉狭窄后低剂量阿司匹林引起的小肠粘膜损伤的发生率:多中心横断面研究

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摘要

Although low-dose aspirin (LDA) is known to induce small intestinal mucosal injury, the effect of dual antiplatelet therapy (DAPT; LDA + clopidogrel) on small intestinal mucosa in patients after percutaneous coronary intervention (PCI) for coronary stenosis is unknown. Fifty-one patients with a history of PCI and LDA use were enrolled, and 45 eligible patients were analyzed. Patients were grouped based on DAPT (DAPT: n = 10 and non-DAPT: n = 35) and proton pump inhibitor (PPI) use (PPI user: n = 22 and PPI-free patients: n = 23) to compare small intestinal endoscopic findings. The relationship between LDA-use period and small intestinal endoscopic findings was also examined. Multivariate analysis was performed to identify risk factors for LDA-induced mucosal injury using age, sex, DAPT, PPI, gastric mucoprotective drug, and LDA-use period. The rate of small intestinal mucosal injury incidence did not significantly differ between DAPT and non-DAPT patients (50% vs 51.1%, respectively; p = 0.94), or PPI users and PPI-free patients (50% vs 52.2%, respectively; p = 0.88). Additionally, LDA-use period of ≤24 months (n = 15) yielded a significantly higher rate of small intestinal mucosal injury incidence than LDA-use period >24 months (n = 30) (80% vs 36.7%, respectively; p = 0.006). Multivariate analysis revealed that a LDA-use period of ≤24 months was a significant risk factor for small intestinal mucosal injury (odds ratio: 19.5, 95% confidence interval: 2.48–154.00, p = 0.005). Following PCI for coronary stenosis, neither DAPT nor PPI affected LDA-induced small intestinal mucosal injury. Moreover, patients who used LDA within the last 24 months were at a greater risk of small intestinal mucosal injury.
机译:尽管已知小剂量阿司匹林(LDA)会引起小肠粘膜损伤,但在针对冠状动脉狭窄的经皮冠状动脉介入治疗(PCI)后,双重抗血小板治疗(DAPT; LDA +氯吡格雷)对小肠粘膜的作用尚不清楚。入选了51名具有PCI和LDA使用史的患者,并对45例合格患者进行了分析。根据DAPT(DAPT:n = 10和非DAPT:n = 35)和使用质子泵抑制剂(PPI)(PPI用户:n = 22和无PPI的患者:n = 23)对患者进行分组以比较小肠内窥镜检查结果。还检查了LDA使用期与小肠内窥镜检查结果之间的关系。使用年龄,性别,DAPT,PPI,胃粘膜保护药物和LDA使用期限,进行多变量分析以识别LDA诱导的粘膜损伤的危险因素。 DAPT和非DAPT患者之间的小肠粘膜损伤发生率没有显着差异(分别为50%和51.1%; p = 0.94),或者PPI使用者和无PPI的患者(分别为50%和52.2%; p = 0.88)。此外,≤24个月(n = 15)的LDA使用期比> 24个月(n = 30)的LDA使用期产生的小肠粘膜损伤发生率显着更高(分别为80%和36.7%; p = 0.006)。多变量分析显示,LDA使用期≤24个月是小肠粘膜损伤的重要危险因素(几率:19.5,95%置信区间:2.48–154.00,p = 0.005)。 PCI治疗冠状动脉狭窄后,DAPT和PPI均未影响LDA引起的小肠粘膜损伤。此外,在过去24个月内使用LDA的患者发生小肠粘膜损伤的风险更大。

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