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在服用氯吡格雷的同时使用质子泵抑制剂并不会增加中国冠心病患者的不良临床结局风险。

Intermittent concurrent use of clopidogrel and proton pump inhibitors did not increase risk of adverse clinical outcomes in Chinese patients with coronary artery disease.

机构信息

Department of Cardiology, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, 107 Yanjiang West Rd., Guangzhou, 510120, Guangdong Province, China.

出版信息

BMC Cardiovasc Disord. 2021 Feb 5;21(1):75. doi: 10.1186/s12872-021-01884-z.

DOI:10.1186/s12872-021-01884-z
PMID:33546595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7863361/
Abstract

BACKGROUND

Proton pump inhibitors (PPIs) are frequently prescribed to patients with coronary heart disease (CHD) under antiplatelet therapy to prevent gastrointestinal (GI) bleeding. However, its clinical impact is still under debate, especially in Asian population. This study was undertaken to explore the effects of concurrent use of clopidogrel and PPIs on the clinical outcomes in Chinese patients with CHD in secondary prevention.

METHODS

A single-center retrospective study was conducted in 638 patients with CHD on consecutive clopidogrel therapy for at least 1 year. After 18-month follow-up, adverse clinical events were collected. Cox regression was used to calculate hazard ratios (HR) and 95% confidence interval (CI) for the effect of PPI use on the outcomes. A total of 638 patients were recruited from 2014 to 2015 in this study, among whom 201 were sustained PPI users, 188 were intermittent PPI users and the remaining 249 were non-PPI users.

RESULTS

Compared with sustained PPI users, intermittent use of PPIs was associated with a lower risk of stroke, major adverse cardiac events (MACE) and net adverse clinical event (NACE) (stroke: adjusted HR: 0.109, 95% CI 0.014-0.878, p = 0.037; MACE: adjusted HR: 0.293, 95% CI 0.119-0.722; p = 0.008; NACE: adjusted HR: 0.357, 95% CI 0.162-0.786, p = 0.011). Subgroup analysis further revealed the benefit of intermittent PPI use was significant in male CHD patients over 60 years old, with hypertension or chronic kidney disease, and undergoing percutaneous coronary intervention during hospitalization.

CONCLUSION

The current findings suggest that the intermittent concurrent use of PPIs and clopidogrel is not associated with an increased risk of 18-month adverse clinical outcomes, and intermittent use of PPIs is associated with a lower rate of MACE and NACE.

摘要

背景

质子泵抑制剂(PPIs)经常被开具给接受抗血小板治疗的冠心病(CHD)患者,以预防胃肠道(GI)出血。然而,其临床影响仍存在争议,尤其是在亚洲人群中。本研究旨在探讨冠心病二级预防中氯吡格雷联合质子泵抑制剂(PPI)的使用对中国患者临床结局的影响。

方法

对 638 例连续接受氯吡格雷治疗至少 1 年的 CHD 患者进行单中心回顾性研究。经过 18 个月的随访,收集不良临床事件。使用 Cox 回归计算 PPI 使用对结局影响的风险比(HR)和 95%置信区间(CI)。本研究共纳入 2014 年至 2015 年期间的 638 例患者,其中持续 PPI 使用者 201 例,间歇性 PPI 使用者 188 例,非 PPI 使用者 249 例。

结果

与持续 PPI 使用者相比,间歇性使用 PPI 与卒中、主要不良心脏事件(MACE)和净不良临床事件(NACE)的风险降低相关(卒中:调整后的 HR:0.109,95%CI 0.014-0.878,p=0.037;MACE:调整后的 HR:0.293,95%CI 0.119-0.722;p=0.008;NACE:调整后的 HR:0.357,95%CI 0.162-0.786,p=0.011)。亚组分析进一步显示,在年龄超过 60 岁、有高血压或慢性肾脏病、住院期间行经皮冠状动脉介入治疗的男性 CHD 患者中,间歇性使用 PPI 的获益更为显著。

结论

目前的研究结果表明,氯吡格雷联合质子泵抑制剂的间歇性同时使用与 18 个月不良临床结局的风险增加无关,且间歇性使用质子泵抑制剂与较低的 MACE 和 NACE 发生率相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/bcb1abb3301a/12872_2021_1884_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/c79ef896efd4/12872_2021_1884_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/1ab58ffc2445/12872_2021_1884_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/4fe0f2cd6eb8/12872_2021_1884_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/e10fd47f1d06/12872_2021_1884_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/d411fc2b3828/12872_2021_1884_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/bcb1abb3301a/12872_2021_1884_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/c79ef896efd4/12872_2021_1884_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/1ab58ffc2445/12872_2021_1884_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/4fe0f2cd6eb8/12872_2021_1884_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/e10fd47f1d06/12872_2021_1884_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/d411fc2b3828/12872_2021_1884_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e6/7863361/bcb1abb3301a/12872_2021_1884_Fig6_HTML.jpg

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