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磷酸二酯酶 5 抑制剂与前列地尔治疗冠心病患者的生存预后比较。

Association of Phosphodiesterase-5 Inhibitors Versus Alprostadil With Survival in Men With Coronary Artery Disease.

机构信息

Department of Medicine Huddinge H7, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.

Functional Area of Emergency Medicine, Karolinska University Hospital, Huddinge, Stockholm, Sweden.

出版信息

J Am Coll Cardiol. 2021 Mar 30;77(12):1535-1550. doi: 10.1016/j.jacc.2021.01.045.

Abstract

BACKGROUND

Phosphodiesterase 5 inhibitor (PDE5i) treatment is associated with reduced mortality compared with no treatment for erectile dysfunction after myocardial infarction (MI).

OBJECTIVES

This study sought to investigate the association between treatment with PDE5i or alprostadil and outcomes in men with stable coronary artery disease.

METHODS

All Swedish men with a prior MI or revascularization who received PDE5i or alprostadil during 2006 through 2013 at >6 months after the event were included, using the Swedish Patient Register and the Swedish Prescribed Drug Register. Cox regression was used to estimate adjusted hazard ratios with 95% confidence intervals for all-cause mortality, MI, heart failure, cardiovascular mortality, noncardiovascular mortality, cardiac revascularization, peripheral arterial disease, and stroke in men treated with PDE5i versus alprostadil.

RESULTS

This study included 16,548 men treated with PDE5i and 1,994 treated with alprostadil. The mean follow-up was 5.8 years, with 2,261 deaths (14%) in the PDE5i group and 521 (26%) in the alprostadil group. PDE5i compared with alprostadil treatment was associated with lower mortality (hazard ratio: 0.88; 95% confidence interval: 0.79 to 0.98) and with similar associations for MI, heart failure, cardiovascular mortality, and revascularization. When quintiles (q) of filled PDE5i prescriptions were compared using q1 as reference, patients in q3, q4, and q5 had lower all-cause mortality. Among alprostadil users, those in q5 had a lower all-cause mortality compared to q1.

CONCLUSIONS

In men with stable coronary artery disease, treatment with PDE5i is associated with lower risks of death, MI, heart failure, and revascularization compared with alprostadil treatment. Although the decrease in all-cause mortality was PDE5i dose dependent, the data do not permit the inference of causality or any clinical benefits of PDE5i because of the observational study design.

摘要

背景

与未接受治疗相比,磷酸二酯酶 5 抑制剂 (PDE5i) 治疗可降低心肌梗死后勃起功能障碍患者的死亡率。

目的

本研究旨在探讨 PDE5i 或前列地尔治疗与稳定型冠状动脉疾病男性患者结局的相关性。

方法

使用瑞典患者登记处和瑞典处方药物登记处,纳入 2006 年至 2013 年期间在事件发生后 >6 个月时接受 PDE5i 或前列地尔治疗的所有瑞典男性心肌梗死或血运重建患者。采用 Cox 回归模型估计 PDE5i 与前列地尔治疗的男性全因死亡率、心肌梗死、心力衰竭、心血管死亡率、非心血管死亡率、心脏血运重建、外周动脉疾病和卒中等所有原因死亡率的调整后危险比及其 95%置信区间。

结果

本研究纳入了 16548 名接受 PDE5i 治疗的男性和 1994 名接受前列地尔治疗的男性。平均随访时间为 5.8 年,PDE5i 组有 2261 例死亡(14%),前列地尔组有 521 例(26%)。与前列地尔治疗相比,PDE5i 治疗与死亡率降低相关(风险比:0.88;95%置信区间:0.79 至 0.98),并且与心肌梗死、心力衰竭、心血管死亡率和血运重建的相关性相似。与 q1 相比,q3、q4 和 q5 的 PDE5i 处方填充量较高时,所有原因死亡率均较低。在前列地尔使用者中,q5 组的全因死亡率低于 q1 组。

结论

在稳定型冠状动脉疾病男性中,与前列地尔治疗相比,PDE5i 治疗可降低死亡、心肌梗死、心力衰竭和血运重建的风险。尽管全因死亡率与 PDE5i 剂量呈剂量依赖性降低,但由于观察性研究设计,数据不能推断 PDE5i 的因果关系或任何临床获益。

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