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螺内酯治疗收缩性心力衰竭的疗效和安全性。

Effectiveness and safety of spironolactone for systolic heart failure.

机构信息

Division of Research, Kaiser Permanente Northern California, Oakland, California; Department of Cardiology, Kaiser Permanente Santa Clara Medical Center, Santa Clara, California; Department of Health Research and Policy, Stanford University School of Medicine, Stanford, California.

出版信息

Am J Cardiol. 2013 Nov 1;112(9):1427-32. doi: 10.1016/j.amjcard.2013.06.039. Epub 2013 Sep 13.

Abstract

Aldosterone receptor antagonists have been shown in randomized trials to reduce morbidity and mortality in adults with symptomatic systolic heart failure. We studied the effectiveness and safety of spironolactone in adults with newly diagnosed systolic heart failure in clinical practice. We identified all adults with newly diagnosed heart failure, left ventricular ejection fraction of <40%, and no previous spironolactone use from 2006 to 2008 in Kaiser Permanente Northern California. We excluded patients with baseline serum creatinine level of >2.5 mg/dl or a serum potassium level of >5.0 mEq/L. We used Cox regression with time-varying covariates to evaluate the independent association between spironolactone use and death, hospitalization, severe hyperkalemia, and acute kidney injury. Among 2,538 eligible patients with a median follow-up of 2.5 years, 521 patients (22%) initiated spironolactone, which was not associated with risk of hospitalization (adjusted hazard ratio 0.91, 95% confidence interval 0.77 to 1.08) or death (adjusted hazard ratio 0.93, confidence interval 0.60 to 1.44). Crude rates of severe hyperkalemia and acute kidney injury during spironolactone use were similar to that seen in clinical trials. Spironolactone was independently associated with a 3.5-fold increased risk of hyperkalemia but not with acute kidney injury. Within a diverse community-based cohort with incident systolic heart failure, use of spironolactone was not independently associated with risks of hospitalization or death. Our findings suggest that the benefits of spironolactone in clinical practice may be reduced compared with other guideline-recommended medications.

摘要

醛固酮受体拮抗剂在随机试验中已被证明可降低有症状的收缩性心力衰竭成人的发病率和死亡率。我们研究了螺内酯在临床实践中对新诊断为收缩性心力衰竭的成年人的有效性和安全性。我们从 2006 年至 2008 年在 Kaiser Permanente Northern California 确定了所有新诊断为心力衰竭、左心室射血分数<40%且以前未使用过螺内酯的成年人。我们排除了基线血清肌酐水平>2.5 mg/dl 或血清钾水平>5.0 mEq/L 的患者。我们使用时变协变量的 Cox 回归来评估螺内酯使用与死亡、住院、严重高钾血症和急性肾损伤之间的独立关联。在中位随访 2.5 年的 2538 名合格患者中,有 521 名患者(22%)开始使用螺内酯,其与住院风险(校正风险比 0.91,95%置信区间 0.77 至 1.08)或死亡风险(校正风险比 0.93,置信区间 0.60 至 1.44)无关。在使用螺内酯期间,严重高钾血症和急性肾损伤的发生率与临床试验相似。螺内酯与高钾血症的风险增加 3.5 倍相关,但与急性肾损伤无关。在一个有事件性收缩性心力衰竭的多样化社区队列中,螺内酯的使用与住院或死亡风险无关。我们的研究结果表明,与其他指南推荐的药物相比,螺内酯在临床实践中的益处可能会降低。

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