Department of Anesthesiology, Division of Cardiology, Vanderbilt University School of Medicine, Nashville, TN, USA.
Crit Care Med. 2012 Oct;40(10):2805-12. doi: 10.1097/CCM.0b013e31825b8be2.
This study tested the hypothesis that interruption of the renin-angiotensin system with either an angiotensin-converting enzyme inhibitor or a mineralocorticoid receptor antagonist will decrease the prevalence of atrial fibrillation after cardiac surgery.
Randomized double-blind placebo-controlled study.
University-affiliated hospitals.
Four hundred forty-five adult patients in normal sinus rhythm undergoing elective cardiac surgery.
One week to 4 days prior to surgery, patients were randomized to treatment with placebo, ramipril (2.5 mg the first 3 days followed by 5 mg/day, with the dose reduced to 2.5 mg/day on the first postoperative day only), or spironolactone (25 mg/day).
The primary endpoint was the occurrence of electrocardiographically confirmed postoperative atrial fibrillation. Secondary endpoints included acute renal failure, hyperkalemia, the prevalence of hypotension, length of hospital stay, stroke, and death.
The prevalence of atrial fibrillation was 27.2% in the placebo group, 27.8% in the ramipril group, and 25.9% in the spironolactone group (p=.95). Patients in the ramipril (0.7%) or spironolactone (0.7%) group were less likely to develop acute renal failure than those randomized to placebo (5.4%, p=.006). Patients in the placebo group tended to be hospitalized longer than those in the ramipril or spironolactone group (6.8±8.2 days vs. 5.7±3.2 days and 5.8±3.4 days, respectively, p=.08 for the comparison of placebo vs. the active treatment groups using log-rank test). Compared with patients in the placebo group, patients in the spironolactone group were extubated sooner after surgery (576.4±761.5 mins vs. 1091.3±3067.3 mins, p=.04).
Neither angiotensin-converting enzyme inhibition nor mineralocorticoid receptor blockade decreased the primary outcome of postoperative atrial fibrillation. Treatment with an angiotensin-converting enzyme inhibitor or mineralocorticoid receptor antagonist was associated with decreased acute renal failure. Spironolactone use was also associated with a shorter duration of mechanical ventilation after surgery.
本研究旨在检验假设,即通过血管紧张素转换酶抑制剂或盐皮质激素受体拮抗剂阻断肾素-血管紧张素系统会降低心脏手术后心房颤动的发生率。
随机、双盲、安慰剂对照研究。
大学附属医院。
445 名窦性心律的成年择期心脏手术患者。
手术前 1 周至 4 天,患者随机接受安慰剂、雷米普利(第 1 至 3 天 2.5mg,随后每天 5mg,仅在术后第 1 天减少至 2.5mg)或螺内酯(25mg/天)治疗。
主要终点是心电图确认的术后心房颤动的发生。次要终点包括急性肾衰竭、高钾血症、低血压的发生率、住院时间、中风和死亡。
安慰剂组、雷米普利组和螺内酯组的心房颤动发生率分别为 27.2%、27.8%和 25.9%(p=0.95)。与随机分配至安慰剂组的患者相比,雷米普利(0.7%)或螺内酯(0.7%)组患者发生急性肾衰竭的可能性较小(5.4%,p=0.006)。与雷米普利或螺内酯组相比,安慰剂组患者的住院时间更长(分别为 6.8±8.2 天、5.7±3.2 天和 5.8±3.4 天,p=0.08,采用对数秩检验比较安慰剂与活性治疗组)。与安慰剂组相比,螺内酯组患者术后拔管更早(576.4±761.5 分钟 vs. 1091.3±3067.3 分钟,p=0.04)。
血管紧张素转换酶抑制或盐皮质激素受体阻断均未降低术后心房颤动的主要结局。血管紧张素转换酶抑制剂或盐皮质激素受体拮抗剂的治疗与急性肾衰竭的减少有关。螺内酯的使用还与术后机械通气时间缩短有关。