Waldo A L, Camm A J, deRuyter H, Friedman P L, MacNeil D J, Pauls J F, Pitt B, Pratt C M, Schwartz P J, Veltri E P
Case Western Reserve University, Cleveland, Ohio, USA.
Lancet. 1996 Jul 6;348(9019):7-12. doi: 10.1016/s0140-6736(96)02149-6.
Left ventricular dysfunction after myocardial infarction is associated with an increased risk of death. Other studies have suggested that a potassium-channel blocker might reduce this risk with minimal adverse effects. We investigated whether d-sotalol, a pure potassium-channel blocker with no clinically significant beta-blocking activity, could reduce all-cause mortality in these high-risk patients.
Patients with a left ventricular ejection fraction of 40% or less and either a recent (6-42 days) myocardial infarction or symptomatic heart failure with a remote (> 42 days) myocardial infarction were randomly assigned d-sotalol (100 mg increased to 200 mg twice daily, if tolerated) or matching placebo twice daily.
After 3121 of the planned 6400 patients had been recruited, the trial was stopped. Among 1549 patients assigned d-sotalol, there were 78 deaths (5.0%) compared with 48 deaths (3.1%) among the 1572 patients assigned placebo (relative risk 1.65 [95% CI 1.15-2.36], p = 0.006). Presumed arrhythmic deaths (relative risk 1.77 [1.15-2.74], p = 0.008) accounted for the increased mortality. The effect was greater in patients with a left ventricular ejection fraction of 31-40% than in those with lower ( <or= 30%) ejection fractions (relative risk 4.0 vs 1.2, p = 0.007).
Among the 1549 patients evaluated, administration of d-sotalol was associated with increased mortality, which was presumed primarily to be due to arrhythmias. The prophylactic use of a specific potassium-channel blocker does not reduce mortality, and may be associated with increased mortality in high-risk patients after myocardial infarction.
心肌梗死后左心室功能障碍与死亡风险增加相关。其他研究表明,钾通道阻滞剂可能以最小的不良反应降低这种风险。我们研究了d - 索他洛尔(一种无临床显著β受体阻断活性的纯钾通道阻滞剂)是否能降低这些高危患者的全因死亡率。
左心室射血分数为40%或更低,且近期(6 - 42天)发生心肌梗死或有症状性心力衰竭且有陈旧性(> 42天)心肌梗死的患者,被随机分配接受d - 索他洛尔(若耐受,100 mg每日两次增至200 mg每日两次)或匹配的安慰剂每日两次。
在计划招募的6400例患者中有3121例入组后,试验停止。在分配接受d - 索他洛尔的1549例患者中,有78例死亡(5.0%),而在分配接受安慰剂的1572例患者中有48例死亡(3.1%)(相对风险1.65 [95% CI 1.15 - 2.36],p = 0.006)。推测为心律失常导致的死亡(相对风险1.77 [1.15 - 2.74],p = 0.008)导致了死亡率增加。左心室射血分数为31 - 40%的患者中该效应比射血分数较低(≤ 30%)的患者更大(相对风险4.0对1.2,p = 0.007)。
在评估的1549例患者中,给予d - 索他洛尔与死亡率增加相关,推测主要是由于心律失常。特定钾通道阻滞剂的预防性使用并不能降低死亡率,且可能与心肌梗死后高危患者的死亡率增加有关。