Division of Cardiology, Duke Clinical Research Institute, Duke University Medical Center #31115, Durham, NC 27710, USA.
Eur Heart J. 2009 May;30(10):1245-53. doi: 10.1093/eurheartj/ehp100. Epub 2009 Mar 31.
Not all patients at risk for sudden cardiac death (SCD) are eligible for, or have access to implantable cardioverter defibrillator (ICD) implantation. There are conflicting data regarding the efficacy and safety of amiodarone for the prevention of SCD.
We conducted a meta-analysis of all randomized controlled trials examining the use of amiodarone vs. placebo/control for the prevention of SCD. We identified 15 trials, which randomized 8522 patients to amiodarone or placebo/control. Amiodarone decreased the incidence of SCD [7.1 vs. 9.7%; OR 0.71 (0.61-0.84), P < 0.001] and cardiovascular death (CVD) [14.0 vs. 16.3%; OR 0.82 (0.71-0.94), P = 0.004]. There was a 1.5% absolute risk reduction in all-cause mortality which did not meet statistical significance (P = 0.093). Amiodarone therapy increased the risk of pulmonary [2.9 vs. 1.5%; OR 1.97, (1.27-3.04), P = 0.002], and thyroid [3.6 vs. 0.4%; OR 5.68, (2.94-10.98), P < 0.001] toxicity.
Amiodarone reduces the risk of SCD by 29% and CVD by 18%, and therefore, represents a viable alternative in patients who are not eligible for or who do not have access to ICD therapy for the prevention of SCD. However, amiodarone therapy is neutral with respect to all-cause mortality and is associated with a two- and five-fold increased risk of pulmonary and thyroid toxicity.
并非所有发生心源性猝死(SCD)风险的患者都适合植入式心脏复律除颤器(ICD)植入,或有条件接受 ICD 植入。关于胺碘酮预防 SCD 的疗效和安全性存在相互矛盾的数据。
我们对所有评估胺碘酮对比安慰剂/对照组用于预防 SCD 的随机对照试验进行了荟萃分析。我们共确定了 15 项试验,这些试验共纳入 8522 例患者,分为胺碘酮组或安慰剂/对照组。胺碘酮降低 SCD 发生率[7.1%比 9.7%;比值比(OR)0.71(0.61-0.84),P<0.001]和心血管死亡(CVD)发生率[14.0%比 16.3%;OR 0.82(0.71-0.94),P=0.004]。全因死亡率的绝对风险降低了 1.5%,但未达到统计学意义(P=0.093)。胺碘酮治疗增加了肺部[2.9%比 1.5%;OR 1.97(1.27-3.04),P=0.002]和甲状腺[3.6%比 0.4%;OR 5.68(2.94-10.98),P<0.001]毒性的风险。
胺碘酮可降低 29%的 SCD 风险和 18%的 CVD 风险,因此,对于不适合或无法接受 ICD 治疗以预防 SCD 的患者,胺碘酮是一种可行的替代治疗方法。然而,胺碘酮治疗在全因死亡率方面无显著影响,且与肺部和甲状腺毒性的风险增加 2 倍和 5 倍相关。