Heart Failure Institute do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Circ Heart Fail. 2010 Jan;3(1):82-8. doi: 10.1161/CIRCHEARTFAILURE.109.882035. Epub 2009 Nov 20.
Peculiar aspects of Chagas cardiomyopathy raise concerns about efficacy and safety of sympathetic blockade. We studied the influence of beta-blockers in patients with Chagas cardiomyopathy.
We examined REMADHE trial and grouped patients according to etiology (Chagas versus non-Chagas) and beta-blocker therapy. Primary end point was all-cause mortality or heart transplantation. Altogether 456 patients were studied; 27 (5.9%) were submitted to heart transplantation and 202 (44.3%) died. Chagas etiology was present in 68 (14.9%) patients; they had lower body mass index (24.1+/-4.1 versus 26.3+/-5.1, P=0.001), smaller end-diastolic left ventricle diameter (6.7+/-1.0 mm versus 7.0+/-0.9 mm, P=0.001), smaller proportion of beta-blocker therapy (35.8% versus 68%, P<0.001), and higher proportion of spironolactone therapy (74.6% versus 57.8%, P=0.003). Twenty-four (35.8%) patients with Chagas disease were under beta-blocker therapy and had lower serum sodium (136.6+/-3.1 versus 138.4+/-3.1 mEqs, P=0.05) and lower body mass index (22.5+/-3.3 versus 24.9+/-4.3, P=0.03) compared with those who received beta-blockers. Survival was lower in patients with Chagas heart disease as compared with other etiologies. When only patients under beta-blockers were considered, the survival of patients with Chagas disease was similar to that of other etiologies. The survival of patients with beta-blockers was higher than that of patients without beta-blockers. In Cox regression model, left ventricle end-diastolic diameter (hazard ratio, 1.78; CI, 1.15 to 2.76; P=0.009) and beta-blockers (hazard ratio, 0.37; CI, 0.14 to 0.97; P=0.044) were associated with better survival.
Our study suggests that beta-blockers may have beneficial effects on survival of patients with heart failure and Chagas heart disease and warrants further investigation in a prospective, randomized trial. Clinical Trial Registration- clinicaltrials.gov. Identifier: NCT00505050.
恰加斯心肌病的特殊表现引起了人们对交感神经阻滞疗效和安全性的关注。我们研究了β受体阻滞剂在恰加斯心肌病患者中的作用。
我们对 REMADHE 试验进行了研究,并根据病因(恰加斯或非恰加斯)和β受体阻滞剂治疗将患者进行分组。主要终点是全因死亡率或心脏移植。共纳入 456 例患者,27 例(5.9%)接受心脏移植,202 例(44.3%)死亡。68 例(14.9%)患者存在恰加斯病因,他们的体重指数较低(24.1±4.1 比 26.3±5.1,P=0.001),左心室舒张末期直径较小(6.7±1.0 毫米比 7.0±0.9 毫米,P=0.001),β受体阻滞剂治疗的比例较低(35.8%比 68%,P<0.001),螺内酯治疗的比例较高(74.6%比 57.8%,P=0.003)。24 例(35.8%)恰加斯病患者接受β受体阻滞剂治疗,血清钠较低(136.6±3.1 比 138.4±3.1 mEq/L,P=0.05),体重指数较低(22.5±3.3 比 24.9±4.3,P=0.03)。与接受β受体阻滞剂治疗的患者相比,恰加斯心脏病患者的生存情况较差。当仅考虑接受β受体阻滞剂治疗的患者时,恰加斯病患者的生存率与其他病因相似。β受体阻滞剂治疗患者的生存率高于未接受β受体阻滞剂治疗的患者。Cox 回归模型显示,左心室舒张末期直径(危险比,1.78;95%置信区间,1.15 至 2.76;P=0.009)和β受体阻滞剂(危险比,0.37;95%置信区间,0.14 至 0.97;P=0.044)与更好的生存相关。
我们的研究表明,β受体阻滞剂可能对心力衰竭和恰加斯心脏病患者的生存有有益影响,值得在一项前瞻性、随机试验中进一步研究。临床试验注册- clinicaltrials.gov。标识符:NCT00505050。