Effect on survival and hospitalization of initiating treatment for chronic heart failure with bisoprolol followed by enalapril, as compared with the opposite sequence - Results of the randomized cardiac insufficiency bisoprolol study (CIBIS) III

被引:244
作者
Willenheimer, R [1 ]
van Veldhuisen, DJ
Silke, B
Erdmann, E
Follath, F
Krum, H
Ponikowski, P
Skene, A
Van de Ven, L
Verkenne, P
Lechat, P
机构
[1] Lund Univ, Dept Cardiol, Malmo Univ Hosp, S-20502 Malmo, Sweden
[2] Univ Groningen Hosp, Dept Cardiol, Thoraxctr, Groningen, Netherlands
[3] St James Hosp, Dept Pharmacol & Therapeut, Trinity Ctr, Dublin 8, Ireland
[4] Univ Cologne, Med Klin 3, Cologne, Germany
[5] Univ Zurich Hosp, CH-8091 Zurich, Switzerland
[6] Monash Univ, Alfred Hosp, Dept Epidemiol & Prevent Med, Melbourne, Vic 3181, Australia
[7] Monash Univ, Alfred Hosp, Dept Med, Melbourne, Vic 3181, Australia
[8] Clin Mil Hosp, Dept Cardiol, Wroclaw, Poland
[9] Nottingham Clin Res Ltd, Nottingham, England
[10] Merck KGaA, Darmstadt, Germany
[11] Hop La Pitie Salpetriere, Serv Pharmacol, Paris, France
关键词
heart failure; drugs; adrenergic beta-antagonists; angiotensin-converting enzyme inhibitors;
D O I
10.1161/CIRCULATIONAHA.105.582320
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - In patients with chronic heart failure (CHF), a beta-blocker is generally added to a regimen containing an angiotensin-converting-enzyme ( ACE) inhibitor. It is unknown whether beta-blockade as initial therapy may be as useful. Methods and Results - We randomized 1010 patients with mild to moderate CHF and left ventricular ejection fraction <= 35%, who were not receiving ACE inhibitor, beta-blocker, or angiotensin receptor blocker therapy, to open-label monotherapy with either bisoprolol ( target dose 10 mg QD; n = 505) or enalapril ( target dose 10 mg BID; n = 505) for 6 months, followed by their combination for 6 to 24 months. The 2 strategies were blindly compared with regard to the combined primary end point of all-cause mortality or hospitalization and with regard to each of these end point components individually. Bisoprolol-first treatment was noninferior to enalapril-first treatment if the upper limit of the ;95% confidence interval (CI) for the absolute between-group difference was < 5%, corresponding to a hazard ratio (HR) of 1.17. In the intention-to-treat sample, the primary end point occurred in 178 patients allocated to bisoprolol-first treatment versus 186 allocated to enalapril-first treatment ( absolute difference - 1.6%, 95% CI - 7.6 to 4.4%, HR 0.94; 95% CI 0.77 to 1.16). In the per-protocol sample, 163 patients allocated to bisoprolol-first treatment had a primary end point, versus 165 allocated to enalapril-first treatment ( absolute difference - 0.7%, 95% CI - 6.6 to 5.1%, HR 0.97; 95% CI 0.78 to 1.21). With bisoprolol-first treatment, 65 patients died, versus 73 with enalapril-first treatment ( HR 0.88; 95% CI 0.63 to 1.22), and 151 versus 157 patients were hospitalized ( HR 0.95; 95% CI 0.76 to 1.19). Conclusion - Although noninferiority of bisoprolol-first versus enalapril-first treatment was not proven in the per-protocol analysis, our results indicate that it may be as safe and efficacious to initiate treatment for CHF with bisoprolol as with enalapril.
引用
收藏
页码:2426 / 2435
页数:10
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