Article ID Journal Published Year Pages File Type
2930155 International Journal of Cardiology 2012 7 Pages PDF
Abstract

BackgroundGuideline-recommended beta-blocker (BB) target doses for patients with chronic heart failure can often not be reached. This secondary analysis of the CIBIS-ELD trial was carried out to better understand reasons for not achieving target doses.MethodsChanges in heart rate (HR) and other parameters during a 12-week up-titration period in 302 BB naïve patients were evaluated in the subgroups achieving 12.5, 25, 50, and 100% of the target dose (groups 1, 2, 3, and 4, respectively).ResultsAchieved doses predominantly depended on baseline HR (means 68, 74, 76, and 84 bpm in groups 1–4, respectively, P < 0.001). HR was consistently reduced with each dose level to 65, 63, and 62 bpm in groups 1–3 and to 71 bpm in group 4 (P < 0.001). When adjusted for baseline, HR reduction achieved in group 3 was better than in group 4 (difference − 5.4 bpm, P < 0.05). More patients in groups 3/4 than in groups 1/2 improved in NYHA class (P = 0.01). NTproBNP increased by 38% in group 4 (P < 0.01) but not in the others (P < 0.05 between groups). Changes in blood pressure, six-minute walk distance and self-rated health were comparable in all groups.ConclusionsThe desired effect of HR reduction appears to be a predominant limitation for BB up-titration. Vice versa, achieving the target dose may be a sign of insufficient response rather than successful treatment. In view of these results and the well-known importance of HR for survival, not target doses, but HR control should be given priority in BB treatment for heart failure.

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