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Heart failure therapy in diabetic patients-comparison with the recent ESC/EASD guideline.

Authors :
Edelmann F
Wachter R
Düngen HD
Störk S
Richter A
Stahrenberg R
Neumann T
Lüers C
Angermann CE
Mehrhof F
Gelbrich G
Pieske B
Source :
Cardiovascular diabetology [Cardiovasc Diabetol] 2011 Feb 08; Vol. 10, pp. 15. Date of Electronic Publication: 2011 Feb 08.
Publication Year :
2011

Abstract

Background: To assess heart failure therapies in diabetic patients with preserved as compared to impaired systolic ventricular function.<br />Methods: 3304 patients with heart failure from 9 different studies were included (mean age 63 ± 14 years); out of these, 711 subjects had preserved left ventricular ejection fraction (≥ 50%) and 994 patients in the whole cohort suffered from diabetes.<br />Results: The majority (>90%) of heart failure patients with reduced ejection fraction (SHF) and diabetes were treated with an ACE inhibitor (ACEi) or angiotensin receptor blocker (ARB) or with beta-blockers. By contrast, patients with diabetes and preserved ejection fraction (HFNEF) were less likely to receive these substance classes (p < 0.001) and had a worse blood pressure control (p < 0.001). In comparison to patients without diabetes, the probability to receive these therapies was increased in diabetic HFNEF patients (p < 0.001), but not in diabetic SHF patients. Aldosterone receptor blockers were given more often to diabetic patients with reduced ejection fraction (p < 0.001), and the presence and severity of diabetes decreased the probability to receive this substance class, irrespective of renal function.<br />Conclusions: Diabetic patients with HFNEF received less heart failure medication and showed a poorer control of blood pressure as compared to diabetic patients with SHF. SHF patients with diabetes were less likely to receive aldosterone receptor blocker therapy, irrespective of renal function.

Details

Language :
English
ISSN :
1475-2840
Volume :
10
Database :
MEDLINE
Journal :
Cardiovascular diabetology
Publication Type :
Academic Journal
Accession number :
21303531
Full Text :
https://doi.org/10.1186/1475-2840-10-15