Publication:
Tolerability and Feasibility of Beta-Blocker Titration in HFpEF Versus HFrEF: Insights From the CIBIS-ELD Trial

dc.contributor.authorEdelmann, Frank (35366308700)
dc.contributor.authorMusial-Bright, Lindy (25642935600)
dc.contributor.authorGelbrich, Goetz (14119833600)
dc.contributor.authorTrippel, Tobias (16834210300)
dc.contributor.authorRadenovic, Sara (57000170900)
dc.contributor.authorWachter, Rolf (12775831800)
dc.contributor.authorInkrot, Simone (35784615000)
dc.contributor.authorLoncar, Goran (55427750700)
dc.contributor.authorTahirovic, Elvis (24339336300)
dc.contributor.authorCelic, Vera (57132602400)
dc.contributor.authorVeskovic, Jovan (56951285600)
dc.contributor.authorZdravkovic, Marija (24924016800)
dc.contributor.authorLainscak, Mitja (9739432000)
dc.contributor.authorApostolović, Svetlana (13610076800)
dc.contributor.authorNeskovic, Aleksandar N. (35597744900)
dc.contributor.authorPieske, Burkert (35499467500)
dc.contributor.authorDüngen, Hans-Dirk (16024171900)
dc.date.accessioned2025-06-12T18:53:05Z
dc.date.available2025-06-12T18:53:05Z
dc.date.issued2016
dc.description.abstractObjectives: This study evaluated the tolerability and feasibility of titration of 2 distinctly acting beta-blockers (BB) in elderly heart failure patients with preserved (HFpEF) and reduced (HFrEF) left ventricular ejection fraction. Background: Broad evidence supports the use of BB in HFrEF, whereas the evidence for beta blockade in HFpEF is uncertain. Methods: In the CIBIS-ELD (Cardiac Insufficiency Bisoprolol Study in Elderly) trial, patients >65 years of age with HFrEF (n = 626) or HFpEF (n = 250) were randomized to bisoprolol or carvedilol. Both BB were up-titrated to the target or maximum tolerated dose. Follow-up was performed after 12 weeks. HFrEF and HFpEF patients were compared regarding tolerability and clinical effects (heart rate, blood pressure, systolic and diastolic functions, New York Heart Association functional class, 6-minute-walk distance, quality of life, and N-terminal pro-B-type natriuretic peptide). Results: For both of the BBs, tolerability and daily dose at 12 weeks were similar. HFpEF patients demonstrated higher rates of dose escalation delays and treatment-related side effects. Similar HR reductions were observed in both groups (HFpEF: 6.6 beats/min; HFrEF: 6.9 beats/min, p = NS), whereas greater improvement in NYHA functional class was observed in HFrEF (HFpEF: 23% vs. HFrEF: 34%, p < 0.001). Mean E/e' and left atrial volume index did not change in either group, although E/A increased in HFpEF. Conclusions: BB tolerability was comparable between HFrEF and HFpEF. Relevant reductions of HR and blood pressure occurred in both groups. However, only HFrEF patients experienced considerable improvements in clinical parameters and left ventricular function. Interestingly, beta-blockade had no effect on established and prognostic markers of diastolic function in either group. Long-term studies using modern diagnostic criteria for HFpEF are urgently needed to establish whether BB therapy exerts significant clinical benefit in HFpEF. (Comparison of Bisoprolol and Carvedilol in Elderly Heart Failure [HF] Patients: A Randomised, Double-Blind Multicentre Study [CIBIS-ELD]; ISRCTN34827306). © 2016 American College of Cardiology Foundation.
dc.identifier.urihttps://doi.org/10.1016/j.jchf.2015.10.008
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84959144458&doi=10.1016%2fj.jchf.2015.10.008&partnerID=40&md5=313c737ec2b12e29efb1da345b6b2d5e
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/7817
dc.subjectBeta-blockers
dc.subjectHeart failure
dc.subjectHFpEF
dc.subjectHFrEF
dc.subjectTolerability
dc.titleTolerability and Feasibility of Beta-Blocker Titration in HFpEF Versus HFrEF: Insights From the CIBIS-ELD Trial
dspace.entity.typePublication

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