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Titration to target dose of bisoprolol vs. carvedilol in elderly patients with heart failure: the CIBIS‐ELD trial

Identifieur interne : 000C71 ( Istex/Corpus ); précédent : 000C70; suivant : 000C72

Titration to target dose of bisoprolol vs. carvedilol in elderly patients with heart failure: the CIBIS‐ELD trial

Auteurs : Hans-Dirk Düngen ; Svetlana Apostolovi ; Simone Inkrot ; Elvis Tahirovi ; Agnieszka Töpper ; Felix Mehrhof ; Christiane Prettin ; Biljana Putnikovi ; Aleksandar N. Neškovi ; Mirjana Krotin ; Dejan Saka ; Mitja Lainš Ak ; Frank Edelmann ; Rolf Wachter ; Thomas Rau ; Thomas Eschenhagen ; Wolfram Doehner ; Stefan D. Anker ; Finn Waagstein ; Christoph Herrmann-Lingen ; Goetz Gelbrich ; Rainer Dietz

Source :

RBID : ISTEX:47222E9C93CF33B0BA8512D96142A5730B23B309

Abstract

Various beta‐blockers with distinct pharmacological profiles are approved in heart failure, yet they remain underused and underdosed. Although potentially of major public health importance, whether one agent is superior in terms of tolerability and optimal dosing has not been investigated. The aim of this study was therefore to compare the tolerability and clinical effects of two proven beta‐blockers in elderly patients with heart failure.

Url:
DOI: 10.1093/eurjhf/hfr020

Links to Exploration step

ISTEX:47222E9C93CF33B0BA8512D96142A5730B23B309

Le document en format XML

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<name sortKey="Neskovi, Aleksandar N" sort="Neskovi, Aleksandar N" uniqKey="Neskovi A" first="Aleksandar N." last="Neškovi">Aleksandar N. Neškovi</name>
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<name sortKey="Neskovi, Aleksandar N" sort="Neskovi, Aleksandar N" uniqKey="Neskovi A" first="Aleksandar N." last="Neškovi">Aleksandar N. Neškovi</name>
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<name sortKey="Saka, Dejan" sort="Saka, Dejan" uniqKey="Saka D" first="Dejan" last="Saka">Dejan Saka</name>
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<name sortKey="Edelmann, Frank" sort="Edelmann, Frank" uniqKey="Edelmann F" first="Frank" last="Edelmann">Frank Edelmann</name>
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<name sortKey="Wachter, Rolf" sort="Wachter, Rolf" uniqKey="Wachter R" first="Rolf" last="Wachter">Rolf Wachter</name>
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<name sortKey="Rau, Thomas" sort="Rau, Thomas" uniqKey="Rau T" first="Thomas" last="Rau">Thomas Rau</name>
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<name sortKey="Eschenhagen, Thomas" sort="Eschenhagen, Thomas" uniqKey="Eschenhagen T" first="Thomas" last="Eschenhagen">Thomas Eschenhagen</name>
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<name sortKey="Doehner, Wolfram" sort="Doehner, Wolfram" uniqKey="Doehner W" first="Wolfram" last="Doehner">Wolfram Doehner</name>
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<name sortKey="Herrmann Ingen, Christoph" sort="Herrmann Ingen, Christoph" uniqKey="Herrmann Ingen C" first="Christoph" last="Herrmann-Lingen">Christoph Herrmann-Lingen</name>
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<mods:affiliation>Department of Psychosomatic Medicine and Psychotherapy, Göttingen University Medical Center, Göttingen, Germany</mods:affiliation>
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<title level="j">European Journal of Heart Failure</title>
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<div type="abstract">Various beta‐blockers with distinct pharmacological profiles are approved in heart failure, yet they remain underused and underdosed. Although potentially of major public health importance, whether one agent is superior in terms of tolerability and optimal dosing has not been investigated. The aim of this study was therefore to compare the tolerability and clinical effects of two proven beta‐blockers in elderly patients with heart failure.</div>
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<name>Frank Edelmann</name>
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<p>Various beta‐blockers with distinct pharmacological profiles are approved in heart failure, yet they remain underused and underdosed. Although potentially of major public health importance, whether one agent is superior in terms of tolerability and optimal dosing has not been investigated. The aim of this study was therefore to compare the tolerability and clinical effects of two proven beta‐blockers in elderly patients with heart failure.</p>
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<p>We performed a double‐blind superiority trial of bisoprolol vs. carvedilol in 883 elderly heart failure patients with reduced or preserved left ventricular ejection fraction in 41 European centres. The primary endpoint was tolerability, defined as reaching and maintaining guideline‐recommended target doses after 12 weeks treatment. Adverse events and clinical parameters of patient status were secondary endpoints. None of the beta‐blockers was superior with regards to tolerability: 24% [95% confidence interval (CI) 20–28] of patients in the bisoprolol arm and 25% (95% CI 21–29) of patients in the carvedilol arm achieved the primary endpoint (P= 0.64). The use of bisoprolol resulted in greater reduction of heart rate (adjusted mean difference 2.1 b.p.m., 95% CI 0.5–3.6, P= 0.008) and more, dose‐limiting, bradycardic adverse events (16 vs. 11%; P= 0.02). The use of carvedilol led to a reduction of forced expiratory volume (adjusted mean difference 50 mL, 95% CI 4–95, P= 0.03) and more, non‐dose‐limiting, pulmonary adverse events (10 vs. 4%; P < 0.001).</p>
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<city>Berlin</city>
<country>Germany</country>
</address>
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<country>Italy</country>
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<country>Germany</country>
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<keyword xml:id="ejhfhfr020-kwd-0001">Heart failure</keyword>
<keyword xml:id="ejhfhfr020-kwd-0002">Beta‐blocker</keyword>
<keyword xml:id="ejhfhfr020-kwd-0003">Elderly</keyword>
<keyword xml:id="ejhfhfr020-kwd-0004">Tolerability</keyword>
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<p>We performed a double‐blind superiority trial of bisoprolol vs. carvedilol in 883 elderly heart failure patients with reduced or preserved left ventricular ejection fraction in 41 European centres. The primary endpoint was tolerability, defined as reaching and maintaining guideline‐recommended target doses after 12 weeks treatment. Adverse events and clinical parameters of patient status were secondary endpoints. None of the beta‐blockers was superior with regards to tolerability: 24% [95% confidence interval (CI) 20–28] of patients in the bisoprolol arm and 25% (95% CI 21–29) of patients in the carvedilol arm achieved the primary endpoint (
<i>P</i>
= 0.64). The use of bisoprolol resulted in greater reduction of heart rate (adjusted mean difference 2.1 b.p.m., 95% CI 0.5–3.6,
<i>P</i>
= 0.008) and more, dose‐limiting, bradycardic adverse events (16 vs. 11%;
<i>P</i>
= 0.02). The use of carvedilol led to a reduction of forced expiratory volume (adjusted mean difference 50 mL, 95% CI 4–95,
<i>P</i>
= 0.03) and more, non‐dose‐limiting, pulmonary adverse events (10 vs. 4%;
<i>P</i>
< 0.001).</p>
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<p>Overall tolerability to target doses was comparable. The pattern of intolerance, however, was different: bradycardia occurred more often in the bisoprolol group, whereas pulmonary adverse events occurred more often in the carvedilol group.</p>
<p>This study is registered with
<url href="http://controlled-trials.com">controlled‐trials.com</url>
, number ISRCTN34827306.</p>
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<abstract>We performed a double‐blind superiority trial of bisoprolol vs. carvedilol in 883 elderly heart failure patients with reduced or preserved left ventricular ejection fraction in 41 European centres. The primary endpoint was tolerability, defined as reaching and maintaining guideline‐recommended target doses after 12 weeks treatment. Adverse events and clinical parameters of patient status were secondary endpoints. None of the beta‐blockers was superior with regards to tolerability: 24% [95% confidence interval (CI) 20–28] of patients in the bisoprolol arm and 25% (95% CI 21–29) of patients in the carvedilol arm achieved the primary endpoint (P= 0.64). The use of bisoprolol resulted in greater reduction of heart rate (adjusted mean difference 2.1 b.p.m., 95% CI 0.5–3.6, P= 0.008) and more, dose‐limiting, bradycardic adverse events (16 vs. 11%; P= 0.02). The use of carvedilol led to a reduction of forced expiratory volume (adjusted mean difference 50 mL, 95% CI 4–95, P= 0.03) and more, non‐dose‐limiting, pulmonary adverse events (10 vs. 4%; P < 0.001).</abstract>
<abstract>Overall tolerability to target doses was comparable. The pattern of intolerance, however, was different: bradycardia occurred more often in the bisoprolol group, whereas pulmonary adverse events occurred more often in the carvedilol group. This study is registered with controlled‐trials.com, number ISRCTN34827306.</abstract>
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