Literature DB >> 33960305

Resting heart rate and real-life treatment modalities in outpatients with left ventricular systolic dysfunction study: A multicenter, prospective, observational, and national registry.

Yüksel Çavuşoğlu1, Ömer Kozan2, Ahmet Temizhan3, Mehmet Serdar Küçükoğlu4.   

Abstract

OBJECTIVE: Heart rate (HR) reduction is associated with improved outcomes in heart failure (HF). This multicenter, prospective, observational, and national registry aimed to evaluate resting HR and the impacts of HR-related medications in real-life clinical practice in patients with HF.
METHODS: The Resting HR and Real-Life Treatment Modalities in Outpatients with Left Ventricular Systolic Dysfunction (REALITY HF) study enrolled 1054 patients with HF and left ventricular ejection fraction (LVEF) of <40% from 16 centers. Clinical characteristics, HR, and medications were noted (enrollment phase). A total of 487 patients with sinus rhythm and HR of ≥70 bpm were included in a further 4-month follow-up (FU) program (V0). Changes in HR and medications were reevaluated at 1-month (V1) and 4-month (V2) FU visits. The Kansas City Cardiomyopathy Questionnaire (KCCQ) was used to assess the quality of life (QoL) of 320 patients in a 4-month FU program.
RESULTS: During enrollment, 794 patients (75.3%) were in sinus rhythm, in whom resting HR was 76.7±14 bpm, 69.1% had a resting HR of ≥70 bpm, 79.1% were receiving beta blocker (BB), and 6.1% were receiving ivabradine. Resting HR was lower in patients receiving BB (75.8±13 vs. 80.4±16 bpm; p=0.001); however, 65.8% of those still had a resting HR of ≥70 bpm. A significant association was found between elevated HR and worse New York Heart Association (NYHA) class, worse QoL, or lower LVEF. During the 4-month FU, adjustment of HR-lowering therapy was left to the physician's discretion. Resting HR significantly reduced from 83.6±12 (80) bpm at V0 to 78.6±13 (77) bpm at V1 (p=0.001) and further decreased to 73.0±11 (73) bpm at V2 (p=0.001). Patients achieving a resting HR of <70 bpm were 21.7% at V1 (p=0.001) and 39.9% at V2 (p=0.001). KCCQ significantly increased from 59.7±23 (62.7) at V0 to 73.1±18 (78.5) at V2 (p=0.001). In addition, patients with NYHA I increased from 22.2% at V0 to 29.2% at V1 and 39.4% at V2 (p=0.01).
CONCLUSION: In real-life clinical practice, elevated HR is highly prevalent in HF despite widely used BB therapy and is associated with worse clinical picture. Therapeutic interventions targeting HR significantly reduce HR, and HR lowering is associated with improved clinical outcomes.

Entities:  

Year:  2021        PMID: 33960305      PMCID: PMC8114622          DOI: 10.14744/AnatolJCardiol.2020.13247

Source DB:  PubMed          Journal:  Anatol J Cardiol        ISSN: 2149-2263            Impact factor:   1.596


  26 in total

1.  EURObservational Research Programme: the Heart Failure Pilot Survey (ESC-HF Pilot).

Authors:  Aldo P Maggioni; Ulf Dahlström; Gerasimos Filippatos; Ovidiu Chioncel; Marisa Crespo Leiro; Jaroslaw Drozdz; Friedrich Fruhwald; Lars Gullestad; Damien Logeart; Marco Metra; John Parissis; Hans Persson; Piotr Ponikowski; Mathias Rauchhaus; Adriaan Voors; Olav Wendelboe Nielsen; Faiez Zannad; Luigi Tavazzi
Journal:  Eur J Heart Fail       Date:  2010-08-29       Impact factor: 15.534

2.  Long-term treatment with ivabradine over 12months in patients with chronic heart failure in clinical practice: Effect on symptoms, quality of life and hospitalizations.

Authors:  C Zugck; S Störk; G Stöckl
Journal:  Int J Cardiol       Date:  2017-04-11       Impact factor: 4.164

3.  Meta-analysis: beta-blocker dose, heart rate reduction, and death in patients with heart failure.

Authors:  Finlay A McAlister; Natasha Wiebe; Justin A Ezekowitz; Alexander A Leung; Paul W Armstrong
Journal:  Ann Intern Med       Date:  2009-06-02       Impact factor: 25.391

4.  Heart rate and cardiac rhythm relationships with bisoprolol benefit in chronic heart failure in CIBIS II Trial.

Authors:  P Lechat; J S Hulot; S Escolano; A Mallet; A Leizorovicz; M Werhlen-Grandjean; G Pochmalicki; H Dargie
Journal:  Circulation       Date:  2001-03-13       Impact factor: 29.690

5.  Heart rate achieved or beta-blocker dose in patients with chronic heart failure: which is the better target?

Authors:  Damien Cullington; Kevin M Goode; Andrew L Clark; John G F Cleland
Journal:  Eur J Heart Fail       Date:  2012-05-22       Impact factor: 15.534

6.  Optimization of heart rate lowering therapy in hospitalized patients with heart failure: Insights from the Optimize Heart Failure Care Program.

Authors:  Yuri M Lopatin; Martin R Cowie; Anna A Grebennikova; Hamayak S Sisakian; Zurab M Pagava; Hamlet G Hayrapetyan; Timur A Abdullaev; Leonid G Voronkov; Anna I Chesnikova; Vira I Tseluyko; Ekaterina I Tarlovskaya; Gülnaz M Dadashova; Salim F Berkinbaev; Maria G Glezer; Natalia A Koziolova; Amina G Rakisheva; Zviad V Kipiani; Alena K Kurlyanskaya
Journal:  Int J Cardiol       Date:  2018-06-01       Impact factor: 4.164

Review 7.  Vascular pathophysiology in response to increased heart rate.

Authors:  Florian Custodis; Stephan H Schirmer; Magnus Baumhäkel; Gerd Heusch; Michael Böhm; Ulrich Laufs
Journal:  J Am Coll Cardiol       Date:  2010-12-07       Impact factor: 24.094

8.  Heart rate and cardiovascular mortality: the Framingham Study.

Authors:  W B Kannel; C Kannel; R S Paffenbarger; L A Cupples
Journal:  Am Heart J       Date:  1987-06       Impact factor: 4.749

9.  The prognostic significance of heart rate in patients hospitalized for heart failure with reduced ejection fraction in sinus rhythm: insights from the EVEREST (Efficacy of Vasopressin Antagonism in Heart Failure: Outcome Study With Tolvaptan) trial.

Authors:  Stephen J Greene; Muthiah Vaduganathan; Jane E Wilcox; Matthew E Harinstein; Aldo P Maggioni; Haris Subacius; Faiez Zannad; Marvin A Konstam; Ovidiu Chioncel; Clyde W Yancy; Karl Swedberg; Javed Butler; Robert O Bonow; Mihai Gheorghiade
Journal:  JACC Heart Fail       Date:  2013-12-02       Impact factor: 12.035

10.  Heart rate as a prognostic risk factor in patients with coronary artery disease and left-ventricular systolic dysfunction (BEAUTIFUL): a subgroup analysis of a randomised controlled trial.

Authors:  Kim Fox; Ian Ford; P Gabriel Steg; Michal Tendera; Michele Robertson; Roberto Ferrari
Journal:  Lancet       Date:  2008-08-29       Impact factor: 79.321

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