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      Rate pressure product and the components of heart rate and systolic blood pressure in hospitalized heart failure patients with preserved ejection fraction: Insights from ASCEND‐HF

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          Abstract

          Background

          Heart rate and systolic blood pressure (SBP) are prognostic markers in heart failure (HF) with reduced ejection fraction (HFrEF). Their combination in rate pressure product (RPP) as well as their role in heart failure with preserved ejection fraction (HFpEF) remains unclear.

          Hypothesis

          RPP and its components are associated with HFpEF outcomes.

          Methods

          We performed an analysis of Acute Study of Clinical Effectiveness of Nesiritide in Subjects With Decompensated Heart Failure (ASCEND‐HF; http://www.clinicaltrials.gov NCT00475852), which studied 7141 patients with acute HF. HFpEF was defined as left ventricular ejection fraction ≥40%. Outcomes were assessed by baseline heart rate, SBP, and RPP, as well as the change of these variables using adjusted Cox models.

          Results

          After multivariable adjustment, in‐hospital change but not baseline heart rate, SBP, and RPP were associated with 30‐day mortality/HF hospitalization (hazard ratio [HR]: 1.17 per 5‐bpm heart rate, HR: 1.20 per 10‐mm Hg SBP, and HR: 1.02 per 100 bpm × mm Hg RPP; all P < 0.05). Baseline SBP was associated with 180‐day mortality (HR: 0.88 per 10‐mm Hg, P = 0.028). Though change in RPP was associated with 30‐day mortality/HF hospitalization, the RPP baseline variable did not provide additional associative information with regard to outcomes when compared with assessment of baseline heart rate and SBP variables alone.

          Conclusions

          An increase in heart rate and SBP from baseline to discharge was associated with increased 30‐day mortality/HF hospitalization in HFpEF patients with acute exacerbation. These findings suggest value in monitoring the trend of vital signs during HFpEF hospitalization.

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          Author and article information

          Contributors
          amanda.verma@wustl.edu
          Journal
          Clin Cardiol
          Clin Cardiol
          10.1002/(ISSN)1932-8737
          CLC
          Clinical Cardiology
          Wiley Periodicals, Inc. (New York )
          0160-9289
          1932-8737
          17 July 2018
          July 2018
          : 41
          : 7 ( doiID: 10.1002/clc.2018.41.issue-7 )
          : 945-952
          Affiliations
          [ 1 ] Department of Cardiology Washington University School of Medicine St. Louis Missouri
          [ 2 ] Department of Statistics Duke University Medical Center Durham North Carolina
          [ 3 ] Department of Cardiology Duke Clinical Research Institute, Duke Hospital Durham North Carolina
          [ 4 ] Department of Cardiology, School of Medicine University of California San Francisco
          [ 5 ] Department of Health Sciences Research Mayo Clinic Rochester Minnesota
          [ 6 ] Division of Cardiology University of Alberta Edmonton Canada
          [ 7 ] Department of Cardiology University Medical Center Groningen Groningen the Netherlands
          [ 8 ] Department of Cardiology Cleveland Clinic Cleveland Ohio
          Author notes
          [*] [* ] Correspondence

          Amanda K. Verma, MD, 660 South Euclid Avenue, Campus Box 8086, St. Louis, MO 63110

          Email: amanda.verma@ 123456wustl.edu

          Author information
          http://orcid.org/0000-0001-9747-3119
          Article
          PMC6103846 PMC6103846 6103846 CLC22981
          10.1002/clc.22981
          6103846
          29781109
          d305992e-8917-4131-bdc5-0a61dd2f13d0
          © 2018 Wiley Periodicals, Inc.
          History
          : 25 February 2018
          : 14 May 2018
          : 16 May 2018
          Page count
          Figures: 1, Tables: 3, Pages: 8, Words: 5719
          Funding
          Funded by: National Institute for Health Research
          Award ID: U10HL110312
          Award ID: R01AG045551‐01A1
          Categories
          Clinical Investigations
          Clinical Investigations
          Custom metadata
          2.0
          clc22981
          July 2018
          Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.2.1 mode:remove_FC converted:30.04.2019

          Heart Failure,Clinical Trials,Blood Pressure Control and Regulation

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