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Worsening renal function and outcome in heart failure patients with reduced and preserved ejection fraction and the impact of angiotensin receptor blocker treatment: data from the CHARM-study programme.

Publication ,  Journal Article
Damman, K; Solomon, SD; Pfeffer, MA; Swedberg, K; Yusuf, S; Young, JB; Rouleau, JL; Granger, CB; McMurray, JJV
Published in: Eur J Heart Fail
December 2016

AIMS: We investigated the association between worsening renal function (WRF) that occurs during renin-angiotensin-aldosterone system inhibition initation and outcome in heart failure (HF) patients with preserved ejection fraction (HFPEF) and compared this with HF patients with reduced ejection fraction (HFREF). METHODS AND RESULTS: We examined changes in estimated glomerular filtration rate (GFR) and the relationship between WRF (defined as ≥26.5 µmol/L and ≥25% increase in serum creatinine from baseline to 6 weeks) and outcome, according to randomized treatment, in patients with HFREF (EF <45%; n = 1569) and HFPEF (EF ≥45%; n = 836) in the CHARM programme. The primary outcome was cardiovascular death or HF hospitalization. Estimated GFR decreased 9.0 ± 21 vs. 4.0 ± 21 mL/min/1.73 m2 with candesartan and placebo, respectively, and this was similar in HFREF and HFPEF. WRF developed more frequently with candesartan, 16% vs. 7%, P < 0.001, with similar findings in patients with HFREF and HFPEF. WRF was associated with a higher risk of the primary outcome: multivariable hazard ratio (HR) 1.26, 95% confidence interval 1.03-1.54, P = 0.022, in both treatment groups, and in both HFREF and HFPEF (P for interaction 0.98). In HFREF, WRF was mostly related to HF hospitalization, while in HFPEF, WRF seemed more associated with mortality. CONCLUSIONS: GFR decreased more and WRF was more common with candesartan compared with placebo, and this was similar in HFREF and HFPEF. WRF was associated with worse outcomes in HFREF and HFPEF. Although no formal interaction was present, the association between candesartan treatment, WRF, and type of clinical outcome was slightly different between HFREF and HFPEF.

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Published In

Eur J Heart Fail

DOI

EISSN

1879-0844

Publication Date

December 2016

Volume

18

Issue

12

Start / End Page

1508 / 1517

Location

England

Related Subject Headings

  • Tetrazoles
  • Stroke Volume
  • Renal Insufficiency
  • Randomized Controlled Trials as Topic
  • Proportional Hazards Models
  • Multivariate Analysis
  • Middle Aged
  • Male
  • Logistic Models
  • Humans
 

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Damman, K., Solomon, S. D., Pfeffer, M. A., Swedberg, K., Yusuf, S., Young, J. B., … McMurray, J. J. V. (2016). Worsening renal function and outcome in heart failure patients with reduced and preserved ejection fraction and the impact of angiotensin receptor blocker treatment: data from the CHARM-study programme. Eur J Heart Fail, 18(12), 1508–1517. https://doi.org/10.1002/ejhf.609
Damman, Kevin, Scott D. Solomon, Marc A. Pfeffer, Karl Swedberg, Salim Yusuf, James B. Young, Jean L. Rouleau, Christopher B. Granger, and John J. V. McMurray. “Worsening renal function and outcome in heart failure patients with reduced and preserved ejection fraction and the impact of angiotensin receptor blocker treatment: data from the CHARM-study programme.Eur J Heart Fail 18, no. 12 (December 2016): 1508–17. https://doi.org/10.1002/ejhf.609.
Damman K, Solomon SD, Pfeffer MA, Swedberg K, Yusuf S, Young JB, Rouleau JL, Granger CB, McMurray JJV. Worsening renal function and outcome in heart failure patients with reduced and preserved ejection fraction and the impact of angiotensin receptor blocker treatment: data from the CHARM-study programme. Eur J Heart Fail. 2016 Dec;18(12):1508–1517.
Journal cover image

Published In

Eur J Heart Fail

DOI

EISSN

1879-0844

Publication Date

December 2016

Volume

18

Issue

12

Start / End Page

1508 / 1517

Location

England

Related Subject Headings

  • Tetrazoles
  • Stroke Volume
  • Renal Insufficiency
  • Randomized Controlled Trials as Topic
  • Proportional Hazards Models
  • Multivariate Analysis
  • Middle Aged
  • Male
  • Logistic Models
  • Humans