4.7 Article

Clinical course and predictive value of congestion during hospitalization in patients admitted for worsening signs and symptoms of heart failure with reduced ejection fraction: findings from the EVEREST trial

Journal

EUROPEAN HEART JOURNAL
Volume 34, Issue 11, Pages 835-843

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/eurheartj/ehs444

Keywords

Heart failure; Signs and symptoms; Hospitalization; Outcomes; Morbidity; Mortality

Funding

  1. Otsuka Inc. (Rockville, Maryland, USA)
  2. Abbott
  3. Merck
  4. PDL BioPharma
  5. Medtronic
  6. Gambro
  7. Novartis
  8. Abbott Labs
  9. Astellas
  10. AstraZeneca
  11. Bayer Schering PharmaAG
  12. CorThera, Inc.
  13. Cytokinetics, Inc.
  14. DebioPharm SA
  15. ErrekappaTerapeutici (Milan, Italy)
  16. Glaxo Smith Kline
  17. JNJ
  18. Novartis Pharma AG
  19. Otsuka
  20. Sigma Tau
  21. Solvay Pharmaceuticals
  22. Pericor Therapeutics
  23. Amgen
  24. Johnson and Johnson
  25. Cardiokine

Ask authors/readers for more resources

Signs and symptoms of congestion are the most common cause for hospitalization for heart failure (HHF). The clinical course and prognostic value of congestion during HHF has not been systemically characterized. A post hoc analysis was performed of the placebo group (n 2061) of the EVEREST trial, which enrolled patients within 48 h of admission (median 24 h) for worsening HF with an EF 40 and two or more signs or symptoms of fluid overload [dyspnoea, oedema, or jugular venous distension (JVD)] for a median follow-up of 9.9 months. Clinician-investigators assessed patients daily for dyspnoea, orthopnoea, fatigue, rales, pedal oedema, and JVD and rated signs and symptoms on a standardized 4-point scale ranging from 0 to 3. A modified composite congestion score (CCS) was calculated by summing the individual scores for orthopnoea, JVD, and pedal oedema. Endpoints were HHF, all-cause mortality (ACM), and ACM HHF. Multivariable Cox regression models were used to evaluate the risk of CCS at discharge on outcomes at 30 days and for the entire follow-up period. The mean CCS obtained after initial therapy decreased from the mean SD of 4.07 1.84 and the median (25th, 75th) of 4 (3, 5) at baseline to 1.11 1.42 and 1 (0, 2) at discharge. At discharge, nearly three-quarters of study participants had a CCS of 0 or 1 and fewer than 10 of patients had a CCS 3. B-type natriuretic peptide (BNP) and amino terminal-proBNP, respectively, decreased from 734 (313, 1523) pg/mL and 4857 (2251, 9642) pg/mL at baseline to 477 (199, 1079) pg/mL, and 2834 (1218, 6075) pg/mL at discharge/Day 7. A CCS at discharge was associated with increased risk (HR/point CCS, 95 CI) for a subset of endpoints at 30 days (HHF: 1.06, 0.951.19; ACM: 1.34, 1.141.58; and ACM HHF: 1.13, 1.031.25) and all outcomes for the overall study period (HHF: 1.07, 1.011.14; ACM: 1.16, 1.091.24; and ACM HHF 1.11, 1.061.17). Patients with a CCS of 0 at discharge experienced HHF of 26.2 and ACM of 19.1 during the follow-up. Among patients admitted for worsening signs and symptoms of HF and reduced EF, congestion improves substantially during hospitalization in response to standard therapy alone. However, patients with absent or minimal resting signs and symptoms at discharge still experienced a high mortality and readmission rate.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available