The first prognostic model for stroke and death in patients with systolic heart failure

Abstract Background Patients with systolic heart failure (HF) are at increased risk of both ischemic stroke and death. Currently, no risk scores are available to identify HF patients at high risk of stroke or death. The Warfarin vs. Aspirin in Reduced Cardiac Ejection Fraction (WARCEF) trial studied...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of cardiology 2016-08, Vol.68 (2), p.100-103
Hauptverfasser: Freudenberger, Ronald S., MD, Cheng, Bin, PhD, Mann, Douglas L., MD, Thompson, John L.P., PhD, Sacco, Ralph L., MD, Buchsbaum, Richard, BS, Sanford, Alexandra, MS, Pullicino, Patrick M., MD, Levin, Bruce, PhD, Teerlink, John R., MD, Graham, Susan, MD, Mohr, J.P., MD, Labovitz, Arthur J., MD, Di Tullio, Marco R., MD, Lip, Gregory Y.H., MD, Estol, Conrado J., MD, PhD, Lok, Dirk J., MD, Ponikowski, Piotr, MD, PhD, Anker, Stefan D., MD, PhD, Homma, Shunichi, MD
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Abstract Background Patients with systolic heart failure (HF) are at increased risk of both ischemic stroke and death. Currently, no risk scores are available to identify HF patients at high risk of stroke or death. The Warfarin vs. Aspirin in Reduced Cardiac Ejection Fraction (WARCEF) trial studied 2305 HF patients, in sinus rhythm, followed for up to 6 years (3.5 ± 1.5 years). This trial showed no overall difference in those treated with warfarin vs aspirin with regard to death or stroke. The present study develops the first prognostic model to identify patients at higher risk of stroke or death based on their overall risk profile. Methods and results A scoring algorithm using 8 readily obtainable clinical characteristics as predictors, age, gender, hemoglobin, blood urea nitrogen, ejection fraction, diastolic blood pressure, diabetes status, and prior stroke or transient ischemic attack (C-index = 0.65, 95% CI: 0.613–0.681), was developed. It was validated internally using a bootstrap method. In predicting 1-year survival for death alone, our 8-predictor model had an AUC of 0.63 (95% CI: 0.579–0.678) while the 14-predictor Seattle model had an AUC of 0.72. The Seattle model did not report stroke. Conclusions This novel prognostic model predicts the overall risk of ischemic stroke or death for HF patients. This model compares favorably for death with the Seattle model and has the added utility of including stroke as an endpoint. Use of this model will help identify those patients in need of more intensive monitoring and therapy and may help identify appropriate populations for trials of new therapies. Clinical Trial Registration http://www.Clinicatrials.gov NCT00041938.
ISSN:0914-5087
1876-4738
DOI:10.1016/j.jjcc.2015.09.014