Incremental value of C‐reactive protein to the MEESSI acute heart failure risk score

Author:

Wussler Desiree12ORCID,Belkin Maria12,Shrestha Samyut12,Wernicke Hannah1,Papachristou Androniki12,Nowak Albina13,Aliyeva Fatima1,Mork Constantin14,Strebel Ivo1,Huré Gabrielle Valerie Francoi1,Weil Dominic1,Michou Eleni15,Kozhuharov Nikola1,Gualandro Danielle M.1,Puelacher Christian1,Miró Oscar6,Rossello Xavier7,Martín‐Sánchez Francisco Javier8,Pocock Stuart J.9,Goudev Assen10,Breidthardt Tobias12,Mueller Christian1

Affiliation:

1. Cardiovascular Research Institute Basel (CRIB) and Department of Cardiology University Hospital Basel, University of Basel Basel Switzerland

2. Department of Internal Medicine University Hospital Basel Basel Switzerland

3. Department of Endocrinology and Clinical Nutrition University Hospital Zurich, University of Zurich Zurich Switzerland

4. University Clinic of Medicine, Cantonal Hospital Baselland Liestal Switzerland

5. Department of Cardiology Cantonal Hospital Aarau Aarau Switzerland

6. Emergency Department Hospital Clínic, University Barcelona Barcelona Spain

7. Cardiology Department Institut d'Investigació Sanitària Illes Balears (IdISBa), Hospital Universitari Son Espases Palma de Mallorca Spain

8. Emergency Department Hospital Clínico San Carlos, Universidad Complutense Madrid Spain

9. Department of Medical Statistics, Department of Epidemiology and Population Health London School of Hygiene and Tropical Medicine London UK

10. Department of Cardiology Queen Ioanna University Hospital Sofia, Medical University of Sofia Sofia Bulgaria

Abstract

AbstractAimsWe hypothesized that the current gold standard for risk stratification of patients with acute heart failure (AHF), the Multiple Estimation of risk based on the Emergency department Spanish Score In patients with AHF (MEESSI‐AHF) risk score, can be further improved by adding systemic inflammation as quantified by C‐reactive protein (CRP).Methods and resultsIn a prospective multicentre diagnostic study (BASEL V), AHF was centrally adjudicated by two independent cardiologists. The MEESSI‐AHF risk score was calculated using an established reduced and recalibrated model containing 12 independent risk factors. Model extension was performed by refitting and adding CRP in the logistic regression model with 30‐day mortality as binary outcome. Discrimination, calibration and clinical usefulness were used to assess the performance of the extended Multiple Estimation of risk based on the Emergency department Spanish Score In patients (MEESSI) model. Validation was performed in an independent, retrospective and single‐centre AHF cohort. Among 1208 AHF patients with complete data allowing calculation of the recalibrated MEESSI and the extended MEESSI models, the prognostic accuracy for 30‐day mortality of the extended MEESSI model (c‐statistic 0.83, 95% confidence interval [CI] 0.79–0.87) was significantly higher compared to the recalibrated model (c‐statistic 0.79, 95% CI 0.75–0.83, p = 0.013). The extended model allowed to stratify a higher percentage of patients into the lowest risk group compared to the recalibrated model (33.1% vs. 20.3%). Demonstrating a calibration plot's slope of 1.00 (95% CI 0.81–1.19) and an intercept of 0.0 (95% CI −0.22 to 0.22), the extended MEESSI model achieved excellent and improved calibration. Results were confirmed in the independent validation cohort (n = 575).ConclusionsQuantifying inflammation using CRP concentration provided incremental value in AHF risk stratification using the established MEESSI model.

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Schweizerische Herzstiftung

Publisher

Wiley

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