Cardiometabolic biomarkers are predictors of readmission and death in patients hospitalized for acute dyspnea

Background: Acute dyspnea affects a large heterogeneous patient group with high mortality and readmission rates. Purpose: To investigate if cardiometabolic biomarkers and clinical characteristics predict readmission and death in patients hospitalized for acute dyspnea. Methods: 65 dyspnea patients at a general internal medicine ward were followed for six months. The combined endpoint was readmission or death. Measurements and results: Cardiometabolic biomarkers at admission were related to the endpoint in Cox proportional hazard models (adjusted for sex, age, oxygen saturation, respiratory rate and C-reactive protein (CRP)). The biomarkers tissue-type plasminogen activator (tPA), prolactin (PRL), tumor necrosis factor receptor superfamily member 6 (FAS) and C-C motif chemokine 3 (CCL3) were independently and significantly related to the endpoint and combined into a biomarker risk score (BRS). Each SD increment of the BRS conferred a hazard ratio (HR) of 2.13 (1.39-3.27) P = 0.001. The top vs bottom tertile of the BRS conferred a HR of 4.75 (1.9311.68) P = 0.001. Dyspnea severity was also associated with worse outcome, HR = 3.43 (1.28-9.20) P = 0.014. However, when mutually adjusted the BRS remained significant (P = 0.004) whereas dyspnea severity was not. The BRS was related to the endpoint among patients with mild to moderate dyspnea (P= 0.016) but not among those with severe dyspnea. Conclusion: A score of tPA, PRL, FAS and CCL3 predicts 6-month death and readmission in patients hospitalized for acute dyspnea and may prove useful to optimize length of stay and follow-up. Although the BRS outweighs dyspnea severity in prediction of the endpoint, its prognostic role is strongest in mild-moderate dyspnea. (C) 2016 The Authors. Published by Elsevier Inc.