A Clinical Prediction Model for Sudden Cardiac Arrest Presenting as Pulseless Electrical Activity
Chugh, H.; Reinier, K.; Uy-Evanado, A.; Nakamura, K.; Sovari, A. A.; Salvucci, A.; Jui, J.; Chugh, S. S.
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BackgroundThe incidence of sudden cardiac arrest (SCA) manifesting as pulseless electrical activity (PEA) has increased, and survival remains extremely low. Methods for early identification and management of high-risk individuals are needed, but no clinical risk scores currently exist to predict PEA-SCA. Our objective was to develop and validate a clinical prediction model for PEA-SCA. MethodsFrom an ongoing prospective, population-based study of SCA in Portland, Oregon (catchment pop. {approx}1 M, 2002-2020), we identified PEA-SCA adults. Lifetime clinical records were compared with those of a control group with >50% prevalence of significant coronary disease. Prediction models were constructed using backwards stepwise logistic regression in a training dataset (67%) and evaluated in a validation dataset (33%). Model discrimination was assessed using receiver operating characteristic curves (C statistic). External validation was performed in a geographically distinct population in Ventura County, California (population {approx}850,000, 2015-2022). ResultsThe final clinical algorithm (PEA-Risk) incorporating 12 clinical, electrocardiogram and medication variables demonstrated strong discrimination in the training dataset (C statistic = 0.860 [95% CI: 0.838-0.881]) and remained robust in internal (C statistic = 0.832 [95% CI: 0.800-0.865]) and external validation datasets (C statistic = 0.704 [95% CI: 0.665-0.743]). ConclusionsWe developed and externally validated a clinical algorithm for predicting PEA-SCA. Given the low rates of successful resuscitation after PEA arrest, this risk prediction tool may enable earlier identification and prevention of PEA-SCA. Clinical PerspectiveO_ST_ABSWhat is knownC_ST_ABSO_LIThe proportion of SCA presenting as pulseless electrical activity (PEA) is increasing, and survival from these events remains extremely low. C_LIO_LIThe are no available methods for clinical risk prediction of these events. C_LI What the study addsO_LIThe present study constructs and replicates a risk score for prediction of SCA manifesting with PEA using widely available clinical and noninvasive markers. C_LIO_LIThese findings have implications for developing prevention and management strategies for individuals at high risk of PEA-SCA. C_LI
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