PERFORMANCE OF THE EARLY WARNING SYSTEM VITAL TO PREDICT UNANTICIPATED HIGHER-LEVEL OF CARE ADMISSION AND IN-HOSPITAL DEATH OF WARD PATIENTS
Author(s)
Correia S1, Gomes A2, Shahriari S1, Almeida JP3, Severo M4, Azevedo A5
1EpiUnit - Institute of Public Health, University of Porto, Porto, Portugal, 2Hospital Epidemiology Center & Dep Internal Medicine - Centro Hospitalar São João, Porto, Portugal, 3Business Intelligence and Data Science Department - Centro Hospitalar São João, Porto, Portugal, 4Department of Public Health and Forensic Sciences, and Medical Education, Faculdade de Medicina Universidade do Porto, Porto, Portugal, 5Hospital Epidemiology Center - Centro Hospitalar São João, Porto, Portugal
OBJECTIVES: Early Warning Scores to predict patients’ clinical deterioration are recommended to improve outcomes. We aimed to validate a tool integrating real-time vital signs and laboratory results in predicting adverse outcomes in patients hospitalized in medical wards. METHODS: VITAL (surVeiIIlance, moniToring and ALert) is a score developed at Centro Hospitalar São João, a tertiary hospital with 1083 beds (Portugal). Each parameter (n=14) was classified as abnormal when below or above a threshold or if a significant change occurred. The algorithm was run in a retrospective dataset of patients admitted from February to June 2013 (402,044 measurements) to test the ability of the score to predict unanticipated admission to higher level of care (HLC) and death within 24 hours. The performance of VITAL (including a modified version with parameters weighing differentially) was assessed by the area under the receiver operating characteristic (AUROC) curve, and the number needed to evaluate (NNE) and rate of alerts for different cut-offs. RESULTS: Admission to HLC and death within 24 hours of score calculation occurred in 0.4% and 0.7% of patients, respectively. The AUROC (95%CI) values were 0.65 (0.62-0.68) for predicting admission to HLC and 0.69 (0.67-0.70) for death. For VITAL ≥3, 5 alerts per 100 patients per day would occur, with a positive predictive value of 1.7% (95%CI; 1.3%-2.0%) and 3.9% (3.4%-4.5%), respectively. VITAL ≥3 would elicit further evaluation of 69 and 33 patients to detect one admission to HLC and one death, respectively. Part of the apparently false positive alerts at 24 hours developed the adverse event in the following 3 to 7 days. CONCLUSIONS: VITAL performed well to identify patients at high short-term risk of admission to HLC and death, with a relatively low additional workload, and would also result in earlier detection of events, contributing to the improvement of patient care.
Conference/Value in Health Info
2018-11, ISPOR Europe 2018, Barcelona, Spain
Value in Health, Vol. 21, S3 (October 2018)
Code
PRM28
Topic
Clinical Outcomes, Methodological & Statistical Research
Topic Subcategory
Clinical Outcomes Assessment, Confounding, Selection Bias Correction, Causal Inference
Disease
Multiple Diseases
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