PREDICTION OF SURVIVAL OF CRITICALLY ILL PATIENTS BY ADMISSION COMORBIDITY

Citation
Rm. Poses et al., PREDICTION OF SURVIVAL OF CRITICALLY ILL PATIENTS BY ADMISSION COMORBIDITY, Journal of clinical epidemiology, 49(7), 1996, pp. 743-747
Citations number
28
Categorie Soggetti
Public, Environmental & Occupation Heath","Medicine, General & Internal
ISSN journal
08954356
Volume
49
Issue
7
Year of publication
1996
Pages
743 - 747
Database
ISI
SICI code
0895-4356(1996)49:7<743:POSOCI>2.0.ZU;2-K
Abstract
The objective of this study was to determine how well the Charlson ind ex of comorbidity would predict mortality of critically ill patients; and how the predictive ability of the index would compare with that of the comorbidity component (Chronic Health Points) of the APACHE II sy stem. This prospective cohort study included in its setting an intensi ve care unit (ICU) and intermediate ICU (IICU) in a teaching hospital. Patients included a previously assembled inception cohort of 201 pati ents consecutively admitted to either unit, followed until death or di scharge from the hospital, excluding patients admitted after coronary artery bypass grafting, for planned dialysis, or transferred to the II CU from another intensive care unit. Main outcome measures were record ed as death in hospital versus survival at discharge. For each patient we had prospectively obtained all data necessary to predict the proba bility of in hospital death using the APACHE II system, and to classif y comorbidity using the Charlson index. The Charlson index had signifi cant ability to discriminate between patients who would live and who w ould die (ROC curve area = 0.67, SE = 0.05). The Chronic Health Points component of APACHE II had no significant discriminating ability (ROC area 0.57, SE = 0.05), although the full APACHE II system was an exce llent predictor (area = 0.87, SE = 0.04). Logistic regression analyses suggested that the Charlson index could contribute significant (p = 0 .03) prognostic information to that obtained from the components of AP ACHE II other than Chronic Health, i.e., acute physiological derangeme nt, age, and reason for admission, but the Chronic Health Points compo nent of APACHE II could not so contribute to the rest of APACHE II (p = 0.19). Our conclusion is that use of the detailed information about comorbidity captured by the Charlson index could improve prognostic pr edictions even for critically ill patients.