Study of clinical course of organ dysfunction in intensive care
- 1 February 2004
- journal article
- research article
- Published by Wolters Kluwer Health in Critical Care Medicine
- Vol. 32 (2) , 384-390
- https://doi.org/10.1097/01.ccm.0000108881.14082.10
Abstract
Objective Multiple organ dysfunction is a common cause of death in intensive care units. We describe the daily course of multiple organ dysfunction measured by the Sequential Organ Failure Assessment score in a population-based cohort of critically ill patients. Design Prospective cohort study. Setting Adult multisystem intensive care units in the Calgary Health Region. Patients A total of 1,436 patients admitted from May 1, 2000 to April 30, 2001. Measurements Temporal change in Sequential Organ Failure Assessment score. Interventions None; observational study. Main Results The mean age was 58 yrs (range, 14–100). The mean ± sd intensive care unit admission Acute Physiology and Chronic Health Evaluation II score was 25 ± 9. The median intensive care unit length of stay was 4 days (interquartile range, 2–8), and the median hospital length of stay was 15 days (interquartile range, 7–32). A total of 20.5% of patients were infected at admission, and 26.0% were immediately postoperative. Intensive care unit mortality was 27.0%, and hospital mortality was 35.1%. The daily Sequential Organ Failure Assessment score was significantly higher in nonsurvivors than survivors. A population-averaged model determined a mean rate of change of Sequential Organ Failure Assessment score to be −0.29 per day (95% confidence interval, −0.32 to −0.25) for survivors and −0.03 per day (95% confidence interval, −0.08 to 0.03) for nonsurvivors (overall regression, p < .0001). Patients with infection had higher admission Sequential Organ Failure Assessment scores compared with patients without infection (difference, 1.8; p < .001), but a similar rate of daily change. Conclusions Multiple organ dysfunction, does not follow a course of progressive and sequential failure. Evidence of differential daily change should further inform the use of organ failure scores as surrogate outcomes in clinical trials.Keywords
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