Multiple organ dysfunction: Baseline and serial component scores

Citation
R. Cook et al., Multiple organ dysfunction: Baseline and serial component scores, CRIT CARE M, 29(11), 2001, pp. 2046-2050
Citations number
38
Categorie Soggetti
Aneshtesia & Intensive Care
Journal title
CRITICAL CARE MEDICINE
ISSN journal
00903493 → ACNP
Volume
29
Issue
11
Year of publication
2001
Pages
2046 - 2050
Database
ISI
SICI code
0090-3493(200111)29:11<2046:MODBAS>2.0.ZU;2-L
Abstract
Objective: The multiple organ dysfunction score (MODS) describes and quanti fies organ-specific physiology. The objective of this study was to examine the relation between six components of MODS (cardiovascular, respiratory, r enal, central nervous system, hepatic, and hematologic) measured at admissi on to the intensive core unit (ICU) and during the ICU stay, with time to d eath in the ICU. Design: Prospective observational cohort study. Setting. Sixteen Canadian ICUs. Patients., A total of 1,200 patients were mechanically ventilated for > 48 hrs. Measurements and Main Results. The six organ systems comprising MODS were m easured at ICU admission (baseline scores) and daily thereafter. The change in organ dysfunction each day (serial scores) were calculated as daily com ponent scores minus the corresponding baseline component scores. In Cox reg ression analyses, the independent explanatory variables were the MODS compo nents measured at baseline and serially, and the dependent variable was the time from admission to ICU mortality. When each organ system was analyzed individually, both the baseline and serial MODS for the cardiovascular, res piratory, renal, central nervous system, and hematologic components were si gnificantly associated with ICU mortality. After adjusting for the serial h epatic score, the baseline hepatic score was unrelated to mortality. After adjusting for all baseline and serial MODS components in aggregate, four or gan systems were significantly associated with ICU mortality: cardiovascula r (baseline relative risk [RR], 1.5; serial RR, 1.4); respiratory (baseline RR, 1.4; serial RR, 1.4); renal (baseline RR, 1.3; serial RR, 1.5); and ce ntral nervous system (baseline RR, 1.6; serial RR, 1.7). We found that the relative risk of mortality related to organ dysfunction varied significantl y over time and among organ systems. Baseline respiratory function was not associated with mortality until the second ICU week (week 1: RR, 1.1 [0.9-1 .4]; week 2 onward: RR, 1.9 [1.5-2.4]); the same was true for the change in respiratory function as measured by the serial respiratory score (week 1: RR, 1.2 [1.0-1.5]; week 2 onward: RR, 1.7 [1.4-2.1]). The serial hepatic sc ore was not associated with mortality until the fourth ICU week (weeks 1-3: RR, 0,9 [0.7-1.1]; week 4 onward: RR, 1.4 [1.0-2.0]). Conclusions: Organ dysfunction scores describe physiology at ICU admission and during ICU stay. Although patterns vary by system, daily MODS component scores provide additional prognostic value over baseline MODS.