TY - JOUR
T1 - Simultaneous prediction of new morbidity, mortality, and survival without new morbidity from pediatric intensive care
T2 - A new paradigm for outcomes assessment
AU - Pollack, Murray M.
AU - Holubkov, Richard
AU - Funai, Tomohiko
AU - Berger, John T.
AU - Clark, Amy E.
AU - Meert, Kathleen
AU - Berg, Robert A.
AU - Carcillo, Joseph
AU - Wessel, David L.
AU - Moler, Frank
AU - Dalton, Heidi
AU - Newth, Christopher J.L.
AU - Shanley, Thomas
AU - Harrison, Rick E.
AU - Doctor, Allan
AU - Jenkins, Tammara L.
AU - Tamburro, Robert
AU - Dean, J. Michael
N1 - Publisher Copyright:
© 2015 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved.
PY - 2015
Y1 - 2015
N2 - Objectives: Assessments of care including quality assessments adjusted for physiological status should include the development of new morbidities as well as mortalities. We hypothesized that morbidity, like mortality, is associated with physiological dysfunction and could be predicted simultaneously with mortality. Design: Prospective cohort study from December 4, 2011, to April 7, 2013. Setting: General and cardiac/cardiovascular PICUs at seven sites. Patients: Randomly selected PICU patients from their first PICU admission. Interventions: None. Measurements and Main Results: Among 10,078 admissions, the unadjusted morbidity rates (measured with the Functional Status Scale and defined as an increase of ? 3 from preillness to hospital discharge) were 4.6% (site range, 2.6-7.7%) and unadjusted mortality rates were 2.7% (site range, 1.3-5.0%). Morbidity and mortality were significantly (p < 0.001) associated with physiological instability (measured with the Pediatric Risk of Mortality III score) in dichotomous (survival and death) and trichotomous (survival without new morbidity, survival with new morbidity, and death) models without covariate adjustments. Morbidity risk increased with increasing Pediatric Risk of Mortality III scores and then decreased at the highest Pediatric Risk of Mortality III values as potential morbidities became mortalities. The trichotomous model with covariate adjustments included age, admission source, diagnostic factors, baseline Functional Status Scale, and the Pediatric Risk of Mortality III score. The three-level goodnessof-fit test indicated satisfactory performance for the derivation and validation sets (p > 0.20). Predictive ability assessed with the volume under the surface was 0.50 ± 0.019 (derivation) and 0.50 ± 0.034 (validation) (vs chance performance = 0.17). Sitelevel standardized morbidity ratios were more variable than standardized mortality ratios. Conclusions: New morbidities were associated with physiological status and can be modeled simultaneously with mortality. Trichotomous outcome models including both morbidity and mortality based on physiological status are suitable for research studies and quality and other outcome assessments. This approach may be applicable to other assessments presently based only on mortality.
AB - Objectives: Assessments of care including quality assessments adjusted for physiological status should include the development of new morbidities as well as mortalities. We hypothesized that morbidity, like mortality, is associated with physiological dysfunction and could be predicted simultaneously with mortality. Design: Prospective cohort study from December 4, 2011, to April 7, 2013. Setting: General and cardiac/cardiovascular PICUs at seven sites. Patients: Randomly selected PICU patients from their first PICU admission. Interventions: None. Measurements and Main Results: Among 10,078 admissions, the unadjusted morbidity rates (measured with the Functional Status Scale and defined as an increase of ? 3 from preillness to hospital discharge) were 4.6% (site range, 2.6-7.7%) and unadjusted mortality rates were 2.7% (site range, 1.3-5.0%). Morbidity and mortality were significantly (p < 0.001) associated with physiological instability (measured with the Pediatric Risk of Mortality III score) in dichotomous (survival and death) and trichotomous (survival without new morbidity, survival with new morbidity, and death) models without covariate adjustments. Morbidity risk increased with increasing Pediatric Risk of Mortality III scores and then decreased at the highest Pediatric Risk of Mortality III values as potential morbidities became mortalities. The trichotomous model with covariate adjustments included age, admission source, diagnostic factors, baseline Functional Status Scale, and the Pediatric Risk of Mortality III score. The three-level goodnessof-fit test indicated satisfactory performance for the derivation and validation sets (p > 0.20). Predictive ability assessed with the volume under the surface was 0.50 ± 0.019 (derivation) and 0.50 ± 0.034 (validation) (vs chance performance = 0.17). Sitelevel standardized morbidity ratios were more variable than standardized mortality ratios. Conclusions: New morbidities were associated with physiological status and can be modeled simultaneously with mortality. Trichotomous outcome models including both morbidity and mortality based on physiological status are suitable for research studies and quality and other outcome assessments. This approach may be applicable to other assessments presently based only on mortality.
KW - Critical care
KW - Functional status
KW - Functional status score
KW - Intensive care
KW - Morbidity
KW - Outcome prediction
KW - Pediatric critical care
KW - Pediatric intensive care
KW - Pediatris
KW - Severity of illness
UR - http://www.scopus.com/inward/record.url?scp=84942540543&partnerID=8YFLogxK
U2 - 10.1097/CCM.0000000000001081
DO - 10.1097/CCM.0000000000001081
M3 - Article
C2 - 25985385
AN - SCOPUS:84942540543
SN - 0090-3493
VL - 43
SP - 1699
EP - 1709
JO - Critical care medicine
JF - Critical care medicine
IS - 8
ER -