Recalibration of the pediatric risk of admission score using a multi-institutional sample

被引:23
作者
Chamberlain, JM
Patel, KM
Pollack, MM
Brayer, A
Macias, CG
Okada, P
Schunk, JE
机构
[1] Childrens Hosp, Childrens Natl Med Ctr, Div Emergency Med, Washington, DC 20010 USA
[2] Childrens Res Inst, Div Emergency Med, Washington, DC 20010 USA
[3] Childrens Res Inst, Div Crit Care Med, Washington, DC 20010 USA
[4] Childrens Res Inst, Dept Pediat, Washington, DC 20010 USA
[5] George Washington Univ, Sch Med & Hlth Sci, Washington, DC USA
[6] Univ Rochester, Sch Med, Dept Emergency Med & Pediat, Rochester, NY 14642 USA
[7] Baylor Coll Med, Texas Childrens Hosp, Dept Emergency Med, Houston, TX 77030 USA
[8] Univ Texas, SW Med Ctr, Dept Pediat, Div Emergency Med, Dallas, TX 75230 USA
[9] Univ Utah, Sch Med, Primary Childrens Med Ctr, Dept Pediat,Div Pediat Emergency Med, Salt Lake City, UT USA
关键词
D O I
10.1016/j.annemergmed.2003.08.001
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Study objective: Case-mix adjustment is a critical component of quality assess ment and benchmarking. The Pediatric Risk of Admission (PRISA) score is composed of descriptive, physiologic, and diagnostic variables that provide a probability of hospital admission as an index of severity. The score was developed and validated in a single tertiary pediatric hospital emergency department (ED) after exclusion of children with minor injuries and illnesses. We provide a multi-institutional recalibration and validation of the PRISA score and test its performance in 4 additional EDs, including patients with minor injuries and illnesses. Methods: Masked, photocopied, randomly selected medical records of ED patients from 2000 were abstracted and were used to test the performance (discrimination and calibration) of the original PRISA score. This sample differed from the original PRISA sample by including 5 hospitals and including patients with minor injuries and minor illnesses. Independent variables included components of acute and chronic history, physiologic variables, and 3 ED therapies. The dependent variable was hospital admission. PRISA was then recalibrated as needed by using an 80% development sample and a 20% validation sample. Area under the curve and the Hosmer-Lemeshow goodness-of-fit test were used to measure, respectively, discrimination and calibration of the PRISA score after recalibration. We then applied the recalibrated PRISA score to secondary outcomes to test construct validity. We reasoned that a valid measure of ED severity should also be associated with the secondary outcomes of mandatory admissions (admissions using greater than or equal to1 inpatient resources) and ICU admissions. Results: The recalibrated PRISA score performed well in all deciles of predicted probability of admission. The area under the curve was 0.81 and the calibration was good (Hosmer-Lemeshow 10.658; df=8; P=.222) for the development sample, and the area under the curve was 0.785 with excellent calibration (Hosmer-Lemeshow 8.341; df=9; P=.500) for the validation sample. The overall development sample had 423.9 admissions predicted and 423 observed; the validation sample had 112.1 predicted and 110 observed. Conclusion: The PRISA score has been recalibrated and performs well in EDs of tertiary pediatric hospitals. Comparison with this benchmark may allow individual EDs to improve their performance and may provide insight into best practices.
引用
收藏
页码:461 / 468
页数:8
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