Adjusting for Congenital Heart Surgery Risk Using Administrative Data

被引:2
|
作者
Jayaram, Natalie [1 ,7 ]
Allen, Philip [2 ]
Hall, Matthew [3 ]
Karamlou, Tara [4 ]
Woo, Joyce [5 ]
Crook, Sarah [6 ]
Anderson, Brett R. [6 ]
机构
[1] Childrens Mercy Kansas City, Kansas City, MO USA
[2] Brigham & Womens Hosp, Boston, MA USA
[3] Childrens Hosp Assoc, Lenexa, KS USA
[4] Cleveland Clin, Cleveland, OH USA
[5] Lurie Childrens Hosp, Chicago, IL USA
[6] NewYork Presbyterian Columbia Univ Irving Med Ctr, New York, NY USA
[7] Childrens Mercy Kansas City, Heart Ctr, 2401 Gillham Rd, Kansas City, MO 64108 USA
关键词
congenital heart surgery; outcomes; risk-adjustment; COMPLEX CHRONIC CONDITIONS; EMPIRICALLY BASED TOOL; CENTER VOLUME; MORTALITY; MODELS; EPIDEMIOLOGY; ADJUSTMENT; CHILDREN; OUTCOMES; SOCIETY;
D O I
10.1016/j.jacc.2023.09.826
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Congenital heart surgery (CHS) encompasses a heterogeneous population of patients and surgeries. Risk standardization models that adjust for patient and procedural characteristics can allow for collective study of these disparate patients and procedures. OBJECTIVES We sought to develop a risk-adjustment model for CHS using the newly developed Risk Stratification for Congenital Heart Surgery for ICD-10 Administrative Data (RACHS-2) methodology.METHODS Within the Kids' Inpatient Database 2019, we identified all CHSs that could be assigned a RACHS-2 score. Hierarchical logistic regression (clustered on hospital) was used to identify patient and procedural characteristics associated with in-hospital mortality. Model validation was performed using data from 24 State Inpatient Databases during 2017. RESULTS Of 5,902,538 total weighted hospital discharges in the Kids' Inpatient Database 2019, 22,310 pediatric cardiac surgeries were identified and assigned a RACHS-2 score. In-hospital mortality occurred in 543 (2.4%) of cases. Using only RACHS-2, the mortality mode had a C-statistic of 0.81 that improved to 0.83 with the addition of age. A final multivariable model inclusive of RACHS-2, age, payer, and presence of a complex chronic condition outside of congenital heart disease further improved model discrimination to 0.87 (P < 0.001). Discrimination in the validation cohort was also very good with a C-statistic of 0.83. CONCLUSIONS We created and validated a risk-adjustment model for CHS that accounts for patient and procedural characteristics associated with in-hospital mortality available in administrative data, including the newly developed RACHS-2. Our risk model will be critical for use in health services research and quality improvement initiatives.
引用
收藏
页码:2212 / 2221
页数:10
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