[HTML][HTML] Development of a diagnosis-and procedure-based risk model for 30-day outcome after pediatric cardiac surgery

S Crowe, KL Brown, C Pagel, N Muthialu… - The Journal of thoracic …, 2013 - Elsevier
S Crowe, KL Brown, C Pagel, N Muthialu, D Cunningham, J Gibbs, C Bull, R Franklin…
The Journal of thoracic and cardiovascular surgery, 2013Elsevier
OBJECTIVE: The study objective was to develop a risk model incorporating diagnostic
information to adjust for case-mix severity during routine monitoring of outcomes for pediatric
cardiac surgery. METHODS: Data from the Central Cardiac Audit Database for all pediatric
cardiac surgery procedures performed in the United Kingdom between 2000 and 2010 were
included: 70% for model development and 30% for validation. Units of analysis were 30-day
episodes after the first surgical procedure. We used logistic regression for 30-day mortality …
OBJECTIVE
The study objective was to develop a risk model incorporating diagnostic information to adjust for case-mix severity during routine monitoring of outcomes for pediatric cardiac surgery.
METHODS
Data from the Central Cardiac Audit Database for all pediatric cardiac surgery procedures performed in the United Kingdom between 2000 and 2010 were included: 70% for model development and 30% for validation. Units of analysis were 30-day episodes after the first surgical procedure. We used logistic regression for 30-day mortality. Risk factors considered included procedural information based on Central Cardiac Audit Database “specific procedures,” diagnostic information defined by 24 “primary” cardiac diagnoses and “univentricular” status, and other patient characteristics.
RESULTS
Of the 27,140 30-day episodes in the development set, 25,613 were survivals, 834 were deaths, and 693 were of unknown status (mortality, 3.2%). The risk model includes procedure, cardiac diagnosis, univentricular status, age band (neonate, infant, child), continuous age, continuous weight, presence of non–Down syndrome comorbidity, bypass, and year of operation 2007 or later (because of decreasing mortality). A risk score was calculated for 95% of cases in the validation set (weight missing in 5%). The model discriminated well; the C-index for validation set was 0.77 (0.81 for post-2007 data). Removal of all but procedural information gave a reduced C-index of 0.72. The model performed well across the spectrum of predicted risk, but there was evidence of underestimation of mortality risk in neonates undergoing operation from 2007.
CONCLUSIONS
The risk model performs well. Diagnostic information added useful discriminatory power. A future application is risk adjustment during routine monitoring of outcomes in the United Kingdom to assist quality assurance.
Elsevier
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