ArticleInternational journal of cardiology. Congenital heart disease2024
Improved complexity stratification in congenital heart disease; the impact of including procedural data on accuracy and reliability.
Article in International journal of cardiology. Congenital heart disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Bridging communication gaps to improve adult congenital heart disease care: patient perspectives from a qualitative study.BMC health services research · 2026Article
- Using big data to search for possible geographic clustering of Congenital Heart Disease (CHD) across Australia.PLOS digital health · 2026Article
- Mortality rates in adults with severe congenital heart disease: insights from the National Congenital Heart Disease Registry of Australia.International journal of cardiology. Congenital heart disease · 2025Article
- A national Australian Congenital Heart Disease registry; methods and initial results.International journal of cardiology. Congenital heart disease · 2024Article
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Authors and funding
6 authors.
Funding
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Abstract
Background: In order to manage a class of diseases as broad as congenital heart disease (CHD), multiple "manually generated" classification systems defining CHDs as mild, moderate and severe have been developed and used to good effect. As databases have grown, however, such "manual" complexity scoring has become infeasible. Though past attempts have been made to determine CHD complexity algorithmically using a list of diagnoses alone, missing data and lack of procedural information have been significant limitations. Methods: We built an algorithm that can stratify the complexity of patients with CHD by integrating their diagnoses with a list of their previous procedures. Specific procedures which address a missing diagnosis or imply a certain operative status were used to supplement the diagnosis list. To verify this algorithm, CHD specialists manually checked the classification of 100 children and 100 adults across four hospitals in Australia. Results: Our algorithm was 99.5% accurate in the manually checked cohort (100% in children and 99% in adults) and was able to automatically classify more than 90% of a cohort of over 24,000 CHD patients, including 92.5% of children (vs 84.4% without procedures, p < 0.0001) and 91.1% of adults (vs 70.4% without procedures; p < 0.0001). Conclusions: CHD complexity scoring is significantly improved by access to procedural history and can be automatically calculated with high accuracy.
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