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Regression Trees Identify Relevant Interactions: Can This Improve the Predictive Performance of Risk Adjustment?
Florian Buchner1,2, Jürgen Wasem1, Sonja Schillo1
1Institute for Health Services and Research CINCH, University of Duisburg-Essen, Essen, Germany.
This study introduces a novel regression tree method to identify complex interactions in risk equalization formulas. While it slightly improves accuracy, incorporating numerous interactions does not significantly enhance predictive performance in German social health insurance.
Area of Science:
- Health economics
- Biostatistics
- Social health insurance
Background:
- Risk equalization formulas are crucial for fair healthcare reimbursement but often overlook complex variable interactions.
- Existing methods struggle to systematically identify and incorporate these interactions due to their complexity.
Purpose of the Study:
- To develop and evaluate a novel method using regression trees to systematically identify and incorporate interactions in risk equalization.
- To assess the impact of including identified interactions on the accuracy of risk adjustment formulas.
Main Methods:
- A two-step approach was applied using a large German social health insurance dataset (nearly 2.9 million individuals).
- Step 1: A regression tree identified interaction effects between different morbidity groups.
- Step 2: Identified interactions were added to a traditional weighted least squares regression model, and coefficients were recalculated.
Main Results:
- The enhanced risk adjustment formula showed a marginal improvement in adjusted R-squared from 25.43% to 25.81% on the evaluation dataset.
- Analysis of predictive ratios for subgroups affected by interactions was performed.
- The inclusion of multiple morbidity interactions resulted in only a minor increase in overall accuracy.
Conclusions:
- The regression tree approach offers a systematic way to explore interactions in risk equalization.
- Despite the marginal R-squared improvement, the study suggests that not accounting for a large number of morbidity interactions does not lead to a significant loss in predictive accuracy at the sample level.
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