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Table · dataset · 2026

<p>S2 Table; Figs S1 and S2; Tables S2-S11.</p>

Listed in ZivaHub and HKU DataHub and DaYta Ya Rona and figshare and Loughborough Research Repository and UP Research Data Repository — shown once because both records carry DOI 10.1371/journal.pone.0359577.s002

<div><p>Choosing an appropriate imputation strategy for clinical datasets requires understanding which missing data mechanism is operative, yet most imputation benchmarks conflate performance across mechanisms.

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The present work addresses this gap by conducting the first mechanism-stratified comparison of three imputation approaches—CHIT, Multiple Imputation by Chained Equations via BayesianRidge (MICE), and Random-Forest-based Iterative Imputation—across Missing Completely at Random (MCAR), Missing at Random (MAR), and Missing Not at Random (MNAR) conditions.

Three health datasets serve as experimental platforms: the Chronic Kidney Disease (CKD) dataset, the Heart Disease Dataset (HDD), and the Mice Protein Expression Dataset (MPED). Domain-knowledge-driven missingness patterns are constructed for each mechanism (Fig 2) at approximately 20–25% overall rates. Eight classifiers—KNN, Logistic Regression, SVC, Decision Tree, Random Forest, Gaussian Naïve Bayes, MLP, and a deep neural network—are trained on imputed data following GridSearchCV optimisation.

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Across all conditions, CHIT achieves near-perfect or perfect downstream classification, with SVC reaching up to 100% accuracy on the CKD dataset under MNAR, and 98.75% under MCAR and MAR. Competing methods degrade by up to 19.38 percentage points under MNAR, while CHIT’s accuracy remains stable. Two structural properties account for this resilience: an iterative enrichment of the regression training set as records are completed, and a within-record prioritisation of the most data-scarce features for model-based filling.

Taken together, these results provide mechanism-specific guidance for imputation selection in health informatics pipelines. Statistical significance of classifier accuracy differences between CHIT and MICE was assessed using McNemar’s test (two-tailed, continuity-corrected chi-square) applied to the exact binary prediction vectors from each experiment [n_test = 80]. Ninety-five percent confidence intervals for all reported accuracy values were computed using the Wilson score method [z = 1.96].

The 42-configuration mean accuracy and standard deviation for CHIT are reported in Supplementary <a href="plosone.org/article/info:doi/10.1371/journal.pone.0359577#pone.0359577.s001" target="_blank">Table S1</a>. Full McNemar results with confidence intervals are in Supplementary <a href="plosone.org/article/info:doi/10.1371/journal.pone.0359577#pone.0359577.s002" target="_blank">Table S2</a>.</p></div>

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Cardiovascular disease 65% · Data management and data science 71% · Disease 75% · Heart 75% · Tabular 65%
Provenance · 6 source records, 55 field assertions
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