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Chiratidzo Rudado Sanyika

Publications and source records attributed to Chiratidzo Rudado Sanyika.

2 recordsLinked to original sources

Comparison of techniques for fine-tuning open-weight models for entity extraction from radiology reports

Converting free-text radiology reports into structured labels supports cohort building, quality assurance, and monitoring of clinical imaging models, but the strongest label extractors are hosted proprietary models whose use raises privacy, cost, and reproducibility concerns. We asked whether a fine-tuned open-weight model (Gemma-3-12B) can match GPT-4o at multi-label intracranial hemorrhage (ICH) acuity extraction from non-contrast head-CT reports, and which ingredients matter. Using a 2x2 design, we crossed two adaptation strategies (a discriminative classification head, CH; generative instruction fine-tuning, IFT) with two training-data sources (distillation of real GPT-4o-labeled reports; synthetic reports generated by GPT-4o from real exemplars), across five training sizes, benchmarked on 100 expert-adjudicated reports against GPT-4o and the un-tuned open-weight base. The distilled instruction-tuned model (DIFT) matched GPT-4o (macro-F1 0.845 vs 0.850; p = 1.000) and exceeded the base model by 0.178. The decisive factor was the training-data source, not the fine-tuning method: both synthetic-data models failed to exceed the un-tuned open-weight base at any training size and underperformed the distilled models across all acuity classes. Fine-tuning and inference fit within the memory envelope of a single 24 GB consumer GPU. For narrow, high-value clinical label-extraction tasks, distilling real reports, rather than generating synthetic ones, is what closes the gap to a hosted model, enabling a private, low-cost, version-stable on-premises alternative.

cs.CL↗

Impact of Label Noise from Large Language Models Generated Annotations on Evaluation of Diagnostic Model Performance

Large language models (LLMs) are increasingly used to generate labels from radiology reports to enable large-scale AI evaluation. However, label noise from LLMs can introduce bias into performance estimates, especially under varying disease prevalence and model quality. This study quantifies how LLM labeling errors impact downstream diagnostic model evaluation. We developed a simulation framework to assess how LLM label errors affect observed model performance. A synthetic dataset of 10,000 cases was generated across different prevalence levels. LLM sensitivity and specificity were varied independently between 90% and 100%. We simulated diagnostic models with true sensitivity and specificity ranging from 90% to 100%. Observed performance was computed using LLM-generated labels as the reference. We derived analytical performance bounds and ran 5,000 Monte Carlo trials per condition to estimate empirical uncertainty. Observed performance was highly sensitive to LLM label quality, with bias strongly influenced by disease prevalence. In low-prevalence settings, small reductions in LLM specificity led to substantial underestimation of sensitivity. For example, at 10% prevalence, an LLM with 95% specificity yielded an observed sensitivity of ~53% despite a perfect model. In high-prevalence scenarios, reduced LLM sensitivity caused underestimation of model specificity. Monte Carlo simulations consistently revealed downward bias, with observed performance often falling below true values even when within theoretical bounds. LLM-generated labels can introduce systematic, prevalence-dependent bias into model evaluation. Specificity is more critical in low-prevalence tasks, while sensitivity dominates in high-prevalence settings. These findings highlight the importance of prevalence-aware prompt design and error characterization when using LLMs for post-deployment model assessment in clinical AI.

stat.ME↗