Guideline2Graph: Profile-Aware Multimodal Parsing for Executable Clinical Decision Graphs
- URL: http://arxiv.org/abs/2604.02477v1
- Date: Thu, 02 Apr 2026 19:21:31 GMT
- Title: Guideline2Graph: Profile-Aware Multimodal Parsing for Executable Clinical Decision Graphs
- Abstract summary: We present a decomposition-first pipeline that converts full-guideline evidence into an executable clinical decision graph.<n>We evaluate on an adjudicated prostate-guideline benchmark with matched inputs and the same underlying VLM backbone.
- Score: 3.459382629188014
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Clinical practice guidelines are long, multimodal documents whose branching recommendations are difficult to convert into executable clinical decision support (CDS), and one-shot parsing often breaks cross-page continuity. Recent LLM/VLM extractors are mostly local or text-centric, under-specifying section interfaces and failing to consolidate cross-page control flow across full documents into one coherent decision graph. We present a decomposition-first pipeline that converts full-guideline evidence into an executable clinical decision graph through topology-aware chunking, interface-constrained chunk graph generation, and provenance-preserving global aggregation. Rather than relying on single-pass generation, the pipeline uses explicit entry/terminal interfaces and semantic deduplication to preserve cross-page continuity while keeping the induced control flow auditable and structurally consistent. We evaluate on an adjudicated prostate-guideline benchmark with matched inputs and the same underlying VLM backbone across compared methods. On the complete merged graph, our approach improves edge and triplet precision/recall from $19.6\%/16.1\%$ in existing models to $69.0\%/87.5\%$, while node recall rises from $78.1\%$ to $93.8\%$. These results support decomposition-first, auditable guideline-to-CDS conversion on this benchmark, while current evidence remains limited to one adjudicated prostate guideline and motivates broader multi-guideline validation.
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