Evidence map›Paper›PMID 42684595›Full record

ArticleAnnals of biomedical engineering2026

Predicting Craniospinal Surgery in Pediatric Achondroplasia: Benchmarking Statistical Inference and Explainable AI Under Rare-Disease Constraints.

Seifollah Gholampour, Jesse Huang, Dylan Keusch, Carolina Lopes, Aseel Masarwy, James Obayashi, Marcella Ruppert-Gomez, Christina M Sayama, Lissa C Baird, Moise Danielpour and 1 more

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Article in Annals of biomedical engineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

11 authors.

Seifollah GholampourDepartment of Neurological Surgery, University of Chicago Medicine, Chicago, IL, USA.
Jesse HuangDepartment of Neurological Surgery, University of Chicago Medicine, Chicago, IL, USA.
Dylan KeuschBoston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Carolina LopesBoston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Aseel MasarwyDepartment of Neurosurgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
James ObayashiDoernbecher Children's Hospital, Oregon Health & Science University, Portland, OR, USA.
Marcella Ruppert-GomezBoston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Christina M SayamaDoernbecher Children's Hospital, Oregon Health & Science University, Portland, OR, USA.
Lissa C BairdBoston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Moise DanielpourDepartment of Neurosurgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
David F BauerDivision of Neurosurgery, Department of Surgery, Texas Children's Hospital/Baylor College of Medicine, Houston, TX, USA. dfbauer@texaschildrens.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo develop a framework that benchmarks penalized statistical inference against explainable artificial intelligence (XAI) methods for predicting cranial and spinal surgical need in pediatric achondroplasia under small-cohort, class-imbalanced, and phenotypically heterogeneous conditions.

methodsWe analyzed 34 clinical, demographic, and imaging variables in a multicenter cohort (four U.S. hospitals) of 150 pediatric patients with achondroplasia. We benchmarked penalized statistical inference (ridge regression and generalized additive models [GAMs]) against nine cost-sensitive classifiers, and applied post hoc SHapley Additive exPlanations (SHAP) to interpret the best-performing classifier.

resultsThe stacked ensemble achieved superior test-set performance (accuracy and macro-F1 = 0.77) with stable generalization and significantly higher discrimination than the GAM baseline (cranial AUROC 0.78 vs. 0.68; spinal AUROC 0.76 vs. 0.66). Calibration was acceptable, and decision curve analysis showed positive net benefit across relevant thresholds for both outcomes. SHAP highlighted class-specific drivers: foramen magnum (FM) stenosis, hydrocephalus, family history, frontal bossing, sleep disturbance, and age for cranial surgery, and spinal stenosis, Chiari malformation, family history, back pain, FM stenosis, and age for spinal surgery. SHAP dependence patterns suggested context-dependent age attributions in relation to FM or spinal stenosis, rather than a consistent standalone age effect. Several SHAP-highlighted predictors (e.g., sleep disturbance, back pain, and age) were nonsignificant in the inferential baselines. Kaplan-Meier curves indicated earlier intervention in high-risk phenotypes.

conclusionIn a reproducible dual-stream benchmark, XAI improved discrimination over conventional inference by capturing clinically contextualized, complex nonlinear predictive dependencies and interactions associated with cranial and spinal surgical risk in achondroplasia using preoperative variables.

Indexed as

AchondroplasiaClinical decision support systemCraniospinal surgeryExplainable artificial intelligence (XAI)Generalized additive models (GAMs)Surgical risk stratification

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.