Evidence map›Paper›PMID 42274982›Full record

ArticleSpine deformity2026

Evolution of multimodal intraoperative neuromonitoring in pediatric spinal deformity surgery over 39 years: are we better?

Gabrielle A Rogie, Hilton C Braithwaite, Chris Bozorgmehr, Leah Rakers, Brian A Kelly, Scott J Luhmann

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Article in Spine deformity, 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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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Gabrielle A RogieDepartment of Orthopedic Surgery, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
Hilton C BraithwaiteDepartment of Orthopedic Surgery, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
Chris BozorgmehrDepartment of Orthopedic Surgery, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
Leah RakersDepartment of Electrophysiology, Barnes-Jewish Hospital, St. Louis, MO, USA.
Brian A KellyDepartment of Orthopedic Surgery, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
Scott J LuhmannDepartment of Orthopedic Surgery, Washington University in St. Louis School of Medicine, St. Louis, MO, USA. luhmanns@wustl.edu.ORCID http://orcid.org/0000-0003-3656-5962

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo describe the incidence and characteristics of multimodal intraoperative neuromonitoring (IONM) in pediatric spinal deformity surgery between two eras (1985-2008 vs. 2008-2024).

methodsA review was conducted of 3316 consecutive pediatric spinal deformity surgeries (2008-2024) at a single institution. Neuromonitoring modalities included somatosensory-evoked potentials (SSEP), transcranial electrical motor-evoked potentials (TCeMEP), and descending neurogenic-evoked potentials (DNEP). Due to inherent cohort heterogeneity and evolving surgical standards over four decades, a descriptive analysis was prioritized to characterize shifts in monitoring performance and case complexity.

resultsIONM alerts were more frequent in 2008-2024 at 4.1% (1 in 24) versus 2.2% (1 in 46). Highest alert rates were in kyphosis/kyphoscoliosis (14.8% vs. 9.3%) and revision procedures (9.5% vs. 3.0%). Most alerts occurred during correction/instrumentation (62.2% vs. 47%). Permanent neurologic deficits were more common in the modern cohort: 16 patients (0.48%, 1 in 207) versus 6 (0.17%, 1 in 573). False negatives occurred at similar frequencies (0.15% vs. 0.2%) but were more consequential, with 80% resulting in permanent deficits versus 14% previously. While lower in comparison to the historic era, IONM was associated with a disparity between alert frequent and observed permanent neurologic deficit rates with alerts occurring in 4.1% of cases and permanent deficits in 0.48% (historic era: 2.2 and 0.17%, respectively). However, this coincided with an increase in case complexity as evidenced by higher prevalence of three-column osteotomies and use of traction.

conclusionMultimodal IONM remains a critical adjunct in pediatric spinal deformity surgery, with alert events occurring in 4.1% of cases and an observed permanent neurologic deficit rate of 0.48%. False negatives, particularly nerve root related, remain a key limitation. Observed differences between eras likely reflect evolving case complexity, surgical techniques, and monitoring practices rather than changes in intrinsic monitoring performance.

Indexed as

Evolution of IONMIntraoperative neuromonitoringNeuromonitoring alertsPediatric spinal deformitySpinal cord monitoring

Identifiers

PMID42274982

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