Evidence map›Paper›PMID 42707645›Full record

ArticleCase reports in anesthesiology2026

Perioperative Management of Presumed Schwartz-Jampel Syndrome During Complex Pediatric Spinal Fusion: A Case Report.

Hannah Shreiner, Anna Booth, Amy McIntosh, Christopher McLeod

Abstract read
In one paragraph

Article in Case reports in anesthesiology, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Hannah ShreinerDepartment of Orthopedics, Scottish Rite for Children, Dallas, Texas, USA.ORCID https://orcid.org/0009-0000-5920-6861
Anna BoothDepartment of Orthopedics, Scottish Rite for Children, Dallas, Texas, USA.ORCID https://orcid.org/0000-0002-6223-4561
Amy McIntoshDepartment of Orthopedics, Scottish Rite for Children, Dallas, Texas, USA.ORCID https://orcid.org/0000-0002-3660-4901
Christopher McLeodDepartment of Orthopedics, Scottish Rite for Children, Dallas, Texas, USA.ORCID https://orcid.org/0000-0002-2561-459X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schwartz-Jampel syndrome (SJS) is associated with neuromuscular and structural abnormalities that can complicate perioperative and anesthetic management. The syndrome has been noted to create increased difficulty in anesthetic airway management with age. We report the perioperative course of a 13-year-old female with presumed SJS undergoing combined anterior and posterior spinal fusion for severe progressive congenital scoliosis. Preoperative evaluation revealed features predictive of a difficult airway, including limited mouth opening and restricted neck mobility, requiring video laryngoscopy for successful intubation. During the anterior thoracoscopic phase, dense pleural adhesions were encountered, requiring extensive pleural dissection and adhesiolysis to allow completion of the release of the anterior spinal column. After repositioning prone for the posterior procedure, the patient developed acute ventilation difficulty with markedly elevated airway pressures and severe hypercarbia. Flexible bronchoscopy revealed a nearly occlusive sanguineous mucus plug within the endotracheal tube, prompting abortion of the procedure. The patient returned 1 week later for completion of surgery, and difficulty with endotracheal tube depth was encountered due to a foreshortened trachea. She otherwise recovered without major complications. This case highlights the perioperative management of a complex pediatric neuromuscular scoliosis patient undergoing combined anterior and posterior spinal procedures. It underscores the importance of anticipating unexpected pulmonary complications in patients with difficult airway anatomy and severe restrictive lung disease. Heightened awareness of endotracheal tube obstruction and malposition is imperative.

Indexed as

case reportcombined anterior and posterior spinal fusionendotracheal tube obstructionpleural adhesionsSchwartz–Jampel syndrome

Identifiers

PMID42707645
PMCPMC13547842

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