Perioperative management and outcomes for posterior spinal fusion in patients with Friedreich ataxia: A single‐center, retrospective study

Author:

O'Brien Elizabeth M.12ORCID,Neiswinter Natalie34,Lin Kimberly Y.25,Lynch David26,Baldwin Keith27,Profeta Victoria6,Flynn John M.27,Muhly Wallis T.12

Affiliation:

1. Department of Anesthesiology and Critical Care Medicine Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

2. Perelman School of Medicine at the University of Pennsylvania Philadelphia Pennsylvania USA

3. Department of Anesthesiology and Perioperative Medicine Penn State Health Hershey Pennsylvania USA

4. Pennsylvania State University College of Medicine Hershey Pennsylvania USA

5. Division of Cardiology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

6. Division of Neurology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

7. Division of Orthopedic Surgery Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

Abstract

AbstractBackgroundFriedreich ataxia is a rare genetic disorder associated with progressive mitochondrial dysfunction leading to widespread sequelae including ataxia, muscle weakness, hypertrophic cardiomyopathy, diabetes mellitus, and neuromuscular scoliosis. Children with Friedreich ataxia are at high risk for periprocedural complications during posterior spinal fusion due to their comorbidities.AimTo describe our single‐center perioperative management of patients with Friedreich ataxia undergoing posterior spinal fusion.MethodsAdolescent patients with Friedreich ataxia presenting for spinal deformity surgery between 2007 and 2023 were included in this retrospective case series performed at the Children's Hospital of Philadelphia. Perioperative outcomes were reviewed along with preoperative characteristics, intraoperative anesthetic management, and postoperative medical management.ResultsSeventeen patients were included in the final analysis. The mean age was 15 ± 2 years old and 47% were female. Preoperatively, 35% were wheelchair dependent, 100% had mild‐to‐moderate hypertrophic cardiomyopathy with preserved systolic function and no left ventricular outflow tract obstruction, 29% were on cardiac medications, and 29% were on pain medications. Intraoperatively, 53% had transesophageal echocardiography monitoring; 12% had changes in volume status on echo but no changes in function. Numerous combinations of total intravenous anesthetic agents were used, most commonly propofol, remifentanil, and ketamine. Baseline neuromonitoring signals were poor in four patients and one patient lost signals, resulting in 4 (24%) wake‐up tests. The majority (75%) were extubated in the operating room. Postoperative complications were high (88%) and ranged from minor complications like nausea/vomiting (18%) to major complications like hypotension/tachycardia (29%) and need for extracorporeal membrane oxygenation support in one patient (6%).ConclusionsPatients with Friedreich ataxia are at high risk for perioperative complications when undergoing posterior spinal fusion and coordinated multidisciplinary care is required at each stage. Future research should focus on the utility of intraoperative echocardiography, optimal anesthetic agent selection, and targeted fluid management to reduce postoperative cardiac complications.

Publisher

Wiley

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