Affiliation:
1. Department of Anesthesiology and Critical Care University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania USA
2. Department of Anesthesiology and Critical Care Medicine Children's Hospital of Philadelphia Philadelphia Pennsylvania USA
3. Division of Neurology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA
4. Department of Neurology University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania USA
Abstract
AbstractBackgroundAlexander disease is a rare, progressive leukodystrophy, which predisposes patients to complications under general anesthesia due to clinical manifestations including developmental delay, seizures, dysphagia, vomiting, and sleep apnea. However, study of anesthetic outcomes is limited.AimsOur aim was to describe patient characteristics, anesthetic techniques, and anesthesia‐related complications for Alexander disease patients undergoing magnetic resonance imaging and/or lumbar puncture at a quaternary‐care children's hospital.MethodsWe performed a retrospective review of anesthetic outcomes in patients with Alexander disease enrolled in a prospective observational study. Included patients had diagnosed Alexander disease and underwent magnetic resonance imaging and/or lumbar puncture at our institution. We excluded anesthetics for other procedures or at outside institutions. Collected data included patient characteristics, anesthetic techniques, medications, and complications under anesthesia and in the subsequent 24 h. We performed descriptive statistics as appropriate.ResultsForty patients undergoing 64 procedures met inclusion criteria. Fifty‐six procedures (87.5%) required general anesthesia or monitored anesthesia care (MAC) and eight (12.5%) did not. The general anesthesia/MAC group tended to be younger than nonanesthetized patients (median age 6 years [IQR 3.8; 9] vs. 14.5 years [IQR 12.8; 17.5]). In both groups, dysphagia (78.6% vs. 87.5%, respectively), seizures (62.5% vs. 25%), and recurrent vomiting (17.9% vs. 25%) were frequently reported preprocedure symptoms. Inhalational induction was common (N = 48; 85.7%), and two (3.6%) underwent rapid sequence induction. Serious complications were rare, with no aspiration or seizures. Hypotension resolving with ephedrine occurred in eight cases (14.3%). One patient each (1.8%) experienced postprocedure emergence agitation or vomiting. Fifty‐three (94.6%) were ambulatory procedures. No inpatients required escalation in acuity of care.ConclusionsIn this single‐center study, patients with Alexander disease did not experience frequent or irreversible complications while undergoing general anesthesia/MAC. Co‐morbid symptoms were not increased postanesthesia. Some patients may not require anesthesia to complete short procedures.
Funder
Ionis Pharmaceuticals
National Institutes of Health