Characterization of sedation and anesthesia complications in patients with alternating hemiplegia of childhood

Alternating hemiplegia of childhood (AHC) pathophysiology suggests predisposition to sedation and anesthesia complications. Hypotheses: 1) AHC patients experience high rates of sedation-anesthesia complications. 2) ATP1A3 mutation genotype positivity, age, and AHC severity correlate with more severe...

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Published inEuropean journal of paediatric neurology Vol. 38; pp. 47 - 52
Main Authors Parker, Lauren E., Wallace, Keri, Thevathasan, Arthur, Funk, Emily, Pratt, Milton, Thamby, Julie, Tran, Linh, Prange, Lyndsey, Uchitel, Julie, Boggs, April, Minton, Melissa, Jasien, Joan, Nagao, Kanae Jennifer, Richards, Amanda, Cruse, Belinda, De-Lisle Dear, Guy, Landstrom, Andrew P., Mikati, Mohamad A.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.05.2022
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Summary:Alternating hemiplegia of childhood (AHC) pathophysiology suggests predisposition to sedation and anesthesia complications. Hypotheses: 1) AHC patients experience high rates of sedation-anesthesia complications. 2) ATP1A3 mutation genotype positivity, age, and AHC severity correlate with more severe complications. 3) Prior short QTc correlates with cardiac rhythm complications. Analysis of 34 consecutive AHC patients who underwent sedation or anesthesia. Classification of complications: mild (not requiring intervention), moderate (intervention), severe (intervention, risk for permanent injury or potential life-threatening emergency). Statistics: Fisher Exact test, Spearman correlations. These patients underwent 129 procedures (3.79 ± 2.75 procedures/patient). Twelve (35%) experienced complications during at least one procedure. Fourteen/129 procedures (11%) manifested one or more complications (2.3% mild, 7% moderate, 1.6% severe). Of the total 20 observed complications, six (33.3%) were severe: apneas (2), seizures (2), bradycardia (1), ventricular fibrillation that responded to resuscitation (1). Moderate complications: non-life-threatening bradycardias, apneas, AHC spells or seizures. Complications occurred during sedation or anesthesia and during procedures or recovery periods. Patients with disease-associated ATP1A3 variants were more likely to have moderate or severe complications. There was no correlation between complications and age or AHC severity. Presence of prior short QTc correlated with cardiac rhythm complications. After this series was analyzed, another patient had severe recurrent laryngeal dystonia requiring tracheostomy following anesthesia with intubation. During sedation or anesthesia, AHC patients, particularly those with ATP1A3 variants and prior short QTc, are at risk for complications consistent with AHC pathophysiology. Increased awareness is warranted during planning, performance, and recovery from such procedures. •Patients with AHC had complications in 11% of sedation-anesthesia procedures.•All recovered without consequences; 2.3% were mild, 7% moderate, 1.6% severe.•Severe complications: apnea, seizures, serious cardiac arrhythmia.•Complications occurred with sedation or anesthesia and during procedure or recovery.•Having ATP1A3 mutation or short QTc increased risk of complications.
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ISSN:1090-3798
1532-2130
DOI:10.1016/j.ejpn.2022.03.007