Analysis of the factors contributing to residual weakness after sugammadex administration in pediatric patients under 2 years of age

Author:

Cates Alexandra C.1,Freundlich Robert E.2,Clifton Jacob C.3,Lorinc Amanda N.1

Affiliation:

1. Department of Anesthesiology Monroe Carell Jr. Children's Hospital at Vanderbilt Nashville Tennessee USA

2. Department of Anesthesiology Vanderbilt University Medical Center Nashville Tennessee USA

3. Department of Anesthesiology & Perioperative Informatics Research Vanderbilt University Medical Center Nashville Tennessee USA

Abstract

AbstractBackgroundSugammadex reverses the neuromuscular blockade induced by rocuronium and vecuronium and is approved by the U.S. Food and Drug Administration for use in patients aged over 2 years. There is, however, a paucity of data regarding its dosing profile in infants and children younger than 2 years.AimsThe aim of this study was to assess the risk of recurarization, or re‐paralysis, in children under 2 years of age to increase awareness on the importance of appropriate neuromuscular blocked monitoring and reversal.MethodsAll patients aged ≤24 months who underwent an operative procedure at a tertiary medical center between January 1, 2018, and December 31, 2021, and received both rocuronium for neuromuscular blockade and sugammadex for neuromuscular blockade reversal, were identified in the electronic medical record. Patients were excluded from analysis if they (1) received vecuronium, cisatracurium, atracurium, or succinylcholine for neuromuscular blockade, (2) received neostigmine for reversal, or (3) underwent more than one operation within 24 h. We performed a survival analysis of sugammadex redose using a Cox proportional hazards model.ResultsWe reviewed 2923 records. Sugammadex was redosed in 123 (4.2%) cases. The median [IQR] time to redose was 7 [4–17] min, and the median [IQR] amount of redose administered was 2.74 [1.96–3.99] mg/kg. Increasing patient age (p < .01) and weight (p < .01) were associated with reduced hazard rate of sugammadex redose. For a patient of median weight, increasing age from 3 to 13 months was associated with a 53% risk reduction (HR: 0.47; 95% CI: 0.24–0.91). For a patient of median age, increasing weight from 4.7 to 9.2 kg was associated with 41% risk reduction (HR: 0.59; 95% CI: 0.32–1.07). We failed to detect any other associations.ConclusionsIn this single‐center, retrospective cohort study of pediatric surgery patients, there was an association between the hazard of sugammadex redose with both increased age and weight.

Publisher

Wiley

Subject

Anesthesiology and Pain Medicine,Pediatrics, Perinatology and Child Health

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