{"title":"Safety of a higher thiamylal induction dose in pediatric sedation for magnetic resonance imaging scans.","authors":"Yi-Shiuan Li, Shih-Pin Lin, Wen-Kuei Chang, Ting Chien-Kun","doi":"10.1186/s40001-025-02332-w","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Previous studies have shown that 3.6 (2.8-4.0) mg/kg of intravenous thiamylal is effective and safe for pediatric sedation during magnetic resonance imaging (MRI) scans, although its success rate (96.6%) is slightly lower than that via propofol (99%). This retrospective study aimed to evaluate whether a higher induction dose of thiamylal can reduce MRI scan interruptions without increasing the incidence of adverse events.</p><p><strong>Methods: </strong>This study included patients aged < 18 years who underwent MRI under thiamylal sedation between January 2021 and December 2022. Intravenous atropine (0.01 mg/kg) and midazolam (0.08 mg/kg) were administered as premedications. An induction intravenous dose of 2-5 mg/kg thiamylal was administered, with additional doses administered as needed. The induction dose was defined as the total amount of thiamylal administered before the scan. Once adequate sedation was achieved, MRI was performed. Any additional doses of thiamylal required because of scan interruption were recorded as rescue doses. Patients who received an induction thiamylal dose of < 3.6 mg/kg were categorized into the lower induction dose group. The primary endpoint was the rate of MRI interruptions. Secondary endpoints included adverse events related to sedation, total thiamylal dose, and total MRI scanning time.</p><p><strong>Results: </strong>A total of 566 patients, with a median age of 56.4 months (range: 24.0-79.2 months) and median weight of 16.0 kg (range: 10.3-21.0 kg), were included in the analysis. The median induction and total dose of thiamylal per body weight were 4.7 (3.8-5.8) mg/kg and 6.0 (4.6-8.1) mg/kg, respectively. No respiratory or other adverse events were recorded. For 30- to 60-min MRI scans, the higher induction dose group had a lower scan interruption rate, and a lower total thiamylal dose was required than that for the lower induction dose group.</p><p><strong>Conclusion: </strong>A higher induction dose of thiamylal (5.4 ± 1.6 mg/kg) is safe and is associated with a reduced scan interruption rate for 30- to 60-min MRI scans, as well as a lower total thiamylal dose requirement. However, thiamylal is not an ideal sedative agent for MRI scans longer than 1 h.</p>","PeriodicalId":11949,"journal":{"name":"European Journal of Medical Research","volume":"30 1","pages":"106"},"PeriodicalIF":2.8000,"publicationDate":"2025-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11829367/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Medical Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s40001-025-02332-w","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Previous studies have shown that 3.6 (2.8-4.0) mg/kg of intravenous thiamylal is effective and safe for pediatric sedation during magnetic resonance imaging (MRI) scans, although its success rate (96.6%) is slightly lower than that via propofol (99%). This retrospective study aimed to evaluate whether a higher induction dose of thiamylal can reduce MRI scan interruptions without increasing the incidence of adverse events.
Methods: This study included patients aged < 18 years who underwent MRI under thiamylal sedation between January 2021 and December 2022. Intravenous atropine (0.01 mg/kg) and midazolam (0.08 mg/kg) were administered as premedications. An induction intravenous dose of 2-5 mg/kg thiamylal was administered, with additional doses administered as needed. The induction dose was defined as the total amount of thiamylal administered before the scan. Once adequate sedation was achieved, MRI was performed. Any additional doses of thiamylal required because of scan interruption were recorded as rescue doses. Patients who received an induction thiamylal dose of < 3.6 mg/kg were categorized into the lower induction dose group. The primary endpoint was the rate of MRI interruptions. Secondary endpoints included adverse events related to sedation, total thiamylal dose, and total MRI scanning time.
Results: A total of 566 patients, with a median age of 56.4 months (range: 24.0-79.2 months) and median weight of 16.0 kg (range: 10.3-21.0 kg), were included in the analysis. The median induction and total dose of thiamylal per body weight were 4.7 (3.8-5.8) mg/kg and 6.0 (4.6-8.1) mg/kg, respectively. No respiratory or other adverse events were recorded. For 30- to 60-min MRI scans, the higher induction dose group had a lower scan interruption rate, and a lower total thiamylal dose was required than that for the lower induction dose group.
Conclusion: A higher induction dose of thiamylal (5.4 ± 1.6 mg/kg) is safe and is associated with a reduced scan interruption rate for 30- to 60-min MRI scans, as well as a lower total thiamylal dose requirement. However, thiamylal is not an ideal sedative agent for MRI scans longer than 1 h.
期刊介绍:
European Journal of Medical Research publishes translational and clinical research of international interest across all medical disciplines, enabling clinicians and other researchers to learn about developments and innovations within these disciplines and across the boundaries between disciplines. The journal publishes high quality research and reviews and aims to ensure that the results of all well-conducted research are published, regardless of their outcome.