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Case report: The art of anesthesiology—Approaching a minor procedure in a child with MPI-CDG
Background: Protein glycosylation plays an important role in post-translational modification, which defines a broad spectrum of protein functions. Accordingly, infants with a congenital disorder of glycosylation (CDG) can have N-glycosylation, O-glycosylation, or combined N- and O-glycosylation defe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798425/ https://www.ncbi.nlm.nih.gov/pubmed/36588700 http://dx.doi.org/10.3389/fphar.2022.1038090 |
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author | Chang, En-Che Chang, Yu-Hsuan Tsai, Yu-Shiun Hung, Yi-Li Li, Min-Jia Wong, Chih-Shung |
author_facet | Chang, En-Che Chang, Yu-Hsuan Tsai, Yu-Shiun Hung, Yi-Li Li, Min-Jia Wong, Chih-Shung |
author_sort | Chang, En-Che |
collection | PubMed |
description | Background: Protein glycosylation plays an important role in post-translational modification, which defines a broad spectrum of protein functions. Accordingly, infants with a congenital disorder of glycosylation (CDG) can have N-glycosylation, O-glycosylation, or combined N- and O-glycosylation defects, resulting in similar but different multisystem involvement. CDGs can present notable gastrointestinal and neurologic symptoms. Both protein-losing enteropathy and hypotonia affect the decision of using anesthetics. We reported a case of MPI-CDG with protein-losing enteropathy and muscular hypotonia that underwent different anesthesia approach strategies of vascular access. Here, we highlight why intubation with sevoflurane anesthesia and sparing use of muscle relaxants is the optimal strategy for such a condition. Case presentation: A 25-month-old girl, weighing 6.6 kg and 64 cm tall, suffered chronic diarrhea, hypoalbuminemia, and hypotonia since birth. Protein-losing enteropathy due to MPI-CDG was documented by whole-exome sequencing. She underwent three sedated surgical procedures in our hospital. The sedation was administered twice by pediatricians with oral chloral hydrate, intravenous midazolam, and ketamine, to which the patient showed moderate to late recovery from sedation and irritability the following night. The most recent one was administered by an anesthesiologist, where endotracheal intubation was performed with sevoflurane as the main anesthetic. The patient regained consciousness immediately after the operation. She had no complications after all three sedation/anesthesia interventions and was discharged 7 days later, uneventful after the third general anesthesia procedure. Conclusion: We performed safe anesthetic management in a 25-month-old girl with MPI-CDG using sevoflurane under controlled ventilation. She awoke immediately after the procedure. Due to the disease entity, we suggested bypassing the intravenous route to avoid excess volume for drug administration and that muscle relaxant may not be necessary for endotracheal intubation and patient immobilization when performing procedures under general anesthesia in CDG patients. |
format | Online Article Text |
id | pubmed-9798425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97984252022-12-30 Case report: The art of anesthesiology—Approaching a minor procedure in a child with MPI-CDG Chang, En-Che Chang, Yu-Hsuan Tsai, Yu-Shiun Hung, Yi-Li Li, Min-Jia Wong, Chih-Shung Front Pharmacol Pharmacology Background: Protein glycosylation plays an important role in post-translational modification, which defines a broad spectrum of protein functions. Accordingly, infants with a congenital disorder of glycosylation (CDG) can have N-glycosylation, O-glycosylation, or combined N- and O-glycosylation defects, resulting in similar but different multisystem involvement. CDGs can present notable gastrointestinal and neurologic symptoms. Both protein-losing enteropathy and hypotonia affect the decision of using anesthetics. We reported a case of MPI-CDG with protein-losing enteropathy and muscular hypotonia that underwent different anesthesia approach strategies of vascular access. Here, we highlight why intubation with sevoflurane anesthesia and sparing use of muscle relaxants is the optimal strategy for such a condition. Case presentation: A 25-month-old girl, weighing 6.6 kg and 64 cm tall, suffered chronic diarrhea, hypoalbuminemia, and hypotonia since birth. Protein-losing enteropathy due to MPI-CDG was documented by whole-exome sequencing. She underwent three sedated surgical procedures in our hospital. The sedation was administered twice by pediatricians with oral chloral hydrate, intravenous midazolam, and ketamine, to which the patient showed moderate to late recovery from sedation and irritability the following night. The most recent one was administered by an anesthesiologist, where endotracheal intubation was performed with sevoflurane as the main anesthetic. The patient regained consciousness immediately after the operation. She had no complications after all three sedation/anesthesia interventions and was discharged 7 days later, uneventful after the third general anesthesia procedure. Conclusion: We performed safe anesthetic management in a 25-month-old girl with MPI-CDG using sevoflurane under controlled ventilation. She awoke immediately after the procedure. Due to the disease entity, we suggested bypassing the intravenous route to avoid excess volume for drug administration and that muscle relaxant may not be necessary for endotracheal intubation and patient immobilization when performing procedures under general anesthesia in CDG patients. Frontiers Media S.A. 2022-12-15 /pmc/articles/PMC9798425/ /pubmed/36588700 http://dx.doi.org/10.3389/fphar.2022.1038090 Text en Copyright © 2022 Chang, Chang, Tsai, Hung, Li and Wong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Chang, En-Che Chang, Yu-Hsuan Tsai, Yu-Shiun Hung, Yi-Li Li, Min-Jia Wong, Chih-Shung Case report: The art of anesthesiology—Approaching a minor procedure in a child with MPI-CDG |
title | Case report: The art of anesthesiology—Approaching a minor procedure in a child with MPI-CDG |
title_full | Case report: The art of anesthesiology—Approaching a minor procedure in a child with MPI-CDG |
title_fullStr | Case report: The art of anesthesiology—Approaching a minor procedure in a child with MPI-CDG |
title_full_unstemmed | Case report: The art of anesthesiology—Approaching a minor procedure in a child with MPI-CDG |
title_short | Case report: The art of anesthesiology—Approaching a minor procedure in a child with MPI-CDG |
title_sort | case report: the art of anesthesiology—approaching a minor procedure in a child with mpi-cdg |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798425/ https://www.ncbi.nlm.nih.gov/pubmed/36588700 http://dx.doi.org/10.3389/fphar.2022.1038090 |
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