Remimazolam Anesthesia for a Pediatric Patient With Glutaric Aciduria Type I: A Case Report

被引:0
|
作者
Tsuruno, Tomoko [1 ]
Tateiwa, Hiroki [1 ]
Hashimoto, Yuki [1 ]
Katsumata, Yoshifumi [1 ]
Kawano, Takashi [1 ]
机构
[1] Kochi Med Sch, Dept Anesthesiol & Intens Care Med, Kochi, Japan
关键词
mitochondrial disorder; perioperative management; general anesthesia; remimazolam; glutaric aciduria type 1; MANAGEMENT;
D O I
10.7759/cureus.66612
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glutaric aciduria type I (GA-1) is a rare metabolic disorder caused by an autosomal, recessive, inherited deficiency of glutaryl-CoA dehydrogenase. Reports on the anesthetic management of patients with GA-1 are limited. It has been suggested that inhalation anesthesia is safer than propofol due to the mitochondrial dysfunction inherent in GA-1. However, inhalation anesthesia poses a risk, albeit rare, of malignant hyperthermia, which can result in severe neurological damage in GA-1 patients. Therefore, we considered that management using remimazolam might be effective and, provided a successful general anesthesia using it for a pediatric patient with GA-1. We report a case of a four-year-old girl with GA-1 who underwent a laparoscopic gastrostomy under general anesthesia. Remimazolam was used for both induction and maintenance of anesthesia. Our perioperative management also included measures to prevent a hypercatabolic condition such as adequate hydration and blood glucose control. The patient had an uneventful perioperative course and was discharged on postoperative day 7. Thus, remimazolam is proposed as a new option for anesthetic management in patients with GA-1. Additionally, tailored perioperative management that addresses the unique characteristics of GA-1 is crucial for favorable outcomes.
引用
收藏
页数:5
相关论文
共 50 条
  • [1] A Case report on aneurometabolic disorder: Glutaric aciduria type I
    Sadehal, Setareh
    Eshraghi, Peyman
    ELECTRONIC JOURNAL OF GENERAL MEDICINE, 2019, 16 (02):
  • [2] Case Report: Hemophagocytic Lymphocytosis in a Patient With Glutaric Aciduria Type IIC
    Huang, Lingtong
    Wu, Wei
    Zhu, Yijing
    Yu, Huili
    Tang, Lingling
    Fang, Xueling
    FRONTIERS IN IMMUNOLOGY, 2022, 12
  • [3] Glutaric aciduria type I: Report of a late diagnosed case.
    Rodriguez, Victor R. de J. Lopez
    Galan, Maria del C. Chima
    Guerrero, Lina M. Parra
    Estrada, Mariana Navarro
    Hernandez, Yuritzi Santillan
    Quevedo, Ericka Vargas
    ACTA PEDIATRICA DE MEXICO, 2023, 44 (04): : 290 - 296
  • [4] GLUTARIC ACIDURIA TYPE-I - A NEW CASE-REPORT
    YACOUB, M
    TABARKI, B
    SALEM, N
    HASSEN, A
    ABROUG, S
    HARBI, A
    ESSOUSSI, AS
    ANNALES DE PEDIATRIE, 1994, 41 (03): : 185 - 187
  • [5] A CASE OF TYPE-I GLUTARIC ACIDURIA
    CARTER, P
    LUSTY, H
    EDMUNDS, AT
    EUROPEAN JOURNAL OF PEDIATRICS, 1986, 144 (06) : 602 - 602
  • [6] Glutaric aciduria type II: A case report
    Domizio, S
    Romanelli, A
    Brindisino, P
    Puglielli, C
    Conte, E
    Domizio, R
    Sgarrella, MC
    Sabatino, G
    INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2005, 18 (04): : 805 - 808
  • [7] GLUTARIC ACIDURIA TYPE I AND GLIOMA: THE FIRST REPORT IN A YOUNG ADULT PATIENT
    Burlina, A. P.
    Danieli, D.
    Malfa, F.
    Manara, R.
    Del Rizzo, M.
    Bordugo, A.
    Burlina, A. B.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2012, 35 : S58 - S58
  • [8] Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review
    Qian, Gu-Ling
    Hong, Fang
    Tong, Fan
    Fu, Hai-Dong
    Liu, Ai-Min
    WORLD JOURNAL OF PEDIATRICS, 2016, 12 (03) : 368 - 371
  • [9] Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review
    Gu-Ling Qian
    Fang Hong
    Fan Tong
    Hai-Dong Fu
    Ai-Min Liu
    World Journal of Pediatrics, 2016, 12 : 368 - 371
  • [10] A Case of Glutaric Aciduria Type I with a Novel Mutation
    Unal, Nilgun Uyduran
    Kor, Deniz
    Yucel, Didem
    Mert, Gulen Gul
    Mungan, Neslihan Onenli
    CUKUROVA MEDICAL JOURNAL, 2013, 38 (04): : 809 - 812