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
  • [31] Severe clinical course with recurrent hyperpyrexia in a patient with glutaric aciduria type I
    Hauser, SEP
    Boneh, A
    NEUROPEDIATRICS, 1999, 30 (01) : 51 - 52
  • [32] Thymine Hyperexcretion in a Patient with Abnormal Newborn Screen for Glutaric Aciduria Type I
    Wongkittichote, Parith
    Edmondson, Andrew
    Hong, Xinying
    CLINICAL CHEMISTRY, 2023, 69 (04) : 431 - 432
  • [33] Glutaric aciduria type I: phenotypic variability. Report of six patients
    Casella, EB
    Bresolin, AU
    Valente, M
    Daniel, DA
    Machado, JJ
    Vieira, MA
    Tenorio, AG
    Chamoles, N
    ARQUIVOS DE NEURO-PSIQUIATRIA, 1998, 56 (3B) : 545 - 552
  • [34] AN UNUSUAL CASE OF GLUTARIC ACIDURIA TYPE II
    Rigal, O.
    Benoist, J-F
    Brivet, M.
    Pasche, J.
    de Baulny, Ogier H.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 : 116 - 116
  • [35] GLUTARIC ACIDURIA - NEW CASE-REPORT
    FLORET, D
    DIVRY, P
    DINGEON, N
    MONNET, P
    ARCHIVES FRANCAISES DE PEDIATRIE, 1979, 36 (05): : 462 - 470
  • [36] General anesthesia with remimazolam in a patient with mitochondrial encephalomyopathy: a case report
    Yuji Suzuki
    Matsuyuki Doi
    Yoshiki Nakajima
    JA Clinical Reports, 7
  • [37] General anesthesia with remimazolam in a patient with mitochondrial encephalomyopathy: a case report
    Suzuki, Yuji
    Doi, Matsuyuki
    Nakajima, Yoshiki
    JA CLINICAL REPORTS, 2021, 7 (01)
  • [38] Colorectal cancer in a patient with glutaric aciduria type 1
    Hayasaka, Kiyoshi
    Numakura, Chikahiko
    Sato, Hiroko
    Meguro, Toru
    Mitsui, Tetsuo
    PEDIATRICS INTERNATIONAL, 2025, 67 (01)
  • [39] A Case of Mistaken Identity: Glutaric Aciduria Type I Masquerading as Postmeningitic Hydrocephalus
    Rajani, Heena
    Grover, Shabnam Bhandari
    Antil, Neha
    Katyan, Amit
    JOURNAL OF CLINICAL IMAGING SCIENCE, 2018, 8
  • [40] Dystonia and choreoathetosis after glutaric aciduria type I
    Bidabadi, E
    MOVEMENT DISORDERS, 2004, 19 : S77 - S77