Literature DB >> 32528202

Sudden cardiac arrest during induction of anaesthesia in paediatric patient with glutaric aciduria type II.

Sema Şanal Baş1, Gonca Kılıç Yıldırım2.   

Abstract

Glutaric aciduria type II (GA2) is an autosomal recessive metabolic disorder of amino acid and lipid metabolism, which is serious and rare. The most serious form is seen in early infancy and is associated with very high mortality rates. Here, we present an 8-month-old male patient with GA2 who had electrocardiographic ST ST-segment depression and sudden cardiac arrest at 10th minute of emergency operation (central venous catheter placement). There is a very scarce amount of data in the literature about anaesthetic management of GA2 patients. There is also no previously published report about cardiac arrest during induction of anaesthesia in this condition. The present report highlights this serious complication.
Copyright © Sudanese Association of Pediatricians.

Entities:  

Keywords:  Anaesthesia; Cardiac arrest; Glutaric aciduria type II

Year:  2020        PMID: 32528202      PMCID: PMC7282425          DOI: 10.24911/SJP.106-1580816331

Source DB:  PubMed          Journal:  Sudan J Paediatr        ISSN: 0256-4408


  10 in total

1.  Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases.

Authors:  Kenji Yamada; Hironori Kobayashi; Ryosuke Bo; Tomoo Takahashi; Jamiyan Purevsuren; Yuki Hasegawa; Takeshi Taketani; Seiji Fukuda; Takuya Ohkubo; Takanori Yokota; Mutsufusa Watanabe; Taiji Tsunemi; Hidehiro Mizusawa; Hiroshi Takuma; Ayako Shioya; Akiko Ishii; Akira Tamaoka; Yosuke Shigematsu; Hideo Sugie; Seiji Yamaguchi
Journal:  Brain Dev       Date:  2015-09-26       Impact factor: 1.961

Review 2.  Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency.

Authors:  Kenji Yamada; Takeshi Taketani
Journal:  J Hum Genet       Date:  2018-11-06       Impact factor: 3.172

3.  Multiple Acyl CoA dehydrogenase deficiency: Uncommon yet treatable disorder.

Authors:  M Pooja; R Subasree; S Sumanth; M Veerendra Kumar; N Gayathri; S Rashmi
Journal:  Neurol India       Date:  2017 Jan-Feb       Impact factor: 2.117

4.  The anesthetic management of ventricular septal defect (VSD) repair in a child with mitochondrial cytopathy.

Authors:  Ehab Farag; Maged Argalious; Samer Narouze; Glenn E DeBoer; Julie Tome
Journal:  Can J Anaesth       Date:  2002-11       Impact factor: 5.063

5.  Propofol-mediated cardioprotection dependent of microRNA-451/HMGB1 against myocardial ischemia-reperfusion injury.

Authors:  Yu-Mei Li; Jin-Guo Sun; Li-Hua Hu; Xian-Chun Ma; Gang Zhou; Xi-Zhao Huang
Journal:  J Cell Physiol       Date:  2019-06-12       Impact factor: 6.384

6.  Glutaric aciduria type II: observations in seven patients with neonatal- and late-onset disease.

Authors:  M A al-Essa; M S Rashed; S M Bakheet; Z J Patay; P T Ozand
Journal:  J Perinatol       Date:  2000-03       Impact factor: 2.521

7.  Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature.

Authors:  Mohit Singla; Grace Guzman; Andrew J Griffin; Saroja Bharati
Journal:  Pediatr Cardiol       Date:  2007-10-03       Impact factor: 1.655

8.  Glutaric acidemia type II: heterogeneity of clinical and biochemical phenotypes.

Authors:  J P Loehr; S I Goodman; F E Frerman
Journal:  Pediatr Res       Date:  1990-03       Impact factor: 3.756

9.  Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II.

Authors:  Brad Angle; Barbara K Burton
Journal:  Mol Genet Metab       Date:  2007-10-31       Impact factor: 4.797

10.  Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency.

Authors:  Rikke K J Olsen; Eliška Koňaříková; Teresa A Giancaspero; Signe Mosegaard; Veronika Boczonadi; Lavinija Mataković; Alice Veauville-Merllié; Caterina Terrile; Thomas Schwarzmayr; Tobias B Haack; Mari Auranen; Piero Leone; Michele Galluccio; Apolline Imbard; Purificacion Gutierrez-Rios; Johan Palmfeldt; Elisabeth Graf; Christine Vianey-Saban; Marcus Oppenheim; Manuel Schiff; Samia Pichard; Odile Rigal; Angela Pyle; Patrick F Chinnery; Vassiliki Konstantopoulou; Dorothea Möslinger; René G Feichtinger; Beril Talim; Haluk Topaloglu; Turgay Coskun; Safak Gucer; Annalisa Botta; Elena Pegoraro; Adriana Malena; Lodovica Vergani; Daniela Mazzà; Marcella Zollino; Daniele Ghezzi; Cecile Acquaviva; Tiina Tyni; Avihu Boneh; Thomas Meitinger; Tim M Strom; Niels Gregersen; Johannes A Mayr; Rita Horvath; Maria Barile; Holger Prokisch
Journal:  Am J Hum Genet       Date:  2016-06-02       Impact factor: 11.025

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.