Literature DB >> 29575534

Perioperative management of children with glycogen storage disease type II-Pompe disease.

Linelot Bosman1, Sanne E Hoeks1, Antonia González Candel2, Hannerieke J M van den Hout3, Ans T van der Ploeg3, Lonneke M Staals2.   

Abstract

BACKGROUND: Pompe disease is a rare metabolic disorder caused by a deficiency of the lysosomal enzyme acid α-glucosidase. Glycogen accumulation damages skeletal, cardiac, and smooth muscles, causing a progressive and debilitating muscle weakness and cardiomyopathy. As life expectancy has much improved since the introduction of enzyme replacement therapy an increasing number of patients are referred for surgical procedures. Due to the potential cardiopulmonary complications, these patients form a high-risk group for the anesthesiologist. AIMS: In this study, we investigated the incidence of perioperative complications in children with Pompe disease treated in our hospital since the introduction of enzyme replacement therapy.
METHODS: Anesthetic and perioperative data of children with Pompe disease treated between 1999 and 2015 in the Erasmus MC-Sophia Children's Hospital, University Medical Centre, Rotterdam, The Netherlands, were collected, retrospectively.
RESULTS: Of the 65 children with Pompe disease, 34 patients underwent in total 77, mostly low-risk, surgical procedures. Twenty-one children had the classic infantile form and 13 had a nonclassic presentation of Pompe disease. In 13 (16.8%) procedures, 1 or more perioperative complications occurred. Perioperative desaturation was the main complication (12.9%), followed by arrhythmia (3.8%) and heart failure requiring diuretic treatment (2.6%). One child died 2 days postoperatively, but this was considered unrelated to the procedure.
CONCLUSION: Despite the potentially high anesthetic risk for children with Pompe disease under enzyme replacement therapy, the incidence of perioperative complications in our study was relatively low. Our data suggest that with proper precautionary measures and a critical choice of timing of the operation, general anesthesia in children with Pompe disease could be relatively safe nowadays.
© 2018 The Authors. Pediatric Anesthesia Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  adverse events; child; congenital anomalies and syndromes; infant; muscle disorders

Mesh:

Year:  2018        PMID: 29575534     DOI: 10.1111/pan.13361

Source DB:  PubMed          Journal:  Paediatr Anaesth        ISSN: 1155-5645            Impact factor:   2.556


  1 in total

1.  Case Report: Anesthetic Management and Electrical Cardiometry as Intensive Hemodynamic Monitoring During Cheiloplasty in an Infant With Enzyme-Replaced Pompe Disease and Preserved Preoperative Cardiac Function.

Authors:  Meng-Chen Liu; Ming-Tse Wang; Philip Kuo-Ting Chen; Dau-Ming Niu; Yu-Hsuan Fan Chiang; Ming-Hui Hsieh; Hsiao-Chien Tsai
Journal:  Front Pediatr       Date:  2021-12-13       Impact factor: 3.418

  1 in total

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