Literature DB >> 23726952

Tracheostomy in mucopolysaccharidosis type II (Hunter's Syndrome).

Vikas Malik1, Jaya Nichani, Michael P Rothera, James Edmond Wraith, Simon A Jones, Robert Walker, Iain A Bruce.   

Abstract

OBJECTIVE: Patients with mucopolysaccharidosis type II (MPS II) may develop progressive multi-level upper airway obstruction. Despite the unique challenges presented by these complex patients, tracheostomy remains an important intervention to safeguard the airway when other interventions have failed or when the airway obstruction involves multiple sites. Airway involvement is largely responsible for the significant anaesthetic risk seen in MPS II. We reviewed our tertiary unit's experience of tracheostomies in patients with MPS II. STUDY
DESIGN: Retrospective study.
METHODS: Case note review of MPS II patients requiring tracheostomy at our tertiary institution. The primary outcome measure used for this study was complications following tracheostomy.
RESULTS: We identified 10 MPS II patients requiring tracheostomy to manage upper airway obstruction. Mean age at which tracheostomy was 11 years 2 months (range 4 years 6 months to 28 years 10 months). Tracheostomy insertion was indicated in 3 scenarios: (1) to safeguard an anticipated difficult airway prior to a planned non-ENT surgical procedure, (2) to treat refractory progressive upper airway obstruction and (3) emergency airway management. Complications recorded included infratip and suprastomal granulations, local wound infection and skin ulceration from mechanical trauma. There were no immediate postoperative complications.
CONCLUSIONS: Progressive upper airway obstruction is common in children with MPS II. Tracheostomy is an effective way of managing airway obstruction when less invasive interventions are no longer adequate. Tracheostomy in these patients can be technically difficult and although the complications of tracheostomy in MPS II do not significantly differ from other patient groups, the implications and management complexity vary considerably. The impact of ERT on airway obstruction is not yet fully understood, with tracheostomies likely to remain an important airway adjunct in some patients who fail to respond to ERT, or in those patients surviving into adulthood. It is vital that a multidisciplinary team, comprising clinicians with experience in managing such patients, are involved in airway management of patients with MPS II to enable the best standard of care to be given. The significant additional implications of a tracheostomy in a patient with MPS II, in terms of safety, aftercare and potentially life-threatening complications must be discussed in detail with the patient's family and/or carers. LEVEL OF EVIDENCE: 2c.
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

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Year:  2013        PMID: 23726952     DOI: 10.1016/j.ijporl.2013.05.002

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  8 in total

1.  Perioperative airway management for aortic valve replacement in an adult with mucopolysaccharidosis type II (Hunter syndrome).

Authors:  Kazuchika Suzuki; Hiroaki Sakai; Kenji Takahashi
Journal:  JA Clin Rep       Date:  2018-03-05

Review 2.  ENT and mucopolysaccharidoses.

Authors:  Pier Marco Bianchi; Renato Gaini; Silvano Vitale
Journal:  Ital J Pediatr       Date:  2018-11-16       Impact factor: 2.638

Review 3.  Anesthesiological risks in mucopolysaccharidoses.

Authors:  Alessandra Moretto; Maria Grazia Bosatra; Laura Marchesini; Simonetta Tesoro
Journal:  Ital J Pediatr       Date:  2018-11-16       Impact factor: 2.638

4.  Otolaryngologists and the Early Diagnosis of Mucopolysaccharidoses: A Cross-Sectional Study.

Authors:  Danielle de Araujo Torres; Anneliese Lopes Barth; Mariana Pires de Mello Valente; Paulo Pires de Mello; Dafne Dain Gandelman Horovitz
Journal:  Diagnostics (Basel)       Date:  2019-11-13

5.  Double Valve Replacement in a Patient With Hunter Syndrome.

Authors:  Suresh Keshavamurthy; Andra Duncan; Akshay Kumar; Carlos Trombetta; Rene Rodriguez; Carmela Tan; Eric Roselli
Journal:  Cureus       Date:  2022-09-08

6.  Enzymatic replacement therapy for Hunter disease: Up to 9 years experience with 17 patients.

Authors:  Rossella Parini; Miriam Rigoldi; Lucia Tedesco; Lucia Boffi; Alessandra Brambilla; Sara Bertoletti; Agata Boncimino; Alessandra Del Longo; Paola De Lorenzo; Renato Gaini; Denise Gallone; Serena Gasperini; Carlo Giussani; Marco Grimaldi; Daniele Grioni; Pamela Meregalli; Grazia Messinesi; Francesca Nichelli; Marco Romagnoli; Pierluigi Russo; Erik Sganzerla; Grazia Valsecchi; Andrea Biondi
Journal:  Mol Genet Metab Rep       Date:  2015-04-22

Review 7.  Non-cardiac Manifestations in Adult Patients With Mucopolysaccharidosis.

Authors:  Karolina M Stepien; Andrew Bentley; Cliff Chen; M Wahab Dhemech; Edward Gee; Peter Orton; Catherine Pringle; Jonathan Rajan; Ankur Saxena; Govind Tol; Chaitanya Gadepalli
Journal:  Front Cardiovasc Med       Date:  2022-03-07

8.  Mediastinal Tracheostoma for Treatment of Tracheostenosis after Tracheostomy in a Patient with Mucopolysaccharidosis-Induced Tracheomalacia.

Authors:  Yasuhiro Chikaishi; Kenichi Kobayashi; Shuichi Shinohara; Akihiro Taira; Yusuke Nabe; Shinji Shinohara; Taiji Kuwata; Masaru Takenaka; Soichi Oka; Ayako Hirai; Kazue Yoneda; Koji Kuroda; Naoko Imanishi; Yoshinobu Ichiki; Fumihiro Tanaka
Journal:  Case Rep Surg       Date:  2017-10-12
  8 in total

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