Literature DB >> 26826883

Neurofibromatosis type 2 service delivery in England.

S K Lloyd1, D G Evans2.   

Abstract

Neurofibromatosis type 2 (NF2) is a complex disease characterized by the development of multiple schwannomas, especially vestibular schwannomas, as well as other types of benign tumours including meningioma and spinal ependymoma. Due to its multisystem nature, the management of NF2 requires a multidisciplinary approach. In England, the delivery of care for NF2 patients has been centralized to four-"hub" centres in Manchester, Cambridge, Oxford and London each having associated "spoke" centres. Each centre has a core multidisciplinary team consisting of genetics, otolaryngology, neurosurgery, paediatrics, neurology, audiology, radiology, psychology, physiotherapy, specialist nurses and administrative staff. In addition, the core team has access to plastic surgery, ophthalmology, peripheral nerve surgery and adult and paediatric oncology. There are weekly multidisciplinary clinics each with six to eight patients. Each patient is discussed during a team meeting and the management decisions that are made are then discussed with the patients. All patients are reviewed at least annually and have annual head magnetic resonance imaging (MRI) and three yearly spinal MRI. Annual audiological assessment is performed. Cochlear implantation and auditory brainstem implantation are offered if indicated. Surgery, stereotactic radiosurgery and bevacizumab therapy are available for the management of intracranial and spinal tumours. The integration of the service in England has provided significant benefits to patient care and, in the long term, will provide robust patient outcome data that will provide an evidence base to assist in optimizing management of patients with NF2.
Copyright © 2016. Published by Elsevier Masson SAS.

Entities:  

Keywords:  Auditory brainstem implantation; Bevacizumab; Bévacizumab; Cochlear implantation; Implant auditif du tronc cérébral; Implantation cochléaire; Neuriniome de l’acoustique; Neurofibromatose de type 2; Neurofibromatosis type 2; Vestibular schwannoma

Mesh:

Year:  2016        PMID: 26826883     DOI: 10.1016/j.neuchi.2015.10.006

Source DB:  PubMed          Journal:  Neurochirurgie        ISSN: 0028-3770            Impact factor:   1.553


  5 in total

1.  Impact of cochlear implantation on the management strategy of patients with neurofibromatosis type 2.

Authors:  Haoyue Tan; Huan Jia; Yun Li; Zhihua Zhang; Weidong Zhu; Yun Cai; Zhaoyan Wang; Hao Wu
Journal:  Eur Arch Otorhinolaryngol       Date:  2018-09-18       Impact factor: 2.503

2.  Prevalence and natural history of schwannomas in neurofibromatosis type 2 (NF2): the influence of pathogenic variants.

Authors:  Daniel Moualed; Jonathan Wong; Owen Thomas; Calvin Heal; Rukhtam Saqib; Cameron Choi; Simon Lloyd; Scott Rutherford; Emma Stapleton; Charlotte Hammerbeck-Ward; Omar Pathmanaban; Roger Laitt; Miriam Smith; Andrew Wallace; Mark Kellett; Gareth Evans; Andrew King; Simon Freeman
Journal:  Eur J Hum Genet       Date:  2022-01-24       Impact factor: 4.246

3.  Treatment Analysis and Overall Survival Outcomes of Patients With Bilateral Vestibular Schwannoma.

Authors:  Khodayar Goshtasbi; Mehdi Abouzari; Tyler M Yasaka; Sina Soltanzadeh-Zarandi; Brooke Sarna; Harrison W Lin; Hamid R Djalilian
Journal:  Otol Neurotol       Date:  2021-04-01       Impact factor: 2.619

Review 4.  Diagnostics and therapy of vestibular schwannomas - an interdisciplinary challenge.

Authors:  Steffen Rosahl; Christopher Bohr; Michael Lell; Klaus Hamm; Heinrich Iro
Journal:  GMS Curr Top Otorhinolaryngol Head Neck Surg       Date:  2017-12-18

5.  Genetic Severity Score predicts clinical phenotype in NF2.

Authors:  Dorothy Halliday; Beatrice Emmanouil; Pieter Pretorius; Samuel MacKeith; Sally Painter; Helen Tomkins; D Gareth Evans; Allyson Parry
Journal:  J Med Genet       Date:  2017-08-28       Impact factor: 6.318

  5 in total

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