In April 2016 Manchester eScholar was replaced by the University of Manchester’s new Research Information Management System, Pure. In the autumn the University’s research outputs will be available to search and browse via a new Research Portal. Until then the University’s full publication record can be accessed via a temporary portal and the old eScholar content is available to search and browse via this archive.

Hearing and facial function outcomes for neurofibromatosis 2 clinical trials.

Plotkin, Scott R; Ardern-Holmes, Simone L; Barker, Fred G; Blakeley, Jaishri O; Evans, D Gareth; Ferner, Rosalie E; Hadlock, Tessa A; Halpin, Chris;

Neurology. 2013;81(21 Suppl 1):S25-32.

Access to files

Full-text and supplementary files are not available from Manchester eScholar. Full-text is available externally using the following links:

Full-text held externally

Abstract

OBJECTIVES: Vestibular schwannomas are the hallmark of neurofibromatosis 2 (NF2), occurring in >95% of patients. These tumors develop on the vestibulocochlear nerve and are associated with significant morbidity due to hearing loss, tinnitus, imbalance, facial weakness, and risk of early mortality from brainstem compression. Although hearing loss and facial weakness have been identified as important functional outcomes for patients with NF2, there is a lack of consensus regarding appropriate endpoints in clinical trials. METHODS: The functional outcomes group reviewed existing endpoints for hearing and facial function and developed consensus recommendations for response evaluation in NF2 clinical trials. RESULTS: For hearing endpoints, the functional group endorsed the use of maximum word recognition score as a primary endpoint, with the 95% critical difference as primary hearing outcomes. The group recommended use of the scaled measurement of improvement in lip excursion (SMILE) system for studies of facial function. CONCLUSIONS: These recommendations are intended to provide researchers with a common set of endpoints for use in clinical trials of patients with NF2. The use of common endpoints should improve the quality of clinical trials and foster comparison among studies for hearing loss and facial weakness.

Bibliographic metadata

Type of resource:
Content type:
Publication type:
Published date:
Journal title:
Abbreviated journal title:
ISSN:
Place of publication:
United States
Volume:
81
Issue:
21 Suppl 1
Pagination:
S25-32
Digital Object Identifier:
10.1212/01.wnl.0000435746.02780.f6
Pubmed Identifier:
24249803
Pii Identifier:
81/21_supplement_1/S25
Access state:
Active

Institutional metadata

University researcher(s):

Record metadata

Manchester eScholar ID:
uk-ac-man-scw:239381
Created by:
Evans, Gareth
Created:
10th November, 2014, 20:22:47
Last modified by:
Evans, Gareth
Last modified:
10th November, 2014, 20:22:47

Can we help?

The library chat service will be available from 11am-3pm Monday to Friday (excluding Bank Holidays). You can also email your enquiry to us.