J Neurol Surg B Skull Base 2012; 73(02): 104-111
DOI: 10.1055/s-0032-1301396
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

The NFTI-QOL: A Disease-Specific Quality of Life Questionnaire for Neurofibromatosis 2

Rachael E. Hornigold
1   National Specialist Commissioning Team Neurofibromatosis Unit, Department of Neurology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
2   Department of ENT, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
,
John F. Golding
3   University of Westminster, London, United Kingdom
,
Guy Leschziner
1   National Specialist Commissioning Team Neurofibromatosis Unit, Department of Neurology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
,
Rupert Obholzer
1   National Specialist Commissioning Team Neurofibromatosis Unit, Department of Neurology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
2   Department of ENT, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
,
Michael J. Gleeson
1   National Specialist Commissioning Team Neurofibromatosis Unit, Department of Neurology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
2   Department of ENT, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
,
Nick Thomas
1   National Specialist Commissioning Team Neurofibromatosis Unit, Department of Neurology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
4   King's College Hospital NHS Trust, London, United Kingdom
,
Daniel Walsh
1   National Specialist Commissioning Team Neurofibromatosis Unit, Department of Neurology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
5   UCL Ear Institute and Royal National Throat, Nose, and Ear Hospital, London, United Kingdom
,
Shakeel Saeed
1   National Specialist Commissioning Team Neurofibromatosis Unit, Department of Neurology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
5   UCL Ear Institute and Royal National Throat, Nose, and Ear Hospital, London, United Kingdom
,
Rosalie E. Ferner
1   National Specialist Commissioning Team Neurofibromatosis Unit, Department of Neurology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom
6   Department of Clinical Neuroscience, Institute of Psychiatry, King's College, London, United Kingdom
› Author Affiliations
Further Information

Publication History

19 June 2011

11 October 2011

Publication Date:
06 February 2012 (online)

Preview

Abstract

The objective of this study was to develop a reliable, validated disease-specific score measuring quality of life (QOL) in clinical practice and treatment trials in Neurofibromatosis 2 (NF2) individuals. In NF2 patients, qualitative interviews (n = 15) and a focus group session (n = 30) generated items for a pilot questionnaire. This was tested and refined (n = 20). The final version (NFTI-QOL) was validated (n = 50) with two generic QOL questionnaires (SF-36 and EuroQOL). The NFTI-QOL was also administered to patients with solitary vestibular schwannoma (SVS) (n = 30) and normal controls (n = 30). The participants were NF2 patients, SVS patients, and normal controls. NFTI-QOL score, SF-36 score, and EuroQOL score were the main outcome measures. Mean NFTI-QOL score was 9.4 (range: 0 to 20, maximum possible score = 24). The NFTI-QOL score correlated strongly with EuroQOL (r = 0.71, p < 0.001) and SF-36 (r = 0.81, p < 0.001). NF2 individuals were significantly worse than the SVS patients, who in turn were worse than the controls on the NIFTI-QOL. The NFTI-QOL showed good internal reliability (Cronbach's α = 0.87). We developed an eight-item disease-specific QOL score for NF2 patients, validated against SF-36 and EuroQOL. It correlated strongly with clinician-rated disease severity in NF2, with better correlation than the SF-36 in this regard.