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Defining unmet clinical need across the pathway of brain tumor care: a patient and carer perspective

Authors Sage W, Fernández-Méndez R, Crofton A, Gifford MJ, Bannykh A, Chrysaphinis C, Tingley E, Bulbeck H, Brahmbhatt M, Pickard JD, Walter FM, Brodbelt A, Price SJ, Joannides AJ

Received 31 May 2018

Accepted for publication 19 November 2018

Published 19 March 2019 Volume 2019:11 Pages 2189—2202

DOI https://doi.org/10.2147/CMAR.S175886

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Justinn Cochran

Peer reviewer comments 3

Editor who approved publication: Dr Kenan Onel


William Sage,1 Rocío Fernández-Méndez,1 Anna Crofton,2 Michael J Gifford,3 Alexey Bannykh,3 Constantinos Chrysaphinis,4 Emma Tingley,4 Helen Bulbeck,5 Mita Brahmbhatt,1 John D Pickard,1 Fiona M Walter,6 Andrew Brodbelt,2 Stephen J Price,1 Alexis J Joannides1

1Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK; 2Department of Neurosurgery, The Walton Centre, Liverpool, UK; 3Mountain Hare Consulting, London, UK; 4The Brain Tumour Charity, Farnborough, UK; 5Brainstrust, Cowes, Isle of Wight, UK; 6Primary Care Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK

Objective: The aim of this study was to determine the experience of patients with brain tumors and their carers across distinct parts of their treatment pathway and identify their views on potential service gaps in need of addressing.
Methods: A structured survey was administered at patient workshops across the UK and online through a charity newsletter. Answers to closed questions were analyzed using descriptive statistics, and open questions were examined using techniques of inductive content analysis.
Results: A total of 136 survey responses were received, representing patients with a variety of diagnoses and geographical locations (30 counties). There was a wide range of opinions on the provision of current neuro-oncology services. Key themes identified included a perceived lack of information provision, a gap in postdischarge psychological and neuropsychological supports, and an unmet willingness for involvement in research.
Conclusion: This national survey enhances our knowledge of current patient and carer experience within neuro-oncology services. A number of areas of unmet clinical need are highlighted providing a basis for informing future patient-centered service improvements and research.

Keywords: patient experience, brain cancer, brain tumors, neuro-oncology pathway


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