Outcomes important to patients with non-infectious posterior segment-involving uveitis: a qualitative study
Autor: | Philip I. Murray, Alastair K Denniston, David Moore, Mohammad O. Tallouzi, Jonathan Mathers, Melanie Calvert, Nicholas Bucknall |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
03 medical and health sciences 0302 clinical medicine lcsh:Ophthalmology medicine 030212 general & internal medicine Functional ability Original Research business.industry Public health public health medicine.disease Focus group Posterior segment of eyeball Clinical trial Ophthalmology inflammation lcsh:RE1-994 treatment other 030221 ophthalmology & optometry Physical therapy business Psychosocial Uveitis Qualitative research |
Zdroj: | BMJ Open Ophthalmology, Vol 5, Iss 1 (2020) BMJ Open Ophthalmology |
ISSN: | 2397-3269 |
Popis: | ObjectiveUveitis, a group of disorders characterised by intraocular inflammation, causes 10%–15% of total blindness in the developed world. The most sight-threatening forms of non-infectious uveitis are those affecting the posterior segment of the eye, collectively known as posterior segment-involving uveitis (PSIU). Numerous different clinical outcomes have been used in trials evaluating treatments for PSIU, but these may not represent patients’ and carers’ concerns. Therefore, the aims of this study were to understand the impact of PSIU on adult patients’ and carers’ lives and to explore what outcomes of treatment are important to them.Methods and AnalysisFour focus group discussions were undertaken to understand the perspectives of adult patients (=18) and carers (10) with PSIU. Participants were grouped according to whether or not their uveitis was complicated by the sight-threatening condition uveitic macular oedema. Discussions were audio-recorded, transcribed and analysed using the framework analytical approach. Outcomes were identified and grouped into outcome domains.ResultsEleven core domains were identified as important to patients and carers undergoing treatment for PSIU, comprising (1) visual function, (2) symptoms, (3) functional ability, (4) impact on relationships, (5) financial impact, (6) psychological morbidity and emotional well-being, (7) psychosocial adjustment to uveitis, (8) doctor/patient/interprofessional relationships and access to healthcare, (9) treatment burden, (10) treatment side effects, and (11) disease control.ConclusionThe domains identified represent patients’ and carers’ experience and perspectives and can be used to reflect on outcomes assessed in PSIU. They will directly inform the development of a core outcome set for PSIU clinical trials. |
Databáze: | OpenAIRE |
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