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Patient-reported outcomes (PRO's) in glaucoma: a systematic review
S Vandenbroeck1, S De Geest, T Zeyen
1Department of Public Health, Centre for Health Services and Nursing Research, Katholieke Universiteit Leuven, Kapucijnenvoer 35/4, Leuven, Belgium.
Eye (London, England)
|March 23, 2011
Summary
This review found most patient-reported outcome (PRO) instruments for glaucoma lack quality and patient input. The Treatment Satisfaction Survey for Intra Ocular Pressure is a high-quality tool for side effect assessment.
Area of Science:
- Ophthalmology
- Patient-Reported Outcomes
- Health Measurement
Background:
- Patient-reported outcome (PRO) instruments are crucial for assessing glaucoma patient experiences.
- Existing PRO instruments vary in quality and applicability to glaucoma.
Purpose of the Study:
- To systematically review and evaluate PRO instruments for glaucoma.
- To provide guidance on best practices for assessing patient outcomes in glaucoma care.
Main Methods:
- A systematic literature review of papers detailing the development and psychometric properties of glaucoma or vision-specific PRO instruments.
- Assessment of 27 identified PRO instruments against a quality criteria framework.
Main Results:
- Most PRO instruments (18 for glaucoma, 9 for other eye conditions) showed partial adherence to quality standards.
- Functional status tools were of poor quality; Glaucoma Quality of Life Questionnaire and Vision Quality of Life Index are well-developed but used classical validation.
- Rasch-scaled QoL tools (IVI, VCM1) require improved item content; adherence questionnaires need better validity. Treatment Satisfaction Survey for Intra Ocular Pressure is high-quality for topical treatment side effects.
Conclusions:
- Many PRO instruments for glaucoma suffer from poor developmental quality, lacking patient perspectives in item generation and conceptual frameworks.
- Psychometric validation predominantly relies on classical techniques, indicating a need for more robust methodologies.
- Further development and validation are needed for most PRO instruments to accurately capture glaucoma patient experiences and outcomes.
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