Abstract
Objectives
To evaluate the measurement properties of the EuroQoL EQ-5D and two condition-specific patient-reported outcome measures—the Symptom Severity Index (SSI) and the Urinary Incontinence-Specific Quality of Life instrument (I-QoL)—in women with urinary incontinence.
Methods
A questionnaire comprising all instruments was completed by women taking part in a clinical trial of physiotherapy for urinary incontinence. Follow-up questionnaires were at 6 weeks and 5 months. Data quality, internal consistency reliability, validity and responsiveness were assessed.
Results
One hundred and seventy-four patients taking part in the clinical trial completed the questionnaire. Instruments had low levels of missing data. The EQ-5D had a large ceiling effect and poor responsiveness. The SSI had poor validity and responsiveness. The I-QoL had levels of reliability that supported application in group assessment, and in some cases, individual assessment, and good evidence of validity. The I-QoL was the most responsive instrument at both 6 weeks and 5 months.
Conclusion
The I-QoL was the best performing instrument and is recommended as a continence-specific measure of quality of life in a clinical trial setting. The SSI and EQ-5D are not recommended. Alternative generic instruments, which support economic evaluation, require further evaluation in trials of female urinary incontinence.
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Acknowledgements
We are very grateful to all of the patients who so willingly gave of their time to complete the various questionnaires, and the healthcare practitioners taking part in the trial. This study was funded by the Physiotherapy Research Foundation.
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On behalf of the West Midlands Incontinence Research Collaboration.
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Haywood, K.L., Garratt, A.M., Lall, R. et al. EuroQol EQ-5D and condition-specific measures of health outcome in women with urinary incontinence: reliability, validity and responsiveness. Qual Life Res 17, 475–483 (2008). https://doi.org/10.1007/s11136-008-9311-z
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DOI: https://doi.org/10.1007/s11136-008-9311-z