Non-surgical management of stress urinary incontinence: ambulatory treatments for leakage associated with stress (ATLAS) trial

Author:

Richter Holly E1,Burgio Kathryn L,Goode Patricia S2,Borello-France Diane3,Bradley Catherine S4,Brubaker Linda5,Handa Victoria L6,Fine Paul M7,Visco Anthony G8,Zyczynski Halina M9,Wei John T10,Weber Anne M11,

Affiliation:

1. Department of Obstetrics and Gynecology, Division of Women's Pelvic Medicine and Reconstructive Surgery University of Alabama at Birmingham

2. Birmingham/Atlanta Geriatric Research, Education and Clinical Center (GRECC), Department of Veterans Affairs Medical Center, Birmingham, AL; Division of Gerontology and Geriatric Medicine, University of Alabama at Birmingham

3. Department of Physical Therapy, Duquesne University

4. Department of Obstetrics and Gynecology, University of Iowa

5. Department of Obstetrics and Gynecology, Loyola University Medical Center, Maywood, IL

6. Department of Obstetrics and Gynecology, Johns Hopkins School of Medicine, Baltimore, MD

7. Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX

8. Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill

9. Division of Gynecology Specialties, University of Pittsburgh

10. Department of Urology, University of Michigan

11. Contraception and Reproductive Health Branch, Center for Population Research, National Institute of Child Health and Human Development, National Institutes of Health

Abstract

Background Non-surgical treatment for stress urinary incontinence (SUI) is recommended as first-line therapy, yet few prospective studies and no randomized trials compare the most common non-surgical treatments for SUI. Purpose To present the design and methodology of the ambulatory treatments for leakage associated with stress (ATLAS) trial, a randomized clinical trial comparing three interventions for predominant SUI in women: intravaginal continence pessary; behavioral therapy (including pelvic floor muscle training and exercise and bladder control strategies); and a combination of the two treatments. Methods Treatment outcome measures, collected at 12 weeks and six and 12 months post randomization, include the Patient Global Impression of Improvement (PGI-I), the Stress Incontinence Scale of the Pelvic Floor Distress Inventory (PFDI), seven-day bladder diaries, Pelvic Floor Impact Questionnaire (PFIQ), Pelvic Organ Prolapse-Urinary Incontinence Sexual Function Questionnaire (PISQ-12), Patient Satisfaction Questionnaire (PSQ) and the Medical Outcomes Study Short Form Health Survey (SF-36). Limitations The study design reduces most common biases, but some degree of selection bias may remain. Conclusion This trial will provide useful information to help counsel women with stress and mixed incontinence about the relative efficacy and satisfaction with pessary, behavioral therapy and both treatments combined.

Publisher

SAGE Publications

Subject

Pharmacology,General Medicine

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