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A randomized trial of retropubic vs single-incision sling among patients undergoing vaginal prolapse repair - 25/05/24

Doi : 10.1016/j.ajog.2024.04.036 
Catherine A. Matthews, MD a, , Charles R. Rardin, MD b, Andrew Sokol, MD c, Cheryl Iglesia, MD c, Sarah Collins, MD d, Cecile Ferrando, MD e, Harvey Winkler, MD f, Kimberly Kenton, MD d, Julia Geynisman-Tan, MD d, Robert E. Gutman, MD c
a Department of Urology, Wake Forest Baptist Health, Winston Salem, NC 
b Department of Obstetrics and Gynecology, Women and Infants Hospital of Rhode Island Providence, RI 
c Department of Obstetrics and Gynecology, MedStar Washington Hospital Center, Georgetown University, Washington DC 
d Department of Obstetrics and Gynecology, Northwestern University, Chicago, IL 
e Obstetrics and Gynecology Institute, Cleveland OH 
f Department of Obstetrics and Gynecology, Hofstra University/Northwell Health, Hempstead, NY 

Corresponding author: Catherine A. Matthews, MD.
Sous presse. Épreuves corrigées par l'auteur. Disponible en ligne depuis le Saturday 25 May 2024

Abstract

Background

The choice of midurethral sling type may impact efficacy and complications in women undergoing transvaginal native tissue repair of pelvic organ prolapse.

Objective

The primary aim was to determine if the single-incision sling is noninferior to retropubic sling for the management of stress urinary incontinence among patients undergoing reconstructive or obliterative native tissue vaginal repair. The secondary aims were to compare adverse events and surgeon ease of use with sling assignment.

Study Design

A multicenter, noninferiority, randomized trial of women with ≥ stage II pelvic organ prolapse and objectively confirmed stress urinary incontinence undergoing reconstructive or obliterative vaginal repair was performed. Women were randomized to concomitant single-incision (Altis sling, Coloplast Minneapolis, MN) with suprapubic sham incisions or retropubic slings. The primary dichotomous outcome was abnormal lower urinary tract function within 12 months postsurgery, defined as bothersome stress urinary incontinence symptoms (>1 Pelvic Floor Distress Inventory question no. 17); retreatment for stress urinary incontinence or treatment for urinary retention. Secondary outcomes were adverse events, Patient Global Impression of Improvement of bladder function, and surgeon ease of use (1, worst; 10, best). All subjects completed validated questionnaires and underwent a Pelvic Organ Prolapse Quantification, cough stress test, and postvoid residual preoperatively, at 6 weeks and 12 months postoperatively. Assuming a subjective cure rate for retropubic of 82%, 80% power, and 1-sided 5% significance level, we estimated that 127 patients in each arm were needed to declare noninferiority of the single-incision sling if the upper bound of the 95% confidence interval for the between-group difference per protocol in abnormal bladder function was <12%. Assuming a 10% loss to follow-up, the total enrollment goal was 280.

Results

Between December 2018 and January 2023, 280 subjects were enrolled across 7 sites, and 255 were randomized: 126 were for single-incision, and 129 were for retropubic sling. There were no preoperative or operative characteristic differences between groups. Overall, 81% had reconstructive, and 19% had obliterative native tissue repairs. The primary outcome, abnormal lower urinary tract function at 12 months, occurred in 29 (25%) of single-incision vs 24 (20%) of the retropubic sling group (risk difference, 0.04472 [95% confidence interval, −0.03 to 0.1133]; P=.001 for noninferiority). Bothersome stress urinary incontinence occurred in 20% vs 17% (P=.27) and was retreated in 4% vs 2% (P=.44) of single-incision vs retropubic groups, respectively. Adverse events were reported in 24 (16%) of single-incision vs 14 (9%) of the retropubic group (95% confidence interval, 0.95–3.29; P=.70) and included de novo or worsening urgency incontinence symptoms, urinary tract infection, mesh exposure, need for prolonged catheter drainage, and de novo pain, without differences between groups. Patient Global Impression of Improvement (very satisfied and satisfied) was 71% vs 67% (P=.43), and median surgeon ease of sling use was 8 (7–10) vs 9 (8–10), P=.03 in single-incision vs retropubic, respectively.

Conclusion

For women undergoing vaginal repair, single-incision was noninferior to retropubic sling for stress urinary incontinence symptoms, and complications, including treatment for urinary retention, did not differ.

Le texte complet de cet article est disponible en PDF.

Key words : colpocleisis, midurethral sling, native tissue vaginal repair, occult stress incontinence, single-incision sling, stress incontinence


Plan


 C.M. has grant support from Coloplast and Boston Scientific (serves on the advisory board for Boston Scientific), is a consultant for Coloplast, and is an expert witness for Johnson & Johnson. R.E.G. serves on the advisory board for Boston Scientific and is an expert witness for Johnson & Johnson. S.C. is an expert witness for Johnson & Johnson and serves as a content expert for MCG Health. C.R.R. has grant support from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (Pelvic Floor Disorders Network) and Reia, LLC. C.F. is a consultant for Collamedix and has grant support from Caldera and Axonics. K.K. has grant support from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (Pelvic Floor Disorders Network) and is an expert witness for Johnson & Johnson. C.I. serves on the advisory board for the Eunice Kennedy Shriver National Institute of Child Health and Human Development Pelvic Floor Disorders Network and on the Obstetrician-Gynecologist Devices Panel for the US Food and Drug Administration. H.W. is a consultant for Boston Scientific, ConTipi, and Kimberly Clark, serves on the Clinical Evaluation Committee for Coloplast, received grant support from Coloplast and Boston Scientific, and is an expert witness for Johnson and Johnson. J.G.T. has grant support from Coloplast. A.S. has no disclosures.
 This study was supported by a grant from the Foundation for Female Health Awareness.
 Clinical Trial ID no. NCT03520114 (NCT03520114); registration date: April 26, 2018; initial participant enrollment: December 12, 2018.
 Cite this article as: Matthews C, Rardin CR, Sokol A, et al. A randomized trial of retropubic vs single-incision sling among patients undergoing vaginal prolapse repair. Am J Obstet Gynecol 2024;XX:x.ex–x.ex.


© 2024  The Authors. Publié par Elsevier Masson SAS. Tous droits réservés.
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