J 2016

Prospective randomized comparison of the transobturator mid-urethral sling with the single-incision sling among women with stress urinary incontinence: 1-year follow-up study

JURÁKOVÁ, Michaela, Martin HUSER, Atanas-Ivan BELKOV, Petr JANKŮ, Robert HUDEČEK et. al.

Basic information

Original name

Prospective randomized comparison of the transobturator mid-urethral sling with the single-incision sling among women with stress urinary incontinence: 1-year follow-up study

Authors

JURÁKOVÁ, Michaela (203 Czech Republic, belonging to the institution), Martin HUSER (203 Czech Republic, guarantor, belonging to the institution), Atanas-Ivan BELKOV (203 Czech Republic, belonging to the institution), Petr JANKŮ (203 Czech Republic, belonging to the institution), Robert HUDEČEK (203 Czech Republic, belonging to the institution), Petr ŠTOURAČ (203 Czech Republic, belonging to the institution), Jiří JARKOVSKÝ (203 Czech Republic, belonging to the institution) and Pavel VENTRUBA (203 Czech Republic, belonging to the institution)

Edition

International urogynecology journal, London, Springer London, 2016, 0937-3462

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30214 Obstetrics and gynaecology

Country of publisher

United Kingdom of Great Britain and Northern Ireland

Confidentiality degree

není předmětem státního či obchodního tajemství

Impact factor

Impact factor: 1.937

RIV identification code

RIV/00216224:14110/16:00089792

Organization unit

Faculty of Medicine

UT WoS

000374572900015

Keywords in English

Stress urinary incontinence; Mid-urethral sling; Single-incision sling ; Efficacy; Patient-reported outcomes; Randomized controlled trial

Tags

Tags

International impact, Reviewed
Změněno: 29/7/2016 15:03, Soňa Böhmová

Abstract

V originále

Introduction and hypothesis The objective was to compare the efficacy and safety of an innovative single-incision sling (SIS) with the inside-out transobturator sling (TOT) in the treatment of female stress urinary incontinence (SUI). Methods A prospective randomized trial was performed in a tertiary referral urogynecology center from January 2012 to December 2013. The study included women with pure urodynamic SUI. Patients were randomized to either the SIS or the TOT anti-incontinence procedure. Surgery duration, blood loss, and groin pain scores were recorded for each patient. The 1-year follow-up visit included objective and subjective cure parameters, postoperative de novo urgency, complications, and the impact on the patient’s life quality.