Detailed Information on Publication Record
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.