Transurethral injection of polyacrylamide hydrogel (Bulkamid (R)) for the treatment of female stress or mixed urinary incontinence
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F14%3A10284800" target="_blank" >RIV/00216208:11110/14:10284800 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00064165:_____/14:10284800
Výsledek na webu
<a href="http://dx.doi.org/10.1016/j.ejogrb.2014.03.033" target="_blank" >http://dx.doi.org/10.1016/j.ejogrb.2014.03.033</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.ejogrb.2014.03.033" target="_blank" >10.1016/j.ejogrb.2014.03.033</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Transurethral injection of polyacrylamide hydrogel (Bulkamid (R)) for the treatment of female stress or mixed urinary incontinence
Popis výsledku v původním jazyce
Objective: The aim of this study was to evaluate the cure effect of a transurethral injection (TUI) of Bulkamid (R) for female urodynamic stress (USI) and stress-predominant mixed urinary incontinence. The hypothesis was that the cure effect of Bulkamid(R) is positive in patients who have undergone previous unsuccessful anti-incontinence surgery and in patients with ISD (Intrinsic Sphincter Deficiency). Study design: This retrospective clinical study was performed on 52 patients for whom previous anti-incontinence surgery had failed (n = 40) and on patients with ISD. Five patients had a reinjection of Bulkamid (R). The efficacy of TUI was evaluated an average of 22 months (minimum - 6 months, maximum - 50 months) after the procedure. Subjective assessment of the leakage of urine was based on the International Consultation on Incontinence Questionnaire - Short Form (ICIQ-UI SF). Objective assessment of leakage of urine was assessed by the cough test. The cure effect of procedures was e
Název v anglickém jazyce
Transurethral injection of polyacrylamide hydrogel (Bulkamid (R)) for the treatment of female stress or mixed urinary incontinence
Popis výsledku anglicky
Objective: The aim of this study was to evaluate the cure effect of a transurethral injection (TUI) of Bulkamid (R) for female urodynamic stress (USI) and stress-predominant mixed urinary incontinence. The hypothesis was that the cure effect of Bulkamid(R) is positive in patients who have undergone previous unsuccessful anti-incontinence surgery and in patients with ISD (Intrinsic Sphincter Deficiency). Study design: This retrospective clinical study was performed on 52 patients for whom previous anti-incontinence surgery had failed (n = 40) and on patients with ISD. Five patients had a reinjection of Bulkamid (R). The efficacy of TUI was evaluated an average of 22 months (minimum - 6 months, maximum - 50 months) after the procedure. Subjective assessment of the leakage of urine was based on the International Consultation on Incontinence Questionnaire - Short Form (ICIQ-UI SF). Objective assessment of leakage of urine was assessed by the cough test. The cure effect of procedures was e
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FK - Gynekologie a porodnictví
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/NT13509" target="_blank" >NT13509: Intrauretrální aplikace Bulkamidu u žen s těžkou inkontinencí moči na podkladě insuficience vnitřního svěrače uretry.</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2014
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
European Journal of Obstetrics, Gynecology and Reproductive Biology
ISSN
0301-2115
e-ISSN
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Svazek periodika
178
Číslo periodika v rámci svazku
July
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
4
Strana od-do
199-202
Kód UT WoS článku
000339036600037
EID výsledku v databázi Scopus
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