Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/36548
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dc.contributor.authorLeitch A.en
dc.contributor.authorRosamilia A.en
dc.contributor.authorLee J.K.en
dc.contributor.authorNikpoor P.en
dc.contributor.authorKarjalainen P.K.en
dc.contributor.authorOw L.L.en
dc.contributor.authorMelendez-Munoz J.en
dc.contributor.authorRyan G.en
dc.date.accessioned2021-05-14T12:24:00Zen
dc.date.available2021-05-14T12:24:00Zen
dc.date.copyright2019en
dc.date.created20190919en
dc.date.issued2019-09-19en
dc.identifier.citationFemale Pelvic Medicine and Reconstructive Surgery. Conference: 2019 Annual Scientific Meetings of the American Urogynecologic Society, AUGS and the International Urogynecological Association, IUGA. Nashville, TN United States. 25 (5 Supplement 1) (pp S92-S93), 2019. Date of Publication: September - October 2019.en
dc.identifier.issn2154-4212en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/36548en
dc.description.abstractObjective: To evaluate 3-year objective and subjective outcomes of single incision and modified transobturator sling in women with stress urinary incontinence. Method(s): Women assessed for stress urinary incontinence surgery were eligible to participate. Exclusion criteria included intrinsic sphincter deficiency, previous failed midurethral or fascial sling, untreated detrusor overactivity or significant voiding dysfunction. Randomization was performed with computer-generated blocks of 4-8, with concealed allocation. Assuming an objective cure rate of 90% for TVT Abbrevo with a power of 80%, a sample size of 79 in each arm was required to detect a clinical difference of 15%, using a 1-sided alpha of 0.05. Allowing for 15% attrition rate, target recruitment was 220. Institution ethics approval (11261B) was obtained. Three year follow up consisted of patient-reported outcomemeasures utilizing ICIQ UI SF, ICIQ OAB, IIQ7, PISQ12& PGII and objective outcomes included POP-Q, cough stress test, assessment of mesh complications and uroflowmetry. Objective cure was defined as a negative cough stress test with a comfortably full bladder. Subjective cure was defined as "no" leakage on section 3 and 5 of ICIQ UI SF Question 6. Result(s): At 3 years data was available for 207 women (MiniArc: 100 and TVT Abbrevo:107) from the original 246 women. Those who were excluded after randomization were described in the 12 month follow up publication. Baseline characteristics of the two groups were comparable. There was no statistically significant difference in subjective (59% vs 69.5%; P: 0.14) or objective (92.6% vs 98.7%; P: 0.12) cure rates between MiniArc and TVTAbbrevo at 3 years, respectively. A sensitivity analysis taking into account all missing data also showed this. No statistically significant differences were found in functional outcomes and incontinence impact scores significantly improved and were greater than theminimally important difference in both groups. Conclusion(s): There are no statistically significant differences in subjective and objective cure rates and a low rate of complications at 3 years between the single incision and modified transobturator sling. (Table Presented).en
dc.languageEnglishen
dc.languageenen
dc.publisherLippincott Williams and Wilkinsen
dc.titleModified transobturator (TVT Abbrevo) and single incision (MiniArc) suburethral sling in women with stress urinary incontinence-A randomised controlled trial: 3 year follow up. [Female Pelvic Medicine and Reconstructive Surgery]en
dc.typeConference Abstracten
dc.type.studyortrialRandomised controlled trial-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1097/SPV.0000000000000767en
local.date.conferencestart2019-09-24en
dc.identifier.source629337314en
dc.identifier.institution(Nikpoor, Karjalainen, Ow, Leitch, Ryan) Monash Health, Melbourne, VIC, Australia (Karjalainen) Central Finland Central Hospital, Jyvaskyla, Finland (Melendez-Munoz) Hospital Universitari Dr. Josep Trueta, Girona, Spain (Lee) St Vincents Clinic, Sydney, NSW, Australia (Rosamilia) Monash Medical Centre, Melbourne, VIC, Australiaen
dc.description.addressP. Nikpoor, Monash Health, Melbourne, VIC, Australiaen
dc.description.publicationstatusCONFERENCE ABSTRACTen
local.date.conferenceend2019-09-28en
dc.rights.statementCopyright 2019 Elsevier B.V., All rights reserved.en
dc.identifier.affiliationext(Karjalainen) Central Finland Central Hospital, Jyvaskyla, Finland-
dc.identifier.affiliationext(Melendez-Munoz) Hospital Universitari Dr. Josep Trueta, Girona, Spain-
dc.identifier.affiliationext(Lee) St Vincents Clinic, Sydney, NSW, Australia-
dc.identifier.affiliationmh(Nikpoor, Karjalainen, Ow, Leitch, Ryan) Monash Health, Melbourne, VIC, Australia-
dc.identifier.affiliationmh(Rosamilia) Monash Medical Centre, Melbourne, VIC, Australia-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeConference Abstract-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptObstetrics and Gynaecology (Monash Women's)-
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