Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/36410
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dc.contributor.authorOw L.L.en
dc.contributor.authorDwyer P.L.en
dc.contributor.authorYoung N.R.en
dc.contributor.authorKulkarni M.en
dc.contributor.authorLee J.K.en
dc.contributor.authorRosamilia A.en
dc.contributor.authorLeitch A.en
dc.date.accessioned2021-05-14T12:20:59Zen
dc.date.available2021-05-14T12:20:59Zen
dc.date.copyright2019en
dc.date.created20200515en
dc.date.issued2020-05-15en
dc.identifier.citationInternational Urogynecology Journal. Conference: 44th Annual Meeting of the American Urogynecologic Society and the International Urogynecological Association, AUGS-IUGA 2019. Nashville, TN United States. 30 (1 Supplement) (pp S96-S97), 2019. Date of Publication: 2019.en
dc.identifier.issn1433-3023en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/36410en
dc.description.abstractObjective: To compare objective and subjective cure rates between Uphold and vaginal hysterectomy. Method(s):Women with symptomatic uterine descent referred for vaginal prolapse surgery were included. Women who chose UpholdTMwere required to have an endometrial assessment. Routine clinic follow-up was scheduled at 6 weeks, 6 & 12 months, involving a clinical review, examination with symptom & quality of life questionnaires. Primary outcome was incidence of stage 2 prolapse in any compartment and a composite cure of no leading edge beyond the hymen, absence of bulge symptoms on questionnaire and no retreatment. Secondary outcomes were qualityof-life measures (PFDI-20, PFIQ-7, PISQ, Patient Global impression of improvement, EQ5D and a health score) Assuming a recurrence rate of 30% for VH, with a power of 80%, a sample size of 49 each arm would be required to detect a clinical difference of 20% with UpholdTM, using a one sidedaof 0.05. Allowing for attrition rate of 15%, we proposedto recruit a total of 114 subjects for the trial. Outcomes were compared with Pearson chi2test for categorical data and Student t test or Wilcoxon rank-sum for continuous data as appropriate. Result(s): We performed 50 VH from August 2011 and November 2013 and 51 Upholds from August 2011 to June 2016, a long recruitment period for Uphold as it coincided with transvaginal mesh FDA notification. Six women from the VH group were lost to follow-up (12%) and 8 from the Uphold (16%). There was balanced demographics and POP-Q measurements between groups. The incidence of stage 2 prolapse in any compartment at 12 months was 48.8%in VH and 33.3% in Uphold. The composite cure rate at 12 months was 79.55% in VH and 72.09% in Uphold. PGI-I was not different between the groups. There was significant change in POPDI-6 (p<0.0001), CRAD-8 (p=0.0004), UDI-6 (p<0.0001), total PFDI 20 (p<0.0001) and PFIQ7 scores (p =0.0004) between the two time points but not between two comparators. There was no significant difference in surgical complication (p=0.1223), assessed using Clavien-Dindo classification. In the Uphold group, there were 9 grade 1 for prolonged catheterization, 3 grade 2 (2x UTI's and 1 mesh exposure that resolved with oestrogen) and 6 grade 3, one mesh exposure requiring excision(2AT2S1), 5 repeat surgery for stress urinary incontinence. In the vaginal hysterectomy group, there was 1 grade 1 for prolonged catheterization, 7 grade 2 (1x vault infection requiring readmission for IVAB, 1 vault haematoma with readmission, 1 PE, 4 UTI's). There was one repeat surgery in the VH group having a repeat anterior repair and mid-urethral sling. Conclusion(s): Uphold uterine suspension and repair and VH, vault suspension and repair appear to have equivalent objective and subjective cure at 12 months with no significant difference in surgical complications. There was a 2% surgery rate for mesh exposure in the Uphold group which occurred prior to adoption of the transverse incision technique. There was a trend to more re-operation for stress urinary incontinence in the Uphold group. Longer-term follow-up is anticipated.en
dc.languageEnglishen
dc.languageenen
dc.publisherSpringeren
dc.relation.ispartofInternational Urogynecology Journalen
dc.subjectincidenceen
dc.subjectoutcome assessmenten
dc.subjectPelvic Organ Prolapse Quantificationen
dc.subjectperoperative complicationen
dc.subjectquality of lifeen
dc.subjectrecurrence risken
dc.subjectreoperationen
dc.subjectretreatmenten
dc.subjectsample sizeen
dc.subjectstress incontinenceen
dc.subjectsurgeryen
dc.subjectsuspensionen
dc.subjecturinary tract infectionen
dc.subject*uterus prolapseen
dc.subject*vaginal hysterectomyen
dc.subjectestrogenen
dc.subjecthymenen
dc.subjectincisionen
dc.subjectadoptionen
dc.subjectadulten
dc.subjectcatheterizationen
dc.subjectclinical assessmenten
dc.subjectClinical Global Impression scaleen
dc.subject*cohort analysisen
dc.subjectcomplicationen
dc.subjectconference abstracten
dc.subjectcontrolled studyen
dc.subjectdemographyen
dc.subjectEuropean Quality of Life 5 Dimensions questionnaireen
dc.subjectexcisionen
dc.subjectfemaleen
dc.subjectfollow upen
dc.subjecthematomaen
dc.subjecthospital readmissionen
dc.subjecthumanen
dc.subjectmajor clinical studyen
dc.subject.meshPelvic Organ Prolapse Quantification-
dc.subject.meshperoperative-
dc.subject.meshquality of life-
dc.subject.meshrecurrence risk-
dc.subject.meshreoperation-
dc.subject.meshretreatment-
dc.subject.meshstress incontinence-
dc.subject.meshsurgery-
dc.subject.meshsuspension-
dc.subject.meshurinary tract infection-
dc.subject.meshuterus prolapse-
dc.subject.meshvaginal hysterectomy-
dc.subject.meshestrogen-
dc.subject.meshhymen-
dc.subject.meshincision-
dc.subject.meshadoption-
dc.subject.meshcatheterization-
dc.subject.meshClinical Global Impression scale-
dc.subject.meshEuropean Quality of Life 5 Dimensions-
dc.subject.meshexcision-
dc.subject.meshhematoma-
dc.subject.meshhospital readmission-
dc.titleHysterectomy or uphold uterine conservation in women with apical prolapse: A parallel cohort study of 12 months.en
dc.typeConference Abstracten
dc.type.studyortrialObservational study (cohort, case-control, cross sectional or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1007/s00192-019-04125-2-
local.date.conferencestart2019-09-24en
dc.identifier.source631723426en
dc.identifier.institution(Young, Kulkarni, Leitch, Ow) Monash Health, Melbourne, VIC, Australia (Lee) St Vincents Clinic, Sydney, NSW, Australia (Rosamilia) Monash Medical Centre, Melbourne, VIC, Australia (Dwyer) Mercy Hospital for Women, Melbourne, VIC, Australiaen
dc.description.addressN.R. Young, Monash Health, Melbourne, VIC, Australiaen
dc.subject.keywordfollow upen
dc.subject.keywordhematomaen
dc.subject.keywordhospital readmissionen
dc.subject.keywordhumanen
dc.subject.keywordhymenen
dc.subject.keywordincidenceen
dc.subject.keywordincisionen
dc.subject.keywordmajor clinical studyen
dc.subject.keywordoutcome assessmenten
dc.subject.keywordPelvic Organ Prolapse Quantificationen
dc.subject.keywordperoperative complicationen
dc.subject.keywordquality of lifeen
dc.subject.keywordrecurrence risken
dc.subject.keywordreoperationen
dc.subject.keywordretreatmenten
dc.subject.keywordsample sizeen
dc.subject.keywordstress incontinenceen
dc.subject.keywordsurgeryen
dc.subject.keywordsuspensionen
dc.subject.keywordurinary tract infectionen
dc.subject.keyword*uterus prolapseen
dc.subject.keywordadoptionen
dc.subject.keyword*vaginal hysterectomyen
dc.subject.keywordadulten
dc.subject.keywordcatheterizationen
dc.subject.keywordclinical assessmenten
dc.subject.keywordClinical Global Impression scaleen
dc.subject.keyword*cohort analysisen
dc.subject.keywordcomplicationen
dc.subject.keywordconference abstracten
dc.subject.keywordcontrolled studyen
dc.subject.keywordfemaleen
dc.subject.keywordexcisionen
dc.subject.keywordEuropean Quality of Life 5 Dimensions questionnaireen
dc.subject.keyworddemographyen
dc.relation.libraryurlLibKey Linken
dc.description.publicationstatusCONFERENCE ABSTRACTen
local.date.conferenceend2019-09-28en
dc.rights.statementCopyright 2020 Elsevier B.V., All rights reserved.en
dc.identifier.affiliationext(Lee) St Vincents Clinic, Sydney, NSW, Australia-
dc.identifier.affiliationext(Dwyer) Mercy Hospital for Women, Melbourne, VIC, Australia-
dc.identifier.affiliationmh(Young, Kulkarni, Leitch, Ow) Monash Health, Melbourne, VIC, Australia-
dc.identifier.affiliationmh(Rosamilia) Monash Medical Centre, Melbourne, VIC, Australia-
item.openairetypeConference Abstract-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
crisitem.author.deptObstetrics and Gynaecology (Monash Women's)-
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