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Richtlijn Sterilisatie van de vrouw - NVOG

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ReferenceType studyCharacteristicsIntervention (I)Outcomemeasured andfollow upResultsQualityassessmentHurskainen,2010SR,searched tilljuly 2008Inclu<strong>de</strong>d:KErin2003,CooperDuffy,Kerin 2004,Ubeda,Litta, LevieEfficacy/effectiveness, adverseevents, costsJamieson 2000prospective,multicentercohortstudyN = 9475Inclusion criteria: 18–44 years old womenscheduled for tubal sterilizations in 15participating institutions in nine cities from1978 to 1987.Exclusion criteria: women who hadconcurrent surgeries other than diagnosticD&C or simple biopsies.Intervallaparoscopicprocedures.The fourmostfrequentmethods ofocclusionwere: bipolarcoagulation,unipolarcoagulation,siliconerubber bandapplication,and springclipapplicationOutcomes:- Overall complicationrates.- six standardcomplicationcategories werechosen:1) uninten<strong>de</strong>d majorsurgery2) transfusion,3) febrile morbidity,4) life threateningevent,5) Rehospitalisation,6) <strong>de</strong>ath)- Standard rates (byinten<strong>de</strong>d method atinitiation of surgeryfor the four mostfrequent methods ofocclusion: bipolarcoagulation, unipolarcoagulation, siliconerubber bandapplication, andspring clipapplication.- Potential predictorsof intraoperative andpostoperativecomplications wereStudy groups clearly <strong>de</strong>fined: +Selectionbias*: ?A<strong>de</strong>quate assesment of exposure *: +A<strong>de</strong>quate assesment of outcomes*: +Assesor of the effect a<strong>de</strong>quately blin<strong>de</strong>d*: -Sufficient length of follow-up*: +Selective loss tofollow-up*: ? not reportedI<strong>de</strong>ntification ofconfoun<strong>de</strong>rs andcorrection in analysis:? Riskfactors were i<strong>de</strong>ntified, but no correctionin effects was performedFinancial support: Supported by an interagencyagreement (3-Y02-HD41075-10) withthe National Institute of Child Health andHuman Development104

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