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Richtlijn Sterilisatie van de vrouw - NVOG

Richtlijn Sterilisatie van de vrouw - NVOG

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ReferenceType studyCharacteristicsIntervention (I)Outcomemeasured andfollow upResultsQualityassessmentEvi<strong>de</strong>nce tabel 2.2 Wat is bekend over <strong>de</strong> effectiviteit en betrouwbaarheid <strong>van</strong> laparoscopische (clips/coagulatie/ringen) enhysteroscopische sterilisatie?Argueta, 1980CohortstudyprospectiveComparitive.No inclusion/exclustion criteria were<strong>de</strong>scribed.Socio<strong>de</strong>mographic characteristics weresimilar between the intervention groups.Mean age: 29 years.Mean parity: 4.Laparoscopicapplicationof springloa<strong>de</strong>d clipsvs tubalrings.Outcomes:- Failure- Surgical time- Surgical difficulties- Pain- Postoperativecomplications andcomplaints- Gynaecologicalevents up to 24months after surgery.- Pregnancy rate.The groups were similar for failure and surgical timeSurgical difficulties:Study groups clearly <strong>de</strong>fined: (?)Selectionbias*: (-), randomisationA<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*: (-),but they did a randomisation for interventionSufficient length of follow-up*: (+), 24 monthsSelective loss tofollow-up*: (-)I<strong>de</strong>ntification ofconfoun<strong>de</strong>rs andcorrection in analysis: (?)Financial support: partial supported.The severity of reported pain was significantly higher for the tubal ringprocedures (6.1 vs 14.2%).Postoperative complications and complaints and gynaecological events (nosignificant differences between the groups):97

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