Risk of fetal loss after chorionic villus sampling in twin pregnancy derived from propensity score matching analysis

dc.contributor.authorGil, M. M.
dc.contributor.authorRodriguez-Fernandez, M.
dc.contributor.authorElger, T.
dc.contributor.authorAkolekar, R.
dc.contributor.authorSyngelaki, A.
dc.contributor.authorDe Paco Matallana, C.
dc.contributor.authorMolina, F. S.
dc.contributor.authorGallardo Arocena, M.
dc.contributor.authorChaveeva, P.
dc.contributor.authorPersico, N.
dc.contributor.authorAccurti, V
dc.contributor.authorKagan, K. O.
dc.contributor.authorProdan, N.
dc.contributor.authorCruz, J.
dc.contributor.authorNicolaides, K. H.
dc.contributor.authoraffiliation[Gil, M. M.] Univ Francisco de Vitoria, Hosp Univ Torrejon, Madrid, Spain
dc.contributor.authoraffiliation[Rodriguez-Fernandez, M.] Univ Francisco de Vitoria, Hosp Univ Torrejon, Madrid, Spain
dc.contributor.authoraffiliation[Gil, M. M.] Univ Francisco de Vitoria, Sch Med, Madrid, Spain
dc.contributor.authoraffiliation[Rodriguez-Fernandez, M.] Univ Francisco de Vitoria, Sch Med, Madrid, Spain
dc.contributor.authoraffiliation[Gil, M. M.] Kings Coll Hosp London, Fetal Med Res Inst, 16-20 Windsor Walk,Denmark Hill, London SE5 8BB, England
dc.contributor.authoraffiliation[Elger, T.] Kings Coll Hosp London, Fetal Med Res Inst, 16-20 Windsor Walk,Denmark Hill, London SE5 8BB, England
dc.contributor.authoraffiliation[Syngelaki, A.] Kings Coll Hosp London, Fetal Med Res Inst, 16-20 Windsor Walk,Denmark Hill, London SE5 8BB, England
dc.contributor.authoraffiliation[Nicolaides, K. H.] Kings Coll Hosp London, Fetal Med Res Inst, 16-20 Windsor Walk,Denmark Hill, London SE5 8BB, England
dc.contributor.authoraffiliation[Akolekar, R.] Medway Maritime Hosp, Gillingham, England
dc.contributor.authoraffiliation[Akolekar, R.] Canterbury Christ Church Univ, Inst Med Sci, Chatham, Kent, England
dc.contributor.authoraffiliation[De Paco Matallana, C.] Hosp Clin Univ Virgen de la Arrixaca, Murcia, Spain
dc.contributor.authoraffiliation[Molina, F. S.] Hosp Univ San Cecilio, Granada, Spain
dc.contributor.authoraffiliation[Gallardo Arocena, M.] Hosp Univ San Cecilio, Granada, Spain
dc.contributor.authoraffiliation[Chaveeva, P.] Shterev Hosp, Sofia, Bulgaria
dc.contributor.authoraffiliation[Persico, N.] Osped Maggiore Policlin, Fdn IRCCS Ca Granda, Milan, Italy
dc.contributor.authoraffiliation[Accurti, V] Osped Maggiore Policlin, Fdn IRCCS Ca Granda, Milan, Italy
dc.contributor.authoraffiliation[Persico, N.] Univ Milan, Dept Clin Sci & Community Hlth, Milan, Italy
dc.contributor.authoraffiliation[Accurti, V] Univ Milan, Dept Clin Sci & Community Hlth, Milan, Italy
dc.contributor.authoraffiliation[Kagan, K. O.] Univ Womens Hosp, Tubingen, Germany
dc.contributor.authoraffiliation[Prodan, N.] Univ Womens Hosp, Tubingen, Germany
dc.contributor.authoraffiliation[Cruz, J.] Ctr Hosp Univ Lisboa Cent, Lisbon, Portugal
dc.contributor.funderFetal Medicine Foundation (UK Charity)
dc.date.accessioned2025-01-07T13:58:57Z
dc.date.available2025-01-07T13:58:57Z
dc.date.issued2022-01-13
dc.description.abstractObjective To estimate the risk of fetal loss associated with chorionic villus sampling (CVS) in twin pregnancy, using propensity score analysis. Methods This was a multicenter cohort study of women with twin pregnancy undergoing ultrasound examination at 11-13 weeks' gestation, performed in eight fetal medicine units in which the leadership were trained at the Harris Birthright Research Centre for Fetal Medicine in London, UK, and in which the protocols for screening, invasive testing and pregnancy management are similar. The risk of death of at least one fetus was compared between pregnancies that had and those that did not have CVS, after propensity score matching (1:1 ratio). This procedure created two comparable groups by balancing the maternal and pregnancy characteristics that lead to CVS being performed, similar to how randomization operates in a randomized clinical trial. Results The study population of 8581 twin pregnancies included 445 that had CVS. Death of one or two fetuses at any stage during pregnancy occurred in 11.5% (51/445) of pregnancies in the CVS group and in 6.3% (515/8136) in the non-CVS group (P
dc.identifier.doi10.1002/uog.24826
dc.identifier.essn1469-0705
dc.identifier.issn0960-7692
dc.identifier.pmid34845786
dc.identifier.unpaywallURLhttp://repositorio.chlc.min-saude.pt/bitstream/10400.17/4499/1/Ultras%20Obstet%20Gynec%202022%20162.pdf
dc.identifier.urihttps://hdl.handle.net/10668/26017
dc.identifier.wosID742107400001
dc.issue.number2
dc.journal.titleUltrasound in obstetrics & gynecology
dc.journal.titleabbreviationUltrasound obstet. gynecol.
dc.language.isoen
dc.organizationSAS - Hospital Universitario San Cecilio
dc.organizationSAS - Hospital Universitario San Cecilio
dc.page.number162-168
dc.publisherWiley
dc.rights.accessRightsopen access
dc.subjectadverse pregnancy outcome
dc.subjectchorionic villus sampling
dc.subjectCVS
dc.subjectfirst-trimester screening
dc.subjectinvasive procedure
dc.subjectinvasive testing
dc.subjectmiscarriage
dc.subjectpregnancy complications
dc.subjectprenatal diagnosis
dc.subjectNuchal translucency
dc.subjectPrediction
dc.subjectModel
dc.titleRisk of fetal loss after chorionic villus sampling in twin pregnancy derived from propensity score matching analysis
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number59
dc.wostypeArticle

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