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  5. Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ
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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/18295
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dc.contributor.authorMakrydimas, G.en
dc.contributor.authorKaponis, A.en
dc.contributor.authorSkentou, C.en
dc.contributor.authorLolis, D.en
dc.date.accessioned2015-11-24T18:51:42Z-
dc.date.available2015-11-24T18:51:42Z-
dc.identifier.issn0960-7692-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/18295-
dc.rightsDefault Licence-
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectAmniocentesis/adverse effects/*methodsen
dc.subjectChi-Square Distributionen
dc.subjectChorionic Villi Sampling/adverse effects/*methodsen
dc.subjectFemaleen
dc.subjectFetal Death/prevention & controlen
dc.subjectHumansen
dc.subjectPregnancyen
dc.subjectPregnancy Complications/prevention & controlen
dc.subjectPregnancy Trimester, Firsten
dc.subjectPrenatal Diagnosis/methodsen
dc.subjectProbabilityen
dc.subjectProspective Studiesen
dc.subjectRisk Assessmenten
dc.subjectSafetyen
dc.subjectSensitivity and Specificityen
dc.subjectStatistics, Nonparametricen
dc.subjectTime Factorsen
dc.titleShort-term safety of celocentesis for the mother and the fetusen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1046/j.1469-0705.2002.00646.x-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/11896943-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1046/j.1469-0705.2002.00646.x/asset/84_ftp.pdf?v=1&t=h0l4afhe&s=7f1b073e7765ee2052e9561f1de10873716a54e5-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2002-
heal.abstractOBJECTIVE: Celocentesis offers the potential for prenatal diagnosis from as early as 6 weeks of gestation. The aim of this study was to examine the short-term safety of celocentesis. METHODS: Eligible for the study were pregnant women with single live fetuses at 6-10 weeks of gestation, requesting pregnancy termination for social indications. At presentation, the patients were asked if they were willing to undergo celocentesis and in those women who agreed the procedure was performed at the time of the initial scan. A second scan was carried out just before termination to measure fetal crown-rump length and heart rate. RESULTS: Four hundred and forty-seven women requested termination of pregnancy and 108 of these agreed to have celocentesis. There were no significant differences between the groups in maternal age, prevalence of primigravidas, cigarette smokers, existence of uterine fibroids, the median fetal crown-rump length or the interval between the initial scan (or celocentesis) at presentation and the pregnancy termination. At the time of termination, ultrasound examination demonstrated fetal death in five (4.7%) of the celocentesis group and nine (2.7%) of the controls (odds ratio, 1.804; 95% confidence interval, 0.5912-5.504). In all other cases, there was normal fetal growth and there were no significant differences between the groups in fetal crown-rump length. CONCLUSIONS: The procedure related fetal loss associated with celocentesis may be approximately 2%.en
heal.journalNameUltrasound Obstet Gynecolen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
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