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dc.creatorGrouzi E., Pouliakis A., Aktypi Α., Christoforidou A., Kotsi P., Αnagnostou G., Foifa A., Papadakis E.en
dc.date.accessioned2023-01-31T08:27:20Z
dc.date.available2023-01-31T08:27:20Z
dc.date.issued2022
dc.identifier10.1186/s12959-022-00419-6
dc.identifier.issn14779560
dc.identifier.urihttp://hdl.handle.net/11615/73725
dc.description.abstractBackground: During pregnancy and puerperium women are at high VTE risk. Current guidelines recommend dynamic VTE-risk assessment during pregnancy. Based on related RCOG-guidelines we constructed a digital VTE-risk assessment tool: PATrisks (www.PATrisks.com). Using this tool, we retrospectively evaluated the thrombotic risk in 742 women from our previous work, women who received thromboprophylaxis based on clinical experience for A) pregnancy complications, B) IVF treatment and C) prothrombotic tendency, in order to investigate whether that practice was justified according to the PATrisks scoring system for VTE prevention. Methods: Women with pregnancy complications [Group-A: 445], women who had undergone IVF [Group-B:132] and women with a prothrombotic tendency (thrombophilia, family history of VTE, other) [Group-C:165] were assessed using the PATrisks scoring system for thrombotic risk. The women were assigned into one of the following risk categories: low (score ≤ 2), intermediate (score = 3) and high (score ≥ 4). Further analysis per risk factor type (pre-existing or obstetric) and for various combinations of them, was also performed. We evaluated thrombotic risk early in pregnancy, and in the peripartum period. Results: The mean risk score antepartum was higher for women in Group B (3.3 in comparison with 1.9 and 2.0 in Group A and Group C respectively). Moreover, the risk score increased significantly postpartum for all Groups. The chi-square test also proved that there was a higher percentage of women at high or intermediate risk in group B compared to C before birth (55.3% vs.26.1% respectively, p < 0.0001, OR: 3.5, 95% CI: 2.2 – 5.7) and similarly after birth (85.6% vs. 56.4%, OR: 4.6, 95%CI: 2.6–8.2, p < 0.0001). In total 12 (1.6%) out of 742 women experienced thrombotic events, whether pre- or post-partum. Conclusions: LMWHs are widely prescribed during pregnancy for a number of indications, even when a proven scientific basis for such a practice is lacking. However, a considerable percentage of women were already at VTE-risk according to PATrisks and might have derived an additional benefit from LMWH in the form of VTE prevention. The rational use of these drugs should be optimized by establishing and implementing routine risk assessment for all pregnant women and by providing the necessary education to healthcare professionals. © 2022, The Author(s).en
dc.language.isoenen
dc.sourceThrombosis Journalen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85139528744&doi=10.1186%2fs12959-022-00419-6&partnerID=40&md5=328f5086268808bcbb4fa211212a7e65
dc.subjectlow molecular weight heparinen
dc.subjectadulten
dc.subjectArticleen
dc.subjectclinical assessmenten
dc.subjectclinical evaluationen
dc.subjectclinical practiceen
dc.subjectcontrolled studyen
dc.subjectdrug useen
dc.subjectfamily historyen
dc.subjectfemaleen
dc.subjecthealth care personnelen
dc.subjecthigh risk patienten
dc.subjecthumanen
dc.subjectin vitro fertilizationen
dc.subjectintermediate risk patienten
dc.subjectlow risk patienten
dc.subjectmajor clinical studyen
dc.subjectmulticenter studyen
dc.subjectpatient educationen
dc.subjectperinatal perioden
dc.subjectpopulation structureen
dc.subjectpregnancyen
dc.subjectpregnant womanen
dc.subjectprescriptionen
dc.subjectpuerperiumen
dc.subjectretrospective studyen
dc.subjectrisk assessmenten
dc.subjectrisk factoren
dc.subjectthrombophiliaen
dc.subjecttreatment indicationen
dc.subjectvenous thromboembolismen
dc.subjectBioMed Central Ltden
dc.titlePregnancy and thrombosis risk for women without a history of thrombotic events: a retrospective study of the real risksen
dc.typejournalArticleen


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