Comparison of two-risk assessment algorithms for preeclampsia in first trimester with consecutive intake of low-dose aspirin in the high-risk group - an observational study.

We analyzed outcome of women screened for preeclampsia with two different multifactorial risk algorithms (Predictor®Software by PerkinElmer, PerkinElmer, Waltham, MA; PERK-group:n = 214 and Viewpoint®by GE Healthcare, Dornstadt, Germany; VIEW-group:n = 209) in first trimester. Women at high risk for...

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Detalles Bibliográficos
Publicado en:Journal of Maternal-Fetal & Neonatal Medicine Vol. 31; no. 5; pp. 549 - 553
Autores principales: Lakovschek, Ioana-Claudia, Csapo, Bence, Kolovetsiou-Kreiner, Vassiliki, Mayer-Pickel, Karoline, Reif, Philipp, Stern, Christina, Ulrich, Daniela, Lang, Uwe, Obermayer-Pietsch, Barbara, Cervar-Zivkovic, Mila
Formato: research Journal Article
Publicado: Taylor & Francis Ltd Mar2018
Acceso en línea:Ver este registro en EBSCOhost
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Sumario:We analyzed outcome of women screened for preeclampsia with two different multifactorial risk algorithms (Predictor®Software by PerkinElmer, PerkinElmer, Waltham, MA; PERK-group:n = 214 and Viewpoint®by GE Healthcare, Dornstadt, Germany; VIEW-group:n = 209) in first trimester. Women at high risk for developing preeclampsia were advised to take low-dose acetylsalicylic acid (LDA). Screening positive rates for early onset preeclampsia differed significantly between the two groups (7.9% versus 26.3%;p = 0.000). According the clinical use of screening test criteria, LDA was prescribed in 63 (29.4%) women in the PE-group and 55 (26.3%) in the VP-group (p = 0.516). There were no differences in onset of preeclampsia [4 (1.9%) versus 6 (2.9%);p = 0.540]. No early or severe preeclampsia occurred in the whole population.