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Combined screening for early and late pre-eclampsia and intrauterine growth restriction by maternal history, uterine artery Doppler, mean arterial pressure and biochemical markers.
Litwinska, Ewelina; Litwinska, Magdalena; Oszukowski, Przemyslaw; Szaflik, Krzysztof; Kaczmarek, Piotr.
Affiliation
  • Litwinska E; Perinatology and Gynecology Department, Polish Mother's Memorial Hospital Research Institute, Lódz, Poland.
  • Litwinska M; Department of Gynecology, Fertility and Fetal Therapy, Polish Mother's Memorial Hospital Research Institute, Lódz, Poland.
  • Oszukowski P; Perinatology and Gynecology Department, Polish Mother's Memorial Hospital Research Institute, Lódz, Poland.
  • Szaflik K; Department of Gynecology, Fertility and Fetal Therapy, Polish Mother's Memorial Hospital Research Institute, Lódz, Poland.
  • Kaczmarek P; Department of Operative Gynecology and Oncological Gynecology, Polish Mother's Memorial Hospital Research Institute, Lódz, Poland.
Adv Clin Exp Med ; 26(3): 439-448, 2017.
Article in En | MEDLINE | ID: mdl-28791818
ABSTRACT

BACKGROUND:

Pre-eclampsia is a systemic disease connected with high maternal and fetal morbidity and mortality. Despite significant progress achieved in perinatal medicine, pre-eclampsia is still one of the most significant current problems in obstetrics.

OBJECTIVES:

The aim of the study was to establish diagnostic algorithms for early and late pre-eclampsia (PE) and intrauterine growth restriction (IUGR). MATERIAL AND

METHODS:

A total of 320 pregnant women between 11 + 0 and 13 + 6 weeks of gestation were recruited for a case-control study. The study group consisted of 22 patients with early PE, 29 patients with late PE and 269 unaffected controls. The following parameters were recorded maternal history, mean arterial pressure (MAP), mean uterine artery pulsatility index (UtA-PI), and the concentrations of placental growth factor (PlGF), pregnancy-associated plasma protein A (PAPP-A) and free beta-human chorionic gonadotropin (free ß-hCG).

RESULTS:

A multivariable stepwise logistic regression analysis indicated that the best screening model for the prediction of early PE is based on a combined analysis of maternal risk factors, UtA-PI and PlGF levels (sensitivity 91%; specificity 84%). The best screening model for the prediction of late PE is based on a combined analysis of maternal risk factors, UtA-PI and MAP (sensitivity 85%; specificity 83%). The most effective screening model for the prediction of IUGR is based on a combined analysis of maternal risk factors, UtA-PI and PlGF concentrations (sensitivity 91%; specificity 83%).

CONCLUSIONS:

The integrated model of screening established in this study can be a valuable method to identify patients at increased risk of developing pre-eclampsia and related complications. The ability to predict the occurrence of pre-eclampsia in early pregnancy would enable maternal and fetal morbidity to be reduced through the introduction of strict obstetric surveillance as well as planned delivery in a reference center.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pre-Eclampsia / Biomarkers / Uterine Artery / Fetal Growth Retardation / Arterial Pressure Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Adult / Female / Humans / Pregnancy Language: En Journal: Adv Clin Exp Med Year: 2017 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pre-Eclampsia / Biomarkers / Uterine Artery / Fetal Growth Retardation / Arterial Pressure Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Adult / Female / Humans / Pregnancy Language: En Journal: Adv Clin Exp Med Year: 2017 Document type: Article Affiliation country:
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