In patients with suspected placental vascular disease who do not require hospitalization, the use of the sFlt-1 (Soluble FMS like tyrosin-kinase-1)/PlGF (Placental Growth Factor)/ assay can most likely help teams to define the best possible management.
Preeclampsia is a serious obstetric condition, affecting 2 to 5% of pregnancies and associated with maternal hypertension and renal dysfunction. It is a constant concern of obstetrical teams in the pre and post partum period. In case of diagnosis in the emergency unit, patients are usually hospitalized. However, in the case of a diagnosis of preeclampsia has been invalidated, but in presence of isolated or frustrated clinical functional signs, in the case of a history of placental vascular pathology, obstetric teams implement surveillance strategies that are binding on the patients. The sFlt-1/ PlGF assay has a high negative predictive value for the coming week. The use in clinical practice of these two biomarkers in the indication of negative prediction at one week could help teams in their management but the interest of this use needs to be evaluated.
Study Type
OBSERVATIONAL
Enrollment
150
During a vascular check-up usually prescribed, an additional blood sample is taken to allow the determination of the sFlt1/PlGf ratio.
Centre Hospitalier Intercommunal de Créteil
Créteil, France
Reconvening period in patients with an sFlt1 (Soluble FMS like tyrosin-kinase-1)/PlGF (Placental Growth Factor) ratio <38 (day)
At the end of pregnancy, calculation of the average time between the 1st consultation and the 1st reconvening in patients with an sFlt1/PlGF ratio \<38, unknown during pregnancy, to determine if consultations could have been avoided.
Time frame: trough participation period, an average of 4 months
reconvening period in patients with an sFlt1/PlGF ratio between 38 and 85 (day)
rate of reconvening
Time frame: trough participation period, an average of 4 months
reconvening period in patients with an sFlt1/PlGF ratio superior to 85 (day)
rate of reconvening
Time frame: trough participation period, an average of 4 months
blood pressure (mmHg)
Blood pressure higher than 140/90 mm Hg
Time frame: trough participation period, an average of 4 months
number of patients with functional signs of hypertension
phosphenes, accouphens, headaches, epigastric bar, edema
Time frame: trough participation period, an average of 4 months
number of patient with abnormal vascular and renal blood tests
platelets, transaminase, uric acid, ionogram
Time frame: trough participation period, an average of 4 months
proteinuria (mg/mmol)
urine protein-creatinine (P/C) ratio, mg/mmol
Time frame: trough participation period, an average of 4 months
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Intra Uterine growth restriction (IUGR)
estimate foetal weight \< 10 percentile or \< 5 percentile
Time frame: trough participation period, an average of 4 months
fetal echography
umbilical and/or cerebral doppler
Time frame: trough participation period, an average of 4 months
term of delivery (weeks of gestation)
Analysis of term delivery with stratification by sFlt-1/PlGF ratio
Time frame: at birth
fetal weight at birth (g)
Analysis of fetal weight with stratification by sFlt-1/PlGF ratio
Time frame: at birth
number of hospitalized new born
Analysis of number of hospitalized new born with stratification by sFlt-1/PlGF ratio
Time frame: at birth