Different screening modalities evaluation to develop algorithms to predict pregnancy complications in twin pregnancies, and evaluation of serologic response to BNT162b2 Pfeizer/BioNTech vaccination.
This is a multi-center study to identify biomarkers or marker combinations for early prediction of pregnancy complications in twin pregnancies in the first, second or third trimester. In the future, the identified patients' risk will enable patients' referrals for proper prevention when such will become available Specifically the investigators aim for * Predicting the risk to develop preeclampsia, IUGR, preterm delivery, gestational Diabetes Melitus * Assessment of major and minor markers for chromosomal and structural anomalies * Identification of placenta accrete spectrum disorders and vasa previa * Diagnosis of specific MC twin complications such as TTTS The investigators will stratify and assess all the above according to chorionicity and delivery with complications at \<32 weeks, \<34 weeks, \<37 weeks, and at any gestation. Screening methods will be conducted in the first, second or third trimester or at any gestation Also the investigators aim to Identify the risk to lose one or both twins at \<32 weeks, \<34 weeks, \<37 weeks and at any gestation, the ability to predict fetal birth weight at \<32 weeks, \<34 weeks, \<37 weeks and at any gestation The investigators also aim for monitoring any of the following maternal complications including placental abruption (clinically or on placental examination), postpartum hemorrhage (defined as blood loss ≥1 L within the first 24 hours after birth) at \<32 weeks, \<34 weeks, \<37 weeks and at any gestation. The investigators will monitor 1. Neonatal morbidity due to intraventricular hemorrhage (IVH) grade II or above - Defined as bleeding into the ventricles, Grade II (moderate) - IVH occupies \<50% of the lateral ventricle volume, Grade III (severe) - IVH occupies ≥50% of the lateral ventricle volume or Grade IV (severe) - Hemorrhagic infarction in periventricular white matter ipsilateral to a large IVH 2. Neonatal sepsis confirmed bacteremia in cultures, anemia defined as low Hemoglobin and / or hematocrit requiring blood transfusion, respiratory distress syndrome defined as need for treatment by surfactant and ventilation, necrotizing enterocolitis requiring surgical intervention, and composite of any of the above 3. Newborn admission to neonatal intensive care units (NICU), length of stay and therapies during the admission. 4. Ventilation defined as a need for a positive pressure (continuous positive airway pressure (CPAP), nasal continuous positive airway pressure (NCPAP)) or intubation and a composite of any of the above 5. Any maternal complications within the first 6-10 weeks post delivery. The investigators will recruit patients in the different sites aiming for 1200 twin pregnancy and will collect the patients' entire pregnancy data for developing an algorithm to calculate the risk to develop the complications 6. Evaluation of serologic response to BNT162b2 Pfeizer/BioNTech vaccination.
Study Type
OBSERVATIONAL
Enrollment
1,200
MC twin anaestemosis separatio by laser. Vasa previa and placenta accreta are treated with steroids or other protocols, Positive trisomies by NIPS undergoes CVS or amniocentesis
CHU Brugmann,
Brussels, Belgium
NOT_YET_RECRUITINGUniversity of Montreal Medical Centre, Canada
Montreal, Canada
NOT_YET_RECRUITINGUniversity Hospital Bonn, Bonn, Germany
Bonn, Germany
RECRUITINGOliver Kagan
Tübingen, Germany
RECRUITINGDepartment of ObGyn, Assaf Harofe-Shamir Medical Center
Zrifin, Israel
RECRUITINGHospital Clinic, Barcelona,
Barcelona, Catalonia, Spain
NOT_YET_RECRUITINGThe Fetal Medicine Foundation
London, United Kingdom
NOT_YET_RECRUITINGAdverse pregnancy outcome
preterm delivery before 37 weeks of gestation , or hypertension of \>90/140, from gestational week 24 and above throughout pregnancy , baby birth weight below the 5 lower centile for the gestation week, or shoulder dyctorcia at delivery, or newborn admission to NICU for any complication or placental position complications such as placenta accreta, or vasa previa, or intra uterine fetal death,
Time frame: through study completion, an average of 1 year
Adverse neonatal outcome
Admission to neonatal intensive care unit, Sepsis, asphyxia, intraventricular hemorrhage, intrauterine growth retardation
Time frame: through study completion, an average of 2 year
Evaluation of serologic response to BNT162b2 Pfeizer/BioNTech vaccination.
Testing blood sample drawn for the study for antybody levels in conjunction to BNT162b2 Pfeizer/BioNTech vaccination
Time frame: through study completion, an average of 2 year including stored samples collected before vaccination was avaluable.
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