Results 111 to 120 of about 39,435 (216)

Cord blood T-Cell imbalances as early predictors of bronchopulmonary dysplasia in extremely preterm neonates. [PDF]

Respir Res
Li Y, Xue Y, Zhang L, Xu Y, Guo X, Zhang X, Li H, Yang Y, Wang Y, Zhu X, Wang H, Jing X, Zhu C, Xu F.   +13 more
europepmc   +1 more source

Study Protocol for a Pilot Randomized Controlled Trial of a Brief, Virtual Exposure‐Based Intervention for Perinatal Posttraumatic Stress Disorder

Research in Nursing &Health, EarlyView.
ABSTRACT Perinatal posttraumatic stress disorder (PPTSD) is a public health concern with serious implications for maternal and infant health outcomes. However, clinical research for PPTSD treatment is minimal. Thus, we aim to help address this gap by evaluating the feasibility, acceptability, and preliminary effectiveness of a tailored PPTSD ...
Michelle L. Miller, Samantha Addante, Sarah A. Greenwell, Avelina C. Padin, David M. Haas   +4 more
wiley   +1 more source

High Prevalence and Limited Perinatal Prediction of Kidney Dysfunction in Adolescents Born Extremely Preterm. [PDF]

Kidney Int Rep
Sanderson KR, Vazquez JE, Flythe JE, Askenazi D, Kosorok MR, Lu M, Makker K, Laughon M, Kistler CE, Fry RC, O'Shea TM.   +10 more
europepmc   +1 more source

Hemolytic Disease of the Fetus and Newborn: Fetal RHD Genotyping, Targeted Prophylaxis, and Prenatal Therapies

Prenatal Diagnosis, EarlyView.
ABSTRACT Hemolytic disease of the fetus and newborn (HDFN) remains a significant concern in prenatal care primarily caused by maternal alloimmunization against fetal red blood cell antigens, most commonly the D antigen. Noninvasive fetal RHD genotyping, used as a screening tool, enables targeted antenatal prophylaxis and has been implemented in several
Emilie Thorup, Steffen Thorsen, Morten Hanefeld Dziegiel, Olav Bjørn Petersen, Frederik Banch Clausen   +4 more
wiley   +1 more source

The Diagnosis and Prenatal Management of Non‐RHD Alloimmunizations

Prenatal Diagnosis, EarlyView.
ABSTRACT Red blood cell (RBC) alloimmunization remains a relevant cause of hemolytic disease of the fetus and newborn (HDFN). Although RhD immunization has significantly decreased since the implementation of systematic prophylaxis, it is still the main cause of alloimmunization in pregnancy.
Mar Bennasar, Antoni Borrell
wiley   +1 more source

Early-life serum protein profiles associated with bronchopulmonary dysplasia in extremely preterm infants. [PDF]

Respir Res
Klevebro S, Panwar MB, Wackernagel D, Hansen Pupp I, Björkander S, Danielsson H, Uhlén M, Vallin L, Sävman K, Pivodic A, Hellström A, Nilsson AK.   +11 more
europepmc   +1 more source

Fetal Intracranial Hemorrhage: What to Tell Expecting Parents?

Prenatal Diagnosis, EarlyView.
ABSTRACT Fetal intracranial hemorrhage (ICH) is a rare but serious prenatal diagnosis, and counseling affected families remains challenging. In this narrative review, we summarize current evidence on the classification, epidemiology, etiology, diagnosis and neurodevelopmental outcomes of fetal ICH, with a primary focus on intraventricular hemorrhage ...
Shiri Shinar, Yada Kunpalin, Elka Miller
wiley   +1 more source

Transplacental Flecainide and/or Digoxin for Fetal Tachyarrhythmias: Therapeutic Efficacy and Clinical Experience

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To assess the efficacy and safety of transplacental flecainide and/or digoxin for fetal tachyarrhythmias when sotalol is unavailable. Method We evaluated transplacental flecainide, digoxin, or combination therapy in a retrospective and prospective cohort across two Thai tertiary centers.
Mukpradab Darakamas, Sanitra Anuwutnavin, Fuanglada Tongprasert, Wisit Chankhunaphas, Kanyarat Nilto, Supaluck Kanjanauthai, Jarupim Soongswang   +6 more
wiley   +1 more source

Automated oxygen control in extremely preterm infants: lessons from a negative trial. [PDF]

Transl Pediatr
Benincasa BC, Silveira RC.
europepmc   +1 more source

Genome‐Wide NIPT With Fetal‐Fraction Enrichment and BinDel: Clinical Cohort Evaluation of Microdeletion and ‐Duplication Detection

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To evaluate the analytical and clinical performance of fetal fraction (FF) enriched genome‐wide noninvasive prenatal testing (GW‐NIPT) for the detection of clinically relevant copy number variants (CNVs) down to 1 Mb. Methods We retrospectively analyzed 10,501 singleton pregnancies tested with FF enrichment‐based GW‐NIPT between ...
Karmen Vaiküll, Priit Paluoja, Signe Mölder, Vadym Gryshchenko, Neeme Tõnisson, Andres Salumets, Kaarel Krjutškov   +6 more
wiley   +1 more source