Risk of emergency cesarean section when giving birth in Sweden: A nationwide cohort study comparing women born in countries practicing female genital mutilation, with Swedish-born women. [PDF]
Eshraghi B, Hermansson J, Marions L.
europepmc +1 more source
"We have a place, and we are present": the journey of male nursing students through obstetric clinical training in Saudi Arabia: a mixed-methods study. [PDF]
Alkhaifi SA.
europepmc +1 more source
ABSTRACT Aim In this article, we present two cases of severe fetal hemolytic anemia based on a beta‐thalassaemia trait inherited from a single parent. Results These cases, presented at 20 and 28 weeks' gestation, necessitated intra‐uterine blood transfusions.
Eva van der Meij +11 more
wiley +1 more source
Peripartum aortic dissection: a rare case of Stanford type B dissection triggered by severe labor pain. [PDF]
Lu Y +5 more
europepmc +1 more source
ABSTRACT Prenatal exome sequencing (ES) can establish rare genetic diagnoses in a fetus but may also lead to occult genetic diagnosis in a biological parent. We present a case of dual fetal and maternal diagnosis by prenatal ES, in a fetus with unexplained anemia and in a pregnant patient with sickle cell disease (SCD) and recurrent unexplained hypoxia.
Matthew A. Shear +6 more
wiley +1 more source
Obstetric-Related Emergency Medical Treatment and Labor Act Violations and No Health Exception Bans.
Woskie LR, Brower N, Shaffer J, Ladin K.
europepmc +1 more source
Evaluation of Operative Vaginal Delivery Practices and Maternal-Neonatal Outcomes. [PDF]
Baloch F, Javed M, Grosu L.
europepmc +1 more source
ABSTRACT Objective To describe the implementation of whole genome sequencing (WGS) in prenatal diagnostics and outline the national guideline system facilitating this. Methods Clinical guidelines for WGS in prenatal diagnostics were developed and implemented by the Danish Fetal Medicine Society.
Ida Vogel +17 more
wiley +1 more source
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa +7 more
wiley +1 more source
Spanish-Language Patient Education Materials for Obstetric Anesthesia: A Comparison of Readability and Quality of Online Spanish-Language Resources. [PDF]
Restrepo M, Pai S, Scott T, Burnett GW.
europepmc +1 more source

