Results 171 to 180 of about 83,716 (331)

Diagnosis of Spontaneous Massive Fetomaternal Hemorrhage: A Case Report and Literature Review

open access: yesJournal of Clinical Ultrasound, EarlyView.
Fetomaternal hemorrhage (FMH) is the passage of fetal blood through the circulatory system of the mother either before or during delivery, and it is rarely diagnosed prenatally. This paper aims to present a comprehensive review of the literature allowing us to offer comprehensive insights into the diagnosis and management of FMH.
Martina Derme   +11 more
wiley   +1 more source

Differential impacts of parental attention deficit/hyperactivity disorder on early maternal‐infant attachment

open access: yesJCPP Advances, EarlyView.
Abstract Background Parental attention deficit/hyperactivity disorder (ADHD) is associated with increased postpartum depressive symptoms and impaired daily functioning, potentially impacting early maternal‐infant attachment (MIA). Methods 78 mothers, half with ADHD, were enrolled during pregnancy or postpartum.
Elyse Mark   +4 more
wiley   +1 more source

Elevation in white blood cell count after corticosteroid use in noninfected hospitalized patients

open access: yesJournal of Hospital Medicine, EarlyView.
Abstract Background It is widely accepted that corticosteroids cause leukocytosis. Clinicians must decide whether a rise in white blood cell (WBC) count is due to steroids versus other processes like developing infection. Objective The objective of this study is to measure the increase in white blood cell count after corticosteroid administration in ...
Erin Sullivan   +2 more
wiley   +1 more source

Developing a Childbirth Preparation Model for Pregnant Women and Supporters

open access: yesJournal of Health Science and Medical Research (JHSMR), 2012
This participatory action research aimed to develop a childbirth preparation model for pregnant womenandsupporters focusingonparticipationof15pairsofpregnant womenandtheirclosesupporters (husband or significant other) as well as 13 professional nurses ...
Warangkana Chatchawet   +4 more
doaj  

Antithrombin: Deficiency, Diversity, and the Future of Diagnostics

open access: yesMass Spectrometry Reviews, EarlyView.
ABSTRACT Our healthcare system provides reactive sick‐care, treating patients after symptoms have appeared by prescription of generic and often suboptimal therapy. This strategy brings along high costs and high pressure which is not sustainable.
Mirjam Kruijt   +2 more
wiley   +1 more source

Synergistic effects of nifedipine and indomethacin in tocolysis: A translational study

open access: yes
International Journal of Gynecology &Obstetrics, EarlyView.
Lucile Yart   +2 more
wiley   +1 more source

β3‐Adrenoceptor Agonist Effects on the Urinary Bladder Beyond Detrusor Relaxation

open access: yesNeurourology and Urodynamics, EarlyView.
ABSTRACT Aims β3‐Adrenoceptor agonists such as mirabegron or vibegron reach pharmacokinetic steady‐state within a few days. However, maximum improvements in symptoms of the overactive bladder syndrome are reached at time points later than 4 weeks, that is, detrusor smooth muscle relaxation cannot fully explain clinical effects.
Martin C. Michel   +2 more
wiley   +1 more source

Heterozygous Beta‐Thalassaemia in Pregnancy: Two Rare Causes of Severe Fetal Anemia Requiring Intrauterine Blood Transfusions

open access: yesPrenatal Diagnosis, EarlyView.
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

Prenatal Exome Sequencing Identifies Dual Maternal‐Fetal Diagnosis of HbF Mission Bay, a Novel HBG2 Variant Associated With Methemoglobinemia, Hypoxia and Hemolytic Anemia

open access: yesPrenatal Diagnosis, EarlyView.
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

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