Publications by authors named "Alberry M"

Background: Postpartum depression and anxiety are the 2 most common perinatal mental health disorders, with prevalence rates higher among women living in the Middle East than in most Western countries. The negative outcomes associated with postpartum depression and anxiety are profound and include less responsive parenting and compromised infant and young child development. Although interventions exist to prevent postpartum depression and anxiety, to date, there have been no studies that have attempted to prevent postpartum depression or anxiety among Arabic-speaking women in the Middle East, including Qatar.

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Introduction This case study aimed to enhance the traceability and retrieval accuracy of ChatGPT-4 in medical text by employing a step-by-step systematic approach. The focus was on retrieving clinical answers from three international guidelines on diabetic ketoacidosis (DKA). Methods A systematic methodology was developed to guide the retrieval process.

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Background This study aimed to evaluate the efficacy of ChatGPT, an advanced natural language processing model, in adapting and synthesizing clinical guidelines for diabetic ketoacidosis (DKA) by comparing and contrasting different guideline sources. Methodology We employed a comprehensive comparison approach and examined three reputable guideline sources: Diabetes Canada Clinical Practice Guidelines Expert Committee (2018), Emergency Management of Hyperglycaemia in Primary Care, and Joint British Diabetes Societies (JBDS) 02 The Management of Diabetic Ketoacidosis in Adults. Data extraction focused on diagnostic criteria, risk factors, signs and symptoms, investigations, and treatment recommendations.

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Article Synopsis
  • The study aims to create a long-term mother-baby cohort to identify biomarkers predicting adverse pregnancy outcomes using advanced multi-omics technologies.
  • One thousand pregnant women in their first trimester will be recruited, monitored throughout pregnancy, and after childbirth, with various biological samples collected for analysis.
  • The findings are expected to enhance understanding of the relationship between molecular profiles and pregnancy complications, as well as the influence of familial and environmental factors on maternal and child health.
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Non invasive prenatal Testing (NIPT) is changing the practice of prenatal diagnosis worldwide. It provides high sensitivity and specificity in screening for common aneuploidies. As a result, it has reduced the number of invasive procedures, thereby reducing their associated risk of pregnancy miscarriage.

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Non-invasive prenatal testing is regularly used to screen for aneuploidies and Rhesus status of a fetus. Since 1997 when free fetal DNA (ffDNA) in the maternal circulation was first identified, it has been hypothesized that it may be possible to use non-invasive prenatal testing (NIPT) to identify high-risk pregnancies including pre-eclampsia, growth restriction and preterm birth. Since then there has been much interest in this area as a way to identify and understand disease processes.

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Background: Three-Dimensional visualization of brain tumors is very useful in both diagnosis and treatment stages of brain cancer.

Discussion: It helps the oncologist/neurosurgeon to take the best decision in Radiotherapy and/or surgical resection techniques. 3D visualization involves two main steps; tumor segmentation and 3D modeling.

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Objective: We sought to determine the factors associated with selection of rotational instrumental vs cesarean delivery to manage persistent fetal malposition, and to assess differences in adverse neonatal and maternal outcomes following delivery by rotational instruments vs cesarean delivery.

Study Design: We conducted a retrospective cohort study over a 5-year period in a tertiary United Kingdom obstetrics center. In all, 868 women with vertex-presenting, single, liveborn infants at term with persistent malposition in the second stage of labor were included.

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Article Synopsis
  • The study aimed to understand cardiac function in small for gestational age and intrauterine growth restricted fetuses, analyzing it in relation to fetal Doppler parameters.
  • It involved measuring various cardiac performance metrics and comparing them among appropriately grown fetuses and those that are small for their gestational age or growth restricted.
  • Findings indicated that small for gestational age and growth-restricted fetuses had significantly higher myocardial performance indices, suggesting altered cardiac function before typical hypoxia-related Doppler abnormalities appeared.
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Recent guidance from the UK National Screening Committee (NSC) and the Fetal Anomaly Screening Programme (FASP) has led to important changes in prenatal ultrasound diagnosis and invasive testing. These relate to prenatal ultrasound investigation of what were previously known as 'soft markers' for Down's syndrome at the time of the detailed anomaly scan and as to whether full karyotype or FISH (fluorescent in situ hybridisation)/QFPCR (quantitative fluorescence PCR) testing for trisomies should be carried out when an invasive test is performed. Neither recommendation is directly related to the other but both in combination could have profound implications for the detection of chromosomal abnormalities other than trisomy 21 (Down's syndrome).

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Diagnosis of foetal lingual cysts is extremely rare. If large enough, it can compromise the upper oropharyngeal airway. A case of a large ventral lingual thyroglossal duct cyst mimicking a ranula was identified at 20 weeks of gestation and excised 11 weeks postnatally using the harmonic scalpel.

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Aim: The aim of this work was to compare the effect of intraumbilical injection of three different uterotonic solutions in the management of retained placenta.

Materials And Methods: This study was conducted in Ain-Shams University Maternity Hospital, Cairo, Egypt. A total of 78 women with retained placenta (>30 min after delivery of the fetus) were included in the study and subdivided into three groups.

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After the revolutionary detection of ffDNA (free fetal DNA) in maternal circulation by real-time PCR in 1997 and advances in molecular techniques, NIPD (non-invasive prenatal diagnosis) is now a clinical reality. Non-invasive diagnosis using ffDNA has been implemented, allowing the detection of paternally inherited alleles, sex-linked conditions and some single-gene disorders and is a viable indicator of predisposition to certain obstetric complications [e.g.

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Article Synopsis
  • The study aimed to evaluate levels of free fetal DNA in maternal plasma during pregnancy and its association with conditions like preeclampsia and fetal growth restriction.
  • Blood samples from 138 singleton male pregnancies were analyzed, categorizing them into normal pregnancies, preeclampsia, and fetal growth restriction to determine gestational age-related DNA levels.
  • Results indicated that free fetal DNA levels rise with gestational age and are notably higher in pregnancies with complications, suggesting its potential as a marker for placental dysfunction, warranting further research.
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There has been a huge effort in the last 2-3 decades to develop non-invasive prenatal diagnosis to avoid the risks to the fetus caused by invasive procedures. Obtaining fetal nucleic material for molecular analysis without the need of invasive procedures has been a goal of prenatal diagnosis for many years; this is now been made possible by the use of non-cellular fetal nucleic acids circulating in maternal blood. The placenta is the primary source of these nucleic acids, raising the possibility that they could be a marker for pregnancy complications resulting from placental disease/dysfunction such as pre-eclampsia and fetal growth restriction.

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Objective: To test the hypothesis that free fetal DNA (ffDNA) circulating in maternal plasma originates mainly from the placenta we studied ffDNA levels in anembryonic pregnancies.

Methods: Maternal blood samples were collected from 15 normal first-trimester pregnancies in which fetal sex was subsequently determined and nine patients with a diagnosis of anembryonic gestation (AG). The Y chromosome DYS14 gene was quantified by real-time quantitative PCR (RT-PCR) for the determination of fetal sex in both plasma and chorionic tissue samples.

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Management of fetal growth restriction.

Arch Dis Child Fetal Neonatal Ed

January 2007

Fetal growth restriction (FGR) is challenging because of the difficulties in reaching a definitive diagnosis of the cause and planning management. FGR is associated not only with a marked increased risk in perinatal mortality and morbidity but also with long-term outcome risks. Combinations of fetal biometry, amniotic fluid volume, heart rate patterns, arterial and venous Doppler, and biophysical variables allow a comprehensive fetal evaluation of FGR.

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