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Showing 1 to 18 of 18 for “"Amniocentesis"”.

  1. Influence of Anchoring On Miscarriage Risk Perception Associated With Amniocentesis

    … ON MISCARRIAGE RISK PERCEPTION ASSOCIATED WITH AMNIOCENTESIS Publication No. ___________ Regina Nuccio, BS Supervisory Professor: Claire N. Singletary, MS, CGC Amniocentesis is the most common invasive procedure performed during pregnancy (Eddleman, et al., 2006). One important factor that women …

    uthsc Repository record for Influence of Anchoring On Miscarriage Risk Perception Associated With Amniocentesis (opens in a new tab)

  2. Effect of Anchoring On Perceived Amniocentesis Related Miscarriage Risk Within A Latina Population

    … risk to have a child with a birth defect. Amniocentesis, the most common type of prenatal diagnostic test, is used to detect chromosomal abnormalities, such as Down syndrome. Amniocentesis is associated with a risk of complications that can lead to a miscarriage, which is typically quoted …

    uthsc Repository record for Effect of Anchoring On Perceived Amniocentesis Related Miscarriage Risk Within A Latina Population (opens in a new tab)

  3. Choices made under reproductive uncertainty: acceptance or rejection of amniocentesis by women at genetic reproductive risk

    … factors that influence women to accept or reject amniocentesis. A sample of 199 acceptors and 50 rejectors of amniocentesis was recruited from pregnant females at genetic reproductive risk (due to advanced maternal age or hereditary genetic disorders) attending a genetic counseling clinic in a …

    iastate Repository record for Choices made under reproductive uncertainty: acceptance or rejection of amniocentesis by women at genetic reproductive risk (opens in a new tab)

  4. the Order of Genetic Counseling and Ultrasound In the Second Trimester For Patients Screen Positive Down Syndrome: Effects On Patient Knowledge, Anxiety, Decision-Making, and Satisfaction

    … and genetic counseling with the option of amniocentesis. Respondents in Group A (n = 14) had ultrasound prior to genetic counseling, while those in Group B (n = 19) had genetic counseling prior to ultrasound. State anxiety, knowledge, and decisional conflict were measured at three times …

    south-carolina Repository record for the Order of Genetic Counseling and Ultrasound In the Second Trimester For Patients Screen Positive Down Syndrome: Effects On Patient Knowledge, Anxiety, Decision-Making, and Satisfaction (opens in a new tab)

  5. ΜΕΛΕΤΗ ΕΠΙ ΤΗΣ ΚΡΥΣΤΑΛΛΩΣΕΩΣ ΤΟΥ ΑΜΝΙΑΚΟΥ ΥΓΡΟΥ

    … WERE TAKEN 61 SAMPLES OF AMNIOTIC FLUID (43 WITH AMNIOCENTESIS AND 16 FROM THE POSTERIOR CUL-DE-SAC AFTER SPONTANEOUS RUPTURE OF THE MEMBRANES. IT WAS NOTICED THAT THE CRYSTALS WHICH WERE FORMED IN A DRY DROP OF AMNIOTICFLUID WERE DIFFERENT IN VARIOUS STAGES OF GESTATION. THEY WERE MORE DISTINCT …

    greece Repository record for ΜΕΛΕΤΗ ΕΠΙ ΤΗΣ ΚΡΥΣΤΑΛΛΩΣΕΩΣ ΤΟΥ ΑΜΝΙΑΚΟΥ ΥΓΡΟΥ (opens in a new tab)

  6. A review of antenatally-diagnosed congenital heart disease in a Western Cape tertiary facility: outcomes and diagnostic discrepancy

    … 19 – 25 weeks) and a mean BMI of 28.1 (± 6.8). Amniocentesis was performed in 43/106 cases (40.6%), with a positive genetic abnormality in 23/43(53.5%), highest in the IUFD group (75.0%). Of the cases diagnosed, 21/106 were terminated (n=19.6%), intrauterine fetal death (IUFD) occurred in 21/106 …

    cape-town Repository record for A review of antenatally-diagnosed congenital heart disease in a Western Cape tertiary facility: outcomes and diagnostic discrepancy (opens in a new tab)

  7. Women’s decision making process regarding prenatal diagnostic testing

    … in the uptake of invasive diagnostic tests - amniocentesis and Chorionic Villus Sampling (CVS) – and taking into account the latest emergence of a Noninvasive Prenatal Testing, NIPT, the primary goal of this study was to explore factors that influence women’s decision to have an invasive, a …

    london-metro Repository record for Women’s decision making process regarding prenatal diagnostic testing (opens in a new tab)

  8. Clinical implementation of first trimester combined test for aneuploidies in patients aged 35 years or older

    … still a large contributor to invasive testing (amniocentesis and villocentesis). However, there are many reasons to abandon screening on the basis of AMA, given its low detection rate (DR), the risk of fetal loss (0,5-1%) and high costs for the national health systems (NHS). The aim of our study …

    catania Repository record for Clinical implementation of first trimester combined test for aneuploidies in patients aged 35 years or older (opens in a new tab)

  9. Diagnosi prenatale non invasiva di malattie monogeniche attraverso la ricerca e l'isolamento di cellule e DNA fetale nel sangue materno

    … fetal samples through villocentesis or amniocentesis. These invasive procedures are associated with 0.5-1% risk for the fetus. Due to it, in recent years, much effort has been made to develop non invasive prenatal diagnosis (NIPD). Two potential non invasive approaches involve the …

    cagliari Repository record for Diagnosi prenatale non invasiva di malattie monogeniche attraverso la ricerca e l'isolamento di cellule e DNA fetale nel sangue materno (opens in a new tab)

  10. Attitudes to ward and Utilization of Non-Invasive Prenatal Testing For Chromosome Aneuploidy Among Ob/Gyns

    … made via invasive procedures such as amniocentesis and chorionic villus sampling (CVS). However, both procedures carry a risk of complications, including miscarriage. Many groups have spent years searching for a way to diagnose a chromosome aneuploidy without putting the fetus or the …

    uthsc Repository record for Attitudes to ward and Utilization of Non-Invasive Prenatal Testing For Chromosome Aneuploidy Among Ob/Gyns (opens in a new tab)

  11. Rhetoric, Disability, and Prenatal Testing: Down Syndrome as an Object of Discourse

    … prenatal testing situation—such as the offer of amniocentesis—operate rhetorically in tacit ways, obscuring the relationship between the choice to undergo genetic screening and perceived meanings of Down syndrome.

    vt Repository record for Rhetoric, Disability, and Prenatal Testing: Down Syndrome as an Object of Discourse (opens in a new tab)

  12. Termination Rates Following Prenatal Diagnosis For Down Syndrome: A Systematic Review

    … such as chorionic villus sampling (CVS) or amniocentesis. </p> <p> The objective of this study was to review the published literature on termination rates among women with a prenatal diagnosis of Down syndrome in the United States. In addition, we aimed to describe temporal trends and …

    south-carolina Repository record for Termination Rates Following Prenatal Diagnosis For Down Syndrome: A Systematic Review (opens in a new tab)

  13. Sviluppo di una piattaforma per la diagnosi prenatale non invasiva di malattie genetiche in epoca gestazionale precoce

    … and monogenic diseases is usually performed by amniocentesis or chorionic villous sampling. However, these procedures are associated with 0.5%-2% risk of miscarriage. The discovery of cell free fetal DNA (cffDNA) in maternal plasma in 1997 has provided a new source of fetal genetic material that …

    cagliari Repository record for Sviluppo di una piattaforma per la diagnosi prenatale non invasiva di malattie genetiche in epoca gestazionale precoce (opens in a new tab)

  14. Inflammatory response in maternal serum during preterm labour

    … an invasive and sometimes risky procedure (e.g. amniocentesis). A non-invasive approach seems to be more relevant to clinical practice because of the feasibility and accessibility. However, few studies have investigated the maternal inflammatory response during preterm labour. Therefore, the …

    ghent Repository record for Inflammatory response in maternal serum during preterm labour (opens in a new tab)

  15. Maternal Biochemical Screening as a Method for Prenatal Genetic Prophylaxis /// Майчин биохимичен скрининг като метод за пренатална генетична профилактика

    Майчин биохимичен скрининг като метод за пренатална генетична профилактика цели навременно осигуряване на максимално точна индивидуална оценка на риска за най-честите и клинично значими анeуплоидии при фетуса. Касае социално значими заболявания асоциирани с тежка клинична картина и/или намален …

    varna Repository record for Maternal Biochemical Screening as a Method for Prenatal Genetic Prophylaxis /// Майчин биохимичен скрининг като метод за пренатална генетична профилактика (opens in a new tab)

  16. Sonographische Softmarker

    Die vorliegende Arbeit beschäftigt sich mit der Wertigkeit von sonographischen Softmarkern und ihrer Aussagekraft im Hinblick auf das Risiko fetaler Chromosomenanomalien. Sonographische Softmarker sind geringfügige Strukturauffälligkeiten in der Anatomie des Feten, welche die Funktion des …

    goettingen Repository record for Sonographische Softmarker (opens in a new tab)