What Is the Optimal Gestational Age for Delivery?
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Risk Factors Associated with Maternal Age and Other Parameters in Assisted Reproductive Technologies - a Brief Review
Available online at www.pelagiaresearchlibrary.com Pelagia Research Library Advances in Applied Science Research, 2017, 8(2):15-19 ISSN : 0976-8610 CODEN (USA): AASRFC Risk Factors Associated with Maternal Age and Other Parameters in Assisted Reproductive Technologies - A Brief Review Shanza Ghafoor* and Nadia Zeeshan Department of Biochemistry and Biotechnology, University of Gujrat, Hafiz Hayat Campus, Gujrat, Punjab, Pakistan ABSTRACT Assisted reproductive technology is advancing at fast pace. Increased use of ART (Assisted reproductive technology) is due to changing living standards which involve increased educational and career demand, higher rate of infertility due to poor lifestyle and child conceivement after second marriage. This study gives an overview that how advancing age affects maternal and neonatal outcomes in ART (Assisted reproductive technology). Also it illustrates how other factor like obesity and twin pregnancies complicates the scenario. The studies find an increased rate of preterm birth .gestational hypertension, cesarean delivery chances, high density plasma, Preeclampsia and fetal death at advanced age. The study also shows the combinatorial effects of mother age with number of embryos along with number of good quality embryos which are transferred in ART (Assisted reproductive technology). In advanced age women high clinical and multiple pregnancy rate is achieved by increasing the number along with quality of embryos. Keywords: Reproductive techniques, Fertility, Lifestyle, Preterm delivery, Obesity, Infertility INTRODUCTION Assisted reproductive technology actually involves group of treatments which are used to achieve pregnancy when patients are suffering from issues like infertility or subfertility. The treatments can involve invitro fertilization [IVF], intracytoplasmic sperm injection [ICSI], embryo transfer, egg donation, sperm donation, cryopreservation, etc., [1]. -
Extended Abstract
Extended abstract Effect of intrauterine development and nutritional status on perinatal, intrauterine and neonatal mortality 1 Péter Berkő, 2 Kálmán Joubert, 3 Éva Gárdos, 4 Gyula Gyenis 1Faculty of Healthcare, Miskolc University, BAZ County and University Teaching Hospital Miskolc, Hungary, - 2Demographic Research Institute, Hungarian Central Statistical Office, Budapest, - 3Hungarian Central Statistical Office, Budapest, - 4Department of Biological Anthropology, Faculty of Science, Eötvös Lorand University, Budapest, Hungary At least 50-60% of 3 million of intrauterine and near 4 million deaths that occur worldwide every year are associated with low birth weight, caused by intrauterine growth restriction, preterm delivery, and genetic abnormalities. Fetal growth restriction is the second leading cause of perinatal morbidity and mortality. The authors study to what extent bodily development and nutritional status influence the viability, or perinatal mortality of foetuses and neonates. In the present study the authors describe their novel method, the MDN system (MDN: Maturity, Development, Nutritional status) and its application: 1./ to determine the nutritional status of a neonate on the basis of its gestational age, length and weight development considered simultaneously; - 2./ to differentiate the most viable and the most endangered neonates on the basis of their development and nutritional status; - 3./ to demonstrate the influence of a neonate’s nutritional status by the gestational age on its perinatal mortality. Method – the MDN system The authors have developed a new method, the MDN system (MDN: Maturity, Development, Nutritional status) to determine the weight and length standard positions of neonates in relation to reference standards on the basis of their gestational ages, birth weights and lengths. -
Evolution of Oviductal Gestation in Amphibians MARVALEE H
THE JOURNAL OF EXPERIMENTAL ZOOLOGY 266394-413 (1993) Evolution of Oviductal Gestation in Amphibians MARVALEE H. WAKE Department of Integrative Biology and Museum of Vertebrate Zoology, University of California,Berkeley, California 94720 ABSTRACT Oviductal retention of developing embryos, with provision for maternal nutrition after yolk is exhausted (viviparity) and maintenance through metamorphosis, has evolved indepen- dently in each of the three living orders of amphibians, the Anura (frogs and toads), the Urodela (salamanders and newts), and the Gymnophiona (caecilians). In anurans and urodeles obligate vivi- parity is very rare (less than 1%of species); a few additional species retain the developing young, but nutrition is yolk-dependent (ovoviviparity) and, at least in salamanders, the young may be born be- fore metamorphosis is complete. However, in caecilians probably the majority of the approximately 170 species are viviparous, and none are ovoviviparous. All of the amphibians that retain their young oviductally practice internal fertilization; the mechanism is cloaca1 apposition in frogs, spermato- phore reception in salamanders, and intromission in caecilians. Internal fertilization is a necessary but not sufficient exaptation (sensu Gould and Vrba: Paleobiology 8:4-15, ’82) for viviparity. The sala- manders and all but one of the frogs that are oviductal developers live at high altitudes and are subject to rigorous climatic variables; hence, it has been suggested that cold might be a “selection pressure” for the evolution of egg retention. However, one frog and all the live-bearing caecilians are tropical low to middle elevation inhabitants, so factors other than cold are implicated in the evolu- tion of live-bearing. -
Management of Neonates Born at ≤34 6/7 Weeks' Gestation with Suspected Or Proven Early-Onset Bacterial Sepsis Karen M
CLINICAL REPORT Guidance for the Clinician in Rendering Pediatric Care ≤ ’ Management of Neonates Born at 34 Karen M. Puopolo, MD, PhD, FAAP, a, b William E. Benitz, MD, FAAP, c Theoklis E. Zaoutis, MD, MSCE, FAAP, a, d 6/7COMMITTEE ONWeeks FETUS AND NEWBORN, GestationCOMMITTEE ON INFECTIOUS DISEASES With Suspected or Proven Early-Onset Bacterial Sepsis Early-onset sepsis (EOS) remains a serious and often fatal illness among abstract infants born preterm, particularly among newborn infants of the lowest gestational age. Currently, most preterm infants with very low birth weight are treated empirically with antibiotics for risk of EOS, often for prolonged aDepartment of Pediatrics, Perelman School of Medicine, University periods, in the absence of a culture-confirmed infection. Retrospective of Pennsylvania, Philadelphia, Pennsylvania; bChildren’s Hospital of studies have revealed that antibiotic exposures after birth are associated Philadelphia, and dRoberts Center for Pediatric Research, Philadelphia, Pennsylvania; and cDivision of Neonatal and Developmental Medicine, with multiple subsequent poor outcomes among preterm infants, making the Department of Pediatrics, School of Medicine, Stanford University, Palo risk/benefit balance of these antibiotic treatments uncertain. Gestational Alto, California age is the strongest single predictor of EOS, and the majority of preterm This document is copyrighted and is property of the American Academy of Pediatrics and its Board of Directors. All authors have births occur in the setting of other factors associated with risk of EOS, filed conflict of interest statements with the American Academy of Pediatrics. Any conflicts have been resolved through a process making it difficult to apply risk stratification strategies to preterm infants. -
Bivariate Analysis of Birth Weight and Gestational Age Depending on Environmental Exposures: Bayesian Distributional Regression with Copulas
Bivariate Analysis of Birth Weight and Gestational Age Depending on Environmental Exposures: Bayesian Distributional Regression with Copulas Jonathan Rathjens1, Arthur Kolbe2, Jürgen Hölzer2, Katja Ickstadt1, and Nadja Klein3 1Technische Universität Dortmund, 2Ruhr-Universität Bochum, 3Humboldt-Universität zu Berlin April 30, 2021 Abstract In this article, we analyze perinatal data with birth weight (BW) as primarily interesting response variable. Gestational age (GA) is usually an important covariate and included in polynomial form. However, in opposition to this univariate regression, bivariate modeling of BW and GA is recommended to distinguish effects on each, on both, and between them. Rather than a parametric bivariate distribution, we apply conditional copula regression, where marginal distributions of BW and GA (not necessarily of the same form) can be estimated independently, and where the dependence structure is modeled conditional on the covariates separately from these marginals. In the resulting distributional regression models, all parame- ters of the two marginals and the copula parameter are observation-specific. Besides biometric and obstetric information, data on drinking water contamination and maternal smoking are in- cluded as environmental covariates. While the Gaussian distribution is suitable for BW, the skewed GA data are better modeled by the three-parametric Dagum distribution. The Clay- ton copula performs better than the Gumbel and the symmetric Gaussian copula, indicating lower tail dependence (stronger dependence when both variables are low), although this non- linear dependence between BW and GA is surprisingly weak and only influenced by Cesarean arXiv:2104.14243v1 [stat.ME] 29 Apr 2021 section. A non-linear trend of BW on GA is detected by a classical univariate model that is polynomial with respect to the effect of GA. -
Glossary of Common MCH Terms and Acronyms
Glossary of Common MCH Terms and Acronyms General Terms and Definitions Term/Acronym Definition Accountable Care Organizations that coordinate and provide the full range of health care services for Organization individuals. The ACA provides incentives for providers who join together to form such ACO organizations and who agree to be accountable for the quality, cost, and overall care of their patients. Adolescence Stage of physical and psychological development that occurs between puberty and adulthood. The age range associated with adolescence includes the teen age years but sometimes includes ages younger than 13 or older than 19 years of age. Antepartum fetal Fetal death occurring before the initiation of labor. death Authorization An act of a legislative body that establishes government programs, defines the scope of programs, and sets a ceiling for how much can be spent on them. Birth defect A structural abnormality present at birth, irrespective of whether the defect is caused by a genetic factor or by prenatal events that are not genetic. Cost Sharing The amount an individual pays for health services above and beyond the cost of the insurance coverage premium. This includes co-pays, co-insurance, and deductibles. Crude birth rate Number of live births per 1000 population in a given year. Birth spacing The time interval from one child’s birth until the next child’s birth. It is generally recommended that at least a two-year interval between births is important for maternal and child health and survival. BMI Body mass index (BMI) is a measure of body weight that takes into account height. -
An EPIC Predictor of Gestational Age and Its Application to Newborns Conceived by Assisted Reproductive Technologies Kristine L
Haftorn et al. Clin Epigenet (2021) 13:82 https://doi.org/10.1186/s13148-021-01055-z RESEARCH Open Access An EPIC predictor of gestational age and its application to newborns conceived by assisted reproductive technologies Kristine L. Haftorn1,2,3* , Yunsung Lee1,2, William R. P. Denault1,2,4, Christian M. Page2,5, Haakon E. Nustad2,6, Robert Lyle2,7, Håkon K. Gjessing2,4, Anni Malmberg8, Maria C. Magnus2,9,10, Øyvind Næss3,11, Darina Czamara12, Katri Räikkönen8, Jari Lahti8, Per Magnus2, Siri E. Håberg2, Astanand Jugessur1,2,4† and Jon Bohlin2,13† Abstract Background: Gestational age is a useful proxy for assessing developmental maturity, but correct estimation of gestational age is difcult using clinical measures. DNA methylation at birth has proven to be an accurate predictor of gestational age. Previous predictors of epigenetic gestational age were based on DNA methylation data from the Illumina HumanMethylation 27 K or 450 K array, which have subsequently been replaced by the Illumina Methylatio- nEPIC 850 K array (EPIC). Our aims here were to build an epigenetic gestational age clock specifc for the EPIC array and to evaluate its precision and accuracy using the embryo transfer date of newborns from the largest EPIC-derived dataset to date on assisted reproductive technologies (ART). Methods: We built an epigenetic gestational age clock using Lasso regression trained on 755 randomly selected non-ART newborns from the Norwegian Study of Assisted Reproductive Technologies (START)—a substudy of the Norwegian Mother, Father, and Child Cohort Study (MoBa). For the ART-conceived newborns, the START dataset had detailed information on the embryo transfer date and the specifc ART procedure used for conception. -
PSBC Obstetric Guideline: Prenatal Screening for Down Syndrome, Trisomy 18, and Open Neural Tube Defects 3 1
Perinatal Services BC Obstetric Guideline: Prenatal Screening for Down Syndrome, Trisomy 18, and Open Neural Tube Defects June 2020 Table of Contents EXECUTIVE SUMMARY � � � � � � � � � � � � � � � � � � � � � � � � � � � � � 2 1� INTRODUCTION � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � 3 SIPS, IPS, Quad, NIPT � � � � � � � � � � � � � � � � � � � � � � � � � � � � 3 Open Neural Tube Defects (ONTDs) � � � � � � � � � � � � � � � � � � � � 4 Counselling � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � 4 Table 1: Summary of Prenatal Genetic Screening Tests � � � � � � � � 5 Table 2: Screening options available through the BC Prenatal Genetic Screening Program � � � � � � � � � � � � � � � � � 6 2� MANAGEMENT � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � 7 3� RESOURCES � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � 10 BC Prenatal Genetic Screening Program Website � � � � � � � � � � 10 Other Useful Websites � � � � � � � � � � � � � � � � � � � � � � � � � � � 10 4� BIBLIOGRAPHY � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � 11 APPENDIX 1 � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � 12 Risk of Down Syndrome and Other Chromosome Abnormalities in Live Births by Maternal Age � � � � � � � � � � � 12 Tel: 604-877-2121 www.bcprenatalscreening.ca APPENDIX 2 � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � � 13 Screen Cut-Offs and Performance of Screening Tests � � � � � � � 13 APPENDIX 3 � � � � � � � � � � � -
Genetic Testing for Reproductive Carrier Screening and Prenatal Diagnosis
Medical Coverage Policy Effective Date ............................................. 7/15/2021 Next Review Date ......................................12/15/2021 Coverage Policy Number .................................. 0514 Genetic Testing for Reproductive Carrier Screening and Prenatal Diagnosis Table of Contents Related Coverage Resources Overview ........................................................ 2 Genetics Coverage Policy ............................................ 2 Genetic Testing Collateral File Genetic Counseling ...................................... 2 Recurrent Pregnancy Loss: Diagnosis and Treatment Germline Carrier Testing for Familial Infertility Services Disease .......................................................... 3 Preimplantation Genetic Testing of an Embryo........................................................... 4 Preimplantation Genetic Testing (PGT-A) .. 5 Sequencing–Based Non-Invasive Prenatal Testing (NIPT) ............................................... 5 Invasive Prenatal Testing of a Fetus .......... 6 Germline Mutation Reproductive Genetic Testing for Recurrent Pregnancy Loss ...... 6 Germline Mutation Reproductive Genetic Testing for Infertility ..................................... 7 General Background .................................... 8 Genetic Counseling ...................................... 8 Germline Genetic Testing ............................ 8 Carrier Testing for Familial Disease ........... 8 Preimplantation Genetic Testing of an Embryo.......................................................... -
Birthweight Between 14 and 42 Weeks' Gestation
Arch Dis Child: first published as 10.1136/adc.60.5.440 on 1 May 1985. Downloaded from Archives of Disease in Childhood, 1985, 60, 440-446 Birthweight between 14 and 42 weeks' gestation D V KEEN AND R G PEARSE Jessop Hospital for Women, Sheffield SUMMARY Data representing fetal weight gain between 14 and 42 weeks' gestation are presented; firstly to provide suitable curves enabling the growth of the very immature infant to be monitored and secondly to examine the influence of the improved techniques of paediatric and obstetric assessment developed since the publication of previous studies. Data have been collected from the 57 866 livebirths in Sheffield between 1976 and 1984 and from therapeutically terminated and spontaneously aborted fetuses over the same period. It seems that preterm livebirths do not form a different population with respect to weight from the fetus still in utero, at least until the beginning of the third trimester. Previous studies have reported a bimodality of weight distribution in preterm infants at each gestational age which has been attributed to errors in gestational assessment. The pattern of distribution of weight in this study suggests that early ultrasonography and paediatric assessment techniques have exerted a considerable influence on the accuracy of gestational assessment. The mean weights of the sample differ considerably from those of the Gairdner and Pearson chart which are, therefore, considered to be inappropriate for the Sheffield population. The importance of accurate data for birthweight at It is now apparent that it is important to identify the lower gestational ages has increased with the those genuinely growth retarded infants who are improving survival of these babies. -
Women's Experience of Prenatal Ultrasound Examination
Journal of Perinatology (2006) 26, 403–408 r 2006 Nature Publishing Group All rights reserved. 0743-8346/06 $30 www.nature.com/jp ORIGINAL ARTICLE Seeing baby: women’s experience of prenatal ultrasound examination and unexpected fetal diagnosis JE Van der Zalm and PJ Byrne John Dossetor Health Ethics Centre, University of Alberta, Edmonton, AB, Canada multiple gestation, congenital fetal abnormalities, fetal growth Objective: Although prenatal ultrasound (US) is a common clinical problems and amniotic fluid or placental abnormalities. Study of undertaking today, little information is available about women’s experience US as a perinatal diagnostic tool has focused on whether US of the procedure from the perspective of women themselves. The objective of improves perinatal outcomes,3–6 the psychological effect on this study was to explore women’s experience of undergoing a routine women and men of such an examination,7–9 perception and prenatal US examination associated with an unexpected fetal diagnosis. receipt of information,10–14 and the experiences of staff who 15,16 Study Design: Qualitative methods were used to explore the prenatal US perform US examinations. A 1998 Cochrane review of routine 17 18 experience of 13 women. Five women were given unexpected news of US focused only on physical outcomes, as did a later work. multiple pregnancy and eight women were given unexpected news of Reviewers of the work suggested a lack of research on women’s 19 congenital fetal abnormality. One in-depth audio-taped interview was experience of this type of procedure. conducted with each woman. Content analysis of interview data identified Other researchers have focused on specific aspects of breaking themes common to women’s experience of US. -
Prenatal Development
2 Prenatal Development Learning Objectives Conception and Genetics 2.5 What behaviors have scientists observed 2.8 How do maternal diseases and 2.1 What are the characteristics of the zygote? in fetuses? environmental hazards affect prenatal 2.1a What are the risks development? associated with assisted Problems in Prenatal Development 2.8a How has technology changed reproductive technology? 2.6 What are the effects of the major dominant, the way that health professionals 2.2 In what ways do genes influence recessive, and sex-linked diseases? manage high-risk pregnancies? development? 2.6a What techniques are used to as- 2.9 What are the potential adverse effects sess and treat problems in prena- of tobacco, alcohol, and other drugs on Development from Conception to Birth tal development? prenatal development? 2.3 What happens in each of the stages of 2.7 How do trisomies and other disorders of 2.10 What are the risks associated with legal prenatal development? the autosomes and sex chromosomes drugs, maternal diet, age, emotional 2.4 How do male and female fetuses differ? affect development? distress, and poverty? efore the advent of modern medical technology, cul- garments that are given to her by her mother. A relative ties tures devised spiritual practices that were intended to a yellow thread around the pregnant woman’s wrist as cer- B ensure a healthy pregnancy with a happy outcome. emony attendees pronounce blessings on the unborn child. For instance, godh bharan is a centuries-old Hindu cere- The purpose of the thread is to provide mother and baby mony that honors a woman’s first pregnancy.