Acr–Acog–Aium Practice Guideline for the Performance of Obstetrical Ultrasound
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Pre-Term Pre-Labour Rupture of Membranes and the Role of Amniocentesis
Fetal and Maternal Medicine Review 2010; 21:2 75–88 C Cambridge University Press 2010 doi:10.1017/S096553951000001X First published online 15 March 2010 PRE-TERM PRE-LABOUR RUPTURE OF MEMBRANES AND THE ROLE OF AMNIOCENTESIS 1,2 ANNA P KENYON, 1,2 KHALIL N ABI-NADER AND 2 PRANAV P PANDYA 1Elizabeth Garrett Anderson Institute for Women’s Health, University College London, 86-96 Chenies Mews, London WCIE 6NX. 2Fetal Medicine Unit, University College London Hospitals NHS Foundation Trust, 235 Euston Rd, London NWI 2BU. INTRODUCTION Pre-labour premature rupture of membranes (PPROM) is defined as rupture of membranes more than 1 hour prior to the onset of labour at <37 weeks gestation. PPROM occurs in approximately 3% of pregnancies and is responsible for a third of all preterm births.1 Once membranes are ruptured prolonging the pregnancy has no maternal physical advantage but fetal morbidity and mortality are improved daily at early gestations: 19% of those infants born <25 weeks develop cerebral palsy (CP) and 28% have severe motor disability.2 Those infants born extremely pre term (<28 weeks) cost the public sector £75835 (95% CI £27906–145508) per live birth3 not to mention the emotional cost to the family. To prolong gestation is therefore the suggested goal: however how and why might we delay birth in those at risk? PPROM is one scenario associated with preterm birth and here we discuss the causative mechanisms, sequelae, latency, strategies to prolong gestation (antibiotics) and consider the role of amniocentesis. We will also discuss novel therapies. PATHOPHYSIOLOGY OF MEMBRANE RUPTURE The membranes, which act to protect and isolate the fetus, are composed of two layers. -
Prenatal and Preimplantation Genetic Diagnosis for Mps and Related Diseases
PRENATAL AND PREIMPLANTATION GENETIC DIAGNOSIS FOR MPS AND RELATED DISEASES Donna Bernstein, MS Amy Fisher, MS Joyce Fox, MD Families who are concerned about passing on genetic conditions to their children have several options. Two of those options are using prenatal diagnosis and preimplantation genetic diagnosis. Prenatal diagnosis is a method of testing a pregnancy to learn if it is affected with a genetic condition. Preimplantation genetic diagnosis, also called PGD, is a newer technology used to test a fertilized embryo before a pregnancy is established, utilizing in vitro fertilization (IVF). Both methods provide additional reproductive options to parents who are concerned about having a child with a genetic condition. There are two types of prenatal diagnosis; one is called amniocentesis, and the other is called CVS (chorionic villus sampling). Amniocentesis is usually performed between the fifteenth and eighteenth weeks of pregnancy. Amniocentesis involves inserting a fine needle into the uterus through the mother's abdomen and extracting a few tablespoons of amniotic fluid. Skin cells from the fetus are found in the amniotic fluid. These cells contain DNA, which can be tested to see if the fetus carries the same alterations in the genes (called mutations) that cause a genetic condition in an affected family member. If the specific mutation in the affected individual is unknown, it is possible to test the enzyme activity in the cells of the fetus. Although these methods are effective at determining whether a pregnancy is affected or not, they do not generally give information regarding the severity or the course of the condition. -
Proteomic Biomarkers of Intra-Amniotic Inflammation
0031-3998/07/6103-0318 PEDIATRIC RESEARCH Vol. 61, No. 3, 2007 Copyright © 2007 International Pediatric Research Foundation, Inc. Printed in U.S.A. Proteomic Biomarkers of Intra-amniotic Inflammation: Relationship with Funisitis and Early-onset Sepsis in the Premature Neonate CATALIN S. BUHIMSCHI, IRINA A. BUHIMSCHI, SONYA ABDEL-RAZEQ, VICTOR A. ROSENBERG, STEPHEN F. THUNG, GUOMAO ZHAO, ERICA WANG, AND VINEET BHANDARI Department of Obstetrics, Gynecology and Reproductive Sciences [C.S.B., I.A.B., S.A.-R., V.A.R., S.F.T., G.Z., E.W.], and Department of Pediatrics [V.B.], Division of Perinatal Medicine, Yale University School of Medicine, New Haven, CT 06520 ABSTRACT: Our goal was to determine the relationship between 4 vein inflammatory cytokine levels, but not maternal serum val- amniotic fluid (AF) proteomic biomarkers (human neutrophil de- ues, correlate with the presence and severity of the placental fensins 2 and 1, calgranulins C and A) characteristic of intra-amniotic histologic inflammation and umbilical cord vasculitis (7). inflammation, and funisitis and early-onset sepsis in premature neo- Funisitis is characterized by perivascular infiltrates of in- nates. The mass restricted (MR) score was generated from AF flammatory cells and is considered one of the strongest hall- obtained from women in preterm labor (n ϭ 123). The MR score marks of microbial invasion of the amniotic cavity and fetal ranged from 0–4 (none to all biomarkers present). Funisitis was graded histologically and interpreted in relation to the MR scores. inflammatory syndrome (8,9). While there is some debate with Neonates (n ϭ 97) were evaluated for early-onset sepsis. -
ENT of UATION MEMOR the HUMAN FETUS Cothelijne Van Heter
PDF hosted at the Radboud Repository of the Radboud University Nijmegen The following full text is a publisher's version. For additional information about this publication click this link. http://hdl.handle.net/2066/146798 Please be advised that this information was generated on 2021-09-24 and may be subject to change. ENT OF UATION MEMOR THE HUMAN FETUS Cothelijne van Heter • DEVELOPMENT OF HABITUATION AND MEMORY IN THE HUMAN FETUS Van Heteren, Cathelijne Francisca - Development of habituation and memory in the human fetus - 2001 Thesis University Nijmegen - with réf.- with summary m Dutch -136 p. ISBN: 90-9015000-5 Print: Grafisch Bedrijf Ponsen &i Looijen BV Wageningen Graphic Design Marie-Louise Dusée No part of this book may be reproduced in any form without permission of the author. This research project was financially supported by ZorgOnderzoek Nederland and the Hersenstichting Nederland. Publication of this thesis was financially supported by ATL Nederland BV, Ferring BV, GlaxoSmithKline, Hitachi Ultrasound BV, Medical Dynamics, Novo Nordisk Farma BV, Organon Nederland BV, Pie Medical Benelux BV, Sanofi-Synthélabo, Schering Nederland BV. DEVELOPMENT OF HABITUATION AND MEMORY IN THE HUMAN ?-f τ'••<, Een wetenschappelijke proeve op het gebied van de Medische Wetenschappen Proefschrift ter verkrijging van de graad van doctor aan de Katholieke Universiteit Nijmegen, volgens besluit van het College van Decanen in het openbaar te verdedigen op vrijdag 5 oktober 2001 des namiddags om 1.30 uur precies door Cathelijne Francisca van Heteren -
The Empire Plan SEPTEMBER 2018 REPORTING ON
The Empire Plan SEPTEMBER 2018 REPORTING ON PRENATAL CARE Every baby deserves a healthy beginning and you can take steps before your baby is even born to help ensure a great start for your infant. That’s why The Empire Plan offers mother and baby the coverage you need. When your primary coverage is The Empire Plan, the Empire Plan Future Moms Program provides you with special services. For Empire Plan enrollees and for their enrolled dependents, COBRA enrollees with their Empire Plan benefits and Young Adult Option enrollees TABLE OF CONTENTS Five Important Steps ........................................ 2 Feeding Your Baby ...........................................11 Take Action to Be Healthy; Breastfeeding and Your Early Pregnancy ................................................. 4 Empire Plan Benefits .......................................12 Prenatal Testing ................................................. 5 Choosing Your Baby’s Doctor; New Parents ......................................................13 Future Moms Program ......................................7 Extended Care: Medical Case High Risk Pregnancy Program; Management; Questions & Answers ...........14 Exercise During Pregnancy ............................ 8 Postpartum Depression .................................. 17 Your Healthy Diet During Pregnancy; Medications and Pregnancy ........................... 9 Health Care Spending Account ....................19 Skincare Products to Avoid; Resources ..........................................................20 Childbirth Education -
Amniocentesis
Amniocentesis Family history of an open neural tube defect Infection About Integrated Genetics If a close relative has been born with an open neural Great care is taken to prevent infection. Therefore, tube defect, such as spina bifida or anencephaly, infection following amniocentesis is very rare. there may be an increased risk to other pregnancies However, a woman with fever or any flu-like symptoms Integrated Genetics has been in the family. after amniocentesis should call her doctor for advice. a leader in genetic testing Abnormal maternal serum screening test Harm to the fetus and counseling services for over 25 years. Screening tests performed on a sample of blood Since the ultrasound image gives the doctor exact from a pregnant woman can identify pregnancies information about the location of the fetus inside the This brochure is provided at risk for the common chromosome abnormalities, uterus, the risk that the needle will harm the fetus is by Integrated Genetics as including Down syndrome and open neural extremely low. an educational service for tube defects. When the screening results show physicians and their patients. Rh problems that a pregnancy has a high risk for one of these For more information on problems, amniocentesis for diagnostic testing is If a woman having an amniocentesis has Rh our genetic testing and recommended. negative blood type, and the baby’s father has Rh positive blood type, the woman should have counseling services, Abnormal ultrasound an injection of Rh immune globulin following the please visit our web sites: If an ultrasound shows an abnormality, procedure. This helps prevent Rh disease in the baby. -
Chapter 12 Vaginal Breech Delivery
FOURTH EDITION OF THE ALARM INTERNATIONAL PROGRAM CHAPTER 12 VAGINAL BREECH DELIVERY Learning Objectives By the end of this chapter, the participant will: 1. List the selection criteria for an anticipated vaginal breech delivery. 2. Recall the appropriate steps and techniques for vaginal breech delivery. 3. Summarize the indications for and describe the procedure of external cephalic version (ECV). Definition When the buttocks or feet of the fetus enter the maternal pelvis before the head, the presentation is termed a breech presentation. Incidence Breech presentation affects 3% to 4% of all pregnant women reaching term; the earlier the gestation the higher the percentage of breech fetuses. Types of Breech Presentations Figure 1 - Frank breech Figure 2 - Complete breech Figure 3 - Footling breech In the frank breech, the legs may be extended against the trunk and the feet lying against the face. When the feet are alongside the buttocks in front of the abdomen, this is referred to as a complete breech. In the footling breech, one or both feet or knees may be prolapsed into the maternal vagina. Significance Breech presentation is associated with an increased frequency of perinatal mortality and morbidity due to prematurity, congenital anomalies (which occur in 6% of all breech presentations), and birth trauma and/or asphyxia. Vaginal Breech Delivery Chapter 12 – Page 1 FOURTH EDITION OF THE ALARM INTERNATIONAL PROGRAM External Cephalic Version External cephalic version (ECV) is a procedure in which a fetus is turned in utero by manipulation of the maternal abdomen from a non-cephalic to cephalic presentation. Diagnosis of non-vertex presentation Performing Leopold’s manoeuvres during each third trimester prenatal visit should enable the health care provider to make diagnosis in the majority of cases. -
Computerized Fetal Heart Rate Analysis, Doppler Ultrasound and Biophysical Profile Score in the Prediction of Acid–Base Status of Growth-Restricted Fetuses
Ultrasound Obstet Gynecol 2007; 30: 750–756 Published online 10 August 2007 in Wiley InterScience (www.interscience.wiley.com). DOI: 10.1002/uog.4101 Computerized fetal heart rate analysis, Doppler ultrasound and biophysical profile score in the prediction of acid–base status of growth-restricted fetuses S. TURAN*†, O. M. TURAN*†, C. BERG‡, D. MOYANO†, A. BHIDE§, S. BOWER†, B. THILAGANATHAN§, U. GEMBRUCH‡, K. NICOLAIDES†, C. HARMAN* and A. A. BASCHAT* *Department of Obstetrics, Gynecology and Reproductive Sciences, University of Maryland, Baltimore, MD, USA, †Harris Birthright Research Centre for Fetal Medicine, King’s College Hospital and §Fetal Medicine Unit, St George’s Hospital Medical School, London, UK and ‡Department of Obstetrics and Prenatal Medicine, Friedrich-Wilhelm University, Bonn, Germany KEYWORDS: arterial Doppler; biophysical profile scoring; computerized CTG; cord pH; fetal growth restriction; non-stress test; venous Doppler ABSTRACT patients with an equivocal or normal BPS. Abnormal DV Doppler correctly identified false positives among Objective To investigate the performance of non-stress patients with an abnormal BPS. cCTG reduced the rate test (NST), computerized fetal heart rate analysis (cCTG), of an equivocal BPS from 16% to 7.1% when substituted biophysical profile scoring (BPS) and arterial and venous for the traditional NST. Elevated DV Doppler index and Doppler ultrasound investigation in the prediction of umbilical venous pulsations predicted a low pH with 73% acid–base status in fetal growth restriction. sensitivity and 90% specificity (P = 0.008). Methods Growth-restricted fetuses, defined by abdomi- Conclusion In fetal growth restriction with placental nal circumference < 5th percentile and umbilical artery insufficiency, venous Doppler investigation provides the (UA) pulsatility index > 95th percentile, were tested by best prediction of acid–base status. -
Increased Incidence of Cytogenetic Abnormalities in Chorionic Villus Samples from Pregnancies Established by in Vitro Fertilization and Embryo Transfer (Ivf-Et)
PRENATAL DIAGNOSIS, VOL. 15: 975-980 (1995) INCREASED INCIDENCE OF CYTOGENETIC ABNORMALITIES IN CHORIONIC VILLUS SAMPLES FROM PREGNANCIES ESTABLISHED BY IN VITRO FERTILIZATION AND EMBRYO TRANSFER (IVF-ET) P. A. I”TVELD, D. VAN OPSTAL, c. VAN DEN BERG, M. VAN OOIJEN, H. BRANDENBURG*, L. PIJPERS*$, M. G. J. JAHODA*, TH. STUNEN? AND F. J. LOS Departments of Clinical Genetics, *Obstetrics and Gynaecology and ?Epidemiology and Biostatistics, University Hospital Dijkzigt and Erasmus University, Rotterdam; SMerwede Hospital, Dordrecht, The Netherlands Received 9 January I995 Revised 23 May 1995 Accepted 18 June 1995 SUMMARY We studied 201 pregnancies that were established by in vitro fertilization and embryo transfer (IVF-ET) and compared the frequency of cytogenetic abnormalities with that found in a large control population matched for indication group (advanced maternal age) and time of sampling. A total of 252 IVF-ET fetuses were cytogenetically analysed by either chorionic villus sampling (CVS; n=80) or amniocentesis (n= 172). Eleven chromosome abnormalities were found in the CVS group (13.8 per cent); among them, a 45,X/46,X,dic(Y)(ql1)/46,X,delCY)(qll) mosaic that was found in an IVF pregnancy established by intracytoplasmic sperm injection (ICSI), four cases of trisomy 21, and three cases of trisomy 7 confined to the placenta. The results indicate a statistically significant three- to five-fold increase in both confined placental abnormalities (P<0.008) and true fetal chromosome anomalies (W0.04).In the amniocentesis group, identical rates (1.7 per cent) of chromosome abnormalities were found in the IVF-ET and control groups. -
Prenatal Care Book – 30 Days of Your Baby’S Birth
August 2014 Prenatal NEW YORK STATE HEALTH INSURANCE PROGRAM Care (NYSHIP) for Empire Plan enrollees and for their enrolled dependents, COBRA enrollees with their Empire Plan Congratulations on your benefits and Young Adult Option enrollees pregnancy! Every baby deserves a healthy beginning. You can take steps before your baby is even born to help Five Important Steps to Having a Healthy Baby ensure a great start for your 1. Call your doctor infant. That’s why The Empire As soon as you think you are pregnant, call your doctor. Plan offers mother and baby You can do the most for your baby during the first three the coverage you need. months of pregnancy, so try to start your doctor visits as When your primary coverage soon as possible. is The Empire Plan, The The Empire Plan covers your maternity care under the Empire Plan Future Moms Medical/Surgical Program. You may choose a participating Program provides you with or non-participating provider for your maternity care. special services. Participating Provider If you choose a participating provider (obstetrician, family practice physician or certified nurse-midwife), there are no copayments for prenatal visits, delivery or your six-week checkup 3 Early Symptoms of Pregnancy after delivery. You pay only your copayment for covered services 4 Take Action to Be Healthy at participating laboratories. Exercise During Pregnancy To locate an Empire Plan participating provider or laboratory, call 5 Prenatal Testing The Empire Plan toll free at 1-877-7-NYSHIP (1-877-769-7447) 6 The Future Moms Program and select the Medical Program. -
Coding for the OB/GYN Practice Coding Principals
12/4/2013 Coding for the OB/GYN Practice NAMAS 5th Annual Auditing Conference Atlanta, GA December 10, 2013 Peggy Y. Green, CMA(AAMA), CPC, CPMA, CPC‐I Coding Principals • Correct coding implies the selection is – What are we doing? Procedures – Why are we doing it? Diagnosis – Supported by documentation – Consistent with coding guidelines 1 12/4/2013 Coding Principals • Reporting Services – IS there physician work or practice expense? – Can it be supported by an ICD‐9 code? – Is it independent of other procedures/services? – Is there documentation of the service? Billing “Rule” • “Not documented” means “Not done” – “Not documented” “Not billable” • Documentation must support type and level of extent of service reported Code Sets • Key Code sets – HCPCS (includes CPT‐4) – ICD‐9‐CM/ICD‐10‐CM • HCPCS dibdescribes “ht”“what” • ICD‐9 CM describes “why” 2 12/4/2013 Who can bill as a Provider? • Change have been made throughout the CPT manual to clarify who may provide certain services with the addition of the phrase “other qualified healthcare professionals”. • Some codes define that a service is limited to professionals or limited to other entities such as hospitals or home health agencies. Providers • CPT defines a “Physician or other qualified health care professional” as an individual who is qualified by education, training, licensure/regulation (when applicable), and facility privileging (when applicable), who performs a professional services within his/her scope of practice and independently reports that professional service. • This is distinct from clinical staff 3 12/4/2013 Providers • Clinical staff members are people who work under the supervision of a physician or other qualified health care professional and who is allowed by law, regulation, and facility policy to perform or assist in the performance of a specified professional service, but who does not individually report that professional service. -
A Guide to Prenatal Testing
Patient Education intermountainhealthcare.org A Guide to Prenatal Testing LIVING AND LEARNING TOGETHER Most news is good news. Most babies are born without major birth defects. Early in your pregnancy, you’ll need to make decisions about prenatal testing. Prenatal tests aim to detect the risk or presence of a birth defect or serious disease in your developing baby. This guide gives you the facts you need to make decisions about testing. Spend some time with this guide. Take it home and read it carefully. At your next prenatal checkup, ask any remaining questions before making your decisions. 2 PRENATAL TESTING What’s Inside: AT A GLANCE .................................................4 TESTS: Options for screening and testing ......6 Maternal serum screening ..........................................6 Cell-free DNA (cfDNA) screening .............................8 Chorionic villus sampling (CVS) and amniocentesis 10 Carrier screening for cystic fibrosis (CF), spinal muscular atrophy (SMA), and other conditions .......................................................13 CONDITIONS: Diseases and disorders discussed in this guide .................................15 Cystic fibrosis (CF) ..................................................15 Spinal muscular atrophy (SMA) ...............................16 Turner syndrome .....................................................17 Down syndrome ......................................................18 Trisomy 18 and 13 ..................................................18 Neural tube defects (NTDs) ....................................19