Perinatal Care Perinatal Care
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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. -
Characteristics of Heart Rate Tracings in Preterm Fetus
medicina Review Characteristics of Heart Rate Tracings in Preterm Fetus Maria F. Hurtado-Sánchez 1, David Pérez-Melero 2, Andrea Pinto-Ibáñez 3 , Ernesto González-Mesa 4 , Juan Mozas-Moreno 1,5,6,7,* and Alberto Puertas-Prieto 1,7 1 Obstetrics and Gynecology Service, Virgen de las Nieves University Hospital, 18014 Granada, Spain; [email protected] (M.F.H.-S.); [email protected] (A.P.-P.) 2 Anesthesiology, Resuscitation and Pain Therapy Service, Virgen de las Nieves University Hospital, 18014 Granada, Spain; [email protected] 3 Obstetrics and Gynecology Service, Poniente Hospital, 04700 El Ejido (Almería), Spain; [email protected] 4 Obstetrics and Gynecology Service, Regional University Hospital of Malaga, 29011 Malaga, Spain; [email protected] 5 Department of Obstetrics and Gynecology, University of Granada, 18016 Granada, Spain 6 Consortium for Biomedical Research in Epidemiology & Public Health (CIBER Epidemiología y Salud Pública-CIBERESP), 28029 Madrid, Spain 7 Biohealth Research Institute (Instituto de Investigación Biosanitaria Ibs.GRANADA), 18014 Granada, Spain * Correspondence: [email protected]; Tel.: +34-958242867 Abstract: Background and Objectives: Prematurity is currently a serious public health issue worldwide, because of its high associated morbidity and mortality. Optimizing the management of these preg- nancies is of high priority to improve perinatal outcomes. One tool frequently used to determine the degree of fetal wellbeing is cardiotocography (CTG). A review of the available literature on fetal heart rate (FHR) monitoring in preterm fetuses shows that studies are scarce, and the evidence thus far is unclear. The lack of reference standards for CTG patterns in preterm fetuses can lead to misinterpretation of the changes observed in electronic fetal monitoring (EFM). -
Neonatal Orthopaedics
NEONATAL ORTHOPAEDICS NEONATAL ORTHOPAEDICS Second Edition N De Mazumder MBBS MS Ex-Professor and Head Department of Orthopaedics Ramakrishna Mission Seva Pratishthan Vivekananda Institute of Medical Sciences Kolkata, West Bengal, India Visiting Surgeon Department of Orthopaedics Chittaranjan Sishu Sadan Kolkata, West Bengal, India Ex-President West Bengal Orthopaedic Association (A Chapter of Indian Orthopaedic Association) Kolkata, West Bengal, India Consultant Orthopaedic Surgeon Park Children’s Centre Kolkata, West Bengal, India Foreword AK Das ® JAYPEE BROTHERS MEDICAL PUBLISHERS (P) LTD. New Delhi • London • Philadelphia • Panama (021)66485438 66485457 www.ketabpezeshki.com ® Jaypee Brothers Medical Publishers (P) Ltd. Headquarters Jaypee Brothers Medical Publishers (P) Ltd. 4838/24, Ansari Road, Daryaganj New Delhi 110 002, India Phone: +91-11-43574357 Fax: +91-11-43574314 Email: [email protected] Overseas Offices J.P. Medical Ltd. Jaypee-Highlights Medical Publishers Inc. Jaypee Brothers Medical Publishers Ltd. 83, Victoria Street, London City of Knowledge, Bld. 237, Clayton The Bourse SW1H 0HW (UK) Panama City, Panama 111, South Independence Mall East Phone: +44-2031708910 Phone: +507-301-0496 Suite 835, Philadelphia, PA 19106, USA Fax: +02-03-0086180 Fax: +507-301-0499 Phone: +267-519-9789 Email: [email protected] Email: [email protected] Email: [email protected] Jaypee Brothers Medical Publishers (P) Ltd. Jaypee Brothers Medical Publishers (P) Ltd. 17/1-B, Babar Road, Block-B, Shaymali Shorakhute, Kathmandu Mohammadpur, Dhaka-1207 Nepal Bangladesh Phone: +00977-9841528578 Mobile: +08801912003485 Email: [email protected] Email: [email protected] Website: www.jaypeebrothers.com Website: www.jaypeedigital.com © 2013, Jaypee Brothers Medical Publishers All rights reserved. No part of this book may be reproduced in any form or by any means without the prior permission of the publisher. -
Association Between First Caesarean Delivery and Adverse Outcomes In
Hu et al. BMC Pregnancy and Childbirth (2018) 18:273 https://doi.org/10.1186/s12884-018-1895-x RESEARCHARTICLE Open Access Association between first caesarean delivery and adverse outcomes in subsequent pregnancy: a retrospective cohort study Hong-Tao Hu1†, Jing-Jing Xu1†, Jing Lin1, Cheng Li1, Yan-Ting Wu2, Jian-Zhong Sheng3, Xin-Mei Liu4,5* and He-Feng Huang2,4,5* Abstract Background: Few studies have explored the association between a previous caesarean section (CS) and adverse perinatal outcomes in a subsequent pregnancy, especially in women who underwent a non-indicated CS in their first delivery. We designed this study to compare the perinatal outcomes of a subsequent pregnancy in women who underwent spontaneous vaginal delivery (SVD) or CS in their first delivery. Methods: This retrospective cohort study included women who underwent singleton deliveries at the International Peace Maternity and Child Health Hospital from January 2013 to December 2016. Data on the perinatal outcomes of all the women were extracted from the medical records. Multivariate logistic regression was conducted to assessed the association between CS in the first delivery and adverse perinatal outcomes in the subsequent pregnancy. Results: CS delivery in the subsequent pregnancy was more likely for women who underwent CS in their first birth than for women with previous SVD (97.3% versus 13.2%). CS in the first birth was also associated with a significantly increased risk of adverse outcomes in the subsequent pregnancy, especially in women who underwent a non- indicated CS. Adverse perinatal outcomes included pregnancy-induced hypertension [adjusted odds ratio (OR), 95% confidence interval (CI): 2.20, 1.59–3.05], gestational diabetes mellitus (1.82, 1.57–2.11), gestational anaemia (1.27, 1. -
SUBCHORIONIC HEMATOMA OR SUBCHORIONIC CLOT Val Catanzarite, MD, Phd San Diego Perinatal Center 8010 Frost Street, Suite 300 San Diego, CA 92123 © 2008
SUBCHORIONIC HEMATOMA OR SUBCHORIONIC CLOT Val Catanzarite, MD, PhD San Diego Perinatal Center 8010 Frost Street, Suite 300 San Diego, CA 92123 © 2008 What is a subchorionic hematoma or subchorionic clot? The “bag of waters” within the uterus is composed of two layers, called the chorion and the amnion. The inner layer, closer to the baby, is the amnion. The outer layer, which is normally against the uterine wall, is the chorion. The term “subchorionic clot” or “subchorionic hematoma” describes a blood clot between the bag of waters and the uterus. How does a subchorionic hematoma look on ultrasound? We see subchorionic hematomas or suspect subchorionic clots in perhaps 1% of pregnancies in the between 13 and 22 weeks. Most of these occur in women who have had vaginal bleeding. These must be distinguished from regions of nonfusion of the membranes to the wall of the uterus, which are very common prior to 16 weeks gestation. Findings which suggest a bleed or hematoma rather than membrane separation include irregular texture to the material seen beneath the membranes, a speckled rather than uniform appearance to the amniotic fluid. The image at left shows a crescent shaped subchorionic clot, indicated by the arrows. The image at right shows a larger, rounded subchorionic clot. Both women had experienced bleeding episodes during the prior week, and had passed blood clots. On rare occasions, we will be able to see the source of the bleeding beneath the membranes. Usually, we cannot. This image is of a region of nonfusion of the membranes, also called chorioamniotic separation. -
G Eneral Introduction
Follow-up studies in prenatal medicine Nagel, H.T.C. Citation Nagel, H. T. C. (2007, February 14). Follow-up studies in prenatal medicine. Retrieved from https://hdl.handle.net/1887/9762 Version: Corrected Publisher’s Version Licence agreement concerning inclusion of doctoral thesis in the License: Institutional Repository of the University of Leiden Downloaded from: https://hdl.handle.net/1887/9762 Note: To cite this publication please use the final published version (if applicable). Proefschrift H. Nagel 11-01-2007 13:34 Pagina 11 C H ! T " # $ * eneral introduction 11 Proefschrift H. Nagel 11-01-2007 13:34 Pagina 12 C H ! T " # $ The %etus in prenatal m edicine ccording to M edline de-initions' a conce.tus is an em ,ryo until a .ostconce.tional age o- 9 1 ee2s (or a gestational age o- $* 1 ee2s) and 1 ill then ,e a -etus until ,irth. =- ,orn via,le' the .erson then ,ecom es an in-ant. The -etus is a uni>ue .atient -or several reasons. 6irst' there is a uni>ue relationshi. ,et1 een the m other and her un,orn child. lthough the -etus has his o1 n rights' he or she can only ,e treated via the m other. There-ore the .ur.orted rights o- $ the -etus can never ta2e .recedence over that o- the m other. ;econd' des.ite advances in m edical care there is stri2ing little 2no1 ledge a,out -etal live. ? uestions such as does the -etus [email protected] .ain' does it have a m em ory' are still unans1 ered. -
Areola-Sparing Mastectomy: Defining the Risks
COLLECTIVE REVIEWS Areola-Sparing Mastectomy: Defining the Risks Alan J Stolier, MD, FACS, Baiba J Grube, MD, FACS The recent development and popularity of skin-sparing to actual risk of cancer arising in the areola and is pertinent mastectomy (SSM) is a likely byproduct of high-quality to any application of ASM in prophylactic operations. autogenous tissue breast reconstruction. Numerous non- 7. Based on clinical studies, what are the outcomes when randomized series suggest that SSM does not add to the risk some degree of nipple-areola complex (NAC) is preserved of local recurrence.1–3 Although there is still some skepti- as part of the surgical treatment? cism,4 SSM has become a standard part of the surgical ar- mamentarium when dealing with small or in situ breast ANATOMY OF THE AREOLA cancers requiring mastectomy and in prophylactic mastec- In 1719, Morgagni first observed that there were mam- tomy in high-risk patients. Some have suggested that SSM mary ducts present within the areola. In 1837, William also compares favorably with standard mastectomy for Fetherstone Montgomery (1797–1859) described the 6 more advanced local breast cancer.2 Recently, areola- tubercles that would bare his name. In a series of schol- sparing mastectomy (ASM) has been recommended for a arly articles from 1970 to 1974, William Montagna and similar subset of patients in whom potential involvement colleagues described in great detail the histologic anat- 7,8 by cancer of the nipple-areola complex is thought to be low omy of the nipple and areola. He noted that there was or in patients undergoing prophylactic mastectomy.5 For “confusion about the structure of the glands of Mont- ASM, the assumption is that the areola does not contain gomery being referred to as accessory mammary glands glandular tissue and can be treated the same as other breast or as intermediates between mammary and sweat 9 skin. -
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. -
What You Need to Know to Successfully Start Breastfeeding Your Baby
BREASTFEEDING SUPPORT WHAT YOU NEED TO KNOW TO SUCCESSFULLY START BREASTFEEDING YOUR BABY Northpoint Pediatrics supports breastfeeding for our patients and offers a full-time lactation expert to help. Breastfeeding is a natural way to feed your baby, but it does not always come easily as mom and baby learn how. Start with this brochure to learn how to get started, how to keep breastfeeding when you return to work, and the best breastfeeding diet. Getting started Don’t panic if your newborn seems to have trouble latching or staying on your nipple. Breastfeeding requires patience and lots of practice. Ask a nurse for help and request a visit from the hospital or Northpoint lactation consultant. Breastfeeding is going well if: Call your doctor if: □ Your baby is breastfeeding at least eight □ Your baby is having fewer than six wet diapers times in 24 hours a day by the sixth day of age □ Your baby has at least six wet diapers □ Your baby is still having meconium (black, every 24 hours tarry stools) on the fourth day of age or is □ Your baby has at least four bowel having fewer than four stools by the sixth day movements every 24 hours of age □ You can hear your baby gulping or □ Your milk supply is full but you don’t hear swallowing at feeds your baby gulping or swallowing frequently during breastfeeding □ Your breasts feel softer after a feed □ Your nipples are painful throughout the feed □ Your nipples are not painful □ Your baby seems to be breastfeeding □ Breastfeeding is an enjoyable experience “all the time” □ You don’t feel that your breasts are full and excreting milk by the fifth day □ Your baby is a “sleepy, good baby” and is hard to wake for feedings NORTHPOINTPEDS.COM — NOBLESVILLE — INDIANAPOLIS — 317-621-9000 1 BREASTFEEDING SUPPORT: WHAT YOU NEED TO KNOW TO SUCCESSFULLY START BREASTFEEDING YOUR BABY Are you nursing correctly? Pumping at work A checklist from the American Academy of Pediatrics. -
Marvel-Phile: Über-Grim-And-Gritty EXTREME Edition!
10 MAR 2018 1 Marvel-Phile: Über-Grim-and-Gritty EXTREME Edition! It was the best of times, it was the worst of times. It 90s, but you’d be wrong. Then we have Nightwatch, a was a dark time for the Republic. In short, it was...the bald-faced ripoff of Todd MacFarlane’s more ‘90s. The 1990s were an odd time for comic books. A successful Spawn. Next, we have Necromancer… the group of comic book artists, including the likes of Jim Dr. Strange of Counter-Earth. And best for last, Lee and hate-favorite Rob Liefield, splintered off from there’s Adam X the X-TREME! Oh dear Lord -- is there Marvel Comics to start their own little company called anything more 90s than this guy? With his backwards Image. True to its name, Image Comics featured comic baseball cap, combustible blood, a costume seemingly books light on story, heavy on big, flashy art (often made of blades, and a title that features not one but either badly drawn or heavily stylized, depending on TWO “X”s, this guy that was teased as the (thankfully who you ask), and a grim and gritty aesthetic that retconned) “third Summers brother” is literally seemed to take all the wrong lessons from renowned everything about the 90s in comics, all rolled into one. works such as Frank Miller’s Dark Knight Returns. Don’t get me wrong, there were a few gems in the It wasn’t long until the Big Two and other publishers 1990s. Some of my favorite indie books were made hopped on the bandwagon, which was fueled by during that time. -
(“Spider-Man”) Cr
PRIVILEGED ATTORNEY-CLIENT COMMUNICATION EXECUTIVE SUMMARY SECOND AMENDED AND RESTATED LICENSE AGREEMENT (“SPIDER-MAN”) CREATIVE ISSUES This memo summarizes certain terms of the Second Amended and Restated License Agreement (“Spider-Man”) between SPE and Marvel, effective September 15, 2011 (the “Agreement”). 1. CHARACTERS AND OTHER CREATIVE ELEMENTS: a. Exclusive to SPE: . The “Spider-Man” character, “Peter Parker” and essentially all existing and future alternate versions, iterations, and alter egos of the “Spider- Man” character. All fictional characters, places structures, businesses, groups, or other entities or elements (collectively, “Creative Elements”) that are listed on the attached Schedule 6. All existing (as of 9/15/11) characters and other Creative Elements that are “Primarily Associated With” Spider-Man but were “Inadvertently Omitted” from Schedule 6. The Agreement contains detailed definitions of these terms, but they basically conform to common-sense meanings. If SPE and Marvel cannot agree as to whether a character or other creative element is Primarily Associated With Spider-Man and/or were Inadvertently Omitted, the matter will be determined by expedited arbitration. All newly created (after 9/15/11) characters and other Creative Elements that first appear in a work that is titled or branded with “Spider-Man” or in which “Spider-Man” is the main protagonist (but not including any team- up work featuring both Spider-Man and another major Marvel character that isn’t part of the Spider-Man Property). The origin story, secret identities, alter egos, powers, costumes, equipment, and other elements of, or associated with, Spider-Man and the other Creative Elements covered above. The story lines of individual Marvel comic books and other works in which Spider-Man or other characters granted to SPE appear, subject to Marvel confirming ownership.