Case Report: a Prenatally Diagnosed Case of Vasa Praevia and Its Subsequent Management
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PLANNED OUT-OF-HOSPITAL BIRTH Approved 11/12/15
HEALTH EVIDENCE REVIEW COMMISSION (HERC) COVERAGE GUIDANCE: PLANNED OUT-OF-HOSPITAL BIRTH Approved 11/12/15 HERC COVERAGE GUIDANCE Planned out-of-hospital (OOH) birth is recommended for coverage for women who do not have high- risk coverage exclusion criteria as outlined below (weak recommendation). This coverage recommendation is based on the performance of appropriate risk assessments1 and the OOH birth attendant’s compliance with the consultation and transfer criteria as outlined below. Planned OOH birth is not recommended for coverage for women who have high risk coverage exclusion criteria as outlined below, or when appropriate risk assessments are not performed, or where the attendant does not comply with the consultation and transfer criteria as outlined below (strong recommendation). High-risk coverage exclusion criteria: Complications in a previous pregnancy: Maternal surgical history Cesarean section or other hysterotomy Uterine rupture Retained placenta requiring surgical removal Fourth-degree laceration without satisfactory functional recovery Maternal medical history Pre-eclampsia requiring preterm birth Eclampsia HELLP syndrome Fetal Unexplained stillbirth/neonatal death or previous death related to intrapartum difficulty Baby with neonatal encephalopathy Placental abruption with adverse outcome Complications of current pregnancy: Maternal Induction of labor Prelabor rupture of membranes > 24 hours 1 Pre-existing chronic hypertension; Pregnancy-induced hypertension with diastolic blood pressure greater than -
Low-Lying Placenta
LOW- LYING PLACENTA LOW-LYING PLACENTA WHAT IS PLACENTA PRAEVIA? The placenta develops along with the baby in the uterus (womb) during pregnancy. It connects the baby with the mother’s blood system and provides the baby with its source of oxygen and nourishment. The placenta is delivered after the baby and is also called the afterbirth. In some women the placenta attaches low in the uterus and may be near, or cover a part, or lie over the cervix (entrance to the womb). If it is shown in early ultrasound scans, it is called a low-lying placenta. In most cases, the placenta moves upwards as the uterus enlarges. For some women the placenta continues to lie in the lower part of the uterus in the last months of pregnancy. This condition is known as placenta praevia. If the placenta covers the cervix, this is known as major placenta praevia. Normal Placenta Placenta Praevia Major Placenta Praevia WHAT ARE THE RISKS TO MY BABY AND ME? When the placenta is in the lower part of the womb, there is a risk that you may bleed in the second half of pregnancy. Bleeding from placenta praevia can be heavy, and so put the life of the mother and baby at risk. However, deaths from placenta praevia are rare. You are more likely to need a caesarean section because the placenta is in the way of your baby being born. HOW IS PLACENTA PRAEVIA DIAGNOSED? A low-lying placenta may be suspected during the routine 20-week ultrasound scan. Most women who have a low-lying placenta at the routine 20-week scan will not go on to have a low-lying placenta later in the pregnancy – only 1 in 10 go on to have a placenta praevia. -
Aspirin Use to Prevent Preeclampsia and Related Morbidity and Mortality: an Evidence Update for the U.S
Evidence Synthesis Number 205 Aspirin Use to Prevent Preeclampsia and Related Morbidity and Mortality: An Evidence Update for the U.S. Preventive Services Task Force Prepared for: Agency for Healthcare Research and Quality U.S. Department of Health and Human Services 5600 Fishers Lane Rockville, MD 20857 www.ahrq.gov Contract No. HHSA-290-2015-00007-I-EPC5, Task Order No. 6 Prepared by: Kaiser Permanente Research Affiliates Evidence-based Practice Center Kaiser Permanente Center for Health Research Portland, OR Investigators: Jillian T. Henderson, PhD, MPH Kimberly K. Vesco, MD, MPH Caitlyn A. Senger, MPH Rachel G. Thomas, MPH Nadia Redmond, MSPH AHRQ Publication No. 21-05274-EF-1 February 2021 This report is based on research conducted by the Kaiser Permanente Research Affiliates Evidence-based Practice Center (EPC) under contract to the Agency for Healthcare Research and Quality (AHRQ), Rockville, MD (Contract No. HHSA-290-2015-00007-I-EPC5, Task Order No. 6). The findings and conclusions in this document are those of the authors, who are responsible for its contents; the findings and conclusions do not necessarily represent the views of AHRQ. Therefore, no statement in this report should be construed as an official position of AHRQ or of the U.S. Department of Health and Human Services. The information in this report is intended to help health care decisionmakers—patients and clinicians, health system leaders, and policymakers, among others—make well-informed decisions and thereby improve the quality of healthcare services. This report is not intended to be a substitute for the application of clinical judgment. Anyone who makes decisions concerning the provision of clinical care should consider this report in the same way as any medical reference and in conjunction with all other pertinent information (i.e., in the context of available resources and circumstances presented by individual patients). -
Antepartum Haemorrhage
OBSTETRICS AND GYNAECOLOGY CLINICAL PRACTICE GUIDELINE Antepartum haemorrhage Scope (Staff): WNHS Obstetrics and Gynaecology Directorate staff Scope (Area): Obstetrics and Gynaecology Directorate clinical areas at KEMH, OPH and home visiting (e.g. Community Midwifery Program) This document should be read in conjunction with this Disclaimer Contents Initial management: MFAU APH QRG ................................................. 2 Subsequent management of APH: QRG ............................................. 5 Management of an APH ........................................................................ 7 Key points ............................................................................................................... 7 Background information .......................................................................................... 7 Causes of APH ....................................................................................................... 7 Defining the severity of an APH .............................................................................. 8 Initial assessment ................................................................................................... 8 Emergency management ........................................................................................ 9 Maternal well-being ................................................................................................. 9 History taking ....................................................................................................... -
Rotation Objectives
Rotation Objectives Obstetrical Ward (Caseroom) Medical Expert 1. Be able to diagnose and manage the following antenatal complications a. Gestational Hypertension and preeclampsia b. Gestational diabetes c. Premature rupture of membranes d. Antepartum Bleeding (after 20 weeks gestation) e. Maternal hypothyroidism f. Intrauterine growth retardation 2. Demonstrate the following skills during antenatal visits: a. Fundal height measurements, b. Leopold manoeuvres, c. Fetal Doppler heart monitoring, d. Cervical exam 3. Be able to assess and triage risk associated with a trial of labour after Cesarian 4. Be able to assess the factors that will influence the decision to induce labour 5. Be able to perform normal risk labour and vaginal deliveries a. Demonstrate accurate cervical exams to determine the stage of labour b. Be able to evaluate for spontaneous rupture of membranes c. Fetal surveillance during labour d. Be able to diagnose non-cephalic fetal presentation using appropriate techniques 6. Be able to recognize and manage the following complications of labour and delivery a. Labour dystocia b. Shoulder dystocia c. Postpartum hemorrhage d. Perineal lacerations e. Vacuum assisted delivery f. Non-cephalic presentation g. Peripartum fever 7. Be able to manage pain in labour Postnatal and neonatal Care *The following objectives are relevant to services in which the resident is responsible for newborn assessments 8. Be able to describe and perform neonatal resuscitation 9. Demonstrate a comprehensive evaluation of a newborn in the first few days of life that will identify complications specific to the newborn period a. Hypoglycemia b. Hyperbilirubinemia c. Neonatal respiratory distress d. Congenital anomalies 10. Be able to provide support for breastfeeding, and anticipatory guidance for new mothers 11. -
Recode - Guidelines for Use the System Is Hierarchical I.E
ReCoDe - Guidelines for use The system is hierarchical i.e. categories at the head of the list take priority over those lower down. However multiple relevant conditions can be recorded. The primary condition is the highest on the list that is applicable to the case. Secondary condition is the next relevant condition down the list e.g. for codes B2, F3, and A7 - the primary code is A7, secondary code is B2 etc. ReCoDe - version 2.0 Group Condition further definition inclusion/exclusion A Fetus A1 Lethal congenital anomaly Lethal or severe. Any structural, genetic, or metabolic defect arising at conception or during embryogenesis incompatible with life or potentially treatable but causing death. A2 Infection Positive fetal microbiologic or serological culture. 2.1 Chronic – e.g. TORCH E.g. congenital or intrauterine pneumonia, cytomegalovirus, 2.2 Acute rubella, herpes. A3 Non-immune hydrops fetalis Presence of any two of the following signs: Ascites pericardial effusion pleural effusion subcutaneous oedema. A4 Iso-immunisation Blood group incompatibility rhesus or non rhesus (ABO). Death ascribable to blood group incompatibility. An indirect Coomb test greater than 1/16 and fetal hydrops (see A3). A5 Fetomaternal haemorrhage Haemorrhage into maternal circulation Kleihauer-Betke test > 0.4%1. A6 Twin-twin transfusion Presence of polyhydramnios (maximum vertical pocket of ≥ 8 cm) and oligohydramnios (maximum vertical pocket of ≤ 2 cm)2. A7 Fetal growth restriction SGA by customised percentile, intrauterine growth retardation. < 10th customised weight for gestational age centile3 OR IUGR reported on clinical or pathological grounds. A8 Other fetus Death due to other specific fetal conditions e.g. -
Antepartum Haemorhhage(Aph)
ANTEPARTUM HAEMORHHAGE(APH) MAJ SAMIA NASREEN CLASSIFIED GYNAECOLOGIST CMH OBJECTIVES OF PRESENTATION • Identify serious causes of vaginal bleeding in the second half of pregnancy • Describe a systematic approach to identify the cause of bleeding • Describe specific treatment options based on diagnosis DEFINITION • Vaginal bleeding after 24weeks and before the delivery of the fetus. • It complicates (3-4%) of all pregnancies. • It is an obstetric emergency because it endanger the life of both the mother and fetus. • Hemorrhage remain the most frequent cause of maternal deaths. • Mild= <50 mL loss of blood, Major= 50-1000mL loss, Massive= >1000mL loss. • Bleeding >1 occasion regarded as recurrent APH. Causes of Late Pregnancy Bleeding • Placenta previa • Placental abruption • Uterine scar disruption Life Threatening • Ruptured vasa previa • Cervical polyp • Bloody show/cervical change • Cervicitis or cervical ectropion • Vaginal trauma • Cervical cancer INITIAL MANAGEMENT • Same initial steps regardless of etiology in all cases of APH • Assess vital signs, circulatory stability • Secure intravenous access, administer fluids HISTORY & EXAMINATION • Targeted history and physical • Abdominal examination for estimated fetal weight (EFW), estimated gestational age (EGA), and fetal presentation Localize tenderness Palpate for uterine contractions • Gentle speculum examination is safe • NO digital vaginal exam unless placental location is known DIAGNOSTIC EVALUATION • Continuous electronic fetal monitoring (CTG) and tocodynamometry • Ultrasound for placental location, presence of clots, and fetal presentation • Obtain baseline laboratory tests Complete blood count Blood type and antibody screen Consider: coagulation studies, blood urea nitrogen (BUN), creatinine, liver function testing, and type and cross • Prepare for possible emergent cesarean delivery PLACENTA PREVIA Grading of placenta previa Grade .1 (lateral placenta): The placenta implanted in the lower uterine segment but not reach the internal os. -
Umbilical Cord Accidents
UMBILICAL CORD ACCIDENTS DR PADMASRI R PROF & HOD, DEPT OF OBSTETRICS & GYNAECOLOGY SAPTHAGIRI INSTITUTE OF MEDICAL SCIENCES 1 • “Cord accident,” defined by obstruction of fetal blood flow through the umbilical cord, is a common ante- or perinatal occurrence. • Obstruction can be either acute, as in cases of cord prolapse during delivery, or sub acute to-chronic, as in cases of grossly abnormal umbilical cords Placental findings in cord accidents. Mana M Parast From Stillbirth Summit 2011, Minneapolis, USA 2 TYPES Acute events Sub Acute on Chronic • Umbilical Cord Prolapse • Loops • Knots • Vasa Praevia • Entanglements • Coiling • Torsion • Rupture • Haematomas, thrombosis • Cysts, tumours • Nuchal Cord • Insertion - velamentous cord CORD COMPRESSION – SUDDEN IUD’s 3 CORD COMPRESSION 2 Principles of asphyxia are: a. Cord compression -preventing venous return to the fetus b. Umbilical vasospasm -preventing venous and arterial blood flow to and from the fetus due to exposure to external environment. 4 Recovery time from compression • 1min, 1 time 100% compression – 5 mins to recover- oxygen levels decrease by 50% • 5 mins comp – 30 mins to recover • Continued 5 min compressions every 30 mins causes fetal decompensation RISK FACTORS FOR CORD PROLAPSE GENERAL PROCEDURE RELATED Artificial rupture of membranes with high Multiparity presenting part Vaginal manipulation of the fetus with ruptured Low birthweight (< 2.5 kg) membranes Preterm labour (< 37+0 External cephalic version (during procedure) weeks) Fetal congenital anomalies Internal podalic version Breech presentation Stabilising induction of labour Transverse, oblique and Insertion of intrauterine pressure transducer unstable lie* Second twin Large balloon catheter induction of labour Polyhydramnios Unengaged presenting part Low-lying placenta RCOG Green-top Guideline No. -
Perinatal Arterial Ischemic Stroke: an Unusual Causal Mechanism
ical C lin as C e f R o l e Russo et al., J Clin Case Rep 2014, 4:8 a p n o r r u t DOI: 10.4172/2165-7920.1000401 s o J Journal of Clinical Case Reports ISSN: 2165-7920 Case Report Open Access Perinatal Arterial Ischemic Stroke: An Unusual Causal Mechanism Francesca Maria Russo1*, Giuseppe Paterlini2 and Patrizia Vergani1 1Department of Obstetrics and Gynecology, University of Milano-Bicocca, Monza, Italy 2Department of Pediatrics and Neonatal Intensive Care Unit, University of Milano-Bicocca, Monza, Italy Abstract Perinatal Arterial Ischemic Stroke (AIS) is an important cause of neurological morbidity in infants. Some risk factors have been identified, but its pathogenesis remains unclear. We present a case of perinatal in which macroscopic examination of the placenta revealed the presence of a vasa praevia. We hypothesize that compression of the vasa praevia during labor could have determined the formation of thrombi, which were subsequently embolized into the fetal circulation causing perinatal AIS. Background increased flow in the districts of the sylvian artery. No cardiac anatomic or functional abnormalities were found. Coagulation studies were Perinatal arterial ischemic stroke (AIS) is estimated to occur in the normal range and disorders of the coagulation pathway were in 1/1600 to 1/5000 births [1]. Even if rare, it is an important cause excluded. Thrombophilias were excluded both in the baby and in the of mortality and morbidity in neonates. A meta-analysis showed mother. that 57% of infants who suffer perinatal AIS develop motor and/or cognitive deficits, and 3% die [2]. -
Third Trimester Bleeding
Third Trimester Bleeding Nicole Sprawka, MD Maternal Fetal Medicine Causes of antepartum bleeding Labor Cervical bleeding Placental abruption Placenta previa Bleeding from a site above the cervix Vasa previa Bleeding in Labor Bleeding during labor is common Effacement and dilation of the cervix causes tearing of small vessels Often called “bloody show” Cervical bleeding Cervix my be friable due pregnancy or infection Cervical polyps Ask about recent intercourse Placental abruption Separation from it’s site of implantation before delivery Occurs 1 in 200 deliveries Cause of fetal death 1 in 1600 10% of all 3rd trimester stillbirth due to abruption Pathology of abruption Initiated by hemorrhage in to the decidua basalis The decidual hematoma leads to separation, compression, and destruction of the adjacent placenta In the early stages there may be no clinical symptoms The blood may dissect the membranes from the uterine wall and escape through the cervix Placental abruption The blood can be retained between the placenta and uterus resulting in a concealed abruption Concealed abruption likely go undiagnosed till delivery and are associated with a higher rate of DIC Risk factors for abruption Prior abruption 10 - 25 Preterm ruptured membranes 2.4 – 4.9 Preeclampsia 2.1 – 4.0 Chronic hypertension 1.8 – 3.0 Multifetal gestation 2.1 Polyhydramnios 2.0 Cigarette smoking 1.4 – 1.9 Increased age and parity 1.3 – 1.5 Cocaine use Uterine fibroids (esp. if behind placental implantation site) Hypertension and abruption Most common -
Management of Obstetric Hemorrhage
MANAGEMENT OF OBSTETRIC HEMORRHAGE AMITAVA RUDRA*, SUMAN CHATTERJEE**, SAIKAT SENGUPTA***, RAVI WANKHEDE***, BIswaJIT NANDI****, GAURAB MAITRA***, AND JAYANTA MITRA**** Abstract Major obstetric hemorrhage is an extremely challenging obstetric emergency associated with significant morbidity and mortality. Pharmacological treatment of uterine atony has not altered much in recent years apart from the increasing use of misoprostol, although controversy surrounds its advantages over other uterotonics. Placenta accreta is becoming more common, a sequel to the rising caesarean section rate. Interventional radiology may reduce blood loss in these cases. Uterine compression sutures, intrauterine tamponade balloons and cell salvage have been introduced in the last decade. Keywords: Antepartum hemorrhage, postpartum hemorrhage, uterotonics. Obstetric hemorrhage is the world’s leading cause of maternal mortality1. Postpartum hemorrhage (PPH) accounts for the majority of these deaths1. The global maternal ratio of 402 deaths per 100,000 live births2 obscures the fact that 99% of these deaths occur in the developing world3. In addition, even in many developed countries, it is also the maternal complication for which the highest rate of substandard care is observed4. Furthermore, Zeeman’s5 study of obstetric critical care provision identifies hemorrhage as one of the most frequent reasons for admission to intensive care unit. Major obstetric hemorrhage accounts for 30% of cases6. Obstetric hemorrhage is often sudden, unexpected, and may be associated with coagulopathy. Blood loss can be notoriously difficult to assess in obstetric bleeds. Bleeding may sometimes be concealed and the presence of amniotic fluid makes accurate estimation challenging. Hence, early recognition and treatment are essential to ensure the best outcome. Therefore, it is important to have a thorough knowledge of the pathophysiology, etiology, and management strategies of obstetric hemorrhage. -
The Identification and Validation of Neural Tube Defects in the General Practice Research Database
THE IDENTIFICATION AND VALIDATION OF NEURAL TUBE DEFECTS IN THE GENERAL PRACTICE RESEARCH DATABASE Scott T. Devine A dissertation submitted to the faculty of the University of North Carolina at Chapel Hill in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the School of Public Health (Epidemiology). Chapel Hill 2007 Approved by Advisor: Suzanne West Reader: Elizabeth Andrews Reader: Patricia Tennis Reader: John Thorp Reader: Andrew Olshan © 2007 Scott T Devine ALL RIGHTS RESERVED - ii- ABSTRACT Scott T. Devine The Identification And Validation Of Neural Tube Defects In The General Practice Research Database (Under the direction of Dr. Suzanne West) Background: Our objectives were to develop an algorithm for the identification of pregnancies in the General Practice Research Database (GPRD) that could be used to study birth outcomes and pregnancy and to determine if the GPRD could be used to identify cases of neural tube defects (NTDs). Methods: We constructed a pregnancy identification algorithm to identify pregnancies in 15 to 45 year old women between January 1, 1987 and September 14, 2004. The algorithm was evaluated for accuracy through a series of alternate analyses and reviews of electronic records. We then created electronic case definitions of anencephaly, encephalocele, meningocele and spina bifida and used them to identify potential NTD cases. We validated cases by querying general practitioners (GPs) via questionnaire. Results: We analyzed 98,922,326 records from 980,474 individuals and identified 255,400 women who had a total of 374,878 pregnancies. There were 271,613 full-term live births, 2,106 pre- or post-term births, 1,191 multi-fetus deliveries, 55,614 spontaneous abortions or miscarriages, 43,264 elective terminations, 7 stillbirths in combination with a live birth, and 1,083 stillbirths or fetal deaths.