Isolated Single Umbilical Artery: Need for Specialist Fetal Echocardiography?
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Multiple Fetal Anomalies: a Case of Complete Triploidy
Holman JLN and McGowan MEB, J Neonatol Clin Pediatr 2020, 7: 045 DOI: 10.24966/NCP-878X/100045 HSOA Journal of Neonatology and Clinical Pediatrics Case Report Multiple Fetal Anomalies: A Case of Complete Triploidy Holman JLN1* and McGowan MEB2 1Department of Neonatology, Brenner Children’s Hospital, Wake Forest Bap- tist Medical Center, Winston-Salem, North Carolina, USA 2Department of Pediatrics, Brenner Children’s Hospital, Wake Forest Baptist Medical Center, Winston-Salem, North Carolina, USA Figure 1: The placenta is enlarged and heterogeneous. The appearance is nonspecific and may be secondary to report triploidy and/or partially due to maternal hyperten- sion. Fetal assessment is limited secondary to the enlarged placenta causing mass effect displacing the fetus towards the right as well as limited due to oligohydramnios. Abstract Complete triploidy is a rare genetic condition characterized by an additional complete chromosome set within all cells. Its presenta- tion is typically lethal, although case reports of infants with partial or complete triploidy surviving hours to days exist. Presentation is as- sociated with multiple congenital anomalies. We herein report a rare presentation of triploidy in a neonatal patient who suffered from pre- maturity, respiratory distress, metabolic acidosis and subsequently expired. Diagnostic tests ultimately revealed complete triploidy. In spite of what is understood about the genetics of the condition, op- tions for the management of this disorder are not well described in the literature, as cases are extremely rare. Case Report Figure 2: The more focal T2 hypointense region about the left side of the thickened placenta is nonspecific, though may be sequelae of prior placental hemorrhage. -
How to Recognize a Suspected Cardiac Defect in the Neonate
Neonatal Nursing Education Brief: How to Recognize a Suspected Cardiac Defect in the Neonate https://www.seattlechildrens.org/healthcare- professionals/education/continuing-medical-nursing-education/neonatal- nursing-education-briefs/ Cardiac defects are commonly seen and are the leading cause of death in the neonate. Prompt suspicion and recognition of congenital heart defects can improve outcomes. An ECHO is not needed to make a diagnosis. Cardiac defects, congenital heart defects, NICU, cardiac assessment How to Recognize a Suspected Cardiac Defect in the Neonate Purpose and Goal: CNEP # 2092 • Understand the signs of congenital heart defects in the neonate. • Learn to recognize and detect heart defects in the neonate. None of the planners, faculty or content specialists has any conflict of interest or will be presenting any off-label product use. This presentation has no commercial support or sponsorship, nor is it co-sponsored. Requirements for successful completion: • Successfully complete the post-test • Complete the evaluation form Date • December 2018 – December 2020 Learning Objectives • Describe the risk factors for congenital heart defects. • Describe the clinical features of suspected heart defects. • Identify 2 approaches for recognizing congenital heart defects. Introduction • Congenital heart defects may be seen at birth • They are the most common congenital defect • They are the leading cause of neonatal death • Many neonates present with symptoms at birth • Some may present after discharge • Early recognition of CHD -
Pulmonary-Atresia-Mapcas-Pavsdmapcas.Pdf
Normal Heart © 2012 The Children’s Heart Clinic NOTES: Children’s Heart Clinic, P.A., 2530 Chicago Avenue S, Ste 500, Minneapolis, MN 55404 West Metro: 612-813-8800 * East Metro: 651-220-8800 * Toll Free: 1-800-938-0301 * Fax: 612-813-8825 Children’s Minnesota, 2525 Chicago Avenue S, Minneapolis, MN 55404 West Metro: 612-813-6000 * East Metro: 651-220-6000 © 2012 The Children’s Heart Clinic Reviewed March 2019 Pulmonary Atresia, Ventricular Septal Defect and Major Aortopulmonary Collateral Arteries (PA/VSD/MAPCAs) Pulmonary atresia (PA), ventricular septal defect (VSD) and major aortopulmonary collateral arteries (MAPCAs) is a rare type of congenital heart defect, also referred to as Tetralogy of Fallot with PA/MAPCAs. Tetralogy of Fallot (TOF) is the most common cyanotic heart defect and occurs in 5-10% of all children with congenital heart disease. The classic description of TOF includes four cardiac abnormalities: overriding aorta, right ventricular hypertrophy (RVH), large perimembranous ventricular septal defect (VSD), and right ventricular outflow tract obstruction (RVOTO). About 20% of patients with TOF have PA at the infundibular or valvar level, which results in severe right ventricular outflow tract obstruction. PA means that the pulmonary valve is closed and not developed. When PA occurs, blood can not flow through the pulmonary arteries to the lungs. Instead, the child is dependent on a patent ductus arteriosus (PDA) or multiple systemic collateral vessels (MAPCAs) to deliver blood to the lungs for oxygenation. These MAPCAs usually arise from the de- scending aorta and subclavian arteries. Commonly, the pulmonary arteries are abnormal, with hypoplastic (small and underdeveloped) central and branch pulmonary arteries and/ or non-confluent central pulmonary arteries. -
Congenital Malformations Associated with a Single Umbilical Artery in Twin Pregnancies
Twin Research and Human Genetics Volume 18 Number 5 pp. 595–600 C The Author(s) 2015 doi:10.1017/thg.2015.59 Congenital Malformations Associated With a Single Umbilical Artery in Twin Pregnancies Sarah E. Mitchell,1 Karen Reidy,2,3,4 Fabricio Da Silva Costa,1,2,3,4 Ricardo Palma-Dias,1,2,3,4 Thomas J. Cade,1 and Mark P. Umstad1,4 1Division of Maternity Services, The Royal Women’s Hospital, Melbourne, Victoria, Australia 2Pregnancy Research Centre, The Royal Women’s Hospital, Melbourne, Victoria, Australia 3Pauline Gandel Imaging Centre, The Royal Women’s Hospital, Melbourne, Victoria, Australia 4Department of Obstetrics and Gynaecology, University of Melbourne, Victoria, Australia A single umbilical artery (SUA) was identified in 1.5% of twin pregnancies. The presence of a SUA in a twin pregnancy was associated with a 50% incidence of fetal anomalies, many of them complex and severe. The embryology and pathophysiological mechanisms associated with a SUA are reviewed. Aneuploidy is relatively common and should be considered, particularly in the presence of associated anomalies. Fetal growth restriction is frequent and preterm delivery is common. Keywords: twins, single umbilical artery, growth restriction, fetal anomalies The incidence of a SUA in singleton pregnancies approxi- review the available literature about the formation of a mates 0.5% (Granese et al., 2007; Hua et al., 2010), with a SUA. We aim to define the common problems encoun- higher prevalence in twin pregnancies (Heifetz, 1984;Klatt tered in these pregnancies and the clinical implications of et al., 2012). There is an association between a SUA and such findings. -
Ceftriaxone Induced Hypersensitivity Reactions Following Intradermal Skin Test: Case Series
DOI: 10.7860/JCDR/2017/29088.10758 Case Series Ceftriaxone Induced Hypersensitivity Section Reactions Following Intradermal Pharmacology Skin Test: Case Series SEREEN ROSE THOMSON1, BALAJI OMMURUGAN2, NAVIN PATIL3 ABSTRACT The incidence of cephalosporin induced hypersensitivity reactions in non-penicillin allergic patients is about 1.7% and in penicillin allergic patients it is about 3-5%. Infact, cephalosporins are considered as the first choice in penicillin allergic patients who need antibiotic therapy intraoperatively. Prompt identification of patients with beta-lactam allergy would lead to an improved utilization of antibiotics and reduced occurrence of resistant strains. We hereby attempt to present a series of cases where ceftriaxone has been implicated in the manifestation of various hypersensitivity reactions. We have also tried to highlight some of the errors, risk factors and other drugs that precipitate a hypersensitivity reaction. Keywords: Adverse drug reaction, Allergic reaction, Broad spectrum antibiotic, Naranjo’s scale Cephalosporin’s are one of the most commonly prescribed antibiotics she started complaining of rashes and itching over the injected along with penicillin’s, because of their broad spectrum of activity. site which subsequently progressed to the shoulder and chest. On As the therapeutic use of cephalosporin’s are increasing, reports examination, urticarial rash and 2 mm wheals were present over of hypersensitivity reactions are also on the rise [1]. Drug induced the injected site, left shoulder and chest associated with itching. allergic reactions can be grouped into IgE mediated and non IgE Her vitals were, pulse rate-70/minute and blood pressure- 130/82 mediated. IgE mediated reactions include angioedema, urticaria, mmHg. -
The Outcome of Adults Born with Pulmonary Atresia: High Morbidity and Mortality Irrespective of Repair
International Journal of Cardiology 280 (2019) 61–66 Contents lists available at ScienceDirect International Journal of Cardiology journal homepage: www.elsevier.com/locate/ijcard The outcome of adults born with pulmonary atresia: High morbidity and mortality irrespective of repair Claudia Montanaro a,1, Assunta Merola a,1, Aleksander Kempny a,b, Belen Alvarez-Alvarez a, Rafael Alonso-Gonzalez a,b, Lorna Swan a,b,AnselmUebinga,b,WeiLia,b, Sonya V. Babu-Narayan a,b, Michael A. Gatzoulis a,b, Konstantinos Dimopoulos a,b,⁎ a Adult Congenital Heart Centre and National Centre for Pulmonary Hypertension, Royal Brompton Hospital, London, UK b NIHR Cardiovascular Biomedical Research Unit, Royal Brompton Hospital and National Heart and Lung Institute, Imperial College London, UK article info abstract Article history: Objectives: To describe the characteristics and long-term outcome of a large adult cohort with pulmonary atresia. Received 8 April 2018 Background: Patients with pulmonary atresia (PA) are a heterogeneous population in terms of anatomy, Received in revised form 15 October 2018 physiology and surgical history, and their management during adulthood remains challenging. Accepted 5 November 2018 Methods: Data on all patients with PA followed in our center between January 2000 and March 2015 were Available online 7 November 2018 recorded. Patients were classified into the following groups: PA with ventricular septal defect (PA-VSD, 1), PA with intact ventricular septum (PA-IVS, 2) and other miscellaneous PA (PA-other, 3). Keywords: fi Pulmonary atresia Results: Two-hundred twenty-seven patients with PA were identi ed, 66.1% female, mean age 25.5 ± 8.7 years. Adult Over a median follow-up of 8.8 years, 49 (21.6%) patients had died: heart failure (n = 21, 42.8%) and sudden Outcome cardiac death (n = 8, 16.3%) were the main causes. -
Single Umbilical Artery (SUA) - Prenatal Sonography Diagnosis and Vascular Imaging
CASE REPORT Bali Medical Journal (Bali MedJ) 2021, Volume 10, Number 1: 8-10 P-ISSN.2089-1180, E-ISSN: 2302-2914 Single Umbilical Artery (SUA) - prenatal sonography diagnosis and vascular imaging Published by Bali Medical Journal features postnatal cord: a case report I Nyoman Hariyasa Sanjaya1*, Cokorda Istri Mirayani Pemayun2, Ni Wayan Dewi Purwanti3, Made Diah Vendita Sakuntari3, Ni Putu Nining Gianni3, Ni Luh Made Diah Mas Cahyani Putri3, Ni Komang Anik Pirgantari3, Ni Luh Md Dwi Laxmi Satriani3, Firsta Sesarina Mintariani3, Ni Luh Putu Yulia Padmawati3, Anak Agung Wahyu Putri3 ABSTRACT Background: Single umbilical artery (SUA) is a rare presentation in obstetrics practice, yet it comprises most of the umbilical anomaly. Despite its rare occurrence, a proper prenatal diagnosis needs to be established timely in order to prevent morbidity 1Department of Obstetrics and and mortality from commonly coexisting abnormalities. This case report presents a delayed diagnosis of SUA by prenatal Gynecology, Faculty of Medicine, sonography diagnosis and vascular imaging features postnatal cord at the third trimester of pregnancy and discusses the Universitas Udayana, Sanglah General proper diagnosis and management of such cases. Hospital, Denpasar, Bali, Indonesia. Case Presentation: We reported a case of a 37 year old pregnant woman who found to have one artery one vein in her 2 Outpatient Clinic,Sanglah General umbilical cord on ultrasound. This is very rare case and precise concern for us. Unfortunately we found this case in the third Hospital, Denpasar, Bali, Indonesia. trimester of pregnancy (37w5d), therefore we have slightly to evaluate. Female baby was born by elective C-section. -
Early Complete Repair of Pulmonary Atresia with Ventricular Septal Defect and Major
ORIGINAL ARTICLES: CONGENITAL HEART SURGERY CONGENITAL HEART SURGERY: The Annals of Thoracic Surgery CME Program is located online at http://www.annalsthoracicsurgery.org/cme/ home. To take the CME activity related to this article, you must have either an STS member or an individual non-member subscription to the journal. Early Complete Repair of Pulmonary Atresia With Ventricular Septal Defect and Major Aortopulmonary Collaterals CONGENITAL HEART Naruhito Watanabe, MD, Richard D. Mainwaring, MD, V. Mohan Reddy, MD, Michal Palmon, BS, MPH, and Frank L. Hanley, MD Division of Pediatric Cardiac Surgery, Lucile Packard Children’s Hospital/Stanford University, Stanford, California Background. Pulmonary atresia with ventricular septal the complete repair demonstrated an average right defect and major aortopulmonary collaterals (PA/VSD/ ventricular peak systolic pressure of 32 ± 5 mm Hg and MAPCAs) is a complex and diverse form of congenital an average right ventricle to aortic pressure ratio of 0.36 ± heart defect. Although most patients with PA/VSD/ 0.06. The median length of hospital stay was 26 days. MAPCAs can wait until they are 3 to 6 months of age to There have been 2 subsequent mortalities (7%), with a undergo surgical reconstruction, there are three specific median follow-up duration of 4 years. Eight of the criteria that merit an earlier repair. These 3 criteria are (1) 27 patients have subsequently undergone conduit unremitting heart failure; (2) a ductus to one lung and replacements at our institution. The hemodynamics at the MAPCAs to the other; and (3) hemitruncus to one lung conclusion of the conduit change were statistically and MAPCAs to the other. -
Pulmonary Atresia / Intact Ventricular Septum
Pulmonary Atresia / Intact Ventricular Septum What is it? In pulmonary atresia, no pulmonary valve exists. Blood can’t flow from the right ventricle into the pulmonary artery and on to the lungs. The right ventricle and tricuspid valve are often poorly developed. What causes it? In most children, the cause isn’t known. Some children can have other heart defects along with pulmonary atresia. (Children with tetralogy of Fallot who also have pulmonary atresia may have treatment similar to others with tetralogy of Fallot.) How does it affect the heart? An opening in the atrial septum lets blood exit the right atrium, so low-oxygen (bluish) blood mixes with the oxygen-rich (red) blood in the left atrium. The left ventricle pumps this mixture of oxygen- poor blood into the aorta and out to the body. The infant appears blue (cyanotic) because there’s less oxygen in the blood. The only source of lung blood flow is the patent ductus arteriosus (PDA), an open passageway between the pulmonary artery and the aorta. How does pulmonary atresia affect my child? If the PDA narrows or closes, the lung blood flow is reduced to critically low levels. This can cause very severe cyanosis. Symptoms may develop soon after birth. What can be done about the defect? Temporary treatment includes a drug to keep the PDA from closing. A surgeon can create a shunt between the aorta and the pulmonary artery that may help increase blood flow to the lungs. A more complete repair depends on the size of the pulmonary artery and right ventricle. -
P-46 Single Umbilical Artery
P-46 Single Umbilical Artery: An Important Marker for Prenatal Suspicion and Detection of Fetal Cardiac Anomalies Babaoğlu K. (1), Kayabey Ö. (1), Doğan Y. (2), Deveci M. (1), Beattie B. (3), Yücesoy G. (2), Uzun O. (3) Kocaeli University, School of Medicine, Department of Pediatrics, Division of Pediatric Cardiology, Kocaeli, Turkey (1); Kocaeli University, School of Medicine, Department of Obstretrics and Gynecology, Division of Perinatology, Kocaeli, Turkey (2); University Hospital of Wales, Department of Paediatric Cardiology, Cardiff, Wales, United Kingdom (3). Objective: To determine the frequency of associations between the single umbilical artery (SUA) and congenital heart disease in two tertiary centers. Methods: The fetuses diagnosed with SUA at mid-trimester detailed ultrasound examination between May 2001 and March 2014 were included in the study. Colour Doppler was used to visualize the umbilical arteries adjacent to the fetal bladder and in a section of the free loop of cord. Results: A total of 265 fetuses with SUA were identified. Complete data were available in 197/265 pregnancies (74.3%). The mean maternal age was 29 years and the average gestational age at diagnosis was 23 weeks. A cardiac anomaly was detected in 58 of these fetuses (29.0%): 34.3% in center-1, and 18.3% in center-2. Detected cardiac abnormalities include 19 ventricular septal defect (14 perimembranous, five muscular), eight tetralogy of Fallot (TOF), seven complete atrioventricular septal defect, five hypoplastic left heart syndromes, five double outlet right ventricle, three coarctation of the aorta, three hypoplastic right heart syndrome, two dextrocardia, and one for each of the following: absent pulmonary valve, aorta-pulmonary window, left atrial isomerism, double aortic arch, aortic stenosis and transposition of the great arteries. -
The Role of ABO-Incompatible Heart Transplantation in the Treatment of Newborn Complex Congenital Heart Disease
The Earlier, The Better: The Role of ABO-Incompatible Heart Transplantation in the Treatment of Newborn Complex Congenital Heart Disease Hannah Hsieh MD, Jasmine Patel MD, Madelyn Kahana MD Montefiore Medical Center, Department of Anesthesiology, Division of Pediatric Anesthesiology Background Discussion With advances in neonatal cardiac surgical repairs and palliative Due to the limited availability of donor organs, the transplantation of ABO procedures, the use of heart transplantation for the treatment of incompatible hearts has become an acceptable approach in infants less congenital heart defects in the newborn period is uncommon. There are a than 15 months of age. There have been several studies that show similar few congenital heart defects that are considered to be incompatible with early survival for ABO incompatible transplants as in ABO compatible surgical repair or palliation: pulmonary atresia with intact ventricular transplants. It is believed that newborn infants do not produce sufficient septum and right ventricular dependent coronary circulation (PA/IVS, isohemagglutinins (serum anti-A or anti-B antibodies) to mount a RVDCC), transposition of the great arteries with a single ventricle and heart hyperacute rejection following transplant until approximately 12 to 14 block, complex heterotaxy syndromes, severe atrioventricular canal or months of age. semilunar valve defects, and in some centers, hypoplastic left heart syndrome. Actuarial graft survival in newborn heart transplant recipients is Allowing ABO incompatible heart transplantation increases organ approximately 59% at age 25. availability in young patients and allows for use of organs from donors Figure 1 Figure 2 who have less common blood types. In summary, heart transplantation in We describe a case of ABO incompatible heart transplant in a newborn with the neonatal patient population poses unique challenges but can be the PA/IVS, RVDCC. -
Early and Intermediate Outcomes After Repair of Pulmonary Atresia With
Early and Intermediate Outcomes After Repair of Pulmonary Atresia With Ventricular Septal Defect and Major Aortopulmonary Collateral Arteries Experience With 85 Patients V. Mohan Reddy, MD; Doff B. McElhinney, MD; Zahid Amin, MD; Phillip Moore, MD; Andrew J. Parry, MD; David F. Teitel, MD; Frank L. Hanley, MD Background—Pulmonary atresia with ventricular septal defect (VSD) and major aortopulmonary collaterals (MAPCAs) is a complex lesion with marked heterogeneity of pulmonary blood supply. Traditional management has involved staged unifocalization of pulmonary blood supply. Our approach has been to perform early 1-stage complete unifocalization in almost all patients. Methods and Results—Since 1992, 85 patients with pulmonary atresia, VSD, and MAPCAs have undergone unifocal- ization (median age, 7 months). Complete 1-stage unifocalization and intracardiac repair were performed through a Downloaded from midline approach in 56 patients, whereas 23 underwent unifocalization in a single stage with the VSD left open, and 6 underwent staged unifocalization through sequential thoracotomies. There were 9 early deaths. During follow-up (1 to 69 months), there were 7 late deaths. Actuarial survival was 80% at 3 years. Among early survivors, actuarial survival with complete repair was 88% at 2 years. Reintervention on the neo–pulmonary arteries was performed in 24 patients. Conclusions—Early 1-stage complete unifocalization can be performed in Ͼ90% of patients with pulmonary atresia and http://circ.ahajournals.org/ MAPCAs, even those with absent true pulmonary arteries, and yields good functional results. Complete repair during the same operation is achieved in two thirds of patients. There remains room for improvement; actuarial survival 3 years after surgery is 80%, and there is a significant rate of reintervention.