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Program PDF Saturday, March 28, 2020 Updated: 02-14-20
Program PDF Saturday, March 28, 2020 Updated: 02-14-20 Special ‐ Events and Meetings Congenital Heart Disease ‐ Scientific Session #5002 Session #602 Fellowship Administrators in Cardiovascular Education and ACHD Cases That Stumped Me Training Meeting, Day 2 Saturday, March 28, 2020, 8:00 a.m. ‐ 9:30 a.m. Saturday, March 28, 2020, 7:30 a.m. ‐ 5:30 p.m. Room S105b Marriott Marquis Chicago, Great Lakes Ballroom A CME Hours: 1.5 / CNE Hours: CME Hours: / CNE Hours: Co‐Chair: C. Huie Lin 7:30 a.m. Co‐Chair: Karen K. Stout Fellowship Administrators in Cardiovascular Education and Training Meeting, Day 2 8:00 a.m. LTGA, Severe AV Valve Regurgitation, Moderately Reduced EF, And Atrial Acute and Stable Ischemic Heart Disease ‐ Scientific Arrhythmia Session #601 Elizabeth Grier Treating Patients With STEMI: What They Didn't Teach You in Dallas, TX Fellowship! Saturday, March 28, 2020, 8:00 a.m. ‐ 9:30 a.m. 8:05 a.m. Room S505a ARS Questions (Pre‐Panel Discussion) CME Hours: 1.5 / CNE Hours: Elizabeth Grier Dallas, TX Co‐Chair: Frederick G. Kushner Co‐Chair: Alexandra J. Lansky 8:07 a.m. Panelist: Alvaro Avezum Panel Discussion: LTGA With AVVR And Reduced EF Panelist: William W. O'Neill Panelist: Jennifer Tremmel Panelist: Jonathan Nathan Menachem Panelist: Joseph A. Dearani 8:00 a.m. Panelist: Michelle Gurvitz Case of a Young Women With STEMI Panelist: David Bradley Jasjit Bhinder Valhalla, NY 8:27 a.m. ARS Questions (Post‐Panel Discussion) 8:05 a.m. Elizabeth Grier Young Women With STEMI: Something Doesn't Make Sense... -
The Increase of the Pulmonary Blood Flow Inhigh-Risk Hypoxic Patients with a Bidirectional Glenn Anastomosis
ORIGINAL ARTICLE The increase of the pulmonary blood flow inhigh-risk hypoxic patients with a bidirectional Glenn anastomosis Jacek Kołcz1, Mirosława Dudyńska2, Aleksandra Morka3, Sebastian Góreczny4, Janusz Skalski1 1Department of Pediatric Cardiac Surgery, Jagiellonian University Medical College, Kraków, Poland 2Department of Pediatric Cardiac Surgery, University Children’s Hospital in Krakow, Kraków, Poland 3Faculty of Health Sciences, Jagiellonian University Medical College, Kraków, Poland 4Department of Pediatric Cardiology, Jagiellonian University Medical College, Kraków, Poland Correspondence to: Jacek Kołcz, MD, PhD, ABSTRACT FECTS, Department of Pediatric Background: An additional shunt in single ventricle patients with Glenn anastomosis may increase Cardiac Surgery, pulmonary flow at the expense of ventricle volume overloading. The performance of the modification Jagiellonian University depends on pulmonary resistance, indicating better results in favorable hemodynamic conditions. Medical College, Wielicka 265, Aims: The study aims at analyzing the influence of precisely adjusted pulsatile shunt in borderline 30–663 Kraków, Poland, phone: +40 12 658 20 11, high-risk Glenn patients on early and late results. e-mail: Methods: The study involved 99 patients (including 21 children) with the bidirectional Glenn and ac- [email protected] cessory pulsatile shunt (BDGS group), and 78 patients with the classic bidirectional Glenn anastomosis Copyright by the Author(s), 2021 (BDG group). Kardiol Pol. 2021; Results: There was 1 death in the BDGS group and 4 deaths in the BDG group. No difference in mortality 79 (6): 638–644; DOI: 10.33963/KP.15939 (P = 0.71) was found. The Fontan completion was achieved in 69 (88.5%) children in the BDG group and Received: 18 (85.7%) patients in the BDGS group, without fatalities. -
The Physiology of the Fontan Circulation ⁎ Andrew Redington
Progress in Pediatric Cardiology 22 (2006) 179–186 www.elsevier.com/locate/ppedcard The physiology of the Fontan circulation ⁎ Andrew Redington Division of Cardiology, The Department of Pediatrics, The Hospital for Sick Children, University of Toronto School of Medicine, Toronto, Ontario, Canada Available online 8 September 2006 Abstract The Fontan circulation, no matter which of its various iterations, is abnormal in virtually every aspect of its performance. Some of these abnormalities are primarily the result of the procedure itself, and others are secondary to the fundamental disturbances of circulatory performance imposed by the ‘single’ ventricle circulation. The physiology of ventricular, systemic arterial and venopulmonary function will be described in this review. © 2006 Elsevier Ireland Ltd. All rights reserved. Keywords: palliation; Fontan circulation; Cavopulmonary anastomosis; Antriopulmonary anastomosis 1. Introduction has the profound consequences for the systemic ventricle that will discussed below. At the same time as the bidirectional In this personal overview, I will discuss the physiology of the cavopulmonary anastomosis was becoming almost uniformly Fontan circulation. Bob Freedom's contribution to our under- adopted, there was abandonment of the ‘classical’ atriopulmon- standing of complex congenital heart disease has meant that ary anastomosis, in favour of the total cavopulmonary con- many more of these patients are surviving with this physiology nection (TCPC). The ‘lateral wall’ TCPC, popularised by Marc than could have been contemplated 30 years ago. Nonetheless, deLeval [1], was shown experimentally and clinically to be they represent a very difficult group of patients and we continue haemodynamically more efficient [1,2] and set the scene for the to learn more about this unique circulation. -
A Better Approach for Left Ventricular Training In
Received: 28 September 2018 | Revised: 7 November 2018 | Accepted: 29 December 2018 DOI: 10.1111/chd.12749 ORIGINAL ARTICLE A better approach for left ventricular training in transposition of the great arteries and intact interventricular septum: Bidirectional cavopulmonary anastomosis and pulmonary artery banding Mehmet Salih Bilal MD1 | Arda Özyüksel MD1,2 | Mustafa Kemal Avşar MD1 | Şener Demiroluk MD3 | Osman Küçükosmanoğlu MD4 | Yalım Yalçın MD5 1Department of Cardiovascular Surgery, Medicana International Hospital, Abstract Istanbul, Turkey Objective: Management of the patients with transposition of the great arteries and 2 Department of Cardiovascular intact ventricular septum may be challenging beyond the newborn period. Herein, we Surgery, Biruni University, Istanbul, Turkey would like to present our alternative strategy for training the left ventricle in these 3Department of Anesthesiology, Medicana International Hospital, Istanbul, Turkey patients. 4Department of Pediatric Methods: Six patients with transposition of the great arteries and intact ventricular Cardiology, Medicana International Hospital, Istanbul, Turkey septum were evaluated in our clinic. Two of them were palliated with Glenn proce- 5Department of Pediatric dure and pulmonary banding as a definitive treatment strategy at other centers. Four Cardiology, Florence Nightingale Hospital, patients were operated on and a bidirectional cavopulmonary anastomosis in combi- Istanbul, Turkey nation with pulmonary artery banding was performed (stage‐1: palliation and ven- Correspondence tricular training) in our center. In four out of these six patients, arterial switch Arda Özyüksel, Department of Cardiovascular Surgery, Medicana operation was performed with takedown and direct re‐anastomosis of the superior International Hospital, Beylikdüzü Caddesi, vena cava to right atrium after an interstage period of 21‐30 months (stage‐2: ana- No:3, Beylikdüzü, Istanbul, Turkey. -
Glenn Surgery: a Safe Procedure in the Path of Univentricular Correction
Boletín Médico del Hospital Infantil de México RESEARCH ARTICLE Glenn surgery: a safe procedure in the path of univentricular correction Guadalupe Hernández-Morales1*, Alejandro Bolio-Cerdán2, Sergio Ruiz-González2, Patricia Romero-Cárdenas2, and Miguel A. Villasís-Keever3 1Departamento de Cirugía Cardiaca en Pediatría, Hospital Militar de Especialidades de la Mujer y Neonatología; 2Departamento de Cirugía Cardiovascular, Hospital Infantil de México Federico Gómez; 3Unidad de Investigación en Epidemiología Clínica, Unidad Médica de Alta Especialidad, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social. Mexico City, Mexico Abstract Background: This study describes 35 years of experience in a tertiary care level hospital that treats cardiac patients with univentricular heart physiology who underwent Glenn surgery. Methods: The study consisted of a retrospective analysis of patients who underwent Glenn surgery, including variables related to pre-operative, intra-operative, and post-operative mor- bidity and mortality. Results: From 1980 to 2015, 204 Glenn surgeries were performed. The most common heart disease was tricuspid atresia IB (19.2%). In 48.1% of the cases, the procedure was performed with antegrade flow. A bilateral Glenn procedure was performed in 12.5% of the cases and 10.3% were carried out without using a cardiopulmonary bypass pump. Reported complications included infections, bleeding, arrhythmias, chylothorax, neurological alterations, and pleural effusion. The mortality rate was 2.9%. Conclusions: Glenn surgery is a palliative surgery with good results. It significantly improves patient quality of life over a long period until a total cavopulmonary shunt is performed. The complications observed are few, and the mortality rate is low. -
Coders' Desk Reference for ICD-10-PCS Procedures
2 0 2 DESK REFERENCE 1 ICD-10-PCS Procedures ICD-10-PCS for DeskCoders’ Reference Coders’ Desk Reference for ICD-10-PCS Procedures Clinical descriptions with answers to your toughest ICD-10-PCS coding questions Sample 2021 optum360coding.com Contents Illustrations ..................................................................................................................................... xi Introduction .....................................................................................................................................1 ICD-10-PCS Overview ...........................................................................................................................................................1 How to Use Coders’ Desk Reference for ICD-10-PCS Procedures ...................................................................................2 Format ......................................................................................................................................................................................3 ICD-10-PCS Official Guidelines for Coding and Reporting 2020 .........................................................7 Conventions ...........................................................................................................................................................................7 Medical and Surgical Section Guidelines (section 0) ....................................................................................................8 Obstetric Section Guidelines (section -
Stenting Arterial Duct
McMullan et al Congenital Heart Disease Modified Blalock-Taussig shunt versus ductal stenting for palliation of cardiac lesions with inadequate pulmonary blood flow David Michael McMullan, MD,a Lester Cal Permut, MD,a Thomas Kenny Jones, MD,b Troy Alan Johnston, MD,b and Agustin Eduardo Rubio, MDb Objective: The modified Blalock-Taussig shunt is the most commonly used palliative procedure for infants with ductal-dependent pulmonary circulation. Recently, catheter-based stenting of the ductus arteriosus has been used by some centers to avoid surgical shunt placement. We evaluated the durability and safety of ductal stenting as an alternative to the modified Blalock-Taussig shunt. Methods: A single-institution, retrospective review of patients undergoing modified Blalock-Taussig shunt versus ductal stenting was performed. Survival, procedural complications, and freedom from reintervention were the primary outcome variables. Results: A total of 42 shunted and 13 stented patients with similar age and weight were identified. Survival to second-stage palliation, definitive repair, or 12 months was similar between the 2 groups (88% vs 85%; P ¼ .742). The incidence of surgical or catheter-based reintervention to maintain adequate pulmonary blood flow was 26% in the shunted patients and 25% in the stented patients (P ¼ 1.000). Three shunted patients (7%) required intervention to address contralateral pulmonary artery stenosis and 3 (7%) required surgical reintervention to address nonpulmonary blood flow-related complications. The need for ipsilateral or juxtaductal pulmonary artery intervention at, or subsequent to, second-stage palliation or definitive repair was similar between the 2 groups. Conclusions: Freedom from reintervention to maintain adequate pulmonary blood flow was similar between infants undergoing modified Blalock-Taussig shunt or ductal stenting as an initial palliative procedure. -
Table of Contents Introduction
Congenital Heart Surgery Database v.3.3 effective July 1, 2015 Training Manual October 2017 Table of Contents Introduction ................................................................................................................................................................2 1. Administrative ...............................................................................................................................................2 2. Demographics ...............................................................................................................................................5 3. Noncardiac Congenital Anatomic Abnormalities ....................................................................................... 21 4. Chromosomal Abnormalities ..................................................................................................................... 22 5. Syndromes ................................................................................................................................................. 23 6. Hospitalization ........................................................................................................................................... 24 7. Preoperative Factors .................................................................................................................................. 28 8. Diagnosis .................................................................................................................................................... 30 9. Procedures ................................................................................................................................................ -
TOPICC Public Use Dataset Annotated Ecrf
Public Use Dataset Annotated eCRF Trichotomous Outcome Prediction in Critical Care (The TOPICC Study) Phase II CPCCRN Protocol Number 034 ____________________________________________________ Collaborative Pediatric Critical Care Research Network Eunice Kennedy Shriver National Institute for Child Health and Human Development (NICHD) Protocol Version 3.0 Version Date: October 10, 2011 Annotated eCRF Version 1.0 Version Date: July 7, 2016 TOPICCII Annotated eCRF, v1.0_07Jul2016 1 Table of Contents Annotations key ............................................................................................................................. 3 Notes ............................................................................................................................................... 4 TOPICC Phase II Physiological Status Logs: .......................................................................... 12 TOPICC Phase II PICU Care Processes: ................................................................................. 16 TOPICC Phase II PICU Discharge Information: .................................................................... 17 TOPICC Phase II Hospital Discharge Information: ............................................................... 22 TOPICC Phase II Limitations/Withdrawals of Care: ............................................................. 26 TOPICC Phase II Cardiopulmonary Resuscitation: ............................................................... 27 TOPICC Phase II Surgery during PICU Course: .................................................................. -
Complex Congenital Cardiac Lesions
SPECIAL ARTICLE Canadian Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: Complex congenital cardiac lesions Candice K Silversides MD1, Omid Salehian (Section Editor) MD2, Erwin Oechslin MD1, Markus Schwerzmann MD3, Isabelle Vonder Muhll MD4, Paul Khairy MD5, Eric Horlick MD1, Mike Landzberg MD6, Folkert Meijboom MD7, Carole Warnes MD8, Judith Therrien MD9 CK Silversides, O Salehian, E Oechslin, et al. Canadian La conférence consensuelle 2009 de la Société Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: Complex canadienne de cardiologie sur la prise en charge congenital cardiac lesions. Can J Cardiol 2010;26(3):e98-e117. des adultes ayant une cardiopathie congénitale : Résumé With advances in pediatric cardiology and cardiac surgery, the population of adults with congenital heart disease (CHD) has increased. In the current era, there are more adults with CHD than children. This population has Étant donné les progrès de la cardiologie pédiatrique et de la chirurgie many unique issues and needs. They have distinctive forms of heart failure cardiaque, la population d’adultes ayant une cardiopathie congénitale and their cardiac disease can be associated with pulmonary hypertension, (CPC) a augmenté. Il y a maintenant plus d’adultes que d’enfants ayant thromboemboli, complex arrhythmias and sudden death. Medical aspects une CPC. Cette population a de nombreux problèmes et besoins that need to be considered relate to the long-term and multisystemic uniques. Ces adultes ont des formes particulières d’insuffisance cardiaque, effects of single ventricle physiology, cyanosis, systemic right ventricles, et leur maladie cardiaque peut s’associer à une hypertension pulmonaire, complex intracardiac baffles and failing subpulmonary right ventricles. -
A One and a Half Ventricular Repair in a Patient Presenting with Cardiac Arrest Reginald Chonoune
Himmelfarb Health Sciences Library, The George Washington University Health Sciences Research Commons Pediatrics Faculty Publications Pediatrics 2017 Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest Reginald Chonoune Adam Lowry Karthik Ramakrishnan Gail D. Pearson George Washington University Jeffrey P. Moak George Washington University See next page for additional authors Follow this and additional works at: https://hsrc.himmelfarb.gwu.edu/smhs_peds_facpubs Part of the Cardiology Commons, and the Cardiovascular Diseases Commons APA Citation Chonoune, R., Lowry, A., Ramakrishnan, K., Pearson, G. D., Moak, J. P., & Nath, D. S. (2017). Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac arrest. Journal of the Saudi Heart Association, (). http://dx.doi.org/10.1016/ j.jsha.2017.03.011 This Journal Article is brought to you for free and open access by the Pediatrics at Health Sciences Research Commons. It has been accepted for inclusion in Pediatrics Faculty Publications by an authorized administrator of Health Sciences Research Commons. For more information, please contact [email protected]. Authors Reginald Chonoune, Adam Lowry, Karthik Ramakrishnan, Gail D. Pearson, Jeffrey P. Moak, and Dilip S. Nath This journal article is available at Health Sciences Research Commons: https://hsrc.himmelfarb.gwu.edu/smhs_peds_facpubs/1977 Uhl’s anomaly: A one and a half ventricular repair in a patient presenting with cardiac CASE REPORT arrest ⇑ Reginald Chounoune a, , Adam Lowry b, Karthik Ramakrishnan a, Gail D. Pearson b, Jeffrey P. Moak b, Dilip S. Nath b a Division of Cardiovascular Surgery, Children’s National Medical Center, Washington, DC b Division of Cardiology, Children’s National Medical Center, Washington, DC a,bUSA Uhl’s anomaly, first reported in 1952, is an extremely rare congenital cardiac defect characterized by partial or complete loss of the right ventricular myocardium and unknown etiology. -
Hypoplastic Left Heart Syndrome: from Comfort Care to Long-Term Survival
Review nature publishing group Open Hypoplastic left heart syndrome: from comfort care to long-term survival Mouhammad Yabrodi1 and Christopher W. Mastropietro1 The management of hypoplastic left heart syndrome (HLHS) chambers along with a small ascending aorta and aortic has changed substantially over the past four decades. In the arch. This defect was not introduced as a syndrome until 1970s, children with HLHS could only be provided with sup- 1958 when Noonan and Nadas described it as a combined portive care. As a result, most of these unfortunate children aortic and mitral atresia malformation (3,4). At birth, an died within the neonatal period. The advent of the Norwood infant with this anatomy can survive as long as the duc- procedure in the early 1980s has changed the prognosis for tus arteriosus (DA) remains patent and a communication these children, and the majority now undergoing a series of between the left and right atria is present, allowing the right three surgical stages that can support survival beyond the neo- ventricle to maintain cardiac output to the systemic circu- natal period and into early adulthood. This review will focus on lation (Figure 1). If the DA closes, systemic blood flow is the Norwood procedure and the other important innovations compromised and clinical deterioration rapidly ensues. In of the last half century that have improved our outlook toward 1979, Yabek and Mann described the first reported use of children born with HLHS. prostaglandin E1 (PGE1) to maintain ductal patency in a patient with HLHS (5). Continuous infusion of PGE1, how- ever, is not a long-term solution.