Congenital Heart Anomaly Procedures Proposals for ICD-10-PCS Changes
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
The Conversion to Rastelli's Type Operation from Patrick-Mcgoon's
General Thoracic and Cardiovascular Surgery (2019) 67:551–553 https://doi.org/10.1007/s11748-018-0942-x CASE REPORT The conversion to Rastelli’s type operation from Patrick-McGoon’s procedure of an adult with Taussig–Bing heart: a case report Keiichi Fujiwara1 · Kousuke Yoshizawa1 · Nobuhisa Ohno1 · Hisanori Sakazaki2 Received: 30 January 2018 / Accepted: 18 May 2018 / Published online: 11 June 2018 © The Japanese Association for Thoracic Surgery 2018 Abstract A 23-year-old female of Taussig–Bing heart with antero-posterior relation of the great arteries was underwent Patrick- McGoon’s intraventricular rerouting at 6 years old of age. The left ventricular outflow obstruction (peak pressure gradient of 100 mmHg) developed, and severe aortic valve regurgitation following bacterial endocarditis was noted. The conversion to Rastelli’s type operation and aortic valve replacement were performed successfully at 23 years old of age. She is doing well without any significant left or right ventricular outflow obstruction at 7 years postoperatively. Keywords Taussig–Bing heart · Intraventricular rerouting · Patrick-McGoon’s operation · Left ventricular outflow obstruction · Adult congenital heart disease Introduction Case Taussig–Bing heart is characterized by double-outlet right A 23-year-old female diagnosed of double outlet right ventricle with subpulmonary ventricular septal defect [1, 2]. ventricle with subpulmonary ventricular septal defect and Currently, the arterial switch procedure as anatomic repair, antero-posterior relation of the great arteries, was referred to connecting the left ventricle to aorta and the right ventricle our hospital for severe left ventricular outflow tract obstruc- to pulmonary artery, is a popular surgical management for tion following Patrick-McGoon’s intraventricular rerouting Taussig–Bing heart regardless of relation of the great arter- and moderate to severe aortic valve regurgitation following ies. -
Usefulness Ofcontinuous Positive Airway Pressure in Differential
Arch Dis Child: first published as 10.1136/adc.53.6.456 on 1 June 1978. Downloaded from Archives of Disease in Childhood, 1978, 53, 456-460 Usefulness of continuous positive airway pressure in differential diagnosis of cardiac from pulmonary cyanosis in newborn infants P. SYAMASUNDAR RAO, BRENDA L. MARINO, AND ALEX F. ROBERTSON III From the Department of Pediatrics, Sections of Pediatric Cardiology and Neonatology, Medical College of Georgia, Augusta, Georgia, USA SUMMARY Differential diagnosis of cyanosis in the neonate is difficult and cardiac catheterisa- tion may be required for a correct diagnosis. It has been suggested that the response of Pao2 to continuous positive airway pressure (CPAP) with 100% oxygen may be useful. The purpose of this study was to test further this hypothesis by studying all neonates investigated for cyanosis with a Pao2 -50 torr in 0 8 to 1 .0 F1o2. Arterial blood samples were obtained in an F1o2 of 0 21-0 .4 and 0 8-1 .0, and in an F1O2 of 0 8-1 0 with 8-10 cm CPAP, and were analysed for Pao2, Paco2, and pH, bicarbonate being calculated. The final diagnoses were congenital heart disease (CHD) 21 cases, pulmonary parenchymal disease (PD) 10 cases, and persistent fetal circulation (PFC) 3 cases. No significant difference in pH, bicarbonate, or Paco2 was observed among the three groups or with CPAP. In the CHD and PFC infants CPAP produced no significant change in Pao2. In the PD babies Pao2 increased by an average of 33 torr (P<0 05). Despite thus attaining statistical significance 2 PD infants had no increase in Pao2 with CPAP. -
Pharmacy Policy Statement
PHARMACY POLICY STATEMENT Ohio Medicaid DRUG NAME Synagis (palivizumab) BILLING CODE 90378 (1 unit = 1 vial) BENEFIT TYPE Medical SITE OF SERVICE ALLOWED Office/Outpatient Hospital/Home COVERAGE REQUIREMENTS Prior Authorization Required (Preferred Product) QUANTITY LIMIT— 1 vial per month (max 5 during respiratory syncytial virus season) LIST OF DIAGNOSES CONSIDERED NOT Click Here MEDICALLY NECESSARY Synagis (palivizumab) is a preferred product and will only be considered for coverage under the medical/pharmacy benefit when the following criteria are met: Members must be clinically diagnosed with one of the following disease states and meet their individual criteria as stated. PREVENTION OF RESPIRATORY TRACT DISEASE CAUSED BY RESPIRATORY SYNCYTIAL VIRUS (RSV) For initial authorization: 1. Request must be made during the RSV season (November 1st through March 31st) AND initiation of injections should be timed with the onset of laboratory confirmed cases of RSV activity in the community, no earlier than November 1, 2017; AND 2. Member is < 12 months old at the beginning of the RSV season AND meet one of the following criteria (chart notes must be provided to support evidence): a) Member was born < 29 weeks, 0 days’ gestation; b) Member has Chronic Lung Disease (CLD) of prematurity (defined as gestational age <32 weeks, 0 days and a requirement for >21% oxygen for at least the first 28 days after birth); c) Member has hemodynamically significant Congenital Heart Disease (CHD) with one or more of the following: i) Acyanotic heart disease (e.g. atrial septal defect (ASD), ventricular septal defect (VSD), patent ductus arteriosus (PDA), etc.), AND member is receiving medication to control congestive heart failure (CHF) AND will require cardiac surgical procedures; ii) Moderate to severe pulmonary hypertension; iii) Cyanotic heart defect (e.g. -
Arterial Switch Operation Surgery Surgical Solutions to Complex Problems
Pediatric Cardiovascular Arterial Switch Operation Surgery Surgical Solutions to Complex Problems Tom R. Karl, MS, MD The arterial switch operation is appropriate treatment for most forms of transposition of Andrew Cochrane, FRACS the great arteries. In this review we analyze indications, techniques, and outcome for Christian P.R. Brizard, MD various subsets of patients with transposition of the great arteries, including those with an intact septum beyond 21 days of age, intramural coronary arteries, aortic arch ob- struction, the Taussig-Bing anomaly, discordant (corrected) transposition, transposition of the great arteries with left ventricular outflow tract obstruction, and univentricular hearts with transposition of the great arteries and subaortic stenosis. (Tex Heart Inst J 1997;24:322-33) T ransposition of the great arteries (TGA) is a prototypical lesion for pediat- ric cardiac surgeons, a lethal malformation that can often be converted (with a single operation) to a nearly normal heart. The arterial switch operation (ASO) has evolved to become the treatment of choice for most forms of TGA, and success with this operation has become a standard by which pediatric cardiac surgical units are judged. This is appropriate, because without expertise in neonatal anesthetic management, perfusion, intensive care, cardiology, and surgery, consistently good results are impossible to achieve. Surgical Anatomy of TGA In the broad sense, the term "TGA" describes any heart with a discordant ven- triculoatrial (VA) connection (aorta from right ventricle, pulmonary artery from left ventricle). The anatomic diagnosis is further defined by the intracardiac fea- tures. Most frequently, TGA is used to describe the solitus/concordant/discordant heart. -
The Arterial Switch Operation for Transposition of the Great Arteries
The Arterial Switch Operation for Transposition of the Great Arteries Richard A. Jonas Transposition of the great arteries, together with tetral- Ijased on the fact that (luring fetal life hoth ventricles ogy of Fallot, is one of the most common congenital are exposed to the same pressure load. Thus, the left cardiac anomalies resulting in cyanosis. It is hardly ventricle is prepared at birth. However, hecause pulnio- surprising, therefore, that shortly after the introduc- nary resistance falls ra1)idlj within 6 to 8 weeks ancl tion of cardiopulmonary hypass in the early 195Os, perhaps as quicltly as within 2 to 4 weeks, the left attempts were made at anatomical correction of transpo- ventricle is no longer prepared. Iiitroduction of an sition, ie, the arterial switch procedure. These early essentially elective complex neonatal operation in 1983 attempts were uniformly unsuccessful for a number of initially met with consitlerahle resistance, particularly reasons : 1)ecause hy this time the surgical mortality for the atrial 1. Microvascular techniques were not adequately level procedures had reached very low levels. However, developed for delicate coronary artery transfer. a prospectivr study conducted Ijy the Congenital Heart 2. Pulmonary vascular disease is common in transpo- Surgeons Society‘ showed that the overall survival of an sition beyond the first year of life. entire population of patients with transposition en- 3. Surgeons failed to appreciate that in the presence rolled in the neonatal period was superior with the of an intact ventricular septum, the left ventricle was neonatal arterial switch approach because of the previ- inadequately prepared to acntely take over the pressure ously uncaptured deaths that occurred before atrial load of the systemic circulation. -
World Journal for Pediatric & Congenital Heart Surgery
World Journal for Pediatric & Congenital Heart Surgery Keywords List A __________________________________________________________________________________ Ablative therapy (all modalities) Acute respiratory distress syndrome (ARDS) Adult Adult Congenital Heart Disease Airway Allograft, homograft Anastomosis Anatomy Anesthesia (includes agents, pharmacology, care and research) Aneurysm (aortic, myocardial, other) Angiogenesis Angiography Angioplasty Angioplasty (balloon dilatation) Animal model Annuloplasty (indicate location) Antibiotics Antibody/antigen Aorta/aortic Aortic arch Aortic dissection (includes ulcers, hematomas) Aortic operation Aortic root Aortic valve, repair Aortic valve, replacement Apoptosis Arrhythmia Arrhythmia surgery (includes Maze) Arterial switch operation Artery/arteries Artificial organs Atherosclerosis Atrial fibrillation, flutter Atrial Septal Defect (ASD) Atrio-ventricular Septal Defect (AVSD) Atrium Autograft Autonomic nervous system B __________________________________________________________________________________ Biochemistry Bioengineering Biomaterials Biopsy (indicate tissue) Blood Blood conservation Blood substitutes Blood transfusion Blood, coagulation/anticoagulation Brain Bronchial arteries Bronchiolitis obliterans Bronchoscopy/bronchus C __________________________________________________________________________________ Calcification Cardiac (use in combination) Cardiac anatomy/pathologic anatomy Cardiac catheterization/intervention Cardiac function Cardiac tumors (includes myxoma, primary, metastases) -
TGA Surgical Techniques: Tips & Tricks
TGA Surgical techniques: tips & tricks (Arterial switch operation) Seoul National University Children’s Hospital Woong-Han Kim Surgical History • 1951 Blalock and Hanlon, atrial septectomy • 1954 Mustard et al. arterial switch op • (monkey lung, 7 patients, 19 days old) • 1958 Senning, Atrial switch operation • 1963 Mustard, Mustard operation • 1966 Raskind and Miller, Balloon atrial septostomy • 1969 Rastelli, Rastelli operation • 1975 Jatene, first successulful ASO in patients with TGA and large VSD • 1977 Yacoub et al. two stage repair • 1983 Quaegebeur and Castaneda, primary repair in neonate • 1988 Boston group, rapid two-stage ASO The wide range of spatial relationships between the great arteries in TGA d-TGA Taussig-Bing (DORV) Posterior TGA Complete Transposition of the Great Arteries . Ventriculoarterial discordance . Also known as d-TGA (d = dextroposition of the bulboventricular loop) . Aorta on the right and anterior • Morphogenesis – Failure of the septum to spiral • Straight septum • Parallel arrangement of RVOT and LVOT – Abnormal growth and development of subaortic infundibulum – Absence of subpulmonic infundibulum growth Major coexisting anomalies * About 75% of neonates presenting TGA have no other cardiac anomalies, other than PFO or ASD and 20% have VSD and only 5% have LVOTO. 1 VSD Conoventricular(not necessarily juxtapulmonary) 55~60% Juxtaaortic 5% Juxtaarterial 5% Inlet septal 5% Juxtatricuspid Juxtacrucial : straddling muscular 25~30% 2 LVOTO It occurs 0.7% in TGA + IVS at birth and 20% in TGA+VSD, and may develop after birth in others and so reach an overall prevalence of 30%. Dynamic type - leftward bulging of septum Anatomic type - subvalvar fibrous ridge, fibrous tags, aneurysm, muscular (malalignment) or fibromuscular obstruction, valvar hypoplasia, combined. -
Review Article Congenital Heart Diseases
KYAMC Journal Vol. 9, No.1, April 2018 Review Article Congenital heart diseases: A review of echocardiogram records Md. Saiful Islam1, Md. Moniruzzaman2 Abstract Congenital heart defect (CHD) means an anatomic malformation of the heart or great vessels which occurs during intrauterine development, irrespective of the age at presentation. They can disrupt the normal blood flow through the heart. The blood flow can slow down, go in the wrong direction or to the wrong place, or be blocked completely. Broadly congenital heart defects can be acyanotic and cyanotic. We have reviewed retrospectively from echocardiogram record nearly two years of period & collected total 404 patients with congenital heart defects. Among them 329 (81.43%) was acyanotic and 75 (18.57%) was cyanotic congenital defects with variety of diagnosis. Ventricular septal defect was the most common acyanotic heart defect and Tetralogy of Fallot was the most common cyanotic heart defect. There was no significant gender deference. Keywords: Acyanotic, Congenital heart disease, Cyanotic. Date of received: 11. 11. 2017 Date of acceptance: 05. 01. 2018 Introduction known. The majority of the defects can be explained by Congenital heart defects (CHD) are reported in almost 1% of multifactorial inheritance hypothesis which states that a live births, and about half of these children need medical or predisposed fetus, when exposed to a given environmental surgical management in infancy1. In the first decade, a further trigger, to which the fetus is sensitive during the critical period 25% require surgery to maintain or improve their life1. Only of cardiac morphogenesis may develop the disease5. A variety 10% survive to adolescence without specific treatment. -
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. -
Appendix A: Surgical Procedure Terms and Definitions
Appendix A: Surgical Procedure Terms and Definitions Anomalous Systemic Venous Connection Anomalous Systemic Venous Connection Repair Repair includes a range of surgical approaches, including, among others: ligation of anomalous vessels, reimplantation of anomalous vessels (with or without use of a conduit), or redirection of anomalous systemic venous flow through directly to the pulmonary circulation (bidirectional Glenn to redirect LSVC or RSVC to left or right pulmonary artery, respectively). Aortic Aneurysm Aortic aneurysm repair Aortic aneurysm repair by any technique. Aortic Dissection Aortic Dissection repair Aortic dissection repair by any technique. Aortic Root Replacement Aortic Root Replacement, Bioprosthetic Replacement of the aortic root (that portion of the aorta attached to the heart; it gives rise to the coronary arteries) with a bioprosthesis (e.g., porcine) in a conduit, often composite. Aortic Root Replacement, Mechanical Replacement of the aortic root (that portion of the aorta attached to the heart; it gives rise to the coronary arteries) with a mechanical prosthesis in a composite conduit. Aortic Root Replacement, Homograft Replacement of the aortic root (that portion of the aorta attached to the heart; it gives rise to the coronary arteries) with a homograft Aortic Root Replacement, Valve sparing Replacement of the aortic root (that portion of the aorta attached to the heart; it gives rise to the coronary arteries) without replacing the aortic valve (using a tube graft). Aortic Valve Disease Ross Procedure Replacement of the aortic valve with a pulmonary autograft and replacement of the pulmonary valve with a homograft conduit. Konno Procedure (with and without aortic valve replacement) Relief of left ventricular outflow tract obstruction associated with aortic annular hypoplasia, aortic valvar stenosis and/or aortic valvar insufficiency via Konno aortoventriculoplasty. -
Fellow in Training Research Abstracts Oral Competition Indiana-ACC Poster Competition Abstract
Fellow in Training Research Abstracts Oral Competition Indiana-ACC Poster Competition Abstract Do NOT write outside the boxes. Any text or images outside the boxes will be deleted. Do NOT alter this form by deleting parts of it (including this text) or adding new boxes. Please structure your clinical research abstract using the following headings: * Background * Objective * Methods * Results (if relevant) * Conclusion Please structure your case study abstract using the following headings: * Introduction/objective * Case presentation * Discussion * Conclusion Title: Multi-Disciplinary Team Approach to Cardiogenic Shock Reduces In-Hospital Mortality Abstract: (Your abstract must use Normal style and must fit into the box. You may not alter the size of this ) Purpose: To determine the effectiveness of a hospital-wide process improvement program labeled as level 1 cardiogenic shock rapid response that enables a concerted coordinated multi-disciplinary team approach to treatment of patients with cardiogenic shock. Methods: Conducted a retrospective analysis of the cardiogenic shock rapid response program (protocol group) comparing to similar cohort of cardiogenic shock patients who did not utilize the shock response program. The program required alerting the advanced heart failure trained cardiologist who advises activation of a burst page to the cardiogenic shock team. This team rapidly institutes protocol-directed therapy and use of advanced support devices if necessary. The primary endpoint was hospital mortality. Secondary endpoint was utilization of advanced therapy (temporary mechanical circulatory support) Results: 471 patients were in the control and 110 in the protocol group. Baseline characteristics were similar and etiology of cardiogenic shock. The protocol group had significant reductions in-hospital mortality (35% to 45% (p< 0.05). -
101St Annual Meeting Share Your Annual Meeting Experience on Twitter: Featuring Aortic Symposium @AATSHQ and Mitral Conclave #AATS2021 a Virtual Learning Experience
TABLE OF CONTENTS AATS Annual Meeting Committees ............................................................................. 2 Accreditation ......................................................................................................................... 5 Scientific Program ...............................................................................................................8 Abstracts ............................................................................................................................108 C. Walton Lillehei Abstracts ..................................................................................341 Case Video Abstracts ..............................................................................................350 PROGRAM BOOK 101st Annual Meeting Share your Annual Meeting experience on Twitter: Featuring Aortic Symposium @AATSHQ and Mitral Conclave #AATS2021 A Virtual Learning Experience April 30-May 2, 2021 This program book went to ePrint on April 29, 2021. Any program changes made after this date are available at aats.org/annualmeeting. President Marc R. Moon *AATS Member ◆AATS New Member 1 101st Annual Meeting AMERICAN ASSOCIATION April 30 – May 2, 2021 | A Virtual Learning Experience FOR THORACIC SURGERY AORTIC SYMPOSIUM AATS – PROMOTING SCHOLARSHIP IN Co-Chairs THORACIC AND CARDIOVASCULAR SURGERY *Joseph S. Coselli *Steven L. Lansman Since 1917, when it was founded as the first organization dedicated to thoracic surgery, the Committee Members American Association for Thoracic Surgery