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And Its Obstructive Form, Idiopathic Hypertrophic Subaortic Stenosis (IHSS), in Pediatrics
Asymmetric septal hypertrophy (ASH) and its obstructive form, idiopathic hypertrophic subaortic stenosis (IHSS), in pediatrics ALBERT K. HARVEY, DD. Oklahoma City, Oklahoma IHSS. The father had no siblings, but two uncles had Although idiopathic hypertrophic died suddenly of heart disease at early ages. subaortic stenosis usually occurs in Case 1 adults, the possibility of its presence in children must not be overlooked. It An 18-year-old white girl said she had not experienced dyspnea, exercise intolerance, syncope, or chest pain. She has been reported even as early as was a senior in high school and had participated in dra- infancy and in stillborn fetuses. The matic and athletic activities. Physical examination condition appears to be genetically showed the pulse rate to be 74 and the blood pressure transmitted, with the natural history 110/64 mm. Hg. Pulses on the upper and lower ex- one of progressive disease. The tremities were strong and symmetric. The point of atypical location of an aortic stenosis maximum intensity (PMI) was not enlarged, and no type murmur is a clue to early thrill or precordial heave was perceptible. There was a diagnosis. Echocardiography is Grade 2/6 harsh systolic ejection murmur along the lower confirmative of a diagnosis. Four case left sternal border, which was transmitted well to the reports are presented. apex. No diastolic component was present. The phono- cardiogram showed an intermittent fourth heart sound. An x-ray film of the chest showed the heart size and vascularity of the lung field to be normal. An elec- trocardiogram (EKG) revealed left ventricular hyper- trophy with marked ST and T wave changes in the left precordial leads. -
Understanding Cardiomyopathy: Practical Guidelines
Chapter 30 Understanding Cardiomyopathy: Practical Guidelines Asha Moorthy, Jain T Kallarakkal HYPERTROPHIC CARDIOMYOPATHY genes predominate in frequency. Beta-myosin heavy chain (the first identified), myosin-binding protein C and cardiac troponin T Hypertrophic cardiomyopathy (HCM) is a genetic cardiac disorder probably comprise more than one half of the genotyped patients to caused by mutations in 1 of the 12 sarcomeric or nonsarcomeric date. Seven other genes each account for fewer cases: regulatory and genes and is recognized as the most common cause of sudden cardiac essential myosin light chains, titin, alpha-tropomyosin, alpha-actin, death (SCD) in the young and an important substrate for disability cardiac troponin I and alpha-myosin heavy chain. at any age. It affects men and women equally and occurs in many races and countries. The clinical diagnosis of HCM is established most easily and reliably with two-dimensional echocardiography by Clinical Course demonstrating left ventricular hypertrophy (LVH) which is typically asymmetric in distribution, and showing virtually any diffuse or Adverse clinical course proceeds along one or more of the following segmental pattern of left ventricular (LV) wall thickening. LV wall pathways, which ultimately dictate treatment strategies: (1) high thickening is associated with a nondilated and hyperdynamic risk for premature, sudden and unexpected death; (2) progressive chamber, in the absence of any other cardiac or systemic disease symptoms like exertional dyspnea, chest pain and impaired -
Cardiac Surgery
NON-PROFIT ORG. U.S. POSTAGE UAB Insight on Heart and Vascular Disease PAID PERMIT NO. 1256 410 • 500 22nd Street South BIRMINGHAM, AL Insight 1530 3rd ave S ON HEART AND VASCULAR DISEASE birmingham al 35294-0104 UAB Division of Cardiovascular Disease medicine.uab.edu/cardiovasculardisease UAB Division of Cardiothoracic Surgery medicine.uab.edu/cardiothoracicsurgery UAB Section of Vascular Surgery and Endovascular Therapy medicine.uab.edu/vascularsurgery Combined Therapy UAB Ambassador Program for Peripheral Vascular Disease The Ambassador Program gives referring physicians complete access to patient notes, letters, reports, and other data through a Catheter Ablation of secure Web portal. To join this program, please contact Physician Tachycardia Services at 1.800.822.6478. Minimally Invasive Pulmonary Thromboendarterectomy Clinic Cardiac Surgery welcOme 3 cOnTents Uab inSighT Welcome to the first issue of UAB Insight on Heart and Vascular On hearT and Disease, designed to keep you informed about UAB’s leading role in Cardiothoracic Surgery VaScUlar diSeaSe evaluation and treatment of cardiac and vascular diseases. UAB con- FALL 2009 sistently ranks among the top 30 cardiac programs rated in U.S. News Minimally Invasive Cardiac Surgery ... 2 & World Reports, and is a regional, national, and international referral VOlUme 1, nUmber 1 center for cardiac and vascular disease diagnosis and treatment. Adult Congenital Heart Disease ........ 3 With expertise in every major area of heart and vascular diseases, and James Kirklin, MD E D I T O R I N C H I E F as home to the Southeast’s largest and most technologically advanced Pulmonary Thromboendarterectomy Julius Linn, MD Heart and Vascular Center, we offer innovative, scientifically based Clinic ................................................. -
Heart & Vascular Institute
Sydell and Arnold Miller Family Heart & Vascular Institute 9500 Euclid Avenue, Cleveland, OH 44195 ClevelandClinic.org 2016 Outcomes 17-OUT-413 108369_CCFBCH_Cov_acg.indd 1 8/31/17 12:22 PM Measuring Outcomes Promotes Quality Improvement This project would not have been possible without the commitment and expertise of a team led by Umesh Khot, MD; Mouin Abdallah, MD; Sandra Hays; and Jagina McIntyre. Graphic design and photography were provided by Brian Kohlbacher and Cleveland Clinic’s Center for Medical Art and Photography. © The Cleveland Clinic Foundation 2017 108369_CCFBCH_Cov_acg.indd 2 9/19/17 10:57 AM Measuring and understanding outcomes of medical treatments promotes quality improvement. Cleveland Clinic has created a series of Outcomes books similar to this one for its clinical institutes. Designed for a physician audience, the Outcomes books contain a summary of many of our surgical and medical treatments, with a focus on outcomes data and a review of new technologies and innovations. The Outcomes books are not a comprehensive analysis of all treatments provided at Cleveland Clinic, and omission of a particular treatment does not necessarily mean we do not offer that treatment. When there are no recognized clinical outcome measures for a specific treatment, we may report process measures associated with improved outcomes. When process measures are unavailable, we may report volume measures; a relationship has been demonstrated between volume and improved outcomes for many treatments, particularly those involving surgical and -
Surgical Septal Myectomy Outcome for Obstructive Hypertrophic Cardiomyopathy After Alcohol Septal Ablation
1065 Original Article Surgical septal myectomy outcome for obstructive hypertrophic cardiomyopathy after alcohol septal ablation Qiulan Yang1^, Changsheng Zhu1, Hao Cui2, Bing Tang3, Shengwei Wang3, Qinjun Yu4, Shihua Zhao5, Yunhu Song1, Shuiyun Wang1 1Department of Cardiovascular Surgery, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China; 2Department of Cardiovascular Surgery, Mayo Clinic, Rochester, MI, USA; 3Department of Cardiac Surgery, Beijing Anzhen Hospital, Capital Medical University & Beijing Institute of Heart, Beijing, China; 4Department of Anesthesiology, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China; 5Department of Magnetic Resonance Imaging, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China Contributions: (I) Conception and design: S Wang; (II) Administrative support: C Zhu, H Cui, B Tang, S Wang, S Zhao; (III) Provision of study materials or patients: C Zhu; (IV) Collection and assembly of data: Q Yang; (V) Data analysis and interpretation: C Zhu, H Cui, B Tang, S Wang, S Zhao; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors. Correspondence to: Shuiyun Wang. Department of Cardiovascular Surgery, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beilishi Road 167, Xicheng District, Beijing 100037, China. Email: [email protected]. Background: Although surgical treatment of residual obstruction after alcohol septal ablation (ASA) is often challenging in patients with obstructive hypertrophic cardiomyopathy (OHCM) there are very few relevant clinical reports. Thus, outcomes of surgical septal myectomy (SSM) in this subgroup of patients remain to be determined. -
Asymmetric Septal Hypertrophy in Patients with Aortic Stenosis: an Adaptive Mechanism Or a Coexistence of Hypertrophic Cardiomyopathy?
View metadata, citation and similar papers at core.ac.uk brought to you by CORE J AM cou,providedCARDIOl by Elsevier - Publisher783 Connector 1983.1(3)783-9 Asymmetric Septal Hypertrophy in Patients With Aortic Stenosis: An Adaptive Mechanism or a Coexistence of Hypertrophic Cardiomyopathy? OTTO M. HESS, MD, JAKOB SCHNEIDER, MD, MARCO TURINA, MD, JOHN D. CARROLL, MD, FACC, MARTIN ROTHLIN, MD, HANS P. KRAYENBUEHL, MD Zurich, Switzerland Myocardial histologic features andventricular left dy• 1 and 2 (26.5 versus 29.1IJ.; NS), but muscle fiber di• namics were assessed in 24 patients with severe aorticameter of the septum in group 1 was significantlysmaller stenosis, 12 with (group 1) and 12 without (group(24.4 2) IJ.; P < 0.01) than that ofanterolateral the wall in associated asymmetric septalhypertrophy.In 10patients group 2. No morphologic abnormalities typical for hy• from group 1,echocardiographyshowed a septal/pos• pertrophic cardiomyopathy (fiberdisarray)were seen in teriorwall ratio of 1.5; in the other 2, asymmetric septalsamples from the patients in either group. By 18 months hypertrophywas diagnosed by direct inspection at thepostoperatively, septal wall thickness had decreased sig• time of surgery. Septal myectomy in all 12 patientsnificantly in from 2.0 to 1.5 em< (p0.01) and posterior group 1 was completed at the time of aortic valvewall re• thickness from 1.4 to 1.2 cm< (p0.05) in group 1. In group 2, septal wall thickness decreased from 1.5 placement. Septal histologicfeatures were assessedfrom to 1.3 em (NS) and posterior wall thickness from 1.4 to surgical specimens in 10 patients in groupTransseptal 1. -
Septal Myectomy for Obstructive Hypertrophic Cardiomyopathy Joseph A
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Septal Myectomy for Obstructive Hypertrophic Cardiomyopathy Joseph A. Dearani, MD, and Gordon K. Danielson, MD ransaortic septal myectomy is currently considered to tion of the LVOT gradient is important so that a compar- Tbe the most appropriate surgical treatment for pa- ison can be made with postmyectomy measurements. tients with obstructive hypertrophic cardiomyopathy Standard cardiopulmonary bypass with mild to moderate (HCM) and severe symptoms unresponsive to medical hypothermia (30-34°C) is used and the left heart is vented therapy.1-18 However, there is a significant learning curve with a catheter inserted through the right superior pulmo- for this procedure, and early surgical experience was as- nary vein. Myocardial protection, especially important be- sociated with complications of complete heart block, ven- cause of the severe ventricular hypertrophy, is begun with tricular septal defect, injury to the aortic or mitral valves, a generous infusion of cold blood cardioplegia (800-1000 and incomplete relief of obstruction. Current surgical re- mL) into the aortic root followed by additional doses given sults are vastly improved, although the reported experi- selectively into the left and right coronary ostia every 20 ence in North America is limited to a few centers. minutes. For more complex and lengthy procedures, top- ical cooling with ice-cold saline is applied, and an insulat- Surgical Technique ing pad is placed behind the left ventricle. After the extended left ventricular septal myectomy is Over the last three decades, our technique of septal myec- performed, the resected area can be deepened with a ron- tomy has evolved from the classic Morrow myectomy (Fig geur. -
Data Element Specifications
California CABG Outcomes Reporting Program (CCORP) Data Element Specifications Version 7.1 May 5, 2019 California CABG Outcomes Reporting Program Data Element Specifications Version 7.1, dated May 5, 2019 (1) Medical Record Number: (A) Format: Alphanumeric, length 12 (B) Valid Values: Free text (C) Category: Demographics (D) Definition/Description: Indicate the patient's medical record number at the hospital where surgery occurred. (2) Type of Coronary Artery Bypass Graft (CABG): (A) Format: Numeric, length 1 (B) Valid Values: 1 = Isolated CABG; 3 = CABG + Valve; 4= Other non-isolated CABG (C) Category: Operative (D) Definition/Description: Indicate the type of CABG. (i) Type of CABG should be coded Isolated CABG if none of the procedures listed in this subsection was performed concurrently with the coronary artery bypass surgery. (a) Valve repairs or replacements (b) Operations on structures adjacent to heart valves (papillary muscle, chordae tendineae, traebeculae carneae cordis, annuloplasty, infundibulectomy) (c) Ventriculectomy when diagnosed preoperatively as a rupture, aneurysm or remodeling procedure. Excludes 1) sites intra-operatively diagnosed, 2) patch applications for site oozing discovered during surgery and 3) prophylactic patch applications to reduce chances of future rupture (d) Repair of atrial and ventricular septa, excluding closure of patent foramen ovale (e) Excision of aneurysm of heart (f) Head and neck, intracranial endarterectomy (g) Other open heart surgeries, such as aortic arch repair, pulmonary endarterectomy -
Severe Mitral Annular Calcification
JACC: CARDIOVASCULAR IMAGING VOL. 9, NO. 11, 2016 ª 2016 BY THE AMERICAN COLLEGE OF CARDIOLOGY FOUNDATION ISSN 1936-878X/$36.00 PUBLISHED BY ELSEVIER http://dx.doi.org/10.1016/j.jcmg.2016.09.001 STATE-OF-THE-ART PAPERS Severe Mitral Annular Calcification Multimodality Imaging for Therapeutic Strategies and Interventions Mackram F. Eleid, MD, Thomas A. Foley, MD, Sameh M. Said, MD, Sorin V. Pislaru, MD, PHD, Charanjit S. Rihal, MD, MBA ABSTRACT Mitral annular calcification (MAC) is a chronic degenerative process associated with advanced age and conditions predisposing to left ventricular hypertrophy. Assessment of mitral valve disease in patients with severe MAC can be a challenge. When severe MAC results in mitral stenosis or regurgitation, multimodality imaging with 2-dimensional, 3-dimensional, and Doppler echocardiography and cardiac computed tomography angiography can delineate the severity and pathoanatomic features to help guide therapeutic strategies. New approaches using computer-assisted simulation of transcatheter valves and novel percutaneous and surgical techniques are being used to devise effective alternative strategies to conventional mitral valve replacement in this high-risk group of patients. (J Am Coll Cardiol Img 2016;9:1318–37) © 2016 by the American College of Cardiology Foundation. itral annular calcification (MAC) is a being investigated, offering hope for this challenging M chronic degenerative process that, when group of patients. severe, can result in mitral stenosis (MS) and/or mitral regurgitation (MR). The prevalence of PATHOPHYSIOLOGY OF MAC significant MS due to severe MAC is increasing in the developed world due to the growing population MAC is a result of slowly progressive calcification of ofelderlypatientsandriskfactorssuchashyperten- the fibrous mitral annulus (Figure 1) (1). -
Magnetic Resonance Imaging of Non‑Ischemic Cardiomyopathies: a Pictorial Essay
Editor-in-Chief: Vikram S. Dogra, MD OPEN ACCESS Department of Imaging Sciences, University of Rochester Medical Center, Rochester, USA HTML format Journal of Clinical Imaging Science For entire Editorial Board visit : www.clinicalimagingscience.org/editorialboard.asp www.clinicalimagingscience.org PICTORIAL ESSAY Magnetic Resonance Imaging of Non‑ischemic Cardiomyopathies: A Pictorial Essay Cristina I Olivas‑Chacon, Carola Mullins, Kevan Stewart, Nassim Akle, Jesus E Calleros, Luis R Ramos‑Duran Department of Radiology, Texas Tech University Health Science Center El Paso, El Paso, Texas, USA Address for correspondence: Dr. Cristina Ivette Olivas Chacon, ABSTRACT Department of Radiology, 4800 Alberta Avenue, El Paso, Non-ischemic cardiomyopathies are defined as either primary or secondary diseases of Texas ‑ 79905, USA. the myocardium resulting in cardiac dysfunction. While primary cardiomyopathies are E‑mail: [email protected] confined to the heart and can be genetic or acquired, secondary cardiomyopathies show involvement of the heart as a manifestation of an underlying systemic disease including metabolic, inflammatory, granulomatous, infectious, or autoimmune entities. Non-ischemic cardiomyopathies are currently classified as hypertrophic, dilated, restrictive, or unclassifiable, including left ventricular non-compaction. Cardiovascular Magnetic Resonance Imaging (CMRI) not only has the capability to assess cardiac morphology and function, but also the ability to detect edema, hemorrhage, fibrosis, and intramyocardial deposits, -
Targeting Alcohol Septal Ablation in Patients with Obstructive
Journal of Clinical Medicine Article Targeting Alcohol Septal Ablation in Patients with Obstructive Hypertrophic Cardiomyopathy Candidates for Surgical Myectomy: Added Value of Three-Dimensional Intracoronary Myocardial Contrast Echocardiography Giovanni La Canna 1,*, Iside Scarfò 1, Irina Arendar 1, Antonio Colombo 2, Lucia Torracca 3, Davide Margonato 4, Matteo Montorfano 4 and Ottavio Alfieri 5 1 Applied Diagnostic Echocardiography Unit, IRCCS Humanitas Clinical and Research Center, 20089 Rozzano, Italy; [email protected] (I.S.); [email protected] (I.A.) 2 Interventional Cardiology Unit, IRCCS Humanitas Clinical and Research Center, 20089 Rozzano, Italy; [email protected] 3 Cardiac Surgery, IRCCS Humanitas Clinical and Research Center, 20089 Rozzano, Italy; [email protected] 4 Interventional Cardiology Unit, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy; [email protected] (D.M.); [email protected] (M.M.) 5 Cardiac Surgery Unit, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy; ottavio.alfi[email protected] * Correspondence: [email protected]; Tel.: +39-33-5674-4319 Citation: La Canna, G.; Scarfò, I.; Abstract: Background: Myocardial contrast two-dimensional echocardiography (MC-2DE) is widely Arendar, I.; Colombo, A.; Torracca, L.; Margonato, D.; Montorfano, M.; used to address alcohol septal ablation (ASA) in obstructive hypertrophic cardiomyopathy (HCM). Alfieri, O. Targeting Alcohol Septal Owing to its limited cut-planes, MC-2DE may inaccurately identify the contrast misplacement Ablation in Patients with Obstructive associated with an unsuccessful or complicated ASA outcome. Objective: The aim of this study Hypertrophic Cardiomyopathy was to assess the added value of myocardial contrast three-dimensional echocardiography (MC- Candidates for Surgical Myectomy: 3DE) compared with MC-2DE to identify the appropriate matching between the target septal zone Added Value of Three-Dimensional (TSZ) and coronary artery branch for safe and long-term effective ASA in HCM patients. -
Hypertrophic Cardiomyopathy 2011 Pocket Guide
ACCF/AHA Pocket Guideline Adapted from the 2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy November 2011 Developed in Collaboration With the American Association for Thoracic Surgery, American Society of Echocardiography, American Society of Nuclear Cardiology, Heart Failure Society of America, Heart Rhythm Society, Society for Cardiovascular Angiography and Interventions, and Society of Thoracic Surgeons © 2011 by the American College of Cardiology Foundation and the American Heart Association, Inc. The following material was adapted from the 2011 ACCF/AHA Guidelines for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy (J Am Coll Cardiol 2011;XX:XX–XX). This pocket guideline is available on the World Wide Web sites of the American College of Cardiology (www.cardiosource. org) and the American Heart Association (my.americanheart.org). For copies of this document, please contact Elsevier Inc. Reprint Department, e-mail: [email protected]; phone: 212-633-3813; fax: 212-633-3820. Permissions: Multiple copies, modification, alteration, enhancement, and/ ordistribution of this document are not permitted without the express permission of the American College of Cardiology Foundation. Please contact Elsevier’s permission department at [email protected]. Contents 1. Introduction .........................................................................................3 2. Clinical Definition ................................................................................6 3. Genetic