Abnormalities Caused by Left Bundle Branch Block - Print Article - JAAPA
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Cardiovascular System 9
Chapter Cardiovascular System 9 Learning Outcomes On completion of this chapter, you will be able to: 1. State the description and primary functions of the organs/structures of the car- diovascular system. 2. Explain the circulation of blood through the chambers of the heart. 3. Identify and locate the commonly used sites for taking a pulse. 4. Explain blood pressure. 5. Recognize terminology included in the ICD-10-CM. 6. Analyze, build, spell, and pronounce medical words. 7. Comprehend the drugs highlighted in this chapter. 8. Describe diagnostic and laboratory tests related to the cardiovascular system. 9. Identify and define selected abbreviations. 10. Apply your acquired knowledge of medical terms by successfully completing the Practical Application exercise. 255 Anatomy and Physiology The cardiovascular (CV) system, also called the circulatory system, circulates blood to all parts of the body by the action of the heart. This process provides the body’s cells with oxygen and nutritive ele- ments and removes waste materials and carbon dioxide. The heart, a muscular pump, is the central organ of the system. It beats approximately 100,000 times each day, pumping roughly 8,000 liters of blood, enough to fill about 8,500 quart-sized milk cartons. Arteries, veins, and capillaries comprise the network of vessels that transport blood (fluid consisting of blood cells and plasma) throughout the body. Blood flows through the heart, to the lungs, back to the heart, and on to the various body parts. Table 9.1 provides an at-a-glance look at the cardiovascular system. Figure 9.1 shows a schematic overview of the cardiovascular system. -
LBBB Cardiomyopathy and His- Bundle Pacing
LBBB Cardiomyopathy and His- Bundle Pacing Rajeev Singh General Cardiology Fellow October 2018 Disclosures • No relevant disclosures Goals of this Presentaon • I. Background: Introduce the audience to the concept of LBBB Cardiomyopathy • II. IU Experience with His Bundle Pacing and LeQ Bundle Branch Cardiomyopathy • III. Novel Concepts and Future Work Background: His Bundle Pacing Carlson, Joe. “Making pacemakers easier on the heart may come down to connections.” Star Tribune. May 27, 2017. Background: LBBB Cardiomyopathy • First proposed in 2013; based on JACC arIcle which retrospecIvely analyzed 375 paents form 2007-2010 • Six Paents were idenIfied that fit pre-exisIng criteria which included 1) History of typical LBBB > 5 years 2) LVEF > 50% 3) Decrease LVEF < 40% and development of HF to NYHA II-IV 4) Major mechanical dyssychrony 4) Idiopathic eIology of cardiomyopathy Vaillant, Caroline, et al. "Resolution of left bundle branch block–induced cardiomyopathy by cardiac resynchronization therapy." Journal of the American College of Cardiology 61.10 (2013): 1089-1095. Background: LBBB HFREF Does Not Respond to ConvenIonal Treatment • January 2018 Duke study; QRS duraon, EF, and OMT studied on 659 paents • Highest HF hospitalizaon, mortality for LBBB, worst response to OMT (3.5% improvement in EF vs 10% ) Sze, Edward, et al. "Impaired recovery of left ventricular function in patients with cardiomyopathy and left bundle branch block." Journal of the American College of Cardiology71.3 (2018): 306-317. 72 Paents who underwent His Bundle Pacing -
Postural Heart Block*
Br Heart J: first published as 10.1136/hrt.44.2.221 on 1 August 1980. Downloaded from Case reports Br Heart J 1980; 44: 221-3 Postural heart block* PETER E SEDA, JOHN H McANULTY, C JOE ANDERSON From the Department of Medicine, University of Oregon Health Sciences Center, Portland, Oregon, USA SUMMARY A patient presented with orthostatic dizziness and syncope caused by postural heart block. When the patient was supine, atrioventricular conduction was normal and he was asymptomatic; when he was standing he developed second degree type II block and symptoms. The left bundle-branch block on his electrocardiogram and intracardiac electrophysiological study findings suggest that this heart block occurred distal to the His bundle. Orthostatic symptoms are usually presumed to be secondary to an inappropriate distribution of intravascular volume or to autonomic nervous system abnormalities. As shown in this patient, these symptoms may be the result of orthostatic heart block. Ambulatory monitoring may be useful in patients with orthostatic neurological symptoms, particularly when conduction abnormalities are present on the electrocardiogram. Orthostatic neurological symptoms usually result minute and regular, and increased to 90 beats a from inadequate cerebral perfusion caused by minute with some irregularity when he was upright. disturbances of the autonomic nervous system,'-3 The carotid pulse was normal, and there were no ineffective or inappropriate shifts in volume carotid bruits. The cardiac impulse was normal. http://heart.bmj.com/ distribution,4 or drugs.5 We report a patient with The second heart sound was paradoxically split. orthostatic dizziness and syncope caused by inter- There was a grade 2/6 apical systolic murmur. -
Resolution of Left Bundle Branch Block–Induced Cardiomyopathy by Cardiac Resynchronization Therapy
Journal of the American College of Cardiology Vol. xx, No. x, 2013 © 2013 by the American College of Cardiology Foundation ISSN 0735-1097/$36.00 Published by Elsevier Inc. http://dx.doi.org/10.1016/j.jacc.2012.10.053 CLINICAL RESEARCH Resolution of Left Bundle Branch Block–Induced Cardiomyopathy by Cardiac Resynchronization Therapy Caroline Vaillant, MD,* Raphaël P. Martins, MD,*† Erwan Donal, MD, PHD,*† Christophe Leclercq, MD, PHD,*† Christophe Thébault, MD,* Nathalie Behar, MD,* Philippe Mabo, MD,*† Claude Daubert, MD, FACC*† Rennes, France Objectives The study sought to describe a specific syndrome characterized by isolated left bundle branch block (LBBB) and a history of progressive left ventricular (LV) dysfunction, successfully treated by cardiac resynchronization ther- apy (CRT). Background Isolated LBBB in animals causes cardiac remodeling due to mechanical dyssynchrony, reversible by biventricular stimulation. However, the existence of LBBB-induced cardiomyopathy in humans remains uncertain. Methods Between 2007 and 2010, 375 candidates for CRT were screened and retrospectively included in this study if they met all criteria of a pre-defined syndrome, including: 1) history of typical LBBB for Ͼ5 years; 2) LV ejection fraction (EF) Ͼ50%; 3) decrease in LVEF to Ͻ40% and development of heart failure (HF) to NYHA functional class II to IV over several years; 4) major mechanical dyssynchrony; 5) no known etiology of cardiomyopathy; and 6) super-response to CRT with LVEF Ͼ45% and decrease in NYHA functional class at 1 year. Results The syndrome was identified in 6 patients (1.6%), 50.5 years of age on average at the time of LBBB diagnosis. -
View Pdf Copy of Original Document
Phenotype definition for the Vanderbilt Genome-Electronic Records project Identifying genetics determinants of normal QRS duration (QRSd) Patient population: • Patients with DNA whose first electrocardiogram (ECG) is designated as “normal” and lacking an exclusion criteria. • For this study, case and control are drawn from the same population and analyzed via continuous trait analysis. The only difference will be the QRSd. Hypothetical timeline for a single patient: Notes: • The study ECG is the first normal ECG. • The “Mildly abnormal” ECG cannot be abnormal by presence of heart disease. It can have abnormal rate, be recorded in the presence of Na-channel blocking meds, etc. For instance, a HR >100 is OK but not a bundle branch block. • Y duration = from first entry in the electronic medical record (EMR) until one month following normal ECG • Z duration = most recent clinic visit or problem list (if present) to one week following the normal ECG. Labs values, though, must be +/- 48h from the ECG time Criteria to be included in the analysis: Criteria Source/Method “Normal” ECG must be: • QRSd between 65-120ms ECG calculations • ECG designed as “NORMAL” ECG classification • Heart Rate between 50-100 ECG calculations • ECG Impression must not contain Natural Language Processing (NLP) on evidence of heart disease concepts (see ECG impression. Will exclude all but list below) negated terms (e.g., exclude those with possible, probable, or asserted bundle branch blocks). Should also exclude normalization negations like “LBBB no longer present.” -
Clinical Implications of Electrocardiographic Bundle Branch Block in Primary Care
Cardiac risk factors and prevention ORIGINAL RESEARCH ARTICLE Heart: first published as 10.1136/heartjnl-2018-314295 on 25 May 2019. Downloaded from Clinical implications of electrocardiographic bundle branch block in primary care Peter Vibe Rasmussen, 1,2 Morten Wagner Skov,2,3 Jonas Ghouse,2,3 Adrian Pietersen,4 Steen Møller Hansen,5 Christian Torp-Pedersen,5,6 Lars Køber,3,7 Stig Haunsø,2,3,7 Morten Salling Olesen,2,8 Jesper Hastrup Svendsen,3,7 Jacob Melgaard,6 Claus Graff,6 Anders Gaardsdal Holst,3,9 Jonas Bille Nielsen2,10,11 ► Additional material is ABSTRact In the primary care setting, patients are referred published online only. To view Objectives Electrocardiographic bundle branch block for 12-lead standard ECG recording based on a please visit the journal online broad range of indications, ranging from typical (http:// dx. doi. org/ 10. 1136/ (BBB) is common but the prognostic implications in heartjnl- 2018- 314295). primary care are unclear. We sought to investigate the symptoms of CV disease to more diffuse symptoms relationship between electrocardiographic BBB subtypes as well as monitoring of medical treatment (eg, QTc For numbered affiliations see and the risk of cardiovascular (CV) outcomes in a primary interval-prolonging drugs) or as part of a routine end of article. care population free of major CV disease. health check. Opportunistic ECG recordings Methods Retrospective cohort study of primary care will often result in identification of various BBB Correspondence to subtypes. However, to the best of our knowledge, Peter Vibe Rasmussen, patients referred for electrocardiogram (ECG) recording Department of Cardiology, between 2001 and 2011. -
Basic ECG Interpretation
12/2/2016 Basic Cardiac Anatomy Blood Flow Through the Heart 1. Blood enters right atrium via inferior & superior vena cava 2. Right atrium contracts, sending blood through the tricuspid valve and into the right ventricle 3. Right ventricle contracts, sending blood through the pulmonic valve and to the lungs via the pulmonary artery 4. Re-oxygenated blood is returned to the left atrium via the right and left pulmonary veins 5. Left atrium contracts, sending blood through the mitral valve and into the left ventricle 6. Left ventricle contracts, sending blood through the aortic Septum valve and to the body via the aorta 1 http://commons.wikimedia.org/wiki/File:Diagram_of_the_human_heart 2 _(cropped).svg Fun Fact….. Layers of the Heart Pulmonary Artery – The ONLY artery in the body that carries de-oxygenated blood Pulmonary Vein – The ONLY vein in the body that carries oxygenated blood 3 4 Layers of the Heart Endocardium Lines inner cavities of the heart & covers heart valves (Supplies left ventricle) Continuous with the inner lining of blood vessels Purkinje fibers located here; (electrical conduction system) Myocardium Muscular layer – the pump or workhorse of the heart “Time is Muscle” Epicardium Protective outer layer of heart (Supplies SA node Pericardium in most people) Fluid filled sac surrounding heart 5 6 http://stanfordhospital.org/images/greystone/heartCenter/images/ei_0028.gif 1 12/2/2016 What Makes the Heart Pump? Electrical impulses originating in the right atrium stimulate cardiac muscle contraction Your heart's -
Ventricular Anatomy for the Electrophysiologist (Part
Ventricular Anatomy for the REVIEW Electrophysiologist (Part II) SPECIAL 서울대학교 의과대학 병리학교실 서정욱 이화여자대학교 의학전문대학원 김문영 ABSTRACT The conduction fibers and Purkinje network of the ventricular myocardium have their peculiar location and immuno-histochemical characteristics. The bundle of His is located at the inferior border of the membranous septum, where the single trunk ramifies into the left and right bundle branches. The left bundle branches are clearly visible at the surface. The right bundles are hidden in the septal myocardium and it is not easy to recognize them. The cellular characters of the conduction bundles are modified myocardial cells with less cytoplasmic filaments. Myoglobin is expressed at the contractile part, whereas CD56 is expressed at the intercalated disc. A fine meshwork of synaptophysin positive processes is noted particularly at the nodal tissue. C-kit positive cells are scattered, but their role is not well understood. Purkinje cells are a peripheral continuation of bundles seen at the immediate subendocardium of the left ventricle. Key words: ■ conduction system ■ Purkinje network ■ pathology ■ arrhythmia ■ electrophysiology Introduction human heart. In this brief review, the histological characteristics of conduction cells, stained by The functional assessment of abnormal cardiac conventional and immuno-histochemical staining, are 3 rhythm and a targeted treatment based on demonstrated in the second part of the review. electrophysiologic studies are successful advances in cardiology.1 Morphological assessment or confirmation The characteristic location of the ventricular of hearts with such abnormalities is rare, not only due conduction system to the limited availability of human hearts but also inherent technological limitations of existing The atrioventricular node is situated in its technology.2 Classical morphological approaches and subendocardial location at the triangle of Koch. -
Cardiology Self Learning Package
Cardiology Self Learning Package Module 1: Anatomy and Physiology of the Module 1: Anatomy and Physiology of the Heart Heart. Page 1 Developed by Tony Curran (Clinical Nurse Educator) and Gill Sheppard (Clinical Nurse Specialist) Cardiology (October 2011) CONTENT Introduction…………………………………………………………………………………Page 3 How to use the ECG Self Learning package………………………………………….Page 4 Overview of the Heart…………………………………………………...…………..…….Page 5 Location, Size and Shape of the Heart…………………………………………………Page 5 The Chambers of the Heart…………….………………………………………..……….Page 7 The Circulation System……………………………………….………………..…………Page 8 The Heart Valve Anatomy………………………….…………………………..…………Page 9 Coronary Arteries…………………………………………….……………………..……Page 10 Coronary Veins…………………………………………………………………..……….Page 11 Cardiac Muscle Tissue……………………………………………………………..……Page 12 The Conduction System………………………………………………………………...Page 13 Cardiac Cycle……………………………………………………………………………..Page 15 References…………………………………………………………………………………Page 18 Module Questions………………………………………………………………………..Page 19 Module Evaluation Form………………………………………………………………..Page 22 [Module 1: Anatomy and Physiology of the Heart Page 2 Developed by Tony Curran (Clinical Nurse Educator) and Gill Sheppard (Clinical Nurse Specialist) Cardiology (October 2011) INTRODUCTION Welcome to Module 1: Anatomy and Physiology of the Heart. This self leaning package is designed to as tool to assist nurse in understanding the hearts structure and how the heart works. The goal of this module is to review: Location , size and shape of the heart The chambers of the heart The circulation system of the heart The heart’s valve anatomy Coronary arteries and veins Cardiac muscle tissue The conduction system The cardiac cycle This module will form the foundation of your cardiac knowledge and enable you to understand workings of the heart that will assist you in completing other modules. Learning outcomes form this module are: To state the position of the heart, the size and shape. -
Hypercalcemia-Induced New Onset Left Bundle Branch Block Mimicking Acute Myocardial Infarction in a Patient with Primary Hyperparathyroidism
Case Report Acta Cardiol Sin 2013;29:188-191 Hypercalcemia-Induced New Onset Left Bundle Branch Block Mimicking Acute Myocardial Infarction in a Patient with Primary Hyperparathyroidism Yu-Tsung Cheng,1 Chieh-Shou Su,1,2 Wei-Chun Chang,1,2 Meng-Hsia Chiang,1,3 Chih-Tai Ting1,2 and Wei-Win Lin1,4 A 78-year-old women with a recent diagnosis of primary hyperparathyroidism presented with vague chest pain, and new onset left bundle block (LBBB) on the electrocardiogram (ECG) mimicking acute myocardial infarction (AMI). LBBB resolved without abnormal Q waves only after correction of hypercalcemia. The cardiac enzymes, including creatine kinase, creatine kinase-MB, and troponin-I were all within normal range. Hypercalcemia provoking ECG changes that mimic acute myocardial infarction is infrequently reported. To our knowledge, this is the first report of hypercalcemia-induced new onset LBBB mimicking AMI. Emergency physicians should include hypercalcemia-induced new onset LBBB on the ECG in the differential diagnosis of AMI. Key Words: Acute myocardial infarction · Hypercalcemia · Hyperparathyroidism · left bundle branch block INTRODUCTION CASE REPORT Acute myocardial infarction (AMI) is an important A 78-year-old female presented to our facility with a differential diagnosis in patients who present with acute 10-year history of hypertension. The patient denied any chest pain and new onset left bundle branch block (LBBB) history of coronary artery disease, diabetes mellitus, or on the electrocardiogram (ECG). Unnecessary treatment hyperlipidemia. She had been hospitalized in another can be harmful in patients who have new onset LBBB institution for a deteriorating level of consciousness and due to conditions other than AMI. -
Intra-His Bundle Block. Clinical, Electrocardiographic, and Electrophysiologic Characteristics
Andréa et al OriginalArq Bras Article Cardiol Intra-His bundle 2002; 79: 532-7. Intra-His Bundle Block. Clinical, Electrocardiographic, and Electrophysiologic Characteristics Eduardo M. Andréa, Jacob Atié, Washington A. Maciel, Nilson A. de Oliveira Jr, Luiz Eduardo Camanho, Luís Gustavo Belo, Hecio Affonso de Carvalho, Leonardo Siqueira, Eduardo Saad, Ana Claudia Venancio Rio de Janeiro, RJ - Brazil Objective - To assess the clinical, electrocardiogra- Atrioventricular block is a conduction disturbance at phic, and electrophysiologic characteristics of patients the axis formed by the atrium, AV node, His bundle, and its (pt) with intra-His bundle block undergoing an electro- branches, which may vary from a mild delay in conduction physiologic study (EPS). (first-degree atrioventricular block) to a conduction block between atria and ventricles (second- and third-degree Methods - We analyzed the characteristics of 16 pt with atrioventricular blocks) 1. second-degree atrioventricular block and symptoms of Atrioventricular block may occur at the 3 following syncope or dyspnea, or both, undergoing conventional EPS. electrophysiological levels: atrioventricular node, within 2 Results - Intra-His bundle block was documented in 16 the His bundle, and below the His bundle . These levels pt during an EPS. In 15 (94%) pt, the atrioventricular block have anatomical correlation with, respectively, the atrioven- was recorded in sinus rhythm; 4 (25%) pt had intra-His tricular node, the penetrating His bundle (within the central Wenckebach phenomenon, which correlated with Mobitz I fibrous body), and nonpenetrating His bundle (out of the (MI) atrioventricular block on the electrocardiogram. Seven central fibrous body). First-degree atrioventricular block (44%) pt had 2:1 atrioventricular block, 2 of whom were usually has a delay in the conduction within the atrioventri- asymptomatic (12.5%). -
The Cardiac Conduction System in the Rat Expresses the A2 and A3
Proc. Nati. Acad. Sci. USA Vol. 89, pp. 99-103, January 1992 Medical Sciences The cardiac conduction system in the rat expresses the a2 and a3 isoforms of the Na+,K+-ATPase (in situ hybridization/heart conduction system/atrioventricular node/Purkinje strand) RAPHAEL ZAHLER*t, MICHAEL BRINES*, MICHAEL KASHGARIANt, E. J. BENZ, JR.*, AND MAUREEN GILMORE-HEBERT§ Departments of *Internal Medicine, SPathology, and §Therapeutic Radiology, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06510 Communicated by Vincent T. Marchesi, September 5, 1991 ABSTRACT The sodium pump is crucial for the function tially expressed in specialized cardiac conduction tissue. This of the heart and of the cardiac conduction system, which conjecture is reasonable because (i) the cardiac effects of initiates the heartbeat. The a (catalytic) subunit of this pump glycosides are especially prominent in the conduction system has three isoforms; the al isoform is ubiquitous, but the a2 and (although this action is also mediated indirectly via the a3 isoforms are localized to excitable tissue. Because rodent a2 nervous system), (ii) Purkinje fibers contain pumps that are and a3 isoforms are relatively sensitive to ouabain, which also more ouabain-sensitive than those of ventricular muscle, slows cardiac conduction, we studied heart-cell-specific expres- both by electrophysiologic and transport criteria (16-18), (iii) sion of pump isoform genes. Multiple conduction-system struc- electrophysiologic parameters have been found to differ tures, including sinoatrial node, bundle branches, and Pur- between Purkinje myocytes and working ventricular fibers kinje strands, had prominent, specific hybridization signal for (19-22). We thus used the technique of in situ hybridization a2 and a3 isoforms compared with adjacent working myo- to address this issue.