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Tag Archives: cardiomyopathy

Amyloid heart disease module 2: management

April 2021 doi:10.5837/bjc.2021.016

Amyloid heart disease module 2: management

Tamer Rezk, Julian D Gillmore

Abstract

Introduction Table 1. Main amyloid types and responsible precursor fibrils Amyloid type Precursor fibril protein Immunoglobulin light chain (AL) Immunoglobulin light chains Hereditary transthyretin (hATTR) Mutations of the transythretin molecules Wild-type transthyretin (wtATTR) Wild-type (non-mutant) transthyretin molecules Hereditary fibrinogen (AFib) Mutations of the fibrinogen molecules Hereditary apolipoprotein (AApoA1) Mutations of apolipoprotein A1 molecules Isolated atrial amyloid (IAA) Atrial natriuretic peptide Systemic AA Serum amyloid A (SAA) protein This table illustrates the most common amyloid types and is

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March 2021 Br J Cardiol 2021;28:37–8 doi:10.5837/bjc.2021.012

Takotsubo syndrome: a predominantly female CV disorder, from the perspective of primary care

Melissa Matthews, Terry McCormack

Abstract

Introduction Takotsubo syndrome (TS) is increasingly recognised by the medical community following its first description in five Japanese patients, mostly male, in 1990 by Sato et al.1 Dote, his colleague, named the syndrome Takotsubo in 1991 due to its characteristic left ventricle (LV) shape in systole (narrow neck and wide base) and similarity to the Japanese octopus trap (takotsubo).2 The syndrome is also termed apical ballooning syndrome, broken heart syndrome and stress cardiomyopathy, among other names. Case one: a woman born in 1947 In January 2018 she was aged 70 and had been diagnosed with hypertension in 1996, but had no other card

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October 2019 Br J Cardiol 2019;26:145–8 doi:10.5837/bjc.2019.035

Clinical CMR: one-year case mix, outcomes and stress-testing accuracy from a regional tertiary centre

Protik Chaudhury, Min Aung, Rossella Barbagallo, Edward Barden, Swamy Gedela, Stuart J Harris, Henry O Savage, Jason N Dungu

Abstract

Introduction Cardiac magnetic resonance (CMR) imaging has developed into a crucial diagnostic tool in all patients with known or suspected heart disease. The role of CMR in differentiating ischaemic from non-ischaemic heart disease is well established and there are extensive data in the literature correlating myocardial fibrosis, as identified by the late gadolinium hyperenhancement technique, with adverse outcomes in patients with cardiomyopathy.1 A regional CMR service for the Essex region in southeast England was established in 2012, serving a population of 1,393,587 (2011 census data) with the benefit of avoiding transfer of patients to L

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January 2019 Br J Cardiol 2019;26:36–7 doi:10.5837/bjc.2019.006

Significant suppression of premature ventricular ectopics with ivabradine in dilated cardiomyopathy

Lal H Mughal, Andrew R Houghton, Jeffrey Khoo

Abstract

Case history A 79-year-old woman with a background history of non-ischaemic dilated cardiomyopathy with severe left ventricular (LV) impairment, left-bundle branch block (LBBB) with QRS duration 130–140 ms and LV dyssynchrony, underwent cardiac resynchronisation device implantation after optimisation of her heart failure medication. She continued to remain breathless (New York Heart Association [NYHA] grade III) even after implantation of the device. Device interrogation revealed only 50% pacing due to interference by predominantly unifocal ventricular ectopics (VEs) with VE load of 20% on 24-hour Holter monitoring (figure 1), which did not

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August 2014 Br J Cardiol 2014;21:(3) Online First

Call to support cardiomyopathy survey

BJCardio Staff

Abstract

The survey can be found at http://www.cardiomyopathysurvey.co.uk/ and the results, along with other research, will be used by the Board of the Association to inform and guide its development. It should take no more than 10 minutes to complete. All views expressed are confidential and will be kept anonymous. The Association is conducting a review of the charity’s strategy, purpose, image and communications to determine how they can support more people affected by this condition. Please also forward this survey link to anyone you feel may have an interest in cardiomyopathy or the work of the charity. For more information, visit http://www

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An update on treatments for amyloid heart disease

July 2013 Br J Cardiol 2013;20:107 doi:10.5837/bjc.2013.024

An update on treatments for amyloid heart disease

Simon W Dubrey

Abstract

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July 2009 Br J Cardiol 2009;16:197–8

An unusual ‘heart attack’ – Takotsubo cardiomyopathy

Jerzy Wojciuk, Ravish Katira, Ranjit S More, Roger W Bury

Abstract

Case report A 59-year-old woman was admitted with symptoms and signs suggesting acute coronary syndrome. A 12-lead electrocardiogram (ECG) demonstrated ST segment elevation in leads V2-V6, I, II and aVL consistent with ST segment elevation myocardial infarction. She underwent emergency coronary angiography, which demonstrated only minor irregularities in coronaries. Chest pain resolved completely after four hours. Figure 1b. Transthoracic echocardiography during the initial admission (apical four-chamber view, diastole) Figure 1a. Transthoracic echocardiography during the initial admission (apical four-chamber view, systole) demonstrating ba

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September 2004 Br J Cardiol 2004;11:393-6

The treatment of peripartum cardiomyopathy

Stephen J Leslie, Yaso Emmanuel, C Mark Francis, Andrew D Flapan

Abstract

No content available

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September 2004 Br J Cardiol 2004;11:388-92

Lowering blood pressure for the secondary prevention of stroke

Joanna K Lovett

Abstract

No content available

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