Literature DB >> 32874753

Clinical Presentation, Cardiac Magnetic Resonance Findings, and Prognosis of Patients with Arrhythmogenic Right Ventricular Cardiomyopathy - An Experience from Pakistan.

Intisar Ahmed1, Fateh Ali Tipoo1.   

Abstract

OBJECTIVES: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart-muscle disease, characterized by fibro-fatty replacement and ventricular arrhythmias, that primarily affects the right ventricle (RV). We aimed to look at the clinical presentation, cardiac magnetic resonance (CMR) imaging findings and prognosis of patients with ARVC in Pakistan.
MATERIAL AND METHODS: It is a retrospective observational study, 17 consecutive patients with CMR and other findings consistent with ARVC, were enrolled from 2010 to 2019 at a single center.
RESULTS: Out of 17 patients, 12 (70.6%) were male with a mean age of 33.5 ± 17.5 years. Family history of sudden cardiac death was present in 3 (17.7%) patients while one (5.9%) patient had family history of ARVC. Syncope was the first presenting symptom in eight (47.1%) patients. On 12 leads ECG, T wave inversion in precordial leads was found in 6 (35.4%) patients, and epsilon wave was present in only 3 (17.7%) patients. On echocardiogram, 13 (76.5%) patients had dilated RV with reduced systolic function. On CMR, majority of patients (n = 14, 82.4%) were found to have RV dilatation with regional dyskinesia and fatty infiltration, 9 (52.9%) of them had left ventricular involvement also. Follow-up was available for 14 patients (82.4%) with a mean follow-up period of 35.5 ± 19.7 months. Three (21.4%) of them died and 10 (71.4%) got admissions for heart failure during follow-up period.
CONCLUSION: Arrhythmia related events are the main presenting symptoms of ARVC in this region, and left ventricular involvement in ARVC is not rare in this population. The mortality is relatively high, probably due to advanced disease at the time of presentation and less medical facilities available.
© 2020 Published by Scientific Scholar on behalf of Journal of Clinical Imaging Science.

Entities:  

Keywords:  Arrhythmogenic; Cardiomyopathy; Pakistan; Prognosis

Year:  2020        PMID: 32874753      PMCID: PMC7451142          DOI: 10.25259/JCIS_109_2020

Source DB:  PubMed          Journal:  J Clin Imaging Sci        ISSN: 2156-5597


  16 in total

1.  Arrhythmogenic right ventricular dysplasia: a United States experience.

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Journal:  Circulation       Date:  2005-12-12       Impact factor: 29.690

2.  Long-term evolution of right ventricular dysplasia-cardiomyopathy. The Heart Muscle Disease Study Group.

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Review 3.  Arrhythmogenic right ventricular cardiomyopathy.

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Journal:  J Am Coll Cardiol       Date:  2001-12       Impact factor: 24.094

Review 4.  Arrhythmogenic cardiomyopathy: etiology, diagnosis, and treatment.

Authors:  Srijita Sen-Chowdhry; Robert D Morgan; John C Chambers; William J McKenna
Journal:  Annu Rev Med       Date:  2010       Impact factor: 13.739

5.  High Arrhythmic Burden but Low Mortality during Long-term Follow-up in Arrhythmogenic Right Ventricular Cardiomyopathy.

Authors:  Andrew Martin; Jackie Crawford; Jonathan R Skinner; Warren Smith
Journal:  Heart Lung Circ       Date:  2015-09-28       Impact factor: 2.975

6.  Left Ventricular Involvement in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Predicts Adverse Clinical Outcomes: A Cardiovascular Magnetic Resonance Feature Tracking Study.

Authors:  Meng-Ting Shen; Zhi-Gang Yang; Kai-Yue Diao; Li Jiang; Yi Zhang; Xi Liu; Yue Gao; Bi-Yue Hu; Shan Huang; Ying-Kun Guo
Journal:  Sci Rep       Date:  2019-10-02       Impact factor: 4.379

7.  Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study.

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Review 8.  Role of cardiovascular magnetic resonance imaging in arrhythmogenic right ventricular dysplasia.

Authors:  Aditya Jain; Harikrishna Tandri; Hugh Calkins; David A Bluemke
Journal:  J Cardiovasc Magn Reson       Date:  2008-06-20       Impact factor: 5.364

Review 9.  The electrocardiographic manifestations of arrhythmogenic right ventricular dysplasia.

Authors:  Li Zhang; Liwen Liu; Peter R Kowey; Guy H Fontaine
Journal:  Curr Cardiol Rev       Date:  2014-08

Review 10.  Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.

Authors:  Ka Hou Christien Li; George Bazoukis; Tong Liu; Guangping Li; William K K Wu; Sunny Hei Wong; Wing Tak Wong; Yat Sun Chan; Martin C S Wong; Katharina Wassilew; Vassilios S Vassiliou; Gary Tse
Journal:  J Arrhythm       Date:  2017-12-21
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  2 in total

Review 1.  Arrhythmogenic Right Ventricular Cardiomyopathy: The Role of Genetics in Diagnosis, Management, and Screening.

Authors:  Mihir Odak; Steven Douedi; Anton Mararenko; Abbas Alshami; Islam Elkherpitawy; Hani Douedi; Eran Zacks; Brett Sealove
Journal:  Cardiol Res       Date:  2022-08-15

2.  Clinical Characteristics, Cardiac Magnetic Resonance Features, and Outcomes of Patients with Dilated Cardiomyopathy - An Experience from a South Asian Country.

Authors:  Pirbhat Shams; Fateh Ali Tipoo Sultan
Journal:  J Clin Imaging Sci       Date:  2021-07-23
  2 in total

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