Literature DB >> 9014792

Spin-echo nuclear magnetic resonance for tissue characterisation in arrhythmogenic right ventricular cardiomyopathy.

L Menghetti1, C Basso, A Nava, A Angelini, G Thiene.   

Abstract

OBJECTIVE: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a myocardial disorder characterised clinically by ventricular arrhythmias that can cause cardiac arrest and morphologically by fatty or fibro-fatty myocardial atrophy of the right ventricle. In vivo tissue characterisation without endomyocardial biopsy would be useful. The aim of this study was to investigate the diagnostic accuracy of spin-echo nuclear magnetic resonance (NMR) for tissue characterisation in ARVC. PATIENTS AND METHODS: Twenty three subjects (15 men and eight women, aged 18-49, mean 34) were studied with spin-echo T1-weighted NMR and multislice scan. Fifteen had a clinical diagnosis of ARVC and eight were controls (age and sex matched subjects). Data were independently evaluated by two expert observers.
RESULTS: In the control group NMR was always negative (100% specificity). Ten of the 15 patients with ARVC had an abnormal NMR result (67% sensitivity), with areas that had a signal intensity close to that of pericardial or subcutaneous fat. In the remaining five cases the NMR signal was inadequate. Nine patients underwent both NMR and endomyocardial biopsy; biopsy was positive in eight (89%) and NMR was positive in five (56%).
CONCLUSIONS: NMR is a useful non-invasive diagnostic tool in the evaluation of fatty replacement in ARVC. The technique can be used with other procedures in the initial diagnostic evaluation and is a useful alternative tool in the long term follow up of patients with ARVC.

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Year:  1996        PMID: 9014792      PMCID: PMC484595          DOI: 10.1136/hrt.76.6.467

Source DB:  PubMed          Journal:  Heart        ISSN: 1355-6037            Impact factor:   5.994


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2.  Familial form of arrhythmogenic right ventricular dysplasia.

Authors:  M Laurent; C Descaves; Y Biron; C Deplace; C Almange; J C Daubert
Journal:  Am Heart J       Date:  1987-03       Impact factor: 4.749

3.  Critical analysis of cineangiographic criteria for diagnosis of arrhythmogenic right ventricular dysplasia.

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4.  Right ventricular dysplasia as a generalized cardiomyopathy? findings on magnetic resonance imaging.

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5.  Arrhythmogenic right and left ventricular disease: evaluation by computed tomography and nuclear magnetic resonance imaging.

Authors:  C Klersy; A Raisaro; J A Salerno; C Montemartini; R Campani
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6.  Familial occurrence of right ventricular dysplasia: a study involving nine families.

Authors:  A Nava; G Thiene; B Canciani; R Scognamiglio; L Daliento; G Buja; B Martini; P Stritoni; G Fasoli
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7.  Right ventricular dysplasia: a report of 24 adult cases.

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8.  Comparison of two-dimensional echocardiographic and angiographic findings in arrhythmogenic right ventricular dysplasia.

Authors:  J H Robertson; G H Bardy; L D German; J J Gallagher; J Kisslo
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9.  Contribution of cross-sectional echocardiography to the diagnosis of right ventricular dysplasia at the asymptomatic stage.

Authors:  R Scognamiglio; G Fasoli; A Nava; G Miraglia; G Thiene; S Dalla-Volta
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Review 4.  Arrhythmogenic right ventricular cardiomyopathy. Contribution of cardiac magnetic resonance imaging to the diagnosis.

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5.  Fibrofatty Changes: Incidence at Cardiac MR Imaging in Patients with Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.

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Review 6.  Arrhythmogenic right ventricular dysplasia/cardiomyopathy: new avenues for diagnosis and treatment.

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7.  Electrocardiographic and morphometric features in patients with ventricular tachycardia of right ventricular origin.

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Review 8.  MRI assessment of right ventricular dysplasia.

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10.  Focal macroscopic fat deposition within the right ventricular wall in asymptomatic patients undergoing screening EBCT coronary calcium scoring examinations.

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