Diagnosing arrhythmogenic right ventricular cardiomyopathy by 2010 Task Force Criteria: clinical performance and simplified practical implementation. Issue 5 (15th April 2020)
- Record Type:
- Journal Article
- Title:
- Diagnosing arrhythmogenic right ventricular cardiomyopathy by 2010 Task Force Criteria: clinical performance and simplified practical implementation. Issue 5 (15th April 2020)
- Main Title:
- Diagnosing arrhythmogenic right ventricular cardiomyopathy by 2010 Task Force Criteria: clinical performance and simplified practical implementation
- Authors:
- Bosman, Laurens P
Cadrin-Tourigny, Julia
Bourfiss, Mimount
Aliyari Ghasabeh, Mounes
Sharma, Apurva
Tichnell, Crystal
Roudijk, Rob W
Murray, Brittney
Tandri, Harikrishna
Khairy, Paul
Kamel, Ihab R
Zimmerman, Stefan L
Reitsma, Johannes B
Asselbergs, Folkert W
van Tintelen, J Peter
van der Heijden, Jeroen F
Hauer, Richard N W
Calkins, Hugh
James, Cynthia A
te Riele, Anneline S J M - Abstract:
- Abstract: Aims: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is diagnosed by a complex set of clinical tests as per 2010 Task Force Criteria (TFC). Avoiding misdiagnosis is crucial to prevent sudden cardiac death as well as unnecessary implantable cardioverter-defibrillator implantations. This study aims to validate the overall performance of the TFC in a real-world cohort of patients referred for ARVC evaluation. Methods and results: We included patients consecutively referred to our centres for ARVC evaluation. Patients were diagnosed by consensus of three independent clinical experts. Using this as a reference standard, diagnostic performance was measured for each individual criterion as well as the overall TFC classification. Of 407 evaluated patients (age 38 ± 17 years, 51% male), the expert panel diagnosed 66 (16%) with ARVC. The clinically observed TFC was false negative in 7/66 (11%) patients and false positive in 10/69 (14%) patients. Idiopathic outflow tract ventricular tachycardia was the most common alternative diagnosis. While the TFC performed well overall (sensitivity and specificity 92%), signal-averaged electrocardiogram (SAECG, P = 0.43), and several family history criteria ( P ≥ 0.17) failed to discriminate. Eliminating these criteria reduced false positives without increasing false negatives (net reclassification improvement 4.3%, P = 0.019). Furthermore, all ARVC patients met at least one electrocardiogram (ECG) or arrhythmia criterionAbstract: Aims: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is diagnosed by a complex set of clinical tests as per 2010 Task Force Criteria (TFC). Avoiding misdiagnosis is crucial to prevent sudden cardiac death as well as unnecessary implantable cardioverter-defibrillator implantations. This study aims to validate the overall performance of the TFC in a real-world cohort of patients referred for ARVC evaluation. Methods and results: We included patients consecutively referred to our centres for ARVC evaluation. Patients were diagnosed by consensus of three independent clinical experts. Using this as a reference standard, diagnostic performance was measured for each individual criterion as well as the overall TFC classification. Of 407 evaluated patients (age 38 ± 17 years, 51% male), the expert panel diagnosed 66 (16%) with ARVC. The clinically observed TFC was false negative in 7/66 (11%) patients and false positive in 10/69 (14%) patients. Idiopathic outflow tract ventricular tachycardia was the most common alternative diagnosis. While the TFC performed well overall (sensitivity and specificity 92%), signal-averaged electrocardiogram (SAECG, P = 0.43), and several family history criteria ( P ≥ 0.17) failed to discriminate. Eliminating these criteria reduced false positives without increasing false negatives (net reclassification improvement 4.3%, P = 0.019). Furthermore, all ARVC patients met at least one electrocardiogram (ECG) or arrhythmia criterion (sensitivity 100%). Conclusion: The TFC perform well but are complex and can lead to misdiagnosis. Simplification by eliminating SAECG and several family history criteria improves diagnostic accuracy. Arrhythmogenic right ventricular cardiomyopathy can be ruled out using ECG and arrhythmia criteria alone, hence these tests may serve as a first-line screening strategy among at-risk individuals. … (more)
- Is Part Of:
- Europace. Volume 22:Issue 5(2020)
- Journal:
- Europace
- Issue:
- Volume 22:Issue 5(2020)
- Issue Display:
- Volume 22, Issue 5 (2020)
- Year:
- 2020
- Volume:
- 22
- Issue:
- 5
- Issue Sort Value:
- 2020-0022-0005-0000
- Page Start:
- 787
- Page End:
- 796
- Publication Date:
- 2020-04-15
- Subjects:
- Arrhythmogenic right ventricular cardiomyopathy -- Diagnosis -- Ventricular arrhythmia -- Cardiomyopathy
Arrhythmia -- Treatment -- Periodicals
Cardiac pacing -- Periodicals
Catheter ablation -- Periodicals
Heart -- Physiology -- Periodicals
Electrophysiology -- Periodicals
617.4120645 - Journal URLs:
- http://europace.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/europace/euaa039 ↗
- Languages:
- English
- ISSNs:
- 1099-5129
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.340450
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