Arrhythmogenic Right Ventricular Dysplasia
Am Fam Physician. 2006 Apr 15;73(8):1391-1398.
Patient information: See related handout on arrhythmogenic right ventricular dysplasia, written by the author of this article.
Arrhythmogenic right ventricular dysplasia (ARVD) is a disorder in which normal myocardium is replaced by fibrofatty tissue. This disorder usually involves the right ventricle, but the left ventricle and septum also may be affected. Although the exact prevalence of ARVD is unknown, it is thought to occur in six per 10,000 persons in certain populations. After hypertrophic heart disease, it is the number one cause of sudden cardiac death in young persons, especially athletes. Patients with ARVD are usually men younger than 35 years who complain of chest pain or rapid heart rate. In some cases, sudden cardiac death is the first presentation. The initial diagnosis of ARVD is based on the presence of major and minor criteria established in 1994. Further confirmation of the diagnosis includes noninvasive studies, such as echocardiography and magnetic resonance imaging of the heart, and invasive studies such as ventricular angiography and endomyocardial biopsy. Patients with ARVD are treated initially with antiarrhythmic agents with serious consideration for automatic implantable cardioverter-defibrillator placement. In patients with persistent symptomatic arrhythmias, radiofrequency ablation, ventriculotomy, or even cardiac transplant may be necessary.
Arrhythmogenic right ventricular dysplasia (ARVD), which was first described in 1977, is a poorly understood yet potentially lethal cause of cardiac disease.1,2 Once thought to be rare, ARVD has been shown to have an incidence of six per 10,000 persons in certain populations.3 In certain Mediterranean and southern U.S. populations, the incidence is as high as 44 per 10,000 persons.3 ARVD accounts for 3 to 4 percent of deaths in sports and 5 percent of sudden cardiac deaths in persons younger than 65 years.4–7 Given the relative frequency of this disorder and its potential for disastrous outcomes, it is important for primary care physicians to be familiar with its presentation, diagnosis, and management.
SORT: KEY RECOMMENDATIONS FOR PRACTICE
SORT: KEY RECOMMENDATIONS FOR PRACTICE
|Clinical recommendation||Evidence rating||References|
Although the best imaging technique is debatable, magnetic resonance imaging of the heart can provide noninvasive localization of structural changes and regional dysfunction.
Electrophysiologic studies can be used to distinguish between idiopathic right ventricular arrhythmias and ARVD.
For chronic management of ARVD, treatment with sotalol (Betapace), beta blockers, propafenone (Rythmol), and amiodarone (Cordarone), alone or in combination, can be used with variable success.
Placement of an automatic implantable cardioverter-defibrillator should be considered strongly in patients with drug-refractory arrhythmias.
ARVD = arrhythmogenic right ventricular dysplasia.
A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, see page 1313 or http://www.aafp.org/afpsort.xml.
A 32-year-old man presented with severe chest pain following exertion. He experienced dizziness, dyspnea, and a tingling sensation in his left arm with the chest pain. He waited for the symptoms to subside but went to the emergency department when the pain had not resolved after 60 minutes. Multiple medical regimens, including lidocaine (Xylocaine) and verapamil (Calan), failed to control his heart rate, and at one point, he required cardioversion because of unstable ventricular tachycardia (VT). His rhythm was finally stabilized using propranolol (Inderal). His event electrocardiography demonstrated no ST-segment changes, but multiple upright premature ventricular contractions were noted in leads II and III and the aVF. Also of note on electrocardiography were negative premature ventricular contractions in leads V1 through V3.
A preliminary diagnosis of right ventricular outflow tract VT was made, and the patient was transferred for cardiac catheterization, cardiac electrophysiologic studies, and magnetic resonance imaging (MRI) of the heart. Results of those studies demonstrated right ventricular dysplasia with a small right lateral wall ventricular aneurysm and inducible sustained monomorphic VT. The diagnosis of ARVD was made, and the patient agreed to receive an automatic implantable cardioverter-defibrillator (AICD) to control future tachycardic events. After AICD implantation, he was discharged on sotalol (Betapace).
Less than a month later, he experienced multiple episodes of sustained VT that were terminated promptly by the AICD. He was readmitted for heart rate control using a combination of intravenous lidocaine and amiodarone (Cordarone) and oral propranolol. Subsequent radiofrequency mapping and ablation, with more than eight arrhythmogenic sites identified and treated in the right ventricle, was successful, and he was discharged on sotalol with no further symptomatic tachycardic events noted.
ARVD is characterized by progressive replacement of the right ventricular myocardium by fibrofatty tissue (Figure 1).8,9 The most common location for this tissue transformation is between the anterior infundibulum, right ventricular apex, and inferior or diaphragmatic aspect of the right ventricle, the so-called “triangle of dysplasia” (Figure 2).2 Dysplasia in this region usually leads to dilatations or aneurysms having paradoxical systolic motion (expansion with systole instead of contraction). On the cellular level, there is transmural loss of myocardium in the right ventricular free wall. The left ventricle and septum usually are spared from the fibrofatty transformation, although they may be involved in more extensive cases.10 In addition, the specialized conduction system of the heart usually is spared. The presence of arrhythmias and characteristic findings on electrocardiography (see Clinical Findings and Diagnosis) can be explained by the dispersal of electrically conducting myocytes that can incite tachycardic events as the dysplastic event progresses.11,12
ARVD appears to have a strong familial association, with more than 30 percent of patients reporting a family history of the disorder. Most of these cases demonstrate an autosomal dominant pattern.3,13 Mutations in genes at three loci have been linked to the presence of ARVD.3,5,14 To date, no specific genetic testing for ARVD is available.
Clinical Findings and Diagnosis
Patients with ARVD may present at any age but are usually young or middle-aged (33 ± 14 years); the majority of patients are men (3:1 ratio).10,15 Because of the progressive nature of the disorder, patients may present with any number of symptoms. Palpitations, fatigue, and syncope appear to be the most common symptoms, but patients may have other nonspecific complaints such as abdominal pain and mental confusion (Table 1). In some cases, cardiac arrest following physical exertion such as participation in sports may be the initial presenting problem.8,16
TABLE 1 Signs and Symptoms of ARVD
Signs and Symptoms of ARVD
Decreased exercise tolerance
Dyspnea (especially with exertion)
Syncope or fainting
ARVD = arrhythmogenic right ventricular dysplasia.
Screening for ARVD begins with a thorough personal and family history, ideally of first- and second-degree relatives. A personal history of palpitations, especially in a young person, or a family history of sudden cardiac death or death at an early age should raise the index of suspicion for ARVD.
The physical examination is normal in at least 50 percent of patients with ARVD. One important diagnostic clue, if present, is a widely split S2.15 An S3 or S4 heart sound may be noted. Rarely, a murmur may be appreciated. If the right ventricle is greatly dilated, asymmetry of the chest wall may be seen.
The diagnosis of ARVD often is made following a work-up for tachycardia in an otherwise healthy adult. Fifty to 90 percent of persons with ARVD will have characteristic findings on a resting electrocardiogram.8,15,17 These findings include T-wave inversion in the anterior precordial leads (V1 through V6), epsilon waves, or VT with a left bundle branch block pattern, although polymorphic and right bundle branch block patterns also have been reported.9,15,18 Epsilon waves are small deflections just beyond the QRS complex (Figure 3); they are best visualized on a signal averaged electrocardiogram in leads V1 through V3. Any potential in leads V1 through V3 that exceeds the QRS duration in lead V6 by more than 25 milliseconds should be considered an epsilon wave.11
In 1994, a scoring system based on major and minor criteria was implemented to help establish the diagnosis of ARVD (Table 2).4,19,20 Although these criteria are specific, they lack sensitivity and have never been validated, in part because there is no single definitive means of making the diagnosis.3,20,21 The preferred method for making the diagnosis is based on histologic evidence of fibrofatty myocardium. Unfortunately, biopsy lacks sufficient sensitivity because of the segmental nature of the disease process. Once ARVD is suspected, early consultation with a cardiologist is recommended so that further testing may be performed to exclude other diagnoses (Table 3).22,23 These tests involve invasive and noninvasive modalities. Noninvasive testing includes Holter monitoring, exercise stress testing, chest radiography, and MRI of the heart. Invasive testing includes right ventricular angiography, contrast echocardiography, electrophysiologic studies, and endomyocardial biopsy.
TABLE 2 Criteria for the Diagnosis of ARVD*
Criteria for the Diagnosis of ARVD*
Global and/or regional dysfunction and structural alterations
Severe dilatation and reduction of right ventricular ejection fraction with no (or only mild) left ventricular impairment
Localized right ventricular aneurysms
Severe segmental dilatation of the right ventricle
Mild global right ventricular dilatation and/or ejection fraction with a normal left ventricle
Mild segmental dilatation of the right ventricle
Regional right ventricular hypokinesis
Tissue characterization of the walls
Fibrofatty replacement of myocardium on endomyocardial biopsy
ECG repolarization abnormalities
Inverted T waves in the right precordial leads (V2 and V3) in patients older than 12 years and in the absence of right bundle branch block
ECG depolarization/conduction abnormalities
Epsilon waves or localized prolongation (greater than 110 milliseconds) of the QRS complex in right precordial leads (V1 through V3)
Late potentials visible on signal-averaged ECG
Sustained or nonsustained left bundle branch block type VT documented on ECG, Holter monitoring, or during exercise stress testing
Frequent ventricular extrasystoles (more than 1,000 per 24 hours on Holter monitoring)
Familial disease confirmed at autopsy or surgery
Family history of premature sudden death (younger than 35 years) caused by suspected AVRD/DC
Family history (clinical diagnosis based on present criteria)
ARVD = arrhythmogenic right ventricular dysplasia; ECG = electrocardiography; VT = ventricular tachycardia; ARVD/C = arrhythmogenic right ventricular dysplasia/cardiomyopathy.
*—The diagnosis of ARVD is made if one of the following is met: two major criteria, one major and two minor criteria, or four minor criteria.
TABLE 3 Differential Diagnosis of ARVD
Differential Diagnosis of ARVD
Atrial septal defect
Naxos disease (ARVD associated with palmoplantar keratosis)
Right ventricular infarct
Right-sided valve insufficiency
Uhl’s anomaly (congenital absence of right ventricular myocardium)
Bundle branch reentry
Dilated cardiomyopathy VT
Idiopathic right ventricular arrhythmia
Ischemic heart disease VT
Right ventricular outflow tract VT
Results of Holter monitoring and exercise stress testing usually are normal. In more advanced cases of ARVD, stress testing may induce VT.15 Chest radiographs usually are normal unless extensive ventricular enlargement is present.
It is debatable which imaging modality is the best for diagnosing ARVD.24 Contrast echocardiography and right ventricular angiography are able to identify ventricular aneurysms and areas of dyskinesis in the triangle of dysplasia but require invasive techniques.25,26 Heart MRI is able to provide noninvasive localization of structural changes and regional dysfunction, although identification of intramyocardial fibrofatty change is difficult.27–30
Electrophysiologic studies are used to detect delayed potentials that can lead to tachycardic events. With these studies, it is possible to determine the number of arrhythmic morphologies, the ease of tachycardia induction, tolerance to tachycardic events, and the capacity for the tachycardia to develop into lethal arrhythmias. Electrophysiologic studies also can be used to distinguish between idiopathic right ventricular arrhythmias, which tend to have a relatively benign course, and ARVD.17,31,32
Endomyocardial biopsy has been considered the preferred method for diagnosis of ARVD. It has a specificity of 92 percent. However, its sensitivity is low (less than 20 percent) because tissue sampling is taken from the septum, where the risk of perforation is low and the likelihood of active disease is minimal.31
One of the major goals when treating ARVD is to prevent sudden cardiac death. Treatment decisions should be made in conjunction with a cardiologist or cardiac electrophysiologist. Although there is no way to cure ARVD, the arrhythmias can be managed. Available therapies include lifestyle modifications, antiarrhythmic medications, radiofrequency ablation, defibrillator implantation, and other surgery (Figure 4).
The first step in management is to educate patients about the disease. Although no definitive evidence exists regarding lifestyle modifications, patients should avoid activities that may trigger a tachycardic event, such as excessive physical exertion. Once effective control of arrhythmias is achieved, physical activities may be increased under close medical supervision.
Antiarrhythmic medications are the initial and most commonly used therapy in ARVD.33 No single drug has been shown to be completely effective in controlling or abolishing the arrhythmias, although intravenous amiodarone reportedly has been effective in terminating acute VT in patients with ARVD.8,10 Sotalol and amiodarone are class III drugs. Other drug regimens include class II antiarrhythmics (beta blockers such as propranolol), alone or in combination with class Ia drugs (procainamide [Pronestyl]) or class Ic drugs (flecainide [Tambocor], propafenone [Rythmol]), class Ic drugs alone, and amiodarone with class Ic or class II drugs. For chronic management of ARVD, treatment with sotalol, beta blockers, propafenone, and amiodarone alone or in combination is used most often with variable success.34,35
Radiofrequency ablation is used in cases of drug refractory or incessant VT, frequent tachycardia following internal defibrillator placement, and localized arrhythmia sites.10,11 The goal of radiofrequency ablation is to eliminate conduction pathways that are critical to the perpetuation of arrhythmias. Because radiofrequency ablation is completely successful in only 30 to 65 percent of cases, many patients will require more than one ablation session. These so-called relapses are often the result of disease progression that creates a new reentrant circuit.
The AICD works by providing antitachycardia pacing and defibrillation shocks as needed when arrhythmias occur. As with optimal antiarrhythmic treatment, the timing of AICD placement is debatable because no reliable risk stratification exists for patients with ARVD.36 In general, placement of an AICD should be considered strongly in patients with drug-refractory arrhythmias.10,37 Other indications for an AICD include younger age at onset, cardiac arrest, and left ventricular involvement (Table 4).37–39 The most significant relative contraindication to AICD placement is incessant VT.37 Other contraindications are listed in Table 4.37–39 Complications of AICD placement are rare but include lead perforation, lead failure, infection, and perioperative mortality.38
TABLE 4 Relative Indications and Contraindications for AICD Placement in ARVD
Relative Indications and Contraindications for AICD Placement in ARVD
Sudden cardiac death or cardiac arrest
VF/VT with hemodynamic compromise
Younger age of onset (less than 35 years)
Left ventricular involvement
Frequent tachyarrhythmias (i.e., sustained VF/VT) not responsive to pacing or anti-arrhythmic medications
VF/VT with a reversible trigger
Life expectancy of less than six months
If the above treatments fail, ventriculotomy and transplantation are options for management. Right ventriculotomy is performed by disconnecting the right ventricle from the rest of the heart. Heart transplantation remains a final option for patients with bilateral ventricular involvement and uncontrollable hemodynamic compromise.40
Prognosis and Course
ARVD is a progressive disease. The fact that it may be found as the cause of sudden cardiac death in young athletes, or as an incidental finding at autopsy in older adults, illustrates the unpredictable course of this disease. Although multiple studies have demonstrated a favorable long-term prognosis in properly treated patients, few long-term prospective studies have been performed to determine if the course of ARVD can be modified.41 Therefore, lifelong monitoring of patients with ARVD by the primary care physician-cardiologist team is recommended.
1. Fontaine GH, Guiraudon G, Frank R, Vedel J, Grosgogeat Y, Calrol C, et al. Stimulation studies and epicardial mapping in ventricular tachycardia: study of mechanisms and selection for surgery. In: Kulbertus HE, ed. Re-entrant arrhythmias: mechanisms and treatment. Baltimore: University Park Press, 1977:334–50.
2. Marcus FI, Fontaine GH, Guiraudon G, Frank R, Laurenceau JL, Malergue C, et al. Right ventricular dysplasia: a report of 24 adult cases. Circulation. 1982;65:384–98.
3. Ahmad F. The molecular genetics of arrhythmogenic right ventricular dysplasiacardiomyopathy. Clin Invest Med. 2003;26:167–78.
4. Thiene G, Nava A, Corrado D, Rossi L, Pennelli N. Right ventricular cardiomyopathy and sudden death in young people. N Engl J Med. 1988;318:129–33.
5. Corrado D, Thiene G, Nava A, Rossi L, Pennelli N. Sudden death in young competitive athletes: clinicopathologic correlations in 22 cases. Am J Med. 1990;89:588–96.
6. Hosey RG, Armsey TD. Sudden cardiac death. Clin Sports Med. 2003;22:51–66.
7. Peters S, Peters H, Thierfelder L. Risk stratification of sudden cardiac death and malignant ventricular arrhythmias in right ventricular dysplasia-cardiomyopathy. Int J Cardiol. 1999;71:243–50.
8. Nava A, Rossi L, Thiene G, eds. Arrhythmogenic right ventricular cardiomyopathy/dysplasia. Amsterdam: Elsevier, 1997.
9. Kayser HW, van der Wall EE, Sivananthan MU, Plein S, Bloomer TN, de Roos A. Diagnosis of arrhythmogenic right ventricular dysplasia: a review. Radiographics. 2002;22:639–50.
10. Ananthasubramaniam K, Khaja F. Arrhythmogenic right ventricular dysplasia/cardiomyopathy: review for the clinician. Prog Cardiovasc Dis. 1998;41:237–46.
11. Fontaine G, Fontaliran F, Hébert JL, Chemla D, Zenati O, Lecarpentier Y, et al. Arrhythmogenic right ventricular dysplasia. Annu Rev Med. 1999;50:17–35.
12. Saliba WI, Natale A. Ventricular tachycardia syndromes. Med Clin North Am. 2001;85:267–304.
13. Wlodarska EK, Konka M, Kepski R, Zaleska T, Ploski R, Ruzyllo W, et al. Familial form of arrhythmogenic right ventricular cardiomyopathy. Kardiol Pol. 2004;60:1–14.
14. Marcus F, Towbin JA, Zareba W, Moss A, Calkins H, Brown M, et al. Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C): a multidisciplinary study design and protocol. Circulation. 2003;107:2975–8.
15. Rossi PA. Arrhythmogenic right ventricular dysplasia—clinical features. Eur Heart J. 1989;10(suppl D):7–9.
16. Coumbe A, Perez-Martinez AL, Fegan AW, Hill IR. Arrhythmogenic right ventricular dysplasia (ARVD): an overlooked and underdiagnosed condition?. Med Sci Law. 1997;37:262–5.
17. O’Donnell D, Cox D, Bourke J, Mitchell L, Furniss S. Clinical and electrophysiological differences between patients with arrhythmogenic right ventricular dysplasia and right ventricular outflow tract tachycardia. Eur Heart J. 2003;24:801–10.
18. Lascault G, Laplaud O, Frank R, Tonet J, Fontaine G, Grosgogeat Y, et al. Ventricular tachycardia features in right ventricular dysplasia. Circulation. 1988;78:300.
19. McKenna WJ, Thiene G, Nava A, Fontaliran F, Blomstrom-Lundqvist C, Fontaine G, et al. Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Br Heart J. 1994;71:215–8.
20. Bomma C, Rutberg J, Tandri H, Nasir K, Roguin A, Tichnell C, et al. Misdiagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. J Cardiovasc Electrophysiol. 2004;15:300–6.
21. Hamid MS, Norman M, Quraishi A, Firoozi S, Thaman R, Gimeno JR, et al. Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteria. J Am Coll Cardiol. 2002;40:1445–50.
22. Richardson P, McKenna W, Bristow M, Maisch B, Mautner B, O’Connell J, et al. Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies. Circulation. 1996;93:841–2.
23. Fontaine G, Fontaliran F, Frank R. Arrhythmogenic right ventricular cardiomyopathies: clinical forms and main differential diagnoses. Circulation. 1998;97:1532–5.
24. Stevenson I, Kalman J. Magnetic resonance imaging in the diagnosis of arrhythmogenic right ventricular cardiomyopathy: the gold standard or just another imaging modality?. J Interv Card Electrophysiol. 2004;10:27–9.
25. Lopez-Fernandez T, Garcia-Fernandez MA, Perez David E, Moreno Yanguela M. Usefulness of contrast echocardiography in arrhythmogenic right ventricular dysplasia. J Am Soc Echocardiogr. 2004;17:391–3.
26. White JB, Razmi R, Nath H, Kay GN, Plumb VJ, Epstein AE. Relative utility of magnetic resonance imaging and right ventricular angiography to diagnose arrhythmogenic right ventricular cardiomyopathy. J Interv Card Electrophysiol. 2004;10:19–26.
27. Blake LM, Scheinman MM, Higgins CB. MR features of arrhythmogenic right ventricular dysplasia. AJR Am J Roentgenol. 1994;162:809–12.
28. Ricci C, Longo R, Pagnan L, Dalla Palma L, Pinamonti B, Camerini F, et al. Magnetic resonance imaging in right ventricular dysplasia. Am J Cardiol. 1992;70:1589–95.
29. Tandri H, Bomma C, Calkins H, Bluemke DA. Magnetic resonance and computed tomography imaging of arrhythmogenic right ventricular dysplasia. J Magn Reson Imaging. 2004;19:848–58.
30. Auffermann W, Wichter T, Breithardt G, Joachimsen K, Peters PE. Arrhythmogenic right ventricular disease: MR imaging vs angiography. AJR Am J Roentgenol. 1993;161:549–55.
31. Iesaka Y, Hiroe M, Aonuma K, Nitta J, Nogami A, Tokunaga T, et al. Usefulness of electrophysiologic study and endomyocardial biopsy in differentiating arrhythmogenic right ventricular dysplasia from idiopathic right ventricular tachycardia. Heart Vessels. 1990;5(suppl):65–9.
32. Niroomand F, Carbucicchio C, Tondo C, Riva S, Fassini G, Apostolo A, et al. Electrophysiological characteristics and outcome in patients with idiopathic right ventricular arrhythmia compared with arrhythmogenic right ventricular dysplasia. Heart. 2002;87:41–7.
33. Wichter T, Borggrefe M, Haverkamp W, Chen X, Breithardt G. Efficacy of antiarrhythmic drugs in patients with arrhythmogenic right ventricular disease. Results in patients with inducible and noninducible ventricular tachycardia. Circulation. 1992;86:29–37.
34. Leclercq JF, Coumel P. Characteristics, prognosis and treatment of the ventricular arrhythmias of right ventricular dysplasia. Eur Heart J. 1989;10(suppl D):61–7.
35. Fontaine G, Gallais Y, Fornes P, Hebert JL, Frank R. Arrhythmogenic right ventricular dysplasia/cardiomyopathy. Anesthesiology. 2001;95:250–4.
36. Fontaine G, Prost-Squarcioni C. Implantable cardioverter defibrillator in arrhythmogenic right ventricular cardiomyopathies. Circulation. 2004;109:1445–7.
37. Gregoratos G, Abrams J, Epstein AE, Freedman RA, Hayes DL, Hlatky MA, et al. ACC/AHA/NASPE 2002 guideline update for implantation of cardiac pacemakers and antiarrhythmia devices—summary article: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2002;40:1703–19.
38. Roguin A, Bomma CS, Nasir K, Tandri H, Tichnell C, James C, et al. Implantable cardioverter-defibrillators in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy. J Am Coll Cardiol. 2004;43:1843–52.
39. Corrado D, Leoni L, Link MS, Della Bella P, Gaita F, Curnis A, et al. Implantable cardioverter-defibrillator therapy for prevention of sudden death in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia. Circulation. 2003;108:3084–91.
40. Gear K, Marcus F. Arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation. 2003;107:e31–3.
41. Harrison TC, Kessler D. Arrhythmogenic right ventricular dysplasia/cardiomyopathy. Heart Lung. 2001;30:360–9.
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