Atrioventricular Block as the Initial Manifestation of Cardiac Sarcoidosis in Middle-Aged Adults
Cardiac Sarcoidosis Presenting as Atrioventricular Block Introduction Atrioventricular block (AVB) can be caused by several conditions, including cardiac sarcoidosis (CS). The prevalence of CS causing this presentation in a North American population has not been investigated and was the purpose of t...
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Published in | Journal of cardiovascular electrophysiology Vol. 25; no. 8; pp. 875 - 881 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.08.2014
Wiley Subscription Services, Inc |
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Abstract | Cardiac Sarcoidosis Presenting as Atrioventricular Block
Introduction
Atrioventricular block (AVB) can be caused by several conditions, including cardiac sarcoidosis (CS). The prevalence of CS causing this presentation in a North American population has not been investigated and was the purpose of this study.
Methods
We prospectively evaluated patients aged 18–60 years presenting with unexplained 2nd or 3rd degree AVB and no previous history of sarcoidosis in any organ. All patients had fluorodeoxyglucose‐positron emission tomography (FDG‐PET) scans for the evaluation of CS. Japanese Ministry of Health Welfare (JMHW) criteria and biopsy results were used to confirm the diagnosis of CS. Subjects with advanced imaging suggestive of CS were investigated for extracardiac involvement. Patients were followed for major adverse cardiac events.
Results
Thirty‐two patients presenting with unexplained AVB underwent cardiac and whole body FDG‐PET for the investigation of CS from February 2010 to June 2013. Mean age was 52.8 ± 6.2 years, and 20 were male. CS was diagnosed in 11/32 (34%) subjects and 11/11 were subsequently diagnosed with extra‐CS. Average follow‐up was 21 ± 9 months. Adverse events were observed in 3 subjects with CS but none in subjects with idiopathic AVB. All 3 patients presented with heart failure, 2 also had recurrent VT resulting in ICD shocks.
Conclusions
In this prospective study of consecutive patients aged ≤60 years presenting with unexplained AVB, we found that 11/32 (34%) had previously undiagnosed CS. Among patients with CS, 3/11 had adverse clinical outcomes compared with 0/21 (P = 0.011). Our data suggest that all patients aged ≤60 years with unexplained AVB should be investigated for CS. Moreover, patients diagnosed with CS should be closely followed. |
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AbstractList | Cardiac Sarcoidosis Presenting as Atrioventricular Block
Introduction
Atrioventricular block (AVB) can be caused by several conditions, including cardiac sarcoidosis (CS). The prevalence of CS causing this presentation in a North American population has not been investigated and was the purpose of this study.
Methods
We prospectively evaluated patients aged 18–60 years presenting with unexplained 2nd or 3rd degree AVB and no previous history of sarcoidosis in any organ. All patients had fluorodeoxyglucose‐positron emission tomography (FDG‐PET) scans for the evaluation of CS. Japanese Ministry of Health Welfare (JMHW) criteria and biopsy results were used to confirm the diagnosis of CS. Subjects with advanced imaging suggestive of CS were investigated for extracardiac involvement. Patients were followed for major adverse cardiac events.
Results
Thirty‐two patients presenting with unexplained AVB underwent cardiac and whole body FDG‐PET for the investigation of CS from February 2010 to June 2013. Mean age was 52.8 ± 6.2 years, and 20 were male. CS was diagnosed in 11/32 (34%) subjects and 11/11 were subsequently diagnosed with extra‐CS. Average follow‐up was 21 ± 9 months. Adverse events were observed in 3 subjects with CS but none in subjects with idiopathic AVB. All 3 patients presented with heart failure, 2 also had recurrent VT resulting in ICD shocks.
Conclusions
In this prospective study of consecutive patients aged ≤60 years presenting with unexplained AVB, we found that 11/32 (34%) had previously undiagnosed CS. Among patients with CS, 3/11 had adverse clinical outcomes compared with 0/21 (P = 0.011). Our data suggest that all patients aged ≤60 years with unexplained AVB should be investigated for CS. Moreover, patients diagnosed with CS should be closely followed. Atrioventricular block (AVB) can be caused by several conditions, including cardiac sarcoidosis (CS). The prevalence of CS causing this presentation in a North American population has not been investigated and was the purpose of this study. We prospectively evaluated patients aged 18-60 years presenting with unexplained 2nd or 3rd degree AVB and no previous history of sarcoidosis in any organ. All patients had fluorodeoxyglucose-positron emission tomography (FDG-PET) scans for the evaluation of CS. Japanese Ministry of Health Welfare (JMHW) criteria and biopsy results were used to confirm the diagnosis of CS. Subjects with advanced imaging suggestive of CS were investigated for extracardiac involvement. Patients were followed for major adverse cardiac events. Thirty-two patients presenting with unexplained AVB underwent cardiac and whole body FDG-PET for the investigation of CS from February 2010 to June 2013. Mean age was 52.8 ± 6.2 years, and 20 were male. CS was diagnosed in 11/32 (34%) subjects and 11/11 were subsequently diagnosed with extra-CS. Average follow-up was 21 ± 9 months. Adverse events were observed in 3 subjects with CS but none in subjects with idiopathic AVB. All 3 patients presented with heart failure, 2 also had recurrent VT resulting in ICD shocks. In this prospective study of consecutive patients aged ≤60 years presenting with unexplained AVB, we found that 11/32 (34%) had previously undiagnosed CS. Among patients with CS, 3/11 had adverse clinical outcomes compared with 0/21 (P = 0.011). Our data suggest that all patients aged ≤60 years with unexplained AVB should be investigated for CS. Moreover, patients diagnosed with CS should be closely followed. Atrioventricular block (AVB) can be caused by several conditions, including cardiac sarcoidosis (CS). The prevalence of CS causing this presentation in a North American population has not been investigated and was the purpose of this study.INTRODUCTIONAtrioventricular block (AVB) can be caused by several conditions, including cardiac sarcoidosis (CS). The prevalence of CS causing this presentation in a North American population has not been investigated and was the purpose of this study.We prospectively evaluated patients aged 18-60 years presenting with unexplained 2nd or 3rd degree AVB and no previous history of sarcoidosis in any organ. All patients had fluorodeoxyglucose-positron emission tomography (FDG-PET) scans for the evaluation of CS. Japanese Ministry of Health Welfare (JMHW) criteria and biopsy results were used to confirm the diagnosis of CS. Subjects with advanced imaging suggestive of CS were investigated for extracardiac involvement. Patients were followed for major adverse cardiac events.METHODSWe prospectively evaluated patients aged 18-60 years presenting with unexplained 2nd or 3rd degree AVB and no previous history of sarcoidosis in any organ. All patients had fluorodeoxyglucose-positron emission tomography (FDG-PET) scans for the evaluation of CS. Japanese Ministry of Health Welfare (JMHW) criteria and biopsy results were used to confirm the diagnosis of CS. Subjects with advanced imaging suggestive of CS were investigated for extracardiac involvement. Patients were followed for major adverse cardiac events.Thirty-two patients presenting with unexplained AVB underwent cardiac and whole body FDG-PET for the investigation of CS from February 2010 to June 2013. Mean age was 52.8 ± 6.2 years, and 20 were male. CS was diagnosed in 11/32 (34%) subjects and 11/11 were subsequently diagnosed with extra-CS. Average follow-up was 21 ± 9 months. Adverse events were observed in 3 subjects with CS but none in subjects with idiopathic AVB. All 3 patients presented with heart failure, 2 also had recurrent VT resulting in ICD shocks.RESULTSThirty-two patients presenting with unexplained AVB underwent cardiac and whole body FDG-PET for the investigation of CS from February 2010 to June 2013. Mean age was 52.8 ± 6.2 years, and 20 were male. CS was diagnosed in 11/32 (34%) subjects and 11/11 were subsequently diagnosed with extra-CS. Average follow-up was 21 ± 9 months. Adverse events were observed in 3 subjects with CS but none in subjects with idiopathic AVB. All 3 patients presented with heart failure, 2 also had recurrent VT resulting in ICD shocks.In this prospective study of consecutive patients aged ≤60 years presenting with unexplained AVB, we found that 11/32 (34%) had previously undiagnosed CS. Among patients with CS, 3/11 had adverse clinical outcomes compared with 0/21 (P = 0.011). Our data suggest that all patients aged ≤60 years with unexplained AVB should be investigated for CS. Moreover, patients diagnosed with CS should be closely followed.CONCLUSIONSIn this prospective study of consecutive patients aged ≤60 years presenting with unexplained AVB, we found that 11/32 (34%) had previously undiagnosed CS. Among patients with CS, 3/11 had adverse clinical outcomes compared with 0/21 (P = 0.011). Our data suggest that all patients aged ≤60 years with unexplained AVB should be investigated for CS. Moreover, patients diagnosed with CS should be closely followed. Cardiac Sarcoidosis Presenting as Atrioventricular Block Introduction Atrioventricular block (AVB) can be caused by several conditions, including cardiac sarcoidosis (CS). The prevalence of CS causing this presentation in a North American population has not been investigated and was the purpose of this study. Methods We prospectively evaluated patients aged 18-60 years presenting with unexplained 2nd or 3rd degree AVB and no previous history of sarcoidosis in any organ. All patients had fluorodeoxyglucose-positron emission tomography (FDG-PET) scans for the evaluation of CS. Japanese Ministry of Health Welfare (JMHW) criteria and biopsy results were used to confirm the diagnosis of CS. Subjects with advanced imaging suggestive of CS were investigated for extracardiac involvement. Patients were followed for major adverse cardiac events. Results Thirty-two patients presenting with unexplained AVB underwent cardiac and whole body FDG-PET for the investigation of CS from February 2010 to June 2013. Mean age was 52.8 ± 6.2 years, and 20 were male. CS was diagnosed in 11/32 (34%) subjects and 11/11 were subsequently diagnosed with extra-CS. Average follow-up was 21 ± 9 months. Adverse events were observed in 3 subjects with CS but none in subjects with idiopathic AVB. All 3 patients presented with heart failure, 2 also had recurrent VT resulting in ICD shocks. Conclusions In this prospective study of consecutive patients aged ≤60 years presenting with unexplained AVB, we found that 11/32 (34%) had previously undiagnosed CS. Among patients with CS, 3/11 had adverse clinical outcomes compared with 0/21 (P = 0.011). Our data suggest that all patients aged ≤60 years with unexplained AVB should be investigated for CS. Moreover, patients diagnosed with CS should be closely followed. [PUBLICATION ABSTRACT] |
Author | GREEN, MARTIN GOLLOB, MICHAEL H. BIRNIE, DAVID H. LEUNG, EUGENE BEANLANDS, ROB S. MCARDLE, BRIAN A. YANG, JIM NERY, PABLO B. DAVIS, DARRYL HEALEY, JEFF S. NAIR, GIRISH M. OHIRA, HIROSHI |
Author_xml | – sequence: 1 givenname: PABLO B. surname: NERY fullname: NERY, PABLO B. email: PNery@ottawaheart.ca organization: Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada – sequence: 2 givenname: ROB S. surname: BEANLANDS fullname: BEANLANDS, ROB S. organization: Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada – sequence: 3 givenname: GIRISH M. surname: NAIR fullname: NAIR, GIRISH M. organization: Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada – sequence: 4 givenname: MARTIN surname: GREEN fullname: GREEN, MARTIN organization: Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada – sequence: 5 givenname: JIM surname: YANG fullname: YANG, JIM organization: Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada – sequence: 6 givenname: BRIAN A. surname: MCARDLE fullname: MCARDLE, BRIAN A. organization: Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada – sequence: 7 givenname: DARRYL surname: DAVIS fullname: DAVIS, DARRYL organization: Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada – sequence: 8 givenname: HIROSHI surname: OHIRA fullname: OHIRA, HIROSHI organization: Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada – sequence: 9 givenname: MICHAEL H. surname: GOLLOB fullname: GOLLOB, MICHAEL H. organization: Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada – sequence: 10 givenname: EUGENE surname: LEUNG fullname: LEUNG, EUGENE organization: Division of Nuclear Medicine, Department of Medicine, University of Ottawa and The Ottawa Hospital, Ottawa, Canada – sequence: 11 givenname: JEFF S. surname: HEALEY fullname: HEALEY, JEFF S. organization: Population Health Research Institute, McMaster University, Ontario, Hamilton, Canada – sequence: 12 givenname: DAVID H. surname: BIRNIE fullname: BIRNIE, DAVID H. organization: Division of Cardiology, Department of Medicine, University of Ottawa Heart Institute, Ottawa, Canada |
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Keywords | prevalence cardiac sarcoidosis implantable cardioverter defibrillator pacing ventricular tachycardia outcomes atrioventricular block middle-aged |
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Notes | ArticleID:JCE12401 istex:19E9499ED2CDE344C7B05B86BE6E704A96C84288 ark:/67375/WNG-24XTLMZP-3 Cardiac Care Network of Ontario R. S. Beanlands serves as consultant to GE Healthcare and Jubilant Draximage. Other authors: No disclosures. D. H. Birnie is a career investigator supported by the Heart and Stroke Foundation of Ontario. R. S. Beanlands is a career investigator supported by the Heart and Stroke Foundation of Ontario and Tier 1 Research Chair supported by the University of Ottawa. This project was supported in part by the Cardiac Care Network of Ontario. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
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PublicationDate | August 2014 |
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PublicationTitle | Journal of cardiovascular electrophysiology |
PublicationTitleAlternate | J Cardiovasc Electrophysiol |
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References | Mc Ardle BA, Birnie DH, Klein R, de Kemp RA, Leung E, Renaud J, DaSilva J, Wells GA, Beanlands RS, Nery PB: Is there an association between clinical presentation and the location and extent of myocardial involvement of cardiac sarcoidosis as assessed by 18f- fluorodeoxyglucose positron emission tomography? Circ Cardiovasc Imaging 2013;6:617-626. Kandolin R, Lehtonen J, Graner M, Schildt J, Salmenkivi K, Kivistö SM, Kupari M: Diagnosing isolated cardiac sarcoidosis. J Intern Med 2011;270:461-468. Barra SN, Providencia R, Paiva L, Nascimento J, Marques AL: A review on advanced atrioventricular block in young or middle-aged adults. Pacing Clin Electrophysiol 2012;35:1395-1405. Redheuil AB, Paziaud O, Mousseaux E: Ventricular tachycardia and cardiac sarcoidosis: Correspondence between MRI and electrophysiology. Eur Heart J 2006;27:1430. Ramachandran V, Stevens MP, Amin M, Appleton D, Abbate A: Bi-fascicular block on EKG as the initial presenting sign of cardiac sarcoidosis. Int J Cardiol 2007;118:e1-e2. Yoshida Y, Morimoto S, Hiramitsu S, Tsuboi N, Hirayama H, Itoh T: Incidence of cardiac sarcoidosis in Japanese patients with high-degree atrioventricular block. Am Heart J 1997;134:382-386. Tavora F, Cresswell N, Li L, Ripple M, Solomon C, Burke A: Comparison of necropsy findings in patients with sarcoidosis dying suddenly from cardiac sarcoidosis versus dying suddenly from other causes. Am J Cardiol 2009;104:571-577. Doughan AR, Williams BR: Cardiac sarcoidosis. Heart 2006;92:282-288. Kavanagh T, Huang S: Cardiac sarcoidosis: An unforeseen cause of sudden death. Can J Cardiol 1995;11:136-138. Banba K, Kusano KF, Nakamura K, Morita H, Ogawa A, Ohtsuka F, Ogo KO, Nishii N, Watanabe A, Nagase S, Sakuragi S, Ohe T: Relationship between arrhythmogenesis and disease activity in cardiac sarcoidosis. Heart Rhythm 2007;4:1292-1299. Kron J, Sauer W, Schuller J, Bogun F, Crawford T, Sarsam S, Rosenfeld L, Mitiku TY, Cooper JM, Mehta D, Greenspon AJ, Ortman M, Delurgio DB, Valadri R, Narasimhan C, Swapna N, Singh JP, Danik S, Markowitz SM, Almquist AK, Krahn AD, Wolfe LG, Feinstein S, Ellenbogen KA: Efficacy and safety of implantable cardiac defibrillators for treatment of ventricular arrhythmias in patients with cardiac sarcoidosis. Europace 2013;15:347-354. Donsky AS, Escobar J, Capehart J, Roberts WC: Heart transplantation for undiagnosed cardiac sarcoidosis. Am J Cardiol 2002;89:1447-1450. Fawcett FJ, Goldberg MJ: Heart block resulting from myocardial sarcoidosis. Br Heart J 1974;36:220-223. Koplan BA, Soejima K, Baughman K, Epstein LM, Stevenson WG: Refractory ventricular tachycardia secondary to cardiac sarcoid: Electrophysiologic characteristics, mapping, and ablation. Heart Rhythm 2006;3:924-929. Sadek M, Yung D, Birnie DH, Beanlands RS, Nery PB: Corticosteroid therapy for cardiac sarcoidosis: A systematic review. Can J Cardiol 2013;29:1034-1041. Kandolin R, Lehtonen J, Kupari M: Cardiac sarcoidosis and giant cell myocarditis as causes of atrioventricular block in young and middle-aged adults. Circ Arrhythm Electrophysiol 2011;4:303-309. Ayyala US, Nair AP, Padilla ML: Cardiac sarcoidosis. Clin Chest Med 2008;29:493-508. Cooper LT Jr, Blauwet LA: When should high-grade heart block trigger a search for a treatable cardiomyopathy? Circ Arrhythm Electrophysiol 2011;4:260-261. Sato H, Woodhead FA, Ahmad T, Grutters JC, Spagnolo P, van den Bosch JM, Maier LA, Newman LS, Nagai S, Izumi T, Wells AU, du Bois RM, Welsh KI: Sarcoidosis HLA class II genotyping distinguishes differences of clinical phenotype across ethnic groups. Hum Mol Genet 2010;19:4100-4111. Spagnolo P, du Bois RM: Genetics of sarcoidosis. Clin Dermatol 2007;25:242-249. Nery PB, Keren A, Healey J, Leug E, Beanlands RS, Birnie DH: Isolated cardiac sarcoidosis: Establishing the diagnosis with electroanatomic mapping-guided endomyocardial biopsy. Can J Cardiol 2012;29:1015e1-1015e3. Rajani R, Prasad S, O'Nunain S, Sohal M, Ghuran A: Heart block: A primary manifestation of sarcoidosis. Europace 2010;12:284-288. Ruiz-Arango A, Sharma GK: Exercise intolerance and multiple conduction abnormalities as first manifestation of cardiac sarcoidosis. South Med J 2008;101:1059-1061. Furushima H, Chinushi M, Sugiura H, Kasai H, Washizuka T, Aizawa Y: Ventricular tachyarrhythmia associated with cardiac sarcoidosis: Its mechanisms and outcome. Clin Cardiol 2004;27:217-222. Felker GM, Hu W, Hare JM, Hruban RH, Baughman KL, Kasper EK: The spectrum of dilated cardiomyopathy. The Johns Hopkins experience with 1,278 patients. Medicine (Baltimore) 1999;78:270-283. Nery PB, Mc Ardle BA, Redpath CJ, Beanlands RS, Birnie DH: Prevalence of cardiac sarcoidosis in patients presenting with monomorphic ventricular tachycardia. Pacing Clin Electrophysiol 2014;37:364-74. doi: 10.1111/pace.12277. Mohsen A, Jimenez A, Hood RE, Dickfeld T, Saliaris A, Shorofsky S, Saba MM: Cardiac sarcoidosis: Electrophysiological outcomes on long-term follow-up and the role of the implantable cardioverter-defibrillator. J Cardiovasc Electrophysiol 2013;24:doi: 10.1111/jce.12302. Britton KA, Stevenson WG, Levy BD, Katz JT, Loscalzo J: Clinical problem-solving. The beat goes on. N Engl J Med 2010;362:1721-1726. Soejima K, Yada H: The work-up and management of patients with apparent or subclinical cardiac sarcoidosis: With emphasis on the associated heart rhythm abnormalities. J Cardiovasc Electrophysiol 2009;20:578-583. Epstein AE, Dimarco JP, Ellenbogen KA, Estes NA 3rd, Freedman RA, Gettes LS, Gillinov AM, Gregoratos G, Hammill SC, Hayes DL, Hlatky MA, Newby LK, Page RL, Schoenfeld MH, Silka MJ, Stevenson LW, Sweeney MO: 2012 ACCF/AHA/HRS Focused update incorporated into the ACCF/AHA/HRS 2008 guidelines for device-based therapy of cardiac rhythm abnormalities. Circulation 2013;127:e283-352. 2006; 92 2010; 12 2013; 29 1974; 36 2009; 20 2010; 19 2004; 27 2013; 24 2013; 127 1995; 11 1997; 134 2010; 362 2006; 3 2011; 4 2008; 101 2012; 35 2013; 6 2011; 270 2007; 118 2013; 15 2002; 89 2006; 27 2008; 29 2014; 37 1999; 78 2012; 29 2007; 4 2007; 25 2009; 104 Kavanagh T (e_1_2_14_7_1) 1995; 11 e_1_2_14_30_1 e_1_2_14_31_1 e_1_2_14_11_1 e_1_2_14_10_1 e_1_2_14_13_1 e_1_2_14_12_1 e_1_2_14_15_1 e_1_2_14_14_1 e_1_2_14_17_1 e_1_2_14_16_1 e_1_2_14_29_1 e_1_2_14_6_1 e_1_2_14_5_1 e_1_2_14_8_1 e_1_2_14_9_1 e_1_2_14_2_1 e_1_2_14_20_1 e_1_2_14_4_1 e_1_2_14_3_1 e_1_2_14_23_1 e_1_2_14_24_1 e_1_2_14_21_1 e_1_2_14_22_1 e_1_2_14_27_1 e_1_2_14_28_1 e_1_2_14_25_1 e_1_2_14_26_1 e_1_2_14_19_1 e_1_2_14_18_1 |
References_xml | – reference: Britton KA, Stevenson WG, Levy BD, Katz JT, Loscalzo J: Clinical problem-solving. The beat goes on. N Engl J Med 2010;362:1721-1726. – reference: Koplan BA, Soejima K, Baughman K, Epstein LM, Stevenson WG: Refractory ventricular tachycardia secondary to cardiac sarcoid: Electrophysiologic characteristics, mapping, and ablation. Heart Rhythm 2006;3:924-929. – reference: Fawcett FJ, Goldberg MJ: Heart block resulting from myocardial sarcoidosis. Br Heart J 1974;36:220-223. – reference: Kavanagh T, Huang S: Cardiac sarcoidosis: An unforeseen cause of sudden death. Can J Cardiol 1995;11:136-138. – reference: Epstein AE, Dimarco JP, Ellenbogen KA, Estes NA 3rd, Freedman RA, Gettes LS, Gillinov AM, Gregoratos G, Hammill SC, Hayes DL, Hlatky MA, Newby LK, Page RL, Schoenfeld MH, Silka MJ, Stevenson LW, Sweeney MO: 2012 ACCF/AHA/HRS Focused update incorporated into the ACCF/AHA/HRS 2008 guidelines for device-based therapy of cardiac rhythm abnormalities. Circulation 2013;127:e283-352. – reference: Tavora F, Cresswell N, Li L, Ripple M, Solomon C, Burke A: Comparison of necropsy findings in patients with sarcoidosis dying suddenly from cardiac sarcoidosis versus dying suddenly from other causes. Am J Cardiol 2009;104:571-577. – reference: Kandolin R, Lehtonen J, Kupari M: Cardiac sarcoidosis and giant cell myocarditis as causes of atrioventricular block in young and middle-aged adults. Circ Arrhythm Electrophysiol 2011;4:303-309. – reference: Redheuil AB, Paziaud O, Mousseaux E: Ventricular tachycardia and cardiac sarcoidosis: Correspondence between MRI and electrophysiology. Eur Heart J 2006;27:1430. – reference: Kron J, Sauer W, Schuller J, Bogun F, Crawford T, Sarsam S, Rosenfeld L, Mitiku TY, Cooper JM, Mehta D, Greenspon AJ, Ortman M, Delurgio DB, Valadri R, Narasimhan C, Swapna N, Singh JP, Danik S, Markowitz SM, Almquist AK, Krahn AD, Wolfe LG, Feinstein S, Ellenbogen KA: Efficacy and safety of implantable cardiac defibrillators for treatment of ventricular arrhythmias in patients with cardiac sarcoidosis. Europace 2013;15:347-354. – reference: Donsky AS, Escobar J, Capehart J, Roberts WC: Heart transplantation for undiagnosed cardiac sarcoidosis. Am J Cardiol 2002;89:1447-1450. – reference: Yoshida Y, Morimoto S, Hiramitsu S, Tsuboi N, Hirayama H, Itoh T: Incidence of cardiac sarcoidosis in Japanese patients with high-degree atrioventricular block. Am Heart J 1997;134:382-386. – reference: Soejima K, Yada H: The work-up and management of patients with apparent or subclinical cardiac sarcoidosis: With emphasis on the associated heart rhythm abnormalities. J Cardiovasc Electrophysiol 2009;20:578-583. – reference: Barra SN, Providencia R, Paiva L, Nascimento J, Marques AL: A review on advanced atrioventricular block in young or middle-aged adults. Pacing Clin Electrophysiol 2012;35:1395-1405. – reference: Furushima H, Chinushi M, Sugiura H, Kasai H, Washizuka T, Aizawa Y: Ventricular tachyarrhythmia associated with cardiac sarcoidosis: Its mechanisms and outcome. Clin Cardiol 2004;27:217-222. – reference: Doughan AR, Williams BR: Cardiac sarcoidosis. Heart 2006;92:282-288. – reference: Sato H, Woodhead FA, Ahmad T, Grutters JC, Spagnolo P, van den Bosch JM, Maier LA, Newman LS, Nagai S, Izumi T, Wells AU, du Bois RM, Welsh KI: Sarcoidosis HLA class II genotyping distinguishes differences of clinical phenotype across ethnic groups. Hum Mol Genet 2010;19:4100-4111. – reference: Mohsen A, Jimenez A, Hood RE, Dickfeld T, Saliaris A, Shorofsky S, Saba MM: Cardiac sarcoidosis: Electrophysiological outcomes on long-term follow-up and the role of the implantable cardioverter-defibrillator. J Cardiovasc Electrophysiol 2013;24:doi: 10.1111/jce.12302. – reference: Cooper LT Jr, Blauwet LA: When should high-grade heart block trigger a search for a treatable cardiomyopathy? Circ Arrhythm Electrophysiol 2011;4:260-261. – reference: Spagnolo P, du Bois RM: Genetics of sarcoidosis. Clin Dermatol 2007;25:242-249. – reference: Ruiz-Arango A, Sharma GK: Exercise intolerance and multiple conduction abnormalities as first manifestation of cardiac sarcoidosis. South Med J 2008;101:1059-1061. – reference: Nery PB, Mc Ardle BA, Redpath CJ, Beanlands RS, Birnie DH: Prevalence of cardiac sarcoidosis in patients presenting with monomorphic ventricular tachycardia. Pacing Clin Electrophysiol 2014;37:364-74. doi: 10.1111/pace.12277. – reference: Felker GM, Hu W, Hare JM, Hruban RH, Baughman KL, Kasper EK: The spectrum of dilated cardiomyopathy. The Johns Hopkins experience with 1,278 patients. Medicine (Baltimore) 1999;78:270-283. – reference: Mc Ardle BA, Birnie DH, Klein R, de Kemp RA, Leung E, Renaud J, DaSilva J, Wells GA, Beanlands RS, Nery PB: Is there an association between clinical presentation and the location and extent of myocardial involvement of cardiac sarcoidosis as assessed by 18f- fluorodeoxyglucose positron emission tomography? Circ Cardiovasc Imaging 2013;6:617-626. – reference: Nery PB, Keren A, Healey J, Leug E, Beanlands RS, Birnie DH: Isolated cardiac sarcoidosis: Establishing the diagnosis with electroanatomic mapping-guided endomyocardial biopsy. Can J Cardiol 2012;29:1015e1-1015e3. – reference: Kandolin R, Lehtonen J, Graner M, Schildt J, Salmenkivi K, Kivistö SM, Kupari M: Diagnosing isolated cardiac sarcoidosis. J Intern Med 2011;270:461-468. – reference: Rajani R, Prasad S, O'Nunain S, Sohal M, Ghuran A: Heart block: A primary manifestation of sarcoidosis. Europace 2010;12:284-288. – reference: Ayyala US, Nair AP, Padilla ML: Cardiac sarcoidosis. Clin Chest Med 2008;29:493-508. – reference: Ramachandran V, Stevens MP, Amin M, Appleton D, Abbate A: Bi-fascicular block on EKG as the initial presenting sign of cardiac sarcoidosis. Int J Cardiol 2007;118:e1-e2. – reference: Sadek M, Yung D, Birnie DH, Beanlands RS, Nery PB: Corticosteroid therapy for cardiac sarcoidosis: A systematic review. Can J Cardiol 2013;29:1034-1041. – reference: Banba K, Kusano KF, Nakamura K, Morita H, Ogawa A, Ohtsuka F, Ogo KO, Nishii N, Watanabe A, Nagase S, Sakuragi S, Ohe T: Relationship between arrhythmogenesis and disease activity in cardiac sarcoidosis. Heart Rhythm 2007;4:1292-1299. – volume: 101 start-page: 1059 year: 2008 end-page: 1061 article-title: Exercise intolerance and multiple conduction abnormalities as first manifestation of cardiac sarcoidosis publication-title: South Med J – volume: 362 start-page: 1721 year: 2010 end-page: 1726 article-title: Clinical problem‐solving. The beat goes on publication-title: N Engl J Med – volume: 29 start-page: 1015e1 year: 2012 end-page: 1015e3 article-title: Isolated cardiac sarcoidosis: Establishing the diagnosis with electroanatomic mapping‐guided endomyocardial biopsy publication-title: Can J Cardiol – volume: 37 start-page: 364 year: 2014 end-page: 74 article-title: Prevalence of cardiac sarcoidosis in patients presenting with monomorphic ventricular tachycardia publication-title: Pacing Clin Electrophysiol – volume: 118 start-page: e1 year: 2007 end-page: e2 article-title: Bi‐fascicular block on EKG as the initial presenting sign of cardiac sarcoidosis publication-title: Int J Cardiol – volume: 127 start-page: e283 year: 2013 end-page: 352 article-title: 2012 ACCF/AHA/HRS Focused update incorporated into the ACCF/AHA/HRS 2008 guidelines for device‐based therapy of cardiac rhythm abnormalities publication-title: Circulation – volume: 20 start-page: 578 year: 2009 end-page: 583 article-title: The work‐up and management of patients with apparent or subclinical cardiac sarcoidosis: With emphasis on the associated heart rhythm abnormalities publication-title: J Cardiovasc Electrophysiol – volume: 270 start-page: 461 year: 2011 end-page: 468 article-title: Diagnosing isolated cardiac sarcoidosis publication-title: J Intern Med – volume: 35 start-page: 1395 year: 2012 end-page: 1405 article-title: A review on advanced atrioventricular block in young or middle‐aged adults publication-title: Pacing Clin Electrophysiol – volume: 78 start-page: 270 year: 1999 end-page: 283 article-title: The spectrum of dilated cardiomyopathy. The Johns Hopkins experience with 1,278 patients publication-title: Medicine (Baltimore) – volume: 3 start-page: 924 year: 2006 end-page: 929 article-title: Refractory ventricular tachycardia secondary to cardiac sarcoid: Electrophysiologic characteristics, mapping, and ablation publication-title: Heart Rhythm – volume: 4 start-page: 303 year: 2011 end-page: 309 article-title: Cardiac sarcoidosis and giant cell myocarditis as causes of atrioventricular block in young and middle‐aged adults publication-title: Circ Arrhythm Electrophysiol – volume: 89 start-page: 1447 year: 2002 end-page: 1450 article-title: Heart transplantation for undiagnosed cardiac sarcoidosis publication-title: Am J Cardiol – volume: 4 start-page: 1292 year: 2007 end-page: 1299 article-title: Relationship between arrhythmogenesis and disease activity in cardiac sarcoidosis publication-title: Heart Rhythm – volume: 29 start-page: 493 year: 2008 end-page: 508 article-title: Cardiac sarcoidosis publication-title: Clin Chest Med – volume: 29 start-page: 1034 year: 2013 end-page: 1041 article-title: Corticosteroid therapy for cardiac sarcoidosis: A systematic review publication-title: Can J Cardiol – volume: 19 start-page: 4100 year: 2010 end-page: 4111 article-title: Sarcoidosis HLA class II genotyping distinguishes differences of clinical phenotype across ethnic groups publication-title: Hum Mol Genet – volume: 12 start-page: 284 year: 2010 end-page: 288 article-title: Heart block: A primary manifestation of sarcoidosis publication-title: Europace – volume: 27 start-page: 217 year: 2004 end-page: 222 article-title: Ventricular tachyarrhythmia associated with cardiac sarcoidosis: Its mechanisms and outcome publication-title: Clin Cardiol – volume: 92 start-page: 282 year: 2006 end-page: 288 article-title: Cardiac sarcoidosis publication-title: Heart – volume: 134 start-page: 382 year: 1997 end-page: 386 article-title: Incidence of cardiac sarcoidosis in Japanese patients with high‐degree atrioventricular block publication-title: Am Heart J – volume: 6 start-page: 617 year: 2013 end-page: 626 article-title: Is there an association between clinical presentation and the location and extent of myocardial involvement of cardiac sarcoidosis as assessed by 18f‐ fluorodeoxyglucose positron emission tomography publication-title: Circ Cardiovasc Imaging – volume: 15 start-page: 347 year: 2013 end-page: 354 article-title: Efficacy and safety of implantable cardiac defibrillators for treatment of ventricular arrhythmias in patients with cardiac sarcoidosis publication-title: Europace – volume: 11 start-page: 136 year: 1995 end-page: 138 article-title: Cardiac sarcoidosis: An unforeseen cause of sudden death publication-title: Can J Cardiol – volume: 27 start-page: 1430 year: 2006 article-title: Ventricular tachycardia and cardiac sarcoidosis: Correspondence between MRI and electrophysiology publication-title: Eur Heart J – volume: 36 start-page: 220 year: 1974 end-page: 223 article-title: Heart block resulting from myocardial sarcoidosis publication-title: Br Heart J – volume: 4 start-page: 260 year: 2011 end-page: 261 article-title: When should high‐grade heart block trigger a search for a treatable cardiomyopathy publication-title: Circ Arrhythm Electrophysiol – volume: 25 start-page: 242 year: 2007 end-page: 249 article-title: Genetics of sarcoidosis publication-title: Clin Dermatol – volume: 24 year: 2013 article-title: Cardiac sarcoidosis: Electrophysiological outcomes on long‐term follow‐up and the role of the implantable cardioverter‐defibrillator publication-title: J Cardiovasc Electrophysiol – volume: 104 start-page: 571 year: 2009 end-page: 577 article-title: Comparison of necropsy findings in patients with sarcoidosis dying suddenly from cardiac sarcoidosis versus dying suddenly from other causes publication-title: Am J Cardiol – ident: e_1_2_14_12_1 doi: 10.1136/hrt.36.2.220 – ident: e_1_2_14_4_1 doi: 10.1093/hmg/ddq325 – ident: e_1_2_14_20_1 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Snippet | Cardiac Sarcoidosis Presenting as Atrioventricular Block
Introduction
Atrioventricular block (AVB) can be caused by several conditions, including cardiac... Atrioventricular block (AVB) can be caused by several conditions, including cardiac sarcoidosis (CS). The prevalence of CS causing this presentation in a North... Cardiac Sarcoidosis Presenting as Atrioventricular Block Introduction Atrioventricular block (AVB) can be caused by several conditions, including cardiac... |
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SubjectTerms | Adolescent Adrenal Cortex Hormones - therapeutic use Adult atrioventricular block Atrioventricular Block - diagnosis Atrioventricular Block - epidemiology Atrioventricular Block - therapy Biopsy cardiac sarcoidosis Cardiology Cardiomyopathies - diagnosis Cardiomyopathies - drug therapy Cardiomyopathies - epidemiology Defibrillators, Implantable Disease-Free Survival Electric Countershock - instrumentation Electrocardiography Female Fluorodeoxyglucose F18 Heart Failure - epidemiology Humans Immunosuppressive Agents - therapeutic use implantable cardioverter defibrillator Male Medical research Middle Aged Ontario - epidemiology outcomes pacing Positron-Emission Tomography Predictive Value of Tests Prevalence Prospective Studies Radiopharmaceuticals Recurrence Risk Factors Sarcoidosis Sarcoidosis - diagnosis Sarcoidosis - drug therapy Sarcoidosis - epidemiology Tachycardia, Ventricular - epidemiology Time Factors Tomography, X-Ray Computed ventricular tachycardia Young Adult |
Title | Atrioventricular Block as the Initial Manifestation of Cardiac Sarcoidosis in Middle-Aged Adults |
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