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      Aetiologies and temporal trends of atrioventricular block in young patients: a 20-year nationwide study

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          Abstract

          Aims

          To describe aetiologies and temporal trends in young patients with atrioventricular block (AVB).

          Methods and results

          We identified all patients in Denmark, receiving their first pacemaker because of AVB before the age of 50 years between 1996 and 2015. Medical records were reviewed and clinical information and diagnostic work-up results were obtained to evaluate the aetiology. We used Poisson regression testing for temporal trends. One thousand and twenty-seven patients were identified, median age at time of implantation was 38 (interquartile range 25–45) years, 584 (56.9%) were male. The aetiologies were complications to cardiac surgery [ n = 157 (15.3%)], congenital AVB [ n = 93 (9.0%)], cardioinhibitory reflex [ n = 52 (5.0%)], congenital heart disease [ n = 43 (4.2%)], complication to radiofrequency ablation [ n = 35 (3.4%)], cardiomyopathy [ n = 31 (3.0%)], endocarditis [ n = 18 (1.7%)], muscular dystrophy [ n = 14 (1.4%)], ischaemic heart disease [ n = 14 (1.4%)], sarcoidosis [ n = 11 (1.1%)], borreliosis [ n = 9 (0.9%)], hereditary [ n = 6 (0.6%)], side-effect to antiarrhythmics [ n = 6 (0.6%)], planned His-ablation [ n = 5 (0.5%)], complication to alcohol septal ablation [ n = 5 (0.5%)], and other known aetiologies [ n = 11 (1.1%)]. The aetiology remained unknown in 517 (50.3%) cases. While the number of patients with unknown aetiology increased during the study period ( P < 0.001), we observed no significant change in the number of patients with identified aetiology ( P = 0.35).

          Conclusion

          In a nationwide cohort, the aetiology of AVB was identified in only half the patients younger than 50 years referred for first-time pacemaker implantation. The number of patients with unknown aetiology increased during the study period. These findings indicate need for better insight into aetiologies of AVB and improved diagnostic work-up guidelines.

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          Most cited references17

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          Sarcoidosis.

          Sarcoidosis is a systemic disease of unknown cause that is characterised by the formation of immune granulomas in various organs, mainly the lungs and the lymphatic system. Studies show that sarcoidosis might be the result of an exaggerated granulomatous reaction after exposure to unidentified antigens in individuals who are genetically susceptible. Several new insights have been made, particularly with regards to the diagnosis and care of some important manifestations of sarcoidosis. The indications for endobronchial ultrasound in diagnosis and for PET in the assessment of inflammatory activity are now better specified. Recognition of unexplained persistent disabling symptoms, fatigue, small-fibre neurological impairment, cognitive failure, and changes to health state and quality of life, has improved. Mortality in patients with sarcoidosis is higher than that of the general population, mainly due to pulmonary fibrosis. Predicted advances for the future are finding the cause of sarcoidosis, and the elucidation of relevant biomarkers, reliable endpoints, and new efficient treatments, particularly in patients with refractory sarcoidosis, lung fibrosis, and those with persistent disabling symptoms. Copyright © 2014 Elsevier Ltd. All rights reserved.
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            Cardiac Sarcoidosis.

            Clinically manifest cardiac involvement occurs in perhaps 5% of patients with sarcoidosis. The 3 principal manifestations of cardiac sarcoidosis (CS) are conduction abnormalities, ventricular arrhythmias, and heart failure. An estimated 20% to 25% of patients with pulmonary/systemic sarcoidosis have asymptomatic cardiac involvement (clinically silent disease). In 2014, the first international guideline for the diagnosis and management of CS was published. In patients with clinically manifest CS, the extent of left ventricular dysfunction seems to be the most important predictor of prognosis. There is controversy in published reports as to the outcome of patients with clinically silent CS. Despite a paucity of data, immunosuppression therapy (primarily with corticosteroids) has been advocated for the treatment of clinically manifest CS. Device therapy, primarily with implantable cardioverter-defibrillators, is often recommended for patients with clinically manifest disease.
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              Atrioventricular Block as the Initial Manifestation of Cardiac Sarcoidosis in Middle-Aged Adults

              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.
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                Author and article information

                Journal
                Europace
                Europace
                europace
                Europace
                Oxford University Press
                1099-5129
                1532-2092
                November 2019
                19 August 2019
                19 August 2019
                : 21
                : 11
                : 1710-1716
                Affiliations
                [1 ] Department of Cardiology, Aarhus University Hospital , Palle Juul-Jensens, Boulevard 99, Aarhus N, Denmark
                [2 ] Department of Clinical Medicine, Health, Aarhus University , Palle Juul-Jensens Boulevard 82, Aarhus N, Denmark
                [3 ] Department of Cardiology, Danish Pacemaker and ICD Registry, Odense University Hospital , J. B. Winsløws Vej 4, Odense, Denmark
                [4 ] Unit for Inherited Cardiovascular Diseases, The Heart Centre, Department of Cardiology B2142, National University Hospital , University of Copenhagen, Blegdamsvej 9, Copenhagen, Denmark
                Author notes
                Corresponding author. Tel: +45 78 45 2262; fax: +45 78 45 2260. E-mail address: jd@ 123456clin.au.dk
                Author information
                http://orcid.org/0000-0003-4979-2566
                http://orcid.org/0000-0003-1802-4302
                Article
                euz206
                10.1093/europace/euz206
                6826204
                31424500
                4c4a99c8-5e76-4b3d-ba60-02b6c7f6ed11
                © The Author(s) 2019. Published by Oxford University Press on behalf of the European Society of Cardiology

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 04 February 2019
                : 09 July 2019
                Page count
                Pages: 7
                Funding
                Funded by: Skibsreder Per Henriksen
                Funded by: R. og hustrus Foundation
                Funded by: Danish Heart Foundation 10.13039/100007405
                Award ID: 16-R107-A6707-22988
                Funded by: Møller Foundation
                Funded by: Novo Nordisk Foundation 10.13039/501100009708
                Award ID: NNF18OC0031258
                Categories
                Clinical Research
                Cardiac Electrophysiology and Ablation

                Cardiovascular Medicine
                atrioventricular block,pacemaker,aetiology,temporal trends,surgical complication,congenital heart block

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