Page 101 - Read Online
P. 101

Porcari et al. Vessel Plus 2022;6:33  https://dx.doi.org/10.20517/2574-1209.2021.134  Page 13 of 14

                   PubMed
               50.      Donnellan E, Elshazly MB, Vakamudi S, et al. No association between CHADS-VASc score and left atrial appendage thrombus in
                   patients with transthyretin amyloidosis. JACC Clin Electrophysiol 2019;5:1473-4.  DOI  PubMed
               51.      Feng D, Syed IS, Martinez M, et al. Intracardiac thrombosis and anticoagulation therapy in cardiac amyloidosis. Circulation
                   2009;119:2490-7.  DOI  PubMed
               52.      Santarone M, Corrado G, Tagliagambe LM, et al. Atrial thrombosis in cardiac amyloidosis: diagnostic contribution of transesophageal
                   echocardiography. J Am Soc Echocardiogr 1999;12:533-6.  DOI  PubMed
               53.      Parsons C, Patel SI, Cha S, et al. CHA DS -VASc score: a predictor of thromboembolic events and mortality in patients with an
                                             2  2
                   implantable monitoring device without atrial fibrillation. Mayo Clin Proc 2017;92:360-9.  DOI  PubMed  PMC
               54.      Ternacle J, Krapf L, Mohty D, et al. Aortic stenosis and cardiac amyloidosis: JACC review topic of the week. J Am Coll Cardiol
                   2019;74:2638-51.  DOI  PubMed
               55.      Galat A, Guellich A, Bodez D, et al. Aortic stenosis and transthyretin cardiac amyloidosis: the chicken or the egg? Eur Heart J
                   2016;37:3525-31.  DOI  PubMed
               56.      Treibel TA, Fontana M, Gilbertson JA, et al. Occult transthyretin cardiac amyloid in severe calcific aortic stenosis: prevalence and
                   prognosis in patients undergoing surgical aortic valve replacement. Circ Cardiovasc Imaging 2016;9:e005066.  DOI  PubMed
               57.      Sperry BW, Jones BM, Vranian MN, Hanna M, Jaber WA. Recognizing transthyretin cardiac amyloidosis in patients with aortic
                   stenosis: impact on prognosis. JACC Cardiovasc Imaging 2016;9:904-6.  DOI  PubMed
               58.      Clavel MA, Magne J, Pibarot P. Low-gradient aortic stenosis. Eur Heart J 2016;37:2645-57.  DOI  PubMed  PMC
               59.      Monticelli FC, Kunz SN, Keller T, Bleiziffer S. Cardiac amyloidosis as a potential risk factor for transapical transcatheter aortic valve
                   implantation. J Card Surg 2014;29:623-4.  DOI  PubMed
               60.      Moreno R, Dobarro D, López de Sá E, et al. Cause of complete atrioventricular block after percutaneous aortic valve implantation:
                   insights from a necropsy study. Circulation 2009;120:e29-30.  DOI  PubMed
               61.      Dubrey SW, Cha K, Anderson J, et al. The clinical features of immunoglobulin light-chain (AL) amyloidosis with heart involvement.
                   QJM 1998;91:141-57.  DOI  PubMed
               62.      Varr BC, Zarafshar S, Coakley T, et al. Implantable cardioverter-defibrillator placement in patients with cardiac amyloidosis. Heart
                   Rhythm 2014;11:158-62.  DOI  PubMed
               63.      Goldsmith YB, Liu J, Chou J, Hoffman J, Comenzo RL, Steingart RM. Frequencies and types of arrhythmias in patients with systemic
                   light-chain amyloidosis with cardiac involvement undergoing stem cell transplantation on telemetry monitoring. Am J Cardiol
                   2009;104:990-4.  DOI  PubMed
               64.      Palladini G, Malamani G, Cò F, et al. Holter monitoring in AL amyloidosis: prognostic implications. Pacing Clin Electrophysiol
                   2001;24:1228-33.  DOI  PubMed
               65.      Giancaterino S, Urey MA, Darden D, Hsu JC. Management of arrhythmias in cardiac amyloidosis. JACC Clin Electrophysiol
                   2020;6:351-61.  DOI  PubMed
               66.      Priori SG, Blomström-Lundqvist C, Mazzanti A, et al; ESC Scientific Document Group. 2015 ESC Guidelines for the management of
                   patients with ventricular arrhythmias and the prevention of sudden cardiac death: the Task Force for the management of patients with
                   ventricular arrhythmias and the prevention of sudden cardiac death of the European society of cardiology (ESC). Endorsed by:
                   Association for European Paediatric and Congenital Cardiology (AEPC). Eur Heart J 2015;36:2793-867.  DOI  PubMed
               67.      Al-Khatib SM, Stevenson WG, Ackerman MJ, et al. 2017 AHA/ACC/HRS guideline for management of patients with ventricular
                   arrhythmias  and  the  prevention  of  sudden  cardiac  death:  executive  summary:  a  report  of  the  American  College  of
                   Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society. Heart Rhythm
                   2018;15:e190-252.  DOI  PubMed
               68.      Ponikowski P, Voors AA, Anker SD, et al; ESC Scientific Document Group. 2016 ESC Guidelines for the diagnosis and treatment of
                   acute and chronic heart failure: the Task Force for the diagnosis and treatment of acute and chronic heart failure of the European
                   Society of Cardiology (ESC)Developed with the special contribution of the Heart Failure Association (HFA) of the ESC. Eur Heart J
                   2016;37:2129-200.  DOI  PubMed
               69.      Hamon D, Algalarrondo V, Gandjbakhch E, et al. Outcome and incidence of appropriate implantable cardioverter-defibrillator therapy
                   in patients with cardiac amyloidosis. Int J Cardiol 2016;222:562-8.  DOI  PubMed
               70.      Lin G, Dispenzieri A, Kyle R, Grogan M, Brady PA. Implantable cardioverter defibrillators in patients with cardiac amyloidosis. J
                   Cardiovasc Electrophysiol 2013;24:793-8.  DOI  PubMed
               71.      Kristen AV, Dengler TJ, Hegenbart U, et al. Prophylactic implantation of cardioverter-defibrillator in patients with severe cardiac
                   amyloidosis and high risk for sudden cardiac death. Heart Rhythm 2008;5:235-40.  DOI  PubMed
               72.      Sayed RH, Rogers D, Khan F, et al. A study of implanted cardiac rhythm recorders in advanced cardiac AL amyloidosis. Eur Heart J
                   2015;36:1098-105.  DOI  PubMed
               73.      Escher F, Senoner M, Doerler J, et al. When and how do patients with cardiac amyloidosis die? Clin Res Cardiol 2020;109:78-88.
                   DOI  PubMed  PMC
               74.      Damy T, Jaccard A, Guellich A, et al. Identification of prognostic markers in transthyretin and AL cardiac amyloidosis. Amyloid
                   2016;23:194-202.  DOI  PubMed
               75.      Donnellan E, Wazni OM, Hanna M, Kanj M, Saliba WI, Jaber WA. Cardiac resynchronization therapy for transthyretin cardiac
                   amyloidosis. J Am Heart Assoc 2020;9:e017335.  DOI  PubMed  PMC
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