Systemic embolism in amyloid transthyretin cardiomyopathy
- PMID: 35650018
- PMCID: PMC9542906
- DOI: 10.1002/ejhf.2566
Systemic embolism in amyloid transthyretin cardiomyopathy
Abstract
Aims: Although systemic embolism is a potential complication in transthyretin amyloid cardiomyopathy (ATTR-CM), data about its incidence and prevalence are scarce. We studied the incidence, prevalence and factors associated with embolic events in ATTR-CM. Additionally, we evaluated embolic events according to the type of oral anticoagulation (OAC) and the performance of the CHA2 DS2 -VASc score in this setting.
Methods and results: Clinical characteristics, history of atrial fibrillation (AF) and embolic events were retrospectively collected from ATTR-CM patients evaluated at four international amyloid centres. Overall, 1191 ATTR-CM patients (87% men, median age 77.1 years [interquartile range-IQR 71.4-82], 83% ATTRwt) were studied. A total of 162 (13.6%) have had an embolic event before initial evaluation. Over a median follow-up of 19.9 months (IQR 9.9-35.5), 41 additional patients (3.44%) had an embolic event. Incidence rate (per 100 patient-years) was 0 among patients in sinus rhythm with OAC, 1.3 in sinus rhythm without OAC, 1.7 in AF with OAC, and 4.8 in AF without OAC. CHA2 DS2 -VASc did not predict embolic events in patients in sinus rhythm whereas in patients with AF without OAC, only those with a score ≥4 had embolic events. There was no difference in the incidence rate of embolism between patients with AF treated with vitamin K antagonists (VKAs) (n = 322) and those treated with direct oral anticoagulants (DOACs) (n = 239) (p = 0.66).
Conclusions: Embolic events were a frequent complication in ATTR-CM. OAC reduced the risk of systemic embolism. Embolic rates did not differ with VKAs and DOACs. The CHA2 DS2 -VASc score did not correlate well with clinical outcome in ATTR-CM and should not be used to assess thromboembolic risk in this population.
Keywords: Anticoagulation; Atrial fibrillation; CHA2DS2-VASc; Cardiac amyloidosis; Embolism; Transthyretin.
© 2022 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.
Figures
Comment in
-
Systemic embolism in transthyretin amyloid cardiomyopathy: how to look into the future.Eur J Heart Fail. 2022 Aug;24(8):1397-1399. doi: 10.1002/ejhf.2610. Epub 2022 Jul 22. Eur J Heart Fail. 2022. PMID: 35790492 No abstract available.
-
Time to reconsider thromboembolic risk and anticoagulation in transthyretin cardiac amyloidosis?Eur J Heart Fail. 2022 Sep;24(9):1716-1718. doi: 10.1002/ejhf.2648. Epub 2022 Aug 14. Eur J Heart Fail. 2022. PMID: 35919942 No abstract available.
References
-
- Feng DL, Edwards WD, Oh JK, Chandrasekaran K, Grogan M, Martinez MW, et al. Intracardiac thrombosis and embolism in patients with cardiac amyloidosis. Circulation. 2007;116:2420–6. - PubMed
-
- González‐López E, Gagliardi C, Dominguez F, Quarta CC, de Haro‐Del Moral FJ, Milandri A, et al. Clinical characteristics of wild‐type transthyretin cardiac amyloidosis: disproving myths. Eur Heart J. 2017;38:1895–904. - PubMed
-
- Cappelli F, Tini G, Russo D, Emdin M, Del Franco A, Vergaro G, et al. Arterial thrombo‐embolic events in cardiac amyloidosis: a look beyond atrial fibrillation. Amyloid. 2021;28:12–8. - PubMed
-
- López‐Sainz Á, Hernandez‐Hernandez A, Gonzalez‐Lopez E, Domínguez F, Restrepo‐Cordoba MA, Cobo‐Marcos M, et al. Clinical profile and outcome of cardiac amyloidosis in a Spanish referral center. Rev Esp Cardiol. 2021;74:149–58. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials
