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Editorial
. 2023 Nov;25(11):2065-2066.
doi: 10.1002/ejhf.3053. Epub 2023 Oct 18.

Tafamidis in patients with severe heart failure due to transthyretin amyloidosis cardiomyopathy: Improved long-term survival

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Editorial

Tafamidis in patients with severe heart failure due to transthyretin amyloidosis cardiomyopathy: Improved long-term survival

Alwin Tubben et al. Eur J Heart Fail. 2023 Nov.
Free article
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References

    1. Maurer MS, Schwartz JH, Gundapaneni B, Elliott PM, Merlini G, Waddington-Cruz M, et al.; ATTR-ACT Study Investigators. Tafamidis treatment for patients with transthyretin amyloid cardiomyopathy. N Engl J Med 2018;379:1007-1016. https://doi.org/10.1056/NEJMoa1805689
    1. Elliott P, Gundapaneni B, Sultan MB, Ines M, Garcia-Pavia P. Improved long-term survival with tafamidis treatment in patients with transthyretin amyloid cardiomyopathy and severe heart failure symptoms. Eur J Heart Fail 2023;25:2060-2064. https://doi.org/10.1002/ejhf.2974
    1. Elliott P, Drachman BM, Gottlieb SS, Hoffman JE, Hummel SL, Lenihan DJ, et al. Long-term survival with tafamidis in patients with transthyretin amyloid cardiomyopathy. Circ Heart Fail 2022;15:e008193. https://doi.org/10.1161/CIRCHEARTFAILURE.120.008193
    1. Rapezzi C, Elliott P, Damy T, Nativi-Nicolau J, Berk JL, Velazquez EJ, et al. Efficacy of tafamidis in patients with hereditary and wild-type transthyretin amyloid cardiomyopathy. JACC Heart Fail 2021;9:115-123. https://doi.org/10.1016/j.jchf.2020.09.011
    1. Li H, Rozenbaum M, Casey M, Sultan MB. Estimating the effect of tafamidis on cardiovascular-related hospitalization in nyha class iii patients with transthyretin amyloid cardiomyopathy in the presence of death. Cardiology 2022;147:398-405. https://doi.org/10.1159/000525883

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