2022 AHA/ACC/HFSA guideline for the management of heart failure: a report of the American College of Cardiology/American Heart Association Joint Committee on …
Abstract Aim The “2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure”
replaces the “2013 ACCF/AHA Guideline for the Management of Heart Failure” and the …
replaces the “2013 ACCF/AHA Guideline for the Management of Heart Failure” and the …
2022 AHA/ACC/HFSA guideline for the management of heart failure: executive summary: a report of the American College of Cardiology/American Heart Association …
Aim: The “2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure” replaces
the “2013 ACCF/AHA Guideline for the Management of Heart Failure” and the “2017 …
the “2013 ACCF/AHA Guideline for the Management of Heart Failure” and the “2017 …
Cardiac amyloidosis: evolving diagnosis and management: a scientific statement from the American Heart Association
Transthyretin amyloid cardiomyopathy (ATTR-CM) results in a restrictive cardiomyopathy
caused by extracellular deposition of transthyretin, normally involved in the transportation of …
caused by extracellular deposition of transthyretin, normally involved in the transportation of …
Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review
FL Ruberg, M Grogan, M Hanna, JW Kelly… - Journal of the American …, 2019 - jacc.org
Transthyretin amyloid cardiomyopathy (ATTR-CM) is an under-recognized cause of heart
failure (HF) in older adults, resulting from myocardial deposition of misfolded transthyretin …
failure (HF) in older adults, resulting from myocardial deposition of misfolded transthyretin …
Redefining the epidemiology of cardiac amyloidosis. A systematic review and meta‐analysis of screening studies
A Aimo, M Merlo, A Porcari… - European journal of …, 2022 - Wiley Online Library
Aims An algorithm for non‐invasive diagnosis of amyloid transthyretin cardiac amyloidosis
(ATTR‐CA) and novel disease‐modifying therapies have prompted an active search for CA …
(ATTR‐CA) and novel disease‐modifying therapies have prompted an active search for CA …
Expert consensus recommendations for the suspicion and diagnosis of transthyretin cardiac amyloidosis
Cardiomyopathy is a manifestation of transthyretin amyloidosis (ATTR), which is an
underrecognized systemic disease whereby the transthyretin protein misfolds to form fibrils …
underrecognized systemic disease whereby the transthyretin protein misfolds to form fibrils …
ASNC/AHA/ASE/EANM/HFSA/ISA/SCMR/SNMMI expert consensus recommendations for multimodality imaging in cardiac amyloidosis: part 1 of 2—evidence base …
S Dorbala, Y Ando, S Bokhari… - Circulation …, 2021 - Am Heart Assoc
Sharmila Dorbala, MD, MPH, FASNC, Chair*; Yukio Ando, MD, PhD†; Sabahat Bokhari,
MD‡; Angela Dispenzieri, MD § ; Rodney H. Falk, MD*; Victor A. Ferrari, MD∥; Marianna …
MD‡; Angela Dispenzieri, MD § ; Rodney H. Falk, MD*; Victor A. Ferrari, MD∥; Marianna …
The pathology of amyloidosis in classification: a review
MM Picken - Acta haematologica, 2020 - karger.com
Background: The amyloidoses are a rare and heterogeneous group of disorders that are
characterized by the deposition of abnormally folded proteins in tissues ultimately leading to …
characterized by the deposition of abnormally folded proteins in tissues ultimately leading to …
Aortic Stenosis and Cardiac Amyloidosis: JACC Review Topic of the Week
J Ternacle, L Krapf, D Mohty, J Magne… - Journal of the American …, 2019 - jacc.org
The prevalence of calcific aortic stenosis (AS) and of cardiac amyloidosis (CA) increases
with age, and their association is not uncommon in the elderly. The identification of CA is …
with age, and their association is not uncommon in the elderly. The identification of CA is …
Systemic amyloidosis recognition, prognosis, and therapy: a systematic review
MA Gertz, A Dispenzieri - Jama, 2020 - jamanetwork.com
Importance Many patients with systemic amyloidosis are underdiagnosed. Overall, 25% of
patients with immunoglobulin light chain (AL) amyloidosis die within 6 months of diagnosis …
patients with immunoglobulin light chain (AL) amyloidosis die within 6 months of diagnosis …