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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Bonderman, D; Pölzl, G; Ablasser, K; Agis, H; Aschauer, S; Auer-Grumbach, M; Binder, C; Dörler, J; Duca, F; Ebner, C; Hacker, M; Kain, R; Kammerlander, A; Koschutnik, M; Kroiss, AS; Mayr, A; Nitsche, C; Rainer, PP; Reiter-Malmqvist, S; Schneider, M; Schwarz, R; Verheyen, N; Weber, T; Zaruba, MM; Badr Eslam, R; Hülsmann, M; Mascherbauer, J.
Diagnosis and treatment of cardiac amyloidosis: an interdisciplinary consensus statement.
Wien Klin Wochenschr. 2020; 132(23-24):742-761 Doi: 10.1007/s00508-020-01781-z [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Ablasser Klemens
Auer-Grumbach Michaela
Rainer Peter
Verheyen Nicolas Dominik
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Abstract:
The prevalence and significance of cardiac amyloidosis have been considerably underestimated in the past; however, the number of patients diagnosed with cardiac amyloidosis has increased significantly recently due to growing awareness of the disease, improved diagnostic capabilities and demographic trends. Specific therapies that improve patient prognosis have become available for certain types of cardiac amyloidosis. Thus, the earliest possible referral of patients with suspicion of cardiac amyloidosis to an experienced center is crucial to ensure rapid diagnosis, early initiation of treatment, and structured patient care. This requires intensive collaboration across several disciplines, and between resident physicians and specialized centers. The aim of this consensus statement is to provide guidance for the rapid and efficient diagnosis and treatment of light-chain amyloidosis and transthyretin amyloidosis, which are the most common forms of cardiac amyloidosis.
Find related publications in this database (using NLM MeSH Indexing)
Amyloid Neuropathies, Familial -
Cardiomyopathies - diagnosis
Cardiomyopathies - therapy
Consensus -
Humans -

Find related publications in this database (Keywords)
Cardiomyopathy
Heart failure
99mTc-DPD scan
Cardiac MRI
Biopsy
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