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Transthyretin amyloid cardiomyopathy: Literature review and red-flag symptom clusters for each cardiology specialty.
Izumiya, Yasuhiro; Kubo, Toru; Endo, Jin; Takashio, Seiji; Minamisawa, Masatoshi; Hamada, Jun; Ishii, Tomonori; Abe, Hajime; Konishi, Hiroaki; Tsujita, Kenichi.
Afiliação
  • Izumiya Y; Department of Cardiovascular Medicine, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
  • Kubo T; Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Endo J; Department of Cardiology and Geriatrics, Kochi Medical School, Kochi University, Kochi, Japan.
  • Takashio S; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
  • Minamisawa M; Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Hamada J; Department of Cardiovascular Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
  • Ishii T; Pfizer Japan Inc., Tokyo, Japan.
  • Abe H; Pfizer Japan Inc., Tokyo, Japan.
  • Konishi H; Pfizer Japan Inc., Tokyo, Japan.
  • Tsujita K; Pfizer Japan Inc., Tokyo, Japan.
ESC Heart Fail ; 2024 Aug 21.
Article em En | MEDLINE | ID: mdl-39168835
ABSTRACT
Wild-type transthyretin amyloid cardiomyopathy (ATTRwt-CM) is a progressive and infiltrative cardiac disorder that may cause fatal consequences if left untreated. The estimated survival time from diagnosis is approximately 3-6 years. Because of the non-specificity of initial symptom manifestation and insufficient awareness among treating physicians, approximately one-third of patients with ATTRwt-CM are initially misdiagnosed with other cardiac diseases. Although heart failure (HF) is the most common initial manifestation of ATTRwt-CM, observed in nearly 70% of affected patients, patients may also present with other cardiologic symptoms, such as atrial fibrillation (AF) and aortic stenosis (AS). This non-specific and diverse nature of the initial ATTRwt-CM presentation indicates that various cardiology subspecialties are involved in patient diagnosis and management. Standard guideline-directed pharmacological treatment for HF is not recommended for patients with ATTRwt-CM because of its limited effectiveness. However, no established algorithms are available regarding HF management in this patient population. This literature review provides an overview of the red flags for ATTRwt-CM and research findings regarding HF management in this patient population. In addition to commonly recognized red flags for ATTRwt-CM (e.g., HF, AF and severe AS), published literature identified potential red flags such as coronary microvascular dysfunction. For HF management in patients with ATTRwt-CM, the use of mineralocorticoid receptor antagonists (MRAs) was reported as a well-tolerated option associated with a low discontinuation rate and reduced mortality. Although there is no concrete evidence for recommendations against sodium-glucose cotransporter 2 inhibitor (SGLT2i) administration, research supporting its use is limited to small-scale studies. Robust evidence is lacking for AF ablation, implantable cardioverter-defibrillators and cardiac resynchronization therapy. Based on the published findings and our clinical experience as Japanese ATTRwt-CM experts, red-flag symptom clusters for each cardiology specialty (HF, arrhythmia and ischaemia/structural heart disease) and a treatment scheme for HF management are presented. As this research area remains at an exploratory stage, our observations would require further discussion among experts worldwide.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article