Management of Arrhythmias and Conduction Disorders in Amyloid Cardiomyopathy

被引:0
|
作者
Holcman, Katarzyna [1 ,2 ]
Zabek, Andrzej [3 ]
Boczar, Krzysztof [3 ]
Podolec, Piotr [2 ]
Kostkiewicz, Magdalena [1 ,2 ]
机构
[1] John Paul 2 Hosp, Dept Nucl Med, PL-31202 Krakow, Poland
[2] Jagiellonian Univ, John Paul II Hosp, Dept Cardiac & Vasc Dis, Med Coll, PL-31202 Krakow, Poland
[3] Jagiellonian Univ, John Paul II Hosp, Dept Electrocardiol, Med Coll, PL-31202 Krakow, Poland
关键词
amyloidosis; amyloid cardiomyopathy; ATTR; AL; TRANSTHYRETIN CARDIAC AMYLOIDOSIS; CARDIOVERTER-DEFIBRILLATOR; ATRIAL-FIBRILLATION; FAMILIAL AMYLOIDOSIS; NATURAL-HISTORY; SYSTEM DISEASE; AL AMYLOIDOSIS; PREVALENCE; DIAGNOSIS; RISK;
D O I
10.3390/jcm13113088
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiac amyloidosis, a condition characterized by abnormal protein deposition in the heart, leads to restrictive cardiomyopathy and is notably associated with an increased risk of arrhythmias and conduction disorders. This article reviews the current understanding and management strategies for these cardiac complications, with a focus on recent advancements and clinical challenges. The prevalence and impact of atrial arrhythmias, particularly atrial fibrillation, are examined, along with considerations for stroke risk and anticoagulation therapy. The article also addresses the complexities of managing rate and rhythm control, outlining the utility and limitations of pharmacological agents and interventions such as catheter ablation. Furthermore, it reviews the challenges in the treatment of ventricular arrhythmias, including the contentious use of implantable cardioverter-defibrillators for primary and secondary prevention. Individualized approaches, considering the unique characteristics of cardiac amyloidosis, are paramount. Continuous research and clinical exploration are essential to refine treatment strategies and improve outcomes in this challenging patient population.
引用
收藏
页数:12
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