Transthyretin Cardiac Amyloidosis An Evolution in Diagnosis and Management of an "Old" Disease

被引:3
|
作者
Smiley, Dia A. [1 ]
Rodriguez, Carlos M. [1 ]
Maurer, Mathew S. [1 ]
机构
[1] Columbia Univ, Irving Med Ctr, New York Presbyterian Hosp, Cardiac Amyloidosis Program, New York, NY 10032 USA
关键词
Amyloidosis; Cardiac amyloidosis; Amyloid cardiomyopathy; Transthyretin; Transthyretin cardiomyopathy; Cardiac scintigraphy; Heart failure with preserved ejection fraction; WILD-TYPE TRANSTHYRETIN; AORTIC-STENOSIS; HEART-FAILURE; ATRIAL ARRHYTHMIAS; PREVALENCE; HISTORY; VARIANT; SCINTIGRAPHY; PREDICTORS; PHENOTYPE;
D O I
10.1016/j.ccl.2022.06.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ATTR-CA is a progressive, infiltrative, and restrictive cardiomyopathy, which remains an under-appreciated and under-diagnosed cause of HFpEF. The importance of enhanced suspicion and early diagnosis cannot be overemphasized, as emerging therapies are more effective early in the course of the disease. Further, because of the unique physiologic and hemodynamic features of CA, patients poorly tolerate traditional heart failure medications and experience worse outcomes compared with other causes of HFpEF. ATTR CA is increasingly recognized due to enhanced clinical awareness, advances in diagnostic imaging that allow noninvasive diagnosis, as well as the recent introduction of novel disease-modifying treatments.
引用
收藏
页码:541 / 558
页数:18
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