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DOI 10.1016/j.jacc.2020.11.006

Медицинская библиотека · Journal of the American College of Cardiology · 2020

Prevalence and Outcomes of Concomitant Aortic Stenosis and Cardiac Amyloidosis.

Nitsche Christian, Scully Paul R, Patel Kush P, Kammerlander Andreas A, Koschutnik Matthias, Dona Carolina, Wollenweber Tim, Ahmed Nida, Thornton George D, Kelion Andrew D, Sabharwal Nikant, Newton James D, Ozkor Muhiddin, Kennon Simon, Mullen Michael, Lloyd Guy, Fontana Marianna, Hawkins Philip N, Pugliese Francesca, Menezes Leon J, Moon James C, Mascherbauer Julia, Treibel Thomas A

СтатьяМногоцентровое исследованиеПеревод пока не подготовлен

Аннотация

BACKGROUND

Older patients with severe aortic stenosis (AS) are increasingly identified as having cardiac amyloidosis (CA). It is unknown whether concomitant AS-CA has worse outcomes or results in futility of transcatheter aortic valve replacement (TAVR).

OBJECTIVES

This study identified clinical characteristics and outcomes of AS-CA compared with lone AS.

METHODS

Patients who were referred for TAVR at 3 international sites underwent blinded research core laboratory 99mtechnetium-3,3-diphosphono-1,2-propanodicarboxylic acid (DPD) bone scintigraphy (Perugini grade 0: negative; grades 1 to 3: increasingly positive) before intervention. Transthyretin-CA (ATTR) was diagnosed by DPD and absence of a clonal immunoglobulin, and light-chain CA (AL) was diagnosed via tissue biopsy. National registries captured all-cause mortality.

RESULTS

A total of 407 patients (age 83.4 ± 6.5 years; 49.8% men) were recruited. DPD was positive in 48 patients (11.8%; grade 1: 3.9% [n = 16]; grade 2/3: 7.9% [n = 32]). AL was diagnosed in 1 patient with grade 1. Patients with grade 2/3 had worse functional capacity, biomarkers (N-terminal pro-brain natriuretic peptide and/or high-sensitivity troponin T), and biventricular remodeling. A clinical score (RAISE) that used left ventricular remodeling (hypertrophy/diastolic dysfunction), age, injury (high-sensitivity troponin T), systemic involvement, and electrical abnormalities (right bundle branch block/low voltages) was developed to predict the presence of AS-CA (area under the curve: 0.86; 95% confidence interval: 0.78 to 0.94; p < 0.001). Decisions by the heart team (DPD-blinded) resulted in TAVR (333 [81.6%]), surgical AVR (10 [2.5%]), or medical management (65 [15.9%]). After a median of 1.7 years, 23% of patients died. One-year mortality was worse in all patients with AS-CA (grade: 1 to 3) than those with lone AS (24.5% vs. 13.9%; p = 0.05). TAVR improved survival versus medical management; AS-CA survival post-TAVR did not differ from lone AS (p = 0.36).

CONCLUSIONS

Concomitant pathology of AS-CA is common in older patients with AS and can be predicted clinically. AS-CA has worse clinical presentation and a trend toward worse prognosis, unless treated. Therefore, TAVR should not be withheld in AS-CA.

Для цитирования: Nitsche Christian, Scully Paul R, Patel Kush P, Kammerlander Andreas A, Koschutnik Matthias, Dona Carolina, Wollenweber Tim, Ahmed Nida, Thornton George D, Kelion Andrew D, Sabharwal Nikant, Newton James D, Ozkor Muhiddin, Kennon Simon, Mullen Michael, Lloyd Guy, Fontana Marianna, Hawkins Philip N, Pugliese Francesca, Menezes Leon J, Moon James C, Mascherbauer Julia, Treibel Thomas A. Prevalence and Outcomes of Concomitant Aortic Stenosis and Cardiac Amyloidosis.. Journal of the American College of Cardiology. 2020. DOI: 10.1016/j.jacc.2020.11.006.

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