Abstract 4349790: Association of Delayed Diagnosis of Transthyretin Cardiomyopathy with Heart Failure Hospitalizations and Mortality
Abstract
Background: Timely diagnosis of transthyretin amyloidosis with cardiomyopathy (ATTR-CM) is important for early treatment, which can improve outcomes. Aim: To characterize the clinical impact of delayed diagnosis of ATTR-CM in real-world populations. Methods: This retrospective cohort study used Medicare fee-for-service and Veterans Health Affairs (VHA) data. We identified patients with ATTR-CM diagnosed between 2016 and 2022. The time-to-diagnosis was defined as the number of days between each patient’s first heart failure (HF) diagnosis and their first ATTR-CM diagnosis. Using multivariable Cox models, we evaluated the association between the time-to-diagnosis and the composite primary outcome of all-cause mortality or heart failure hospitalization (HFH). Secondary outcomes were HFH, all- cause mortality and cardiovascular death (VHA cohort only). Results: We identified 7,770 Medicare beneficiaries and 2,557 Veterans with HF and ATTR-CM. The mean age at the time of ATTR-CM diagnosis was 81 years (interquartile range [IQR] 76, 86) for the Medicare cohort and 81 years in the VHA (IQR 74, 87). This included 1,775 (22.8%) women in the Medicare cohort and 13 (0.5%) in the VHA cohort. The median time-to-diagnosis for ATTR-CM was 494 days (IQR 63, 1340) in the Medicare cohort and 490 days in the VHA (IQR 69, 1286). After adjustment for sociodemographics, diagnostic delays of 6 months to 2 years were associated with a 41% increased risk for the primary outcome in the Medicare cohort (HR 1.41; CI 1.30-1.54) and a 66% increased risk in the VHA cohort (HR 1.66;CI 1.49-1.86) compared with a time-to-diagnosis < 6 months. The results were similar after adjusting for clinical comorbidities. After adjustment, each one-year delay in diagnosis was associated with a 7% increased risk of the composite outcome for both cohorts (Medicare HR 1.07; 95% CI 1.06-1.08 and VHA HR 1.07; 95% CI 1.05-1.09). Each one-year delay was associated with a 7-8% increase in risk of HFH (Medicare HR 1.08; CI 1.06, 1.09 and VHA HR 1.07; 1.04, 1.09) and a 7-8% increase in risk of death (Medicare HR 1.07; CI 1.06-1.09 and VHA HR 1.08; 1.06, 1.10). Conclusions: The significant delays between incident HF and diagnosis of ATTR-CM are associated with an increased risk of heart failure hospitalization and mortality. This highlights the critical need for education around ATTR-CM and novel approaches to shorten the diagnostic delay, initiate early treatment and improve outcomes for patients with ATTR-CM.
Article Details
Authors (14)
Gabriela Spencer-Bonilla
Stanford University, Stanford, California, United States
Jun Fan
Department of Materials Science and Engineering
Paul Cheng
Natasha Din
Veterans Affairs Palo Alto Health Care System, Palo Alto, California, United States
Fatima Rodriguez
Anubodh Varshney
Stanford University, Stanford, California, United States
Marie Davies
AstraZeneca, Greenville, Delaware, United States
John Venditto
AstraZeneca, Greenville, Delaware, United States
Mia Papas
AstraZeneca, Greenville, Delaware, United States
Joanna Huang
AstraZeneca, Greenville, Delaware, United States
Ronald Witteles
Stanford University, Stanford, California, United States
Paul Heidenreich
Stanford University, Stanford, California, United States
Alexander Sandhu
Stanford University, Stanford, California, United States
Kevin Alexander
Division of Cardiovascular Medicine, Department of Medicine, Stanford Center for Clinical Research, Stanford University School of Medicine, Palo Alto, California, United States