Abstract 4365864: Post-Discharge Outcomes and Healthcare Costs for Patients Hospitalized for Heart Failure with Transthyretin Amyloid Cardiomyopathy: Findings From GWTG–HF

S Satoshi Shoji (Duke Clinical Research Institute, Chapel Hill, North Carolina, United States) U Uchechukwu Ikeaba (Duke Clinical Research Institute, Durham, North Carolina, United States) G Gregg Fonarow (UCLA MEDICAL CENTER, Los Angeles, California, United States) S Senthil Selvaraj (Duke University, Durham, Pennsylvania, United States) S Sabra Lewsey (Johns Hopkins University, Baltimore, Maryland, United States) A Ambarish Pandey M Michel Khouri (Duke University School of Medicine, Durham, North Carolina, United States) B Brooke Alhanti (Duke University, Durham, North Carolina, United States) J Jim McDermott (AstraZeneca / BioPharmaceuticals Medical CVRM, Wilmiton, Delaware, United States) J Jason Wright (AstraZeneca, Bryn Mawr, Pennsylvania, United States) M Muthiah Vaduganathan (Division of Cardiovascular Medicine Brigham and Women’s Hospital, Harvard Medical School, Boston, MA (M.V.).) S Stephen Greene (Duke Clinical Research Institute, Durham, North Carolina, United States)

Abstract

Background: Transthyretin amyloid cardiomyopathy (ATTR-CM) is associated with high risk for heart failure (HF) hospitalization. However, little is known regarding post-discharge outcomes and healthcare costs for patients with underlying ATTR-CM, as compared with the general HF population. Methods: We analyzed Medicare beneficiaries hospitalized for HF in the Get With The Guidelines-Heart Failure (GWTG-HF) registry and discharged alive from January 1, 2021, to June 30, 2023. Patients were compared according to the presence or absence of an ATTR-CM diagnosis, as documented in the GWTG-HF case report form. All-cause mortality, HF readmission, and all-cause readmission over 1-year post-discharge were assessed in unadjusted and adjusted risk models. Inpatient, outpatient (excluding medications), and total per-patient healthcare costs over the 1-year post-discharge were calculated from payments made by Medicare. Results: Among 102,160 patients across 563 US hospitals, 190 (0.2%) carried a diagnosis of ATTR-CM. Compared to those without ATTR-CM, patients with an ATTR-CM diagnosis were older (82 [76–87] vs 80 [73–87] years), more likely to be male (68.9% vs 47.0%), and had lower ejection fraction (45 [30–57] vs 53 [35–60]%). Patients with ATTR-CM were significantly more likely to be discharged on a mineralocorticoid receptor antagonist (29.5% vs 20.4%) and SGLT2 inhibitor (21.6% vs 14.1%), and significantly less likely to be discharged on a beta-blocker (52.1% vs 77.6%). After adjustment, ATTR-CM was associated with higher risk of 1-year HF readmission (36.8% vs. 28.2%; HR 1.28, 95% CI 1.01–1.61, p=0.04), but not all-cause mortality (40.0% vs. 34.2%; HR 1.08, 95% CI 0.88–1.31, p=0.47) or all-cause readmission (64.2% vs. 63.4%; HR 0.98, 95% CI 0.83–1.17, p=0.85) (Table 1) . Mean 1-year total per-patient Medicare costs were higher among patients with ATTR-CM than those without ($60,373 vs $50,247; p=0.04), primarily driven by significant differences in outpatient costs ($20,866 vs $16,358]; p=0.03) (Table 2) . Conclusion: Among older adults hospitalized for HF in the US, patients with underlying ATTR-CM experience similarly high rates of post-discharge mortality, but face greater risks of HF readmission and accrue higher post-discharge healthcare costs. These findings highlight a disproportionate clinical and economic burden of ATTR-CM compared with the general HF population, further supporting the need for earlier identification and tailored care strategies.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (12)

S

Satoshi Shoji

Duke Clinical Research Institute, Chapel Hill, North Carolina, United States

U

Uchechukwu Ikeaba

Duke Clinical Research Institute, Durham, North Carolina, United States

G

Gregg Fonarow

UCLA MEDICAL CENTER, Los Angeles, California, United States

S

Senthil Selvaraj

Duke University, Durham, Pennsylvania, United States

S

Sabra Lewsey

Johns Hopkins University, Baltimore, Maryland, United States

A

Ambarish Pandey

M

Michel Khouri

Duke University School of Medicine, Durham, North Carolina, United States

B

Brooke Alhanti

Duke University, Durham, North Carolina, United States

J

Jim McDermott

AstraZeneca / BioPharmaceuticals Medical CVRM, Wilmiton, Delaware, United States

J

Jason Wright

AstraZeneca, Bryn Mawr, Pennsylvania, United States

M

Muthiah Vaduganathan

Division of Cardiovascular Medicine Brigham and Women’s Hospital, Harvard Medical School, Boston, MA (M.V.).

S

Stephen Greene

Duke Clinical Research Institute, Durham, North Carolina, United States