Cost-effectiveness of systematic screening and treatment of transthyretin amyloid cardiomyopathy (ATTR-CM) in patients with heart failure with preserved ejection fraction (HFpEF) in United States.

Int J Cardiol

Department of Pharmacy Systems, Outcomes and Policy, University of Illinois Chicago, Chicago, IL, United States of America; Center for Pharmacoepidemiology and Pharmacoeconomic Research, University of Illinois Chicago, Chicago, IL, United States of America. Electronic address:

Published: March 2024

AI Article Synopsis

  • Transthyretin amyloid cardiomyopathy (ATTR-CM) is a common but often undiagnosed cause of heart failure, and using Tc-pyrophosphate scintigraphy (PYP-scan) helps improve its detection and enables early treatment with tafamidis.
  • A comparison between universal systematic screening (USS) and standard-of-care (SoC) for ATTR-CM in older patients revealed that while USS slightly improves quality adjusted life-years (QALYs), it significantly raises lifetime costs ($124,380 vs. $70,412).
  • The study concluded that due to the high cost of tafamidis, USS for detecting ATTR-CM in older heart failure patients is unlikely to be cost-effective.

Article Abstract

Background: Transthyretin amyloid cardiomyopathy (ATTR-CM) is an underdiagnosed cause of heart failure in clinical practice. Tc-pyrophosphate scintigraphy (PYP-scan) improves the accuracy of ATTR-CM detection, enabling timely initiation of tafamidis, a drug that slows the progression of ATTR-CM and lowers the risk of adverse cardiac events. PYP-scans, serum free light-chain (FLC) test and immunofixation electrophoresis (IFE) are critical components of a systematic screening. We assessed the cost-effectiveness of universal systematic screening (USS) compared to standard-of-care (SoC) selected clinical referrals for the systematic screening in patients aged 60 years or older with heart failure with preserved ejection fraction (HFpEF) and ventricular wall thickness of at least 12 mm.

Methods: Two screening strategies, USS versus SoC screening for ATTR-CM were compared in a model-based assessment. Treatment decisions were based upon the accuracy of each screening strategy, which was followed by Markov state transitions across New York Heart Association (NYHA) functional classes and death. Model inputs were identified from a literature review. We calculated lifetime cost in 2022 US dollars and quality adjusted life-years (QALYs) of each strategy. The primary outcome was the incremental cost-effectiveness ratio (ICER).

Results: The USS was associated with a significant increase in lifetime costs ($124,380 vs. $70,412) and modest improvement in QALYs (4.42 QALYs vs 4.36 QALYs). The ICER for the USS was $919,509 per QALY gained. ICER was sensitive to the age at the time of ATTR-CM diagnosis, true prevalence rate of ATTR-CM, and daily cost of tafamidis.

Conclusions: Owing to the high cost of treatment with tafamidis, USS along with PYP scan for ATTR-CM in older HFpEF patients with ventricular wall thickening is unlikely to become a cost-effective strategy at a liberal WTP threshold.

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Source
http://dx.doi.org/10.1016/j.ijcard.2023.131598DOI Listing

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