# Trends in diagnostic testing in Medicare patients with wild-type transthyretin amyloid cardiomyopathy

**Authors:** Ronald M. Witteles, Haechung Chung, Feng Dai, Cynthia Gutierrez, Andrew Rava, Sameer Swarup, Abbas Ebrahim, Cindi Pankratova

PMC · DOI: 10.3389/fcvm.2025.1638380 · Frontiers in Cardiovascular Medicine · 2025-10-29

## TL;DR

This study examines how Medicare patients are diagnosed with a type of heart disease called wild-type transthyretin amyloid cardiomyopathy and finds that many are not diagnosed using recommended methods.

## Contribution

The study provides new insights into the real-world diagnostic practices for ATTRwt-CM among elderly Medicare patients.

## Key findings

- Annual new diagnoses of ATTRwt-CM nearly tripled from 2018 to 2022.
- Only 14% of patients underwent the recommended noninvasive diagnostic testing.
- Use of cardiac biopsy declined significantly over the study period.

## Abstract

Most patients with wild-type transthyretin amyloid cardiomyopathy (ATTRwt-CM) are diagnosed noninvasively, using nuclear imaging and monoclonal protein testing. However, concerns have been raised that some may receive an ATTRwt-CM diagnosis based on incomplete evaluations (not based on current consensus recommendations). Using a cohort of US Medicare Fee-for-Service patients, we aimed to examine the frequency and cadence of diagnostic testing for ATTRwt-CM.

In this retrospective observational cross-sectional study, administrative de-identified claims data from 2018 to 2022 were derived from patients aged ≥65 years who had at least one claim for ATTRwt-CM and heart failure or cardiomyopathy, and ≥2 years of continuous Medicare enrollment before the first ATTRwt-CM diagnosis. Patients with claims for any other form of amyloidosis, multiple myeloma, or plasma cell dyscrasias were excluded.

Among 2,050 patients with ATTRwt-CM, mean (SD) age was 80.0 (6.9) years, and 75.5% were men. Annual new ATTRwt-CM diagnoses nearly tripled over the study period (2018, n = 198; 2022, n = 578). Technetium-99m pyrophosphate (PYP) scintigraphy use was performed in approximately half of diagnosed patients by the end of the study period (2018, 30%; 2022, 49%). Cardiac biopsy use declined from 14% in patients diagnosed in 2018 to 5% in those diagnosed in 2022. A small minority (14%) of patients underwent the recommended noninvasive diagnostic testing comprised of PYP scintigraphy and complete monoclonal protein testing.

Based on Medicare claims data, most patients diagnosed with ATTRwt-CM have not been diagnosed following consensus-recommended pathways.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252), cardiomyopathy (MONDO:0004994), amyloidosis (MONDO:0019065), multiple myeloma (MONDO:0009693)

## Full-text entities

- **Diseases:** amyloidosis (MESH:D000686), cardiomyopathy (MESH:D009202), plasma cell dyscrasias (MESH:D010265), multiple myeloma (MESH:D009101), transthyretin amyloid cardiomyopathy (MESH:C567782), heart failure (MESH:D006333)
- **Chemicals:** PYP (MESH:C107241), Technetium-99m pyrophosphate (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12606490/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12606490/full.md

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Source: https://tomesphere.com/paper/PMC12606490