Key result
Hypothetical optimal pathways can cut ATTR-CM diagnosis time by ~1.7 years per patient.
Why the study?
The healthcare resource use, diagnostic timeline, and costs associated with diagnosing transthyretin amyloidosis cardiomyopathy, along with the potential benefits of an optimized diagnostic pathway, required evaluation.
Observational (n=38)
Yes
Diagnosis of transthyretin amyloidosis cardiomyopathy is delayed by an average of 2.74 years, and optimizing the diagnostic pathway could significantly reduce time to diagnosis and healthcare costs.
Suggests opportunities to shorten diagnostic delays in transthyretin amyloidosis cardiomyopathy; leaves open prospective validation of outcome benefits.
OBJECTIVES: Our primary aim was to evaluate the healthcare resource use associated with the diagnosis of transthyretin amyloidosis cardiomyopathy. Second, we aim to assess the effect of the number of diagnostic tests and clinical contact points on the total time and costs between symptom onset and diagnosis defining a quantitative hypothetical optimized diagnostic pathway. SETTING: Clinical and cost data were collected from patients presenting between 2010 and 2018 in a tertiary referral institution in South London involving two participating hospitals. PARTICIPANTS: Thirty-eight adult patients with a definite diagnosis of transthyretin amyloidosis cardiomyopathy were included, mostly male (n = 28, 74%) and of African-Caribbean descent (n = 23, 64%). We excluded patients without a confirmed transthyretin amyloidosis cardiomyopathy or those on inotersen, patisiran, or diflunisal at point of referral. PRIMARY AND SECONDARY OUTCOME MEASURES: The average time between first presentation and final diagnosis, and the cost per patient per month. By comparing to a more optimal clinical pathway towards diagnosis, we considered what could be the theoretical gain in terms of time to diagnosis and financial savings. RESULTS: The average time between first presentation and final diagnosis was 2.74 years. The average cost per patient per month was higher with progressive heart failure symptoms. A hypothetical optimal pathway reduces time to diagnosis of 1.65 to 1.74 years per patient. The potential financial savings are estimated within the range of £3000 to £4800 per patient. CONCLUSIONS: Patients diagnosed with transthyretin amyloidosis cardiomyopathy have substantial healthcare resource utilization and costs starting from symptom onset. Higher costs were observed with progression in symptoms and appear linked to a delayed diagnosis. The number of additional diagnostic tests and clinical contact points may contribute to this and could represent a path to explore further for important health and cost savings, with more efficient pathways for these patients to be managed.
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Asher et al. (2022) conducted an observational in transthyretin amyloidosis cardiomyopathy (n=38). Current diagnostic pathway vs. Hypothetical optimized diagnostic pathway was evaluated on Average time between first presentation and final diagnosis, and the cost per patient per month. The average time to diagnosis for transthyretin amyloidosis cardiomyopathy was 2.74 years, which a hypothetical optimal pathway could reduce by 1.65 to 1.74 years per patient.
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