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Healthcare resource use associated with the diagnosis of transthyretin amyloidosis cardiomyopathy

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 d...

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Autores principales: Asher, Clint, Guilder, Andrew, Finocchiaro, Gherardo, Carr‐White, Gerry, Rodríguez‐Guadarrama, Yael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733838/
https://www.ncbi.nlm.nih.gov/pubmed/35024457
http://dx.doi.org/10.1002/hsr2.466
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author Asher, Clint
Guilder, Andrew
Finocchiaro, Gherardo
Carr‐White, Gerry
Rodríguez‐Guadarrama, Yael
author_facet Asher, Clint
Guilder, Andrew
Finocchiaro, Gherardo
Carr‐White, Gerry
Rodríguez‐Guadarrama, Yael
author_sort Asher, Clint
collection PubMed
description 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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spelling pubmed-87338382022-01-11 Healthcare resource use associated with the diagnosis of transthyretin amyloidosis cardiomyopathy Asher, Clint Guilder, Andrew Finocchiaro, Gherardo Carr‐White, Gerry Rodríguez‐Guadarrama, Yael Health Sci Rep Research Articles 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. John Wiley and Sons Inc. 2022-01-06 /pmc/articles/PMC8733838/ /pubmed/35024457 http://dx.doi.org/10.1002/hsr2.466 Text en © 2022 The Authors. Health Science Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Asher, Clint
Guilder, Andrew
Finocchiaro, Gherardo
Carr‐White, Gerry
Rodríguez‐Guadarrama, Yael
Healthcare resource use associated with the diagnosis of transthyretin amyloidosis cardiomyopathy
title Healthcare resource use associated with the diagnosis of transthyretin amyloidosis cardiomyopathy
title_full Healthcare resource use associated with the diagnosis of transthyretin amyloidosis cardiomyopathy
title_fullStr Healthcare resource use associated with the diagnosis of transthyretin amyloidosis cardiomyopathy
title_full_unstemmed Healthcare resource use associated with the diagnosis of transthyretin amyloidosis cardiomyopathy
title_short Healthcare resource use associated with the diagnosis of transthyretin amyloidosis cardiomyopathy
title_sort healthcare resource use associated with the diagnosis of transthyretin amyloidosis cardiomyopathy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733838/
https://www.ncbi.nlm.nih.gov/pubmed/35024457
http://dx.doi.org/10.1002/hsr2.466
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