Cargando…

Modeling the Cost and Health Impacts of Diagnostic Strategies in Patients with Suspected Transthyretin Cardiac Amyloidosis

BACKGROUND: Transthyretin cardiac amyloidosis (ATTR‐CMP) is an increasingly recognized and treatable cause of heart failure with preserved ejection fraction. Multimodality cardiac imaging is recommended for ATTR‐CMP diagnosis, but its cost‐effectiveness in current clinical practice has not been well...

Descripción completa

Detalles Bibliográficos
Autores principales: Ge, Yin, Pandya, Ankur, Cuddy, Sarah A. M., Singh, Amitoj, Singh, Avinainder, Dorbala, Sharmila
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/PMC9683684/
https://www.ncbi.nlm.nih.gov/pubmed/36102240
http://dx.doi.org/10.1161/JAHA.122.026308
_version_ 1784835106965291008
author Ge, Yin
Pandya, Ankur
Cuddy, Sarah A. M.
Singh, Amitoj
Singh, Avinainder
Dorbala, Sharmila
author_facet Ge, Yin
Pandya, Ankur
Cuddy, Sarah A. M.
Singh, Amitoj
Singh, Avinainder
Dorbala, Sharmila
author_sort Ge, Yin
collection PubMed
description BACKGROUND: Transthyretin cardiac amyloidosis (ATTR‐CMP) is an increasingly recognized and treatable cause of heart failure with preserved ejection fraction. Multimodality cardiac imaging is recommended for ATTR‐CMP diagnosis, but its cost‐effectiveness in current clinical practice has not been well studied. METHODS AND RESULTS: Using a microsimulation model, we compared the cost‐effectiveness of a combination of strategies involving (99m)technetium pyrophosphate (PYP), cardiac magnetic resonance imaging, and endomyocardial biopsy for the diagnosis of ATTR‐CMP. We developed a decision analytic model to project health care costs and lifetime quality‐adjusted life years for symptomatic, older patients who present with congestive heart failure, with an increased left ventricular wall thickness and a 13% prevalence of ATTR‐CMP. Rates of clinical events, costs, and quality‐of‐life values were estimated from published literature. The analysis was conducted from a US health care system perspective with health and cost outcomes discounted annually at 3%. In the base‐case scenario, using a fixed tafamidis price of $16 000 annually (previously identified cost‐effective price), total health care costs per person were lowest for the PYP‐only strategy ($209 415) and highest for endomyocardial biopsy strategy ($215 881). Of the 7 strategies examined, the PYP‐only strategy had the highest net monetary benefit using a willingness‐to‐pay threshold of $100 000/quality‐adjusted life year. Results were sensitive to variations in model inputs for PYP and cardiac magnetic resonance imaging specificity, cost of tafamidis, and willingness‐to‐pay thresholds. CONCLUSIONS: Our model‐based analyses showed that a PYP‐only strategy to diagnose ATTR‐CMP is the most cost‐effective strategy, at willingness‐to‐pay threshold of $100 000/quality‐adjusted life year. At higher threshold ($150 000/quality‐adjusted life year), sequential tests involving PYP and cardiac magnetic resonance imaging may be considered cost effective.
format Online
Article
Text
id pubmed-9683684
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-96836842022-11-25 Modeling the Cost and Health Impacts of Diagnostic Strategies in Patients with Suspected Transthyretin Cardiac Amyloidosis Ge, Yin Pandya, Ankur Cuddy, Sarah A. M. Singh, Amitoj Singh, Avinainder Dorbala, Sharmila J Am Heart Assoc Original Research BACKGROUND: Transthyretin cardiac amyloidosis (ATTR‐CMP) is an increasingly recognized and treatable cause of heart failure with preserved ejection fraction. Multimodality cardiac imaging is recommended for ATTR‐CMP diagnosis, but its cost‐effectiveness in current clinical practice has not been well studied. METHODS AND RESULTS: Using a microsimulation model, we compared the cost‐effectiveness of a combination of strategies involving (99m)technetium pyrophosphate (PYP), cardiac magnetic resonance imaging, and endomyocardial biopsy for the diagnosis of ATTR‐CMP. We developed a decision analytic model to project health care costs and lifetime quality‐adjusted life years for symptomatic, older patients who present with congestive heart failure, with an increased left ventricular wall thickness and a 13% prevalence of ATTR‐CMP. Rates of clinical events, costs, and quality‐of‐life values were estimated from published literature. The analysis was conducted from a US health care system perspective with health and cost outcomes discounted annually at 3%. In the base‐case scenario, using a fixed tafamidis price of $16 000 annually (previously identified cost‐effective price), total health care costs per person were lowest for the PYP‐only strategy ($209 415) and highest for endomyocardial biopsy strategy ($215 881). Of the 7 strategies examined, the PYP‐only strategy had the highest net monetary benefit using a willingness‐to‐pay threshold of $100 000/quality‐adjusted life year. Results were sensitive to variations in model inputs for PYP and cardiac magnetic resonance imaging specificity, cost of tafamidis, and willingness‐to‐pay thresholds. CONCLUSIONS: Our model‐based analyses showed that a PYP‐only strategy to diagnose ATTR‐CMP is the most cost‐effective strategy, at willingness‐to‐pay threshold of $100 000/quality‐adjusted life year. At higher threshold ($150 000/quality‐adjusted life year), sequential tests involving PYP and cardiac magnetic resonance imaging may be considered cost effective. John Wiley and Sons Inc. 2022-09-14 /pmc/articles/PMC9683684/ /pubmed/36102240 http://dx.doi.org/10.1161/JAHA.122.026308 Text en © 2022 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Ge, Yin
Pandya, Ankur
Cuddy, Sarah A. M.
Singh, Amitoj
Singh, Avinainder
Dorbala, Sharmila
Modeling the Cost and Health Impacts of Diagnostic Strategies in Patients with Suspected Transthyretin Cardiac Amyloidosis
title Modeling the Cost and Health Impacts of Diagnostic Strategies in Patients with Suspected Transthyretin Cardiac Amyloidosis
title_full Modeling the Cost and Health Impacts of Diagnostic Strategies in Patients with Suspected Transthyretin Cardiac Amyloidosis
title_fullStr Modeling the Cost and Health Impacts of Diagnostic Strategies in Patients with Suspected Transthyretin Cardiac Amyloidosis
title_full_unstemmed Modeling the Cost and Health Impacts of Diagnostic Strategies in Patients with Suspected Transthyretin Cardiac Amyloidosis
title_short Modeling the Cost and Health Impacts of Diagnostic Strategies in Patients with Suspected Transthyretin Cardiac Amyloidosis
title_sort modeling the cost and health impacts of diagnostic strategies in patients with suspected transthyretin cardiac amyloidosis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9683684/
https://www.ncbi.nlm.nih.gov/pubmed/36102240
http://dx.doi.org/10.1161/JAHA.122.026308
work_keys_str_mv AT geyin modelingthecostandhealthimpactsofdiagnosticstrategiesinpatientswithsuspectedtransthyretincardiacamyloidosis
AT pandyaankur modelingthecostandhealthimpactsofdiagnosticstrategiesinpatientswithsuspectedtransthyretincardiacamyloidosis
AT cuddysaraham modelingthecostandhealthimpactsofdiagnosticstrategiesinpatientswithsuspectedtransthyretincardiacamyloidosis
AT singhamitoj modelingthecostandhealthimpactsofdiagnosticstrategiesinpatientswithsuspectedtransthyretincardiacamyloidosis
AT singhavinainder modelingthecostandhealthimpactsofdiagnosticstrategiesinpatientswithsuspectedtransthyretincardiacamyloidosis
AT dorbalasharmila modelingthecostandhealthimpactsofdiagnosticstrategiesinpatientswithsuspectedtransthyretincardiacamyloidosis