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Navigating the Complex Web of Prescribing Amyloidosis Therapeutics: A Primer

Advancement in the diagnosis and treatment of transthyretin amyloid cardiomyopathy has made great strides in recent years. Novel therapeutics for transthyretin amyloidosis such as tafamidis, patisiran, and inotersen have shown significant benefits in a not‐so‐rare disease but come with high listing...

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Autores principales: Chen, Hongya, Chandrashekar, Pranav, Fischer, Katherine, Carlson, Dayna, Narayan, Urja, Chen, Jack, Masri, Ahmad
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/PMC9075432/
https://www.ncbi.nlm.nih.gov/pubmed/35301856
http://dx.doi.org/10.1161/JAHA.121.023895
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author Chen, Hongya
Chandrashekar, Pranav
Fischer, Katherine
Carlson, Dayna
Narayan, Urja
Chen, Jack
Masri, Ahmad
author_facet Chen, Hongya
Chandrashekar, Pranav
Fischer, Katherine
Carlson, Dayna
Narayan, Urja
Chen, Jack
Masri, Ahmad
author_sort Chen, Hongya
collection PubMed
description Advancement in the diagnosis and treatment of transthyretin amyloid cardiomyopathy has made great strides in recent years. Novel therapeutics for transthyretin amyloidosis such as tafamidis, patisiran, and inotersen have shown significant benefits in a not‐so‐rare disease but come with high listing price tags ranging from a quarter to more than a half million dollars per year. These costs create significant financial barriers for the majority of patients, especially those with existing Medicare insurance plans. Of 72 patients reviewed, 67% were Medicare beneficiaries. Financial assistance was explored for the majority, and 37 (51%) patients with Medicare Part D received financial assistance that reduced their copayments to $0. Only one‐third of our patients were able to afford these medications without any forms of financial assistance. Of these patients, 4 (6%) had the highest copayments ranging from $13 000 to $15 000 per year. To navigate the complexities of prescribing and affordability in amyloidosis, a multidisciplinary team including a dedicated clinical pharmacist is crucial in guaranteeing patients’ success to secure these novel therapeutics. In this article, we discuss our experiences with prescribing, acquiring insurance authorizations, and financing these life‐saving medications based on patient‐specific insurance plans and socioeconomic status.
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spelling pubmed-90754322022-05-10 Navigating the Complex Web of Prescribing Amyloidosis Therapeutics: A Primer Chen, Hongya Chandrashekar, Pranav Fischer, Katherine Carlson, Dayna Narayan, Urja Chen, Jack Masri, Ahmad J Am Heart Assoc Mini‐Review Advancement in the diagnosis and treatment of transthyretin amyloid cardiomyopathy has made great strides in recent years. Novel therapeutics for transthyretin amyloidosis such as tafamidis, patisiran, and inotersen have shown significant benefits in a not‐so‐rare disease but come with high listing price tags ranging from a quarter to more than a half million dollars per year. These costs create significant financial barriers for the majority of patients, especially those with existing Medicare insurance plans. Of 72 patients reviewed, 67% were Medicare beneficiaries. Financial assistance was explored for the majority, and 37 (51%) patients with Medicare Part D received financial assistance that reduced their copayments to $0. Only one‐third of our patients were able to afford these medications without any forms of financial assistance. Of these patients, 4 (6%) had the highest copayments ranging from $13 000 to $15 000 per year. To navigate the complexities of prescribing and affordability in amyloidosis, a multidisciplinary team including a dedicated clinical pharmacist is crucial in guaranteeing patients’ success to secure these novel therapeutics. In this article, we discuss our experiences with prescribing, acquiring insurance authorizations, and financing these life‐saving medications based on patient‐specific insurance plans and socioeconomic status. John Wiley and Sons Inc. 2022-03-18 /pmc/articles/PMC9075432/ /pubmed/35301856 http://dx.doi.org/10.1161/JAHA.121.023895 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 Mini‐Review
Chen, Hongya
Chandrashekar, Pranav
Fischer, Katherine
Carlson, Dayna
Narayan, Urja
Chen, Jack
Masri, Ahmad
Navigating the Complex Web of Prescribing Amyloidosis Therapeutics: A Primer
title Navigating the Complex Web of Prescribing Amyloidosis Therapeutics: A Primer
title_full Navigating the Complex Web of Prescribing Amyloidosis Therapeutics: A Primer
title_fullStr Navigating the Complex Web of Prescribing Amyloidosis Therapeutics: A Primer
title_full_unstemmed Navigating the Complex Web of Prescribing Amyloidosis Therapeutics: A Primer
title_short Navigating the Complex Web of Prescribing Amyloidosis Therapeutics: A Primer
title_sort navigating the complex web of prescribing amyloidosis therapeutics: a primer
topic Mini‐Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075432/
https://www.ncbi.nlm.nih.gov/pubmed/35301856
http://dx.doi.org/10.1161/JAHA.121.023895
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