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Economic Evaluation of Multiple-Pharmacogenes Testing for the Prevention of Adverse Drug Reactions in People Living with HIV

PURPOSE: Pharmacogenetics (PGx) testing is one of the methods for determining whether individuals are at risk of adverse drug reactions (ADRs). It has been reported that multiple-PGx testing, a sequencing technology, has a higher predictive value than single-PGx testing. Therefore, this study aimed...

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Autores principales: Turongkaravee, Saowalak, Praditsitthikorn, Naiyana, Ngamprasertchai, Thundon, Jittikoon, Jiraphun, Mahasirimongkol, Surakameth, Sukasem, Chonlaphat, Udomsinprasert, Wanvisa, Wu, Olivia, Chaikledkaew, Usa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272846/
https://www.ncbi.nlm.nih.gov/pubmed/35832304
http://dx.doi.org/10.2147/CEOR.S366906
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author Turongkaravee, Saowalak
Praditsitthikorn, Naiyana
Ngamprasertchai, Thundon
Jittikoon, Jiraphun
Mahasirimongkol, Surakameth
Sukasem, Chonlaphat
Udomsinprasert, Wanvisa
Wu, Olivia
Chaikledkaew, Usa
author_facet Turongkaravee, Saowalak
Praditsitthikorn, Naiyana
Ngamprasertchai, Thundon
Jittikoon, Jiraphun
Mahasirimongkol, Surakameth
Sukasem, Chonlaphat
Udomsinprasert, Wanvisa
Wu, Olivia
Chaikledkaew, Usa
author_sort Turongkaravee, Saowalak
collection PubMed
description PURPOSE: Pharmacogenetics (PGx) testing is one of the methods for determining whether individuals are at risk of adverse drug reactions (ADRs). It has been reported that multiple-PGx testing, a sequencing technology, has a higher predictive value than single-PGx testing. Therefore, this study aimed to determine the most cost-effective PGx testing strategies for preventing drug-induced serious ADRs in human immunodeficiency virus (HIV)-infected patients. PATIENTS AND METHODS: Potential strategies, including 1) single-PGx esting (ie, HLA-B*57:01 testing before prescribing abacavir, HLA-B*13:01 testing before prescribing co-trimoxazole and dapsone, and NAT2 testing before prescribing isoniazid) and 2) multiple-PGx testing as a combination of four single-gene PGx tests in one panel, were all compared to no PGx testing (current practice). To evaluate total cost in Thai baht (THB) and quality-adjusted life years (QALYs) for each strategy-based approach to a societal perspective, a hybrid decision tree and Markov model was constructed. Incremental cost-effectiveness ratios (ICERs) were estimated. Uncertainty, threshold, and scenario analyses were all performed. RESULTS: Before prescribing HIV therapy, providing single or multiple-PGx testing might save roughly 68 serious ADRs per year, and the number needed to screen (NNS) to avoid one serious ADR was 40. Consequently, approximately 35% and 40% of the cost of ADR treatment could be avoided by the implementation of single- and multiple-PGx testing, respectively. Compared with no PGx testing strategy, the ICERs were 146,319 THB/QALY gained for single-PGx testing and 152,014 THB/QALY gained for multiple-PGx testing. Moreover, the probability of multiple-PGx testing being cost-effective was 45% at the Thai willingness to pay threshold of 160,000 THB per QALY. Threshold analyses showed that multiple-PGx testing remained cost-effective under the range of cost, sensitivity at 0.95–1.00 and specificity at 0.98–1.00. CONCLUSION: Single and multiple-PGx testing might be cost-effective options for reducing the incidence of drug-induced serious ADRs in people living with HIV.
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spelling pubmed-92728462022-07-12 Economic Evaluation of Multiple-Pharmacogenes Testing for the Prevention of Adverse Drug Reactions in People Living with HIV Turongkaravee, Saowalak Praditsitthikorn, Naiyana Ngamprasertchai, Thundon Jittikoon, Jiraphun Mahasirimongkol, Surakameth Sukasem, Chonlaphat Udomsinprasert, Wanvisa Wu, Olivia Chaikledkaew, Usa Clinicoecon Outcomes Res Original Research PURPOSE: Pharmacogenetics (PGx) testing is one of the methods for determining whether individuals are at risk of adverse drug reactions (ADRs). It has been reported that multiple-PGx testing, a sequencing technology, has a higher predictive value than single-PGx testing. Therefore, this study aimed to determine the most cost-effective PGx testing strategies for preventing drug-induced serious ADRs in human immunodeficiency virus (HIV)-infected patients. PATIENTS AND METHODS: Potential strategies, including 1) single-PGx esting (ie, HLA-B*57:01 testing before prescribing abacavir, HLA-B*13:01 testing before prescribing co-trimoxazole and dapsone, and NAT2 testing before prescribing isoniazid) and 2) multiple-PGx testing as a combination of four single-gene PGx tests in one panel, were all compared to no PGx testing (current practice). To evaluate total cost in Thai baht (THB) and quality-adjusted life years (QALYs) for each strategy-based approach to a societal perspective, a hybrid decision tree and Markov model was constructed. Incremental cost-effectiveness ratios (ICERs) were estimated. Uncertainty, threshold, and scenario analyses were all performed. RESULTS: Before prescribing HIV therapy, providing single or multiple-PGx testing might save roughly 68 serious ADRs per year, and the number needed to screen (NNS) to avoid one serious ADR was 40. Consequently, approximately 35% and 40% of the cost of ADR treatment could be avoided by the implementation of single- and multiple-PGx testing, respectively. Compared with no PGx testing strategy, the ICERs were 146,319 THB/QALY gained for single-PGx testing and 152,014 THB/QALY gained for multiple-PGx testing. Moreover, the probability of multiple-PGx testing being cost-effective was 45% at the Thai willingness to pay threshold of 160,000 THB per QALY. Threshold analyses showed that multiple-PGx testing remained cost-effective under the range of cost, sensitivity at 0.95–1.00 and specificity at 0.98–1.00. CONCLUSION: Single and multiple-PGx testing might be cost-effective options for reducing the incidence of drug-induced serious ADRs in people living with HIV. Dove 2022-07-07 /pmc/articles/PMC9272846/ /pubmed/35832304 http://dx.doi.org/10.2147/CEOR.S366906 Text en © 2022 Turongkaravee et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Turongkaravee, Saowalak
Praditsitthikorn, Naiyana
Ngamprasertchai, Thundon
Jittikoon, Jiraphun
Mahasirimongkol, Surakameth
Sukasem, Chonlaphat
Udomsinprasert, Wanvisa
Wu, Olivia
Chaikledkaew, Usa
Economic Evaluation of Multiple-Pharmacogenes Testing for the Prevention of Adverse Drug Reactions in People Living with HIV
title Economic Evaluation of Multiple-Pharmacogenes Testing for the Prevention of Adverse Drug Reactions in People Living with HIV
title_full Economic Evaluation of Multiple-Pharmacogenes Testing for the Prevention of Adverse Drug Reactions in People Living with HIV
title_fullStr Economic Evaluation of Multiple-Pharmacogenes Testing for the Prevention of Adverse Drug Reactions in People Living with HIV
title_full_unstemmed Economic Evaluation of Multiple-Pharmacogenes Testing for the Prevention of Adverse Drug Reactions in People Living with HIV
title_short Economic Evaluation of Multiple-Pharmacogenes Testing for the Prevention of Adverse Drug Reactions in People Living with HIV
title_sort economic evaluation of multiple-pharmacogenes testing for the prevention of adverse drug reactions in people living with hiv
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272846/
https://www.ncbi.nlm.nih.gov/pubmed/35832304
http://dx.doi.org/10.2147/CEOR.S366906
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