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Cost-effectiveness of CYP2C19-guided P2Y12 inhibitors in Veterans undergoing percutaneous coronary intervention for acute coronary syndromes.
Dong, Olivia M; Friede, Kevin A; Chanfreau-Coffinier, Catherine; Voora, Deepak.
Afiliação
  • Dong OM; Duke Center for Applied Genomics & Precision Medicine, Department of Medicine, Duke University School of Medicine, 101 Science Dr. CIEMAS Building, Durham, NC 27708, USA.
  • Friede KA; Durham VA Health Care System, 508 Fulton St, Durham, NC 27705, USA.
  • Chanfreau-Coffinier C; Duke Center for Applied Genomics & Precision Medicine, Department of Medicine, Duke University School of Medicine, 101 Science Dr. CIEMAS Building, Durham, NC 27708, USA.
  • Voora D; VA Informatics and Computing Infrastructure (VINCI), Salt Lake City VA Health Care System, 500 Foothill Blvd, Salt Lake City, UT 84148, USA.
Eur Heart J Qual Care Clin Outcomes ; 9(3): 249-257, 2023 04 26.
Article em En | MEDLINE | ID: mdl-35652783
AIMS: CYP2C19-guided P2Y12 inhibitor selection can reduce cardiovascular (CV) events and bleeding in patients with acute coronary syndromes (ACSs) post-percutaneous coronary intervention (PCI). The 12-month cost-effectiveness of CYP2C19-guided P2Y12 inhibitor selection for Veterans post-ACS/PCI was evaluated from the Veterans Health Administration's (VHA) perspective. METHODS AND RESULTS: Using average annualized PCI volumes and P2Y12 inhibitor use from VA data, a decision-analytic model simulated CYP2C19 testing vs. no testing outcomes in 2800 hypothetical Veterans receiving PY212 inhibitor for 12 months post-ACS/PCI (74% clopidogrel, 5% prasugrel, and 21% ticagrelor use at baseline without testing). CYP2C19 loss-of-function (LOF) carrier prevalence was 28%. Model inputs were from studies (bleeding/ischaemic events, CYP2C19-guided therapy effect, health state utilities, CYP2C19 LOF carrier prevalence) and VHA administrative data (costs of events, drugs, CYP2C19 testing; PCI volumes, and P2Y12 inhibitor prescriptions). The primary outcome was cost (2020 US${\$}$) per quality-adjusted life year (QALY) gained. Base-case scenarios, probabilistic sensitivity analyses, and scenario analyses were completed. CYP2C19-guided therapy resulted in 496 (24%) escalations (clopidogrel to prasugrel/ticagrelor) and 465 (65%) de-escalations (prasugrel/ticagrelor to clopidogrel). CYP2C19 testing averted 1 stroke, 27 myocardial infarctions, 8 CV-related deaths, and caused 3 bleeds. CYP2C19 testing (vs. no testing) was dominant in the base-case scenario (0.0027 QALYs gained, ${\$}$527 saved/person) and in 97.1% of simulations, making it cost-effective and high-value. In scenario analyses, de-escalation in conjunction with escalation is required for CYP2C19 testing to be cost-effective and high-value. CONCLUSION: In Veterans post-ACS/PCI, CYP2C19-guided P2Y12 inhibitor selection can improve CV outcomes and lower costs for the VHA within 12 months of implementation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Veteranos / Síndrome Coronariana Aguda / Intervenção Coronária Percutânea Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Veteranos / Síndrome Coronariana Aguda / Intervenção Coronária Percutânea Idioma: En Ano de publicação: 2023 Tipo de documento: Article