药物基因组学
氯吡格雷
CYP2C19型
医学
华法林
成本效益
重症监护医学
VKORC1型
循证医学
药物经济学
循证实践
药店
梅德林
心房颤动
阿司匹林
内科学
CYP2C9
药理学
替代医学
风险分析(工程)
家庭医学
病理
新陈代谢
细胞色素P450
法学
政治学
作者
Ye Zhu,Kristi M. Swanson,Ricardo L. Rojas,Zhen Wang,Jennifer L. St. Sauver,Sue L. Visscher,Larry J. Prokop,Suzette J. Bielinski,Liewei Wang,Richard Weinshilboum,Bijan J. Borah
标识
DOI:10.1038/s41436-019-0667-y
摘要
To examine the evidence on the cost-effectiveness of implementing pharmacogenomics (PGx) in cardiovascular disease (CVD) care.We conducted a systematic review using multiple databases from inception to 2018. The titles and abstracts of cost-effectiveness studies on PGx-guided treatment in CVD care were screened, and full texts were extracted.We screened 909 studies and included 46 to synthesize. Acute coronary syndrome and atrial fibrillation were the predominantly studied conditions (59%). Most studies (78%) examined warfarin-CYP2C9/VKORC1 or clopidogrel-CYP2C19. A payer's perspective was commonly used (39%) for cost calculations, and most studies (46%) were US-based. The majority (67%) of the studies found PGx testing to be cost-effective in CVD care, but cost-effectiveness varied across drugs and conditions. Two studies examined PGx panel testing, of which one examined pre-emptive testing strategies.We found mixed evidence on the cost-effectiveness of PGx in CVD care. Supportive evidence exists for clopidogrel-CYP2C19 and warfarin-CYP2C9/VKORC1, but evidence is limited in other drug-gene combinations. Gaps persist, including unclear explanation of perspective and cost inputs, underreporting of study design elements critical to economic evaluations, and limited examination of PGx panel and pre-emptive testing for their cost-effectiveness. This review identifies the need for further research on economic evaluations of PGx implementation.
科研通智能强力驱动
Strongly Powered by AbleSci AI