Hyland Andrew, Ambrose Bridget K, Conway Kevin P, Borek Nicolette, Lambert Elizabeth, Carusi Charles, Taylor Kristie, Crosse Scott, Fong Geoffrey T, Cummings K Michael, Abrams David, Pierce John P, Sargent James, Messer Karen, Bansal-Travers Maansi, Niaura Ray, Vallone Donna, Hammond David, Hilmi Nahla, Kwan Jonathan, Piesse Andrea, Kalton Graham, Lohr Sharon, Pharris-Ciurej Nick, Castleman Victoria, Green Victoria R, Tessman Greta, Kaufman Annette, Lawrence Charles, van Bemmel Dana M, Kimmel Heather L, Blount Ben, Yang Ling, O'Brien Barbara, Tworek Cindy, Alberding Derek, Hull Lynn C, Cheng Yu-Ching, Maklan David, Backinger Cathy L, Compton Wilson M
Roswell Park Cancer Institute, Buffalo, New York, USA.
Center for Tobacco Products, US Food and Drug Administration, Silver Spring, Maryland, USA.
Tob Control. 2017 Jul;26(4):371-378. doi: 10.1136/tobaccocontrol-2016-052934. Epub 2016 Aug 8.
This paper describes the methods and conceptual framework for Wave 1 of the Population Assessment of Tobacco and Health (PATH) Study data collection. The National Institutes of Health, through the National Institute on Drug Abuse, is partnering with the Food and Drug Administration's (FDA) Center for Tobacco Products to conduct the PATH Study under a contract with Westat.
The PATH Study is a nationally representative, longitudinal cohort study of 45 971 adults and youth in the USA, aged 12 years and older. Wave 1 was conducted from 12 September 2013 to 15 December 2014 using Audio Computer-Assisted Self-Interviewing to collect information on tobacco-use patterns, risk perceptions and attitudes towards current and newly emerging tobacco products, tobacco initiation, cessation, relapse behaviours and health outcomes. The PATH Study's design allows for the longitudinal assessment of patterns of use of a spectrum of tobacco products, including initiation, cessation, relapse and transitions between products, as well as factors associated with use patterns. Additionally, the PATH Study collects biospecimens from consenting adults aged 18 years and older and measures biomarkers of exposure and potential harm related to tobacco use.
The cumulative, population-based data generated over time by the PATH Study will contribute to the evidence base to inform FDA's regulatory mission under the Family Smoking Prevention and Tobacco Control Act and efforts to reduce the Nation's burden of tobacco-related death and disease.
本文介绍了烟草与健康人口评估(PATH)研究第一轮数据收集的方法和概念框架。美国国立卫生研究院通过国家药物滥用研究所,与美国食品药品监督管理局(FDA)烟草制品中心合作,根据与韦斯塔特公司签订的合同开展PATH研究。
PATH研究是一项具有全国代表性的纵向队列研究,研究对象为美国45971名年龄在12岁及以上的成年人和青少年。第一轮研究于2013年9月12日至2014年12月15日进行,采用音频计算机辅助自我访谈,收集有关烟草使用模式、风险认知以及对现有和新出现烟草制品的态度、烟草起始、戒烟、复吸行为和健康结果等信息。PATH研究的设计允许对一系列烟草制品的使用模式进行纵向评估,包括起始、戒烟、复吸以及不同产品之间的转换,以及与使用模式相关的因素。此外,PATH研究从18岁及以上同意参与的成年人中收集生物标本,并测量与烟草使用相关的接触生物标志物和潜在危害。
PATH研究随着时间推移所产生的基于人群的累积数据,将为证据库做出贡献,以支持FDA根据《家庭吸烟预防与烟草控制法案》履行监管使命,并为减轻国家烟草相关死亡和疾病负担的努力提供依据。