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评估一种电子蒸气产品在现实环境中被吸烟者使用两年的安全性状况。

Evaluation of the safety profile of an electronic vapour product used for two years by smokers in a real-life setting.

机构信息

Fontem Ventures, Barbara Strozzilaan 101, 1083 HN Amsterdam, The Netherlands.

Covance Clinical Research Unit, Hyde Street, Leeds, LS2 9LH, UK.

出版信息

Regul Toxicol Pharmacol. 2018 Feb;92:226-238. doi: 10.1016/j.yrtph.2017.12.010. Epub 2017 Dec 14.

DOI:10.1016/j.yrtph.2017.12.010
PMID:29248487
Abstract

The safety profile of Puritane™, a closed system electronic vapour product (EVP), was evaluated when used by smokers of conventional cigarettes (CCs) for 24 months in a real-life setting. The study was a two-centre ambulatory clinical study with 209 healthy volunteers. Outcome measures included adverse events (AEs), vital signs, electrocardiogram, lung function tests, exposure to nicotine and selected smoke constituents, nicotine withdrawal effects and smoking desire. No serious AEs related to EVP use were observed. The most frequently reported AEs were headache, nasopharyngitis, sore throat and cough, reported by 28.7%, 28.7%, 19.6% and 16.7% of subjects, respectively, which dissipated over time. Small decreases in lung function were not considered clinically relevant. No clinically relevant findings were observed in the other safety parameters. From Month 2, nicotine withdrawal symptoms decreased. Smoking desire and CC consumption steadily decreased over time in all subjects. EVP use was associated with reduced exposure to cigarette smoke constituents, whereas urinary nicotine levels remained close to baseline. Body weight did not increase in CC subjects switching to the EVP. In conclusion, the aerosol of the EVP at study was well tolerated and not associated with any clinically relevant health concerns after usage for up to 24 months.

摘要

在真实环境中,吸烟者使用封闭式电子蒸气产品(EVP)Puritane™ 长达 24 个月时,评估其安全性概况。该研究是一项具有 2 个中心的门诊临床研究,共有 209 名健康志愿者参与。主要观察终点包括不良事件(AE)、生命体征、心电图、肺功能检查、尼古丁和选定的烟雾成分暴露情况、尼古丁戒断效应和吸烟欲望。未观察到与 EVP 使用相关的严重 AE。报告发生率最高的 AE 分别为头痛(28.7%)、鼻咽炎(28.7%)、咽痛(19.6%)和咳嗽(16.7%),这些 AE 随时间推移而缓解。肺功能的轻微下降被认为不具有临床相关性。其他安全性参数未观察到具有临床意义的发现。从第 2 个月开始,尼古丁戒断症状减少。所有受试者的吸烟欲望和 CC 消耗量随时间推移逐渐下降。EVP 使用与减少香烟烟雾成分的暴露有关,而尿中尼古丁水平仍接近基线。转换为 EVP 的 CC 受试者的体重没有增加。总之,在长达 24 个月的使用过程中,EVP 的气溶胶耐受性良好,不会引起任何具有临床意义的健康问题。

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