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长期有效性和安全性的瓦伦尼克林和尼古丁替代疗法在有神经发育障碍的人:前瞻性队列研究。

Long-term effectiveness and safety of varenicline and nicotine replacement therapy in people with neurodevelopmental disorders: A prospective cohort study.

机构信息

Medical Research Council Integrative Epidemiology Unit at the University of Bristol, Bristol, BS8 2BN, United Kingdom.

School of Psychological Science, 12a Priory Road, Bristol, BS8 1TU, United Kingdom.

出版信息

Sci Rep. 2019 Dec 20;9(1):19488. doi: 10.1038/s41598-019-54727-5.

DOI:10.1038/s41598-019-54727-5
PMID:31862899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6925148/
Abstract

This study aimed to determine the effectiveness and safety of varenicline versus NRT for smoking cessation in people with neurodevelopmental disorders, compared to those without, at up to four years after exposure. We analysed electronic medical records from the Clinical Practice Research Datalink using three different statistical approaches: multivariable logistic regression, propensity score matching (PSM), and instrumental variable analysis. Exposure was prescription of varenicline versus NRT and the primary outcome was smoking cessation at 2-years. We included 235,314 people aged 18 and above with eligible smoking cessation prescriptions in the effectiveness analysis. Smokers with neurodevelopmental disorders were 48% less likely (95% confidence interval: 42%, 54%) to be prescribed varenicline than NRT, compared to smokers without neurodevelopmental disorders. At 2-year follow-up, smokers with neurodevelopmental disorders prescribed varenicline were 38% more likely to quit smoking (95% confidence interval: 6%, 78%). Similar results were obtained using PSM and instrumental variable analyses. There was little evidence showing that varenicline increased the likelihood of mental health related adverse events in people with neurodevelopmental disorders. Varenicline is less likely to be prescribed to people with neurodevelopmental disorders despite results suggesting it is more effective than NRT and little evidence of increased likelihood of mental health related adverse events.

摘要

本研究旨在确定与无神经发育障碍者相比,在接触后长达四年的时间内,与尼古丁替代疗法(NRT)相比,用伐伦克林戒烟对神经发育障碍者的有效性和安全性。我们使用三种不同的统计方法,即多变量逻辑回归、倾向评分匹配(PSM)和工具变量分析,对来自临床实践研究数据库的电子病历进行了分析。暴露因素为处方用伐伦克林与 NRT,主要结局为 2 年时的戒烟情况。我们在有效性分析中纳入了 235314 名年龄在 18 岁及以上且有合格戒烟处方的患者。与无神经发育障碍的吸烟者相比,有神经发育障碍的吸烟者处方用伐伦克林的可能性低 48%(95%置信区间:42%,54%),而处方用 NRT 的可能性高 48%。在 2 年的随访中,有神经发育障碍的吸烟者处方用伐伦克林的戒烟可能性高 38%(95%置信区间:6%,78%)。使用 PSM 和工具变量分析也得到了类似的结果。几乎没有证据表明,伐伦克林会增加有神经发育障碍者出现心理健康相关不良事件的可能性。尽管有研究表明伐伦克林比 NRT 更有效,但有神经发育障碍者使用伐伦克林的可能性较小,且几乎没有证据表明心理健康相关不良事件的发生几率会增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582c/6925148/dc2d2eac6a62/41598_2019_54727_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582c/6925148/cfcea292698c/41598_2019_54727_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582c/6925148/913443e5b67b/41598_2019_54727_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582c/6925148/dc2d2eac6a62/41598_2019_54727_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582c/6925148/cfcea292698c/41598_2019_54727_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582c/6925148/913443e5b67b/41598_2019_54727_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582c/6925148/dc2d2eac6a62/41598_2019_54727_Fig3_HTML.jpg

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本文引用的文献

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Neuropsychiatric Safety and Efficacy of Varenicline, Bupropion, and Nicotine Patch in Smokers With Psychotic, Anxiety, and Mood Disorders in the EAGLES Trial.在EAGLES试验中,伐尼克兰、安非他酮和尼古丁贴片对患有精神病性、焦虑和情绪障碍的吸烟者的神经精神安全性和有效性。
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