高剂量使用唑吡坦会增加随后发生良性脑肿瘤的风险。

Tomor Harnod, Yu-Fen Li, Cheng-Li Lin, Shih-Ni Chang, Fung-Chang Sung, Chia-Hung Kao
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引用次数: 5

摘要

本研究确定了37,810例焦虑或睡眠障碍患者(平均年龄=53.2岁,SD=16.0岁),这些患者从2000年1月1日至2009年12月31日服用唑吡坦至少2个月。根据估计的治疗概率(倾向得分)与唑吡坦组按1:1匹配选择另一个非唑吡坦组。唑吡坦组与非唑吡坦组相比,良性脑肿瘤的发病率更高,尤其是老年患者。匹配倾向评分分析显示,与未服用唑吡坦的参与者相比,唑吡坦暴露≥520 mg/年的参与者发生良性脑肿瘤的风险最高(风险比=1.85,95%可信区间=1.21-2.82)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Higher-dose uses of zolpidem will increase the subsequent risk of developing benign brain tumors.

This study identified 37,810 patients with anxiety or sleep disorder (mean age=53.2 years, SD=16.0 years) who had zolpidem prescribed for at least 2 months from January 1, 2000 through December 31, 2009. Another non-zolpidem cohort was selected by 1:1 matching with the zolpidem cohort on the estimated probability (propensity score) of being treated. The zolpidem cohort had a higher incidence of benign brain tumors compared with the non-zolpidem cohort, particularly for elderly patients. The matched propensity score analysis showed that the highest risk of benign brain tumors occurred in participants with zolpidem exposure ≥520 mg/year (hazard ratio=1.85, 95% confidence interval=1.21-2.82) compared with those not taking zolpidem.

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