Department of Pharmacy, Okayama Saiseikai General Hospital, 2-25 Kokutaicho, Kita-ku, Okayama-shi, Okayama, 700-8511, Japan.
Int J Clin Pharm. 2023 Oct;45(5):1252-1259. doi: 10.1007/s11096-023-01639-0. Epub 2023 Sep 15.
An association between adrenergic alpha-1 receptor antagonists and delirium has been suggested, but the details are unclear.
This study investigated the association between adrenergic alpha-1 receptor antagonists and delirium in patients with benign prostatic hyperplasia using the Japanese Adverse Drug Event Report database.
First, disproportionality analysis compared the frequency of delirium in the adrenergic alpha-1 receptor antagonists silodosin, tamsulosin, and naftopidil. Next, multivariate logistic analysis was performed to examine the association between delirium and adrenergic alpha-1 receptor antagonists where disproportionality was detected.
A disproportionality in delirium was observed in patients receiving tamsulosin (reporting odds ratio [ROR] 1.85, 95% confidence interval [CI] 1.38-2.44, P < 0.01) compared with those who did not, and also in patients receiving naftopidil (ROR 2.23, 95% CI 1.45-3.28, P < 0.01) compared with those who did not. Multivariate logistic analysis revealed that in addition to previously reported risk factors for delirium, delirium in patients receiving tamsulosin was significantly increased with concomitant use of anticholinergics (odds ratio 2.73, 95% CI 1.41-5.29, P < 0.01) and delirium in patients receiving naftopidil was significantly increased with concomitant use of beta3-adrenergic receptor agonists (odds ratio 4.19, 95% CI 1.66-10.6, P < 0.01).
Anticholinergics or beta3-adrenergic receptor agonists to treat overactive bladder in patients receiving tamsulosin and naftopidil was strongly associated with delirium. Confirming the medical history and concomitant medications of patients receiving tamsulosin or naftopidil may contribute to preventing delirium in patients with benign prostatic hyperplasia and to improving their outcomes.
已有研究提示,肾上腺素能α1受体拮抗剂与谵妄之间存在关联,但具体细节尚不清楚。
本研究利用日本药品不良反应报告数据库,调查良性前列腺增生患者使用肾上腺素能α1受体拮抗剂(包括司洛多辛、坦索罗辛和萘哌地尔)与谵妄之间的关系。
首先,采用比例失衡分析比较了司洛多辛、坦索罗辛和萘哌地尔导致谵妄的频率。其次,对存在比例失衡的药物采用多变量逻辑回归分析,调查谵妄与肾上腺素能α1受体拮抗剂之间的关系。
与未使用这些药物的患者相比,使用坦索罗辛的患者发生谵妄的比例失衡更为明显(报告比值比 [ROR] 1.85,95%置信区间 [CI] 1.38-2.44,P<0.01),使用萘哌地尔的患者发生谵妄的比例失衡也更为明显(ROR 2.23,95% CI 1.45-3.28,P<0.01)。多变量逻辑回归分析显示,除了谵妄的已知危险因素外,坦索罗辛与抗胆碱能药物合用的患者发生谵妄的风险显著增加(比值比 2.73,95% CI 1.41-5.29,P<0.01),而萘哌地尔与β3肾上腺素能受体激动剂合用的患者发生谵妄的风险显著增加(比值比 4.19,95% CI 1.66-10.6,P<0.01)。
在坦索罗辛和萘哌地尔使用者中,抗胆碱能药物或β3肾上腺素能受体激动剂治疗膀胱过度活动症与谵妄密切相关。在坦索罗辛或萘哌地尔使用者中,确认其病史和合并用药情况可能有助于预防良性前列腺增生患者发生谵妄,改善其预后。