アブストラクト
Japanese
Title | アリピプラゾールによる急性アカシジア発現のリスク因子に関する臨床調査 |
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Subtitle | 一般論文 |
Authors | 白濱雅史1, 石田茂1, 永田健一郎1, 渡邊裕之1, 辻敏和1, 宮崎恭輔2, 江頭伸昭1 |
Authors (kana) | |
Organization | 1九州大学病院薬剤部, 2九州大学病院精神科神経科 |
Journal | 医療薬学 |
Volume | 46 |
Number | 8 |
Page | 414-420 |
Year/Month | 2020 / 8 |
Article | 報告 |
Publisher | 日本医療薬学会 |
Abstract | 「緒言」アカシジアは抗精神病薬の投与によって生じる錐体外路症状の1つであり, 不安や焦燥感, 下肢のむずむず感といった主観的症状と, 落ち着きなく足を揺する, 歩き回るといった客観的症状を特徴とする. アカシジアは急性アカシジア, 遅発性アカシジア, 離脱性アカシジア, 慢性アカシジアに分類され, 最も頻度が高い急性アカシジアは抗精神病薬の開始, 増量, 抗コリン薬の中断によって生じる. 急性アカシジアの治療では原因薬剤の減量, ほかの抗精神病薬への変更が推奨されており, 必要に応じてアカシジア症状の緩和のためにβ遮断薬, 抗コリン薬やベンゾジアゼピン系薬などが用いられる. アカシジアは患者にとって不快感が強く, 治療拒否などアドヒアランス低下につながるだけでなく, 自殺衝動を高める可能性が報告されていることから, 抗精神病薬の使用に際し特に注意を要する副作用の1つとなっている. |
Practice | 薬学 |
Keywords | aripiprazole, acute akathisia, risk factors, extrapyramidal symptoms |
English
Title | Identification of Risk Factors Associated with Aripiprazole-induced Acute Akathisia |
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Subtitle | |
Authors | Masafumi Shirahama1, Shigeru Ishida1, Kenichiro Nagata1, Hiroyuki Watanabe1, Toshikazu Tsuji1, Kyosuke Miyazaki2, Nobuaki Egashira1 |
Authors (kana) | |
Organization | 1Department of Pharmacy, Kyushu University Hospital, 2Department of Neuropsychiatry, Kyushu University Hospital |
Journal | Japanese Journal of Pharmaceutical Health Care and Sciences |
Volume | 46 |
Number | 8 |
Page | 414-420 |
Year/Month | 2020 / 8 |
Article | Report |
Publisher | Japanese Society of Pharmaceutical Health Care and Sciences |
Abstract | Akathisia is one of the extrapyramidal side effects induced by antipsychotics, such as aripiprazole (ARP). Although ARP is used widely in the treatment of various psychiatric disorders, such as schizophrenia, mood disorders, and autism spectrum disorders, there is a higher risk of developing akathisia following treatment with ARP than with other second-generation antipsychotics. However, the risk factors for acute akathisia induced by individual antipsychotics, including ARP, have not been fully established. In this study, we retrospectively analyzed the risk factors for the development of acute akathisia in patients treated with ARP. In total, the study included 160 patients who received ARP between April 2010 and March 2017. We found that 16.3% of all patients (n = 26) experienced ARP-induced acute akathisia within 6 weeks of receiving the first dose. There were significant differences in age (P < 0.01), sex (P = 0.04), and diazepam equivalent dose (P < 0.01) between patient groups with and without akathisia. Moreover, multivariate analysis indicated that age (younger than or equal to 31 years of age, P < 0.01) and diazepam equivalent dose (less than or equal to 4.2 mg, P = 0.03) were relevant factors in the development of ARP-induced acute akathisia. The results of this study suggest that scrupulous clinical attention should be paid to younger patients and patients receiving a relatively low diazepam equivalent dose during treatment with ARP to prevent the development of acute akathisia. |
Practice | Pharmaceutical sciences |
Keywords | aripiprazole, acute akathisia, risk factors, extrapyramidal symptoms |
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