Usefulness of Gabapentin as an Alternative/Adjunct Therapy for Delirium: A Retrospective Observational Study

被引:0
|
作者
Nakajima-Ohyama, Kakusho Chigusa [1 ,2 ]
Shizusawa, Yoshie [3 ,4 ]
Uchiyama, Shotaro [1 ]
Kishi, Yasuhiro [1 ]
Tanimukai, Hitoshi [5 ]
机构
[1] Nippon Med Sch, Musashi Kosugi Hosp, Dept Neuropsychiat, 1383 Kosugi Cho,Nakahara Ku, Kawasaki, Kanagawa 2118533, Japan
[2] Ikeda Municipal Hosp, Dept Neuropsychiat, Osaka, Japan
[3] Ikeda Municipal Hosp, Dept Palliat Med, Osaka, Japan
[4] Osaka Gyoumeikan Hosp, Dept Palliat Med, Osaka, Japan
[5] Kyoto Univ, Sch Human Hlth Sci, Grad Sch Med, Kyoto, Japan
关键词
gabapentin; delirium; POSTOPERATIVE DELIRIUM; TRIAL; METAANALYSIS; ACID; DRUG; GABA;
D O I
10.1272/jnms.JNMS.2024_91-214
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Antipsychotics are commonly used to treat delirium but can adversely affect the extrapyramidal and cardiac conduction systems. Antipsychotic use has also been reported to be associated with increased mortality in older adults. Therefore, alternative and adjunct medications for delirium are necessary. We retrospectively assessed the efficacy and safety of gabapentin (GBP) as an alternative and adjunct medication for delirium. Methods: We retrospectively investigated the records of patients with delirium treated with GBP (71 patients; median age, 81 years; interquartile range, 76-87.5 years; 54.9% males) at a general hospital. We examined duration to delirium improvement, as assessed by the Intensive Care Delirium Screening Checklist (ICDSC) and DSM-5 criteria, as well as adverse events. Results: The median (interquartile range) GBP dose was 200 mg (150-350 mg)/day. A total of 71.8% and 85.9% of the patients failed to meet the diagnostic criteria for delirium at 2 days and 5 days after initial administration, respectively (p<0.05). In subgroup analysis, patients with a history of epilepsy or cerebrovascular disease responded better to GBP than did those without such histories, suggesting that patients with abnormal/borderline neuronal activity respond to GBP even though they do not exhibit seizures. GBP did not induce extrapyramidal symptoms, cardiac conduction disturbances, hyperglycemia, or epilepsy but caused sleepiness and myoclonus. Conclusions: GBP may improve delirium with fewer adverse effects and may be a safe alternative or adjunct treatment for delirium. Dosage adjustment may be necessary to prevent sleepiness.
引用
收藏
页码:233 / 240
页数:8
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