Department of Consultation Liaison Psychiatry and Medical Psychiatry, Bellevue Hospital Center, New York University Langone Medical Center, New York, New York, USA.
Palliat Support Care. 2011 Dec;9(4):351-7. doi: 10.1017/S1478951511000368.
The purpose of this study was to examine the efficacy and safety of aripiprazole in the treatment of delirium in hospitalized cancer patients, and to examine differential responses based on delirium subtypes.
We conducted an analysis of 21 hospitalized cancer patients at Memorial Sloan-Kettering Cancer Center (MSKCC) who had been evaluated and treated for delirium with aripiprazole, using an MSKCC Institutional Review Board (IRB) approved Clinical Delirium Database. Measures used were the Memorial Delirium Assessment Scale (MDAS), the Karnofsky Scale of Performance Status (KPS), and side effect rating at baseline (T1), 2-3 days (T2), and 4-7 days (T3). All measurements were integrated into the routine clinical care of patients. Doses of aripiprazole were adjusted based on clinical response.
Patients treated for delirium with aripiprazole experienced significant improvement and resolution of delirium, with MDAS scores declining from a mean of 18.0 at baseline (T1) to mean of 10.8 at T2 and a mean of 8.3 at T3. KPS scores improved from 28.1 at baseline (T1) to 35.2 at T2 and 41 at T3. Delirium resolved (based on MDAS < 10) in 52.4% of cases at T2 and in 76.2% at T3. The mean dosage of aripiprazole required was 18.3 mg (range of 5-30) daily at T3. In our cohort of patients with hypoactive delirium, we observed a delirium resolution rate of 100% compared to the cohort of patients with hyperactive delirium (58.3% rate of delirium resolution). MDAS scores improved from 15.6 at T1 to 5.7 at T3 in hypoactive delirium and from 19.9 at T1 to 10.2 at T3 in hyperactive delirium. In patients with pre-morbid cognitive deficits and the hyperactive subtype of delirium, we observed a more limited treatment response to aripiprazole treatment for delirium. There were no clinically significant side effects noted.
Aripiprazole is effective and safe in the treatment of delirium in hospitalized cancer patients. These preliminary finding suggest that aripiprazole may be most effective in resolving delirium of the hypoactive subtype.
本研究旨在探讨阿立哌唑治疗住院癌症患者谵妄的疗效和安全性,并根据谵妄亚型探讨差异反应。
我们对 Memorial Sloan-Kettering Cancer Center(MSKCC)的 21 名住院癌症患者进行了分析,这些患者使用 MSKCC 机构审查委员会(IRB)批准的临床谵妄数据库,使用阿立哌唑对谵妄进行了评估和治疗。使用的测量方法是纪念谵妄评估量表(MDAS)、卡诺夫斯基表现状态评分(KPS)以及基线(T1)、2-3 天(T2)和 4-7 天(T3)时的副作用评分。所有测量均纳入患者的常规临床护理。根据临床反应调整阿立哌唑的剂量。
接受阿立哌唑治疗谵妄的患者的谵妄明显改善和缓解,MDAS 评分从基线时的平均 18.0 分(T1)下降到 T2 时的平均 10.8 分和 T3 时的平均 8.3 分。KPS 评分从基线时的 28.1 分(T1)提高到 T2 时的 35.2 分和 T3 时的 41 分。T2 时 52.4%的病例和 T3 时 76.2%的病例谵妄缓解(根据 MDAS<10)。T3 时阿立哌唑的平均剂量为 18.3mg(范围 5-30)每日。在我们的低活动型谵妄患者队列中,我们观察到谵妄缓解率为 100%,而高活动型谵妄患者队列的缓解率为 58.3%。MDAS 评分在低活动型谵妄中从 T1 的 15.6 分提高到 T3 的 5.7 分,在高活动型谵妄中从 T1 的 19.9 分提高到 T3 的 10.2 分。在有预先存在的认知缺陷和高活动型谵妄亚型的患者中,我们观察到阿立哌唑治疗谵妄的治疗反应更为有限。没有注意到临床上显著的副作用。
阿立哌唑在治疗住院癌症患者谵妄方面有效且安全。这些初步发现表明,阿立哌唑可能在缓解低活动型谵妄方面最有效。