Aupperle Peter M, Koumaras Barbara, Chen Michael, Rabinowicz Adrian, Mirski Dario
Division of Geriatric Psychiatry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway, NJ, USA.
Curr Med Res Opin. 2004 Oct;20(10):1605-12. doi: 10.1185/030079904125004204.
To evaluate the safety and efficacy of long-term treatment with rivastigmine (3-12 mg/day) and its effects on neuropsychiatric and behavioral disturbances in nursing home patients with moderate to severe probable Alzheimer's disease (AD).
A prospective, multicenter 26-week open-label extension to a 26-week open-label study (52 week results) of rivastigmine treatment in patients with Mini-Mental State Examination (MMSE) scores of 6-15 inclusive, residing in nursing homes at 13 centers in the US. Effects of treatment with rivastigmine for up to 52 weeks on neuropsychiatric and behavioral symptoms were examined using the Neuropsychiatric Inventory-Nursing Home (NPI-NH) scale. Cognitive function was assessed by the MMSE, and the Naming Objects and Fingers Test (NOFT) subset of the Alzheimer's Disease Assessment Scale -- Cognitive subscale (ADAS-Cog). Global functioning was assessed using the simplified Clinician's Interview-Based Impression of Change Plus Caregiver Input (CIBIC-Plus).
Rivastigmine (3-12 mg/day) significantly improved neuropsychiatric and behavioral symptoms compared to baseline (in patients with specific behavioral disturbances at baseline) in observed cases (OC) and last observation carried forward (LOCF) analyses. Over 52 weeks, treatment with rivastigmine significantly improved 10 of 12 individual NPI-NH domains from baseline in LOCF patients with symptoms present at baseline. Cognitive function was stable, indicated by the lack of decline in MMSE and the NOFT. Global function was stabilized or improved in greater than half of the patients as indicated by the simplified CIBIC-Plus scores.
Rivastigmine showed potential benefit in the long-term treatment of behavioral symptoms as well as cognitive and global functioning in nursing home residents with moderate to severe AD with concurrent behavioral symptoms present at baseline. Although these results suggest that treatment with rivastigmine may have beneficial behavioral effects and cognitive benefits on patients with moderate to severe AD, they are subject to the limitations of an open-label study.
评估卡巴拉汀长期治疗(3 - 12毫克/天)对中度至重度可能患有阿尔茨海默病(AD)的养老院患者的安全性和有效性,以及其对神经精神和行为障碍的影响。
一项前瞻性、多中心的研究,是对一项为期26周的开放标签研究(52周结果)的26周开放标签扩展研究,研究对象为美国13个中心养老院中简易精神状态检查表(MMSE)评分在6至15分(含)之间的患者。使用神经精神科问卷 - 养老院版(NPI - NH)量表检查卡巴拉汀治疗长达52周对神经精神和行为症状的影响。认知功能通过MMSE以及阿尔茨海默病评估量表 - 认知分量表(ADAS - Cog)的命名物体和手指测试(NOFT)子量表进行评估。整体功能使用简化的基于临床医生访谈的变化印象加照顾者意见(CIBIC - Plus)进行评估。
在观察病例(OC)和末次观察结转(LOCF)分析中,与基线相比(针对基线时有特定行为障碍的患者),卡巴拉汀(3 - 12毫克/天)显著改善了神经精神和行为症状。在52周内,对于基线时有症状的LOCF患者,卡巴拉汀治疗使12个NPI - NH单项领域中的10个从基线水平显著改善。MMSE和NOFT未出现下降,表明认知功能稳定。简化的CIBIC - Plus评分显示,超过半数的患者整体功能稳定或改善。
对于基线时伴有行为症状的中度至重度AD养老院居民,卡巴拉汀在长期治疗行为症状以及认知和整体功能方面显示出潜在益处。尽管这些结果表明卡巴拉汀治疗可能对中度至重度AD患者具有有益的行为和认知益处,但它们受到开放标签研究的局限性。