Table 1.
Source, Reference, Year | No. of Patients, Age | Medication | Trial Length in Weeks | Primary Outcomes |
---|---|---|---|---|
Wilkinson, et al. [71], 2003 | n = 616 Mean age, 75 years | Donepezil | 24 | 2.2-Point improvement on the ADAS-cog among treated patients (10 mg dose) vs a 0.1-point improvement for those receiving placebo (2.1-point treatment difference; p < 0.001); 1.8-point improvement on the ADAS-cog among treated patients (5 mg dose) vs placebo (1.7-point treatment difference; p < 0.01). Patients treated with 5 mg (39%) and those treated with 10 mg (32%) showed improvement on the CIBIC-plus vs 25% of those receiving placebo (p = 0.004 for 5 mg comparison, and p = 0.047 for 10 mg) |
Black, et al. [70], 2003 | n = 603 Mean age, 74 years | Donepezil | 24 | 2.0-Point improvement on the ADAS-cog among treated patients (10 mg dose) vs a 0.3-point decrease for those receiving placebo (2.3-point treatment difference; P < 0.001); 1.6-point improvement on the ADAS-cog among treated patients (5 mg dose) vs placebo (1.9-point treatment difference; p < 0.01). Patients treated with 5 mg (38%) and those treated with 10 mg (31%) showed improvement on the CIBIC-plus vs 32% of those receiving placebo (p < 0.05 for 5 mg comparison, but not significant for 10 mg comparison) |
Roman, et al. [72], 2010 | n = 974, Mean age, 73 years | Donepezil | 24 | 1.0-Point improvement on the V-ADAS-cog among treated patients (5 mg dose) vs a 0.1-point decrease for those receiving placebo (1.2-point treatment difference; P < 0.01); no significant difference in the CIBIC-plus score |
Auchus, et al. [79], 2007 | n = 788 Mean age, 72 years | Galantamine | 26 | 1.8-Point improvement on the ADAS-cog among treated patients vs a 0.3-point improvement for those receiving placebo (1.5-point treatment difference; p < 0.001); no significant difference in the ADCS-ADL score |
Ballard, et al. [82], 2008 | n = 710 Mean age, 73 years | Rivastigmine | 24 | 0.7-Point improvement on the V-ADAS-cog among treated patients vs a 0.6-point decrease for those receiving placebo (1.3-point treatment difference; p = 0.028); no significant difference in the ADCS-CGIC score |
Orgogozo, et al. [86], 2002 | n = 321 Mean age, 76 years | Memantine | 28 | 0.4-Point improvement on the ADAS-cog among treated patients vs a 1.6-point decline for those receiving placebo (2.0-point treatment difference; p = 0.002); no significant difference in the CIBIC-plus score |
Wilcock, et al. [87], 2002 | n = 579 Mean age, 77 years | Memantine | 28 | 0.5-Point decline on the ADAS-cog among treated patients vs a 2.3-point decline for those receiving placebo (1.8-point treatment difference; p < 0.001); no significant difference in the CGIC score. |
Vascular dementia (VaD) was determined by the National Institute of Neurological Disorders and Stroke (NINDS) and the Association Internationale pour la Recherche et l’Enseignement en Neurosciences (NINDS-AIREN) criteria for vascular dementia and computed tomography or magnetic resonance imaging evidence in all trials. The Vascular-Alzheimer’s Disease Assessment Scale-cognitive subscale (V-ADAS-cog) comprises the Alzheimer’s Disease Assessment Scale-cognitive subscale (ADAS-cog) plus the Maze and Number Cancellation test (NCT) to assess executive function
ADCS-ADL = Alzheimer’s Disease Cooperative Study-Activities of Daily Living inventory total score; ADCS-CGIC = Alzheimer’s Disease Cooperative Study-Clinician’s Global Impression of Change; CGIC = Clinical Global Impression of Change; CIBIC-plus = Clinician’s Interview-Based Impression of Change plus Caregiver Input