Donepezil as add-on treatment of psychotic symptoms in patients with dementia of the Alzheimer's type

被引:20
作者
Bergman, J
Brettholz, I
Shneidman, M
Lerner, V
机构
[1] Mental Hlth Ctr Tirat Carmel, Haifa, Israel
[2] Ben Gurion Univ Negev, Fac Hlth Sci, Minist Hlth, Mental Hlth Ctr, Beer Sheva, Israel
关键词
dementia of the Alzheimer's type; psychotic symptoms; augmentation; donepezil;
D O I
10.1097/00002826-200303000-00008
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Traditionally, the neuropsychiatric symptoms of Alzheimer's disease (AD) have been managed with neuroleptics or benzodiazepines, which have serious side effects. Preliminary observations suggest the possible value of cholinesterase inhibitors in the amelioration of psychotic symptoms in patients with dementia of the Alzheimer's type, dementia with Lewy bodies, and in patients with Parkinson's disease. Twelve inpatients with AD with psychotic symptoms and lack of improvement of their delusions/hallucinations during perphenazine treatment (8 mg/day) for 3 weeks received random open-label donepezil 5 mg daily in addition to an ongoing treatment of 8 mg/day perphenazine or 16 mg/day perphenazine. Assessments conducted at baseline and after weeks 2 and 4 included the Mini-Mental State Examination, the Global Deterioration Scale, the Positive and Negative Symptoms Scale, and the Clinical Global Impressions scale. Frequency of extrapyramidal symptoms was measured according to the Abnormal Involuntary Movement Scale. The donepezil-perphenazine group exhibited substantially greater and clinical improvements in mental state. At the end of the trial (4 weeks), Positive and Negative Symptoms Scale scores revealed significant differences between both groups (p = 0.006). The Clinical Global Impressions scale and the Mini-Mental State Examination scores also showed significant differences between the donepezil-perphenazine group and the perphenazine group (p = 0.028 and p = 0.027 respectively). No significant differences were found in the Global Deterioration Scale scores. Abnormal Involuntary Movement Scale scores showed a significant deterioration in extrapyramidal symptoms in the perphenazine group compared with the donepezil-perphenazine group (p = 0.016). Donepezil augmentation of neuroleptics may be appropriate for those patients for whom neuroleptic monotherapy either does not lead to symptom remission or is associated with intolerable adverse effects. This was an open-label study and there is need for larger studies with double-blind control and a long-term study design to define the efficacy of donepezil for patients with AD and psychotic symptoms.
引用
收藏
页码:88 / 92
页数:5
相关论文
共 30 条
[1]  
[Anonymous], 1986, POSITIVE NEGATIVE SY
[2]   Successful use of donepezil for the treatment of psychotic symptoms in patients with Parkinson's disease [J].
Bergman, J ;
Lerner, V .
CLINICAL NEUROPHARMACOLOGY, 2002, 25 (02) :107-110
[3]   Effects of xanomeline, a selective muscarinic receptor agonist, on cognitive function and behavioral symptoms in Alzheimer disease [J].
Bodick, NC ;
Offen, WW ;
Levey, AI ;
Cutler, NR ;
Gauthier, SG ;
Satlin, A ;
Shannon, HE ;
Tollefson, GD ;
Rasmussen, K ;
Bymaster, FP ;
Hurley, DJ ;
Potter, WZ ;
Paul, SM .
ARCHIVES OF NEUROLOGY, 1997, 54 (04) :465-473
[4]  
Burke WJ, 1999, AM J PSYCHIAT, V156, P1117
[5]   The effects of donepezil in Alzheimer's disease -: Results from a multinational trial [J].
Burns, A ;
Rossor, M ;
Hecker, J ;
Gauthier, S ;
Petit, H ;
Möller, HJ ;
Rogers, SL ;
Friedhoff, LT .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 1999, 10 (03) :237-244
[6]   Donepezil and related cholinesterase inhibitors as mood and behavioral controlling agents. [J].
Burt T. .
Current Psychiatry Reports, 2000, 2 (6) :473-478
[7]  
Casey DE, 1996, J CLIN PSYCHIAT, V57, P40
[8]   PHYSOSTIGMINE AMELIORATES THE DELUSIONS OF ALZHEIMERS-DISEASE [J].
CUMMINGS, JL ;
GORMAN, DG ;
SHAPIRA, J .
BIOLOGICAL PSYCHIATRY, 1993, 33 (07) :536-541
[9]  
Doody RS, 1999, GERONTOLOGY, V45, P1
[10]   Donepezil - A review of its use in Alzheimer's disease [J].
Dooley, M ;
Lamb, HM .
DRUGS & AGING, 2000, 16 (03) :199-226