Ma Hui, Huang Yinglin, Cong Zhengtu, Wang Yuan, Jiang Wenhai, Gao Shuhe, Zhu Gang
Department of Psychiatry, The First Affiliated Hospital of China Medical University, Shenyang, China Center for Mental Health, Yanshan University, Qinhuangdao, China.
Department of Psychiatry, The First Affiliated Hospital of China Medical University, Shenyang, China Department of Psychiatry, Shengjing Hospital of China Medical University, Shenyang, China.
J Alzheimers Dis. 2014;42(3):915-37. doi: 10.3233/JAD-140579.
The application of atypical antipsychotics (SGAs) for treatment of psychiatric and behavioral symptoms of dementia is controversial since their efficacy might be offset by their adverse events (AEs).
To assess the efficacy, safety, and tolerability of SGAs for treatment of psychological and behavioral symptoms of dementia.
Two researchers searched MEDLINE, PsychINFO, and the Cochrane Central Register of Controlled Trials independently for double-blind, placebo-controlled, randomized controlled trials (DB-PC-RCTs) as of June 2013, written in English. Efficacy was measured using the Brief Psychiatric Rating Scale (BPRS), Cohen-Mansfield Agitation Inventory (CMAI), Neuropsychiatric Inventory (NPI), Clinical Global Impression of Change (CGI-C), and (or) Clinical Global Impression of Severity (CGI-S). Safety and tolerability were measured by frequencies of drop-outs, AEs, and death. In total, 19 treatment comparisons drawn from 16 DB-PC-RCTs were included, and 3,343 patients randomized to the antipsychotic group and 1,707 to the placebo group were assessed.
This meta-analysis demonstrated a significant efficacy of atypical antipsychotics on BPRS (MD = -1.58, 95% CI = -2.52 - -0.65), CMAI (-1.84, -3.01 - -0.61), NPI (-2.81, -4.35 - -1.28), CGI-C (-0.32, -0.44 - -0.20), and CGI-S (-0.19, -0.30 - -0.09), compared to placebo (p < 0.01 for all). Patients receiving atypical antipsychotics showed no difference in risk for discontinuation (p > 0.05), significantly higher risks (p < 0.05 for all) for somnolence (OR = 2.95), extrapyramidal symptoms (1.74), cerebrovascular AEs (2.50), urinary tract infection (1.35), edema (1.80), gait abnormality (3.35), and death (1.52), and a lower risk for agitation (OR = 0.80, p = 0.03).
The higher risks for AEs and mortality may offset the efficacy of atypical antipsychotics for treatment of dementia. Efficacy, safety, and tolerability thus should be carefully considered against clinical need.
非典型抗精神病药物(SGA)用于治疗痴呆的精神和行为症状存在争议,因为其疗效可能会被不良事件(AE)抵消。
评估SGA治疗痴呆心理和行为症状的疗效、安全性及耐受性。
两名研究人员独立检索截至2013年6月的MEDLINE、PsychINFO和Cochrane对照试验中央注册库,查找英文撰写的双盲、安慰剂对照、随机对照试验(DB-PC-RCT)。疗效通过简明精神病评定量表(BPRS)、科恩-曼斯菲尔德激越量表(CMAI)、神经精神科问卷(NPI)、临床总体印象变化量表(CGI-C)和(或)临床总体印象严重程度量表(CGI-S)进行衡量。安全性和耐受性通过脱落率、AE和死亡频率来衡量。总共纳入了来自16项DB-PC-RCT的19项治疗比较,评估了3343例随机分配至抗精神病药物组的患者和1707例随机分配至安慰剂组的患者。
该荟萃分析表明,与安慰剂相比,非典型抗精神病药物在BPRS(MD=-1.58,95%CI=-2.52--0.65)、CMAI(-1.84,-3.01--0.61)、NPI(-2.81,-4.35--1.28)、CGI-C(-0.32,-0.44--0.20)和CGI-S(-0.19,-0.30--0.09)方面具有显著疗效(所有p<0.01)。接受非典型抗精神病药物治疗的患者在停药风险方面无差异(p>0.05),在嗜睡(OR=2.95)、锥体外系症状(1.74)、脑血管AE(2.50)、尿路感染(1.35)、水肿(1.80)、步态异常(3.35)和死亡(1.52)方面的风险显著更高(所有p<0.05),而激越风险较低(OR=0.80,p=0.03)。
AE和死亡的较高风险可能会抵消非典型抗精神病药物治疗痴呆的疗效。因此,应根据临床需求仔细考虑疗效、安全性和耐受性。