Department of Psychiatry and Behavioural Neurosciences (BS, SS), McMaster University, Hamilton, Ontario, Canada; Schlegel-UW Research Institute for Aging (BS, JM-W), Waterloo, Ontario, Canada; GeriMedRisk (BS, JM-W, TJ), Waterloo, Ontario, Canada.
Schlegel-UW Research Institute for Aging (BS, JM-W), Waterloo, Ontario, Canada; GeriMedRisk (BS, JM-W, TJ), Waterloo, Ontario, Canada; Department of Medicine (JM-W), McMaster University, Waterloo, Ontario, Canada.
Am J Geriatr Psychiatry. 2024 Oct;32(10):1259-1270. doi: 10.1016/j.jagp.2024.05.004. Epub 2024 May 16.
Behavioral and psychological symptoms of dementia (BPSD) are common and impart a significant burden to patients, caregivers, and the health system. However, there are few pharmacological options for treating BPSD. We conducted a systematic review of clinical trials examining the efficacy of anticonvulsants in BPSD.
We searched five electronic databases through January 2023, for randomized controlled trials and systematic reviews evaluating the efficacy of non-benzodiazepine anticonvulsants for the treatment of BPSD. We used the Cochrane risk of bias tool to ascertain the risk of bias in included trials. Because statistical pooling of results using meta-analysis was not feasible, we synthesized findings using the Cochrane Synthesis Without Meta-analysis reporting guidelines.
We identified 12 studies, including randomized controlled trials (RCTs) and 1 systematic review. Five RCTs evaluating valproic acid were synthesized by a recent Cochrane review which concluded that this drug is likely ineffective for BPSD. We extracted data from 6 trials involving 248 individuals comparing non-benzodiazepine anticonvulsants to either placebo or risperidone. Four trials (n = 97 participants) evaluated carbamazepine, only one of which demonstrated an improvement in the Brief Psychiatric Rating Scale measuring agitation, hostility, psychosis, and withdrawal/depression (effect size: 1.13; 95% confidence interval [CI]: 0.54-1.73) relative to placebo. Adverse effects were more common in patients receiving carbamazepine (20/27; 74%) relative to placebo (5/24; 21%). There is low quality evidence that oxcarbazepine is likely ineffective and that topiramate may be comparable to risperidone.
Anticonvulsants are unlikely to be effective in BPSD, although the quality of existing evidence is low.
痴呆的行为和心理症状(BPSD)很常见,给患者、护理人员和医疗系统带来了巨大负担。然而,治疗 BPSD 的药物选择有限。我们对评估非苯二氮䓬类抗惊厥药治疗 BPSD 疗效的临床试验进行了系统评价。
我们通过电子数据库检索,搜索了截至 2023 年 1 月的随机对照试验和系统评价,评估了非苯二氮䓬类抗惊厥药治疗 BPSD 的疗效。我们使用 Cochrane 偏倚风险工具来确定纳入试验的偏倚风险。由于使用荟萃分析进行结果的统计学汇总不可行,我们根据 Cochrane 无荟萃分析报告指南综合了研究结果。
我们确定了 12 项研究,包括随机对照试验(RCT)和 1 项系统评价。最近的 Cochrane 综述综合了 5 项评估丙戊酸的 RCT,结论是该药可能对 BPSD 无效。我们从涉及 248 人的 6 项试验中提取了数据,这些试验将非苯二氮䓬类抗惊厥药与安慰剂或利培酮进行了比较。四项试验(n = 97 名参与者)评估了卡马西平,其中只有一项试验显示在测量激越、敌意、精神病和戒断/抑郁的简明精神病评定量表上有改善(效应量:1.13;95%置信区间[CI]:0.54-1.73),与安慰剂相比。与安慰剂(5/24;21%)相比,接受卡马西平的患者(20/27;74%)不良反应更常见。现有证据质量低,表明奥卡西平可能无效,托吡酯可能与利培酮相当。
抗惊厥药治疗 BPSD 可能无效,尽管现有证据质量较低。