Lawrence Christopher, Roberts Chloe, Galides Chloe, Chamberlain Samuel R, Hou Ruihua
Faculty of Medicine, Clinical and Experimental Sciences, University of Southampton, Southampton, UK.
Hampshire and Isle of Wight Healthcare NHS Foundation Trust, Southampton, UK.
J Psychopharmacol. 2025 Feb;39(2):132-140. doi: 10.1177/02698811241303652. Epub 2024 Dec 10.
Schizophrenia is considered to have a lifetime prevalence of around 1%. Up to 30% of patients diagnosed with schizophrenia are subsequently categorised as treatment resistant. Current guidelines advise against the use of antipsychotic polypharmacy (APP) or high-dose antipsychotic therapy (HDAT) in the treatment of schizophrenia; however, these treatment approaches continue to be used in up to 25% of cases.
This review was to evaluate the evidence for the efficacy and tolerability of APP and HDAT as an alternative to antipsychotic monotherapy at standard doses in the treatment of schizophrenia.
This is a systematic review. We searched PubMed, EMBASE and PsycINFO, for eligible trials published prior to 24 March 2023. The protocol was registered on PROSPERO (CRD42023408785). Quality assessment was conducted using the Revised Cochrane risk-of-bias tool for randomised trials.
A total of 14 studies were included in this review. Two studies demonstrated clinically significant improvement with APP compared to standard treatment. There was no clear evidence that APP or HDAT is definitively less tolerable than antipsychotic monotherapy at a standard dose.
This review found limited evidence for the efficacy of APP and HDAT in the treatment of schizophrenia over the use of antipsychotic monotherapy at a standard dose. The relative tolerability was unclear. Management of treatment-resistant schizophrenia remains a prominent clinical issue and further research, including high-quality large-scale Randomised Controlled Trials (RCTs) of APP and HDAT in patients who have been unresponsive to clozapine, would be of significant benefit to the field of psychiatry.
精神分裂症的终生患病率约为1%。在被诊断为精神分裂症的患者中,高达30%随后被归类为难治性患者。目前的指南不建议在精神分裂症治疗中使用抗精神病药物联合治疗(APP)或高剂量抗精神病药物治疗(HDAT);然而,这些治疗方法仍在高达25%的病例中使用。
本综述旨在评估APP和HDAT作为标准剂量抗精神病单一疗法的替代方法治疗精神分裂症的疗效和耐受性证据。
这是一项系统综述。我们检索了PubMed、EMBASE和PsycINFO,以查找2023年3月24日前发表的符合条件的试验。该方案已在PROSPERO(CRD42023408785)上注册。使用修订后的Cochrane随机试验偏倚风险工具进行质量评估。
本综述共纳入14项研究。两项研究表明,与标准治疗相比,APP有临床显著改善。没有明确证据表明APP或HDAT在耐受性上肯定低于标准剂量的抗精神病单一疗法。
本综述发现,与标准剂量的抗精神病单一疗法相比,APP和HDAT治疗精神分裂症的疗效证据有限。相对耐受性尚不清楚。难治性精神分裂症的管理仍然是一个突出的临床问题,进一步的研究,包括对氯氮平无反应的患者进行APP和HDAT的高质量大规模随机对照试验(RCT),将对精神病学领域有重大益处。