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口服抗精神病药转换为每月注射一次棕榈酸帕利哌酮(PP1M)治疗精神分裂症的疗效和安全性:系统评价和荟萃分析。

Effectiveness and Safety of Switching from Oral Antipsychotics to Once-Monthly Paliperidone Palmitate (PP1M) in the Management of Schizophrenia: A Systematic Review and Meta-Analysis.

机构信息

Peking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Centre for Mental Disorders (Peking University Sixth Hospital), Beijing, China.

Xi'an Janssen Pharmaceutical Ltd., Chaoyang District, Beijing, China.

出版信息

CNS Drugs. 2023 Aug;37(8):695-713. doi: 10.1007/s40263-023-01028-1. Epub 2023 Jul 25.

DOI:10.1007/s40263-023-01028-1
PMID:37490267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10439041/
Abstract

BACKGROUND

Considering the improvement in adherence and convenience, once-monthly paliperidone palmitate (PP1M) has been increasingly used in the treatment of schizophrenia. However, the outcomes for patients who switch from oral antipsychotics (OAPs) to PP1M have not been reliably assessed. The objective of this systematic review and meta-analysis was to investigate the efficacy and safety of PP1M in the management of patients with schizophrenia with a prior history of OAP use.

METHODS

We conducted a systematic search in PubMed, EMBASE, and the Cochrane Library on 19 July 2022 to identify eligible studies. All studies that examined the effectiveness and safety of switching from OAPs to PP1M in patients with schizophrenia were included. The primary outcomes were relapse rate, hospitalisation rate, and the change from baseline in the Positive and Negative Syndrome Scale (PANSS) total score. The secondary outcomes included the changed number of inpatient visits, changed length of stay hospitalisation, change from baseline in the Clinical Global Impressions-Severity (CGI-S) score and the personal and social performance (PSP) total score, response rate, proportion of treatment discontinuation, and adverse events. We included randomised-controlled trials (RCTs), single-arm studies, and observational studies. Case reports, case series, and reviews were excluded. The quality assessment of included studies was performed using the Revised Cochrane risk-of-bias tool for randomised trials (RoB2), the 9-point Newcastle-Ottawa Scale (NOS) instrument for non-randomised studies and cohort studies, and the 12-item National Institutes of Health (NIH) quality assessment tool for before-after (Pre-Post) study without control group. Follow-up times were reported as short- (≤ 13 weeks), medium- (14-26 weeks), and long term (≥ 27 weeks). Data were pooled using meta-analysis.

RESULTS

Fifteen studies with a total of 4740 patients were included. The long-term relapse rates and hospitalisation rates were 12% (95% CI 0.07-0.18) and 18% (95% CI 0.15-0.20), respectively. The short-, medium-, and long-term change in PANSS total score was - 21.69 (95% CI - 30.02 to -13.36), - 14.98 (95% CI - 21.45 to - 8.51) and - 17.88 (95% CI - 31.94 to -3.82), respectively. Approximately 50% of patients reported at least a 30% reduction in the PANSS score at the short-term follow-up. Improvements in CGI-S and PSP score were observed during various periods. There was a reduction in the length of stay hospitalisation and the number of inpatient visits at the medium- and long-term follow-ups. Low discontinuation and adverse event rates were reported.

CONCLUSION

Based on our findings, this study may support the efficacy and safety of switching from OAPs to PP1M for the treatment of patients with schizophrenia. Future large-scale studies are warranted to confirm our findings.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/606c/10439041/76b29c725ef1/40263_2023_1028_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/606c/10439041/995890460323/40263_2023_1028_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/606c/10439041/211a437ae8a3/40263_2023_1028_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/606c/10439041/8b6d4790b670/40263_2023_1028_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/606c/10439041/76b29c725ef1/40263_2023_1028_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/606c/10439041/995890460323/40263_2023_1028_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/606c/10439041/211a437ae8a3/40263_2023_1028_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/606c/10439041/8b6d4790b670/40263_2023_1028_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/606c/10439041/76b29c725ef1/40263_2023_1028_Fig4_HTML.jpg
摘要

背景

鉴于依从性和便利性的提高,每月一次的棕榈酸帕利哌酮(PP1M)已越来越多地用于治疗精神分裂症。然而,从口服抗精神病药物(OAPs)转为使用 PP1M 的患者的结局尚未得到可靠评估。本系统评价和荟萃分析的目的是调查在有 OAP 使用史的精神分裂症患者中使用 PP1M 的疗效和安全性。

方法

我们于 2022 年 7 月 19 日在 PubMed、EMBASE 和 Cochrane 图书馆进行了系统检索,以确定合格的研究。所有研究均评估了将精神分裂症患者从 OAP 转换为 PP1M 的有效性和安全性。主要结局为复发率、住院率和阳性和阴性综合征量表(PANSS)总分的变化。次要结局包括住院就诊次数、住院时间、临床总体印象严重程度(CGI-S)评分和个人和社会表现(PSP)总分的变化、应答率、停药比例和不良事件。我们纳入了随机对照试验(RCTs)、单臂研究和观察性研究。排除病例报告、病例系列和综述。使用修订后的 Cochrane 随机试验偏倚风险工具(RoB2)、非随机研究和队列研究的 9 分纽卡斯尔-渥太华量表(NOS)仪器以及无对照组的 NIH 12 项质量评估工具(Pre-Post)对纳入研究的质量进行评估研究。随访时间报告为短期(≤13 周)、中期(14-26 周)和长期(≥27 周)。使用荟萃分析汇总数据。

结果

纳入了 15 项共 4740 名患者的研究。长期复发率和住院率分别为 12%(95%CI 0.07-0.18)和 18%(95%CI 0.15-0.20)。PANSS 总分的短期、中期和长期变化分别为-21.69(95%CI-30.02 至-13.36)、-14.98(95%CI-21.45 至-8.51)和-17.88(95%CI-31.94 至-3.82)。大约 50%的患者在短期随访时报告至少 30%的 PANSS 评分降低。在各个时期均观察到 CGI-S 和 PSP 评分的改善。在中期和长期随访时,住院时间和住院就诊次数减少。报告的停药和不良事件发生率较低。

结论

根据我们的发现,本研究可能支持将 OAP 转换为 PP1M 治疗精神分裂症患者的疗效和安全性。需要进行大规模的未来研究来证实我们的发现。

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