Li Kanglai, Liao Yingtao, Yang Zhihua, Yang Caishuang, Chen Minhua, Wu Xiuhua, Gan Zhaoyu
Very Important Patients Department, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Department of Psychiatry, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Front Psychiatry. 2021 Jan 8;11:529672. doi: 10.3389/fpsyt.2020.529672. eCollection 2020.
Medication non-adherence is prevalent in patients with bipolar disorder (BD). Long-acting injectable antipsychotics (LAIAs) are widely used to improve compliance with treatment. This study aimed to illustrate the effectiveness, compliance, and safety profile of once-monthly paliperidone palmitate (PP1M), a novel therapeutic LAIA, in the management of bipolar I disorder (BDI). A prospective follow-up was arranged to 11 BDI patients who were prescribed PP1M as monotherapy or adjunctive treatment. Severity of symptoms, disturbing behavior, status of employment, 17-item Hamilton Depression Rating Scale (HAMD-17), and Young Mania Rating Scale (YMRS) were evaluated at the baseline and the endpoint of follow-up. Clinical Global Impression-Bipolar Disorder-Severity of Illness Scale (CGI-BP) and Treatment Emergent Symptom Scale (TESS) were measured at each injection of PP1M. Compliance, relapse or switch, and new hospitalization were monitored through the period of follow-up. The median duration of treatment was 14 months, ranging from 5 to 22 months. The scores (mean ± standard deviation) of HAMD-17, YMRS, and CGI-BP generally decreased from the baseline (16.1 ± 10.3, 30.9 ± 12.6, 5.3 ± 0.7) to the endpoint (7.4 ± 5.7, 3.7 ± 3.2, 2.3 ± 0.7). No disturbing behavior was detected at the endpoint. Neither new hospitalization nor manic/mixed episode occurred during treatment, whereas mild to moderate depressive episodes were reported in three cases. The status of employment of 10 participants (90.9%) was improved, and no new safety concern was detected. PP1M might offer a new valid treatment option in the long-term management of BDI, especially for those with poor compliance with oral medication. However, more studies are needed to further justify such role.
双相情感障碍(BD)患者中药物治疗依从性不佳的情况很普遍。长效注射用抗精神病药物(LAIA)被广泛用于提高治疗依从性。本研究旨在阐明新型治疗性LAIA——每月注射一次的棕榈酸帕利哌酮(PP1M)在双相I型障碍(BDI)管理中的有效性、依从性和安全性。对11例接受PP1M单药治疗或辅助治疗的BDI患者进行了前瞻性随访。在随访的基线和终点评估症状严重程度、干扰行为、就业状况、17项汉密尔顿抑郁量表(HAMD-17)和杨氏躁狂量表(YMRS)。在每次注射PP1M时测量临床总体印象-双相情感障碍-疾病严重程度量表(CGI-BP)和治疗中出现的症状量表(TESS)。在随访期间监测依从性、复发或转相以及再次住院情况。治疗的中位持续时间为14个月,范围为5至22个月。HAMD-17、YMRS和CGI-BP的评分(均值±标准差)总体上从基线时的(16.1±10.3、30.9±12.6、5.3±0.7)降至终点时的(7.4±5.7、3.7±3.2、2.3±0.7)。在终点时未检测到干扰行为。治疗期间既没有再次住院,也没有出现躁狂/混合发作,而有3例报告了轻度至中度抑郁发作。10名参与者(90.9%)的就业状况得到改善,未发现新的安全问题。PP1M可能为BDI的长期管理提供一种新的有效治疗选择,特别是对于那些口服药物依从性差的患者。然而,需要更多研究来进一步证实这种作用。