Olsen Roy E, Kroken Rune A, Bjørhovde Sigmund, Aanesen Kristina, Jørgensen Hugo A, Løberg Else-Marie, Johnsen Erik
Roy E Olsen, Rune A Kroken, Sigmund Bjørhovde, Kristina Aanesen, Erik Johnsen, Division of Psychiatry, Haukeland University Hospital, 5021 Bergen, Norway.
World J Psychiatry. 2016 Dec 22;6(4):442-448. doi: 10.5498/wjp.v6.i4.442.
To investigate whether differential influence on the QTc interval exists among four second generation antipsychotics (SGAs) in psychosis.
Data were drawn from a pragmatic, randomized head-to-head trial of the SGAs risperidone, olanzapine, quetiapine, and ziprasidone in acute admissions patients with psychosis, and with follow-up visits at discharge or maximally 6-9 wk, 3, 6, 12 and 24 mo. Electrocardiograms were recorded on all visits. To mimic clinical shared decision-making, the patients were randomized not to a single drug, but to a sequence of the SGAs under investigation. The first drug in the sequence defined the randomization group, but the patient and/or clinician could choose an SGA later in the sequence if prior negative experiences with the first one(s) in the sequence had occurred. The study focuses on the time of, and actual use of the SGAs under investigation, that is until treatment discontinuation or change, in order to capture the direct medication effects on the QTc interval. Secondary intention-to-treat (ITT) analyses were also performed.
A total of 173 patients, with even distribution among the treatment groups, underwent ECG assessments. About 70% were males and 43% had never used antipsychotic drugs before the study. The mean antipsychotic doses in milligrams per day with standard deviations (SD) were 3.4 (1.2) for risperidone, 13.9 (4.6) for olanzapine, 325.9 (185.8) for quetiapine, and 97.2 (42.8) for ziprasidone treated groups. The time until discontinuation of the antipsychotic drug used did not differ in a statistically significant way among the groups (Log-Rank test: = 0.171). The maximum QTc interval recorded during follow-up was 462 ms. Based on linear mixed effects analyses, the QTc interval change per day with standard error was -0.0030 (0.0280) for risperidone; -0.0099 (0.0108) for olanzapine; -0.0027 (0.0170) for quetiapine, and -0.0081 (0.0229) for ziprasidone. There were no statistically significant differences among the groups in this regard. LME analyses based on ITT groups (the randomization groups), revealed almost identical slopes with -0.0063 (0.0160) for risperidone, -0.0130 (0.0126) for olanzapine, -0.0034 (0.0168) for quetiapine, and -0.0045 (0.0225) for ziprasidone.
None of the SGAs under investigation led to statistically significant QTc prolongation. No statistically significant differences among the SGAs were found.
研究四种第二代抗精神病药物(SGA)对精神病患者QTc间期的影响是否存在差异。
数据来自一项务实的、随机的、头对头试验,该试验纳入了患有精神病的急性入院患者,他们被随机分配接受利培酮、奥氮平、喹硫平和齐拉西酮这几种SGA治疗,并在出院时或最长6 - 9周、3个月、6个月、12个月和24个月时进行随访。每次随访均记录心电图。为模拟临床共同决策,患者并非随机分配至单一药物,而是随机分配至一系列正在研究的SGA。序列中的第一种药物定义随机分组,但如果患者和/或临床医生在序列中第一种药物上有过负面经历,则可在序列中选择其他SGA。本研究关注正在研究的SGA的使用时间及实际使用情况,即直至治疗中断或更改,以捕捉药物对QTc间期的直接影响。还进行了次要意向性治疗(ITT)分析。
共有173例患者接受了心电图评估,各治疗组分布均匀。约70%为男性,43%在研究前从未使用过抗精神病药物。利培酮治疗组、奥氮平治疗组、喹硫平治疗组和齐拉西酮治疗组每天的平均抗精神病药物剂量(毫克)及标准差分别为3.4(1.2)、13.9(4.6)、325.9(185.8)和97.2(42.8)。各治疗组中抗精神病药物停用时间在统计学上无显著差异(对数秩检验:P = 0.171)。随访期间记录到的最大QTc间期为462毫秒。基于线性混合效应分析,利培酮组每天QTc间期变化及标准误为 -0.0030(0.0280);奥氮平组为 -0.0099(0.0108);喹硫平组为 -0.0027(0.0170);齐拉西酮组为 -0.0081(0.0229)。在这方面,各治疗组间无统计学显著差异。基于ITT组(随机分组)的LME分析显示,斜率几乎相同,利培酮组为 -0.0063(0.0160),奥氮平组为 -0.0130(0.0126),喹硫平组为 -0.0034(0.0168),齐拉西酮组为 -0.0045(0.0225)。
所研究的SGA均未导致具有统计学意义的QTc延长。未发现SGA之间存在统计学显著差异。