Cousin F R, Chabannes J P, Guedj M J, Lachaux B, Pascal J C
CHI de Poissy-Saint-Germain-en-Laye.
Encephale. 2006 Jul-Aug;32(4 Pt 1):466-73. doi: 10.1016/s0013-7006(06)76188-7.
A retrospective observational pharmaco-epidemiological survey was conducted during 24 weeks between October 2004 and March 2005 in metropolitan France (384 investigators) to more clearly define the use of loxapine in acute and chronic psychotic states. The objective of this national survey was to specify the clinical and therapeutic profile of patients managed by this antipsychotic in two cohorts of adult patients: one in "acute phase" (prescription of loxapine during the previous 4 weeks), the other in "maintenance phase" (prescription of loxapine for more than 8 weeks). The two groups of the recruited population (1,511 patients) presented identical sociodemographic data. Selection criteria were adapted to the data collected to ensure statistically relevant analysis: 696 patients in acute phase and 633 patients in maintenance phase. The acute phase group was predominantly composed of known patients (82% of patients had a psychotic history) with schizophrenia (47%) or mood disorders (57%) who had already presented acute episodes (an average of 5.4). The current episode consisted of a state of agitation (88%) lasting an average of two weeks, requiring hospitalization (87%), scheduled admission [HDT (admission at the request of another person) in 47.5% of cases and HO (statutory admission) in 40.8% of cases] and prescription of loxapine monotherapy (56%) at a mean daily dose of 177,3 mg. The maintenance phase group comprised a population of known patients (87.5%), schizophrenics (63%), presenting psychotic symptoms (dissociation 82%, delusions 74%) or mood disorders (71%) requiring voluntary hospitalization (78%) for a mean duration of 180 days and a prescription of loxapine monotherapy in 28% of cases at a mean daily dose of 131.6 mg. The loxapine-haloperidol combination (21%) was prescribed more frequently in the second group in the case of chronic disorders; in the other cases, loxapine was coprescribed with the main second generation antipsychotics: risperidone (16%), olanzapine (16%), amisulpride (11%). CGI assessment of the overall study population revealed a marked or very marked clinical improvement with no significant adverse effects in more than 80% of cases.
2004年10月至2005年3月期间,在法国大都市地区开展了一项为期24周的回顾性观察性药物流行病学调查(384名调查人员参与),以更明确地界定洛沙平在急性和慢性精神病状态中的使用情况。这项全国性调查的目的是明确在两组成年患者中使用这种抗精神病药物治疗的患者的临床和治疗特征:一组处于“急性期”(过去4周内开具洛沙平处方),另一组处于“维持期”(开具洛沙平处方超过8周)。招募人群的两组(1511名患者)呈现出相同的社会人口统计学数据。选择标准根据收集的数据进行调整,以确保进行具有统计学意义的分析:急性期696名患者,维持期633名患者。急性期组主要由已知患者(82%的患者有精神病病史)组成,患有精神分裂症(47%)或情绪障碍(57%),且已经出现过急性发作(平均5.4次)。当前发作表现为激动状态(88%),平均持续两周,需要住院治疗(87%),计划入院(47.5%的病例为HDT(应他人要求入院),40.8%的病例为HO(法定入院)),并开具洛沙平单一疗法(56%),平均日剂量为177.3毫克。维持期组包括已知患者群体(87.5%),精神分裂症患者(63%),表现出精神病症状(解离82%,妄想74%)或情绪障碍(71%),需要自愿住院治疗(78%),平均住院时间为180天,28%的病例开具洛沙平单一疗法,平均日剂量为131.6毫克。在慢性疾病的情况下,第二组更频繁地开具洛沙平 - 氟哌啶醇联合用药(21%);在其他情况下,洛沙平与主要的第二代抗精神病药物联合开具:利培酮(16%)、奥氮平(16%)、氨磺必利(11%)。对整个研究人群的CGI评估显示,超过80%的病例有显著或非常显著的临床改善,且无明显不良反应。