Altamura A C, Mauri M C, De Novellis F, Percudani M, Vampini V
Department of Clinical Psychiatry, University of Milan, Italy.
Pharmacopsychiatry. 1989 Nov;22(6):246-9. doi: 10.1055/s-2007-1014608.
A naturalistic study was performed on 44 schizophrenic outpatients diagnosed according to DSM III-R and presenting neuroleptic-induced extrapyramidal side-effects. All patients had been treated continuously for the previous 10-12 weeks with haloperidol (HL) combined with orphenadrine (ORD). The dosages of HL and ORD remained unchanged for at least four weeks before the evaluations. All patients were assessed for depressive features (HRS-D), extrapyramidal (EPSE) and anticholinergic (ACS check list) side-effects. The plasma levels of ORD and its metabolite tofenacine (TOF) were determined by gas chromatography. There was a positive relationship between HRS-D and EPSE total scores, while there was a negative relationship between age and EPSE total scores. No relationship between the administered dose and plasma levels of ORD was found. The HL daily dose (mg/kg), ORD plasma levels and the TOF/ORD plasma level ratio seem to influence significantly the severity of residual extrapyramidal side-effects.
对44名根据《精神疾病诊断与统计手册》第三版修订版(DSM III-R)诊断为精神分裂症的门诊患者进行了一项自然主义研究,这些患者存在抗精神病药物引起的锥体外系副作用。所有患者在之前的10至12周内一直接受氟哌啶醇(HL)与奥芬那君(ORD)联合治疗。在评估前,HL和ORD的剂量至少四周保持不变。对所有患者进行了抑郁特征(汉密尔顿抑郁量表,HRS-D)、锥体外系(锥体外系症状评定量表,EPSE)和抗胆碱能(抗胆碱能症状检查表,ACS)副作用的评估。通过气相色谱法测定ORD及其代谢产物托芬那辛(TOF)的血浆水平。HRS-D总分与EPSE总分之间呈正相关,而年龄与EPSE总分之间呈负相关。未发现ORD的给药剂量与血浆水平之间存在关联。HL每日剂量(mg/kg)、ORD血浆水平以及TOF/ORD血浆水平比值似乎对残留锥体外系副作用的严重程度有显著影响。