Dale R, Longdon M, Seeman M V
Wellborn Baptist Hospital, Evansville, Indiana.
J Psychiatry Neurosci. 1994 Jul;19(4):278-81.
In order to determine the safety of reducing maintenance neuroleptic dose in long-term ambulatory schizophrenia, a step-wise depot reduction study was carried out on patients over a six month period. Doses were reduced by 1/8 of original approximately every two months for a total of three reductions. At the end of dose reduction and at six month follow-up, relapse rate was calculated. Relapse in this study was defined as the clinical decision to either increase neuroleptic dose or to hospitalize. Approximately 50% of the patients relapsed. There was no association with life events as measured by the Paykel scale. Where relapse occurred, it was usually seen subsequent to the second dose reduction. Patients who survived dose reduction had been maintained for a significantly longer period on depot neuroleptics and tended to suffer from a form of schizophrenia which required the co-administration of antidepressants. The findings show that, for a population on long-term depot medication, the risk of symptom exacerbation after gradual step-wise neuroleptic reduction is 50%. The results help to delineate which patients will fall into that 50%.
为了确定在长期非住院精神分裂症患者中减少维持性抗精神病药物剂量的安全性,我们对患者进行了一项为期六个月的逐步长效针剂减量研究。剂量大约每两个月减少原剂量的1/8,总共减少三次。在剂量减少结束时和六个月随访时,计算复发率。本研究中的复发定义为增加抗精神病药物剂量或住院治疗的临床决定。约50%的患者复发。复发与通过佩克尔量表测量的生活事件无关。复发通常发生在第二次剂量减少之后。在剂量减少过程中存活下来的患者使用长效抗精神病药物维持治疗的时间明显更长,并且倾向于患有需要联合使用抗抑郁药的精神分裂症类型。研究结果表明,对于长期使用长效针剂药物的人群,逐步减少抗精神病药物剂量后症状加重的风险为50%。这些结果有助于确定哪些患者会属于这50%的人群。