Kéri Szabolcs, Kelemen Oguz, Janka Zoltán
Szegedi Tudományegyetem, Szent-Györgyi Albert Orvos- és Gyógyszerésztudományi Központ, Altalános Orvostudományi Kar, Pszichiátriai Klinika, Szeged.
Orv Hetil. 2006 Feb 5;147(5):201-4.
Recent evidence raised the possibility that low-dose antipsychotic treatment during the prodromal phase may prevent the development of full-blown psychosis.
To investigate the effectiveness of low-dose antipsychotic medication in the prevention of psychosis.
Fifty-two persons who fulfilled the PACE (Personal Assessment and Crisis Evaluation) criteria of ultra-high risk for psychosis participated in the study. Low-dose antipsychotic treatment (haloperidol or risperidone, 0.5-2 mg/day) was provided for 6 months together with psychoeducation and supportive psychotherapy. Participants were assessed at baseline, 6 months, and 12 months. Antidepressive therapy was provided as needed.
Forty-two persons completed the study from whom 3 (7.1%) developed schizophrenia during the 6-month treatment period. New psychotic episodes were not observed during the 6-month follow-up period. Side effects were mild and transient, appearing in the first 4 weeks of treatment. The participants were satisfied with the treatment.
Given that without a specific treatment, 30-60% of persons with ultra-high risk develop frank psychosis, low-dose antipsychotic treatment seems to be effective in the prevention or delay of psychosis.
最近的证据表明,在前驱期进行低剂量抗精神病药物治疗可能会预防全面性精神病的发生。
研究低剂量抗精神病药物预防精神病的有效性。
52名符合精神病超高风险PACE(个人评估与危机评估)标准的人参与了该研究。提供为期6个月的低剂量抗精神病药物治疗(氟哌啶醇或利培酮,0.5 - 2毫克/天),同时进行心理教育和支持性心理治疗。在基线、6个月和12个月时对参与者进行评估。根据需要提供抗抑郁治疗。
42人完成了研究,其中3人(7.1%)在6个月的治疗期内发展为精神分裂症。在6个月的随访期内未观察到新的精神病发作。副作用轻微且短暂,出现在治疗的前4周。参与者对治疗感到满意。
鉴于在没有特定治疗的情况下,30 - 60%的超高风险人群会发展为明显的精神病,低剂量抗精神病药物治疗似乎在预防或延迟精神病方面有效。