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阿立哌唑治疗首发精神分裂症的临床观察

The Effect of Aripiprazole on First-onset Schizophrenia
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摘要 目的了解阿立哌唑对首发精神分裂症患者的疗效与耐受性。方法用阿立哌唑治疗56例首发精神分裂症(包括分裂样精神障碍)患者6周,采用阳性与阴性症状量表(PANSS)、副反应量表(TESS)评定疗效及不良反应。结果56例患者治疗后,临床显效率为82.14%,有效率达94.64%,治疗前后患者的PANSS减分率间差别有显著性意义(P<0.01),不良反应主要有轻度的锥体外系症状(EPS)、头痛、失眠、焦虑等,患者的血糖、血脂、体重治疗前后间差别均无显著性意义(P>0.05)。结论阿立哌唑治疗首发精神分裂症患者疗效肯定,不良反应少,依从性较好。 Objective To investigate the effect and side effects of aripiprazole on first - onset schizophrenia. Methods 56 patients with first - onset schizophrenia were treated with arripiprazole for 6 weeks, to evaluate its effect by PANSS and TESS. Results After six - week treatment, the rate of clinical effect was 82 14%, and the effective rate was 94 64%. Significant difference was found in rate of reduction between pre - treatment and post - treatment ( P 〈 0. 01 ), and untoward effects were mainly mild EPS, headache, insomnia and anxiety etc. There was no significant difference in blood gluoose, lipid, body weight and laboratory indexes between pre - treatment and post - treatment. Conclusion The results confirm the effect of arripiprazole on patients with first -onset schizophrenia, with little untoward effects and good obedience.
出处 《中国全科医学》 CAS CSCD 2007年第18期1559-1560,共2页 Chinese General Practice
关键词 阿立哌唑 精神分裂症 治疗结果 Aripiprazole Schizophrenia Treatment outcome
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  • 1[1]Kikuchi T, Tottori K, Uwahodo Y, et al. 7-(4-[4-(2,3-Dichlorophenyl)-1-piperazinyl] butyloxy)-3,4-dihydro-2 ( 1H)-quinolinone (OPC-14597), a new putative antipsychotic drug with both presynaptic dopamine autoreceptor agonistic activity and postsynaptic D2 receptor antagonistic activity. J Pharmacol Exp Ther, 1995 Jul, 274( 1 ) :329 ~ 336
  • 2[2]Fleishhacker WW. New developments in the pharmacotherapy of schizophrenia. J Neural transm Suppl, 2003, 105 ~ 117
  • 3[3]Oshiro Y, Sato S, Kurahashi N, et al. Novel antipsychotic agents with dopamine autoreceptor agonist properties: synthesis and pharmacology of 7-[ 4-( 4-phenyl-1-piperazinyl ) butoxy ]-3, 4-dthydro-2 (1H)-quinolinone derivatives. J Med Chem, 1998 Feb, 41 : 658 ~667
  • 4[4]Matsubayashi H, Amano T, Sasa M. Inhibition by aripiprazole of dopaminergic inputs to striatal neurons from substantia nigra. Psychopharmacolgy (Berl), 1999 Sep, 146(2) : 139 ~ 143
  • 5[5]Lawler CP, Prioleau C, Lewis MM, et al. Interactions of the novel antipsychotic aripiprazole (OPC-14597) with dopamine and serotonin receptor subtypes. Neuropschopharmacolgy, 1999 Jun, 20(6) : 612~627
  • 6[6]Inoue A, Seto M, Sugita S, et al. differential effects on D2 dopamine receptor and prolactin gene expression by haloperidol and aripiprazole in the rat ptiuitary. Brain Res Mol Brain Res, 1998 apr, 55 : 285 ~292
  • 7[7]Shapiro DA, Renock S, Arrington E, et al. Aripiprazole, a novel atypical antipsychotic drug with a unique and robust pharmacology.Neuropsychopharmacology, 2003 May
  • 8[8]Jordan S, Koprivica V, Chen R, et al. The antipsychotic aripiprazole is a potent, partial agonist at the human 5-HT ( 1 A) receptor. Eur J Pharmacol, 2002 Apr 26,441(3) : 137 ~140
  • 9[9]Goodnick P J, Jerry JM. aripiprazole: profile on efficacy and safety.Expert Opin Pharmacother, 2002 Dec, 3(12) : 1773 ~ 1781
  • 10[10]Stahl SM. dopamine system stabilizers, aripiprazole, and the next generation of antipsychotics, part 1, "Goldilocks" actions at dopamine receptors. J Clin Psychiatry, 2001 Nov, 62 (11 ) : 841 ~ 842

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