PMID- 19419595 OWN - NLM STAT- MEDLINE DCOM- 20091123 LR - 20161020 IS - 1469-5111 (Electronic) IS - 1461-1457 (Linking) VI - 12 IP - 9 DP - 2009 Oct TI - Remission in schizophrenia: 196-week, double-blind treatment with ziprasidone vs. haloperidol. PG - 1233-48 LID - 10.1017/S1461145709000352 [doi] AB - To compare the remission rate and its time-course over 196 wk of double-blind treatment with an atypical antipsychotic, ziprasidone (80-160 mg/d given b.i.d., or 80-120 mg/d given q.d.), or a conventional antipsychotic, haloperidol (5-20 mg/d). Outcome assessments included attainment of remission (Andreasen criteria) by longitudinal analysis. Positive and Negative Syndrome Scale (PANSS) scores, Global Assessment of Functioning Scale (GAF) scores, and quality-of-life (QLS) were also assessed in the initial 40-wk study phase (n=599) and the 3-yr extension study (n=186). Discontinuation rates in the initial 40-wk core and follow-up extension studies were comparable between groups: 64% and 65% for the 80-160 mg/d ziprasidone group, 65% and 58% for the 80-120 mg/d ziprasidone group, and 60% and 66% for the 5-20 mg/d haloperidol group, respectively. Mean change scores from baseline to LOCF endpoint (week 40 or early termination) for PANSS negative and GAF (primary efficacy variables) were not statistically significantly different between ziprasidone and haloperidol. During the 3-yr extension study, ziprasidone-treated subjects (80-160 mg/d) were more likely to achieve remission (51%) than haloperidol-treated (40%) subjects (p=0.04), while there was a favourable trend associated with 80-120 mg/d ziprasidone (48%). Compared to the haloperidol group, subjects assigned to the 80-160 mg/d ziprasidone group showed a gradual and persistent improvement in remission (p=0.006) and quality-of-life (p=0.004) in the longitudinal analyses. Significant differences in the trajectory of PANSS total and GAF scores favouring the 80-160 mg/d ziprasidone group were also observed. In this long-term, double-blind study, ziprasidone treatment was more likely to result in remission than haloperidol treatment, and was associated with greater improvement in quality-of-life. FAU - Potkin, Steven G AU - Potkin SG AD - Department of Psychiatry and Human Behavior, University of California, Irvine, CA, USA. sgpotkin@uci.edu FAU - Weiden, Peter J AU - Weiden PJ FAU - Loebel, Antony D AU - Loebel AD FAU - Warrington, Lewis E AU - Warrington LE FAU - Watsky, Eric J AU - Watsky EJ FAU - Siu, Cynthia O AU - Siu CO LA - eng PT - Comparative Study PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't DEP - 20090507 PL - England TA - Int J Neuropsychopharmacol JT - The international journal of neuropsychopharmacology JID - 9815893 RN - 0 (Antipsychotic Agents) RN - 0 (Piperazines) RN - 0 (Thiazoles) RN - 6UKA5VEJ6X (ziprasidone) RN - J6292F8L3D (Haloperidol) SB - IM MH - Adolescent MH - Adult MH - Aged MH - Aged, 80 and over MH - Antipsychotic Agents/adverse effects/*therapeutic use MH - Double-Blind Method MH - Female MH - Haloperidol/adverse effects/*therapeutic use MH - Humans MH - Male MH - Middle Aged MH - Patient Dropouts MH - Piperazines/adverse effects/*therapeutic use MH - Psychiatric Status Rating Scales MH - Quality of Life MH - Remission Induction MH - Schizophrenia/*drug therapy MH - *Schizophrenic Psychology MH - Thiazoles/adverse effects/*therapeutic use MH - Time Factors MH - Treatment Outcome MH - Young Adult EDAT- 2009/05/08 09:00 MHDA- 2009/12/16 06:00 CRDT- 2009/05/08 09:00 PHST- 2009/05/08 09:00 [entrez] PHST- 2009/05/08 09:00 [pubmed] PHST- 2009/12/16 06:00 [medline] AID - S1461145709000352 [pii] AID - 10.1017/S1461145709000352 [doi] PST - ppublish SO - Int J Neuropsychopharmacol. 2009 Oct;12(9):1233-48. doi: 10.1017/S1461145709000352. Epub 2009 May 7.