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. 2011 Feb 7;2011:631690. doi: 10.1155/2011/631690

Table 2.

Psychopathology and clinical improvement measures at baseline, week 4 (end of Phase I) and week 8 (end of Phase II).

Measure, mean (SD) Total sample N = 63 Fast responders *N = 37 Slow responders *N = 26
BPRS total Baseline 54.8 (9.2) 55.1 (9.5) 54.4 (8.9)
Week 4 41.4 (9.8)a 35.9 (5.0)a 49.2 (9.6)a
Week 8 39.1 (9.3)b,c 35.7 (6.9)c 43.9 (10.3)b,c

BPRS psychotic subscale Baseline 14.6 (2.9) 14.3 (2.9) 15.0 (2.8)
Week 4 9.9 (4.0)a 7.3 (1.4)a 13.7 (3.4)
Week 8 8.6 (3.5)b,c 7.4 (2.6)c 10.4 (3.9)b,c

BPRS negative symptoms subscale Baseline 6.3 (2.2) 6.1 (2.2) 6.6 (2.1)
Week 4 5.7 (1.7)a 5.3 (1.4) 6.2 (2.0)
Week 8 5.7 (1.7)c 5.1 (1.2)c 6.5 (1.9)

CGI-S Baseline 4.5 (0.7) 4.5 (0.8) 4.5 (0.7)
Week 4 3.2 (1.1)a 2.5 (0.6)a 4.2 (0.8)a
Week 8 2.8 (1.1)b,c 2.5 (1.0)c 3.3 (1.1)b,c

QLS Baseline 58.8 (20.1) 57.9 (20.9) 60.0 (19.3)
Week 4 68.3 (19.1)a 75.1 (18.0)a 58.5 (16.3)
Week 8 67.9 (20.8)c 74.8 (20.0)c 58.1 (18.1)

*Responder status determined after 4 weeks of risperidone at a dose of 2 mg/day.

Week 8 scores are on an LOCF basis for all measures.

aSignificant change from baseline to week 4, P ≤ .05.

bSignificant change from week 4 to week 8, P ≤ .05.

cSignificant change from baseline to week 8, P ≤ .05.

BPRS: the Brief Psychiatric Rating Scale, CGI-S: Clinical Global Impression Severity Scale, QLS: Quality of Life Scale.