Page 138 - Drug Class Review
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Page 99 of 205
             Drug Effectiveness Review Project
                                                    treatment in excess of that for placebo treatment was 9% (95% CI: 6% – 10%) excluding one study because
                                       unspecified QOL scale, IDDD; global response defined as improved on a global assessment scale (CGIC or
                                                 Global responders extracted from 9 studies: pooled mean proportion of global responders to ChE inhibitor
                                DON 1-10 mg/d given for 12-54 weeks; RIV 1-12 mg/d given for 13-26 weeks; GAL 8-36 mg/d given for
                                          CIBIC plus) and cognitive responders were defined as subjects with a 4-point or greater improvement in
                                    3-6 months; outcome measures included CGIC; CIBIC; ADAS-Cog, MMSE, NPI, DAD, FRS, PDS,
                                                        of heterogeneity; proportion of cognitive responders could be extracted from 5 studies: pooled mean
















































                                                              10% (95% CI: 4% – 17%)  proportion of cognitive responders to ChE inhibitor treatment in excess of that for placebo treatment was  Compared with those receiving placebo, significantly more subjects receiving ChE inhibitor treatment had  adverse advents (8%) (95% CI: 5% – 11%), dropped out (8%) (95% CI: 5% – 11%) and dropped out  because of adverse events (7%) (95% CI: 3% – 10%)  MEDLINE and EMBASE searches from January 1980 to May 2002; key words ChE inhibitor and AD, and  the limits were RCT, English and human; Cochrane library also searched  Trials included if t








                                              ADAS-Cog                                                meta analysis   Good



















             Final Report Update 1     Authors:  Lanctot et al.   Year: 2003   CHARACTERISTICS OF   INTERVENTIONS:      MAIN RESULTS:      ADVERSE EVENTS:      COMPREHENSIVE  LITERATURE SEARCH   STRATEGY:  STANDARD METHOD OF  APPRAISAL OF STUDIES:         QUALITY RATING:            Alzheimer's Drugs
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