University of Iowa Carver College of Medicine, Iowa City, Iowa
University of Pennsylvania School of Medicine and the Department of Veterans Affairs Medical Center, Philadelphia, Pennsylvania
Quintiles Inc, North Carolina
Yale University School of Medicine, West Haven, Connecticut
Duke University Medical Center, Durham, North Carolina
Mental Health Advocates, Inc, Boca Raton, Florida
Mount Sinai School of Medicine-James J. Peter VAMC, Bronx, New York
State University of New York Downstate Medical Center, Brooklyn, New York
Duke University Medical Center, Durham, North Carolina
North Carolina School of Medicine, Neurosciences Hospital, Chapel Hill, North Carolina
Columbia University College of Physicians and Surgeons, New York, New York, USA
the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) Investigators
Correspondence: Del D. Miller, University of Iowa Carver College of Medicine, Psychiatry Research, #2-105 MEB, 500 Newton Road, Iowa City, IA 52242–1000, USA. Email: del-miller{at}uiowa.edu
AstraZeneca Pharmaceuticals, Bristol-Myers Squibb, Forest Pharmaceuticals Inc, Janssen Pharmaceutica, Eli Lilly & Co, Otsuka Pharmaceutical Co, Ltd, Pfizer Inc, and Zenith Goldline Pharmaceuticals provided medications for the study. Authors declare receipt of funding and/or fees from the following (details in Acknowledgements): AstraZeneca Pharmaceuticals (D.D.M., R.A.R., J.P.McE., B.L.S., M.H.C., M.S.S., R.S.E.K., J.A.L.); Bristol-Myers Squibb (D.D.M., S.N.C., R.A.R., J.P.McE., M.S.S., R.S.E.K., T.S.S., J.A.L.); Eli Lilly & Co (R.A.R., J.P.McE., M.S.S., R.S.E.K., T.S.S., J.A.L.); Forest Laboratories (R.S.E.K.); Forest Pharmaceutical Co (J.A.L.); Forest Research Institute (J.P.McE., J.A.L.); GlaxoSmithKline (T.S.S., J.A.L.); Janssen Pharmaceutica (D.D.M., R.A.R., J.P.McE., B.L.S., M.H.C., R.S.E.K., T.S.S., J.A.L.); Novartis (B.L.S., J.A.L.); Organon (D.D.M., M.H.C.); Ortho-McNeil Neurologics (S.N.C.); Pfizer Inc (D.D.M., S.N.C., J.P.McE., M.H.C., M.S.S., R.S.E.K., J.A.L.); Solvay (M.H.C., J.A.L.). S.M.D is an employee of Quintiles.
Background
There are claims that second-generation antipsychotics produce fewer extrapyramidal side-effects (EPS) compared with first-generation drugs.
Aims
To compare the incidence of treatment-emergent EPS between second-generation antipsychotics and perphenazine in people with schizophrenia.
Method
Incidence analyses integrated data from standardised rating scales and documented use of concomitant medication or treatment discontinuation for EPS events. Mixed model analyses of change in rating scales from baseline were also conducted.
Results
There were no significant differences in incidence or change in rating scales for parkinsonism, dystonia, akathisia or tardive dyskinesia when comparing second-generation antipsychotics with perphenazine or comparing between second-generation antipsychotics. Secondary analyses revealed greater rates of concomitant antiparkinsonism medication among individuals on risperidone and lower rates among individuals on quetiapine, and lower rates of discontinuation because of parkinsonism among people on quetiapine and ziprasidone. There was a trend for a greater likelihood of concomitant medication for akathisia among individuals on risperidone and perphenazine.
Conclusions
The incidence of treatment-emergent EPS and change in EPS ratings indicated that there are no significant differences between second-generation antipsychotics and perphenazine or between second-generation antipsychotics in people with schizophrenia.
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R. A. Rosenheck and M. J. Sernyak Developing A Policy For Second-Generation Antipsychotic Drugs Health Aff., September 1, 2009; 28(5): w782 - w793. [Abstract] [Full Text] [PDF] |
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