Impact of antipsychotic medication on family burden in schizophrenia: Longitudinal results of CATIE trial

被引:10
|
作者
Perlick, Deborah A. [1 ,2 ]
Rosenheck, Robert A. [3 ,4 ,5 ]
Kaczynski, Richard [4 ,5 ]
Swartz, Marvin S. [6 ]
Canive, Jose M. [7 ,8 ]
Lieberman, Jeffrey A. [9 ]
机构
[1] Mt Sinai Sch Med, Dept Psychiat, New York, NY 10029 USA
[2] James J Peters VA Med Ctr, Mental Illness Res Educ & Clin Ctr, Bronx, NY 10468 USA
[3] VA Connecticut Hlth Care Syst, New England Mental Illness, Res Educ & Clin Ctr, West Haven, CT 06516 USA
[4] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT 06510 USA
[5] Yale Univ, Sch Med, Dept Epidemiol & Publ Hlth, New Haven, CT 06510 USA
[6] Duke Univ, Dept Psychiat & Behav Sci, Durham, NC 27708 USA
[7] Univ New Mexico, Dept Psychiat, VA Med Ctr, Albuquerque, NM 87108 USA
[8] Univ New Mexico, New Mexico VA Hlth Care Syst, VA Med Ctr, Albuquerque, NM 87108 USA
[9] Columbia Univ Coll Phys & Surg, Dept Psychiat, New York, NY 10032 USA
关键词
Schizophrenia; Family burden; Second-generation antipsychotics; BIPOLAR DISORDER; MENTAL-HEALTH; OLANZAPINE; SCALE; DRUGS;
D O I
10.1016/j.schres.2009.09.026
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: This study evaluated the effectiveness of first- and second-generation antipsychotics in reducing family burden associated with schizophrenia. Methods: The family caregivers of 623 SCID-diagnosed patients enrolled in the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) randomly assigned to a first-generation antipsychotic (perphenazine) or one of four second-generation drugs (olanzapine, quetiapine, risperidone or ziprasidone) were interviewed about resources provided and stresses experienced at baseline and followed for 18 months. Patient symptoms, side effects and service use were assessed as well. Hierarchical regression analyses evaluated the effect of treatment assignment on four burden factors: problem behavior, resource demands and disruption, impairment in activities of daily living and patient helpfulness. Intention-to-treat analyses with all available observations classified based on initial treatment assignment, including observations after medications changed were followed by secondary analyses excluding observations after the first medication change, i.e. only considering initial medication. Results: Despite significant reductions on the problem behavior and resource demands/disruption factors, there were no significant differences between perphenazine and any of the second-generation medications. When only initial treatment period observations were included, patients were perceived as more helpful when medicated with perphenazine as compared to risperidone. in comparisons between second-generation drugs, patients on quetiapine were perceived as more helpful than those on risperidone (p = 0.004). Conclusion: In this 18-month randomized trial. there was no evidence of superiority of second-generation antipsychotics in relieving family burden. (C) 2009 Published by Elsevier B.V.
引用
收藏
页码:118 / 125
页数:8
相关论文
共 50 条
  • [1] The CATIE schizophrenia trial: Results, impact, controversy
    Manschreck, Theo C.
    Boshes, Roger A.
    HARVARD REVIEW OF PSYCHIATRY, 2007, 15 (05) : 245 - 258
  • [2] Impact of the CATIE trial on antipsychotic prescribing
    Citrome, Leslie
    SCHIZOPHRENIA RESEARCH, 2012, 138 (2-3) : 295 - 295
  • [3] Impact of antipsychotic treatment on nonfasting triglycerides in the CATIE Schizophrenia Trial phase 1
    Meyer, Jonathan M.
    Davis, Vicki G.
    McEvoy, Joseph P.
    Goff, Donald C.
    Nasrallah, Henry A.
    Davis, Sonia M.
    Daumit, Gail L.
    Hsiao, John
    Swartz, Marvin S.
    Stroup, T. Scott
    Lieberman, Jeffrey A.
    SCHIZOPHRENIA RESEARCH, 2008, 103 (1-3) : 104 - 109
  • [4] Predictors of antipsychotic dose changes in the CATIE schizophrenia trial
    Hermes, Eric
    Rosenheck, Robert
    PSYCHIATRY RESEARCH, 2012, 199 (01) : 1 - 7
  • [5] INFLAMMATORY MARKERS IN SCHIZOPHRENIA: COMPARING ANTIPSYCHOTIC EFFECTS IN THE CATIE SCHIZOPHRENIA TRIAL
    Nasrallah, Henry A.
    Meyer, J. M.
    McEvoy, J. P.
    Davis, V. G.
    Goff, D. C.
    Davis, S. M.
    SCHIZOPHRENIA BULLETIN, 2009, 35 : 37 - 37
  • [6] Discontinuing and switching antipsychotic medications: Understanding the CATIE schizophrenia trial
    Weiden, Peter J.
    JOURNAL OF CLINICAL PSYCHIATRY, 2007, 68 : 12 - 19
  • [7] Insight and medication adherence in schizophrenia: An analysis of the CATIE trial
    Kim, Julia
    Ozzoude, Miracle
    Nakajima, Shinichiro
    Shah, Parita
    Caravaggio, Fernando
    Iwata, Yusuke
    De Luca, Vincenzo
    Graff-Guerrero, Ariel
    Gerretsen, Philip
    NEUROPHARMACOLOGY, 2020, 168
  • [8] Results of phase 3 of the CATIE schizophrenia trial
    Stroup, T. Scott
    Lieberman, Jeffrey A.
    McEvoy, Joseph R.
    Davis, Sonia M.
    Swartz, Marvin S.
    Keefe, Richard S. E.
    Miller, Alexander L.
    Rosenheck, Robert A.
    Hsiao, John K.
    SCHIZOPHRENIA RESEARCH, 2009, 107 (01) : 1 - 12
  • [9] Longitudinal decision making capacity in the CATIE schizophrenia trial
    Stroup, TS
    SCHIZOPHRENIA RESEARCH, 2006, 81 : 284 - 285
  • [10] Neurocognitive effects of antipsychotic medications in patients with chronic schizophrenia in the CATIE trial
    Keefe, Richard S. E.
    Bilder, Robert M.
    Davis, Sonia M.
    Harvey, Philip D.
    Palmer, Barton W.
    Gold, James M.
    Meltzer, Herbert Y.
    Green, Michael F.
    Capuano, George
    Stroup, T. Scott
    McEvoy, Joseph P.
    Swartz, Marvin S.
    Roscnheck, Robert A.
    Perkins, Diana O.
    Davis, Clarence E.
    Hsiao, John K.
    Lieberman, Jcffrey A.
    ARCHIVES OF GENERAL PSYCHIATRY, 2007, 64 (06) : 633 - 647