Medication Adherence and Persistence in Patients with Severe Major Depressive Disorder with Psychotic Features: Antidepressant and Second-Generation Antipsychotic Therapy Versus Antidepressant Monotherapy

被引:11
作者
Kim-Romo, Dawn N. [1 ]
Rascati, Karen L. [1 ]
Richards, Kristin M. [2 ]
Ford, Kentya C. [1 ]
Wilson, James P. [1 ]
Beretvas, Susan N. [3 ]
机构
[1] Univ Texas Austin, Coll Pharm, Hlth Outcomes & Pharm Practice, 1 Univ Stn,A1900, Austin, TX 78712 USA
[2] Univ Texas Austin, Coll Pharm, Ctr Pharmacoecon Studies, Austin, TX 78712 USA
[3] Univ Texas Austin, Coll Educ, Res & Grad Studies, Austin, TX 78712 USA
关键词
DOUBLE-BLIND; CONTROLLED-TRIAL; PLUS PLACEBO; OLANZAPINE; COMBINATION; PREVALENCE; QUETIAPINE; SERTRALINE; PATTERNS;
D O I
10.18553/jmcp.2016.22.5.588
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
BACKGROUND: Major depressive disorder with psychotic features, or psychotic depression, is a severe mental health disorder often associated with a worse depression-related symptom profile when compared with major depressive disorder without psychotic features. While combination pharmacotherapy with an antidepressant and an antipsychotic is recommended as first-line therapy, antidepressant monotherapy has been found to be useful and efficacious in psychotic depression. OBJECTIVE: To assess the rates of antidepressant adherence and antidepressant persistence in Texas Medicaid patients with psychotic depression who used antidepressant plus second-generation antipsychotic (AD/SGA) therapy or antidepressant (AD) monotherapy. METHODS: Using Texas Medicaid prescription and medical claims data from September 2007 to December 2012, adult patients aged 18-63 years were included if they had no confounding psychiatric disorders, no antidepressant claims during a 6-month pre-index period, and at least 1 diagnosis for severe major depressive disorder with psychotic features (ICD-9-CM codes 296.24 and 296.34). The first claim date for an antidepressant served as the index date. All patients were required to have at least 2 antidepressant claims, and those in the AD/SGA cohort were required to have 2 or more claims for an SGA. Study covariates included age, gender, race/ethnicity, residence, Charison Comorbidity Index (CCI) score, and tobacco use/dependence. Statistical analyses included descriptive statistics, univariate analyses, logistic regression, and Cox proportional hazards regression. RESULTS: A total of 926 patients met study criteria (AD cohort=510; AD/SGA cohort=416). The overall sample had a mean [+/- SD] age of 40.5 [+/- 13.2] years and was primarily female (66.8%) and non-Caucasian (74.8%). When compared with the AD cohort, patients in the AD/SGA cohort had a 52.3% higher likelihood of being adherent to antidepressant therapy based on proportion of days covered (PDC; OR=1.523; 95% CI=1.129-2.053; P=0.006). Similarly, antidepressant adherence was 42.0% higher for the AD/SGA cohort based on medication possession ratio (MPR; OR=1.420; 95% CI=1.062-1.898; P=0.018). Younger patients, African Americans, and tobacco users/dependents had significantly worse likelihoods of antidepressant medication adherence based on PDC and MPR. The risk of antidepressant nonpersistence was 23.2% lower for patients in the AD/SGA cohort (HR=0.768; 95% CI = 0.659-0.896; P=0.001), compared with those in the AD cohort. Antidepressant nonpersistence was significantly higher in younger patients, African Americans, Hispanics, and tobacco users/dependents. CONCLUSIONS: Better antidepressant adherence and persistence outcomes were associated with combination pharmacotherapy with an AD and an SGA antipsychotic. This study provides real-world estimates that support the current first-line treatment recommendations for psychotic depression; however, it should be noted that the majority of study patients used AD therapy only. Future research in psychotic depression is needed. Copyright 2016, Academy of Managed Care Pharmacy. All rights reserved.
引用
收藏
页码:588 / 596
页数:9
相关论文
共 35 条
  • [1] [Anonymous], PRACT GUID TREATM PA
  • [2] [Anonymous], 2000, DIAGN STAT MAN MENT, DOI DOI 10.1176/APPI.BOOKS.9780890425787
  • [3] Bauer MS, 2002, HARVARD REV PSYCHIAT, V10, P138, DOI 10.1080/10673220216217
  • [4] Treatment of mood-congruent psychotic depression with imipramine
    Bruijin, JA
    Moleman, P
    Mulder, PGH
    van den Broek, WW
    [J]. JOURNAL OF AFFECTIVE DISORDERS, 2001, 66 (2-3) : 165 - 174
  • [5] Psychotic versus non-psychotic major depressive disorder: A comparative naturalistic study
    Buoli, Massimiliano
    Caldiroli, Alice
    Altamura, Alfredo Carlo
    [J]. ASIAN JOURNAL OF PSYCHIATRY, 2013, 6 (04) : 333 - 337
  • [6] Methods for evaluating patient adherence to antidepressant therapy - A real-world comparison of adherence and economic outcomes
    Cantrell, CR
    Eaddy, MT
    Shah, MB
    Regan, TS
    Sokol, MC
    [J]. MEDICAL CARE, 2006, 44 (04) : 300 - 303
  • [7] THE CLINICAL AND NEUROENDOCRINE FEATURES OF PSYCHOTIC DEPRESSION
    CORYELL, W
    PFOHL, B
    ZIMMERMAN, M
    [J]. JOURNAL OF NERVOUS AND MENTAL DISEASE, 1984, 172 (09) : 521 - 528
  • [8] Medication use patterns and two-year outcome in first-admission patients with major depressive disorder with psychotic features
    Craig, Thomas J.
    Grossman, Steven
    Bromet, Evelyn J.
    Fochtmann, Laura J.
    Carlson, Gabrielle A.
    [J]. COMPREHENSIVE PSYCHIATRY, 2007, 48 (06) : 497 - 503
  • [9] First-episode psychosis: An epidemiological survey comparing psychotic depression with schizophrenia
    Crebbin, Kathleen.
    Mitford, Emma
    Paxton, Roger
    Turkington, Douglas
    [J]. JOURNAL OF AFFECTIVE DISORDERS, 2008, 105 (1-3) : 117 - 124
  • [10] The Texas Medication Algorithm Project: Report of the Texas Consensus Conference Panel on medication treatment of major depressive disorder
    Crismon, ML
    Trivedi, M
    Pigott, TA
    Rush, AJ
    Hirschfeld, RMA
    Kahn, DA
    DeBattista, C
    Nelson, JC
    Nierenberg, AA
    Sackeim, HA
    Thase, ME
    [J]. JOURNAL OF CLINICAL PSYCHIATRY, 1999, 60 (03) : 142 - 156