Literature DB >> 10537966

Medical resource use and cost of venlafaxine or tricyclic antidepressant therapy. Following selective serotonin reuptake inhibitor therapy for depression.

R I Griffiths1, E M Sullivan, R G Frank, M J Strauss, R J Herbert, J Clouse, H H Goldman.   

Abstract

OBJECTIVE: An analysis of administrative and claims data was performed to compare the resource use and costs to a managed-care organisation of venlafaxine, a serotonin and norepinephrine reuptake inhibitor (SNRI), versus tricyclic antidepressant (TCA) therapy, after switching from a selective serotonin reuptake inhibitor (SSRI).
DESIGN: One-year costs and frequencies of all medical services, and of services coded for depression, were compared between patients who received venlafaxine and TCA therapy as second-line therapy using bivariate and multivariate statistical analyses.
SETTING: Data were obtained from 9 individual health plans with more than 1.1 million covered lives affiliated with a national managed-care organisation. PATIENTS AND PARTICIPANTS: Health plan members were included if they had a diagnosis of depression between July 1993 and February 1997. They also had to have at least 2 months of prescriptions for SSRI therapy followed by at least 2 months of venlafaxine or TCA therapy, and continuous enrollment in the plan from at least 6 months prior to 12 months following initiation of venlafaxine or TCA therapy. 188 patients who received venlafaxine and 172 patients who received TCAs met the inclusion criteria. MAIN OUTCOME MEASURES AND
RESULTS: Patients who received TCAs were slightly but significantly older (43 vs 40 years) than venlafaxine recipients and, during 6 months prior to initiating therapy, had significantly higher mean costs coded for depression ($US451 vs $US311) and costs not coded for depression ($US4500 vs $US2090). Psychiatrists prescribed a significantly higher proportion of venlafaxine than TCA prescriptions (46.3 vs 25.0%). Prior to adjusting for confounding characteristics, during 12 months following initiation of therapy, mean depression-coded costs were significantly higher for venlafaxine than TCA recipients ($US1948 vs $US1396) and mean costs not coded for depression were significantly lower ($US4595 vs $US6677). Overall costs were not significantly different ($US6543 for venlafaxine vs $US8073 for TCA). Significant cost differences were observed with primary care physicians as initial prescribers of second-line therapy but not with psychiatrists. However, costs between the 2 groups were similar after adjusting for confounding variables, including prior 6-month costs and initial prescriber of second-line therapy.
CONCLUSIONS: Payer costs are similar among patients receiving venlafaxine and TCA therapy following SSRI therapy. Higher costs of venlafaxine pharmacotherapy relative to TCA therapy may be offset by lower costs of other medical services. Differences in prescribing patterns and costs between primary care physicians and psychiatrists warrant further investigation.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10537966     DOI: 10.2165/00019053-199915050-00007

Source DB:  PubMed          Journal:  Pharmacoeconomics        ISSN: 1170-7690            Impact factor:   4.981


  12 in total

1.  Pharmacoeconomic analysis of venlafaxine in the treatment of major depressive disorder.

Authors:  T R Einarson; A Addis; M Iskedjian
Journal:  Pharmacoeconomics       Date:  1997-08       Impact factor: 4.981

2.  A randomized, double-blind comparison of a rapidly escalating dose of venlafaxine and imipramine in inpatients with major depression and melancholia.

Authors:  O Benkert; G Gründer; H Wetzel; D Hackett
Journal:  J Psychiatr Res       Date:  1996 Nov-Dec       Impact factor: 4.791

Review 3.  Striking a balance between safety and efficacy: experience with the SSRI sertraline.

Authors:  D E Casey
Journal:  Int Clin Psychopharmacol       Date:  1994-06       Impact factor: 1.659

4.  Long-term safety and clinical acceptability of venlafaxine and imipramine in outpatients with major depression.

Authors:  R K Shrivastava; C Cohn; J Crowder; J Davidson; D Dunner; J Feighner; A Kiev; R Patrick
Journal:  J Clin Psychopharmacol       Date:  1994-10       Impact factor: 3.153

5.  Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Results from the National Comorbidity Survey.

Authors:  R C Kessler; K A McGonagle; S Zhao; C B Nelson; M Hughes; S Eshleman; H U Wittchen; K S Kendler
Journal:  Arch Gen Psychiatry       Date:  1994-01

Review 6.  Evolutionary trends in the pharmacotherapeutic management of depression.

Authors:  C B Nemeroff
Journal:  J Clin Psychiatry       Date:  1994-12       Impact factor: 4.384

7.  Antidepressant pharmacotherapy: economic outcomes in a health maintenance organization.

Authors:  D A Sclar; L M Robison; T L Skaer; R F Legg; N L Nemec; R S Galin; T E Hughes; D P Buesching
Journal:  Clin Ther       Date:  1994 Jul-Aug       Impact factor: 3.393

8.  A comparison of the cost-effectiveness of sertraline versus tricyclic antidepressants in primary care.

Authors:  J Forder; S Kavanagh; A Fenyo
Journal:  J Affect Disord       Date:  1996-06-05       Impact factor: 4.839

9.  Venlafaxine for treatment-resistant unipolar depression.

Authors:  A A Nierenberg; J P Feighner; R Rudolph; J O Cole; J Sullivan
Journal:  J Clin Psychopharmacol       Date:  1994-12       Impact factor: 3.153

Review 10.  Safety and tolerance profile of venlafaxine.

Authors:  P Danjou; D Hackett
Journal:  Int Clin Psychopharmacol       Date:  1995-03       Impact factor: 1.659

View more
  1 in total

Review 1.  Economic considerations in the prescribing of third-generation antidepressants.

Authors:  Stuart Montgomery; John J Doyle; Lee Stern; Christopher R McBurney
Journal:  Pharmacoeconomics       Date:  2005       Impact factor: 4.981

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.