Literature DB >> 10155603

Paroxetine. A pharmacoeconomic evaluation of its use in depression.

M I Wilde1, R Whittington.   

Abstract

There has been intense debate about whether the use of paroxetine or other selective serotonin reuptake inhibitors (SSRIs) as alternatives to tricyclic antidepressants for first-line treatment of depression can be justified, considering their higher acquisition costs. The rationale for using paroxetine in the treatment of depression lies in its more favourable tolerability profile than tricyclic antidepressants and its lower risk of death on overdosage. Depression is one of the most common psychiatric disorders and is associated with substantial direct, indirect and intangible costs. Indirect costs account for the majority of costs associated with depression, while drug costs account for only 9 to 25% of direct costs. Therefore, increased recognition and treatment of depression has the potential to greatly reduce the overall cost of this disease. Pharmacoeconomic data on paroxetine and other SSRIs in the treatment of depression are scarce. Available studies are limited to considerations of direct costs alone and are primarily based on retrospective data from clinical trials. Nevertheless, in terms of costs per successfully-treated patient, available data suggest that the treatment costs associated with paroxetine are similar to those of amitriptyline and possibly less than those of imipramine. Paroxetine treatment costs also appear to be similar to those of amitriptyline and imipramine in terms of expected costs per patient. While one group of investigators suggested that the overall cost of administering paroxetine may also be less than that for fluoxetine and sertraline when drug costs and labour costs associated with dosage adjustment are taken into account, more data are required before conclusions on the relative pharmacoeconomic merits of SSRIs can be made. Despite the lower risk of death from overdosage with SSRIs, switching from an established tricyclic antidepressant to a newer tricyclic or related antidepressant in an attempt to avoid suicide appears to be more cost effective than switching to an SSRI. Thus, evidence available to date indicate that despite higher acquisition costs paroxetine and other SSRIs are no more costly than tricyclic antidepressants when total costs per successfully treated patient or expected costs per patient are considered. With its favourable tolerability profile and low risk of death on overdosage, paroxetine should therefore be considered as an effective alternative to tricyclic antidepressant agents as a first-line treatment of depression.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1995        PMID: 10155603     DOI: 10.2165/00019053-199508010-00008

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


  79 in total

1.  Cost-effectiveness of antidepressants.

Authors:  J T O'Brien
Journal:  Br J Psychiatry       Date:  1994-09       Impact factor: 9.319

Review 2.  Epidemiology of adolescent depression.

Authors:  V J Schoenbach; C Z Garrison; B H Kaplan
Journal:  Public Health Rev       Date:  1984

3.  Sex and depression in the National Comorbidity Survey. I: Lifetime prevalence, chronicity and recurrence.

Authors:  R C Kessler; K A McGonagle; M Swartz; D G Blazer; C B Nelson
Journal:  J Affect Disord       Date:  1993 Oct-Nov       Impact factor: 4.839

Review 4.  Paroxetine. A review of its pharmacology, therapeutic use in depression and therapeutic potential in diabetic neuropathy.

Authors:  S M Holliday; G L Plosker
Journal:  Drugs Aging       Date:  1993 May-Jun       Impact factor: 3.923

5.  Psychiatric status and 9-year mortality data in the New Haven Epidemiologic Catchment Area Study.

Authors:  M L Bruce; P J Leaf; G P Rozal; L Florio; R A Hoff
Journal:  Am J Psychiatry       Date:  1994-05       Impact factor: 18.112

6.  An 11-year follow-up study of 110 depressed patients.

Authors:  H E Lehmann; F R Fenton; M Deutsch; S Feldman; F Engelsmann
Journal:  Acta Psychiatr Scand       Date:  1988-07       Impact factor: 6.392

Review 7.  Epidemiology of depression: prevalence, risk factors and treatment situation.

Authors:  V Lehtinen; M Joukamaa
Journal:  Acta Psychiatr Scand Suppl       Date:  1994

8.  Selective serotonin reuptake inhibitors: meta-analysis of efficacy and acceptability.

Authors:  F Song; N Freemantle; T A Sheldon; A House; P Watson; A Long; J Mason
Journal:  BMJ       Date:  1993-03-13

Review 9.  Comparative tolerability profiles of the newer versus older antidepressants.

Authors:  M V Rudorfer; H K Manji; W Z Potter
Journal:  Drug Saf       Date:  1994-01       Impact factor: 5.606

10.  Epidemiology of depressive symptoms in elderly primary care attenders.

Authors:  S Evans; C Katona
Journal:  Dementia       Date:  1993 Nov-Dec
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  5 in total

Review 1.  Fluoxetine. A pharmacoeconomic review of its use in depression.

Authors:  M I Wilde; P Benfield
Journal:  Pharmacoeconomics       Date:  1998-05       Impact factor: 4.981

2.  Cost effectiveness of fluvoxamine in the treatment of recurrent depression in France.

Authors:  M Nuijten; L Hadjadjeba; C Evans; J van den Berg
Journal:  Pharmacoeconomics       Date:  1998-10       Impact factor: 4.981

3.  A comparison of the direct costs and cost effectiveness of serotonin reuptake inhibitors and associated adverse drug reactions.

Authors:  Patrick W Sullivan; Robert Valuck; Joseph Saseen; Holly M MacFall
Journal:  CNS Drugs       Date:  2004       Impact factor: 5.749

4.  Overview and emerging trends.

Authors:  Sandeep Grover; Ajit Avasthi; Subho Chakrabarti; Paramanand Kulhara
Journal:  Indian J Psychiatry       Date:  2005-10       Impact factor: 1.759

5.  Paroxetine : a review of its pharmacology and therapeutic potential in the management of panic disorder.

Authors:  R H Foster; K L Goa
Journal:  CNS Drugs       Date:  1997-08       Impact factor: 5.749

  5 in total

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