SELECTIVE COX 2 INHIBITORS AND NSAID PRESCRIBING PATTERNS IN IRELAND M. Teeling, K. Bennett, J. Feel - PowerPoint PPT Presentation

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SELECTIVE COX 2 INHIBITORS AND NSAID PRESCRIBING PATTERNS IN IRELAND M. Teeling, K. Bennett, J. Feel

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Adjustments for age, gender and polypharmacy were made. Conclusions (1) ... in those with a higher rate of polypharmacy (as noted from the GMS database in Ireland) ... – PowerPoint PPT presentation

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Title: SELECTIVE COX 2 INHIBITORS AND NSAID PRESCRIBING PATTERNS IN IRELAND M. Teeling, K. Bennett, J. Feel


1
SELECTIVE COX 2 INHIBITORS AND NSAID
PRESCRIBING PATTERNS IN IRELANDM. Teeling, K.
Bennett, J. Feely,Dept of Pharmacology and
Therapeutics, Trinity College, St Jamess
Hospital, Dublin 8, Ireland.
2
Introduction
  • Non steroidal anti inflammatory drugs (NSAIDs)
    are among the most commonly used medicines in the
    world
  • Use is associated with gastrointestinal (GI)
    toxicity
  • Selective COX-2 inhibitors are thought to reduce
    GI toxicity

3
Aim of this Study
  • To investigate what effect, if any,
  • the availability of selective COX-2 inhibitors
    has had on NSAID prescribing patterns in Ireland

4
Methods (1)
  • The General Medical Services(GMS) scheme provides
    free health service to 31 of the Irish
    population(1.2M)
  • Eligibility is means tested
  • The GMS provide details on prescription claims
    and also demographic data on patients such as age
    and sex
  • Total annual cost of prescription items was 434
    million in 2001.

5
Methods (2)
  • GMS database was reviewed from Dec 1999-Nov 2001
  • First 6 months lead-in phase
  • (NSAID and anti-PU drug users excluded)
  • Next 12 months study period
  • ( patients gt 3 prescriptions of the same NSAID
    identified)
  • Final 6 months follow-up period
  • Information on age,sex and on co-prescribing
    of other medications, in particular anti-PU
    drugs, collected from study and follow-up periods

6
Methods (3)
  • The WHO ATC (Anatomical Therapeutic Chemical)
    classification was used to identify drugs in the
    database as follows
  • M01A (Anti-inflammatory and anti-rheumatic
    products, non-steroids)
  • A02B (Drugs for treatment of peptic ulcers)
  • NSAIDs were classified as selective or
    non-selective
  • Odds ratios were calculated, using logistic
    regression (SAS package)

7
(No Transcript)
8
Results
9
Table 1 Prescription of NSAIDs effect of age
10
Table 2 Prescription of NSAIDs - number of
other prescriptions
11
Table 3 ORs for co-prescribing of anti PU drugs
on or after the first month of NSAIDs versus no
NSAIDs
  • NSAID OR (95C1)
  • No NSAIDs 1.00
  • Celecoxib 2.04 (1.67,2.49)
  • Rofecoxib 2.11 (1.83,2.24)
  • Nimesulide 2.09 (1.95,2.24)
  • Diclofenac 1.36 (1.30,1.43)
  • Mefanamic Acid 1.31 (1.22,1.40)
  • Naproxen 1.53 (1.34,1.74)
  • Figures adjusted for age, gender and
    polypharmacy

12
Discussion (1)
  • The selective COX-2 inhibitors (celecoxib and
    rofecoxib) together with nimesulide accounted for
    approximately 25 of the GMS prescriptions for
    NSAIDs and almost 50 (7.3 million) of the total
    cost for anti-inflammatory and anti-rheumatic
    products in 2001
  • Expenditure on anti-PU drugs accounted for over
    8 of total drug costs under the GMS in 2001
    (36.9 million)

13
Discussion (2)
  • Cost of COX-2 inhibitors greatly exceed those of
    conventional non-selective NSAIDs as follows
    (DDD/month)
  • Indomethacin 3.50
  • Ibuprofen 7.00
  • Diclofenac 11.00
  • Mefanamic acid 8.00
  • Naproxen 9.00
  • Nimesulide 21.00
  • Rofecoxib 34.50
  • Celecoxib 32.00
  • defined daily dose (WHO)

14
Discussion (3)
  • Limitations of the study
  • Database records number of prescriptions
    dispensed.
  • Database does not have access to diagnoses.
  • BUT
  • Records were included only if gt 3 prescriptions
    dispensed during the study period and
  • Adjustments for age, gender and polypharmacy were
    made

15
Conclusions (1)
  • In this study, Cox-2 selective inhibitors were
    prescribed more frequently in older age groups
    and in those with a higher rate of polypharmacy
    (as noted from the GMS database in Ireland)
  • These findings suggest that COX-2 inhibitors are
    preferentially prescribed to the more vulnerable
    patients.

16
Conclusions (2)
  • However, even when the figures were adjusted for
    age, gender and polypharmacy, anti-PU drugs were
    still co-prescribed more frequently in the Cox-2
    selective inhibitor group
  • This suggests that there may be other unaccounted
    for risk factors or
  • that prescribers are still uncertain of the
    safety of COX-2 selective inhibitors in
    vulnerable patient groups

17
Conclusions (3)
  • Since selective COX-2 inhibitors are more
    expensive than many of the conventional
    non-selective NSAIDs, these results suggest that
    COX-2 inhibitors may not be cost-effective.
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