Jk. Marshall et al., Incremental cost-effectiveness analysis comparing rofecoxib with nonselective NSAIDs in osteoarthritis - Ontario ministry of health perspective, PHARMACOECO, 19(10), 2001, pp. 1039-1049
Background: Clinical trials have shown rofecoxib, a selective inhibitor of
cyclooxygenase-2, to be associated with fewer gastrointestinal complication
s than nonselective nonsteroidal anti-inflammatory drugs (NSAIDs).
Objective: To evaluate the potential clinical and economic consequences of
rofecoxib prescription in Ontario, Canada, for patients with osteoarthritis
(OA) aged > 65 years who did not respond to paracetamol (acetaminophen) th
erapy.
Design: Decision analytic modelling study.
Methods: A model was constructed to compare rofecoxib and nonselective NSAI
Ds with respect to their gastrointestinal complications in patients with OA
. The model had a 1-year horizon and considered direct medical costs from t
he perspective of the Ontario Ministry of Health. Event rates were estimate
d from a pooled analysis of 8 phase IIb/III clinical trials. The number of
perforations, ulcers and bleeds (PUBs) with each strategy was used as the p
rimary measure of effectiveness.
Results: In the base-case scenario, the expected total cost per patient-day
on nonselective NSAIDs was 1.60 Canadian dollars ($Can) versus $Can1.67 on
rofecoxib (1999 values). Rofecoxib was associated with 0.0109 fewer PUBs p
er patient per year. The incremental cost to avoid I additional PUB by subs
tituting rofecoxib for nonselective NSAIDs was $Can2247. The rofecoxib stra
tegy became dominant if a gastroprotective agent was prescribed to more tha
n 27.5% of the patients receiving nonselective NSAIDs.
Conclusion: For patients with OA aged > 65 years in whom paracetamol therap
y has failed. rofecoxib may represent a cost-effective alternative to nonse
lective NSAIDs. Increased costs for drug acquisition are offset, in part, b
y avoidance of gastrointestinal complications and reduced use of gastroprot
ective agents. Rofecoxib may offer increased benefit among patients at a hi
gher risk of serious gastrointestinal events.