Thirteen patients with osteoid osteoma were enrolled in a prospective trial
to test whether rofecoxib, a selective cyclooxygenase-2 inhibitor, is as e
ffective for pain control as acetylsalicylic acid. Each patient documented
the pain level using a visual analog scale, with 0 being no pain and 10 bei
ng unbearable pain, during 2 days of no pain medication, 4 days of 500 mg a
cetylsalicylic acid three times a day, and 10 days of 25 mg rofecoxib once
a day. Oral administration of 500 mg acetylsalicylic acid three times a day
led to a significant decrease in pain at night, pain at rest, and pain ind
uced by exercise. Twenty-five milligrams rofecoxib given once a day at midd
ay showed the same remarkable improvement in pain at night, pain at rest, a
nd pain induced by exercise. Rofecoxib in comparison with acetylsalicylic a
cid showed a trend toward lower pain levels in all categories. Rofecoxib of
fered a significantly better reduction in pain at rest during the day than
did acetylsalicylic acid. Results of the current study suggest that pain in
duction in osteoid osteoma is related to cyclooxygenase-2, an enzyme that i
s blocked by acetylsalicylic acid and rofecoxib. Conservative medical treat
ment with rofecoxib for osteoid osteoma is recommended when percutaneous in
tervention is associated with significant morbidity.