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Odontalgia 315<br />

pain, trial evidence has found either ibuprofen (400 mg PO) or ketorolac (10<br />

mg PO) provides relief superior to that achieved with acetaminophen (paracetamol;<br />

600 mg PO) alone or in combination with codeine (60 mg PO). 2<br />

Another study found that ketorolac (10 mg PO) monotherapy was signifi-<br />

cantly more efficacious than treatment with acetaminophen (625 mg) plus<br />

codeine (15 mg PO). 3 Other trials in OP have demonstrated the equivalence<br />

or superiority of ibuprofen (400 mg PO) to acetaminophen (600 mg), aspirin<br />

(650 mg PO), codeine (up to 60 mg PO), and even combination therapy<br />

comprising codeine (60 mg PO) and either aspirin or ibuprofen. 4,5 Given<br />

the efficacy of the 400 mg PO of ibuprofen, and the increased incidence of<br />

adverse effects associated with higher doses, we recommend 400 mg of this<br />

NSAID as the initial approach for OP.<br />

The literature fails to identify any significant differences in efficacy<br />

between the various NSAID classes for OP. There are, however, several<br />

NSAIDs (e.g. naproxen, etodolac, piroxicam) that are attractive for OP use<br />

given their extended dosing intervals.<br />

Among the NSAIDs demonstrated to provide better pain relief than placebo<br />

is parenteral ketorolac. 6 While ketorolac’s general acute care efficacy may<br />

not differ from that achieved with other NSAIDs, assessments of the agent’s<br />

parenteral use in acute care suggest it is highly effective in OP. 7 <strong>This</strong> agent’s<br />

IV or IM administration may be useful when patients, owing to oral pain or<br />

other reason, cannot take PO therapy. The full effect of ketorolac analgesia,<br />

which can take as long as an hour even after IV administration, can be<br />

accelerated and even augmented by administering the NSAID directly into<br />

the periapical space. 8–10 The periapical injection of ketorolac is promising for<br />

application in acute care, but its recommendation for ED use must await<br />

further safety and efficacy data.<br />

Trials suggest that there is no reason to employ the COX-2 selective<br />

NSAIDs. Compared with these agents, nonselective NSAIDs such as ibuprofen<br />

provide superior pain relief while incurring no extra short-term side effects.<br />

Consequently, we agree with dental expert reviews that find no reason to use<br />

the COX-2 selective NSAIDs in lieu of agents such as ibuprofen. 11,12<br />

Although the action mechanism is unknown, it is clear that addition of<br />

caffeine improves ibuprofen’s analgesic efficacy in OP. The combination of

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