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Tension-type headache 385<br />

superior to placebo for TH relief, although there appears little reason to use<br />

these drugs for single-dose therapy in the ED. 5<br />

Compared with migraine headache, TH is less likely associated with nausea<br />

and an inability to tolerate oral analgesia. Therefore, the need to provide<br />

injectable NSAIDs is less important, but parenteral agents such as ketorolac<br />

and metamizol (not available in the USA because of potential bone marrow<br />

suppression) have been found to outperform placebo. 7,12<br />

There are conflicting data on the question of whether NSAIDs or acetaminophen<br />

(paracetamol) provide better TH relief. Two trials have found equivalence<br />

between acetaminophen (1000 mg PO) and aspirin (1000 mg PO) or<br />

naproxen (375 mg PO). 9,13 Other studies report mixed results from comparison<br />

of acetaminophen (1000 mg PO) with ketoprofen (25 mg PO); in one<br />

trial, the agents performed equally and in the other the NSAID was superior.<br />

8,14 Some of the inconsistency in the results may reflect the time of<br />

assessment of the pain relief endpoint. There is suggestion that NSAIDs<br />

such as ibuprofen (400 mg PO) provide faster (although not necessarily<br />

more profound) TH relief than acetaminophen. 15,16<br />

Overall, it appears unlikely that there are clinically important efficacy<br />

differences between individual NSAIDs, or between the NSAIDs and acetaminophen.<br />

These agents should be tried on a case-by-case basis, with the<br />

clinician maintaining therapeutic flexibility (an individual patient may<br />

respond differently to different agents in the same class).<br />

The “tension”-type pain of TH is sometimes treated with benzodiazepines.<br />

However, a multicenter RCT of TH patients could detect no overall<br />

benefit from adding a benzodiazepine (etizolam, 0.5 mg PO) to NSAID<br />

monotherapy (mefenamic acid, 250 mg PO). 17<br />

Muscle relaxants such as cyclobenzaprine, chlormezanone, and tizanidine<br />

have been investigated for TH, but the existing evidence does not<br />

support their use in the ED. 18–20<br />

The anti-dopaminergic effects of chlorpromazine (0.1 mg/kg IV) probably<br />

mediate this agent’s reported effectiveness in relieving TH pain, but side<br />

effects limit broad use of this agent. 21<br />

Some drugs, such as mirtazapine, have promise for prophylaxis of chronic<br />

TH but there is no ED role for these agents. 22,23 Other drugs reportedly useful

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