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Reflections on ED analgesia 79<br />

interpreting) pain research. One of the most important confounders deals<br />

with the population – patients with extremity fractures – making up many<br />

pain studies. While the common practice of focusing analgesia studies on<br />

these patients is sensible, clinical experience teaches us that a significant<br />

proportion of such patients achieve pain relief if the extremity is simply left at<br />

rest (even without splinting). The smaller the study number, the more likely<br />

the presence of residual confounding that may be missed by even prospective<br />

methodology.<br />

Therefore, in studying pain, we must allow for the fact that no two patients<br />

perceive pain in the same way; that certain kinds of injury that produce<br />

maximum pain as perceived by some patients produce none in others. We<br />

must also understand that we have no objective method of measuring pain,<br />

or its relief. We are forced to rely on what the patient tells us about the<br />

individual perception of pain.<br />

As well, there are the methodologic difficulties in our science of pain relief.<br />

Because of issues of the type just described, it is hard to constitute a uniform<br />

control group. Nevertheless, even assuming that we have a large enough<br />

patient population to allow for these vagaries of perception in the control<br />

group, we often make errors in the study group. While we are the first to<br />

applaud planning and execution of RCTs in acute care analgesia, such trials<br />

are not infallible, and emergency physicians should be wary of common<br />

shortcomings. When an ED clinician encounters RCT results that contradict<br />

years of experience, a vigilant search for oft-encountered study flaws can be<br />

enlightening.<br />

For example, if one attempts to compare the efficacy of morphine with that<br />

of meperidine (pethidine), what do you think would be the outcome if the<br />

morphine were administered IV in a dose of 10 mg, and the meperidine IM in<br />

a dose of 50 mg? Even if the 50 mg meperidine dose were to be given IV, the<br />

outcome of such a study is predictable. Yet there are many studies that<br />

commit precisely that kind of relative dosing error. The effective dose of<br />

meperidine is 1–1.5 mg/kg; how many patients will achieve relief from a dose<br />

of 50 mg?<br />

Non-analgesic adjunctive care also makes a difference to a pain management<br />

study. We cannot take a population of humans and alter only one

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