''Breakthrough pain'' is a common clinical term that has not been conc
lusively defined or described. Breakthrough pain is a transitory flare
of pain experienced when baseline pain has been reduced to a mild or
moderate level. Breakthrough pain may be characterized by its relation
ship to a fixed around-the-clock (ATC) opioid dose, rapid onset and sh
ort duration, precipitating events, predictability: pathophysiology (w
ith nociceptive pain being most easily controlled), and etiology. The
only prospective study of breakthrough pain conducted to date found a
63% prevalence of breakthrough pain in cancer patients referred to a p
ain service. Although prevalence figures from other studies vary widel
y, partly due to the populations chosen, all of the studies verify tha
t breakthrough pain is a serious problem in cancer patients. In fact,
several studies have listed incident pain, a subset of breakthrough pa
in as a predictor of poor response to analgesic therapy. Breakthrough
pain is currently managed with ornl or parenteral breakthrough pain me
dications given in addition to the ATC analgesic regimen. The A TC dos
age may also be increased until limited by side effects, Newer agents
with a more rapid onset of analgesia and shorter duration of effect ma
y help irt the management of breakthrough pain.