Sa. Schendel et M. Stephanides, TREATMENT OF PERIORBITAL EDEMA WITH HUMAN CORTICOTROPIN-RELEASING FACTOR AFTER BLEPHAROPLASTY, Journal of the American College of Surgeons, 182(3), 1996, pp. 226-232
BACKGROUND: This prospective study of 32 patients was undertaken to ev
aluate the formation of postoperative periorbital edema after administ
ration of human corticotropin-releasing factor (hCRF), Human corticotr
opin-releasing. factor has strong antiedematous properties as a result
of direct action on blood vessels independent of endocrine function a
nd has been shown to have a positive effect on vascular permeability i
n animal studies independent of corticosteroid effects. STUDY DESIGN:
Human corticotropin-releasing factor was administered intravenously pr
eoperatively to patients undergoing blepharoplasty in doses of 2, 4, a
nd 8 mu g/kg body weight as a randomized, double-blind, placebo-contro
lled study, The periorbital edema was measured by the use of a three-d
imensional laser scanner to determine facial and eyelid volume changes
at specified times postoperatively. RESULTS: Human corticotropin-rele
asing factor was well tolerated when administered intravenously over a
ten-minute period to healthy patients undergoing blepharoplasty. Mild
transitory flushing and hypotension were the most common adverse even
ts, Transient decreases in systolic and diastolic blood pressure and i
ncreases in heart rate occurred at hCRF doses greater than 2 mu g/kg a
nd were most prominent at 8 mu g/kg. The 8 mu g/kg. hCRF dose also sho
wed a trend toward less postoperative edema but this was not statistic
ally significant at the p<0.05 level, CONCLUSIONS: Human corticotropin
-releasing factor appears to be safe for intravenous use in patients u
ndergoing blepharoplasty; however, its efficacy in reducing postoperat
ive edema as a single preoperative administration was not conclusively
demonstrated in this study, Further research with a larger study popu
lation and other dosing regimens is indicated.