Study Objective: To compare the efficacy and safety of four commercial prop
ofol solutions marketed in Israel.
Design: Prospective, randomized, double-blind study.
Setting: University-affiliated medical center, Patients: 120 ASA physical s
tatus I and II nullipara patients undergoing dilatation and curettage for i
nterrupted pregnancy.
Interventions: Patients were randomized into four groups of 30 patients eac
h. Group I was anesthetized with Diprivan (AstraZeneca, UK), group 2 with R
ecofol (Leiras Gy, Finland), group 3 with Propofol (Abbott), and group 4 wi
th Diprofol (Taro, Israel).
Measurements and Main Results: The four study groups were similar in mean a
ge and weight. There were no statistically significant differences in the a
dministered doses, quality of anesthesia, recovery time, or adverse effects
among the four groups.
Conclusions: Diprivan, Recofol, Diprofol, and Propofol Abbott are equally e
ffective as anesthesia induction drugs for dilation and curettage, with a s
imilar incidence of adverse effects. Because cost limitations have become a
significant factor in medical care, the choice of drug in this group shoul
d be based solely on cost considerations. (C) 2001 by Elsevier Science Inc.