What is the role of propofol in ambulatory surgery?
Propofol may be used to provide sedation during
a regional anesthetic, to induce general anesthesia, and to maintain general
anesthesia. It is a water-insoluble, highly protein bound, lipophilic compound
that has unique phar-macokinetic characteristics that render it ideal for use
with ambulatory surgery. It is rapidly redistributed, and hepatic and
extrahepatic clearance (pulmonary) permit rapid recovery of cognitive function
with less postoperative sedation and drowsiness compared with the traditionally
employed ultra-short-acting barbiturates. Depressant effects on the central
nervous system are dose-dependent and range from mild sedation to sleep and
unconsciousness. Neither retro-grade nor anterograde amnesia is associated with
this drug. For the induction of anesthesia, propofol can be adminis-tered as a
bolus dose (2–2.5 mg/kg slowly), and its effect can be maintained via a
continuous intravenous infusion (0.1–0.2 mg/kg/min). Dosages are reduced for
debilitated patients and for the geriatric population. For sedation during regional
anesthesia, incremental doses of 10–20 mg (0.3 mg/kg) may be given, or an
infusion begun. There is a known relationship between propofol (as well as
other intravenous agents) serum drug levels and therapeutic effects. For
propofol, the target concentration is between 3 and 6 μg/ml to provide surgical anesthesia.
When administered as the sole agent, propofol
may not provide amnesia 100% of the time, and intraoperative awareness has been
reported. Therefore, it is often used in conjunction with nitrous oxide, a
volatile anesthetic, or midazolam. Propofol has no muscle relaxant or analgesic
properties. For total intravenous anesthesia, a continuous infusion of a
short-acting opioid, such as remifentanil, can be administered along with an
infusion of propofol. Additional bolus doses of propofol can be infused to
rap-idly deepen the level of anesthesia. Another major advan-tage of propofol
appears to be a significantly diminished incidence of postoperative nausea and
vomiting. Propofol’s inherent anti-emetic properties allow earlier discharge of
patients, even when emesis occurs in the PACU. When used for both induction and
maintenance of anesthesia in cases lasting approximately 1 hour, faster
recovery time is noted when compared with a thiopental induction followed by
maintenance with isoflurane and nitrous oxide. Patients anesthetized with
propofol appear to awaken with a posi-tive mood, and they regain equilibrium
including the ability to ambulate early. The requirement for pain medication in
the postoperative period appears to be reduced, which may be related to an
overall feeling of well-being.
Two disadvantages of propofol include the lack
of anal-gesic properties and pain on injection. As for the former, the
combination of propofol with an opioid, such as remifentanil or fentanyl, will
provide required analgesia. The discomfort associated with administration can
be avoided by infusion into large-bore veins as well as pre-treatment with
intravenous lidocaine. Injecting lidocaine, 10–25 mg intravenously, before
giving propofol or drawing up the lidocaine into the syringe after first
filling it with propofol will ameliorate or eliminate completely the discomfort
in most patients.
Infectious hazards associated with propofol
have been well documented because the base, which is composed of an emulsion of
soybean oil and egg phosphatides, serves as an excellent culture medium for the
growth of bacteria. It is important to draw up the drug in an aseptic fashion
and shortly before it is to be administered. Additionally, it is imperative that
the syringe be discarded after single patient use. Repeated use of the same
syringe throughout the day for multiple patients has been associated with
clusters of cases of bacterial septicemia.
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