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A Total Intravenous Anesthetic Technique for
Outpatient Facial laser Resurfacing

Katherine R. Blakeley, MD*, Kevin W. Klein, MD*, Paul F. White, phD, MD, fanzca*, Suzanne Trott, MD, and Rod J. Rohrich, MD, FACs

The increasing use of minimally invasive surgical techniques has facilitated recovery after a wide variety of ambulatory surgical procedures. It has also created new challenges for anesthesia practitioners. For example, the highly specialized surgical equipment required to perform these procedures has created unique anesthetic requirements. The carbon dioxide (CO,) laser used for facial "resurfacing" (socalled laser abrasion) procedures requires intense analgesia with minimal distortion of the skin by anesthesia
equipment and avoidance of supplemental oxygen (0,). Because conventional anesthetic and sedative-analgesic techniques require the use of supplementa 0,, a technique was developed that involves
using a combination of IV anesthetic and nonopioid analgesics to achieve adequate intraoperative patient comfort while minimizing the need for opioid compounds and for interventions to manage airwayrelated problems (e.g., desaturation, airway obstruction).
Total IV anesthesia (TIVA) is well suited for outpatient plastic surgery procedures (1). In an effort to avoid opioid-induced respiratory depression, ketamine has become an increasingly popular
alternative because of its unique sedative/ amnestic/analgesic profile and absence of clinically significant ventilatory depression (e.g., respiratory rate <8 breaths/min and/or hemoglobin oxygen saturation
value ~85%). Unfortunately, the use of ketamine is also associated with cardiovascular stimulation and psychomimetic emergence reactions (2). Concomitant administration of the benzodiazepines
diazepam and midazolam has been reported to be effective in minimizing these side effects during plastic surgery (3). More recently, propofol has also been reported to prevent ketamine-induced cardiovascular stimulation and psycho mimetic emergence reactions when administered as part of a TIVA technique (4). In
outpatients premeditated with midazolam l-4 mg IV, Friedberg (5) described a technique involving the use of a propofol infusion, 100 pg * kg-l * mini (range 20-226 pg * kg-' * mini) in combination with intermittent bolus doses of ketamine (50 mg IV). However, this technique provided inadequate analgesia for the facial laser procedures despite extensive supplementation with local anesthetic solutions (data not reported). Therefore, it was necessary to supplement the basic midazolam/ketamine/propofol anesthetic technique with both opioid and nonopioid analgesic drugs.

We describe a TIVA technique that has facilitated the performance of facial resurfacing procedures inthe ambulatory setting without producing excessive cardiorespiratory depression (>80”/0 of baseline values) or prolonged recovery times.

Anesthetic Technique

On arrival in the day surgery unit 60-90 min before surgery, all patients were premeditated with oral clonidine 0.2 mg (~65 kg), 0.3 mg (65-80 kg), or 0.4 mg (>80 kg), and diazepam 5-10 mg PO. Before transporting the patient to the operating room, midazolam 2-5 mg, dexamethasone 5-10 mg, ketorolac 30-60 mg, and glyco pyrrol ate 0.3-0.5 mg were administered IV. All patients received 500 mL of fluid IV before the induction of anesthesia. Maintenance fluid therapy was administered at a rate of approximately 750 mL/h. Anesthesia was induced with propofol 1 mg/kg IV administered over 60 s, followed by a maintenance infusion of 100 Fg * kg-' * mini'. Before initiating the local anesthetic injections, ketamine 0.5 mg * kg-i was injected, followed by an infusion at an initial rate of 35 pg * kg-' * mine'. The subsequent infusion rates of propofol and ketamine were varied to maintain an adequate depth of hypnosis (i.e., eyes at a rate of 12-
20 breaths/min) and analgesia (i.e., absence of facial grimacing, vocalization, purposeful movements), respectively.
Heart rate values >lOO bpm and mean arterial pressure values >lOO mm Hg were treated with propranolol 0.25-0.5 mg IV and labetalol
5-10 mg IV, respectively. If the cardiostimulatory activity persisted, supplemental bolus doses of propran- 0101 (0.25 mg IV) and labetalol (5 mg IV) were administered.

A local anesthetic solution (lidocaine 0.5%) containing epinephrine 1:400,000 was infiltrated to block the supraorbital, supratrochlear, and mental nerves. In addition, a field block was performed around the entire perimeter of the face. This approach provided adequate analgesia except when the surgeon was lasering the upper eyelids, the brow, and the nasolabial folds. Therefore, small bolus doses of fentanyl (12.5- 25 pg IV) were administered 2-3 min before initiating
the lasering process in these highly sensitive areas.

The doses of the anesthetic drugs administered to the first 20 patients undergoing the laser abrasion procedure are summarized in Table 1. None of the patients managed with this anesthetic
regimen required supplemental oxygen to maintain a room air oxygen saturation value >85%. However, transient upper airway obstruction occurred in four patients and was treated with intermittent jaw thrust maneuvers by the surgical assistant (to avoid having to contaminate the surgical field). When the obstructive signs were not relieved by lifting the mandible, the patient's head was transiently rotated to the side.

Approximately 20-30 min before the end of the operation, the ketamine infusion was discontinued, and the propofol infusion was terminated on completion of the lasering procedure. All patients were
awake and oriented at the time of discharge from the operating room. Despite the local anesthesia, >70% of the patients required analgesic medication before discharge home from the day surgery unit. Although <lo% of the patients developed postoperative emetic
symptoms, one-third required antinausea medication. Although 90% of the patients were highly satisfied with the anesthetic technique, two of the patients who experienced "vivid dreams" would prefer to receive a different anesthetic for a future operation.

Discussion

The adjunctive use of nonopioid compounds reduced the need for traditional opioid analgesics during these painful procedures. Clonidine, ketorolac, and steroids all reduce opioid-related side effects and thereby improve recovery from anesthesia (6-8). Combining these nontraditional drugs with ketamine minimized the need for intraoperative fentanyl and reduced the risk of clinically significant respiratory depression during the procedure. Although both midazolam and propofol were administered during the procedure, 15% of patients still experienced ketamine-induced emergence reactions (described as "vivid but pleasant dreams").

This small series of cases demonstrates the feasibility of performing painful procedures under TIVA with minimal doses of potent opioid analgesics. The use of nonopioid anesthetic and analgesic drugs minimizes the risk of respiratory depression, as well as the adverse effects of these compounds on the central nervous system, gastrointestinal, and genitourinary systems. Given its rapid onset and ultra-short duration of effect, small bolus doses of remifentanil (lo-20 pg IV) may be a useful alternative to fentanyl as a rescue analgesic during the transient painful aspects of these procedures (9). An investigational parenteral formulation of acetaminophen (propacetamol) could also prove to be a useful adjuvant to this TIVA technique (10). In conclusion, the use of a combination of nonopioid IV anesthetics and analgesics to supplement local anesthesia provided an adequate depth of anesthesia for facial laser resurfacing without the need for supplemental oxygen or assisted ventilation.

References

  1. Smith I, White PF. Total intravenous anesthesia. In: Hahn CEW,
    Adams AP, eds. Principles and practice series. London: BMJ,
    1998;Slp97.
  2. White PF, Way WL, Trevor AJ. Ketamine: its pharmacology and
    therapeutic uses. Anesthesiology 1982;56:119-36.
  3. White PF, Vasconez LO, Mathes S, et al. Comparison of midazolam
    and diazepam for sedation during plastic surgery. J Plast
    ReconstrSurg 1988;81:703-10.
  4. Guit JB, Koning HM, Coster ML, et al. Ketamine as an analgesic
    for total intravenous anesthesia with propofol. Anaesthesia
    1991;46:24-7.
  5. Friedberg BL. Hypnotic doses of propofol block ketamineinduced
    hallucinations [letter]. J Plast Reconstr Surg 1993;91:196-7.
  6. Richard MJ, Skues MA, Jarvis AI', Prys-Roberts C. Total iv.
    anaesthesia with propofol and alfentanil: dose requirements for
    propranolol and the effect of premeditation with clonidine. Br J
    Anaesth 1990;65:157-63.
  7. Bosek KV, Smith DB, Endicott J, et al. Comparison of intravenous ketorolac and alfentanil as supplements to propofol anesthesia for diagnostic panendoscopy. J Clin Anesth 1995;7:40-3.
  8. Aasboe V, Raeder JC, Groegaard B. Betamethasone reduces
    postoperative pain and nausea after ambulatory surgery.
    Anesth Analg 1998;87:319-23.
  9. Sa Rego M, Inagaki Y, White PF. Use of remifentanil during
    lithotripsy: intermittent boluses vs continuous infusion. Anesth
    Analg 1998;84:5541.
  10. Delbos A, Boccard E. The morphine-sparing effect of propacetamol in orthopedic postoperative pain. J Pain Sympt AManag 1995;10:279-84.



 
 

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