Transcript Slide 1
Does the time to
administration of
lidocaine-propofol
admixtures affect
induction times?
CDR Gregory G. Nezat, PhD, CRNA
Naval Medical Center Portsmouth
Professional Military Education Directorate
And
Department of Anesthesia
Disclaimer
The views expressed in
this article are those of
the author(s) and do not
reflect the official policy
or position of the
Department of the Navy,
Department of Defense,
or the United States
Government.
Introduction
• Propofol is the most commonly used
induction agent in the United States
• Induction agents are medications which
induce loss of consciousness within 30-45
seconds
Hypothesis
The addition of lidocaine to propofol will
increase induction times.
Methods of Induction
• The standard induction
– Induction agent ==> confirmation of induction
==> muscle relaxant
• The rapid sequence induction
– Induction agent ==> muscle relaxant
Clinical Practice
• Intravenous Propofol causes pain and
burning upon administration
• Propofol and Lidocaine commonly mixed
• 10:1 ratio usually reduces burning/pain
• Impacts the chemical formulation of
propofol
Untoward Chemical
Interaction
•
•
•
•
Propofol is a substituted isoprophylphenol
Only slightly soluble in water
Formulated as an oil-in-water emulsion
Emulsion composed of soybean oil,
glycerol, and egg lecithin
Laboratory Research
• Adding lidocaine to propofol decreases the
zeta potential (electrostatic repulsive
forces) within the emulsion
• Increases droplet size within emulsion in a
linear fashion over time
Clinical Implication
• Possible clinical effect—prolongation of
induction of general anesthesia
• Allow the muscle relaxant to work prior to
the induction
• Predispose patients to recall or awareness
during intubation
Research Question
• Does induction time increase in patients
administered a lidocaine-propofol
admixture when prepared >60 minutes
before induction?
Methods
• Experimental, prospective, randomized study
• Subjects were randomly assigned to the control
group or the experimental group
• Control - propofol 2mg/kg plus 0.2-mg/kg
lidocaine formulated 10 minutes prior to
administration
• Experimental group received the same
formulation prepared approximately 110 minutes
before induction
Methods
• Inclusion
Criteria
– Convenience
sample
– Physical status I
or II (generally
healthy)
– Male or female
– Scheduled for
surgery under
GA
– Ages 18-60
Exclusion criteria
-Pregnancy
-Risk of aspiration of
gastric contents and/or
GERD
-Suspected or known
difficult airway
-Presence of central
nervous system disease
-Significant cardiac or
liver dysfunction
-Morbid obesity (body
mass index >30kg/m2)
Methods
• Subject held fluid-filled syringe between
index finger and thumb of dominant hand
• Admixture administered via rapid IV bolus
• Timer started as admixture given
• Timing ended with the syringe drop
Results
• A total of 116 subjects were included in
final analysis
– No significant differences in demographic
variables or other measured variables
– Statistically significant difference noted in time
to syringe drop (p < .001)
Time to Induction
(p < .001)
70
Time to Induction in Seconds
60
50
40
30
20
10
0
Control
Experimental
Group
Clinical Implications
• The 14 second difference may be
clinically significant during rapid
sequence induction in trauma cases
• Patient may have partial or full muscle
relaxation, but not be completely
unconscious possibly leading to
awareness under anesthesia
Recommendations
• Consider not mixing lidocaine with
propofol when dealing with trauma
patients
• Consider administering IV lidocaine prior
to propofol
• If they are mixed, consider administering
them soon after mixing (<10min)
Does the time to
administration of
lidocaine-propofol
admixtures affect
induction times?
Does the time to
administration of
lidocaine-propofol
admixtures affect
induction times?
Yes