Pg. Atanassoff et al., Ropivacaine 0.2% and lidocaine 0.5% for intravenous regional anesthesia inoutpatient surgery, ANESTHESIOL, 95(3), 2001, pp. 627-631
Citations number
24
Categorie Soggetti
Aneshtesia & Intensive Care","Medical Research Diagnosis & Treatment
Background: A longer-acting local anesthetic agent, such as ropivacaine, ma
y offer advantages over lidocaine for intravenous regional anesthesia. The
objectives of this study were to evaluate whether the findings of volunteer
investigations with intravenous regional anesthesia with ropivacaine (whic
h have shown prolonged analgesia after release of the tourniquet) translate
s into improved pain control after surgery.
Methods: With Human Investigation Committee approval and a double-blind stu
dy design, 20 healthy patients with American Society of Anesthesiologists p
hysical status I or II classification who were scheduled to undergo forearm
and hand surgery were randomly assigned to administration of 40 nil of eit
her 0.2% ropivacaine or 0.5% lidocaine for intravenous regional anesthesia.
Evidence of central nervous system side effects, such as tightheadedness,
tinnitus, and metallic taste, as well as cardiac arrhythmias, were evaluate
d and treated (if necessary) after local anesthetic administration, before
and during surgery, and after release of the tourniquet until discharge fro
m the postanesthesia care unit. Regression of sensory anesthesia in the ner
ve distributions of the forearm and hand was recorded. Verbal numerical pai
n scores were monitored and quantified until the patients were discharged t
o home from the postanesthesia care unit. Patient pain scores, side effect
profiles, time to first oral intake, and total amount of oral analgesics we
re recorded 24 h postoperatively.
Results: Intravenous regional anesthesia with 0.2% ropivacaine and 0.5% lid
ocaine provided equivalent levels of surgical anesthesia. After release of
the tourniquet, the first evidence for return of sensation in the distribut
ion of the five peripheral nerves occurred later in the ropivacaine group (
median, 20 min; range, 15-40 min) than in the lidocaine group (median, 1 mi
n; range, 1-25 min). Verbal numerical pain scores were significantly lower
at the time of admission, whereas during the remainder of the postanesthesi
a care unit stay and later at home, the difference in verbal numerical pain
scores between the two groups was no longer statistically significant.
Conclusions. Ropivacaine 0.2% may be an alternative to 0.5% lidocaine for i
ntravenous regional anesthesia in the outpatient surgical setting. Longer-l
asting analgesia in the Immediate postoperative period may be due to a more
profound and prolonged tissue binding effect of ropivacaine.