Purpose: To assess and compare the onset time and duration of neuroblockade
obtained after ropivacaine or bupivacaine in infants undergoing major abdo
minal surgery. We also evaluated the efficacy and safety of employing ropiv
acaine instead of bupivacaine to provide operative anesthesia and postopera
tive analgesia.
Methods: In a prospective double blind study 28 infants, aged 1-12 months,
undergoing elective major abdominal surgery, were randomly allocated to rec
eive, after induction of general anesthesia, either 0.7 ml.kg(-1) bupivacai
ne 0.25% (group B) or ropivacaine 0.2%, (group R) via lumbar epidural block
, The onset time, total surgical time and duration of analgesia were record
ed.
Results: No differences were noted in demographic data, hemodynamic variabl
es or duration of surgery. The onset time for sensory blockade was 13.1 min
+/- 2.1 (group B) and 11.7 +/- 2.4 min (group R). The duration-of analgesi
a was 491 +/- 291 (group R) and 456 min +/- 247 (group B). Eight patients i
n group B and six in group R needed codeine and acetaminophen rescue on at
least one occasion during the 24 hr study period. No major side effects wer
e noted in either groups.
Conclusions: In infants undergoing major abdominal surgery under combined e
pidural/light general anesthesia, ropivacaine 0.2% produces sensory and mot
or blockade similar in onset, duration of action and efficacy to that obtai
ned from an equal volume, 0.7 ml.kg(-1), of bupivacaine 0.25%.