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Neostigmine versus fentanyl administration with ropivacaine by patient-controlled epidural analgesia for the management of labor pain
Aim The aim of this study was to evaluate the use of epidural Neostigmine (4 mcg/ml) in patientcontrolled epidural anesthesia ( PCEA) in the management of labor pain. Patients and methods This randomized double-blind controlled prospective study was designed to compare PCEA Ropivacaine 0.15%+Fentany...
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Published in: | Ain-Shams journal of anesthesiology 2015-04, Vol.8 (2), p.211-216 |
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Main Author: | |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Aim
The aim of this study was to evaluate the use of epidural Neostigmine (4 mcg/ml) in patientcontrolled
epidural anesthesia ( PCEA) in the management of labor pain.
Patients and methods
This randomized double-blind controlled prospective study was designed to compare
PCEA Ropivacaine 0.15%+Fentanyl 2 mcg/ml (F group) with PCEA Ropivacaine
0.15%+Neostigmine 4 mcg/ml (N group). The study included 60 ASA I–II laboring
mothers. Pain, sedation, nausea, maternal vital signs, motor power, and fetal heart rate
were evaluated every 5 min after epidural bolus for the fi rst 30 min, and then every 2 h
until delivery. The incidence of shivering was documented. Apgar scores at 1 and 5 min
were documented.
Results
There were no differences in maternal and labor characteristics between groups. Progress
of labor and modes of delivery were the same (P = 0.47). Pain scores were signifi cantly
reduced 20 min after initiation of analgesia compared with baseline in both groups (P < 0.001)
and did not differ between groups at any time during the study (P = 0.21–0.43). Addition of
Neostigmine reduced the mean hourly epidural dose of Ropivacaine by 11% compared with
the Fentanyl group (P = 0.003). There were no differences in maternal vital signs between
groups. The sedation score increased compared with baseline through the fi rst 20 min after
initiation of analgesia in both groups (Fentanyl P = 0.043 – Neostigmine P = 0.04). There was
no signifi cant difference in sedation scores between groups at any time or compared with
baseline (P = 0.23–0.46). The incidence of nausea, shivering, pruritus, and motor block was
similar in both groups.
Conclusion
Neostigmine 4 mcg/ml can be used as a safe adjuvant with Ropivacaine 0.15% by PCEA for
the management of labor pain. Its analgesic properties are comparable to that of epidural
Fentanyl. It causes temporary sedation within the fi rst 20 min. This sedation is comparable to
that of Fentanyl. Epidural low-dose Neostigmine infusion did not increase the risk for nausea
during labor. |
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ISSN: | 1687-7934 2090-925X |
DOI: | 10.4103/1687-7934.156689 |