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Application Of Low-dose Naloxone In The Post-operative Analgesia Of Butorphanol

Posted on:2017-05-13Degree:MasterType:Thesis
Country:ChinaCandidate:Y H HeFull Text:PDF
GTID:2284330503989677Subject:Anesthesia
Abstract/Summary:PDF Full Text Request
Objective: To observe the influence of low-dose naloxone on the analgesic efficacy and adverse reactions of butorphanol used for the PCIA of puerperants.Methods: 80 puerperants undergone cesarean section with combined spinal-epidural anesthesia were randomly divided into 4 groups: Group N0(0.14 mg/kg butorphanol and normal saline 100 ml), Group N1(adding 0.10 μg·kg-1·h-1 naloxone based on Group N0), Group N2(adding 0.20 μg·kg-1·h-1 naloxone based on Group N0), Group N3(adding 0.30 μg·kg-1·h-1 naloxone based on Group N0), 20 cases in each group. The scores of satisfaction of postoperative analgesia and visual analogue scales(VAS), Ramsay sedation grades, respiratory depression, somnolence, dizziness, nausea, vomiting and pruritus were respectively recorded at 3 h, 6 h, 12 h, 24 h, 36 h and 48 h of the analgesia.Results:(1)There were no significant differences in the general data and VAS score between the 4 groups at each time point(P>0.05), but the score of satisfaction of postoperative analgesia in Group N0 and N1 was much lower than that in Group N2 and N3(P<0.05); while the post-operation average stay in Group N0 and N1 was obviously higher than that in Group N2 and N3(P<0.05);(2)The Ramsay score in Group N2 and N3 was significantly lower than that in Group N0 at each time point(P<0.05). But compared with Group N1,the score in Group N2 and N3 was lower at 3 h(P<0.05); The difference was absent between Group N0 and N1 at 3 h(P>0.05), but the score in Group N1 was lower than that in Group N0 at the rest of the time points(P<0.05);(3)The occurring rate of somnolence and dizziness in Group N0 and that of nausea with vomit in Group N0 and N1 was higher(P<0.05). There was no case appearing respiratory depression and pruritus.Conclusion: There was no influence on the analgesic efficacy of butorphanol combined with low-dose naloxone for the patient-controlled intravenous analgesia of puerperants and the incidence rates of butorphanol’s adverse reactions including somnolence, dizziness, nausea and vomiting could be more effectively inhibited by 0.200.30 μg·kg-1·h-1 naloxone.
Keywords/Search Tags:naloxone, butorphanol, patient-controlled intravenous analgesia, puerperants
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