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Article: Analgesia after caesarean section with intramuscular ketorolac or pethidine

TitleAnalgesia after caesarean section with intramuscular ketorolac or pethidine
Authors
KeywordsPethidine
Ketorolac
Postoperative
Analgesics
Analgesia
Issue Date1993
Citation
Anaesthesia and Intensive Care, 1993, v. 21, n. 4, p. 420-423 How to Cite?
AbstractWe compared, in a double-blind randomised study, intramuscular ketorolac 30 mg (n = 49) and intramuscular pethidine 75 mg (n = 51) for analgesia after elective caesarean section under general anaesthesia. Anaesthesia was induced with thiopentone and suxamethonium and maintained with atracurium, nitrous oxide and isofluarane. Intravenous fentanyl 100 μg was given after delivery of the neonate. In the recovery ward, patients who requested analgesia were allocated randomly to receive ketorolac 30 mg or pethidine 75 mg intramuscularly. Analgesia was assessed at intervals up to six hours, using a visual analogue scale and a four-point verbal scale, while duration of analgesia was taken as the time until the patient requested additional analgesia. There was no difference in the duration of analgesia between groups (Mann-Whitney test P = 0.27, Mantel-Haentszel test P = 0.17). Twenty-six patients in the ketorolac group and 17 patients in the pethidine group requested further analgesia by 90 minutes. However, four patients in the ketorolac group and six patients in the pethidine group requested no further analgesia within 24 hours. Pain VAS and overall assessment of analgesia was similar between groups, although more side effects (nausea, dizziness) were noted in the pethidine group. Ketorolac 30 mg and pethidine 75 mg provided similar but variable quality of analgesia after caesarean section.
Persistent Identifierhttp://hdl.handle.net/10722/280449
ISSN
2023 Impact Factor: 1.1
2023 SCImago Journal Rankings: 0.534
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorGin, T.-
dc.contributor.authorKan, A. F.-
dc.contributor.authorLam, K. K.-
dc.contributor.authorO'Meara, M. E.-
dc.date.accessioned2020-02-17T14:34:04Z-
dc.date.available2020-02-17T14:34:04Z-
dc.date.issued1993-
dc.identifier.citationAnaesthesia and Intensive Care, 1993, v. 21, n. 4, p. 420-423-
dc.identifier.issn0310-057X-
dc.identifier.urihttp://hdl.handle.net/10722/280449-
dc.description.abstractWe compared, in a double-blind randomised study, intramuscular ketorolac 30 mg (n = 49) and intramuscular pethidine 75 mg (n = 51) for analgesia after elective caesarean section under general anaesthesia. Anaesthesia was induced with thiopentone and suxamethonium and maintained with atracurium, nitrous oxide and isofluarane. Intravenous fentanyl 100 μg was given after delivery of the neonate. In the recovery ward, patients who requested analgesia were allocated randomly to receive ketorolac 30 mg or pethidine 75 mg intramuscularly. Analgesia was assessed at intervals up to six hours, using a visual analogue scale and a four-point verbal scale, while duration of analgesia was taken as the time until the patient requested additional analgesia. There was no difference in the duration of analgesia between groups (Mann-Whitney test P = 0.27, Mantel-Haentszel test P = 0.17). Twenty-six patients in the ketorolac group and 17 patients in the pethidine group requested further analgesia by 90 minutes. However, four patients in the ketorolac group and six patients in the pethidine group requested no further analgesia within 24 hours. Pain VAS and overall assessment of analgesia was similar between groups, although more side effects (nausea, dizziness) were noted in the pethidine group. Ketorolac 30 mg and pethidine 75 mg provided similar but variable quality of analgesia after caesarean section.-
dc.languageeng-
dc.relation.ispartofAnaesthesia and Intensive Care-
dc.subjectPethidine-
dc.subjectKetorolac-
dc.subjectPostoperative-
dc.subjectAnalgesics-
dc.subjectAnalgesia-
dc.titleAnalgesia after caesarean section with intramuscular ketorolac or pethidine-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1177/0310057X9302100409-
dc.identifier.pmid8214547-
dc.identifier.scopuseid_2-s2.0-0027179211-
dc.identifier.volume21-
dc.identifier.issue4-
dc.identifier.spage420-
dc.identifier.epage423-
dc.identifier.isiWOS:A1993LW16100009-
dc.identifier.issnl0310-057X-

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