Preoperative Paracetamol Improves Post-Cesarean Delivery Pain Management: A Prospective, Randomized, Double-Blind, Placebo-Controlled Trial

dc.contributor.authorOzmete, Ozlem
dc.contributor.authorBali, Cagla
dc.contributor.authorCok, Oya Yalcin
dc.contributor.authorErgenoglu, Pinar
dc.contributor.authorOzyilkan, Nesrin Bozdogan
dc.contributor.authorAkin, Sule
dc.contributor.authorKalayci, Hakan
dc.contributor.authorAribogan, Anis
dc.contributor.orcID0000-0003-3004-2626en_US
dc.contributor.orcID0000-0002-4973-8132en_US
dc.contributor.orcID0000-0002-6366-941Xen_US
dc.contributor.orcID0000-0001-5845-699Xen_US
dc.contributor.orcID0000-0001-6423-1076en_US
dc.contributor.orcID0000-0003-2615-1918en_US
dc.contributor.orcID0000-0002-4419-5693en_US
dc.contributor.pubmedID27555133en_US
dc.contributor.researcherIDAAI-8790-2021en_US
dc.contributor.researcherIDS-8336-2019en_US
dc.contributor.researcherIDAAI-7998-2021en_US
dc.contributor.researcherIDJ-5282-2013en_US
dc.contributor.researcherIDAAI-7779-2021en_US
dc.contributor.researcherIDAAJ-2094-2021en_US
dc.contributor.researcherIDAAI-7880-2021en_US
dc.contributor.researcherIDGON-8465-2022en_US
dc.date.accessioned2023-07-07T11:49:10Z
dc.date.available2023-07-07T11:49:10Z
dc.date.issued2016
dc.description.abstractStudy Objective: To evaluate the analgesic effect of preoperative single dose intravenous paracetamol on postoperative pain and analgesic consumption within 24 hours after elective cesarean surgery. Design: Prospective, randomized, double-blind, placebo-controlled clinical trial. Setting: University Teaching Hospital. Patients: American Society of Anesthesiologists (ASA) I and II 60 patients between 18-40 years of age who were scheduled to undergo elective cesarean section. Interventions: Patients were randomized into two groups to receive either intravenous 1 g paracetamol (100 mL) (Group P) or 0.9% NaCl solution (100 mL) (Group C) 15 minutes before the induction of general anesthesia. After delivery of newborn 0.15 mg kg(-1) morphine was administered to all patients in both groups. Postoperative analgesia was provided with patient-controlled intravenous analgesia with morphine in the postoperative period. Measurements: Pain which is the primary outcome measure was assessed at 15th, 30th minutes and 1st, 2nd, 4th, 6th, 12th, 24th hours by the Visual Analogue Scale. Patients' demographics, hemodynamics, Apgar score, additional analgesic requirement, side effects, patients' satisfaction and postoperative total morphine consumption within 24 hours were recorded. Main Results: Median visual analogue scale for pain in Group P was significantly lower compared to Group C at all time points except for the score at 24th h postoperatively (P <.05). Additional analgesic requirement during postoperative first hour was lower in Group P (P <.05). Total morphine consumption was higher in Group C compared with Group P (P <.05). There was no difference between groups with respect to Apgar scores, side effects, and patient satisfaction (P >.05). Conclusions: Preoperative use of single-dose intravenous 1 g paracetamol was found to be effective in reducing the severity of pain and opioid requirements within 24 hours after cesarean section. (C) 2016 Elsevier Inc. All rights reserved.en_US
dc.identifier.eissn1873-4529en_US
dc.identifier.endpage57en_US
dc.identifier.issn0952-8180en_US
dc.identifier.scopus2-s2.0-84962920060en_US
dc.identifier.startpage51en_US
dc.identifier.urihttp://hdl.handle.net/11727/9886
dc.identifier.volume33en_US
dc.identifier.wos000382421800010en_US
dc.language.isoengen_US
dc.relation.isversionof10.1016/j.jclinane.2016.02.030en_US
dc.relation.journalJOURNAL OF CLINICAL ANESTHESIAen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPreoperative analgesiaen_US
dc.subjectParacetamolen_US
dc.subjectCesarean deliveryen_US
dc.subjectGeneral anesthesiaen_US
dc.titlePreoperative Paracetamol Improves Post-Cesarean Delivery Pain Management: A Prospective, Randomized, Double-Blind, Placebo-Controlled Trialen_US
dc.typearticleen_US

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