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dc.contributor.authorAbdollahi, Mohammad-Hasan
dc.contributor.authorForuzan-nia, Khalil
dc.contributor.authorBehjati, Mostafa
dc.contributor.authorBagheri, Babak
dc.contributor.authorKhanbabayi-Gol, Mehdi
dc.contributor.authorDareshiri, Shahla
dc.contributor.authorPishgahi, Alireza
dc.contributor.authorZarezadeh, Rafie
dc.contributor.authorLotfi-Naghsh, Nazgol
dc.contributor.authorLotfi-Naghsh, Ainaz
dc.contributor.authorNaghavi-Behzad, Mohammad
dc.date.accessioned2019-12-12T06:46:25Z
dc.date.available2019-12-12T06:46:25Z
dc.date.issued2014
dc.identifier.issn0300-1652
dc.identifier.urihttps://doi.org/10.4103/0300-1652.140376
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4178333/
dc.identifier.urihttp://hdl.handle.net/11655/16992
dc.description.abstractBackground: Post-operative fever is a common complication of cardiac operations, which is known to be correlated with a greater degree of cognitive dysfunction 6 weeks after cardiac surgery. The aim of the present study was to examine efficacy and safety of single dose intravenous Paracetamol in treatment of post-operative fever in children undergoing cardiac surgery. Materials and Methods: In this randomised, double-blind, placebo-controlled clinical trial, 80 children, aged 1-12 years, presenting for open heart surgery were entered in the trial and randomly allocated into two groups: Placebo and Paracetamol. After induction of anaesthesia, 15 mg/kg intravenous Paracetamol solution was infused during 1 h in the Paracetamol group. Patients in placebo group received 15 mg/kg normal saline infusion during the same time. Since the end of operation until next 24 h in intensive care unit, axillary temperature of the two group patients was recorded in 4-h intervals. Any fever that occurred during this period had been treated with Paracetamol suppository (125 mg) and the amount of antipyretic drug consumption for each patient had been recorded. In order to examine the safety of Paracetamol, patients were evaluated for drug complication at the same time. Results: Mean axillary temperature during first 24 h after operation was significantly lower in Paracetamol group compared with placebo group (P = 0.001). Overall fever incidence during 24 h after operation was higher in placebo group compared with Paracetamol group (P = 0.012). Of Paracetamol group patients, 42.5% compared with 15% of placebo group participants had no consumption of antipyretic agent (Paracetamol suppository) during 24 h after operation (P = 0.001). Conclusion: This study suggests that single dose administration of intravenous Paracetamol before paediatric cardiac surgeries using cardiopulmonary bypass; reduce mean body temperature in the first 24 h after operation.
dc.relation.isversionof10.4103/0300-1652.140376
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleThe Effect Of Preoperative Intravenous Paracetamol Administration On Postoperative Fever In Pediatrics Cardiac Surgery
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalNigerian Medical Journal : Journal of the Nigeria Medical Association
dc.contributor.departmentAnesteziyoloji ve Reanimasyon
dc.identifier.volume55
dc.identifier.issue5
dc.identifier.startpage379
dc.identifier.endpage383
dc.description.indexPubMed


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