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Patient controlled ıntermittent epidural bolus versus epidural ınfusion for posterior spinal fusion after adolescent ıdiopathic scoliosis

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dc.contributor.author Erdoğan, Mehmet Ali
dc.contributor.author Özgül, Ülkü
dc.contributor.author Ucar, Muharrem
dc.contributor.author Korkmaz, Mehmet Fatih
dc.contributor.author Aydogan, Mustafa Said
dc.contributor.author Özkan, Ahmet Selim
dc.contributor.author Çolak, Cemil
dc.contributor.author Durmuş, Mahmut
dc.date.accessioned 2017-12-19T12:45:39Z
dc.date.available 2017-12-19T12:45:39Z
dc.date.issued 2016
dc.identifier.citation Erdoğan, M. A., Özgül, Ü., Uçar, M., Korkmaz, M. F., Aydoğan, M. S., Özkan, A. S., … Durmuş, M. (2016). Patient Controlled Intermittent Epidural Bolus Versus Epidural Infusion For Posterior Spinal Fusion After Adolescent Idiopathic Scoliosis. Spıne, 1(1), 1–6. tr_TR
dc.identifier.uri https://insights.ovid.com/pubmed?pmid=27792112
dc.identifier.uri http://hdl.handle.net/11616/7906
dc.description SPINE Volume 42, Number 12, pp 882–886. tr_TR
dc.description.abstract Study Design. A prospective, randomized, double-blinded study. Objective. The aim of this study was to compare the efficacy and side effects of patient-controlled intermittent bolus epidural analgesia (PCIEA) and patient-controlled continuous epidural analgesia (PCCEA) for postoperative pain control in adolescent idiopathic scoliosis. Summary of Background Data. Epidural analgesia is an accepted efficacious and safe procedure for postoperative pain management in scoliosis surgery. However, the PCIEA has not been adequately investigated for postoperative pain control in adolescent idiopathic scoliosis. Methods. Forty-seven patients, 8 to 18 years of age, who were undergoing posterior spinal fusion for idiopathic scoliosis were randomized to either the PCIEA or PCCEA group. An epidural catheter was inserted by a surgeon under direct visualization. The PCIEA group received 0.2 mg/mL of morphine, 0.25 mL/kg of morphine bolus, additional doses of 0.25 mL/kg morphine with a 1-hour lockout given by patient-controlled demand, and no infusion. The PCCEA group received the following: 0.2 mg/ mL morphine, an initial morphine loading set at 0.1 mL/kg, followed by a 0.05 mL/kg/h continuous infusion of morphine, and a 0.025 mL/kg bolus dose of morphine. There was a 30-minute lockout interval. The primary outcome was morphine usage. The secondary outcomes were pain score, postoperative nausea and vomiting, and pruritus. Results. Cumulative morphine consumption was lower in the PCIEA group than in the PCCEA group. Both methods provided effective pain control. There were no differences in pain scores between the groups. Postoperative nausea, vomiting, and pruritus were lower in the PCIEA group. Conclusion. The two epidural analgesia techniques studied are both safe and effective methods for postoperative pain control after posterior spinal fusion in idiopathic scoliosis. Nausea, vomiting and pruritus were considerably higher in the PCCEA group. Concerns regarding side effects associated with epidural opioids can be avoided by an intermittent bolus with a relatively lower amount of opioid. tr_TR
dc.language.iso eng tr_TR
dc.publisher SPINE Volume 42, Number 12, pp 882–886. tr_TR
dc.relation.isversionof 10.1097/BRS.0000000000001937 tr_TR
dc.rights info:eu-repo/semantics/openAccess tr_TR
dc.subject Pain Management tr_TR
dc.subject Patient-controlled tr_TR
dc.subject Epidural analgesia tr_TR
dc.title Patient controlled ıntermittent epidural bolus versus epidural ınfusion for posterior spinal fusion after adolescent ıdiopathic scoliosis tr_TR
dc.type article tr_TR
dc.relation.journal SPINE Volume 42, Number 12, pp 882–886. tr_TR
dc.contributor.department İnönü Üniversitesi tr_TR
dc.contributor.authorID 116272 tr_TR
dc.contributor.authorID 45360 tr_TR
dc.contributor.authorID 113863 tr_TR
dc.contributor.authorID 41818 tr_TR
dc.contributor.authorID 9217 tr_TR
dc.contributor.authorID 9837 tr_TR
dc.identifier.volume 42 tr_TR
dc.identifier.issue 12 tr_TR
dc.identifier.startpage 882 tr_TR
dc.identifier.endpage 886 tr_TR


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