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Comparison of Propofol, Propofol-Remifentanil, and Propofol-Fentanyl Administrations with Each Other Used for the Sedation of Patients to Undergo ERCP

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dc.contributor.authors Haytural, C; Aydinli, B; Demir, B; Bozkurt, E; Parlak, E; Disibeyaz, S; Sarac, A; Ozgok, A; Kazanci, D;
dc.date.accessioned 2020-02-27T08:45:39Z
dc.date.available 2020-02-27T08:45:39Z
dc.date.issued 2015
dc.identifier.citation Haytural, C; Aydinli, B; Demir, B; Bozkurt, E; Parlak, E; Disibeyaz, S; Sarac, A; Ozgok, A; Kazanci, D; (2015). Comparison of Propofol, Propofol-Remifentanil, and Propofol-Fentanyl Administrations with Each Other Used for the Sedation of Patients to Undergo ERCP. BIOMED RESEARCH INTERNATIONAL, , -
dc.identifier.issn 2314-6133
dc.identifier.uri https://doi.org/10.1155/2015/465465
dc.identifier.uri https://hdl.handle.net/20.500.12619/66858
dc.description.abstract Introduction. Using single anesthetic agent in endoscopic retrograde cholangiopancreatography (ERCP) may lead to inadequate analgesia and sedation. To achieve the adequate analgesia and sedation the single anesthetic agent doses must be increased which causes undesirable side effects. For avoiding high doses of single anesthetic agent nowadays combination with sedative agents is mostly a choice for analgesia and sedation for ERCP. Aim. The aim of this study is to investigate the effects of propofol alone, propofol + remifentanil, and propofol + fentanyl combinations on the total dose of propofol to be administered during ERCP and on the pain scores after the process. Materials and Method. This randomized study was performed with 90 patients (ASA I-II-III) ranging between 18 and 70 years of age who underwent sedation/analgesia for elective ERCP. The patients were administered only propofol (1.5mg/kg) in Group., remifentanil (0.05 mu g/kg) + propofol (1.5mg/kg) combination in Group II, and fentanyl (1 mu g/kg) + propofol (1.5mg/kg) combination in Group III. All the patients' sedation levels were assessed with the Ramsey Sedation Scale (RSS). Their recovery was assessed with the Aldrete and Numerical Rating Scale Score (NRS) at 10 min intervals. Results. The total doses of propofol administered to the patients in the three groups in this study were as follows: 375mg in Group I, 150mg in Group II, and 245mg in Group III. Conclusion. It was observed that, in the patients undergoing ERCP, administration of propofol in combination with an opioid provided effective and reliable sedation, reduced the total dose of propofol, increased the practitioner satisfaction, decreased the pain level, and provided hemodynamic stability compared to the administration of propofol alone.
dc.language English
dc.publisher HINDAWI PUBLISHING CORP
dc.subject Research & Experimental Medicine
dc.title Comparison of Propofol, Propofol-Remifentanil, and Propofol-Fentanyl Administrations with Each Other Used for the Sedation of Patients to Undergo ERCP
dc.type Article
dc.contributor.department Sakarya Üniversitesi/Tıp Fakültesi/Dahili Tıp Bilimleri Bölümü
dc.contributor.saüauthor Parlak, Erkan
dc.relation.journal BIOMED RESEARCH INTERNATIONAL
dc.identifier.wos WOS:000364066300001
dc.identifier.doi 10.1155/2015/465465
dc.identifier.eissn 2314-6141
dc.contributor.author Candan Haytural
dc.contributor.author Bahar Aydinli
dc.contributor.author Berna Demir
dc.contributor.author Elif Bozkurt
dc.contributor.author Parlak, Erkan
dc.contributor.author Selcuk Disibeyaz
dc.contributor.author Ahmet Sarac
dc.contributor.author Aysegul Ozgok
dc.contributor.author Dilek Kazanci


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