Burcin Ozturk's scientific contributions

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Publications (2)


Comparison of troponin values between groups; P∗<0.05. Group I: general anesthesia, Group II: combined general anesthesia and HTEA with levobupivacaine, troponin 1: preoperatively, troponin 2: 6 hours after arrival in the intensive care unit, and troponin 3: 24 hours after arrival in the intensive care unit.
Comparison of CK-MB values between groups; P∗<0.05. Group I: general anesthesia, Group II: combined general anesthesia and HTEA with levobupivacaine, CK-MB 1: preoperatively, CK-MB 2: 6 hours after arrival in the intensive care unit, and CK-MB3:  24 hours after arrival in the intensive care unit.
Comparison of VAS values between groups; P∗<0.05. Group I: general anesthesia, Group II: combined general anesthesia and HTEA with levobupivacaine, VAS: visual analog scale, VAS 0: arrival in the intensive care unit, VAS 4: 4 hours after arrival in the intensive care unit, VAS 8: 8 hours after arrival in the intensive care unit, VAS 12: 12 hours after arrival in the intensive care unit, VAS 16: 16 hours after arrival in the intensive care unit, VAS 20: 20 hours after arrival in the intensive care unit, and VAS 24: 24 hours after arrival in the intensive care unit.
Does High Thoracic Epidural Analgesia with Levobupivacaine Preserve Myocardium? A Prospective Randomized Study
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March 2015

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66 Reads

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7 Citations

BioMed Research International

BioMed Research International

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Umit Karadeniz

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Background: Our study aimed to compare HTEA and intravenous patient-controlled analgesia (PCA) in patients undergoing coronary bypass graft surgery (CABG), based on haemodynamic parameters and myocardial functions. Materials and methods: The study included 34 patients that were scheduled for elective CABG, who were randomly divided into 2 groups. Anesthesia was induced and maintained with total intravenous anesthesia in both groups while intravenous PCA with morphine was administered in Group 1 and infusion of levobupivacaine was administered from the beginning of the anesthesia in Group 2 by thoracic epidural catheter. Blood samples were obtained presurgically, at 6 and 24 hours after surgery for troponin I, creatinine kinase-MB (CK-MB), total antioxidant capacity, and malondialdehyde. Postoperative pain was evaluated every 4 hours until 24 hours via VAS. Results: There were significant differences in troponin I or CK-MB values between the groups at postsurgery 6 h and 24 h. Heart rate and mean arterial pressure in Group 1 were significantly higher than in Group 2 at all measurements. Cardiac index in Group 2 was significantly higher than in Group 1 at all measurements. Conclusion: Patients that underwent CABG and received HTEA had better myocardial function and perioperative haemodynamic parameters than those who did not receive HTEA.

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Postoperative pain therapy in beating-heart coronary revascularization patients who were applied the fast-track protocol: A randomized, placebo controlled study

April 2011

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65 Reads

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2 Citations

Turkish Journal of Thoracic and Cardiovascular Surgery

Background: The present study aimed to investigate the effects of the use of dexketoprofen trometamol and diclofenac sodium in combination with tramadol analgesia on postoperative pain control, sedation, and use of tramadol, as well as their possible side effects that may occur due to nonsteroidal anti-inflammatory drug (NSAID) use in patients having beating-heart coronary artery bypass surgery. Methods: In this randomized, placebo-controlled study, which was approved by the hospital ethics committee, patients who were planned to undergo elective beating-heart coronary artery bypass surgery were divided into three groups (n=15). During the closure of sternum's skin 1 mg/kg-1 intramuscular and 20 mg intravenous tramadol were administered to the patients. During transfer, the dose of remifentanil infusion was decreased by 50% and remifentanil infusion was stopped after the transfer of the patient to the intensive care unit (ICU). During the closure of sternum's skin, in addition to tramadol, group 1 received 1 ampoule (50 mg) intramuscular (i.m.) dexketoprofen trometamol; group 2 received 1 ampoule (75 mg) i.m. diclofenac sodium; and, group 3 received i.m. physiological saline solution. The patient groups were planned and medications were administered by a doctor other than both anesthesiologist and the ICU specialist who attended the patient. Pain visual analogue scale (VAS) and Ramsey sedation scores were recorded at the postoperative 1, 3, 6, 12, and 24 hours. At the same measurement points, nausea, vomiting, gastrointestinal complaints, the need for anti-emetics, tramadol requirement, and bleeding amounts were also recorded. Patients with VAS >3 in ICU were administered 1 mg kg-1 i.m. tramadol. Results: No difference was observed between groups in terms of age, sex, weight, and operation time. There was no significant difference between groups in terms of VAS values recorded at postoperative 1, 6, and 24 hours. The VAS values recorded at the postoperative 3rd hour were significantly higher in groups 2 and 3 compared to group 1. Visual analog scale values recorded at postoperative 12 hours were significantly lower in group 1 compared to group 3. No difference was observed between groups in terms of Ramsey sedation scale scores, nausea/vomiting, anti-emetic medication, and gastrointestinal complaints. Bleeding amount determined at postoperative 12 and 24 hours was significantly higher in group 3 compared to groups 1 and 2. Conclusion: Good quality analgesia is essential for early extubation and short-ICU stay of patients undergoing coronary surgery. We found that dexketoprofen trometamol + tramadol combination that we used for this purpose was more effective than both diclofenac + tramadol and placebo + tramadol combinations.