Dilek Özcengiz
Çukurova University
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Publication
Featured researches published by Dilek Özcengiz.
European Journal of Pharmacology | 2002
Tufan Mert; Yasemin Güneş; Mustafa Güven; Ismail Gunay; Dilek Özcengiz
The experiments were done on frog sciatic nerves, using a sucrose-gap recording technique. The aim of our study was to investigate and to compare the tonic and phasic conduction blocking potency of tramadol and lidocaine on whole nerve and their interactions with Ca(2+). The concentration of a tramadol solution producing the same amount of tonic and phasic conduction blocks was three and six times higher than that needed for lidocaine, respectively. Increasing the Ca(2+) concentration in the test solution enhanced the conduction blocking potency of tramadol, but decreased that of lidocaine. It is concluded that tramadol blocks nerve conduction like a local anesthetic but with a weaker effect than that of lidocaine. Interactions of Ca(2+) and these drugs suggested that these drugs might have either different binding sites or different action mechanisms.
Pediatric Anesthesia | 2001
Dilek Özcengiz; Murat Gündüz; Hayri Özbek; G. Isik
Objectives: We compared the quality and duration of analgesia, the effect on perioperative sevoflurane requirement after a single, presurgical caudal block with either tramadol or morphine in children undergoing inguinal herniorrhaphy. Our study was also designed to evaluate the preemptive analgesic efficacy of morphine administered caudally in children.
Pediatric Anesthesia | 2005
M. Ozalevli; H. Unlugenc; Ülkü Tuncer; Yasemin Güneş; Dilek Özcengiz
Background : Tramadol is an alternative to other opioids for postoperative pain management. This prospective, randomized, double‐blind study was designed to compare the analgesic efficacy of patient‐controlled tramadol with patient‐controlled morphine for postoperative pain after tonsillectomy in children.
Pediatric Anesthesia | 2004
Yasemin Güneş; Murat Gündüz; H. Unlugenc; M. Ozalevli; Dilek Özcengiz
Background : In this study we compared caudal with intravenous (i.v.) tramadol given pre‐ or postoperatively for pain relief in boys having hypospadias repair.
Pediatric Anesthesia | 2004
Yasemin Güneş; Seçen M; Dilek Özcengiz; Murat Gündüz; Okan Balcioglu; G. Isik
Background : The aim of this study was to compare the effect of single‐dose caudal ropivacaine, ropivacaine plus ketamine and ropivacaine plus tramadol in children for postoperative pain management.
Pediatric Anesthesia | 2001
Murat Gündüz; Dilek Özcengiz; Hayri Özbek; G. Isik
Background: Our aim was to compare the effect of single dose caudal tramadol, tramadol plus bupivacaine and bupivacaine on the management of postoperative pain in children.
Pediatric Anesthesia | 2006
Murat Gündüz; M. Ozalevli; Hayri Özbek; Dilek Özcengiz
Background: This study was designed to investigate whether the addition of tramadol or lidocaine to ketamine would enhance the quality of intra‐ and postoperative analgesia for hypospadias surgery in children.
Pediatric Anesthesia | 2002
Hayri Özbek; Ahmet Bilen; Dilek Özcengiz; Yasemin Güneş; M. Ozalevli; H. Akman
Background: Our aim was to compare the effect of single dose caudal ketamine, alfentanil or a mixture of both drugs in the treatment of pain after hypospadias repair surgery in children.
Journal of Anaesthesiology Clinical Pharmacology | 2011
Murat Gündüz; Sefika Sakalli; Yasemin Güneş; Erol Kesiktas; Dilek Özcengiz; G. Isik
Objective: The aim of this randomized, controlled study was to compare the sedoanalgesic effects of ketamine-dexmedetomidine and ketamine-midazolam on dressing changes of burn patients. Materials and Methods: Following Ethics Committee approval and informed patient consent, 90 ASA physical statuses I and II adult burn patients were included in the study. Patients were randomly divided into three groups. Ten minutes before dressing change, the dexmedetomidine group (group KD) (n = 30) received a continuous infusion of dexmedetomidine at a rate of 1 μg kg-1, the midazolam group (group KM) (n = 30) received a continuous infusion of midazolam at a rate of 0.05 mg kg-1 and the saline group (group KS) (n = 30) received a continuous infusion of saline intravenously. One minute before dressing change, each patient was administered 1 mg kg-1 ketamine intravenously. Hemodynamic variables, pain and sedation scores, the number of patients requiring additional ketamine, time to dressing change and recovery time were recorded. Results: Systolic blood pressure (SBP) values were significantly lower at, before and after ketamine administration; and 5, 10 and 15 minutes after the procedure in group KD in comparison with the other groups (P <0.05). There was no significant difference in pain scores among the groups during the study period. Sedation scores were significantly higher in group KD than in groups KM and KS at the end of the first hour (P <0.05). Time to dressing change and recovery time were similar in all the groups Conclusion: In burn patients undergoing dressing changes, although both combinations ketamine-dexmedetomidine and ketamine-midazolam offered an effective sedoanalgesia without causing any significant side effect, the former resulted in higher sedation and lower hemodynamic discrepancy.
European Journal of Anaesthesiology | 2006
H. Unlugenc; M. Ozalevli; Yasemin Güneş; S. Olguner; C. Evrüke; Dilek Özcengiz; H. Akman
Background: In this prospective, randomized, double‐blind, controlled study, we investigated the sensory, motor and analgesic block characteristics of S(+) ketamine, fentanyl and saline given intrathecally (IT) in addition to 0.5% plain bupivacaine (10 mg) for spinal analgesia. Methods: Ninety ASA I or II adult patients undergoing Caesarean section were randomly allocated to receive 1.0 mL of 0.9% saline in Group S (n = 30), 0.05 mg kg−1 of S(+) ketamine (1.0 mL) in Group K (n =30) or 25 μg (1.0 mL) of fentanyl in Group F (n =30) following 10 mg of plain bupivacaine 0.5% IT. We recorded onset and duration of sensory and motor block, time to reach the maximal dermatomal level of sensory block and duration of spinal analgesia. Results: The onset time of sensory and motor block was significantly shorter in Groups K and F than in Group S (P < 0.014). Their duration was significantly longer in Group F than in Groups K and S (P < 0.009). The time to reach the maximal dermatomal level of sensory block was significantly shorter in Groups K and F than in Group S (P < 0.001). The duration of spinal analgesia was significantly longer in Group F than in Groups K and S (P < 0.001). Conclusion: In patients undergoing Caesarean section with spinal analgesia, the addition of S(+) ketamine (0.05 mg kg−1) IT to 10 mg of spinal plain bupivacaine (0.5%) led to rapid onset of both sensory and motor blockade and enhanced the segmental spread of spinal block without prolonging the duration of spinal analgesia, whereas fentanyl provided prolonged analgesia.