Yazar "Özmen, S." seçeneğine göre listele
Listeleniyor 1 - 4 / 4
Sayfa Başına Sonuç
Sıralama seçenekleri
Öğe A Comperative Study on Allergic Reactions Related to Various Anaesthetic Agents(1997) Altındiş, M.; Tuncer, S.; Özmen, S.; Ökeşli, S.; Sütçü, A.; Baysal, B.This study was designed to determine and compare allergic reactions due to IV anaesthetic agents used during surgical operations. From the Departments of general surgery, urology and orthopaedics 60 adults patients (27 male and 33 female with 35.9±12.5 mean age) having no tumoral-endocrine pathology or allergy/athopy history and being classified as ASA I and II were included to the study. They were divided into four groups as equal in number. The groups were similar demographically. After permission of the hospital's ethic comittee, the 4 groups were respectively infused with propofol (2.5 mg/kg) thiopentone (5 mg/kg), etomidate (0.3 mg/kg) and midazolam (0.3 mg/kg) for induction. Serum IgE levels (by ELISA using EIA-Bioclone, Australia) and eosinophil and basophil counts (by using autoanalyser) were measured in blood samples drawn both just before, after induction and 24 hrs later. As a result, we detected thiopentone to cause significant increase in serum IgE levels and eosinophil and basophil counts more than those of the other 3 agents (p<0.05). We concluded that, instead of using thiopentone, propofol, etomidate or midazolam may be a safer alternative for patients with an allergy/athopy history.Öğe EEG Findings in Etomidate Anaesthesia(1992) Özmen, S.; Ökeşli, S.; İlhan, N.; Akhan, G.; Otelcioğlu, S.; Ünal, F.This study included 30 volunteer cases (19 male, 11 female) in ASA-I group with normal electroancephalographic findings. All cases divided in 3 groups randomly and 45 minutessd prior to administration of etomidate, first group was premedicated with 0.5 mg Atropine, second group with 0.5 mg Atropine and 10 mg Diazepam and third group with 0.5 mg Atropine and 01. mg Fentanyl. Induction has been succeeded by IV 0.4 mg/kg etomidate. In order to maintain anaesthesia 0.1 mg/kg etomidate was administered intravenously at 5th minute and EEG was obtained for 15 mintures after first dosage of etomidate. The EEG findings of etomidate anaesthesia and the relation of myoclonia (the main side effect) with CNS was evaluated by EEG records. EEG findings were not affected with premedication methods and no correlation between myoclonia and EEG signs was established. However, myoclonia was decreased significantly in patients who received Fentanyl as premedication. Instead of the irregular alpha and fast activities were observed on control EEG recordings in patients anaesthetised with etomidate. The sharp waves and the suppression burst activities appeared in some cases. In conclusion attention must be paid during etomidate anaesthesia in epileptic patients or it should be avoided using etomidate in patients who has a history of epilepsy because of the possibility of provocating the seizures.Öğe The Effects on Blood Glucose, İnsulin and Cortisol Levels of Using Etomidate and Thiopentone in IV Anaesthesia(1991) Okesli, S.; Özmen, S.; Otelcioğlu, S.; Gürbilek, M.; Karabacak, H.[Abstract not Available]Öğe The Reliability and Validity of Turkish Version of Childhood Asthma Control Test(SPRINGER, 2012) Şekerel, B. E.; Soyer, O. U.; Keskin, O.; Uzuner, N.; Yazıcıoğlu, M.; Kılıç, M.; Artaç, H.; Özmen, S.; Can, D.; Zeyrek, D.; Çokuğraş, H.; Canıtez, Y.; Aydoğan, M.; Kuyucu, S.; İnal, A.; Gürkan, F.; Orhan, F.; Yılmaz, O.; Boz, A. B.; Tahan, F.; Cevit, O.Introduction The reliability and validity of Turkish version of Childhood Asthma Control Test (C-ACT). Purpose The management of asthma is an important as well as difficult issue of physician's daily practice particularly in busy clinical settings. C-ACT was created to identify asthma control levels in children aged 4-11 years. Our aim was to evaluate the reliability, validity and responsiveness of C-ACT in a Turkish sample of children with asthma. Method In this multicenter study, 368 children were enrolled. C-ACT was completed every month by parents and patients who were evaluated in 3 visits within 2 month intervals. At each visit, physicians interpret the control level and decided for the treatment step as established in GINA guidelines. Results The internal consistency reliability of the Turkish version of C-ACT (C-ACT1 to C-ACT5) was found to be 0.82, 0.83, 0.82, 0.82 and 0.80, respectively (reliability statistics, Cronbach's alpha). Test-retest reliability was 0.71. There was significant correlation between C-ACT and physician's assessment of asthma control at visit 1 (r = 0.65, P < 0.001). Conclusions Turkish version of C-ACT is an accurate and reliable tool to evaluate asthma control in children aged 4-11 years. Its widespread use may facilitate appropriate assessment of asthma control and may lead to decrease the number of uncontrolled patients.