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81.
Aim: Failure of dental treatment caused by anxiety is a common problem in children. Oral midazolam has been the most commonly used premedication for pediatric patient but the use of midazolam may be associated with paradoxical reactions in children. Melatonin may induce a natural sleepiness and improve sedation. We have investigated premedication with melatonin compared with midazolam in children under nitrous oxide/oxygen (N2O/O2) sedation for dental treatment. Methods: In a randomized study, 60 children received either 3 mg of melatonin [Melatonina (3 mg®) 60 min before the procedure (n = 15); group I], 0.5 mg·kg?1 melatonin 60 min before the procedure (n = 15; group II), 0.75 mg·kg?1 midazolam [Dormicum (15 mg/3 ml ®) 15 min before the procedure (n = 15); group III] or 3 ml of 0.09 NaCl 15 min (n = 7) or 60 min before the procedure (n = 8; group IV) orally. The children were sedated with 40/60% N2O/O2 inhalation. The heart rate and O2 saturation were monitored during the treatment period. The level of sedation was assessed according to the Ramsay Sedation Scale. The children’s sedation success during dental treatment was classified. The sedation success and other sedation‐related events recorded. Comparisons among the four groups were made using one‐way anova or Kruskal–Wallis test, and if any significant differences were noted, the Tukey’s HSD or Mann–Whitney U‐test were used for intergroup comparisons. All differences were considered significant at P < 0.05. Results: The evaluation of sedation success was as follows: group I: satisfactory (n = 1), average satisfactory (n = 4), and unsatisfactory (n = 10); group II: satisfactory (n = 2), average satisfactory (n = 3), and unsatisfactory (n = 10); group III: satisfactory (n = 9), average satisfactory (n = 6); and group IV: satisfactory (n = 1), average satisfactory (n = 3), and unsatisfactory (n = 11). Conclusion: In these doses and clinical conditions, melatonin was similar to that of placebo and did not contribute to N2O/O2 sedation of anxious children. 相似文献
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84.
Dede F Onec B Ayli D Gonul II Onec K 《Scandinavian journal of urology and nephrology》2008,42(2):178-180
Mycophenolate mofetil (MMF) is considered to be a promising therapeutic agent in primary glomerulonephritis but there are no data on the use of MMF in Henoch-Sch?nlein nephritis (HSN). Herein we report the first adult crescentic HSN patient in whom long-term complete remission was achieved after MMF therapy. 相似文献
85.
A. Idil A. Gürler A. Boyvat D. Çaliskan Ö. Özdemir A. Isik 《Ophthalmic epidemiology》2013,20(5):325-331
PURPOSE The aim of this study was to determine the prevalence of Behçet’s disease above the age of 10 years by means of a population-based study. METHODS The epidemiological investigation (cross-sectional study) was made between May 1997 and May 1998 at the Park Primary Health Care Center, which is one of the education and research divisions of the Department of Public Health, Faculty of Medicine, Ankara University. The research aimed to cover all 17,256 (49.2% male, 50.8% female) inhabitants over 10 years of age living in this area. The screening team first surveyed and selected patients with recurrent aphthous stomatitis. These patients were further examined, free of charge, in the Preventive Ophthalmology Unit of the Public Health Center, at Ibni Sina Hospital’s Behçet Center or in other clinics if necessary. In this study the International Study Group For Behçet’s disease Criteria were used. RESULTS As the final result of the screening, 11 female and 5 male patients with Behçet’s disease were found (female/male = 2.2). These patients represented 9 already known and 7 newly diagnosed cases of Behçet’s disease. The prevalence of Behçet’s disease over 10 years of age is 0.11%. CONCLUSION The existing regional prevalance studies conducted in Turkey have indicated that the real number of Behçet’s patients in our country is markedly higher than the number of registered patients. Therefore the National Behçet’s Disease Commity and Surveillance System was founded by our research group in December 1999. 相似文献
86.
Ozgur H. Harmanli Vani Dandolu Ebru F. Isik Uma R. Panganamamula Jeffrey Lidicker 《Archives of gynecology and obstetrics》2011,283(4):795-798
Objective
To evaluate the effects of obesity on the perioperative outcomes in women who underwent vaginal hysterectomy. 相似文献87.
88.
Evaluating the accuracy of functional biomarkers for detecting histological changes in chronic allograft nephropathy 总被引:1,自引:0,他引:1
Serdar Yilmaz Ipek Isik Marjan Afrouzian Mauricio Monroy Aylin Sar Hallgrimur Benediktsson Kevin McLaughlin 《Transplant international》2007,20(7):608-615
The most common cause of late kidney transplant failure is chronic allograft nephropathy (CAN). Much research has focused on identifying biomarkers (or correlates) that would predict subsequent CAN and allow timely intervention. Functional biomarkers such as serum creatinine and estimated glomerular filtration rate (eGFR) have been widely adopted, even though they have not been rigorously evaluated as surrogate markers. This study evaluated serum creatinine and eGFR for predicting the early histopathological changes seen in transplant protocol biopsies (TPB). We prospectively followed 289 kidney transplant patients in the Southern Alberta Transplant Program who had TPB at 6-12 months post-transplant. Tissue samples (n = 280) were independently examined by renal pathologists. The ability of serum creatinine or eGFR to predict the threshold level for abnormal histopathology was evaluated by calculating the area under the receiver operator characteristic curve. Serum creatinine and eGFR had poor predictive value (most confidence intervals included 0.5, indicating no predictive ability) for ten individual histological measurements (Banff 97 scores), and the Chronic Allograft Damage Index. We conclude that serum creatinine and eGFR have a limited clinical role in predicting the early histopathological changes that precede CAN and should not be used for this purpose. 相似文献
89.
Propofol — not thiopental or etomidate — with remifentanil provides adequate intubating conditions in the absence of neuromuscular blockade 总被引:10,自引:0,他引:10
Elvan Erhan Gulden Ugur Ilkben Gunusen Isik Alper Bulent Ozyar 《Journal canadien d'anesthésie》2003,50(2):108-115
PURPOSE: Administration of remifentanil followed by propofol provides adequate conditions for tracheal intubation without muscle relaxants. Other hypnotic drugs have not been thoroughly investigated in this regard. Intubating conditions with remifentanil followed by propofol, thiopentone or etomidate are compared in this study. METHODS: In a randomized, double-blind study 45 healthy males were assigned to one of three groups (n = 15). After iv atropine, remifentanil 3 microg x kg(-1) were injected over 90 sec followed by propofol 2 mg x kg(-1) (Group I), thiopentone 6 mg x kg(-1) (Group II) or etomidate 0.3 mg x kg(-1) (Group III). Ninety seconds after the administration of the hypnotic agent, laryngoscopy and intubation were attempted. Intubating conditions were assessed as excellent, good or poor on the basis of ease of ventilation, jaw relaxation, position of the vocal cords, and patient response to intubation and slow inflation of the endotracheal tube cuff. RESULTS: One patient in Group I, three patients in Group II and five patients in Group III could not be intubated on the first attempt. Clinically acceptable intubating conditions were observed in 93.3%, 66.7%, 40.0% of patients in Groups I, II and III, respectively. Overall conditions at intubation were significantly (P < 0.05) better, and the frequency of excellent conditions was significantly (P < 0.05) higher in the propofol group compared with the thiopentone and etomidate groups. No patient was treated for hypotension or bradycardia. CONCLUSION: Propofol 2 mg x kg(-1) was superior to thiopentone 6 mg x kg(-1) and etomidate 0.3 mg x kg(-1) for tracheal intubation when combined with remifentanil 3 microg x kg(-1) and no muscle relaxant. 相似文献
90.
Koca SS Isik A Ozercan IH Ustundag B Evren B Metin K 《Rheumatology (Oxford, England)》2008,47(2):172-175
OBJECTIVES: To evaluate the effects of etanercept and thalidomide in the mouse model of bleomycin-induced scleroderma (BLM-IS). METHODS: This study involved four groups (n = 8 mice in each group). Dermal sclerosis was induced by repeated subcutaneous injections of BLM (10 microg) for 4 weeks in BALB/c mice. Control group received only phosphate-buffered saline. The second group received only BLM; the third and fourth groups were also given an intraperitoneal injection of 100 microg etanercept or 150 mg/kg thalidomide, respectively. RESULTS: BLM increased serum TGF-beta1, tissue hydroxyproline levels and expression of alpha-smooth muscle actin (alpha-SMA), and dermal fibrosis was histopathologically prominent. Although thalidomide had no significant effect, etanercept caused decreases in levels of serum TGF-beta1, tissue hydroxyproline and number of alpha-SMA-positive cells. CONCLUSION: Inhibition of TNF-alpha with etanercept in BLM-IS was resulted in a significant reduction of the dermal sclerosis, collagen accumulation and the number of infiltrating myofibroblastic cells. TNF-alpha may play a key role in the progression of BLM-IS and TNF-alpha antagonists may be useful in the management of scleroderma. 相似文献