Taner Karakas
Karadeniz Technical University
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Publication
Featured researches published by Taner Karakas.
Pediatrics International | 2007
Murat Cakir; Ilke Mungan; Taner Karakas; Ilknur Girisken; and Aysenur Okten
Background: Menstrual disorders may affect the life of adolescents and young adult women, and may sometimes cause serious problems. The patterns of menstrual cycles were analyzed for association with age of menarche, prevalence of menstrual irregularity, dysmenorrhea, prolonged menstrual bleeding, and effect of menstrual disorders, especially dysmenorrhea, on social activities and school attendance among the female students.
Clinical & Experimental Allergy | 2009
Fazil Orhan; Taner Karakas; M. Cakir; A. Aksoy; A. Baki; Y. Gedik
Background The prevalence of adverse reactions to food in childhood in Turkey is not known.
Pediatric Allergy and Immunology | 2007
Fazil Orhan; Taner Karakas; Murat Cakir; Nevzat Akkol; Elif Bahat; Fatma Mujgan Sonmez; Yusuf Gedik
Epidemiologic studies about the prevalence of adverse drug reactions in children are scarce compared to reports in adults. To assess the prevalence of parental‐reported drug allergy in 6‐ to 9‐yr‐old urban school children, we performed a cross‐sectional study of 6‐ to 9‐yr‐old urban children from the eastern Black Sea region of Turkey during the year 2004, using a self‐administered questionnaire by parents. Response rate was 81.6% (2855/3500). The prevalence of parental‐reported drug allergy was 2.8% (81/2855). The most common parental‐reported drugs were penicillins and other β‐lactams (59.3%), trimethoprim–sulfamethoxazole (11.1%), and acetylsalicylic acid and other non‐steroidal anti‐inflammatory drugs (NSAIDs) (9.9%). The most commonly reported clinical manifestations were cutaneous (n = 76, 93.8%) followed by gastrointestinal (n = 17, 21%) symptoms. In 19 (23.5%) children, the reaction involved more than one organ system. Of these 19 children, 14 used β‐lactams. Systemic reactions were not reported with NSAIDs. Medications were taken by mouth in 88.9% of the reactions. Most of the reported allergic reactions occurred in the first day of treatment (61.7%). The reported time to reaction after the last intake of the drug was <2 h in 35 (43.2%) children and 2–24 h in 45 (55.6%). Oral reactions occurred later than reactions to parentally administered drugs. Parents of 58 children (71.6%) reported that they completely avoided the suspected culprit drug following the reaction. Relapse occurred after re‐administration of the drug in 21 (25.9%) children. A diagnostic approach for drug allergy was not undertaken in any of the children. This study may provide some information about the prevalence of drug allergy, although it is based on parental perception and results are unlikely to conform well to true prevalence.
Allergy and Asthma Proceedings | 2008
Murat Cakir; Seker Akcay; Taner Karakas; Yusuf Gedik; Ayşenur Ökten; Fazil Orhan
The prevalence of allergic diseases such as asthma, hay fever, and atopic dermatitis has increased over the past few decades, especially in developed countries. They are characterized by a chronic inflammatory reaction mediated by T helper 2 (Th2) cells. Two common chronic diseases of childhood-an autoimmune disease, type 1 diabetes mellitus (DM), and a chronic viral infection, hepatitis B virus (HBV) carriers-are associated with a Th1-dominant and Th1-insufficient cytokine profile, respectively. The purpose of this study was to analyze the frequency of allergic disease in patients with type 1 DM and, in HBV carriers, to evaluate the role of Th1-type immune response in atopy and allergic disease. The study included patients with type 1 DM (group I, n = 52), HBV carriers (group III, n = 47), and a healthy control group (group III, n = 209). Participants were screened for allergic disease and atopic sensitization. Symptoms of asthma, eczema, and atopy were found more commonly in HBV carrier children compared with those with DM and healthy controls. This study supports the Th1/Th2 model. The prevalence of allergic disease and atopy is decreased in Th1-mediated autoimmune disease, type 1 DM, and, conversely, is increased in insufficient Th1 response, chronic HBV carriers. Additional studies are needed to evaluate the effect of atopy and allergic diseases in glycemic control and long-term complications in patients with type 1 DM and the effect of atopy on progression of chronic HBV infection.
Pediatric Allergy and Immunology | 2009
Ozge Soyer; Nazım Ercüment Beyhun; Esen Demir; S. Yıldırım; A. Bingöl Boz; N. Altınel; Ömer Cevit; Taner Karakas; Y. Anlar; A. Söğüt; Derya Ufuk Altıntaş; Yakup Canitez; Z. Büyükdereli; Bulent Enis Sekerel
Many surveys worldwide have consistently demonstrated a low level of asthma control and under‐utilization of preventive asthma drugs. However, these studies have been frequently criticized for using population‐based samples, which include many patients with no or irregular follow‐ups. Our aim, in this study, was to define the extent of asthma drug utilization, control levels, and their determinants among children with asthma attending to pediatric asthma centers in Turkey. Asthmatic children (age range: 6–18 yr) with at least 1‐yr follow‐up seen at 12 asthma outpatient clinics during a 1‐month period with scheduled or unscheduled visits were included and were surveyed with a questionnaire‐guided interview. Files from the previous year were evaluated retrospectively to document control levels and their determinants. From 618 children allocated, most were mild asthmatics (85.6%). Almost 30% and 15% of children reported current use of emergency service and hospitalization, respectively; and 51.4% and 53.1% of children with persistent and intermittent disease, respectively, were on daily preventive therapy, including inhaled corticosteroids. Disease severity [odds ratio: 12.6 (95% confidence intervals: 5.3–29.8)], hospitalization within the last year [3.4 (1.4–8.2)], no use of inhaled steroids [2.9 (1.1– 7.3)], and female gender [2.3 (1.1–5.4)] were major predictors of poor asthma control as defined by their physicians. In this national pediatric asthma study, we found a low level of disease control and discrepancies between preventive drug usage and disease severity, which shows that the expectations of guidelines have not been met even in facilitated centers, thus indicating the need to revise the severity‐based approach of asthma guidelines. Efforts to implement the control‐based approach of new guidelines (Global Initiative for Asthma 2006) would be worthwhile.
Acta Paediatrica | 2007
Murat Cakir; Taner Karakas; Fazil Orhan; Ayşenur Ökten; Yusuf Gedik
Aim: To investigate whether immune responses against chronic HBV infection in children have an effect on prevalence of allergic diseases and atopy.
Pediatric Hematology and Oncology | 2006
Erol Erduran; Yavuz Tekelioglu; Taner Karakas; Yusuf Gedik; Fatih Mehmet Mert
The authors compare the apoptotic effect on the lymphoblasts and the proliferative effect on the myeloid lineage cells of a short-course high-dose methylprednisolone (HDMP) and the conventional-dose prednisolone treatments in children with acute lymphoblastic leukemia (ALL). The patients were divided into 2 groups. Group I (n = 10) received HDMP (30 mg/kg/day for 7 days) in a single dose before 6 a.m. perorally. Group II (n = 10) received prednisolone (2 mg/kg/day for 7 days) in 3 doses. The apoptotic percentages of lymphpblasts and the percentages of blasts and myeloid lineage cells were determined after performing the bone marrow aspiration (BMA) at diagnosis on the 0th, 3rd, and 7th days of the treatments in all patients. The mean apoptotic percentages of the lymphoblasts on the 3rd day were significantly higher than those on the 0th and 7th days in both groups (p <. 05). The highest apoptosis was determined on the 3rd day in group I. The mean percentages of the blast cells on the 7th day were significantly lower than those on the 0th and the 3rd days in both groups (p <. 05). The lowest lymphoblast percentage was determined on the 7th day in group I. The mean percentages of the CD13+ and CD33+ cells on the 7th day were significantly higher than those on the 0th and the 3rd days in both groups (p <. 05). The highest percentages of the CD13+ and CD33+ cells were found on the 7th day in group I. Prednisolone and HDMP showed no proliferative effect on the CD14+ cells. These findings indicate that a short-course HDMP treatment shows a more effective apoptosis on the lymphoblasts and on the increase of the myeloid lineage cells when compared to the prednisolone treatment. The authors suggest that HDMP may be used in the treatment of patients with ALL instead of prednisolone.
The Journal of Allergy and Clinical Immunology | 2016
Mehtap Haktanir Abul; Fazil Orhan; Zekiye İlke Kılıç Topçu; Taner Karakas
The Journal of Allergy and Clinical Immunology | 2015
Mehtap Haktanir Abul; Fazil Orhan; Taner Karakas; Zekiye İlke Kılıç Topçu
Asthma Allergy Immunology | 2012
Elif Acar Arslan; Fazil Orhan; Taner Karakas; İlke Kılıç Topçu; Emine Can; Murat Cakir