73 results on '"Yarar C"'
Search Results
52. Massage Therapy Produces Short-term Improvements in Balance, Neurological, and Cardiovascular Measures in Older Persons.
- Author
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Sefton JM, Yarar C, and Berry JW
- Abstract
Background: Falls are the primary cause of accidental death in older persons, producing increased morbidity, decreased independence, and billions in medical costs annually. Massage therapy (MT) may produce adaptations that decrease risk of falling. If MT can improve stability in older persons, it may provide a new intervention for this issue., Purpose: Determine the acute effects of a 60-minute MT treatment on static and functional balance, neurological measures, heart rate, and blood pressure in healthy, older individuals., Setting: Laboratory, Research Design: A 2 by 4 (treatment by time) mixed factorial experimental design for the cardiovascular and postural control variables; independent variables were treatment with two levels (control, MT) and time with four levels (pretreatment baseline, immediate post-treatment, 20-minute post-treatment, 60-minute post-treatment). Neurological measures utilized a 2 by 2 mixed design, with testing conducted pre- and 60-minutes post-treatment., Participants: Thirty-five healthy, older volunteers (19 male and 16 female; ages 62.9 ± 4.6)., Intervention: A 60-minute full-body therapeutic massage. The control group rested quietly in the treatment room., Main Outcome Measures: Static (double-legged) and functional (single-legged) postural control with eyes-open and eyes-closed; Hoffmann-reflex measures; heart rate, and systolic and diastolic blood pressure., Results: MT significantly decreased rectangular displacement area in both the eyes-open and eyes-closed, double-legged stance conditions (p < 0.05); displacement velocity in both eyes-open conditions (p < .05); and systolic and diastolic blood pressure (p < .05), while increasing heart rate (p < .05). MT also significantly lowered H(max)/M(max) ratios compared to controls (p = .002). Decreased H(max)/M(max) measures were correlated to improved stability., Conclusions: A single, 60-minute, full-body massage therapy treatment was shown to have a stabilizing effect on measures of static and dynamic balance and physiological factors related to stability in older adults. MT should be investigated as a potential intervention to decrease falls in older individuals.
- Published
- 2012
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53. Six weeks of massage therapy produces changes in balance, neurological and cardiovascular measures in older persons.
- Author
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Sefton JM, Yarar C, and Berry JW
- Abstract
Objectives: Falls in older adults represent a primary cause of decreased mobility and independence, increased morbidity, and accidental death. Research and clinical reports indicate that therapeutic massage (TM) may positively influence suggested causative factors. The second in a two-part study, this project assessed the effects of six weeks of TM treatment on balance, nervous system, and cardiovascular measures in older adults., Design: A randomized controlled trial assessed the effects of six weekly 60-minute sessions of TM on balance, cardiovascular, and nervous system measures. Thirty-five volunteers (19 male and 16 female; ages 62.9 ± 4.6) were randomly assigned to relaxation control or TM groups. A 2 × 4 [treatment condition X time (week 1 and 6)] mixed factorial experimental design was utilized for cardiovascular/balance variables assessed at pretreatment baseline, immediate post-treatment, and 20- and 60-minutes post-treatment; nervous system measures were assessed only at pretreatment and at 60-minute follow-up (2 × 2 mixed design). Long-term benefits were assessed by comparing the TM and control groups on pretreatment baseline measures at week six and a follow-up assessment at week seven (2 × 3 mixed design)., Setting: Laboratory, Intervention: Six weekly 60-minute, full-body TM., Outcome Measures: Postural control/cardiovascular measures were assessed weeks one, six, and seven; pretreatment and immediate, 20- and 60-minutes post-treatment. Motoneuron pool excitability was assessed pretreatment and 60 minutes post-treatment., Results: The TM group showed significant differences relative to controls in cardiovascular and displacement area/velocity after the week six session, with decreasing blood pressure and increasing stability over time from immediate post-TM to 60 minutes post-TM. The TM group revealed lower H-max/M-max ratios 60-minutes post-treatment. Long-term differences between the groups were detected at week seven in displacement area/velocity and systolic blood pressure., Conclusions: Results suggest six weeks of TM resulted in immediate and long-term improvements in postural stability and blood pressure, compared to a controlled condition.
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- 2012
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54. Physiological and clinical changes after therapeutic massage of the neck and shoulders.
- Author
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Sefton JM, Yarar C, Carpenter DM, and Berry JW
- Subjects
- Adult, Cross-Over Studies, Female, Humans, Male, Musculoskeletal Diseases diagnostic imaging, Musculoskeletal Diseases physiopathology, Neck Muscles diagnostic imaging, Range of Motion, Articular, Shoulder diagnostic imaging, Ultrasonography, Young Adult, Massage methods, Musculoskeletal Diseases therapy, Neck Muscles physiology, Shoulder physiology
- Abstract
Little is known regarding the physiological and clinical effects of therapeutic massage (TM) even though it is often prescribed for musculoskeletal complaints such as chronic neck pain. This study investigated the influence of a standardized clinical neck/shoulder TM intervention on physiological measures assessing α-motoneurone pool excitability, muscle activity; and the clinical measure of range of motion (ROM) compared to a light touch and control intervention. Flexor carpi radialis (FCR) α-motoneurone pool excitability (Hoffmann reflex), electromyography (EMG) signal amplitude of the upper trapezius during maximal muscle activity, and cervical ROM were used to assess possible physiological changes and clinical effects of TM. Sixteen healthy adults participated in three, 20 min interventions: control (C), light touch (LT) and therapeutic massage (TM). Analysis of Covariance indicated a decrease in FCR α-motoneurone pool excitability after TM, compared to both the LT (p = 0.0003) or C (p = 0.0007) interventions. EMG signal amplitude decreased after TM by 13% (p < 0.0001), when compared to the control, and 12% (p < 0.0001) as compared to LT intervention. The TM intervention produced increases in cervical ROM in all directions assessed: flexion (p < 0.0001), lateral flexion (p < 0.0001), extension (p < 0.0001), and rotation (p < 0.0001). TM of the neck/shoulders reduced the α-motoneurone pool excitability of the flexor carpi radialis after TM, but not after the LT or C interventions. Moreover, decreases in the normalized EMG amplitude during MVIC of the upper trapezius muscle; and increases in cervical ROM in all directions assessed occurred after TM, but not after the LT or C interventions., (Copyright © 2011 Elsevier Ltd. All rights reserved.)
- Published
- 2011
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55. Serum asymmetric dimethylarginine (ADMA), homocysteine, vitamin B(12), folate levels, and lipid profiles in epileptic children treated with valproic acid.
- Author
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Ozdemir O, Yakut A, Dinleyici EC, Aydogdu SD, Yarar C, and Colak O
- Subjects
- Adolescent, Anticonvulsants pharmacology, Arginine blood, Biomarkers blood, Case-Control Studies, Child, Child, Preschool, Cholesterol blood, Cross-Sectional Studies, Drug Administration Schedule, Epilepsy blood, Female, Folic Acid blood, Humans, Male, Triglycerides blood, Valproic Acid pharmacology, Vitamin B 12 blood, Anticonvulsants therapeutic use, Arginine analogs & derivatives, Epilepsy drug therapy, Homocysteine blood, Lipids blood, Valproic Acid therapeutic use, Vitamin B Complex blood
- Abstract
Recent reports have demonstrated elevated serum homocysteine (Hcy) levels in children receiving valproic acid (VPA) therapy. Elevated Hcy levels might play a potential role in the resistance to antiepileptic drugs, and might lead to an increased risk for a vascular disease. It has been reported that elevated total homocysteine (tHcy) levels are associated with elevated asymmetric dimethylarginine (ADMA) levels, which are factors that may be better indicators of endothelial dysfunction compared to serum homocysteine levels, because they are less sensitive to changes, such as fasting status, physical activity, and other factors. In this study, we aim to evaluate serum ADMA, Hcy, lipid, folate, and vitamin B₁₂ levels in epileptic children, receiving VPA monotherapy. Forty-four epileptic children, receiving VPA monotherapy for at least 6 months and 28 healthy children aged between 4 and 16 years, were recruited. Serum lipids, lipoproteins, folate, vitamin B₁₂, Hcy, and ADMA levels were analyzed in both study groups. Serum Hcy, ADMA, and vitamin B₁₂ levels were higher in patients than in controls (p < 0.001 for tHcy and ADMA levels; p < 0.05 for vitamin B₁₂ levels); however, serum lipid, lipoprotein, and folate levels were similar. According to the duration of epilepsy, serum tHcy, ADMA, and triglyceride (TG) levels were higher in patients with epilepsy for ≥ 2 years than in patients with epilepsy for < 2 years (p < 0.001 for serum ADMA levels, p < 0.01 for tHcy levels, and p < 0.05 for serum TG levels). Similarly, with respect to the duration of VPA therapy, serum tHcy, ADMA, and TG levels were higher in patients who had received VPA therapy for more than 2 years (p < 0.001 for serum ADMA levels, p < 0.05 for serum tHcy levels, p < 0.01 for TG levels). Serum ADMA levels were significantly higher in patients receiving VPA at the dose of 25-30 mg/kg/day than in those receiving 20 mg/kg/day (p < 0.01). In conclusion, our study found increased serum ADMA levels and increased tHcy levels in epileptic children receiving VPA monotherapy. Increased serum ADMA levels were demonstrated in epileptic children who have had a seizure history greater than 2 years, and have used VPA therapy for more than 2 years, and have received higher doses of VPA. Routine monitoring of serum ADMA and tHcy levels might have beneficial effects for patients receiving long-term VPA therapy, especially in children who have other potential risk factors for vascular diseases. Further studies are needed to investigate serum ADMA and Hcy levels, and the presence of vascular disease, as well as the potential interactions between serum ADMA levels and seizure control.
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- 2011
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56. Infant with chromhidrosis.
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Carman KB, Aydogdu SD, Sabuncu I, Yarar C, Yakut A, and Oztelcan B
- Subjects
- Age of Onset, Color, Female, Humans, Infant, Sweat, Sweat Gland Diseases diagnosis, Sweat Gland Diseases epidemiology
- Published
- 2011
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57. Six weeks of balance training improves sensorimotor function in individuals with chronic ankle instability.
- Author
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Sefton JM, Yarar C, Hicks-Little CA, Berry JW, and Cordova ML
- Subjects
- Adult, Chronic Disease, Electromyography, Female, H-Reflex physiology, Humans, Joint Instability physiopathology, Male, Motor Neurons physiology, Muscle, Skeletal innervation, Muscle, Skeletal physiology, Ankle Joint physiopathology, Joint Instability therapy, Physical Therapy Modalities, Postural Balance physiology, Proprioception physiology
- Abstract
Study Design: Prospective cohort study., Objective: To assess the effect of 6 weeks of balance training on sensorimotor measures previously found to be deficient in participants with chronic ankle instability (CAI)., Background: CAI is the tendency toward repeated ankle sprains and recurring symptoms, occurring in 40% to 70% of individuals who have previously sustained a lateral ankle sprain. Recent studies have found deficits in sensorimotor measures in individuals with CAI. As balance training is a common component of ankle rehabilitation, understanding its effect on the sensorimotorsystem in individuals with CAI may enable us to optimize protocols to better utilize this rehabilitation method., Methods: Twelve participants with CAI and 9 healthy volunteers participated. Independent variables were group (CAI, control) and time (pretraining, posttraining). Participants with CAI who completed a 6-week balance training program and healthy controls who did not get any training were pretested and posttested at the beginning and at the end of 6 weeks., Results: The individuals in the CAI group who performed balance training demonstrated better performance than control participants on baseline adjusted posttraining measures of dynamic balance in the anterior medial (P = .021), medial (P = .048), and posterior medial directions (P = .030); motoneuron pool excitability Hmax/Mmax ratio (P = .044) and single-limb presynaptic inhibition (P = .012); and joint position sense inversion variable error (P = .017). It may be of note that no systematic differences were detected for static balance or plantar flexion joint position sense tasks., Conclusions: After 6 weeks of balance training, individuals with CAI demonstrated enhanced dynamic balance, inversion joint position sense, and changes in motoneuron pool excitability compared to healthy controls who did not train., Level of Evidence: Therapy, level 2b.
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- 2011
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58. Relapsing acute disseminated encephalomyelitis in children: further evaluation of the diagnosis.
- Author
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Dundar NO, Anlar B, Guven A, Serdaroglu A, and Yarar C
- Subjects
- Adolescent, Age Factors, Child, Child, Preschool, Diagnosis, Differential, Encephalomyelitis, Acute Disseminated physiopathology, Female, Follow-Up Studies, Humans, Male, Multiple Sclerosis physiopathology, Retrospective Studies, Secondary Prevention, Encephalomyelitis, Acute Disseminated diagnosis, Multiple Sclerosis diagnosis
- Abstract
We examined our cases of relapsing acute disseminated encephalomyelitis (n = 13) in which diagnosis was made before the publication of the International Pediatric Multiple Sclerosis Study Group criteria in 2007, with the aim of reevaluating the primary diagnosis, examining any features indicative of other disorders, and determining the final diagnosis. Mean duration of follow-up was 9.4 (range, 2-20) years. Most (n = 11) were multiphasic, and 2 were recurrent cases. The final diagnosis changed in only 2 patients, both in the multiphasic group: one multiple sclerosis, and one other possible central nervous system vasculitis. All others are still being followed up as relapsing acute disseminated encephalomyelitis and had no further attacks. Six patients in this category did not have encephalopathy at first episode, which suggested the requirement for encephalopathy might be restrictive for certain cases. These results suggest the diagnosis of relapsing acute disseminated encephalomyelitis can be made correctly in most cases by clinical and imaging features.
- Published
- 2010
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59. Therapeutic massage of the neck and shoulders produces changes in peripheral blood flow when assessed with dynamic infrared thermography.
- Author
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Sefton JM, Yarar C, Berry JW, and Pascoe DD
- Subjects
- Adult, Arm blood supply, Back blood supply, Cross-Over Studies, Female, Humans, Male, Neck, Shoulder, Thermography methods, Thorax blood supply, Young Adult, Massage, Regional Blood Flow, Skin Temperature
- Abstract
Objective: This study's objective was to determine the effect of therapeutic massage on peripheral blood flow utilizing dynamic infrared thermography in a constant temperature/humidity thermal chamber to assess noncontact skin temperature., Design: The design was a repeated-measures crossover experimental design; the independent variable was treatment condition (massage, light touch, control)., Setting: The study setting was a university research laboratory., Subjects: Seventeen (17) healthy volunteers (8 males/9 females; age = 23.29 +/- 3.06) took part in the study., Interventions: One (1) 20-minute neck and shoulder therapeutic massage treatment was performed for each of the three treatment conditions., Outcome Measures: The dependent variable was noncontact, mean skin temperature in 15 regions measured at 6 time points (pretest and 15, 25, 35, 45, and 60 minutes post-test) for each treatment condition., Results: The massage treatment produced significant elevations in temperature in five regions: anterior upper chest (p = 0.04), posterior neck (p = 0.0006), upper back (p = 0.0005), posterior right arm (p = 0.03), and middle back (p = 0.02). Massage therapy produced significant increases in temperature over time, compared to the other conditions, in the anterior upper chest, and posterior neck, upper back, right arm, and the middle back. Additionally, the temperatures remained above baseline levels after 60 minutes. Interestingly, the massage treatment produced significant temperature elevations in two nonmassaged areas posterior right arm and middle back., Conclusions: These changes in temperature suggest corresponding changes in peripheral blood flow in the treated areas as well as in adjacent not-massaged areas. Moreover, the results suggest dynamic infrared thermography as a useful tool to measure noninvasive, noncontact changes in peripheral blood flow for massage therapy research.
- Published
- 2010
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60. Septo-optic dysplasia plus: a patient with diabetes insipidus.
- Author
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Carman KB, Yarar C, Yakut A, and Adapinar B
- Subjects
- Child, Preschool, Female, Humans, Magnetic Resonance Imaging, Syndrome, Diabetes Insipidus pathology, Lissencephaly pathology, Malformations of Cortical Development pathology, Septo-Optic Dysplasia pathology
- Abstract
The association of septo-optic dysplasia and cortical dysplasia is described as septo-optic dysplasia-plus. Reports on patients with septo-optic dysplasia-plus have been rare. We describe a 4-year-old girl with septo-optic dysplasia-plus syndrome, characterized by septo-optic dysplasia with schizencephaly, pachygyria, and diabetes insipidus.
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- 2010
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61. Magnetic resonance imaging at first episode in pediatric multiple sclerosis retrospective evaluation according to KIDMUS and lesion dissemination in space criteria.
- Author
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Kurne A, Oguz KK, Oz Aksu A, Yarar C, Duman O, Kurul SH, Serdaroglu A, and Anlar B
- Subjects
- Adolescent, Child, Female, Follow-Up Studies, Humans, Male, Sensitivity and Specificity, Young Adult, Brain pathology, Magnetic Resonance Imaging methods, Multiple Sclerosis diagnosis, Multiple Sclerosis pathology
- Abstract
Background: Several diagnostic imaging criteria are being described and examined in pediatric multiple sclerosis (MS). Compared to adults, children are more likely to experience acute or relapsing demyelinating episodes of various etiologies which show similar clinical and magnetic resonance imaging (MRI) findings., Aim: To investigate the fulfillment of MRI diagnostic criteria at initial episode in pediatric MS., Methods: We reviewed our series of children and adolescents with the final diagnosis of clinically definite MS and applied the McDonald dissemination in space (DIS) and KIDMUS criteria to their initial MRI scans., Results: Thirty patients (17 girls, 13 boys), most with brainstem dysfunction and polysymptomatic presentation, were included in the study. Twenty-five (83.3%) patients fulfilled both McDonald and KIDMUS criteria. Patients who did not meet any McDonald DIS criteria did not meet KIDMUS criteria either. Only one patient met the McDonald criteria but not the KIDMUS criteria because of the absence of lesions perpendicular to corpus callosum., Conclusions: Our results show 5/30 (16.6%) of MS patients may not present the diagnostic MRI features initially. The variable sensitivity observed for the current MRI criteria in different series can be due to referral biases, differences between populations and length of follow-up, and the definition of MS patients by two attacks only., (Copyright (c) 2009 Elsevier B.V. All rights reserved.)
- Published
- 2010
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62. Spontaneous acute subdural hematoma and chronic epidural hematoma in a child with F XIII deficiency.
- Author
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Vural M, Yarar C, Durmaz R, and Atasoy MA
- Subjects
- Child, Chronic Disease, Female, Hematoma, Epidural, Cranial diagnostic imaging, Hematoma, Subdural, Acute diagnostic imaging, Hematoma, Subdural, Intracranial diagnostic imaging, Humans, Tomography, X-Ray Computed, Factor XIII Deficiency complications, Hematoma, Epidural, Cranial etiology, Hematoma, Subdural, Acute etiology, Hematoma, Subdural, Intracranial etiology
- Abstract
Factor XIII (F XIII) deficiency is a rare autosomal recessive congenital disorder that can cause spontaneous subdural or epidural hematomas. Due to its low incidence, F XIII deficiency may well be under-diagnosed. A 7-year-old girl with no history of medical problems presented with progressive headache of 3 days. Cerebral computed tomography (CT) scans revealed a large right acute parietooccipital subdural hematoma with a significant midline shift. After an emergent parietooccipital craniotomy and evacuation of the subdural hematoma, a screening test for factor XIII was performed. The results of the test were abnormal. She had full recovery and was discharged with a follow-up treatment of monthly transfusion of fresh frozen plasma as the replacement and prophylactic therapy. Ten months later, she was referred to our center with headache after a minor head trauma. Her medical history revealed that she had not received fresh frozen plasma for the last 2 months. CT scan showed a chronic right parietal epidural hematoma beneath the craniotomy flap. The present case indicates that although its incidence is very rare, F XIII deficiency can cause acute or chronic subdural and epidural hematomas. Therefore, in acute or chronic subdural and epidural hematomas with no underlying cause, the presence of a potential F XIII deficiency should be suspected as a cause of hemorrhagic diathesis., (Copyright 2010 Elsevier Inc. All rights reserved.)
- Published
- 2010
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63. MIDAS (microphthalmia, dermal aplasia, sclerocornea) syndrome with central nervous system abnormalities.
- Author
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Carman KB, Yakut A, Sabuncu I, and Yarar C
- Subjects
- Central Nervous System Diseases pathology, Child, Child, Preschool, Cornea pathology, Female, Humans, Magnetic Resonance Imaging, Microphthalmos pathology, Skin Abnormalities pathology, Syndrome, Abnormalities, Multiple pathology, Central Nervous System Diseases complications, Cornea abnormalities, Microphthalmos complications, Skin Abnormalities complications
- Published
- 2009
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64. Analysis of the features of acute carbon monoxide poisoning and hyperbaric oxygen therapy in children.
- Author
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Yarar C, Yakut A, Akin A, Yildiz B, and Dinleyici EC
- Subjects
- Acute Disease, Adolescent, Carbon Monoxide Poisoning physiopathology, Child, Child, Preschool, Female, Humans, Infant, Male, Retrospective Studies, Carbon Monoxide Poisoning therapy, Hyperbaric Oxygenation
- Abstract
The aim of this study was to make a retrospective descriptive analysis of the features of children with acute carbon monoxide poisoning (COP). We evaluated 74 children (43 girls, 31 boys; age range 1 to 17.8 years) who were consecutively admitted to our emergency unit and hospitalized with accidental acute COP between June 2003 and June 2005. All patients received normobaric oxygen therapy until their carboxyhemoglobin (COHb) levels were decreased below 2% and their symptoms resolved. Thirty-eight of 74 patients (51.4%) also received hyperbaric oxygen (HBO) therapy as indicated by signs and symptoms or COHb levels. COHb levels were significantly higher and hospitalization period was longer in the children who had abnormal neurological findings (p<0.05 for both). All patients showed complete recovery without neurological sequelae except one who had visual impairment at discharge, and antiepileptic therapy was started because of epilepsy after seven months. Acute COP is an important health problem in our country, especially in winter, because of poorly functioning heating systems. The clinical spectrum including neurological findings varies during childhood. We suggest that HBO therapy could be used safely in children.
- Published
- 2008
65. Serum amyloid A, procalcitonin, tumor necrosis factor-alpha, and interleukin-1beta levels in neonatal late-onset sepsis.
- Author
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Ucar B, Yildiz B, Aksit MA, Yarar C, Colak O, Akbay Y, and Colak E
- Subjects
- Biomarkers blood, C-Reactive Protein, Calcitonin Gene-Related Peptide, Female, Humans, Male, Pregnancy, ROC Curve, Sensitivity and Specificity, Calcitonin blood, Infant, Newborn blood, Infant, Newborn, Diseases blood, Interleukin-1beta blood, Protein Precursors blood, Sepsis blood, Sepsis diagnosis, Serum Amyloid A Protein, Tumor Necrosis Factor-alpha blood
- Abstract
Background: Sepsis is an important cause of mortality in newborns. However, a single reliable marker is not available for the diagnosis of neonatal late-onset sepsis (NLS). The aim of this study is to evaluate the value of serum amyloid A (SAA) and procalcitonin (PCT) in the diagnosis and follow-up of NLS., Methods: 36 septic and healthy newborns were included in the study. However, SAA, PCT, TNF-alpha, IL-1beta, and CRP were serially measured on days 0, 4, and 8 in the patients and once in the controls. Töllner's sepsis score (TSS) was calculated for each patient., Results: CRP, PCT, and TNF-alpha levels in septic neonates at each study day were significantly higher than in the controls (P = .001). SAA and IL-1beta levels did not differ from healthy neonates. The sensitivity and specificity were 86.8% and 97.2% for PCT, 83.3% and 80.6% for TNF-alpha, 75% and 44.4% for SAA on day 0., Conclusion: Present study suggests that CRP seems to be the most helpful indicator and PCT and TNF-alpha may be useful markers for the early diagnosis of NLS. However, SAA, IL-1beta, and TSS are not reliable markers for the diagnosis and follow-up of NLS.
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- 2008
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66. Antibiotic resistance in children with complicated urinary tract infection.
- Author
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Yildiz B, Kural N, Durmaz G, Yarar C, Ak I, and Akcar N
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- Adolescent, Child, Child, Preschool, Cohort Studies, Female, Humans, Infant, Male, Recurrence, Urinary Tract Infections etiology, Urinary Tract Infections pathology, Drug Resistance, Bacterial, Urinary Tract Infections drug therapy
- Abstract
Objective: To determine the resistance of antibiotics for complicated urinary tract infection (UTI), including urinary tract anomaly (UTA), for empirical antibiotic therapy of complicated UTI., Methods: Four hundred and twenty urine isolates were obtained from 113 patients with recurrent UTI, who used prophylactic antibiotics between February 1999 and November 2004 in the Eskisehir Osmangazi University, Eskisehir, Turkey., Results: Reflux was found to be the most important predisposing factor for recurrent UTI (31.9%). Renal scar was detected more in patients with UTA than without UTA (59.2% versus 12.4%, p<0.05). Gram-negative organisms were dominant in patients with and without UTA (91.5% and 79.2%). Enterococci and Candida spp. were more prevalent in children with UTA than without UTA (p<0.001). Isolates were significantly more resistant to ampicillin, trimethoprim-sulfamethoxazole, amikacin, co-amoxiclav, ticarcillin-clavulanate, and piperacillin-tazobactam in patients with UTA than without UTA. We found low resistance to ciprofloxacin and nitrofurantoin in UTI with and without UTA. Enterococci spp. was highly resistance to ampicillin and amikacin in patients with UTA., Conclusion: Aztreonam, meropenem, and ciprofloxacin seemed to be the best choice for treatment of UTI with UTA due to Escherichia coli and Klebsiella spp. Nitrofurantoin and nalidixic acid may be first choice antibiotics for prophylaxis in UTI with and without UTA. The UTI with UTA caused by Enterococci spp. might not benefit from a combination of amikacin and ampicillin, it could be treated with glycopeptides.
- Published
- 2007
67. Pericardial effusion due to hypothyroidism in Down syndrome: report of four cases.
- Author
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Dinleyici EC, Ucar B, Kilic Z, Dogruel N, and Yarar C
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- Child, Preschool, Congenital Hypothyroidism diagnosis, Congenital Hypothyroidism drug therapy, Female, Follow-Up Studies, Humans, Infant, Male, Pericardial Effusion diagnosis, Pericardial Effusion drug therapy, Thyroid Function Tests, Thyroxine therapeutic use, Congenital Hypothyroidism complications, Down Syndrome complications, Pericardial Effusion etiology
- Abstract
Pericardial effusion may be the first sign of congenital or acquired hypothyroidism and will completely resolve after thyroxin therapy. Hypothyroidism is more common in Down syndrome population than normal population. In this report we present four infants with Down syndrome who have pericardial effusion due to congenital hypothyroidism. All of these children with Down syndrome were admitted to our clinic with pericardial effusion. Pericardial effusion was completely resolved with thyroxin therapy without pericardiosentesis. Any child with Down syndrome who present with dyspnea and cardiomegaly should be suspected of having pericardial effusion due to hypothyroidism and echocardiography examination should be performed immediately. Pericardial effusion due to hypothyroidism will completely resolve with L-thyroxin therapy without pericardiosentesis. In conclusion, since a delayed diagnosis of hypothyroidism is likely and may favor the development of massive pericardial effusion and because of the difficult diagnosis of the hypothyroidism in Down syndrome, periodic follow-up of thyroid function tests are important.
- Published
- 2007
68. Bell's palsy and hepatitis infection.
- Author
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Yildiz B, Yakut A, Bor O, and Yarar C
- Subjects
- Child, Preschool, Female, Humans, Bell Palsy complications, Hepatitis A complications, Hepatitis B complications
- Published
- 2006
- Full Text
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69. Neuhauser syndrome and Peters' anomaly.
- Author
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Yarar C, Yakut A, Yildirim N, Yildiz B, and Basmak H
- Subjects
- Craniofacial Abnormalities complications, Heart Defects, Congenital complications, Humans, Infant, Male, Microcephaly complications, Muscle Hypotonia complications, Syndrome, Abnormalities, Multiple pathology, Cornea abnormalities, Intellectual Disability complications
- Abstract
We report a 9-month-old boy with major features of Neuhauser syndrome, including megalocornea, mental motor retardation, hypotonia, dysmorphic findings (high-arched palate, broad nasal bridge, epicanthus), who also had additional findings such as Peters' anomaly, microcephaly, undescended testicle, patent ductus arteriosus and atrial septal defects. Ophthalmologic examination demonstrated central opacity of the left cornea and lens and iris adhesions extending from the pupillary margin to the borders of the opacity. Keratoplasty operation was done for the right eye owing to central corneal opacity. Neuhauser syndrome should be considered in the differential diagnosis of the patients with megalocornea, hypotonia and mental and motor retardation who have dysmorphic findings. To the best of our knowledge, Peters' anomaly has not been reported in Neuhauser syndrome previously.
- Published
- 2006
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70. Serum leptin levels in children with cerebral palsy: relationship with growth and nutritional status.
- Author
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Yakut A, Dinleyici EC, Idem S, Yarar C, Dogruel N, and Colak O
- Subjects
- Adolescent, Anthropometry, C-Peptide blood, Cerebral Palsy complications, Cerebral Palsy physiopathology, Child, Child Nutrition Disorders etiology, Child Nutrition Disorders physiopathology, Child, Preschool, Energy Metabolism, Female, Growth Disorders etiology, Growth Disorders physiopathology, Human Growth Hormone blood, Humans, Hydrocortisone blood, Male, Cerebral Palsy metabolism, Child Nutrition Disorders metabolism, Growth Disorders metabolism, Leptin blood, Nutritional Status
- Abstract
Aim: Children with Cerebral Palsy (CP) are generally undernourished and growth retarded than normal children. The reasons of malnutrition are not only due to poor nutritional status but also nonnutritional factors including negative neurotrophic effects and indirect factor such as immobility, endocrinological abnormalities or spasticity that energy requirements might be contributing factors. Several studies indicated that leptin which is produced by adipocytes, might regulate energy intake and expenditure. The aim of this study is to determine serum leptin levels in children with CP and to investigate the relationship between nutritional status and anthropometric measurements., Methods: Forty children with CP and 18 healthy controls were included in this study. The weight, height, body mass index (BMI), upper arm length (UAL) and triceps skinfold thickness (TST) was measured in all children. Serum leptin, growth hormone, C-peptide and cortisol levels were studied. Based on TST measurement CP patients were divided as DSF group (decreased subcutaneous fat) and non-DSF group (nondecreased subcutaneous fat)., Results: UAL were shorter and TST measurements were thinner than control group (p<0.05, p<0.01). Group DSF had lower leptin concentrations compared to Group non-DSF and controls (p<0.001, p<0.001). On the other hand non DSF group had higher leptin levels than controls (p<0.05). There was a positive and significant correlation between leptin and anthropometric measurements, especially TST in children with CP. Serum leptin levels were also lower in non-ambulatory children than ambulatory children with CP (p<0.05)., Conclusion: This study has shown that triceps skinfold thickness is better index for the evaluation of nutritional status in children with CP. Serum leptin levels were lower in CP, especially in DSF group. The possible explanation of this finding may not only related with malnutrition, but also immobility related other factors such as bone metabolism and spasticity. We concluded that leptin which regulates energy intake might have a role of nutritional disorders in cerebral palsy. To better understand this relationship further studies are needed.
- Published
- 2006
71. A patient with cystinosis presenting transient features of Bartter syndrome.
- Author
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Yildiz B, Durmuş-Aydoğdu S, Kural N, Bildirici K, Başmak H, and Yarar C
- Subjects
- Bartter Syndrome diagnosis, Diagnosis, Differential, Humans, Infant, Male, Fanconi Syndrome diagnosis
- Abstract
A 16-month-old boy was admitted to the clinic because of vomiting and growth failure. His weight and height measurements were under the fifth percentile. He had fair hair and skin, enlarged wrists and rachitic rosaries. The presence of metabolic alkalosis, hypokalemia, hypochloremia, and high renin and aldosterone levels were suggestive of Bartter syndrome. However, in view of the growth failure, fair hair and skin, proteinuria, polyuria and active rickets, cystinosis was considered. Bone marrow smear examination was normal, despite the existence of suspicious crystals in the cornea. Cystine crystals were seen in the conjunctiva biopsy and increased leukocyte cystine level was measured; therefore, definitive cystinosis diagnosis was made. Renal Fanconi syndrome with metabolic acidosis is prominent in cystinosis; however, in rare instances, if sodium-dependent trans-tubular transport defect is present, patients could have Bartter syndrome findings such as hypochloremic metabolic alkalosis. Our case is a good example demonstrating that metabolic alkalosis should not exclude cystinosis and the other signs and symptoms of the patient should be thoroughly evaluated.
- Published
- 2006
72. [Investigation of TT virus-DNA in multitransfused children and healthy children].
- Author
-
Yarar C, Bör O, Us T, Akgün Y, and Akgün NA
- Subjects
- Adolescent, Alanine Transaminase blood, Aspartate Aminotransferases blood, Case-Control Studies, Child, Child, Preschool, DNA Primers, DNA Virus Infections diagnosis, Hepatitis, Viral, Human epidemiology, Hepatitis, Viral, Human transmission, Humans, Infant, Open Reading Frames, Polymerase Chain Reaction, Sensitivity and Specificity, Torque teno virus genetics, Transfusion Reaction, Turkey epidemiology, Blood Transfusion statistics & numerical data, DNA Virus Infections epidemiology, DNA Virus Infections transmission, DNA, Viral analysis, Hepatitis, Viral, Human virology, Torque teno virus isolation & purification
- Abstract
TT virus (TTV) is a naked, single stranded DNA virus, which has been discovered in the serum of a patient with posttransfusion hepatitis of unknown etiology. TTV is widespread in the population, however, the mode of its transmission is unclear. This study was conducted to search for TTV-DNA positivity rates and its relationship with the clinical outcomes of recipients who underwent multiple blood or blood product transfusion, together with healthy children. TTV-DNA was investigated in 52 multitransfused pediatric patients (age range: 3 mnths - 17.5 yrs, mean age: 9.2 +/- 5.7 years) and 18 healthy children (age range: 1 mnth - 16.5 yrs, mean age: 8.1 +/- 4.9 years), by qualitative in-house semi-nested polymerase chain reaction (PCR) with the primers NG059, NG061 and NG063, generated from ORF1 region of the viral genome. TTV-DNA was found positive in 30.8% of multitransfused, and 16.7% of healthy children. The differences of TTV-DNA positivity rates between the multitransfused and control groups, and ALT values between the patients with positive and negative TTV-DNA, were statistically insignificant (p>0.05). As a result, no relationship was detected between TTV positivity and hepatitis, although there was a statistically insignificant increase of TTV-DNA positivity in multitransfused children. However, since the primers of ORF1 N22 region used in our PCR method did not have enough sensitivity for the detection of TTV-DNA, it has been concluded that more sensitive primers such as UTR primers, should be used for more reliable evaluation of the results.
- Published
- 2005
73. Atypical hemolytic uremic syndrome associated with group A beta hemolytic streptococcus.
- Author
-
Yildiz B, Kural N, and Yarar C
- Subjects
- Child, Female, Humans, Hemolytic-Uremic Syndrome complications, Streptococcal Infections complications, Streptococcus pyogenes
- Published
- 2004
- Full Text
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