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1.
Pediatr Obes ; 13(5): 301-306, 2018 05.
Article in English | MEDLINE | ID: mdl-28371539

ABSTRACT

BACKGROUND: There are no data regarding the Internet addiction (IA) rates and patterns in youth with obesity. OBJECTIVE: This study aimed to explore the prevalence and patterns of IA in children and adolescents with obesity. The relationship between IA and body mass index (BMI) was also investigated. METHODS: Study includes 437 children and adolescents with age ranging from 8 to 17 years: 268 with obesity and 169 with healthy controls. The Internet addiction scale (IAS) form was administered to all participants. The obesity group also completed a personal information form including Internet usage habits and goals. Linear regression analysis was utilized to assess the contributions of Internet use habits and goals to BMI in the obesity group and IAS scores to BMI in both groups. RESULTS: A total of 24.6% of the obese children and adolescents were diagnosed with IA according to IAS, while 11.2% of healthy peers had IA (p < 0.05). The mean IAS scores for the obesity group and the control group were 53.71 ± 25.04 and 43.42 ± 17.36, respectively (p < 0.05). The IAS scores (t = 3.105) and spending time more than 21 h week-1 on the Internet (t = 3.262) were significantly associated with increased BMI in the obesity group (p < 0.05). Other Internet habits and goals were not associated with BMI (p > 0.05). The IAS scores (t = 8.719) were also found to be associated with increased BMI in the control group (p < 0.05). CONCLUSIONS: The present study suggests that obese children and adolescents were found to have higher IA rates than their healthy peers, and the results indicate an association between IA and BMI.


Subject(s)
Adolescent Behavior , Behavior, Addictive/epidemiology , Internet/statistics & numerical data , Pediatric Obesity/etiology , Adolescent , Behavior, Addictive/complications , Body Mass Index , Child , Cross-Sectional Studies , Female , Humans , Male , Prevalence
2.
Indian J Med Microbiol ; 23(4): 259-61, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16327124

ABSTRACT

This report presents a case of brain abscess due to Haemophilus aphrophilus in a six-year old boy. He was admitted to our hospital suffering from left-sided weakness. The initial radiological diagnosis was an intracranial abscess. Purulent material was obtained by puncturing the subcortical lesion and the sample was cultured on conventional media. H. aphrophilus was isolated in pure culture, identified according to conventional methods and confirmed by Becton Dickinson Laboratory (BBL) crystal system. After surgical drainage and eight weeks of antibiotic therapy, the neurological findings improved. The presented case is an example of H. aphriphilus causing brain abscess in the first decade without cardiac predisposition and with good outcome.


Subject(s)
Brain Abscess/microbiology , Haemophilus Infections/diagnosis , Haemophilus/isolation & purification , Meningitis, Haemophilus/diagnosis , Brain Abscess/diagnosis , Child , Humans , Male , Meningitis, Haemophilus/microbiology , Tomography, X-Ray Computed
4.
Pediatr Pulmonol ; 30(5): 429-33, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11064435

ABSTRACT

Morgagni hernia (MH) is the least common type of congenital diaphragmatic hernias. Although its course is often asymptomatic, it may be associated with various respiratory and gastrointestinal symptoms. We describe 7 children with MH during a 5-year period in three pediatric centers in Turkey. All children had acute or chronic respiratory symptoms; cough was the most frequent. The diagnosis was made by posterior-anterior (PA) and lateral chest X-rays. The PA chest X-rays showed a homogenous mass in 2 and a gas-filled cystic image in 3 children in the right cardiophrenic angle. A retrocardiac homogeneous density in one child, and bilateral consolidation in lower lung areas in another child were also seen. All lateral chest X-rays showed gas-filled bowel loops above the diaphragm. The diagnosis was confirmed by barium-contrast radiograph. Four patients had five additional anomalies, i.e., ventricular septal defect, right inguinal hernia, congenital hip dislocation, pectus carinatum, and obstruction of the uretero-pelvic junction. All of the hernias were repaired by an abdominal approach. There were no complications or recurrences during follow-up. In conclusion, MH should be considered in the differential diagnosis of cases of long-standing respiratory symptoms and/or when an unexplained radiological image, especially on the right cardiophrenic area, is present.


Subject(s)
Hernia, Diaphragmatic/diagnosis , Hernias, Diaphragmatic, Congenital , Respiration Disorders/etiology , Barium Compounds , Child , Child, Preschool , Cough/etiology , Diagnosis, Differential , Female , Hernia, Diaphragmatic/complications , Hernia, Diaphragmatic/surgery , Humans , Infant , Lung/diagnostic imaging , Male , Radiography , Turkey
5.
Pediatr Pulmonol ; 30(5): 434-6, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11064436
7.
Pediatr Nephrol ; 15(3-4): 266-70, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11149123

ABSTRACT

Children with Bartter syndrome have lower than normal vascular reactivity with normotension in spite of biochemical and hormonal abnormalities which are typical of hypertension. Nitric oxide (NO) is a potent endogenous vasodilator, and plays an important role in the control of vascular tone. Adrenomedullin (AM) is a novel hypotensive peptide originally isolated from human pheochromocytoma. The possible role of NO and AM in maintaining this reduced vascular reactivity was examined by studying plasma and urinary nitrite, a stable metabolite of NO, and AM levels in ten children with Bartter syndrome, ten healthy controls, and five children with hypokalemia of causes other than Bartter syndrome (pseudo-Bartter). Urinary excretion of nitrite (mumol/mg urinary creatinine) was 8.9 +/- 1.2 in children with Bartter syndrome, 4.7 +/- 0.9 in healthy controls, and 2.9 +/- 0.8 in pseudo-Bartter (P < 0.05). Plasma nitrite levels (mumol/l) were 101.9 +/- 23.4, 59.9 +/- 14.7, and 65.0 +/- 29.7, respectively (P < 0.05), in the three groups. Urinary excretion of AM (pmol/mg urinary creatinine) was 187 +/- 40, 65 +/- 10, and 160 +/- 50, respectively (P < 0.05), in the three groups. Plasma AM levels were 47.4 +/- 1.8, 39.9 +/- 5.9, and 42.4 +/- 3.9, respectively (P > 0.05), in the three groups. The same parameters were repeated in the two groups of controls and in the Bartter patients in the 6th month of therapy. Urinary nitrite and AM levels were still higher in the Bartter patients than in the other groups. We conclude that in Bartter syndrome the increased NO production may be responsible for the reduced vascular response of the disease. Initially, increased levels of AM in Bartter syndrome and pseudo-Bartter may be a compensatory response to acute hypokalemia; however, continuation of a high level of urinary excretion of AM in children with Bartter syndrome may suggest also the possible role of AM in the reduced vascular response of the disease.


Subject(s)
Bartter Syndrome/metabolism , Nitrites/metabolism , Peptides/metabolism , Adolescent , Adrenomedullin , Bartter Syndrome/blood , Bartter Syndrome/urine , Child , Child, Preschool , Female , Humans , Hypokalemia/blood , Hypokalemia/metabolism , Hypokalemia/urine , Infant , Male , Nitrites/blood , Nitrites/urine , Peptides/blood , Peptides/urine , Potassium/blood
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