1.Screening tools for bacteraemia in a selected population of febrile children.
Hayri Levent YILMAZ ; Riza Dincer YILDIZDAS ; Nazan ALPARSLAN ; Kenan OZCAN ; Akgun YAMAN ; Filiz KIBAR
Annals of the Academy of Medicine, Singapore 2008;37(3):192-199
INTRODUCTIONThis is a prospective, observational study. The aims of the study were to determine the rate of bacteraemia in febrile children in Turkey, and to evaluate the usefulness of white blood cell (WBC) count and manual differential counts of peripheral blood smears and a RISK score in predicting bacteraemia among these children.
MATERIALS AND METHODSA total of 377 febrile children aged 3 to 36 months were included in the study. Complete blood cell (CBC) count, manual differential counts and blood cultures were performed in all patients. The main outcome measures used to evaluate the usefulness of the RISK score were sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), odds ratio (OR), posterior probability, areas under receiver operator characteristic curves (AUC) and miss-to-diagnosis ratio (MDR).
RESULTSAmong the patients, 4.4% had bacteraemia and the predominant pathogen was Streptococcus pneumoniae. The Yale Observation Scale scores, percentages of neutrophil and bands, band-neutrophil ratio, absolute neutrophil count and absolute band count were found to be statistically significant predictors of bacteraemia. When the RISK score was 2 or higher, sensitivity was 93.8%, false positive ratio 35.8%, PPV 10.6%, NPV 99.5%, OR 26.2 (95% CI, 3.4 to 200.8), MDR 0.066 and posterior probability value 10%.
CONCLUSIONSWe conclude that determination of the RISK score will significantly decrease unnecessary blood culture sampling, antibiotherapy and hospitalisation among febrile patients aged 3 to 36 months without an identifiable focus of infection.
Bacteremia ; complications ; diagnosis ; drug therapy ; microbiology ; Bacteria ; isolation & purification ; Child ; Child, Preschool ; Fever ; complications ; Humans ; Infant ; Leukocyte Count ; Neutrophils ; Predictive Value of Tests ; ROC Curve ; Risk Assessment ; Sensitivity and Specificity
2.Possible association of the 5-HTTLPR serotonin transporter promoter gene polymorphism with premature ejaculation in a Turkish population.
Emin OZBEK ; Ali I TASCI ; Volkan TUGCU ; Yusuf O ILBEY ; Abdulmuttalip SIMSEK ; Levent OZCAN ; Emre C POLAT ; Vedat KOKSAL
Asian Journal of Andrology 2009;11(3):351-355
We evaluated the genotypes of the serotonin transporter gene (5-HTT) in patients with premature ejaculation (PE) to determine the role of genetic factors in the etiopathogenesis of PE and possibly to identify the patient subgroups. A total of 70 PE patients and 70 controls were included in this study. All men were heterosexual, had no other disorders and were either married or in a stable relationship. PE was defined as ejaculation that occurred within 1 min of vaginal intromission. Genomic DNA from patients and controls was analyzed using polymerase chain reaction, and allelic variations of the promoter region of the serotonin transporter gene (5-HTTLPR) were determined. The 5-HTTLPR (serotonin transporter promoter gene) genotypes in PE patients vs. controls were distributed as follows: L/L 16% vs. 17%, L/S 30% vs. 53% and S/S 54% vs. 28%. We examined the haplotype analysis for three polymorphisms of the 5-HTTLPR gene: LL, LS and SS. The appropriateness of the allele frequencies in the 5-HTTLPR gene was analyzed by the Hardy-Weinberg equilibrium using the chi2-test. The short (S) allele of the 5-HTTLPR gene was significantly more frequent in PE patients than in controls (P<0.05). We suggest that the 5-HTTLPR gene plays a role in the pathophysiology of all primary PE cases. Further studies are needed to evaluate the relationship between 5-HTTLPR gene polymorphism and patient subgroup (such as primary and secondary PE) responses to selective serotonin reuptake inhibitors as well as ethnic differences.
Adult
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Ejaculation
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Genotype
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Humans
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Male
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Middle Aged
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Polymorphism, Genetic
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Serotonin Plasma Membrane Transport Proteins
;
genetics
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Sexual Dysfunction, Physiological
;
genetics
;
physiopathology
;
Turkey
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Young Adult