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    <title>Versteegh, F.G.</title>
    <link>http://repub.eur.nl/res/aut/15449/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Clinical impact of RT-PCR for pediatric acute respiratory infections: A controlled clinical trial (Article)</title>
      <link>http://repub.eur.nl/res/pub/33224/</link>
      <pubDate>2011-11-01T00:00:00Z</pubDate>
      <description>OBJECTIVE: Real-time polymerase chain reaction (RT-PCR) testing is a quick sensitive method for detecting respiratory pathogens. We evaluated the diagnostic yield of RT-PCR assays and measured the effect of rapid reporting on patient care. METHODS: In a controlled clinical trial, nasal wash specimens were obtained from patients &lt;12 years of age with suspected acute respiratory infections. In addition to the standard hospital protocol, RT-PCR assays for 17 pathogens were performed. The RT-PCR results were communicated to the clinicians within 12 to 36 hours in the intervention group and after 4 weeks in the control group. RESULTS: A total of 583 patients were included (mean age: 8.1 months [range: 0 -107.5 months]): 298 in the intervention group and 285 in the control group. Eighty-two percent of nasal wash specimens tested positive for ≥1 pathogen. Respiratory syncytial virus was the most frequently encountered (55%) pathogen. There were no significant differences between the groups with respect to hospital admissions (intervention group: 223 admissions; control group: 211 admissions; P = .825), length of hospital stay (mean ± SD: 3.68 ± 2.68 days [intervention group] and 3.96 ± 2.67 days [control group]; P = .178), or duration of antibiotic use (mean ± SD: 6.52 ± 2.15 days [intervention group] and 6.97 ± 2.86 days [control group]; P = .490), when antibiotic treatment had been initiated. CONCLUSIONS: RT-PCR testing has a high yield of viral diagnoses, but rapid communication does not lead to decreases in hospital admissions, shorter hospital stays, or less antibiotic use for children with acute respiratory infections. Copyright </description>
    </item> <item>
      <title>Growth charts for children with Ellis-van Creveld syndrome (Article)</title>
      <link>http://repub.eur.nl/res/pub/31724/</link>
      <pubDate>2011-02-01T00:00:00Z</pubDate>
      <description>Ellis-van Creveld (EvC) syndrome is a congenital malformation syndrome with marked growth retardation. In this study, specific growth charts for EvC patients were derived to allow better follow-up of growth and earlier detection of growth patterns unusual for EvC. With the use of 235 observations of 101 EvC patients (49 males, 52 females), growth charts for males and females from 0 to 20 years of age were derived. Longitudinal and cross-sectional data were collected from an earlier review of growth data in EvC, a database of EvC patients, and from recent literature. To model the growth charts, the GAMLSS package for the R statistical program was used. Height of EvC patients was compared to healthy children using Dutch growth charts. Data are presented both on a scale for age and on a scale for the square root of age. Compared to healthy Dutch children, mean height standard deviation score values for male and female EvC patients were -3.1 and -3.0, respectively. The present growth charts should be useful in the follow-up of EvC patients. Most importantly, early detection of growth hormone deficiency, known to occur in EvC, will be facilitated. </description>
    </item> <item>
      <title>Efficacy of fluticasone propionate on lung function and symptoms in wheezy infants. (Article)</title>
      <link>http://repub.eur.nl/res/pub/13567/</link>
      <pubDate>2005-02-15T00:00:00Z</pubDate>
      <description>The role of inhaled corticosteroids in the treatment of recurrent or
      persistent wheeze in infancy remains unclear. We evaluated the effect of 3
      months of treatment with inhaled fluticasone propionate, 200 microg daily
      (FP200), on lung function and symptom scores in wheezy infants. Moreover,
      we evaluated whether infants with atopy and/or eczema respond better to
      FP200 as compared with non-atopic infants. Forced expiratory flow
      (Vmax(FRC)) was measured at baseline and after treatment. Sixty-five
      infants were randomized to receive FP200 or placebo, and 62 infants (mean
      age, 11.3 months) completed the study. Mean Vmax(FRC), expressed as a Z
      score, was significantly below normal at baseline and after treatment in
      both groups. The change from baseline of Vmax(FRC) was not different
      between the two treatment arms. After 6 weeks of treatment, and not after
      13 weeks, the FP200 group had a significantly higher percentage of
      symptom-free days and a significant reduction in mean daily cough score
      compared with placebo. Separate analysis of treatment effect in infants
      with atopy or eczema showed no effect modification. We conclude that in
      wheezy infants, after 3 months of treatment with fluticasone, there was no
      improvement in lung function and no reduction in respiratory symptoms
      compared with placebo.</description>
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