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    <title>Kerrebijn, K.F.</title>
    <link>http://repub.eur.nl/res/aut/4548/</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>Inhaled corticosteroids and growth of airway function in asthmatic children (Article)</title>
      <link>http://repub.eur.nl/res/pub/10351/</link>
      <pubDate>2004-01-01T00:00:00Z</pubDate>
      <description>Airway inflammation and remodelling play an important role in the
      pathophysiology of asthma. Remodelling may affect childhood lung function,
      and this process may be reversed by anti-inflammatory treatment. The
      current study assessed longitudinally whether asthma affects growth of
      airway function relative to airspaces, and if so whether this is redressed
      by inhaled corticosteroids (ICS). Every 4 months for up to 3 yrs, lung
      function was assessed in 54 asthmatic children (initial age 7-16 yrs), who
      inhaled 0.2 mg salbutamol t.i.d. and 0.2 mg budesonide t.i.d.
      (beta2-agonist (BA)+ICS), or placebo (PL) t.i.d. (BA+PL) in a randomised,
      double-blind design. Measurements were carried out before and after
      maximal bronchodilation. Airway growth was assessed from the change of
      forced expiratory volume in one second and of maximal expiratory flows (at
      60% and 40% of total lung capacity (TLC) remaining in the lung) relative
      to TLC, as measures of more central, intermediate and more peripheral
      airways. Growth patterns were compared with the longitudinal findings in
      376 healthy children. Airway patency after maximal bronchodilation in
      patients on BA+PL remained reduced compared to healthy subjects, whereas
      in patients on BA+ICS a marked improvement was observed to subnormal. No
      differences between patients and controls could be demonstrated for growth
      patterns of central and intermediate airway function. Compliance with
BA+ICS was 75% of the prescribed dose, resulting in significant, sustained
      improvement of symptoms and postbronchodilator calibre of central and
      intermediate airways to subnormal within 2 months, but postbronchodilator
      small airway patency remained reduced, though improved compared to
      patients on BA+PL. Anti-inflammatory treatment of asthmatic children is
      associated with normal functional development of central and intermediate
      airways. The persistently reduced postbronchodilator patency of peripheral
      airways may reflect remodelling, or insufficient anti-inflammatory
      treatment.</description>
    </item> <item>
      <title>Addition of salmeterol versus doubling the dose of beclomethasone in children with asthma. The Dutch Asthma Study Group (Article)</title>
      <link>http://repub.eur.nl/res/pub/8853/</link>
      <pubDate>1998-01-01T00:00:00Z</pubDate>
      <description>Studies in adults revealed that addition of salmeterol to a moderate dose
          of inhaled corticosteroid resulted in better symptom control and higher
          PEF compared with doubling the dose of inhaled corticosteroid. The aim of
          this three group study was to compare the effects of a moderate dose of
          beclomethasone, the same dose of beclomethasone with salmeterol, and a
          doubling dose of beclomethasone on lung function and symptoms in children
          with moderate asthma. A total of 177 children already treated with inhaled
          corticosteroids, were randomized in a double-blind parallel study either
          to salmeterol 50 microg twice daily (BDP400+salm), beclomethasone 200
          microg twice daily (BDP800), or placebo (BDP400) in addition to
          beclomethasone 200 microg twice daily. No significant differences between
          groups were found in FEV1, PD20 methacholine, symptom scores, and
          exacerbation rates after 1 yr. Salmeterol resulted in slightly better PEF
          in the first months of treatment. FEV1, and PD20 methacholine
          significantly improved in all groups. After 1 yr mean changes in FEV1,
          percent predicted were 4.3% (95% CI 1.3; 7.2), 5.8% (95% CI 2.9; 8.7), and
          4.3% (95% CI 2.1; 6.5) for BDP400+salm, BDP800, and BDP400, respectively.
          Changes in airway responsiveness were 0.60 (95% CI 0.05; 1.14), 1.30 (95%
          CI 0.73; 1. 87), and 0.80 (95% CI 0.33; 1.27) doubling doses. Growth was
          significantly slower in the BDP800 group. We conclude that no additional
          benefit was found of adding either salmeterol or more beclomethasone to a
          daily dose of 400 microg beclomethasone in this group of children with
          excellent compliance of medication.</description>
    </item> <item>
      <title>One year treatment with salmeterol compared with beclomethasone in children with asthma. The Dutch Paediatric Asthma Study Group (Article)</title>
      <link>http://repub.eur.nl/res/pub/8720/</link>
      <pubDate>1997-01-01T00:00:00Z</pubDate>
      <description>The aim of this study was to compare the effects of salmeterol and
          beclomethasone on lung function and symptoms in children with mild to
          moderate asthma. Sixty-seven children not treated with inhaled
          corticosteroids were randomized in a double-blind parallel study either to
          salmeterol 50 micrograms b.i.d. or beclomethasone 200 micrograms b.i.d.
          After one year, FEV1 significantly increased in the beclomethasone group,
          whereas in the salmeterol group there was a small reduction. Differences
          between groups were 14.2% predicted (p &lt; 0.0001) and 7.0% predicted (p =
          0.007) for pre- and postbronchodilator FEV1 values, respectively. PD20
          methacholine decreased by 0.73 DD (p = 0.05) in the salmeterol group and
          increased by 2.02 DD (p &lt; 0.0001) in the beclomethasone group. Morning and
          evening PEF and symptom scores improved in both groups, although more in
          the beclomethasone group. Asthma exacerbations, for which prednisolone was
          needed, were more frequent in the salmeterol group (17 versus two), as
          were the number of withdrawals due to exacerbations (six versus one).
          However, growth was significantly slower in the beclomethasone group
          (-0.28 SDS) compared with that in the salmeterol group (-0.03 SDS) (p =
          0.001). We conclude that treatment with a moderate dose of beclomethasone
          is superior to salmeterol in children with mild to moderate asthma and
          recommend that salmeterol should not be used as monotherapy.</description>
    </item> <item>
      <title>Naar een Erasmus Medisch Centrum: de tijd dringt (Farewell Lecture)</title>
      <link>http://repub.eur.nl/res/pub/7463/</link>
      <pubDate>1994-03-24T00:00:00Z</pubDate>
      <description></description>
    </item>
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