<?xml version="1.0" encoding="UTF-8"?><mods xmlns="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" version="3.2" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd"><titleInfo><title>Aerosol delivery from spacers in wheezy infants: a daily life study</title></titleInfo><name><namePart>Janssens, H.M. (Hettie)</namePart></name><name><namePart>Heijnen, E.M.</namePart></name><name><namePart>Jong, de V.M.</namePart></name><name><namePart>Hop, W.C.J. (Wim)</namePart></name><name><namePart>Holland, W.P. (Wim)</namePart></name><name><namePart>Jongste, de J.C. (Johan)</namePart></name><name><namePart>Tiddens, H.A.W.M. (Harm)</namePart></name><subject lang="nl"><topic>Comparative Study</topic><topic>Humans</topic><topic>Research Support, Non-U.S. Gov&apos;t</topic><topic>Child, Preschool</topic><topic>Patient Compliance</topic><topic>Infant</topic><topic>Equipment Design</topic><topic>Bronchodilator Agents/*administration &amp; dosage/therapeutic use</topic><topic>Budesonide/*administration &amp; dosage/therapeutic use</topic><topic>Cross-Over Studies</topic><topic>Coated Materials, Biocompatible</topic><topic>Anti-Asthmatic Agents/*administration &amp; dosage/therapeutic use</topic><topic>Aerosols</topic><topic>Androstadienes/*administration &amp; dosage/therapeutic use</topic><topic>Detergents</topic><topic>Electricity</topic><topic>Respiratory Sounds/*drug effects</topic></subject><accessCondition></accessCondition><location><url>http://hdl.handle.net/1765/9563</url></location><language><languageTerm type="text">en</languageTerm></language><genre authority="local">journalArticle</genre><identifier type="issn">0903-1936</identifier><abstract>The aims of this study were to assess and compare dose delivery and dose
          variability of pressurized metered dose inhalers (pMDI)/spacers in wheezy
          infants in daily life and to investigate factors influencing aerosol
          delivery. In an open randomized crossover study in 25 wheezy infants aged
          5-26 months, a metal spacer (Nebuchamber), a detergent coated (DC) and a
          non-detergent coated (nonDC) plastic spacer (Babyhaler) were tested at
          home for 7 days each. Budesonide (200 microg b.i.d) was administered via a
          Nebuchamber or fluticasone (125 microg b.i.d) via a Babyhaler. Aerosol was
          trapped in filters, positioned between the spacer and face mask.
          Cooperation was scored on diary cards. Electrostatic charge (ESC) of the
          spacers was measured. Evaluations of the administration technique were
          made from video recordings. Median (range) dose delivery of the filters
          expressed as per cent (%) of nominal dose, was 34% (3-59), 23% (1-49), and
          41% (12-55) for the Nebuchamber, nonDC-Babyhaler, and DC-Babyhaler
          respectively. Considerable dose variability was found, median (range)
          within-subject dose variability, expressed as coefficient of variation,
          for the Nebuchamber (49% (15-249)) was significantly higher when compared
          with both nonDC- (36% (12-325)) and DC-Babyhalers (27% (10-122)), for
          which dose variabilities were similar. Detergent coating was effective to
          reduce electrostatic charge, and to increase dose delivery, but had no
          effect on dose variability. Bad cooperation was an important cause for
          high dose variability for all spacers (r=0.5-0.6, p&lt;0.02). Many mistakes
          were made during the administration procedure.</abstract><relatedItem type="host"><titleInfo><title>The European Respiratory Journal</title></titleInfo><originInfo><dateIssued>2000-01-01</dateIssued>
</originInfo><identifier type="issn">0903-1936</identifier>
<identifier type="doi">urn:NBN:nl:ui:15-1765/9563</identifier>
<part><extent unit="page"></extent></part></relatedItem></mods>
