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Elective high-frequency oscillatory versus conventional ventilation in preterm infants: a systematic review and meta-analysis of individual patients' data

Identifieur interne : 002452 ( PascalFrancis/Checkpoint ); précédent : 002451; suivant : 002453

Elective high-frequency oscillatory versus conventional ventilation in preterm infants: a systematic review and meta-analysis of individual patients' data

Auteurs : Filip Cools [Belgique] ; Lisa M. Askie [Australie] ; Martin Offringa [Pays-Bas] ; Jeanette M. Asselin [États-Unis] ; Sandra A. Calvert [Royaume-Uni] ; Sherry E. Courtney [États-Unis] ; Carlo Dani [Italie] ; David J. Durand [États-Unis] ; Dale R. Gerstmann [États-Unis] ; David J. Henderson-Smart [Australie] ; Neil Marlow [Royaume-Uni] ; Janet L. Peacock [Royaume-Uni] ; J. Jane Pillow [Australie] ; Roger F. Soll [États-Unis] ; Ulrich H. Thome [Allemagne] ; Patrick Truffert [France] ; Michael D. Schreiber [États-Unis] ; Patrick Van Reempts [Belgique] ; Valentina Vendettuoli [Italie] ; Giovanni Veneto [Italie]

Source :

RBID : Pascal:10-0307348

Descripteurs français

English descriptors

Abstract

Background Population and study design heterogeneity has confounded previous meta-analyses, leading to uncertainty about effectiveness and safety of elective high-frequency oscillatory ventilation (HFOV) in preterm infants. We assessed effectiveness of elective HFOV versus conventional ventilation in this group. Methods We did a systematic review and meta-analysis of individual patients' data from 3229 participants in ten randomised controlled trials, with the primary outcomes of death or bronchopulmonary dysplasia at 36 weeks' postmenstrual age, death or severe adverse neurological event, or any of these outcomes. Findings For infants ventilated with HFOV, the relative risk of death or bronchopulmonary dysplasia at 36 weeks' postmenstrual age was 0.95 (95% CI 0.88-1.03), of death or severe adverse neurological event 1.00 (0.88-1.13), or any of these outcomes 0.98 (0.91-1.05). No subgroup of infants (eg, gestational age, birthweight for gestation, initial lung disease severity, or exposure to antenatal corticosteroids) benefited more or less from HFOV. Ventilator type or ventilation strategy did not change the overall treatment effect. Interpretation HFOV seems equally effective to conventional ventilation in preterm infants. Our results do not support selection of preterm infants for HFOV on the basis of gestational age, birthweight for gestation, initial lung disease severity, or exposure to antenatal corticosteroids.


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Pascal:10-0307348

Le document en format XML

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<name sortKey="Schreiber, Michael D" sort="Schreiber, Michael D" uniqKey="Schreiber M" first="Michael D." last="Schreiber">Michael D. Schreiber</name>
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<name sortKey="Vendettuoli, Valentina" sort="Vendettuoli, Valentina" uniqKey="Vendettuoli V" first="Valentina" last="Vendettuoli">Valentina Vendettuoli</name>
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<name sortKey="Veneto, Giovanni" sort="Veneto, Giovanni" uniqKey="Veneto G" first="Giovanni" last="Veneto">Giovanni Veneto</name>
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<title xml:lang="en" level="a">Elective high-frequency oscillatory versus conventional ventilation in preterm infants: a systematic review and meta-analysis of individual patients' data</title>
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<name sortKey="Courtney, Sherry E" sort="Courtney, Sherry E" uniqKey="Courtney S" first="Sherry E." last="Courtney">Sherry E. Courtney</name>
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<name sortKey="Dani, Carlo" sort="Dani, Carlo" uniqKey="Dani C" first="Carlo" last="Dani">Carlo Dani</name>
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<name sortKey="Durand, David J" sort="Durand, David J" uniqKey="Durand D" first="David J." last="Durand">David J. Durand</name>
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<name sortKey="Gerstmann, Dale R" sort="Gerstmann, Dale R" uniqKey="Gerstmann D" first="Dale R." last="Gerstmann">Dale R. Gerstmann</name>
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<country>États-Unis</country>
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<name sortKey="Henderson Smart, David J" sort="Henderson Smart, David J" uniqKey="Henderson Smart D" first="David J." last="Henderson-Smart">David J. Henderson-Smart</name>
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<s1>Centre for Perinatal Health Services Research, University of sydney</s1>
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</inist:fA14>
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<settlement type="city">Sydney</settlement>
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</placeName>
<orgName type="university">Université de Sydney</orgName>
</affiliation>
</author>
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<name sortKey="Marlow, Neil" sort="Marlow, Neil" uniqKey="Marlow N" first="Neil" last="Marlow">Neil Marlow</name>
<affiliation wicri:level="4">
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<s1>Department of Academic Neonatology, University College London, Elizabeth Garrett Anderson Institute for Women's Health</s1>
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</inist:fA14>
<country>Royaume-Uni</country>
<placeName>
<settlement type="city">Londres</settlement>
<region type="country">Angleterre</region>
<region type="région" nuts="1">Grand Londres</region>
<settlement type="city">Londres</settlement>
</placeName>
<orgName type="university">University College de Londres</orgName>
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<term>Prematurity</term>
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<term>Ventilation haute fréquence</term>
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<term>Prématurité</term>
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<div type="abstract" xml:lang="en">Background Population and study design heterogeneity has confounded previous meta-analyses, leading to uncertainty about effectiveness and safety of elective high-frequency oscillatory ventilation (HFOV) in preterm infants. We assessed effectiveness of elective HFOV versus conventional ventilation in this group. Methods We did a systematic review and meta-analysis of individual patients' data from 3229 participants in ten randomised controlled trials, with the primary outcomes of death or bronchopulmonary dysplasia at 36 weeks' postmenstrual age, death or severe adverse neurological event, or any of these outcomes. Findings For infants ventilated with HFOV, the relative risk of death or bronchopulmonary dysplasia at 36 weeks' postmenstrual age was 0.95 (95% CI 0.88-1.03), of death or severe adverse neurological event 1.00 (0.88-1.13), or any of these outcomes 0.98 (0.91-1.05). No subgroup of infants (eg, gestational age, birthweight for gestation, initial lung disease severity, or exposure to antenatal corticosteroids) benefited more or less from HFOV. Ventilator type or ventilation strategy did not change the overall treatment effect. Interpretation HFOV seems equally effective to conventional ventilation in preterm infants. Our results do not support selection of preterm infants for HFOV on the basis of gestational age, birthweight for gestation, initial lung disease severity, or exposure to antenatal corticosteroids.</div>
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