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Permissive hypercapnia in extremely low birthweight infants (PHELBI): a randomised controlled multicentre trial.
Thome, Ulrich H; Genzel-Boroviczeny, Orsolya; Bohnhorst, Bettina; Schmid, Manuel; Fuchs, Hans; Rohde, Oliver; Avenarius, Stefan; Topf, Hans-Georg; Zimmermann, Andrea; Faas, Dirk; Timme, Katharina; Kleinlein, Barbara; Buxmann, Horst; Schenk, Wilfried; Segerer, Hugo; Teig, Norbert; Gebauer, Corinna; Hentschel, Roland; Heckmann, Matthias; Schlösser, Rolf; Peters, Jochen; Rossi, Rainer; Rascher, Wolfgang; Böttger, Ralf; Seidenberg, Jürgen; Hansen, Gesine; Zernickel, Maria; Alzen, Gerhard; Dreyhaupt, Jens; Muche, Rainer; Hummler, Helmut D.
Afiliação
  • Thome UH; Division of Neonatology, University Hospital for Children and Adolescents, University of Leipzig, Leipzig, Germany. Electronic address: uhthome@web.de.
  • Genzel-Boroviczeny O; Division of Neonatology, Dr. von Hauner University Children's Hospital, Ludwig Maximilian University of Munich, Munich, Germany.
  • Bohnhorst B; Division of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
  • Schmid M; Division of Neonatology and Pediatric Critical Care, University Hospital for Children and Adolescents, University of Ulm, Ulm, Germany.
  • Fuchs H; Division of Neonatology and Pediatric Critical Care, University Hospital for Children and Adolescents, Albert Ludwigs University Freiburg, Freiburg, Germany.
  • Rohde O; Division of Neonatology and Pediatric Critical Care, Elisabeth Children's Hospital, Klinikum Oldenburg, Medical Campus, Carl von Ossietzky University of Oldenburg, Oldenburg, Germany.
  • Avenarius S; Hospital for General Pediatrics and Neonatology, Otto von Guericke University Magdeburg, Magdeburg, Germany.
  • Topf HG; Division of Neonatology, University Hospital for Children and Adolescents, Friedrich-Alexander University Erlangen, Erlangen, Germany.
  • Zimmermann A; Mutter-Kind-Zentrum, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
  • Faas D; University Hospital for General Pediatrics and Neonatology, Justus Liebig University Giessen, Giessen, Germany.
  • Timme K; Division of Neonatology, Hospital for Children and Adolescents, Vivantes-Hospital Neukölln, Berlin, Berlin, Germany.
  • Kleinlein B; Hospital for Children and Adolescents, Children's Hospital of the Third Order, Munich, Germany.
  • Buxmann H; Division of Neonatology, University Hospital for Children and Adolescents of the J.W. Goethe University Frankfurt am Main, Frankfurt am Main, Germany.
  • Schenk W; Hospital for Children and Adolescents, Central Hospital Augsburg, Augsburg, Germany.
  • Segerer H; St. Hedwig Hospital, University of Regensburg, Regensburg, Germany.
  • Teig N; Department of Neonatology and Pediatric Intensive Care, Katholisches Klinikum, Ruhr University Bochum, Bochum, Germany.
  • Gebauer C; Division of Neonatology, University Hospital for Children and Adolescents, University of Leipzig, Leipzig, Germany.
  • Hentschel R; Division of Neonatology and Pediatric Critical Care, University Hospital for Children and Adolescents, Albert Ludwigs University Freiburg, Freiburg, Germany.
  • Heckmann M; Division of Neonatology and Pediatric Critical Care, University Hospital for Children and Adolescents, Ernst Moritz Arndt University Greifswald, Greifswald, Germany.
  • Schlösser R; Division of Neonatology, University Hospital for Children and Adolescents of the J.W. Goethe University Frankfurt am Main, Frankfurt am Main, Germany.
  • Peters J; Hospital for Children and Adolescents, Children's Hospital of the Third Order, Munich, Germany.
  • Rossi R; Division of Neonatology, Hospital for Children and Adolescents, Vivantes-Hospital Neukölln, Berlin, Berlin, Germany.
  • Rascher W; Division of Neonatology, University Hospital for Children and Adolescents, Friedrich-Alexander University Erlangen, Erlangen, Germany.
  • Böttger R; Hospital for General Pediatrics and Neonatology, Otto von Guericke University Magdeburg, Magdeburg, Germany.
  • Seidenberg J; Division of Neonatology and Pediatric Critical Care, Elisabeth Children's Hospital, Klinikum Oldenburg, Medical Campus, Carl von Ossietzky University of Oldenburg, Oldenburg, Germany.
  • Hansen G; Division of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
  • Zernickel M; Division of Neonatology and Pediatric Critical Care, University Hospital for Children and Adolescents, University of Ulm, Ulm, Germany.
  • Alzen G; Division of Pediatric Radiology, University Hospital of the Justus Liebig University Giessen, Giessen, Germany.
  • Dreyhaupt J; Institute of Epidemiology and Medical Biometry, University of Ulm, Ulm, Germany.
  • Muche R; Institute of Epidemiology and Medical Biometry, University of Ulm, Ulm, Germany.
  • Hummler HD; Division of Neonatology and Pediatric Critical Care, University Hospital for Children and Adolescents, University of Ulm, Ulm, Germany.
Lancet Respir Med ; 3(7): 534-43, 2015 Jul.
Article em En | MEDLINE | ID: mdl-26088180
ABSTRACT

BACKGROUND:

Tolerating higher partial pressure of carbon dioxide (pCO2) in mechanically ventilated, extremely low birthweight infants might reduce ventilator-induced lung injury and bronchopulmonary dysplasia. We aimed to test the hypothesis that higher target ranges for pCO2 decrease the rate of bronchopulmonary dysplasia or death.

METHODS:

In this randomised multicentre trial, we recruited infants from 16 tertiary care perinatal centres in Germany with birthweight between 400 g and 1000 g and gestational age 23-28 weeks plus 6 days, who needed endotracheal intubation and mechanical ventilation within 24 h of birth. Infants were randomly assigned to either a high target or control group. The high target group aimed at pCO2 values of 55-65 mm Hg on postnatal days 1-3, 60-70 mm Hg on days 4-6, and 65-75 mm Hg on days 7-14, and the control target at pCO2 40-50 mmHg on days 1-3, 45-55 mm Hg on days 4-6, and 50-60 mm Hg on days 7-14. The primary outcome was death or moderate to severe bronchopulmonary dysplasia, defined as need for mechanical pressure support or supplemental oxygen at 36 weeks postmenstrual age. Cranial ultrasonograms were assessed centrally by a masked paediatric radiologist. This trial is registered with the ISRCTN registry, number ISRCTN56143743.

RESULTS:

Between March 1, 2008, and July 31, 2012, we recruited 362 patients of whom three dropped out, leaving 179 patients in the high target and 180 in the control group. The trial was stopped after an interim analysis (n=359). The rate of bronchopulmonary dysplasia or death in the high target group (65/179 [36%]) did not differ significantly from the control group (54/180 [30%]; p=0·18). Mortality was 25 (14%) in the high target group and 19 (11%; p=0·32) in the control group, grade 3-4 intraventricular haemorrhage was 26 (15%) and 21 (12%; p=0·30), and the rate of severe retinopathy recorded was 20 (11%) and 26 (14%; p=0·36).

INTERPRETATION:

Targeting a higher pCO2 did not decrease the rate of bronchopulmonary dysplasia or death in ventilated preterm infants. The rates of mortality, intraventricular haemorrhage, and retinopathy did not differ between groups. These results suggest that higher pCO2 targets than in the slightly hypercapnic control group do not confer increased benefits such as lung protection.

FUNDING:

Deutsche Forschungsgemeinschaft.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Displasia Broncopulmonar / Dióxido de Carbono / Recém-Nascido de Peso Extremamente Baixo ao Nascer / Lactente Extremamente Prematuro Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Displasia Broncopulmonar / Dióxido de Carbono / Recém-Nascido de Peso Extremamente Baixo ao Nascer / Lactente Extremamente Prematuro Idioma: En Ano de publicação: 2015 Tipo de documento: Article