Whole pulmonary assessment 1 year after paediatric acute respiratory distress syndrome: prospective multicentre study.

ARDS Child Computed tomography Long-term outcomes Pulmonary function

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
20 Aug 2022
Historique:
received: 22 03 2022
accepted: 03 08 2022
entrez: 20 8 2022
pubmed: 21 8 2022
medline: 21 8 2022
Statut: epublish

Résumé

Long-term pulmonary sequelae, including 1-year thoracic computed tomography (CT) sequelae of paediatric acute respiratory distress syndrome (ARDS) remain unknown. The purpose of the study was to determine pulmonary abnormalities in child survivors of pulmonary (p-ARDS) and extra-pulmonary ARDS (ep-ARDS) 1 year after paediatric intensive care unit discharge (PICUD). Prospective multicentre study in four paediatric academic centres between 2005 and 2014. Patients with ARDS were assessed 1 year after PICUD with respiratory symptom questionnaire, thoracic CT and pulmonary function tests (PFT). 39 patients (31 p-ARDS) aged 1.1-16.2 years were assessed. Respiratory symptoms at rest or exercise and/or respiratory maintenance treatment were reported in 23 (74%) of children with p-ARDS but in 1 (13%) of those with ep-ARDS. Thoracic CT abnormalities were observed in 18 (60%) of children with p-ARDS and 4 (50%) of those with ep-ARDS. Diffuse and more important CT abnormalities, such as ground glass opacities or mosaic perfusion patterns, were observed in 5 (13%) of children, all with p-ARDS. PFT abnormalities were observed in 30 (86%) of patients: lung hyperinflation and/or obstructive pattern in 12 (34%) children, restrictive abnormalities in 6 (50%), mild decrease in diffusing capacity in 2 (38%) and 6-min walking distance decrease in 11 (73%). Important PFT abnormalities were observed in 7 (20%) children, all with p-ARDS. Increasing driving pressure (max plateau pressure-max positive end-expiratory pressure) was correlated with increasing CT-scan abnormalities and increasing functional residual capacity (more hyperinflation) (p < 0.005). Children surviving ARDS requiring mechanical ventilation present frequent respiratory symptoms, significant CT-scan and PFT abnormalities 1 year after PICUD. This highlights the need for a systematic pulmonary assessment of these children. Trial registration The study was registered on Clinical Trials.gov PRS (ID NCT01435889).

Sections du résumé

BACKGROUND BACKGROUND
Long-term pulmonary sequelae, including 1-year thoracic computed tomography (CT) sequelae of paediatric acute respiratory distress syndrome (ARDS) remain unknown. The purpose of the study was to determine pulmonary abnormalities in child survivors of pulmonary (p-ARDS) and extra-pulmonary ARDS (ep-ARDS) 1 year after paediatric intensive care unit discharge (PICUD).
METHODS METHODS
Prospective multicentre study in four paediatric academic centres between 2005 and 2014. Patients with ARDS were assessed 1 year after PICUD with respiratory symptom questionnaire, thoracic CT and pulmonary function tests (PFT).
RESULTS RESULTS
39 patients (31 p-ARDS) aged 1.1-16.2 years were assessed. Respiratory symptoms at rest or exercise and/or respiratory maintenance treatment were reported in 23 (74%) of children with p-ARDS but in 1 (13%) of those with ep-ARDS. Thoracic CT abnormalities were observed in 18 (60%) of children with p-ARDS and 4 (50%) of those with ep-ARDS. Diffuse and more important CT abnormalities, such as ground glass opacities or mosaic perfusion patterns, were observed in 5 (13%) of children, all with p-ARDS. PFT abnormalities were observed in 30 (86%) of patients: lung hyperinflation and/or obstructive pattern in 12 (34%) children, restrictive abnormalities in 6 (50%), mild decrease in diffusing capacity in 2 (38%) and 6-min walking distance decrease in 11 (73%). Important PFT abnormalities were observed in 7 (20%) children, all with p-ARDS. Increasing driving pressure (max plateau pressure-max positive end-expiratory pressure) was correlated with increasing CT-scan abnormalities and increasing functional residual capacity (more hyperinflation) (p < 0.005).
CONCLUSIONS CONCLUSIONS
Children surviving ARDS requiring mechanical ventilation present frequent respiratory symptoms, significant CT-scan and PFT abnormalities 1 year after PICUD. This highlights the need for a systematic pulmonary assessment of these children. Trial registration The study was registered on Clinical Trials.gov PRS (ID NCT01435889).

Identifiants

pubmed: 35986824
doi: 10.1186/s13613-022-01050-4
pii: 10.1186/s13613-022-01050-4
pmc: PMC9392829
doi:

Banques de données

ClinicalTrials.gov
['NCT01435889']

Types de publication

Journal Article

Langues

eng

Pagination

79

Subventions

Organisme : The study was supported, in part, by grant from the French Ministry of Health (Programme Hospitalier de Recherche Clinique Régional)
ID : 2005/1906

Informations de copyright

© 2022. The Author(s).

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pubmed: 11887027

Auteurs

Véronique Nève (V)

Pulmonary Function Testing Department, CHU Lille, 2 avenue Oscar Lambret, 59000, Lille, France. veronique.neve@chru-lille.fr.
Univ. Lille, ULR 4483, IMPECS, 59000, Lille, France. veronique.neve@chru-lille.fr.
Institut Pasteur de Lille, 59000, Lille, France. veronique.neve@chru-lille.fr.

Ahmed Sadik (A)

Réanimation pédiatrique, CHU Lille, 59000, Lille, France.

Laurent Petyt (L)

Imaging Department, University Hospital, 59000, Lille, France.

Stéphane Dauger (S)

Pediatric Intensive Care Unit, Assistance Publique, Hôpitaux de Paris, Robert Debré University Hospital, Université de Paris, Paris, France.

Ahmed Kheniche (A)

Imaging Department, Assistance Publique, Hôpitaux de Paris, Robert Debré University Hospital, Paris, France.

André Denjean (A)

Pulmonary Function Testing Department, Assistance Publique, Hôpitaux de Paris, Robert Debré University Hospital, Université de Paris, Paris, France.

Pierre-Louis Léger (PL)

Pediatric and Neonatal Intensive Care Unit, Assistance Publique, Hôpitaux de Paris, Armand-Trousseau Hospital, Sorbonne University, Paris, France.

François Chalard (F)

Imaging Department, Assistance Publique, Hôpitaux de Paris, Armand-Trousseau Hospital, Sorbonne University, Paris, France.

Michèle Boulé (M)

Pulmonary Function Testing Department, Assistance Publique, Hôpitaux de Paris, Armand- Trousseau University Hospital, Sorbonne University, Paris, France.

Etienne Javouhey (E)

Pediatric Intensive Care Unit, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Université Lyon1, Lyon, France.

Philippe Reix (P)

Pediatric Pulmonology Department, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Université Lyon1, Lyon, France.

Isabelle Canterino (I)

Imaging Department, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Université Lyon1, Lyon, France.

Valérie Deken (V)

Service de Biostatistique et Data Management, CHU Lille, 59000, Lille, France.
Évaluation des technologies de santé et des pratiques médicales, Univ. Lille, ULR 2694, METRICS, 59000, Lille, France.

Régis Matran (R)

Pulmonary Function Testing Department, CHU Lille, 2 avenue Oscar Lambret, 59000, Lille, France.
Univ. Lille, ULR 4483, IMPECS, 59000, Lille, France.
Institut Pasteur de Lille, 59000, Lille, France.

Stéphane Leteurtre (S)

Réanimation pédiatrique, CHU Lille, 59000, Lille, France.
Évaluation des technologies de santé et des pratiques médicales, Univ. Lille, ULR 2694, METRICS, 59000, Lille, France.

Francis Leclerc (F)

Réanimation pédiatrique, CHU Lille, 59000, Lille, France.
Évaluation des technologies de santé et des pratiques médicales, Univ. Lille, ULR 2694, METRICS, 59000, Lille, France.

Classifications MeSH