Diffuse alveolar haemorrhage in children: an international multicentre study.


Journal

ERJ open research
ISSN: 2312-0541
Titre abrégé: ERJ Open Res
Pays: England
ID NLM: 101671641

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 22 12 2022
accepted: 05 02 2023
medline: 27 4 2023
pubmed: 27 4 2023
entrez: 27 4 2023
Statut: epublish

Résumé

Paediatric diffuse alveolar haemorrhage (DAH) is a rare heterogeneous condition with limited knowledge on clinical presentation, treatment and outcome. A retrospective, descriptive multicentre follow-up study initiated from the European network for translational research in children's and adult interstitial lung disease (Cost Action CA16125) and chILD-EU CRC (the European Research Collaboration for Children's Interstitial Lung Disease). Inclusion criteria were DAH of any cause diagnosed before the age of 18 years. Data of 124 patients from 26 centres (15 counties) were submitted, of whom 117 patients fulfilled the inclusion criteria. Diagnoses were idiopathic pulmonary haemosiderosis (n=35), DAH associated with autoimmune features (n=20), systemic and collagen disorders (n=18), immuno-allergic conditions (n=10), other childhood interstitial lung diseases (chILD) (n=5), autoinflammatory diseases (n=3), DAH secondary to other conditions (n=21) and nonspecified DAH (n=5). Median (IQR) age at onset was 5 (2.0-12.9) years. Most frequent clinical presentations were anaemia (87%), haemoptysis (42%), dyspnoea (35%) and cough (32%). Respiratory symptoms were absent in 23%. The most frequent medical treatment was systemic corticosteroids (93%), hydroxychloroquine (35%) and azathioprine (27%). Overall mortality was 13%. Long-term data demonstrated persistent abnormal radiology and a limited improvement in lung function. Paediatric DAH is highly heterogeneous regarding underlying causes and clinical presentation. The high mortality rate and number of patients with ongoing treatment years after onset of disease underline that DAH is a severe and often chronic condition. This large international study paves the way for further prospective clinical trials that will in the long term allow evidence-based treatment and follow-up recommendations to be determined.

Sections du résumé

Background UNASSIGNED
Paediatric diffuse alveolar haemorrhage (DAH) is a rare heterogeneous condition with limited knowledge on clinical presentation, treatment and outcome.
Methods UNASSIGNED
A retrospective, descriptive multicentre follow-up study initiated from the European network for translational research in children's and adult interstitial lung disease (Cost Action CA16125) and chILD-EU CRC (the European Research Collaboration for Children's Interstitial Lung Disease). Inclusion criteria were DAH of any cause diagnosed before the age of 18 years.
Results UNASSIGNED
Data of 124 patients from 26 centres (15 counties) were submitted, of whom 117 patients fulfilled the inclusion criteria. Diagnoses were idiopathic pulmonary haemosiderosis (n=35), DAH associated with autoimmune features (n=20), systemic and collagen disorders (n=18), immuno-allergic conditions (n=10), other childhood interstitial lung diseases (chILD) (n=5), autoinflammatory diseases (n=3), DAH secondary to other conditions (n=21) and nonspecified DAH (n=5). Median (IQR) age at onset was 5 (2.0-12.9) years. Most frequent clinical presentations were anaemia (87%), haemoptysis (42%), dyspnoea (35%) and cough (32%). Respiratory symptoms were absent in 23%. The most frequent medical treatment was systemic corticosteroids (93%), hydroxychloroquine (35%) and azathioprine (27%). Overall mortality was 13%. Long-term data demonstrated persistent abnormal radiology and a limited improvement in lung function.
Conclusions UNASSIGNED
Paediatric DAH is highly heterogeneous regarding underlying causes and clinical presentation. The high mortality rate and number of patients with ongoing treatment years after onset of disease underline that DAH is a severe and often chronic condition. This large international study paves the way for further prospective clinical trials that will in the long term allow evidence-based treatment and follow-up recommendations to be determined.

Identifiants

pubmed: 37101741
doi: 10.1183/23120541.00733-2022
pii: 00733-2022
pmc: PMC10123512
pii:
doi:

Types de publication

Journal Article

Langues

eng

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright ©The authors 2023.

Déclaration de conflit d'intérêts

Conflicts of interest: T. Bandeira reports personal fees from Sanofi and other support from Boehringer Ingelheim, outside the submitted work. Conflicts of interest: E.D. Manali reports other from Boehringer Ingelheim, other from Bering, other from Hoffman la Roche, outside the submitted work. Conflicts of interest: S. Papiris reports grants and other support from Boehringer Ingelheim and Hoffman la Roche, and other support from Savara, outside the submitted work. Conflicts of interest: M. Griese reports grants, personal fees and nonfinancial support from Boehringer Ingelheim for an advisory board on nintedanib, outside the submitted work. Conflicts of interest: The remaining authors have nothing to disclose.

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Auteurs

Astrid Madsen Ring (AM)

Paediatric Pulmonary Service, Dept of Paediatrics and Adolescent Medicine, Copenhagen, University Hospital, Rigshospitalet, Copenhagen, Denmark.

Nicolaus Schwerk (N)

Clinic for Paediatric Pneumology, Allergology and Neonatology, Hannover Medical School, German Center for Lung Research (DZL), Hannover, Germany.

Nural Kiper (N)

Hacettepe University Faculty of Medicine, Department of Pediatric Pulmonology, Ankara, Turkey.

Ayse Tana Aslan (AT)

Gazi University Faculty of Medicine, Department of Pediatric Pulmonology, Ankara, Turkey.

Paul Aurora (P)

Respiratory Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.

Roser Ayats (R)

Pediatric Pulmonology and Allergology Department, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT), Universitat Autónoma de Barcelona, Barcelona, Spain.

Ines Azevedo (I)

Departamento de Ginecologia Obstetrícia e Pediatria, Faculdade de Medicina, Universidade do Porto and Serviço de Pediatria, Centro Hospitalar Universitário de S. João, Porto, Portugal.

Teresa Bandeira (T)

Department of Pediatrics, Respiratory Unit, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Lisbon, Portugal.

Julia Carlens (J)

Clinic for Paediatric Pneumology, Allergology and Neonatology, Hannover Medical School, German Center for Lung Research (DZL), Hannover, Germany.

Silvia Castillo-Corullon (S)

Pediatric Pulmonology, Clinical Hospital of Valencia, Valencia, Spain.

Nazan Cobanoglu (N)

Department of Pediatrics, Pediatric Pulmonology Division, Ankara University Faculty of Medicine, Ankara, Turkey.

Basil Elnazir (B)

CHI at Tallaght University Hospital, Dublin, Ireland.

Nagehan Emiralioğlu (N)

Hacettepe University Faculty of Medicine, Department of Pediatric Pulmonology, Ankara, Turkey.

Tugba Sismanlar Eyuboglu (TS)

Gazi University Faculty of Medicine, Department of Pediatric Pulmonology, Ankara, Turkey.

Michael Fayon (M)

Pediatric Pulmonology Department, CHU Bordeaux, Bordeaux, France.

Tugba Ramaslı Gursoy (TR)

Gazi University Faculty of Medicine, Department of Pediatric Pulmonology, Ankara, Turkey.

Claire Hogg (C)

Royal Brompton Hospital, London, UK.

Karsten Kötz (K)

Devision of Paediatrics, Drottning Silvias Barn- och Ungdomssjukhus, University of Gothenburg, Gothenburg, Sweden.

Bülent Karadag (B)

Division of Paediatric Pulmonology, Marmara University Faculty of Medicine, Istanbul, Turkey.

Vendula Látalová (V)

Department of Pediatrics, University Hospital Olomouc, Olomouc, Czech Republic.

Katarzyna Krenke (K)

Department of Pediatric Pneumonology and Allergy, Medical University of Warsaw, Warsaw, Poland.

Joanna Lange (J)

Department of Pediatric Pneumonology and Allergy, Medical University of Warsaw, Warsaw, Poland.

Effrosyni D Manali (ED)

2nd Pulmonary Medicine Department, General University Hospital, Athens Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Borja Osona (B)

Pediatric Pulmonology Department, Son Espases University Hospital, Palma de Mallorca, Spain.

Spyros Papiris (S)

2nd Pulmonary Medicine Department, General University Hospital, Athens Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Marijke Proesmann (M)

Pediatric Pulmonology, KUL UZ Gasthuisberg, Leuven, Belgium.

Philippe Reix (P)

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

Lea Roditis (L)

Dept of Pediatric Pulmonology and Allergy, Children's University Hospital, Toulouse, France.

Sune Rubak (S)

Danish Center of Pediatric Pulmonology and Allergology, Department of Pediatrics and Adolescents Medicine, University Hospital of Aarhus, Aarhus, Denmark.

Nisreen Rumman (N)

Pediatric Department, Makassed Hospital, East Jerusalem, Palestine.

Deborah Snijders (D)

Dipartimento Salute della Donna e del Bambino, Università degli Studi di Padova, Padua, Italy.

Florian Stehling (F)

Clinic for Paediatrics III, University Hospital Essen, Essen, Germany.

Laurence Weiss (L)

Strasbourg University, Hôpital de Hautepierre, Pediatric Pulmonology Department, Strasbourg, France.

Ebru Yalcın (E)

Hacettepe University Faculty of Medicine, Department of Pediatric Pulmonology, Ankara, Turkey.

Fazilcan Zirek (F)

Department of Pediatrics, Pediatric Pulmonology Division, Ankara University Faculty of Medicine, Ankara, Turkey.

Andrew Bush (A)

Imperial College London and Paediatric Respiratory Medicine, Royal Brompton and Harefield NHS Foundation Trust, London, UK.

Annick Clement (A)

Sorbonne Université, Pediatric Pulmonology and Reference Center for rare lung diseases RespiRare, Inserm U933 Laboratory of childhood genetic diseases, Armand Trousseau Hospital, APHP, Paris, France.

Matthias Griese (M)

Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Frederik Fouirnaies Buchvald (FF)

Paediatric Pulmonary Service, Dept of Paediatrics and Adolescent Medicine, Copenhagen, University Hospital, Rigshospitalet, Copenhagen, Denmark.

Nadia Nathan (N)

Sorbonne Université, Pediatric Pulmonology and Reference Center for rare lung diseases RespiRare, Inserm U933 Laboratory of childhood genetic diseases, Armand Trousseau Hospital, APHP, Paris, France.
These authors contributed equally.

Kim Gjerum Nielsen (KG)

Paediatric Pulmonary Service, Dept of Paediatrics and Adolescent Medicine, Copenhagen, University Hospital, Rigshospitalet, Copenhagen, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
These authors contributed equally.

Classifications MeSH