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Published in: Orphanet Journal of Rare Diseases 1/2015

Open Access 01-12-2015 | Research

Categorizing diffuse parenchymal lung disease in children

Authors: Matthias Griese, Armin Irnstetter, Meike Hengst, Helen Burmester, Felicitas Nagel, Jan Ripper, Maria Feilcke, Ingo Pawlita, Florian Gothe, Matthias Kappler, Andrea Schams, Traudl Wesselak, Daniela Rauch, Thomas Wittmann, Peter Lohse, Frank Brasch, Carolin Kröner

Published in: Orphanet Journal of Rare Diseases | Issue 1/2015

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Abstract

Background

Aim of this study was to verify a systematic and practical categorization system that allows dynamic classification of pediatric DPLD irrespective of completeness of patient data.

Methods

The study was based on 2322 children submitted to the kids-lung-register between 1997 and 2012. Of these children 791 were assigned to 12 DPLD categories, more than 2/3 belonged to categories manifesting primarily in infancy. The work-flow of the pediatric DPLD categorization system included (i) the generation of a final working diagnosis, decision on the presence or absence of (ii) DPLD and (iii) a systemic or lung only condition, and (iv) the allocation to a category and subcategory. The validity and inter-observer dependency of this workflow was re-tested using a systematic sample of 100 cases.

Results

Two blinded raters allocated more than 80 % of the re-categorized cases identically. Non-identical allocation was due to lack of appreciation of all available details, insufficient knowledge of the classification rules by the raters, incomplete patient data, and shortcomings of the classification system itself.

Conclusions

This study provides a suitable workflow and hand-on rules for the categorization of pediatric DPLD. Potential pitfalls were identified and a foundation was laid for the development of consensus-based, international categorization guidelines.
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Metadata
Title
Categorizing diffuse parenchymal lung disease in children
Authors
Matthias Griese
Armin Irnstetter
Meike Hengst
Helen Burmester
Felicitas Nagel
Jan Ripper
Maria Feilcke
Ingo Pawlita
Florian Gothe
Matthias Kappler
Andrea Schams
Traudl Wesselak
Daniela Rauch
Thomas Wittmann
Peter Lohse
Frank Brasch
Carolin Kröner
Publication date
01-12-2015
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2015
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-015-0339-1

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