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Categorizing diffuse parenchymal lung disease in children
Orphanet Journal of Rare Diseases volume 10, Article number: 122 (2015)
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.
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.
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.
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.
Childhood interstitial lung diseases (ILD) represent a large spectrum of individually rare diffuse parenchymal lung diseases (DPLD), prevalent in children of all ages [1–3]. They comprise more than 200 different disease entities which are treated by pediatricians and general practitioners in general and specialized (children´s) hospitals. Due to the similarity of symptoms it is often difficult to differentiate these rare patients from children with more common respiratory diseases . Clinical presentation of the disease may further be blurred by recurrent infections or allergies. Childhood DPLD may thus easily be underdiagnosed. Correct classification of all patients is however indispensable for the appropriate treatment, for a better understanding of the underlying pathophysiology, for the identification of biomarkers and for long-term studies and cohort investigations.
Several categorization systems of childhood DPLD have been proposed over time [1, 5–7]. The majority of the recent systems are based on lung histology, related to the study by Deutsch et al. , which classifies the broad spectrum of patients into eight disease categories containing various diagnoses . The categorization system has in the meantime been expanded to the entire pediatric age range  and has been shown useful for pathological studies . In a single center study the system was also used for cases not diagnosed by biopsy .
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. The work-flow and validity of the categorization system was tested, basis were all cases submitted to the kids-lung-register (KLR) between 1997 and 2012 . The kids-lung-register is, an open, non-profit register for rare lung diseases in childhood and adolescence (www.kids-lung-register.eu). On average 147 children with lung diseases per year are referred to the kids-lung-register for consultation and laboratory services from diverse European centers. Based on the kids-lung-register a European management platform was established in 2013 for childhood interstitial lung diseases (http://www.klinikum.uni-muenchen.de/Child-EU/en/index.html) comprising 10 academic partners from 5 European countries.
DPLD are entities originating from abnormalities of lung interstitial tissue components. These structures in the periphery of the lungs include the alveolar epithelium, the vessel endothelium and the tissues between these structures. More centrally they include peribronchiolar and peribronchial tissues . Airways may be involved secondary in the disease process. DPLD disorders more prevalent in infancy (A) and disorders occurring at all ages (B) are differentiated. Diseases which affect the parenchymal tissue, but are localized gross structural abnormalities of the lungs, either congenital (C1) or acquired (C2) are not classified as DPLD. Further separated are disorders which primarily affect the airways (airway disorders (D)), the pleural tissues (pleural diseases (E)), diseases caused by lung infections (F) or neoplasms (G), which may also involve the parenchyma.
Workflow for patient categorization during routine operation of the KLR
For the cases referred to the KLR the categorization system for DPLD suggested by Deutsch et al.  was further developed; three additional categories were introduced (Additional file 1: Table S1) to accommodate cases with “unclear respiratory distress syndrome” in the mature neonate (Ax) and in the almost mature neonate (Ay) and “unclear respiratory distress syndrome” in the non-neonate (By). These categories allow the future analysis of unclear cases. In addition, the rather wide category “disorders masquerading as ILD” was dissolved into two more specific categories: “DPLD related to lung vessels structural processes” (B4) and “DPLD related to reactive lymphoid lesions” (B5) (Fig. 1).
Practical categorization rules were initially set up by the KLR (Table 1) to assure consistent categorization. 2322 children were referred to the KLR between 1997 and 2012. DPLD was suspected in a child with (1) respiratory symptoms and signs such as cough, tachy-/dyspnea at rest or with exercise, crackles, retractions, digital clubbing, failure to thrive, or respiratory failure, and (2) hypoxemia, and (3) diffuse radiological abnormalities and (4) if feasible and available, abnormalities in pulmonary function testing. Minimum duration of symptoms was 4 weeks.
During capture of the cases with suspected DPLD the referring physician mostly specialized in pediatric pulmonology on the level of a tertiary or university hospital diagnosed the patients in cooperation with the radiologist and in cases with biopsy the pathologist. Available material included a clinical history, biochemical, radiological, histological and genetic data of varying level of detail. A diagnosis was independently also established by each of the KLR experts: F. B., a pathologist; P. L. a geneticist; M. G., a pediatric clinician and pulmonologist (Additional file 2: Figure S1).
A four-step algorithm was used for categorization (Table 1 ): in a first step, a “final working diagnosis” was defined by consensus discussion, entered into the data-base and used for categorization and sub-categorization. In a second step it was analyzed if the final working diagnosis was related to DPLD. In a third step it was decided whether the patient suffered from a lung only condition or if the lung disease was part of a systemic disease. Of note, the latter are not restricted to the diagnosis of category B1. Other organ systems than the lungs may also be involved in diseases of categories B3, B4, B5, A1 and in particular A2 (Fig. 1, Additional file 1: Table S1). In a fourth step, the appropriate category and subcategory were selected, preferring the strongest causal explanation of the condition and the most conclusive supporting evidence taking into account the categorization rules shown in Table 1. A total of 791 children of 2322 children in the KLR qualified for childhood DPLD and were further categorized into one of the 12 DPLD categories (Fig. 1, Additional file 1: Table S1) and the respective subcategories.
Workflow for re-rating of selected DPLD cases retrieved from the KLR
The validity and observer-dependency was tested in 2012 using a systematic sample of 100 DPLD cases from the cohort of 791 children previously categorized according to the KLR algorithm. 100 cases were selected randomly and in proportion to their frequency in the KLR categories. All 100 cases were pseudonymized for blinded and independent re-categorization by two pediatric pneumologists, familiar with the KLR categorization system (Fig. 1, red lowever part, Additional file 3: Tables S2, Additional file 4: Table S3). One of the physicians involved in re-rating was already involved in the initial categorization, the other was an independent physician. A final working diagnosis was newly established by each re-rater and allocated in the KLR categorization system, again according to the rules indicated in Table 1 and the workflow detailed in Additional file 2: Figure S1, red part. As re-rating of the categorization was the goal of the study the initial categorization obtained during routine work-flow was set as the correct one. The overall frequencies of diagnostics available for the establishment of the final working diagnosis, categorization and sub-categorization are indicated in Additional file 5: Table S4.
All participants gave their written informed consent to participate in the KLR consultation and diagnosis program. The retrospective analysis of the data was approved by the institutional review board (EK 026–06). Prospective collection and analysis of data was approved in the GOLD.net project (EK 257–10), and analysis was performed under the project FP7-305653-chILD-EU (EK 111–13).
Of 2322 children referred to the KLR between 1997 and 2012, 861 were related to DPLD and included into this cohort. Subjects with insufficient information were excluded. 791 remaining subjects were assigned to the 12 DPLD categories (Fig. 1). Of these subjects 55 % were male; their age at presentation was 4.2 ± 5.5 years (median 1.0 years, range 0 to 20). 549 subjects had a lung disease manifesting primarily in infancy, of which the largest number (294) was assigned to the category A4 (DPLD–related to alveolar surfactant region) (Fig. 1).
Re-categorization of 100 cases was in agreement with the first allocation in more than 80 % (Table 2). Analysis of deviation in allocation showed that four kinds of allocation mistakes were made (Table 2): (1) one source for error was a lack of appreciation of all details available in the medical records; most of these mistakes were associated with wrong allocation of subcategories. (2) a second rater-related source of error was too little knowledge of and erroneous application of the categorization rules. For example, chromosomal abnormalities are listed as an independent category in A2 because they are present at birth and mainly manifest in infancy, and not in B1, i.e. related to systemic disease processes. (3) For some cases previously categorized, the re-rater decided that data was insufficient. In one case for instance, clinical and radiological data was available, however no genetic or histologic information. Information on low levels of hydrophobic surfactant protein content of BAL was not judged to be helpful (4).
Lastly, shortcomings of the categorization system itself lead to non-correct categorization: main deficits of the categorization system were observed for the differentiation of chronic tachypnea of infancy (A3), and for diseases involving the parenchyma but also or primarily the peripheral airways. The latter, such as post-infectious obliterative bronchiolitis and Mac-Leod-Swyer-James-Syndrome, both for immune-competent and immune-compromised hosts, were frequently categorized as airway disorders and not as DPLD. The former, i.e. infants with tachypnea were identified as neuroendocrine cell hyperplasia, even if there was no biopsy available. A comprehensive list of erroneous classification is displayed in Additional files 3 and 4: Tables S2, S3.
Here we describe an algorithm to categorize children with DPLD; we defined and assessed rules for categorization and suggest a tool for establishing large cohorts of consistently categorized subjects with rare pulmonary diseases. We thus provide an important basis for the development of consensus-based, international guidelines for categorization and management of pediatric DPLD. Consistent categorization is indispensable for handling individual cases in registries and biobanks appropriately. It allows to combine or split diagnosis groups and to compare subcategories and categories. A consistent categorization system is the basis for future adjustments, such as the inclusion of new molecular disease entities or of novel diagnostic methods. A specific working diagnosis may change over time or knowledge may evolve on a particular subject, however, the allocation rules should not change, representing an important constant term.
In this study, several important barriers to a consistent categorization of rare lung diseases were identified. It was shown that consistent categorization needs to be repeatedly practiced especially for the use in large registers. Continuous evaluation of the categorization process within a register will be an important element of quality control.
Lack of sufficient data in a case is a common problem in clinical practice, hindering the establishment of a correct diagnosis. Data may be insufficient for many reasons, such as high costs for diagnostic testing, invasiveness of tests (e.g. lung biopsy), missing data or poor quality of the data (e.g. incomplete history, CT scans performed in infants with improper technique). The problem of insufficient data should not distract from making a diagnosis. Appreciating all information and details available will yield a final working diagnosis, which should be clearly indicated. Even if the diagnosis leaves open questions e.g. “unclear RDS in the mature neonate”, these cases must nevertheless be categorized. For this purpose the categories Ax, Ay, Bx were created (Fig. 1, Additional file 1: Table S1). The cases in these categories can (and must) be systematically revisited and if more information becomes available, should be allocated into more specific categories. These patients can furthermore be included into non-hypothesis based screening projects, like exome sequencing or disease marker identification projects, with the aim to identify previously unknown disease causes or to determine disease activity.
Any classification system is continuously evolving. Increasing knowledge on molecular disease mechanisms allows the definition of new entities, which must be easily accommodated in the categorization system, as is the case for the current system.
It is furthermore essential to continuously take note of potential areas of uncertainty within the system and to clarify these: there are for example entities for which no precise diagnostic criteria are available, such as the differentiation of infants with chronic tachypnea in the absence of a lung biopsy (See examples in Additional file 3: Table S2). Another area which needs clarification is the categorization of diffuse parenchymal diseases which also involve the distal airways. These patients overlap with those presenting primarily as obstructive airway diseases, but cannot merely be classified as such, because the remodeling of the lung tissue component is dominant. A precise definition of all subcategories is not yet available but will be significant to be developed as “gold-standard”.
Lastly, a rating of the confidence level of the quality of the data used for establishing the working diagnosis for the individual cases would be a valuable additional indicator and is desirable to be established in the future.
Using a clinically oriented categorization system such as the one presented here has the advantage that different registries or studies using the same definitions and rules may be compared or combined for analysis. Consistent application of a clinically oriented categorization system is prerequisite for the establishment of urgently needed larger cohorts of patients with rare pediatric lung diseases.
We present hands-on rules for the categorization of all pediatric DPLD, independent of the presence or absence of a lung biopsy or the quality of diagnostic data. We empirically identify pitfalls of categorization and suggest solutions for improvement with the aim to provide the basis for the development of consensus-based, international guidelines for the categorization and management of pediatric DPLD.
Diffuse parenchymal lung disease
Respiratory distress syndrome
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We thank all institutions and physicians contributing cases to this project. A complete listing is indicated in Additional file 6: Table S5.
The work of M.G. was supported by chILD-EU (FP7, No. 305653) and the “Else Kröner-Fresenius-Stiftung”.
The authors declare to have no competing interests.
MG designed the study, organized long term collection of subjects, patient recruitment and evaluation, data analysis, and drafted the manuscript. He is the guarantee of the work. AI was involved in patient evaluation; re-review of patients sample, chart review, data analysis, and revisions of the manuscript. MH, HB, FN, JR, MF, IP, FG, MK evaluated patients, made chart reviews, and revised the manuscript. AS, TW, DR, TW organized the study logistics, did laboratory analysis, sample and patient organization, and made critical revisions of the manuscript. PL did chart review, the genetic analyses and revised the manuscript. FB evaluated patients with biopsies, performed histo-pathological analyses and revised the manuscript. CK did patient evaluations, chart review, data analysis, and revised the manuscript. All authors read and approved the final manuscript.
Definitions of diffuse parenchymal lung diseases (DPLD) - disease categories and subcategories. (DOCX 26 kb)
Routine work-flow used in the Kids lung register (KLR) to obtain a final working diagnosis and to categorize and subcategorize cases with suspected DPLD (black and red). The work-flow used for re-rating is depicted in red. *reference pathologist was Frank Brasch, **genetical diagnosis was made by Peter Lohse and ***lavage report on surfactant protein analysis, as well as the establishment of the final working diagnosis during routine KLR workflow were done by Matthias Griese. (PDF 176 kb)
Blinded and independent re-rating of a random sample of 100 DPLD cases from the kids-lung register. Only differences to the original categorization are indicated; empty cells indicate correct categorization. (DOCX 35 kb)
Summary of reasons for incorrect categorization. (DOCX 15 kb)
Overall frequencies of diagnostics available for the establishment of the final working diagnosis, categorization and sub-categorization. Note that not all tests were performed in all patients. (DOCX 15 kb)
Centers and physicians contributing cases to the kids-lung-register. (DOCX 34 kb)
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Griese, M., Irnstetter, A., Hengst, M. et al. Categorizing diffuse parenchymal lung disease in children. Orphanet J Rare Dis 10, 122 (2015). https://doi.org/10.1186/s13023-015-0339-1
- Childhood interstitial lung disease
- Diffuse parenchymal lung disease
- Rare pediatric lung disease