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Jornal Brasileiro de Pneumologia

Print version ISSN 1806-3713On-line version ISSN 1806-3756

J. bras. pneumol. vol.45 no.5 São Paulo  2019  Epub Oct 10, 2019

http://dx.doi.org/10.1590/1806-3713/e20190060 

LETTER TO THE EDITOR

Clinical, functional, and cytological evaluation of sputum in postinfectious bronchiolitis obliterans: a possible overlap with asthma?

Sarah Angélica Maia1 
http://orcid.org/0000-0002-2908-4653

Denise Eli2 
http://orcid.org/0000-0003-3470-2599

Roberta Cunha2 
http://orcid.org/0000-0001-7406-5286

Elessandra Bitencourt2 
http://orcid.org/0000-0002-7501-0647

Carlos Antônio Riedi1 
http://orcid.org/0000-0002-6044-3327

Herberto José Chong Neto1 
http://orcid.org/0000-0002-7960-3925

Débora Carla Chong e Silva1 
http://orcid.org/0000-0002-7385-4598

Nelson Augusto Rosário Filho1 
http://orcid.org/0000-0002-8550-8051

1. Universidade Federal do Paraná, Curitiba (PR) Brasil.

2. Complexo do Hospital de Clínicas, Universidade Federal do Paraná, Curitiba (PR) Brasil.


DEAR EDITOR:

Postinfectious bronchiolitis obliterans (PIBO) is a chronic obstructive pulmonary disease associated with inflammation of the lower airways. The inflammatory process is secondary to infectious bronchiolitis, which can be caused by viruses, atypical germs (especially Mycoplasma pneumoniae), and other bacteria.1,2 Although the clinical manifestations of PIBO can vary widely, its main characteristic is that patients with the condition present with signs and symptoms of a severe and persistent lower airway obstruction.2

The objective of the present study was to evaluate the clinical presentation, pulmonary function, CT findings, and sputum cellularity in patients with PIBO, as well as to correlate sputum cell pattern with spirometry and other imaging findings, clinical manifestations, and atopy.

This is a cross-sectional analytical study with patients diagnosed with PIBO and under follow-up at the Pediatric Pulmonology Center of the Clinical Hospital Complex of the Federal University of Paraná, Curitiba, state of Paraná, Brazil. The study included patients under 21 years of age with a diagnosis of PIBO related to a history of severe viral bronchiolitis before the onset of the respiratory symptoms and imaging studies with radiological findings showing involvement of the small airways and/or spirometry characterizing an obstructive defect. Exclusion criteria were the presence of other lung diseases, such as cystic fibrosis, primary or secondary immunodeficiencies, and other chronic pulmonary diseases.

After selection, patients underwent an initial clinical evaluation followed by complete spirometry-satisfying the acceptability and repeatability criteria established by international guidelines3-and post-bronchodilator (salbutamol, 400 µg) evaluation. The classification of the obstructive ventilatory defect into mild or moderate followed the recommendations of the American Thoracic Society.4 The bronchodilator test was considered positive when the difference in FEV1 was greater than 12% of the predicted value, as recommended by the Global Initiative for Asthma.5 Sputum was induced via inhalation of a hypertonic saline solution, using a 2 L/min oxygen cylinder, and with the assistance of a physical therapist. The process used a hypertonic saline solution with concentrations gradually increasing from 3% to 5% and 7%, when necessary, and lasted a minimum of 20 min per patient. After the minimum time, patients were stimulated to cough and expectorate into a sterile vial. The processes of sputum induction and sample processing followed a laboratory technique described by Pizzichini et al.6 Only samples with cell viability above 50% were considered for the analysis.7 The patterns found were divided into eosinophilic (eosinophils > 2.5% and neutrophils ≤ 54%), neutrophilic (eosinophils ≤ 2.5%, neutrophils > 54%), and mixed (eosinophilic/neutrophilic; eosinophils > 2.5% and neutrophils > 54%).8 The study was approved by the research ethics committee of the institution (Protocol No. 2.062.062). All parents/guardians gave written informed consent.

Our sample was initially composed of 23 patients with a clinical and radiological diagnosis of PIBO, who also met all other inclusion criteria. Of these, 1 patient refused to participate, and we were unable to get hold of another 9 patients. Therefore, 13 patients were enrolled in the study (8 of them male), with a median age of 12.1 years (range: 7-20 years). All 13 patients (100%) had been hospitalized in their first year of life due to a disease whose manifestations were compatible with acute viral bronchiolitis. In addition, 8 (61.5%) had a positive skin prick test for at least one aeroallergen, 7 (53.8%) had rhinitis and/or atopic dermatitis, and 9 (69.2%) were making use of inhaled corticosteroids.

All study participants had undergone at least one chest CT scan. The most prevalent CT finding was a mosaic pattern, found in 11 patients (84%); followed by bronchial wall thickening, in 10 (76%); bronchiectasis, in 4 (30%); and atelectasis, in 4 (30%).

Of the 12 participants who underwent complete spirometry, 11 (91.6%) had obstructive ventilatory defect. Of these, 7 (63.6%) were classified as mild (60% < FEV1 < 90%) and 4 (36.4%) as moderate (40% < FEV1 < 60%). Four patients had a positive bronchodilator test (33.3%).

As for sputum cytology, the samples of 3 patients were considered inadequate for cytology studies for not having sufficient cell viability. Of the 10 samples considered viable, 4 (40%) had a neutrophilic pattern; 4 (40%) had a neutrophilic/eosinophilic pattern (mixed); and 2 (20%) had an eosinophilic pattern. One of the samples was considered neutrophilic in spite of having a neutrophil rate below 54% because of its high cell viability and absence of eosinophils.

Sputum cytological patterns were compared with the CT findings, skin prick test results, presence or absence of daily symptoms and/or symptoms when exercising (especially dry cough and dyspnea), and bronchodilator test results (Table 1).

Table 1 Clinical, functional, and CT variables in relation to sputum cell pattern (N = 10). 

Variables Cell pattern
Neutrophilic Eosinophilic/neutrophilic Eosinophilic
(n = 4) (n = 4) (n = 2)
Positive skin prick test 3 3 2
Daily symptoms 2 1 1
Symptoms when exercising 1 2 2
Bronchiectasis 0 2 0
Ground-glass opacities 1 2 0
Positive bronchodilator test 1 2 1

PIBO is a rare chronic lung disease resulting from severe lung injury following acute infectious bronchiolitis that causes varying degrees of inflammation with narrowing or total obliteration of the small airways in susceptible individuals.9

Supposedly, sputum cytology findings should be similar to those of previous bronchoalveolar lavages,10 with a marked increase in the number of neutrophils. However, only 4 patients presented an exclusively neutrophilic pattern, and, in 2, the pattern was predominantly eosinophilic, contrary to the initial assumption. Such disagreement was seen in atopic patients with a positive skin prick test and a diagnosis of concomitant rhinitis, indicating a probable coexistence of allergic asthma with previously diagnosed PIBO, an overlap suggested in a previous study.11

The bronchodilator test turned out positive in all cytological patterns, including the exclusively neutrophilic one, corroborating studies with long-term follow-up of patients with PIBO.12,13 Those studies have shown severe and permanent impairment of lung function, though air trapping slowly decreased with patient growth.1,12,13

There were no significant correlations between sputum cellularity and the clinical, functional, and CT variables studied. The lack of statistical correlation between the variables in the present study was probably due to the small sample size; the low prevalence of the disease represents an analytical challenge.

The lack of predominance of a specific cytological pattern could suggest a potential overlap of PIBO and asthma, which can indicate a need for new diagnostic and therapeutic approaches aimed at controlling both diseases. A deeper understanding of PIBO will favor an individualized approach of these cases. Similar multicenter studies may help deepen our understanding by providing us with the possibility of evaluating larger samples of such a rare disease.

ACKNOWLEDGMENTS

We would like to give special thanks to our medical student, Thaísa Vieira Sonnberg, for proofreading and conforming the text to the journal’s standards.

REFERENCES

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