Chest
Volume 116, Issue 2, August 1999, Pages 543-548
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Preliminary Report
Aerosol-Derived Airway Morphometry and Aerosol Bolus Dispersion in Patients With Lung Fibrosis and Lung Emphysema

https://doi.org/10.1378/chest.116.2.543Get rights and content

Objective

Patients with lung emphysema show increased aerosol-derived dimensions of peripheral airspaces and increased aerosol bolus dispersion (AD). To apply these tests in epidemiologic studies, the objective of this pilot study was to investigate whether morphometric changes caused by lung fibrosis can be distinguished from those caused by emphysema.

Design

This study was designed as a cross-sectional study in which airspace dimensions and AD in patients with emphysema and in patients with fibrosis were compared. Forty patients participated in the study: 20 patients had high-resolution CT (HRCT)-proved lung emphysema and 20 patients had HRCT-proved lung fibrosis. All patients underwent conventional lung function tests, aerosol-derived airway morphometry (ADAM), and AD measurements.

Results

Patients with lung emphysema showed normal dimensions of small airways but enlarged airspace dimensions in the lung periphery. Patients with fibrosis showed in all lung depths increased airspace dimensions. AD was increased in patients with emphysema but was normal in patients with fibrosis.

Conclusions

These results show that when using ADAM and AD, morphometric changes caused by emphysema can be distinguished from those caused by fibrosis with high sensitivity and specificity.

Section snippets

Subjects

Twenty patients with chronic interstitial pulmonary fibrosis (IPF; 13 men, 7 women) and 20 patients with pulmonary emphysema (PE; 13 men, 7 women) participated in the study (Table 1). Anamnestic data were evaluated by a questionnaire based on American Thoracic Society recommendations.12 The smoking habits of the patients were quantified by using the cumulative cigarette consumption expressed as pack-years.

The diagnosis of chronic IPF was based on clinical, histologic, and radiographic (CT of

Results

Patients with IPF and PE showed no differences in anthropometric data (age, weight, height; Table 1).

In patients with IPF, lung volumes VC and TLC were mild to moderately reduced. RV was relatively well preserved. Because 50% of the patients were current or former smokers, a moderate airflow obstruction with decreased FEV1, MEF25, and MEF50 was observed. The Tlco was reduced.

Patients with PE showed chronic irreversible hyperinflation inferred from elevated levels of TLC and ITGV, clear signs of

Discussion

AD is increased in patients with PE, but is normal in patients with IPF. In both patient groups, ADAM showed increased airspace dimensions compared with the control group. However, the pattern of increased airspace dimensions was different between the two patient groups. Patients with PE showed normal EAD values in proximal lung depth. Inasmuch as this lung depth (Vp,r = 0.04) is, for the patients with PE, on average about 200 to 250 cm3, this likely represents the most peripheral parts of the

Conclusions

The presence of PE can be detected with ADAM and AD. IPF can be distinguished from PE by differences in AD and a different pattern of changes in ADAM. Therefore, in epidemiologic studies and in occupational medicine, both techniques seem to be useful for the detection of PE in humans. The specificity of the aerosol tests is not impaired by subjects with changes in lung morphometry caused by fibrosis. The practical value of these results should be confirmed by further prospective studies.

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