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Uncovering the beneficial effects of inhaled bronchodilator in COPD: beyond forced spirometry

BACKGROUND

It is a common clinical observation that many patients with COPD in whom FEV1 and/or FVC improve less than 200 mL and 12% after the use of inhaled bronchodilator (BD) did report less dyspnea during daily life when exposed to this medication. This state of affairs has shed negative light on the ability of pulmonary function tests to predict a positive clinical response to BDs.

OVERVIEW

A 75-year-old long-term smoker was referred for spirometry with a specific query for diagnosis of COPD-modified Medical Research Council (mMRC) scale score 3. Forced spirometry confirmed moderate-to-severe airflow limitation without a “significant” response to a short-acting BD.11 Lung function testing: selection of reference values and interpretative strategies. American Thoracic Society. Am Rev Respir Dis. 1991;144(5):1202-18. https://doi.org/10.1164/ajrccm/144.5.1202
https://doi.org/10.1164/ajrccm/144.5.120...
,22 Pellegrino R, Viegi G, Brusasco V, Crapo RO, Burgos F, Casaburi R, et al. Interpretative strategies for lung function tests. Eur Respir J. 2005;26(5):948-68. https://doi.org/10.1183/09031936.05.00035205
https://doi.org/10.1183/09031936.05.0003...
Despite these negative results, the patient reported marked improvement in daily exertional symptoms (mMRC scale score 1) after 4 weeks of treatment with a combination of a long-acting β2 agonist (LABA) and a long-acting antimuscarinic agent (LAMA). He was subsequently enrolled in a cross-over, randomized clinical trial contrasting the effects of the same LABA/LAMA combination against placebo. As shown in Figure 1A, the lack of “significant” changes in FEV1 and/or FVC after the use of the medication coexisted with a marked decrease in gas trapping (lower RV). As lung hyperinflation-? functional residual capacity (FRC)-improved to a greater extent than did thoracic hyperinflation (? TLC), inspiratory capacity (IC) increased significantly. The latter was maintained throughout the exercise test (Figure 1B), being associated with lower dyspnea scores and increased tolerance to physical effort.

Figure 1
In A, pulmonary function test results (forced and slow expiratory maneuvers and body plethysmography) before and after the administration of a combination of a long-acting β2-agonist (LABA) and a long-acting antimuscarinic agent (LAMA). In B, results of endurance cardiopulmonary exercise tests performed after the use of placebo (PL; white symbols) and bronchodilators (BD; black symbols) on different days to determine symptom limitation with serial measurements of inspiratory capacity (IC) in order to track end-expiratory (squares) and end-inspiratory (circles) lung volumes. See text for detailed discussion. FRC: functional residual capacity, IC: inspiratory capacity; and IRV: inspiratory reserve volume.

Exertional dyspnea arises when the descending motor drive to the inspiratory muscles is increased and the respiratory system fails to meet this increased demand.33 O'Donnell DE, James MD, Milne KM, Neder JA. The Pathophysiology of Dyspnea and Exercise Intolerance in Chronic Obstructive Pulmonary Disease. Clin Chest Med. 2019;40(2):343-366. https://doi.org/10.1016/j.ccm.2019.02.007
https://doi.org/10.1016/j.ccm.2019.02.00...
During exercise, the expiratory time becomes too short to fully exhale what has been inspired. Thus, expiratory flow limitation worsens gas trapping, leading to an upward shift in the operational lung volumes (i.e., those theoretically available for breathing). This, in turn, causes tidal volume to become progressively constrained as it approaches the “ceiling” (TLC).33 O'Donnell DE, James MD, Milne KM, Neder JA. The Pathophysiology of Dyspnea and Exercise Intolerance in Chronic Obstructive Pulmonary Disease. Clin Chest Med. 2019;40(2):343-366. https://doi.org/10.1016/j.ccm.2019.02.007
https://doi.org/10.1016/j.ccm.2019.02.00...
In this context, BDs fundamentally work as pharmacological deflators: there is more room for tidal volume expansion (IC) when the “floor” (end-expiratory lung volume) drops more than the “ceiling” (Figure 1B).

Why is it possible that forced spirometry may fail to show these beneficial effects on lung volumes? FEV1 is biased to reflect the function of the larger airways, i.e. the “fast component” of expiration, which, by definition, empties first.44 Newton MF, O'Donnell DE, Forkert L. Response of lung volumes to inhaled salbutamol in a large population of patients with severe hyperinflation. Chest. 2002;121(4):1042-50. https://doi.org/10.1378/chest.121.4.1042
https://doi.org/10.1378/chest.121.4.1042...
RV and FRC, in contrast, are strongly influenced by the mechanical properties of the smaller airways which need a longer time to empty (the “slow component”).44 Newton MF, O'Donnell DE, Forkert L. Response of lung volumes to inhaled salbutamol in a large population of patients with severe hyperinflation. Chest. 2002;121(4):1042-50. https://doi.org/10.1378/chest.121.4.1042
https://doi.org/10.1378/chest.121.4.1042...
Thus, an improvement in the flow rates of the “slow component” might not be detected by the maximal flow parameters from forced spirometry.55 O'Donnell DE, Lam M, Webb KA. Spirometric correlates of improvement in exercise performance after anticholinergic therapy in chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 1999;160(2):542-9. https://doi.org/10.1164/ajrccm.160.2.9901038
https://doi.org/10.1164/ajrccm.160.2.990...

CLINICAL MESSAGE

Adding a slow maneuver to forced spirometry to obtain IC (and, if feasible, measurements of static lung volumes) significantly enhances the clinical usefulness of pulmonary function tests in identifying the COPD patients who are poised to benefit from use of inhaled BDs as pertaining to exertional dyspnea and exercise intolerance.

REFERENCES

  • 1
    Lung function testing: selection of reference values and interpretative strategies. American Thoracic Society. Am Rev Respir Dis. 1991;144(5):1202-18. https://doi.org/10.1164/ajrccm/144.5.1202
    » https://doi.org/10.1164/ajrccm/144.5.1202
  • 2
    Pellegrino R, Viegi G, Brusasco V, Crapo RO, Burgos F, Casaburi R, et al. Interpretative strategies for lung function tests. Eur Respir J. 2005;26(5):948-68. https://doi.org/10.1183/09031936.05.00035205
    » https://doi.org/10.1183/09031936.05.00035205
  • 3
    O'Donnell DE, James MD, Milne KM, Neder JA. The Pathophysiology of Dyspnea and Exercise Intolerance in Chronic Obstructive Pulmonary Disease. Clin Chest Med. 2019;40(2):343-366. https://doi.org/10.1016/j.ccm.2019.02.007
    » https://doi.org/10.1016/j.ccm.2019.02.007
  • 4
    Newton MF, O'Donnell DE, Forkert L. Response of lung volumes to inhaled salbutamol in a large population of patients with severe hyperinflation. Chest. 2002;121(4):1042-50. https://doi.org/10.1378/chest.121.4.1042
    » https://doi.org/10.1378/chest.121.4.1042
  • 5
    O'Donnell DE, Lam M, Webb KA. Spirometric correlates of improvement in exercise performance after anticholinergic therapy in chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 1999;160(2):542-9. https://doi.org/10.1164/ajrccm.160.2.9901038
    » https://doi.org/10.1164/ajrccm.160.2.9901038

Publication Dates

  • Publication in this collection
    27 June 2019
  • Date of issue
    2019
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