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. 2024 Oct;6(5):e240041.
doi: 10.1148/ryct.240041.

Low-Dose Whole-Chest Dynamic CT for the Assessment of Large Airway Collapsibility in Patients with Suspected Tracheobronchial Instability

Affiliations

Low-Dose Whole-Chest Dynamic CT for the Assessment of Large Airway Collapsibility in Patients with Suspected Tracheobronchial Instability

Arved Bischoff et al. Radiol Cardiothorac Imaging. 2024 Oct.

Abstract

Purpose To quantify tracheal collapsibility using low-dose four-dimensional (4D) CT and to compare visual and quantitative 4D CT-based assessments with assessments from paired inspiratory-expiratory CT, bronchoscopy, and spirometry. Materials and Methods The authors retrospectively analyzed 4D CT examinations (January 2016-December 2022) during shallow respiration in 52 patients (mean age, 66 years ± 12 [SD]; 27 female, 25 male), including 32 patients with chronic obstructive pulmonary disease (mean forced expiratory volume in 1 second percentage predicted [FEV1%], 50% ± 27), with suspected tracheal collapse. Paired CT data were available for 27 patients and bronchoscopy data for 46 patients. Images were reviewed by two radiologists in consensus, classifying patients into three groups: 50% or greater tracheal collapsibility, less than 50% collapsibility, or fixed stenosis. Changes in minimal tracheal lumen area, tracheal volume, and lung volume from inspiration to expiration were quantified using YACTA software. Tracheal collapsibility between groups was compared employing one-way analysis of variance (ANOVA). For related samples within one group, ANOVA with repeated measures was used. Spearman rank order correlation coefficient was calculated for collapsibility versus pulmonary function tests. Results At 4D CT, 25 of 52 (48%) patients had tracheal collapsibility of 50% or greater, 20 of 52 (38%) less than 50%, and seven of 52 (13%) had fixed stenosis. Visual assessment of 4D CT detected more patients with collapsibility of 50% or greater than paired CT, and concordance was 41% (P < .001). 4D CT helped identify more patients with tracheal collapsibility of 50% or greater than did bronchoscopy, and concordance was 74% (P = .39). Mean collapsibility of tracheal lumen area and volume at 4D CT were higher for 50% or greater visually assessed collapsibility (area: 53% ± 9 and lumen: 52% ± 10) compared with the less than 50% group (27% ± 9 and 26% ± 6, respectively) (P < .001), whereas both tracheal area and volume were stable for the fixed stenosis group (area: 16% ± 12 and lumen: 21% ± 11). Collapsibility of tracheal lumen area and volume did not correlate with FEV1% (rs = -0.002 to 0.01, P = .99-.96). Conclusion The study demonstrated that 4D CT is feasible and potentially more sensitive than paired CT for central airway collapse. Expectedly, FEV1% was not correlated with severity of tracheal collapsibility. Keywords: CT-Quantitative, Tracheobronchial Tree, Chronic Obstructive Pulmonary Disease, Imaging Postprocessing, Thorax Supplemental material is available for this article. © RSNA, 2024.

Keywords: CT-Quantitative; Chronic Obstructive Pulmonary Disease; Imaging Postprocessing; Thorax; Tracheobronchial Tree.

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Conflict of interest statement

Disclosures of conflicts of interest: A.B. No relevant relationships. O.W. Airway analysis technology is licensed to Imbio. A.D. No relevant relationships. R.R. No relevant relationships. H.U.K. Support for the present manuscript from the German Center of Lung Research, paid to author’s institution. D.G. Grant from Olympus for bronchoscopy courses; lecture fees from Pulmonx, Olympus, AstraZeneca, Chiesi, Berlin Chemie, MSD, and Boehringer Ingelheim. R.E. No relevant relationships. F.T. No relevant relationships. C.P.H. Consultation or other fees from Schering-Plough (2009, 2010), Pfizer (2008–2014), Basilea (2008, 2009, 2010), Boehringer Ingelheim (2010–2024), Novartis (2010, 2012, 2014), Roche (2010), Astellas (2011, 2012), Gilead (2011–2015), MSD (2011–2013), Lilly (2011), Intermune (2013–2014), and Fresenius (2013–2014); research funding from Siemens (2012–2014), Pfizer (2012–2014), MeVis (2012, 2013), Boehringer Ingelheim (2014), and Exscientia (2023–2024); lecture fees from Gilead (2008–2014), Essex (2008, 2009, 2010), Schering-Plough (2008, 2009, 2010), AstraZeneca (2008–2014, 2022), Lilly (2008, 2009, 2012), Roche (2008, 2009), MSD (2009–2014), Pfizer (2010–2014, 2023–2024), Bracco (2010, 2011), MEDA Pharma (2011), Intermune (2011–2014), Chiesi (2012), Siemens (2012), Covidien (2012), Pierre Fabre (2012), Boehringer Ingelheim (2012–2024), Grifols (2012), Novartis (2013–2016), Basilea (2015, 2016), and Bayer (2016); patent: “Method and Device for Representing the Microstructure of the Lungs,” IPC8 class: AA61B5055FI, PAN: 20080208038, co-inventor; committee membership on the Chest Working Group of the German Roentgen Society; consultant of ECIL-3, ECCMID, and EORTC/MSG; founding member of the working team in infections in immunocompromised hosts of the German Society of Hematology/Oncology; faculty member of the European Society of Thoracic Radiology (ESTI), European Respiratory Society (ERS), and European Imaging Biomarkers Alliance (EIBALL); editor of Medizinische Klinik, Intensivmedizin und Notfallmedizin (Springer); stock or stock options in GSK. F.J.F.H. No relevant relationships. M.H. No relevant relationships. F.F. Support for the present manuscript from the University of Lübeck; grants or contracts from the University of Lübeck; payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from Technische Hochscule Lübeck; support for attending meetings and/or travel from the University of Lübeck; receipt of equipment, material, drugs, medical writing, gifts, or other services from the University of Lübeck. M.O.W. Study grant from Vertex Pharmaceuticals, paid to author’s institution; consulting fees from Vertex Pharmaceuticals, paid to author’s institution; leadership or fiduciary role in ESTI, IWPFI, and DRG (unpaid).

Figures

None
Graphical abstract
Study flowchart. Patients were grouped as having fixed stenosis or
tracheal collapsibility, the latter with a threshold of 50% or greater
reduction of minimal lumen area. The most frequent diagnosis was
tracheobronchomalacia (TBM), and its most frequent subtype was crescent-type
collapse. (E)DAC = (excessive) dynamic airway collapse.
Figure 1:
Study flowchart. Patients were grouped as having fixed stenosis or tracheal collapsibility, the latter with a threshold of 50% or greater reduction of minimal lumen area. The most frequent diagnosis was tracheobronchomalacia (TBM), and its most frequent subtype was crescent-type collapse. (E)DAC = (excessive) dynamic airway collapse.
Quantification of (A) minimal tracheal lumen area, (B) tracheal
volume, and (C) lung volume during the respiratory cycle by using
four-dimensional (4D) CT. Patients were grouped according to visual degree
of collapsibility. Relative changes during free shallow breathing are shown
with the respiratory cycle separated into 21 discrete time points equal to
5%-wide steps at 4D CT. Symbols represent group means, and whiskers indicate
standard error of the mean; statistical significance is given for maximum
inspiration versus end expiration, with * indicating P < .001.
Comparisons of tracheal collapsibility between groups along the 21 steps of
the respiratory cycle were made by one-way analysis of variance (ANOVA). For
related samples within the patient groups, ANOVA with repeated measures was
used. P < .05 was accepted as statistically significant, including
corrections for multiple comparisons by Bonferroni method.
Figure 2:
Quantification of (A) minimal tracheal lumen area, (B) tracheal volume, and (C) lung volume during the respiratory cycle by using four-dimensional (4D) CT. Patients were grouped according to visual degree of collapsibility. Relative changes during free shallow breathing are shown with the respiratory cycle separated into 21 discrete time points equal to 5%-wide steps at 4D CT. Symbols represent group means, and whiskers indicate standard error of the mean; statistical significance is given for maximum inspiration versus end expiration, with * indicating P < .001. Comparisons of tracheal collapsibility between groups along the 21 steps of the respiratory cycle were made by one-way analysis of variance (ANOVA). For related samples within the patient groups, ANOVA with repeated measures was used. P < .05 was accepted as statistically significant, including corrections for multiple comparisons by Bonferroni method.
Low concordance of paired inspiratory-expiratory CT with
four-dimensional (4D) CT. The top row represents paired
inspiratory-expiratory CT (noncontrast, lung window) in (A) inspiratory and
(B) expiratory breath hold in axial plane in a 77-year-old male patient. The
bottom row shows the same patient under shallow breathing at 4D CT
(noncontrast, lung window) in (C) maximum inspiration and (D) end expiration
in axial plane. Note that the tracheal collapsibility was less than 50% at
paired inspiratory-expiratory CT but 50% or greater at 4D CT. The level of
strongest collapse varied slightly between paired CT and 4D CT.
Figure 3:
Low concordance of paired inspiratory-expiratory CT with four-dimensional (4D) CT. The top row represents paired inspiratory-expiratory CT (noncontrast, lung window) in (A) inspiratory and (B) expiratory breath hold in axial plane in a 77-year-old male patient. The bottom row shows the same patient under shallow breathing at 4D CT (noncontrast, lung window) in (C) maximum inspiration and (D) end expiration in axial plane. Note that the tracheal collapsibility was less than 50% at paired inspiratory-expiratory CT but 50% or greater at 4D CT. The level of strongest collapse varied slightly between paired CT and 4D CT.
Representative example of circumferential-type tracheobronchomalacia
(TBM). (A) Image from four-dimensional (4D) CT (noncontrast, lung window) in
a 72-year-old male patient with circumferential-type TBM at the level of
maximum observed tracheal collapsibility at representative selected time
points of the respiratory cycle. The upper row shows axial view, the lower
row sagittal view. The axial view demonstrates the circular collapse of the
trachea because of cartilaginous malacia. (B) Graph shows the changes of
minimal tracheal lumen area, tracheal volume, and lung volume in the same
patient over the respiratory cycle with 21 time points in 5%-wide steps at
4D CT. (C) Image from correlated bronchoscopy.
Figure 4:
Representative example of circumferential-type tracheobronchomalacia (TBM). (A) Image from four-dimensional (4D) CT (noncontrast, lung window) in a 72-year-old male patient with circumferential-type TBM at the level of maximum observed tracheal collapsibility at representative selected time points of the respiratory cycle. The upper row shows axial view, the lower row sagittal view. The axial view demonstrates the circular collapse of the trachea because of cartilaginous malacia. (B) Graph shows the changes of minimal tracheal lumen area, tracheal volume, and lung volume in the same patient over the respiratory cycle with 21 time points in 5%-wide steps at 4D CT. (C) Image from correlated bronchoscopy.
Representative example of excessive dynamic airway collapse (EDAC).
(A) Images from four-dimensional (4D) CT (noncontrast, lung window) in a
51-year-old female patient with EDAC at the level of maximum observed
tracheal collapsibility at representative selected time points of the
respiratory cycle. The upper row shows axial view, the lower row sagittal
view. The axial view demonstrates the inward bowing of the posterior
membrane while the cartilage retains its normal shape. (B) Graph shows the
changes of minimal tracheal lumen area, tracheal volume, and lung volume of
the same patient over the respiratory cycle with 21 time points in 5%-wide
steps at 4D CT. (C) Image from correlated bronchoscopy.
Figure 5:
Representative example of excessive dynamic airway collapse (EDAC). (A) Images from four-dimensional (4D) CT (noncontrast, lung window) in a 51-year-old female patient with EDAC at the level of maximum observed tracheal collapsibility at representative selected time points of the respiratory cycle. The upper row shows axial view, the lower row sagittal view. The axial view demonstrates the inward bowing of the posterior membrane while the cartilage retains its normal shape. (B) Graph shows the changes of minimal tracheal lumen area, tracheal volume, and lung volume of the same patient over the respiratory cycle with 21 time points in 5%-wide steps at 4D CT. (C) Image from correlated bronchoscopy.
Representative example of fixed tracheal stenosis. (A) Images from
four-dimensional (4D) CT (noncontrast, lung window) in a 53-year-old female
patient with fixed tracheal stenosis at the level of maximum observed
tracheal narrowing at representative selected time points of the respiratory
cycle. The upper row shows axial view, the lower row sagittal view. No
dynamic changes were observed. (B) Graph shows the changes of minimal
tracheal lumen area, tracheal volume, and lung volume of the same patient
over the respiratory cycle with 21 time points in 5%-wide steps at 4D CT.
(C) Image from correlated bronchoscopy.
Figure 6:
Representative example of fixed tracheal stenosis. (A) Images from four-dimensional (4D) CT (noncontrast, lung window) in a 53-year-old female patient with fixed tracheal stenosis at the level of maximum observed tracheal narrowing at representative selected time points of the respiratory cycle. The upper row shows axial view, the lower row sagittal view. No dynamic changes were observed. (B) Graph shows the changes of minimal tracheal lumen area, tracheal volume, and lung volume of the same patient over the respiratory cycle with 21 time points in 5%-wide steps at 4D CT. (C) Image from correlated bronchoscopy.

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