AI Article Synopsis

  • The study evaluates the use of electrical impedance tomography (EIT) as a bedside tool to assess treatment effectiveness in hospitalized patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD).
  • EIT measurements showed significant improvements in regional lung function during hospitalization, while conventional spirometry metrics like forced vital capacity (FVC) and forced expiratory volume (FEV1) showed little significant change.
  • Overall, patients reported better symptom relief, and EIT parameters correlated well with these patient-reported outcomes, suggesting it could be a valuable tool for managing COPD in clinical settings.

Article Abstract

For patients with chronic obstructive pulmonary disease (COPD), the assessment of the treatment efficacy during hospitalization is of importance to the optimization of clinical treatments. Conventional spirometry might not be sensitive enough to capture the regional lung function development. The study aimed to evaluate the feasibility of using electrical impedance tomography (EIT) as an objective bedside evaluation tool for the treatment of acute exacerbation of COPD (AECOPD). Consecutive patients who required hospitalization due to AECOPD were included prospectively. EIT measurements were conducted at the time of admission and before the discharge simultaneously when a forced vital capacity maneuver was conducted. EIT-based heterogeneity measures of regional lung function were calculated based on the impedance changes over time. Surveys for attending doctors and patients were designed to evaluate the ease of use, feasibility, and overall satisfaction level to understand the acceptability of EIT measurements. Patient-reported outcome assessments were conducted. User's acceptance of EIT technology was investigated with a five-dimension survey. A total of 32 patients were included, and 8 patients were excluded due to the FVC maneuver not meeting the ATS criteria. Spirometry-based lung function was improved during hospitalization but not significantly different (FEV1 %pred.: 35.8% ± 6.7% vs. 45.3% ± 8.8% at admission vs. discharge; = 0.11. FVC %pred.: 67.8% ± 0.4% vs. 82.6% ± 5.0%; = 0.15. FEV1/FVC: 0.41 ± 0.09 vs. 0.42 ± 0.07, = 0.71). The symptoms of COPD were significantly improved, but the correlations between the improvement of symptoms and spirometry FEV1 and FEV1/FVC were low (R = 0.1 and -0.01, respectively). The differences in blood gasses and blood tests were insignificant. All but one EIT-based regional lung function parameter were significantly improved after hospitalization. The results highly correlated with the patient-reported outcome assessment (R > 0.6, < 0.001). The overall acceptability score of EIT measurement for both attending physicians and patients was high (4.1 ± 0.8 for physicians, 4.5 ± 0.5 for patients out of 5). These results demonstrated that it was feasible and acceptable to use EIT as an objective bedside evaluation tool for COPD treatment efficacy.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10982416PMC
http://dx.doi.org/10.3389/fphys.2024.1352391DOI Listing

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