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DOI 10.1080/21678421.2024.2434174

Медицинская библиотека · Amyotrophic lateral sclerosis & frontotemporal degeneration · 2024

Thoracic electrical impedance tomography for assessing progression of pulmonary dysfunction in ALS.

Rutkove Seward B, McIlduff Courtney E, Stommel Elijah, Levy Sean, Smith Christy, Gutierrez Hilda, Verga Sarah, Samaan Soleil, Yator Chebet, Nanda Ajitesh, Sonbas-Cobb Buket, Capella Teresa, Pastel Lisa, Doussan Allaire, Phipps Kathy, Murphy Ethan, Halter Ryan

СтатьяПоддержка NIH: внешняя программаПеревод пока не подготовлен

Аннотация

Objective

We compared thoracic electrical impedance tomography (EIT) with slow vital capacity (SVC) to determine if EIT could monitor pulmonary function in ALS patients longitudinally.

Methods

Of 32 ALS patients and 32 age- and sex-matched healthy controls (HCs) initially enrolled in the Pulmonary Function via Impedance Tomography (PuFIT) study, 22 ALS and 20 HCs returned for a follow-up visit ∼3.9 months later. All participants had thoracic EIT measurements performed simultaneously with standard SVC in upright and supine positions at both visits. EIT data from each measurement were summarized as a single parameter, the impedance-SVC (zSVC), representing an averaged impedance change across both lungs. We assessed alterations over time for both cohorts of participants.

Results

Sufficient quality EIT and SVC data were available for 18 of the patients with ALS and 19 HCs. Over time, mean upright SVC significantly declined by 5% in the ALS group and did not change in the healthy group. Supine SVC showed no change in either group. Although mean trajectories of zSVC mirrored mean SVC trajectories in both participant cohorts, changes in zSVC in ALS patients did not reach significance, due to greater variability in the repeated measures.

Conclusion

Despite strong cross-sectional correlations to SVC, EIT did not detect a decline in pulmonary function over approximately four months. Increased variability in EIT data explains the lack of sensitivity to change. Technological improvements and special care with electrode placement will be needed for EIT to reach its full potential in longitudinal assessment of pulmonary function in ALS.

Для цитирования: Rutkove Seward B, McIlduff Courtney E, Stommel Elijah, Levy Sean, Smith Christy, Gutierrez Hilda, Verga Sarah, Samaan Soleil, Yator Chebet, Nanda Ajitesh, Sonbas-Cobb Buket, Capella Teresa, Pastel Lisa, Doussan Allaire, Phipps Kathy, Murphy Ethan, Halter Ryan. Thoracic electrical impedance tomography for assessing progression of pulmonary dysfunction in ALS.. Amyotrophic lateral sclerosis & frontotemporal degeneration. 2024. DOI: 10.1080/21678421.2024.2434174.

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