Spirometry parameter prediction using Acoustic characteristics of Cough

Abstract

Spirometry evaluates lung function by measuring airflow post-maximal inspiration, using parameters like FEV1, FVC, and the FEV1/FVC ratio for respiratory disease classification and severity monitoring. Cough, by inducing intrathoracic pressure changes, reflects respiratory pathology, impacting airflow velocities and cough sound properties. A correlation exists between spirometry values representing air flow-volume properties and acoustic features of cough sounds. The present study explores the correlation between cough sounds and spirometry values (FEV1, FVC, and FEV1/FVC ratio) for assessing respiratory health. Utilizing machine learning models, trained on cough sound data labelled with corresponding spirometry pathologies, the research demonstrates, ability of swaasa in predicting spirometry values. The regression algorithm for predicting spirometry parameters, yields optimal results with FEV1/FVC prediction showing 70.47% accuracy, 77.37% sensitivity, and 68.54% specificity. FVC prediction demonstrates 66.04% accuracy, 87% sensitivity, and 48.38% specificity. The study underscores the potential of AI-based cough sound analysis for detecting respiratory abnormalities, offering a promising avenue for diagnosis in resource-limited settings.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

CTRI/2021/04/032742

Funding Statement

This study is supported by Biotechnology Industry Research Assistance Council (BIRAC) [grant number - BT/BIPP1335/BIPP-49/20].

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study was registered under Clinical Trials Registry- India (CTRI/2021/04/032742) and was begun after getting the approval [Ethics Approval number - IRB Min. No. 13566 (DIAGNO)] from the CMC- IRB (Institutional Review Board).

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data availability statement

Due to the nature of this research, participants of this study did not agree for their data to be shared publicly. However, the detailed analysis can be shared by the author “NRS” upon reasonable request.

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