Multimodal Deep Learning for ARDS Detection

Abstract

Objective Poor outcomes in acute respiratory distress syndrome (ARDS) can be alleviated with tools that support early diagnosis. Current machine learning methods for detecting ARDS do not take full advantage of the multimodality of ARDS pathophysiology. We developed a multimodal deep learning model that uses imaging data, continuously collected ventilation data, and tabular data derived from a patient’s electronic health record (EHR) to make ARDS predictions.

Materials and Methods A chest radiograph (x-ray), at least two hours of ventilator waveform (VWD) data within the first 24 hours of intubation, and EHR-derived tabular data were used from 220 patients admitted to the ICU to train a deep learning model. The model uses pretrained encoders for the x-rays and ventilation data and trains a feature extractor on tabular data. Encoded features for a patient are combined to make a single ARDS prediction. Ablation studies for each modality assessed their effect on the model’s predictive capability.

Results The trimodal model achieved an area under the receiver operator curve (AUROC) of 0.86 with a 95% confidence interval of 0.01. This was a statistically significant improvement (p<0.05) over single modality models and bimodal models trained on VWD+tabular and VWD+x-ray data.

Discussion and Conclusion Our results demonstrate the potential utility of using deep learning to address complex conditions with heterogeneous data. More work is needed to determine the additive effect of modalities on ARDS detection. Our framework can serve as a blueprint for building performant multimodal deep learning models for conditions with small, heterogeneous datasets.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study was funded by NIH grant R01HL16351.

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:

IRB 647002-8 and IRB 19-28933 of the University of California Davis gave ethical approval for this work.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the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

Yes

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

Footnotes

sabroeckerucdavis.edu

jyadamshealth.ucdavis.edu

gkumucdavis.edu

racallcuthealth.ucdavis.edu

yuaniucdavis.edu

strohmermath.ucdavis.edu

1 for first 24 hours post first ICU admission

Data Availability

Data for this study are not publicly available.

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