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Original research
Workflow improvements from automated large vessel occlusion detection algorithms are dependent on care team engagement
  1. Emmanuel C Ebirim1,
  2. Ngoc Mai Le2,
  3. Joseph N Samaha2,
  4. Hussain Azeem2,
  5. Ananya Iyyangar2,
  6. Anjan N Ballekere2,
  7. Saagar Dhanjani3,
  8. Luca Giancardo4,
  9. Eunyoung Lee2,
  10. Sunil A Sheth2
  1. 1The University of Texas Medical Branch at Galveston, Galveston, Texas, USA
  2. 2Department of Neurology, UTHealth Houston McGovern Medical School, Houston, Texas, USA
  3. 3Rice University, Houston, Texas, USA
  4. 4McWilliams School of Biomedical Informatics at UTHealth Houston, Houston, Texas, USA
  1. Correspondence to Dr Sunil A Sheth; Sunil.A.Sheth{at}uth.tmc.edu

Abstract

Background Automated machine learning (ML)‐based large vessel occlusion (LVO) detection algorithms have been shown to improve in‐hospital workflow metrics including door-to-groin time (DTG). The degree to which care team engagement and interaction are required for these benefits remains incompletely characterized.

Methods This analysis was conducted as a pre‐planned post-hoc analysis of a randomized prospective clinical trial. ML‐based LVO detection software was implemented at four comprehensive stroke centers (CSCs) from January 1, 2021, to February 27, 2022. Patients were included if they underwent endovascular thrombectomy for LVO acute ischemic stroke. ML software utilization was quantified as the total number of active users and the ratio of the number of comments to the number of patients analyzed by the software by site per week. Primary outcome was the reduction in DTG relative to pre‐ML implementation by hospital utilization level. Data are expressed as median (IQR).

Results Among 101 patients who met the inclusion criteria, the median age was 71 years (IQR 59–79), with 48.5% being female. CSC 4 had the greatest number of total active users per week (32.5 (27.5–34.5)), and comment-to-patient ratio per week (5.8 (4.6–6.9)). Increased ML software utilization was associated with improvements in DTG reduction. For every 1 unit increase in the comment-to-patient ratio, DTG time decreased by 2.6 (95% CI −5.09 to –0.13) min, while accounting for site-level random effects. Number of users-to-patient was not associated with a reduction in DTG time (β=−0.22, 95% CI −1.78 to 1.33).

Conclusions In this post-hoc analysis, user engagement with software, rather than total number of users, was associated with site-specific improvements in DTG time.

  • Stroke
  • Thrombectomy
  • Technology
  • CT Angiography

Data availability statement

Data are available upon reasonable request.

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Data availability statement

Data are available upon reasonable request.

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Footnotes

  • Contributors ECE contributed to drafting the manuscript. NML was responsible for data analysis and drafting the manuscript. JS, HA, SD and ANB contributed to drafting the manuscript, with ASI and ANB also collecting data. LG and SAS were involved in drafting the manuscript and collecting data, while EL contributed to data analysis and drafting the manuscript. SAS also conceptualized and designed the study, supervised the research, and serves as the guarantor.

  • Funding Foundation for the National Institutes of Health - 1R01NS138765.

  • Competing interests SAS reports funding from the National Institutes of Health as well as consultancy fees from Penumbra, Viz.AI and Imperative Care for unrelated topics.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.