Post Induction Hypotension prediction during general anesthesia using Machine Learning Techniques

Abstract

Background Intraoperative hypotension burden not equally distributed during various periods of a general anesthetic. Post-induction hypotension usually has an iatrogenic cause and is related to the combination of drug doses used for induction of anesthesia. Predicting post-induction blood pressures, prior to induction, may inform anesthesiologists on the most judicious selection of anesthetic drugs and dosages. Our objective was to explore patterns of post-induction hypotension, apply machine learning (ML) to predict the mean blood pressure (MBP) immediately after induction, and develop a prototype of a clinical tool that can implement the ML model.

Materials and Methods We extracted data from preoperative and intraoperative anesthetic episodes over an 8-year period at the University of Pittsburgh Medical Center. The dataset consisted of 93,037 anesthetic episodes, which was partitioned into training, validation, and test sets. Preoperative and pre-induction predictor variables included demographics, comorbidities, laboratory test values, pre-induction MBP, and administrations of induction drugs. The target consisted of 15 minutes of MBP values immediately after induction.

Results The best-performing model was extreme-gradient boosted trees (XGB), with an R-squared value of 0.31 and a mean absolute error of 11.96, which is a moderately good performance. The performance of the model decreased over each minute post-induction.

Conclusion ML modeling to predict post-induction MBP is feasible, and a clinical tool that incorporates ML can potentially aid in preventing hypotension in the operating room.

Competing Interest Statement

Shyam Visweswaran and Harikesh Subramanian have an invention disclosure related to the work described in this manuscript

Funding Statement

This research was supported in part by the University of Pittsburgh Center for Research Computing through the resources provided. Specifically, this work used the HTC cluster, which is supported by NIH award number S10OD028483.

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 of University of Pittsburgh waived 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

Data Availability

All data produced in the present study are available upon reasonable request to the authors after IRB review

Comments (0)

No login
gif