Evidence map›Paper›PMID 38278825›Full record

ArticleScientific reports2024

Improving the precision of shock resuscitation by predicting fluid responsiveness with machine learning and arterial blood pressure waveform data.

Chitrabhanu B Gupta, Debraj Basu, Timothy K Williams, Lucas P Neff, Michael A Johnson, Nathan T Patel, Aravindh S Ganapathy, Magan R Lane, Fatemeh Radaei, Chen-Nee Chuah and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.4field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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  4. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Chitrabhanu B Gupta *Department of Electrical and Computer Engineering, University of California Davis, Davis, CA, USA.
Debraj Basu *Department of Electrical and Computer Engineering, University of California Davis, Davis, CA, USA.
Timothy K WilliamsDepartment of Vascular and Endovascular Surgery, Wake Forest University, Winston-Salem, NC, USA.
Lucas P NeffDepartment of General Surgery, Wake Forest University, Winston-Salem, NC, USA.
Michael A JohnsonDepartment of Emergency Medicine, University of Utah, Salt Lake City, UT, USA.
Nathan T PatelDepartment of General Surgery, Wake Forest University, Winston-Salem, NC, USA.
Aravindh S GanapathyDepartment of General Surgery, Wake Forest University, Winston-Salem, NC, USA.
Magan R LaneDepartment of General Surgery, Wake Forest University, Winston-Salem, NC, USA.
Fatemeh RadaeiMeta Platforms, Inc., Menlo Park, CA, USA.
Chen-Nee ChuahDepartment of Electrical and Computer Engineering, University of California Davis, Davis, CA, USA.
Jason Y AdamsDivision of Pulmonary, Critical Care, and Sleep Medicine, University of California Davis, 4150 V Street, Suite 3400, Sacramento, CA, 95817, USA. jyadams@ucdavis.edu.
Wake Forest University · USUniversity of California, Davis · USMeta (United States) · USUniversity of Utah · USWells Fargo (United States) · US

Funding

U.S. Department of Defense W81XWH-18-0072
6 · The paper itself

Abstract

Fluid bolus therapy (FBT) is fundamental to the management of circulatory shock in critical care but balancing the benefits and toxicities of FBT has proven challenging in individual patients. Improved predictors of the hemodynamic response to a fluid bolus, commonly referred to as a fluid challenge, are needed to limit non-beneficial fluid administration and to enable automated clinical decision support and patient-specific precision critical care management. In this study we retrospectively analyzed data from 394 fluid boluses from 58 pigs subjected to either hemorrhagic or distributive shock. All animals had continuous blood pressure and cardiac output monitored throughout the study. Using this data, we developed a machine learning (ML) model to predict the hemodynamic response to a fluid challenge using only arterial blood pressure waveform data as the input. A Random Forest binary classifier referred to as the ML fluid responsiveness algorithm (MLFRA) was trained to detect fluid responsiveness (FR), defined as a ≥ 15% change in cardiac stroke volume after a fluid challenge. We then compared its performance to pulse pressure variation, a commonly used metric of FR. Model performance was assessed using the area under the receiver operating characteristic curve (AUROC), confusion matrix metrics, and calibration curves plotting predicted probabilities against observed outcomes. Across multiple train/test splits and feature selection methods designed to assess performance in the setting of small sample size conditions typical of large animal experiments, the MLFRA achieved an average AUROC, recall (sensitivity), specificity, and precision of 0.82, 0.86, 0.62. and 0.76, respectively. In the same datasets, pulse pressure variation had an AUROC, recall, specificity, and precision of 0.73, 0.91, 0.49, and 0.71, respectively. The MLFRA was generally well-calibrated across its range of predicted probabilities and appeared to perform equally well across physiologic conditions. These results suggest that ML, using only inputs from arterial blood pressure monitoring, may substantially improve the accuracy of predicting FR compared to the use of pulse pressure variation. If generalizable, these methods may enable more effective, automated precision management of critically ill patients with circulatory shock.

Indexed as

Arterial PressureShockAnimalsBlood PressureCardiac OutputHemodynamicsHumansRespiration, ArtificialResuscitationRetrospective StudiesROC CurveStroke VolumeSwine

Identifiers

PMID38278825
PMCPMC10817926
OpenAlexW4391262634

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.