Evidence map›Paper›PMID 38559667›Full record

ArticleBiomedical signal processing and control2024

Parsimonious Waveform-derived Features consisting of Pulse Arrival Time and Heart Rate Variability Predicts the Onset of Septic Shock.

Moamen M Soliman, Curtis Marshall, Jacob P Kimball, Tilendra Choudhary, Gilles Clermont, Michael R Pinsky, Timothy G Buchman, Craig M Coopersmith, Omer T Inan, Rishikesan Kamaleswaran

Abstract read
In one paragraph

Article in Biomedical signal processing and control, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Observational
  4. Review
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

10 authors.

Moamen M SolimanSchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, 30332, GA, USA.
Curtis MarshallDepartment of Biomedical Informatics, Emory University School of Medicine, Atlanta, 30322, GA, USA.
Jacob P KimballSchool of Biomedical and Electrical Engineering, University of Portland, Portland, 97203, OR, USA.
Tilendra ChoudharyDepartment of Biomedical Informatics, Emory University School of Medicine, Atlanta, 30322, GA, USA.
Gilles ClermontSchool of Medicine, University of Pittsburgh, Pittsburgh, 15213, PA, USA.
Michael R PinskySchool of Medicine, University of Pittsburgh, Pittsburgh, 15213, PA, USA.
Timothy G BuchmanDepartment of Surgery and Emory Critical Care Center, Emory University School of Medicine, Atlanta, 30322, GA, USA.
Craig M CoopersmithDepartment of Surgery and Emory Critical Care Center, Emory University School of Medicine, Atlanta, 30322, GA, USA.
Omer T InanSchool of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, 30332, GA, USA.
Rishikesan KamaleswaranThe Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, 30332, GA, USA.

Funding

Mechanisms of Intestinal Integrity in Sepsis and ShockR01GM072808 · NIGMS · WASHINGTON UNIVERSITY · PI COOPERSMITH, CRAIG M · 2005 to 2021
$5.1M
Sepsis Physiomarkers for Appropriate Risk Knowledge of monitored patients in the ICU (SPARK-ICU)R01GM139967 · NIGMS · EMORY UNIVERSITY · PI KAMALESWARAN, RISHIKESAN · 2021 to 2025
$2.8M
The Impact of Chronic Alcohol Abuse on the Pathophysiology of SepsisR01AA027396 · NIAAA · EMORY UNIVERSITY · PI Craig M Coopersmith, Mandy L Ford · 2019 to 2026
$2.8M
The Impact of Cancer on the Pathophysiology of SepsisR01GM104323 · NIGMS · EMORY UNIVERSITY · PI COOPERSMITH, CRAIG M, FORD, MANDY L · 2013 to 2021
$2.4M
The Gut as a Target to Improve Outcomes in SepsisR35GM148217 · NIGMS · EMORY UNIVERSITY · PI Craig M Coopersmith · 2023 to 2026
$2.2M
NIAAA NIH HHS R01 AA027396NIGMS NIH HHS R01 GM072808NIGMS NIH HHS R01 GM104323NIGMS NIH HHS R01 GM139967NIGMS NIH HHS R35 GM148217
6 · The paper itself

Abstract

Sepsis is a major public health emergency and one of the leading causes of morbidity and mortality in critically ill patients. For each hour treatment is delayed, shock-related mortality increases, so early diagnosis and intervention is of utmost importance. However, earlier recognition of shock requires active monitoring, which may be delayed due to subclinical manifestations of the disease at the early phase of onset. Machine learning systems can increase timely detection of shock onset by exploiting complex interactions among continuous physiological waveforms. We use a dataset consisting of high-resolution physiological waveforms from intensive care unit (ICU) of a tertiary hospital system. We investigate the use of mean arterial blood pressure (MAP), pulse arrival time (PAT), heart rate variability (HRV), and heart rate (HR) for the early prediction of shock onset. Using only five minutes of the aforementioned vital signals from 239 ICU patients, our developed models can accurately predict septic shock onset 6 to 36 hours prior to clinical recognition with area under the receiver operating characteristic (AUROC) of 0.84 and 0.8 respectively. This work lays foundations for a robust, efficient, accurate and early prediction of septic shock onset which may help clinicians in their decision-making processes. This study introduces machine learning models that provide fast and accurate predictions of septic shock onset times up to 36 hours in advance. BP, PAT and HR dynamics can independently predict septic shock onset with a look-back period of only 5 mins.

Indexed as

Early warning scoreFast sepsis detectionIntensive care unitMachine learning for SepsisSeptic shock prediction

Identifiers

PMID38559667
PMCPMC10977921

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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.