Evidence map›Paper›PMID 37195623›Full record

Observational studyJournal of clinical monitoring and computing2023

Deviations in continuously monitored electrodermal activity before severe clinical complications: a clinical prospective observational explorative cohort study.

Andreas Ohrt Johansen, Jesper Mølgaard, Søren Straarup Rasmussen, Ying Gu, Katja Kjær Grønbæk, Helge B D Sørensen, Eske Kvanner Aasvang, Christian Sylvest Meyhoff

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Journal of clinical monitoring and computing, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 4 institutions in 1 country.

Andreas Ohrt JohansenDepartment of Anaesthesia and Intensive Care, Copenhagen University Hospital-Bispebjerg and Frederiksberg, Copenhagen, Denmark. andreasohrt93@gmail.com.ORCID 0000-0002-7391-9945
Jesper MølgaardDepartment of Anaesthesiology, Centre for Cancer and Organ Dysfunction, Copenhagen University Hospital-Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0003-2062-9570
Søren Straarup RasmussenDepartment of Health Technology, Technical University of Denmark, Kgs. Lyngby, Denmark.ORCID 0000-0002-6297-2871
Ying GuDepartment of Health Technology, Technical University of Denmark, Kgs. Lyngby, Denmark.ORCID 0000-0003-4220-8902
Katja Kjær GrønbækDepartment of Anaesthesia and Intensive Care, Copenhagen University Hospital-Bispebjerg and Frederiksberg, Copenhagen, Denmark.ORCID 0000-0003-3045-6909
Helge B D Sørensen *Department of Health Technology, Technical University of Denmark, Kgs. Lyngby, Denmark.ORCID 0000-0001-5716-7600
Eske Kvanner AasvangDepartment of Anaesthesiology, Centre for Cancer and Organ Dysfunction, Copenhagen University Hospital-Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0002-7131-2461
Christian Sylvest Meyhoff *Department of Anaesthesia and Intensive Care, Copenhagen University Hospital-Bispebjerg and Frederiksberg, Copenhagen, Denmark.ORCID 0000-0002-4885-4609
Technical University of Denmark · DKFrederiksberg Hospital · DKUniversity of Copenhagen · DKCopenhagen University Hospital · DK

Funding

Innovationsfonden 8056-00055BKræftens Bekæmpelse R150-A9865-16-S48
6 · The paper itself

Abstract

Monitoring of high-risk patients in hospital wards is crucial in identifying and preventing clinical deterioration. Sympathetic nervous system activity measured continuously and non-invasively by Electrodermal activity (EDA) may relate to complications, but the clinical use remains untested. The aim of this study was to explore associations between deviations of EDA and subsequent serious adverse events (SAE). Patients admitted to general wards after major abdominal cancer surgery or with acute exacerbation of chronic obstructive pulmonary disease were continuously EDA-monitored for up to 5 days. We used time-perspectives consisting of 1, 3, 6, and 12 h of data prior to first SAE or from start of monitoring. We constructed 648 different EDA-derived features to assess EDA. The primary outcome was any SAE and secondary outcomes were respiratory, infectious, and cardiovascular SAEs. Associations were evaluated using logistic regressions with adjustment for relevant confounders. We included 714 patients and found a total of 192 statistically significant associations between EDA-derived features and clinical outcomes. 79% of these associations were EDA-derived features of absolute and relative increases in EDA and 14% were EDA-derived features with normalized EDA above a threshold. The highest F1-scores for primary outcome with the four time-perspectives were 20.7-32.8%, with precision ranging 34.9-38.6%, recall 14.7-29.4%, and specificity 83.1-91.4%. We identified statistically significant associations between specific deviations of EDA and subsequent SAE, and patterns of EDA may be developed to be considered indicators of upcoming clinical deterioration in high-risk patients.

Indexed as

Clinical DeteriorationGalvanic Skin ResponseCohort StudiesHumansSympathetic Nervous SystemContinuous monitoringElectrodermal activityGalvanic skin responsePhysiological abnormalitiesVital signsWireless electronic devices

Identifiers

PMID37195623
PMCPMC10651525
OpenAlexW4376871514

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.