Evidence map›Paper›PMID 27039298›Full record

Observational studyJournal of clinical monitoring and computing2017

Heart rate time series characteristics for early detection of infections in critically ill patients.

T Tambuyzer, F Guiza, E Boonen, P Meersseman, H Vervenne, T K Hansen, M Bjerre, G Van den Berghe, D Berckmans, J M Aerts and 1 more

Open access · greenAbstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Journal of clinical monitoring and computing, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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 2 institutions in 2 countries.

T TambuyzerDivision Animal and Human Health Engineering, Department of Biosystems, KU Leuven, Kasteelpark Arenberg 30, 3001, Louvain, Belgium.
F GuizaLaboratory of Intensive Care Medicine, Division Cellular and Molecular Medicine, Clinical Department, KU Leuven, Herestraat 49, 3000, Louvain, Belgium.
E BoonenLaboratory of Intensive Care Medicine, Division Cellular and Molecular Medicine, Clinical Department, KU Leuven, Herestraat 49, 3000, Louvain, Belgium.
P MeerssemanLaboratory of Intensive Care Medicine, Division Cellular and Molecular Medicine, Clinical Department, KU Leuven, Herestraat 49, 3000, Louvain, Belgium.
H VervenneLaboratory of Intensive Care Medicine, Division Cellular and Molecular Medicine, Clinical Department, KU Leuven, Herestraat 49, 3000, Louvain, Belgium.
T K HansenImmunoendocrine Research Unit, Medical Department M, Aarhus University Hospital, Norrebrogade 44, 8000, Aarhus C, Denmark.
M BjerreImmunoendocrine Research Unit, Medical Department M, Aarhus University Hospital, Norrebrogade 44, 8000, Aarhus C, Denmark.
G Van den BergheLaboratory of Intensive Care Medicine, Division Cellular and Molecular Medicine, Clinical Department, KU Leuven, Herestraat 49, 3000, Louvain, Belgium.
D BerckmansDivision Animal and Human Health Engineering, Department of Biosystems, KU Leuven, Kasteelpark Arenberg 30, 3001, Louvain, Belgium.
J M AertsDivision Animal and Human Health Engineering, Department of Biosystems, KU Leuven, Kasteelpark Arenberg 30, 3001, Louvain, Belgium. jean-marie.aerts@biw.kuleuven.be.
G MeyfroidtLaboratory of Intensive Care Medicine, Division Cellular and Molecular Medicine, Clinical Department, KU Leuven, Herestraat 49, 3000, Louvain, Belgium.
KU Leuven · BEAarhus University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is difficult to make a distinction between inflammation and infection. Therefore, new strategies are required to allow accurate detection of infection. Here, we hypothesize that we can distinguish infected from non-infected ICU patients based on dynamic features of serum cytokine concentrations and heart rate time series. Serum cytokine profiles and heart rate time series of 39 patients were available for this study. The serum concentration of ten cytokines were measured using blood sampled every 10 min between 2100 and 0600 hours. Heart rate was recorded every minute. Ten metrics were used to extract features from these time series to obtain an accurate classification of infected patients. The predictive power of the metrics derived from the heart rate time series was investigated using decision tree analysis. Finally, logistic regression methods were used to examine whether classification performance improved with inclusion of features derived from the cytokine time series. The AUC of a decision tree based on two heart rate features was 0.88. The model had good calibration with 0.09 Hosmer-Lemeshow p value. There was no significant additional value of adding static cytokine levels or cytokine time series information to the generated decision tree model. The results suggest that heart rate is a better marker for infection than information captured by cytokine time series when the exact stage of infection is not known. The predictive value of (expensive) biomarkers should always be weighed against the routinely monitored data, and such biomarkers have to demonstrate added value.

Indexed as

Critical IllnessHeart RateAdultAgedAged, 80 and overArea Under CurveBiomarkersCalibrationCritical CareCross InfectionCytokinesDecision TreesHumansIntensive Care UnitsMaleMiddle AgedBiomarkersCytokinesCytokinesHeart rateICUInfection monitoring

Identifiers

PMID27039298
OpenAlexW2325332565

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.