Evidence map›Paper›PMID 33266577›Full record

ArticleEntropy (Basel, Switzerland)2018

Model Selection for Body Temperature Signal Classification Using Both Amplitude and Ordinality-Based Entropy Measures.

David Cuesta-Frau, Pau Miró-Martínez, Sandra Oltra-Crespo, Jorge Jordán-Núñez, Borja Vargas, Paula González, Manuel Varela-Entrecanales

Abstract read
In one paragraph

Article in Entropy (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

7 authors.

David Cuesta-FrauTechnological Institute of Informatics, Universitat Politècnica de València, 03801 Alcoi Campus, Spain.ORCID 0000-0002-0076-0515
Pau Miró-MartínezDepartment of Statistics, Universitat Politècnica de València, 03801 Alcoi Campus, Spain.
Sandra Oltra-CrespoTechnological Institute of Informatics, Universitat Politècnica de València, 03801 Alcoi Campus, Spain.ORCID 0000-0003-1995-2557
Jorge Jordán-NúñezDepartment of Statistics, Universitat Politècnica de València, 03801 Alcoi Campus, Spain.ORCID 0000-0001-8178-9987
Borja VargasInternal Medicine Department, Teaching Hospital of Móstoles, 28935 Madrid, Spain.ORCID 0000-0002-5553-8372
Paula GonzálezInternal Medicine Department, Teaching Hospital of Móstoles, 28935 Madrid, Spain.
Manuel Varela-EntrecanalesInternal Medicine Department, Teaching Hospital of Móstoles, 28935 Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many entropy-related methods for signal classification have been proposed and exploited successfully in the last several decades. However, it is sometimes difficult to find the optimal measure and the optimal parameter configuration for a specific purpose or context. Suboptimal settings may therefore produce subpar results and not even reach the desired level of significance. In order to increase the signal classification accuracy in these suboptimal situations, this paper proposes statistical models created with uncorrelated measures that exploit the possible synergies between them. The methods employed are permutation entropy (PE), approximate entropy (ApEn), and sample entropy (SampEn). Since PE is based on subpattern ordinal differences, whereas ApEn and SampEn are based on subpattern amplitude differences, we hypothesized that a combination of PE with another method would enhance the individual performance of any of them. The dataset was composed of body temperature records, for which we did not obtain a classification accuracy above 80% with a single measure, in this study or even in previous studies. The results confirmed that the classification accuracy rose up to 90% when combining PE and ApEn with a logistic model.

Indexed as

approximate entropybody temperaturelogistic regressionpermutation entropysample entropysignal classification

Identifiers

PMID33266577
PMCPMC7512415

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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.