Evidence map›Paper›PMID 40469569›Full record

ArticleBiochemia medica2025

Evaluation of the impact of reducing fasting hours on laboratory results in a mediterranean population.

Gemma Solé-Enrech, Ruth Cano-Corres, Raquel Escribano-Tembleque, Eva Martínez-Sevilla, Núria Busquets-Carmona, Carlos García-Miralles

Abstract read
In one paragraph

Article in Biochemia medica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Gemma Solé-EnrechClinical laboratory, Biochemistry Department, Parc Taulí Research and Innovation Institute Foundation (I3PT), Sabadell, Spain.
Ruth Cano-CorresClinical laboratory, Biochemistry Department, Parc Taulí Research and Innovation Institute Foundation (I3PT), Sabadell, Spain.
Raquel Escribano-TemblequeClinical laboratory, Biochemistry Department, Parc Taulí Research and Innovation Institute Foundation (I3PT), Sabadell, Spain.
Eva Martínez-SevillaClinical laboratory, Biochemistry Department, Parc Taulí Research and Innovation Institute Foundation (I3PT), Sabadell, Spain.
Núria Busquets-CarmonaClinical laboratory, Biochemistry Department, Parc Taulí Research and Innovation Institute Foundation (I3PT), Sabadell, Spain.
Carlos García-MirallesClinical laboratory, Biochemistry Department, Parc Taulí Research and Innovation Institute Foundation (I3PT), Sabadell, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: One of the critical points of the preanalytical phase is the patient's adherence to the required fasting duration before undergoing medical analysis. Although many laboratories have already protocols for blood-sample collection that require only a 6-hour fast, clinical guidelines remain unclear on this aspect, and fasting periods of 12 hours are sometimes still recommended. The aim of this study was to evaluate whether there are significant differences between the results obtained in patients' serum samples obtained post-fasting, 4 hours post-meal, and 6 hours post-meal for different predetermined parameters. Materials and methods: 30 volunteers (16 females and 14 males) aged between 23 and 62 years were selected for this study. Each participant underwent an initial analysis after a 10-hour fast (baseline), a second analysis 4 hours after a controlled meal, and a third analysis 6 hours after the meal. The parameters studied correspond to previously selected biochemical, hematological, and coagulation tests. To assess if there are significant differences in the results obtained for each analyte, criteria based on the total allowable error (TEa) and the reference change value (RCV) were used. Results: All parameters evaluated in this study met the criteria based on the RCV at both 4 and 6 hours, although some parameters did not meet TEa criteria. Conclusions: The results obtained in this study demonstrated that a fasting period of 4 or 6 hours is sufficient to obtain reliable results. This could significantly improve the quality of life for patients undergoing analysis without compromising the quality of their results.

Indexed as

Blood Specimen CollectionFastingAdultFemaleHumansMaleMediterranean RegionMiddle AgedTime FactorsYoung Adultfasting hourspreanalytical phasevenous blood sampling

Identifiers

PMID40469569
PMCPMC12131384

What Socratic 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 Socratic graph.