Evidence map›Paper›PMID 42652061›Full record

ReviewBiomedicines2026

Cellular and Molecular Mechanisms of Hemorrhagic Shock: Biological Rationale for Individualized Fluid Resuscitation Strategies and Multimodal Monitoring.

Stelian Adrian Ritiu, Sonia Elena Popovici, Marius Papurica, Dorel Sandesc, Adelina Baloi, Daiana Toma, Norbert Wellmann, Petru Bucuras, Claudiu Rafael Barsac, Ovidiu Bedreag

Abstract readReview
In one paragraph

Review in Biomedicines, 2026. 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
–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

0 citing papers in PubMed.

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

10 authors.

Stelian Adrian RitiuDoctoral School, Victor Babes University of Medicine and Pharmacy, 300041 Timisoara, Romania.ORCID 0000-0002-8751-6813
Sonia Elena PopoviciDoctoral School, Victor Babes University of Medicine and Pharmacy, 300041 Timisoara, Romania.ORCID 0000-0001-5195-3993
Marius PapuricaFaculty of Medicine, Victor Babes University of Medicine and Pharmacy, 300041 Timisoara, Romania.ORCID 0000-0002-4065-3650
Dorel SandescFaculty of Medicine, Victor Babes University of Medicine and Pharmacy, 300041 Timisoara, Romania.
Adelina BaloiDoctoral School, Victor Babes University of Medicine and Pharmacy, 300041 Timisoara, Romania.
Daiana TomaDoctoral School, Victor Babes University of Medicine and Pharmacy, 300041 Timisoara, Romania.ORCID 0009-0007-1034-923X
Norbert WellmannPulmonology University Clinic, Clinical Hospital of Infectious Diseases and Pneumophthisiology Dr. Victor Babeș, 300310 Timisoara, Romania.ORCID 0009-0004-0749-8232
Petru BucurasAnaesthesia and Intensive Care Research Center Timisoara, Victor Babes University of Medicine and Pharmacy, 300041 Timisoara, Romania.
Claudiu Rafael BarsacDoctoral School, Victor Babes University of Medicine and Pharmacy, 300041 Timisoara, Romania.ORCID 0000-0001-7591-7241
Ovidiu BedreagFaculty of Medicine, Victor Babes University of Medicine and Pharmacy, 300041 Timisoara, Romania.ORCID 0000-0002-3432-9168

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemorrhagic shock is a leading cause of preventable death following multiple trauma, driven by a cascade of interacting cellular and molecular disturbances that extend well beyond simple volume loss. Acute blood loss initiates tissue hypoperfusion and cellular hypoxia, setting in motion the lethal triad of hypothermia, acidosis, and coagulopathy through several converging pathways: complement activation with excessive C3a and C5a production; neutrophil-mediated tissue injury; NADPH-oxidase-driven reactive oxygen species (ROS) overproduction that overwhelms superoxide dismutase defenses; mitochondrial respiratory chain impairment; dysregulation of the pro-inflammatory cytokine network; and endothelial apoptosis with degradation of the endothelial glycocalyx and disruption of interendothelial junctions, with consequent vascular hyperpermeability. These mechanisms provide the biological rationale for the resuscitation strategy. Each class of fluid acts on these pathways in a distinct way: crystalloids modulate acid-base homeostasis, chloride-mediated renal vasoconstriction, and coagulation factor activity; colloids influence oncotic pressure, endothelial integrity, and microvascular perfusion; and blood products, particularly plasma and whole blood, actively modulate mitochondrial metabolism, endothelial permeability, and pro-apoptotic signaling beyond their volume-expanding role. Translating this biology to the bedside requires a multimodal monitoring framework that converts molecular endpoints into real-time therapeutic targets, integrating lactate and base excess as markers of cellular oxygen debt, dynamic preload indices such as pulse pressure and stroke volume variation, advanced hemodynamic platforms, point-of-care ultrasonography, viscoelastic coagulation testing, and near-infrared spectroscopy of tissue oxygenation. This review synthesizes the biological basis of hemorrhagic shock and its translation into an individualized, goal-directed resuscitation strategy for the critically ill polytrauma patient.

Indexed as

cellular mechanismsfluid resuscitationglycocalyxhemorrhagic shockmultimodal monitoringoxidative stresstraumatrauma-induced coagulopathy

Identifiers

PMID42652061
PMCPMC13509298

What OpenQuestion holds

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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.