Evidence map›Paper›PMID 33999297›Full record

ReviewAnnals of intensive care2021

The autonomic nervous system in septic shock and its role as a future therapeutic target: a narrative review.

Marta Carrara, Manuela Ferrario, Bernardo Bollen Pinto, Antoine Herpain

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Annals of intensive care, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07470775 (A Prospective Study on the Effects of Early Dexmedetomidine Administration on Sympathetic Nervous System Activity, Pathophysiological Mechanisms, and Clinical Outcomes in Sepsis), which is not on this map. Cited by 67 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 2 pooled it
10.7field-weighted citation impact, top 1% 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.

NCT07470775 phase4not yet recruitingnot on this mapstarted 2026, after this paper: background citation

A Prospective Study on the Effects of Early Dexmedetomidine Administration on Sympathetic Nervous System Activity, Pathophysiological Mechanisms, and Clinical Outcomes in Sepsis

TypeinterventionalSponsorSichuan Academy of Medical SciencesRan2026 to 2028Enrolled168ConditionsSepsis, Septic ShockArmsDexmedetomidine (DEX), Placebo
3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 2 syntheses or guidelines pooled it, 104 citations in OpenAlex.

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  10. Vasopressor Strategy in Pediatric Sepsis: A Clinical Pharmacology Perspective.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2026
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7 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 4 countries.

Marta Carrara *Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milan, Italy.
Manuela Ferrario *Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milan, Italy. manuela.ferrario@polimi.it.ORCID http://orcid.org/0000-0001-7371-3624
Bernardo Bollen PintoDepartment of Acute Medicine, Geneva University Hospitals, Geneve, Switzerland.
Antoine HerpainDepartment of Intensive Care, Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Politecnico di Milano · ITUniversité Libre de Bruxelles · BEUniversity of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The autonomic nervous system (ANS) regulates the cardiovascular system. A growing body of experimental and clinical evidence confirms significant dysfunction of this regulation during sepsis and septic shock. Clinical guidelines do not currently include any evaluation of ANS function during the resuscitation phase of septic shock despite the fact that the severity and persistence of ANS dysfunction are correlated with worse clinical outcomes. In the critical care setting, the clinical use of ANS-related hemodynamic indices is currently limited to preliminary investigations trying to predict and anticipate imminent clinical deterioration. In this review, we discuss the evidence supporting the concept that, in septic shock, restoration of ANS-mediated control of the cardiovascular system or alleviation of the clinical consequences induced by its dysfunction (e.g., excessive tachycardia, etc.), may be an important therapeutic goal, in combination with traditional resuscitation targets. Recent studies, which have used standard and advanced monitoring methods and mathematical models to investigate the ANS-mediated mechanisms of physiological regulation, have shown the feasibility and importance of monitoring ANS hemodynamic indices at the bedside, based on the acquisition of simple signals, such as heart rate and arterial blood pressure fluctuations. During the early phase of septic shock, experimental and/or clinical studies have shown the efficacy of negative-chronotropic agents (i.e., beta-blockers or ivabradine) in controlling persistent tachycardia despite adequate resuscitation. Central α-2 agonists have been shown to prevent peripheral adrenergic receptor desensitization by reducing catecholamine exposure. Whether these new therapeutic approaches can safely improve clinical outcomes remains to be confirmed in larger clinical trials. New technological solutions are now available to non-invasively modulate ANS outflow, such as transcutaneous vagal stimulation, with initial pre-clinical studies showing promising results and paving the way for ANS modulation to be considered as a new potential therapeutic target in patients with septic shock.

Indexed as

Autonomic dysfunctionAutonomic nervous systemBaroreflexDesensitizationDysautonomiaSepsisSeptic shockSympathetic overstimulationTachycardiaVagal stimulation

Identifiers

PMID33999297
PMCPMC8128952
OpenAlexW3162635100

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.