Evidence map›Paper›PMID 38870103›Full record

ArticlePloS one2024

The REPERFUSE study protocol: The effects of vasopressor therapy on renal perfusion in patients with septic shock-A mechanistically focused randomised control trial.

Rory McDonald, James Watchorn, Reena Mehta, Marlies Ostermann, Sam Hutchings

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06234592 (The Effect of Vasopressor Therapy on Renal Perfusion in Patients With Septic Shock - a Mechanistically Focussed Randomized Control Study), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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.

NCT06234592 narecruitingnot on this map

The Effect of Vasopressor Therapy on Renal Perfusion in Patients With Septic Shock - a Mechanistically Focussed Randomized Control Study

TypeinterventionalSponsorKing's College Hospital NHS TrustRan2024 to 2026Enrolled45ConditionsSeptic Shock, Acute Kidney InjuryArmsAngiotensin II, Vasopressin, Norepinephrine
3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. New Kidneys Do Not Tolerate Hypotension.Anesthesiology open · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Review
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

5 authors.

Rory McDonaldDepartment of Inflammation Biology, School of Immunology and Microbial Sciences, King's College London, London, United Kingdom.ORCID 0009-0005-4241-5065
James WatchornAcademic Department of Anaesthesia and Critical Care, Royal Centre for Defence Medicine, Birmingham, United Kingdom.
Reena MehtaDepartment of Critical Care, King's College Hospital, London, United Kingdom.ORCID 0000-0001-6517-7403
Marlies OstermannDepartment of Inflammation Biology, School of Immunology and Microbial Sciences, King's College London, London, United Kingdom.ORCID 0000-0001-9500-9080
Sam HutchingsDepartment of Inflammation Biology, School of Immunology and Microbial Sciences, King's College London, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAcute kidney injury (AKI) is a common complication of septic shock and together these conditions carry a high mortality risk. In septic patients who develop severe AKI, renal cortical perfusion is deficient despite normal macrovascular organ blood flow. This intra-renal perfusion abnormality may be amenable to pharmacological manipulation, which may offer mechanistic insight into the pathophysiology of septic AKI. The aim of the current study is to investigate the effects of vasopressin and angiotensin II on renal microcirculatory perfusion in a cohort of patients with septic shock. METHODS AND ANALYSIS: In this single centre, mechanistically focussed, randomised controlled study, 45 patients with septic shock will be randomly allocated to either of the study vasopressors (vasopressin or angiotensin II) or standard therapy (norepinephrine). Infusions will be titrated to maintain a mean arterial pressure (MAP) target set by the attending clinician. Renal microcirculatory assessment will be performed for the cortex and medulla using contrast-enhanced ultrasound (CEUS) and urinary oxygen tension (pO2), respectively. Renal macrovascular flow will be assessed via renal artery ultrasound. Measurement of systemic macrovascular flow will be performed through transthoracic echocardiography (TTE) and microvascular flow via sublingual incident dark field (IDF) video microscopy. Measures will be taken at baseline, +1 and +24hrs following infusion of the study drug commencing. Blood and urine samples will also be collected at the measurement time points. Longitudinal data will be compared between groups and over time. DISCUSSION: Vasopressors are integral to the management of patients with septic shock. This study aims to further understanding of the relationship between this therapy, renal perfusion and the development of AKI. In addition, using CEUS and urinary pO2, we hope to build a more complete picture of renal perfusion in septic shock by interrogation of the constituent parts of the kidney. Results will be published in peer-reviewed journals and presented at academic meetings.

trial registrationThe REPERFUSE study was registered on Clinical Trials.gov (NCT06234592) on the 30th Jan 24.

Indexed as

Acute Kidney InjuryMicrocirculationShock, SepticVasoconstrictor AgentsAdultAngiotensin IIFemaleHumansKidneyMaleMiddle AgedNorepinephrineRenal CirculationVasopressinsAngiotensin IINorepinephrineVasoconstrictor AgentsVasopressins

Identifiers

PMID38870103
PMCPMC11175393

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.