Evidence mapPaperPMID 40729501Full record

ArticleShock (Augusta, Ga.)2026

Tissue Perfusion and Fluid Responsiveness Assessment in Critically Ill Patients. A Feasibility Pilot Study Using the Ikorus Urothelial Plethysmography Device (The Target-Up Study).

Adrian Wong, Rory McDonald, Nurul Liana Roslan, Kate Bramham, Sam Hutchings

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Article in Shock (Augusta, Ga.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Adrian WongDepartment of Critical Care King's College Hospital, London United Kingdom.ORCID 0000-0003-4968-7328
Rory McDonaldDepartment of Critical Care King's College Hospital, London United Kingdom.
Nurul Liana RoslanDepartment of Emergency Medicine, Kuala Lumpur Malaysia.
Kate BramhamSchool of Life Course and Population Sciences and School of Immunology and Microbial Science Faculty of Life Sciences and Medicine, King's College, London, United Kingdom.
Sam HutchingsDepartment of Critical Care King's College Hospital, London United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate assessment of tissue perfusion is challenging. Commonly used markers like lactate levels and central venous oxygen saturation are indirect, intermittent, and provide a global picture of circulatory status which may not reflect perfusion at the organ level. The Urethral Perfusion Index (UPi), measured through a specialized urinary catheter, is a novel technique that offers continuous, real-time monitoring of perfusion in a central tissue bed, potentially providing more immediate and targeted clinical information.

objectives1. The aims of the study were (1) to assess the correlation between changes to left ventricular outflow tract velocity time integral (LVOT VTi) and UPi following a fluid challenge and (2) To assess the relationship between UPi and other markers of tissue perfusion.

designInterventional, feasibility pilot study.

settingSingle-center, study conducted at a tertiary-level institution in the United Kingdom. All patients were mechanically ventilated adults, whom the primary clinical team thought would benefit from a fluid challenge.

interventionA fluid challenge (FC) was defined as a 250 mL bolus of crystalloid solution.

main outcome measuresFocused transthoracic echocardiogram measured LVOT VTi and UPi, measured before and after FC.

resultsThere were no reported complications associated with device use or insertion. Mean duration of data recorded was 19 h and the Signal Quality Index of the UPi trace was high (93%). There was a moderate positive correlation between the time matched values of UPi and LVOT VTi (Spearman r = 0.55, P  < 0.0001), R 2 value of 0.272. However, there was no discernible correlation seen between change in UPi and VTi following fluid (Spearman r = 0.24, P  = 0.14). Patients with below-average UPi at baseline had evidence of poorer systemic tissue perfusion, as measured by lactate concentration and capillary refill time, and received more vasoactive drugs.

conclusionUPi may be a marker of tissue perfusion in a diverse group of critically ill patients. With further evaluation it may, therefore, present a future therapeutic target. Although there is some relationship between LVOT VTi and UPi, it is not precise enough to be used as a marker of fluid responsiveness.

trial registrationLondon Southeast Research and Ethics Committee (22/LO/0911).

Indexed as

Critical IllnessFluid TherapyAdultAgedFeasibility StudiesFemaleHumansMaleMiddle AgedPilot ProjectsFluid challengePerfusion Indextissue perfusionUrethral Perfusion Index

Identifiers

PMID40729501
PMCPMC12757123

What Socratic holds

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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 Socratic graph.