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Early detection of oliguric events in critically ill patients in the ICU with a novel continuous urine flow measurement device: results of an initial validation study

Objectives: Urine output is used to evaluate fluid status and is an important marker for acute kidney injury (AKI). Our primary aim was to validate a new automatic urine output monitoring device by comparison to the current practice – the standard urometer. Methods: We conducted a prospective observ...

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Autores principales: Fishman, Guy, Ram, Eilon, Gorfil, Dan, Kassif, Yigal, David, Rachel, Hershko, Tzlil, Malbrain, Manu L.N.G., Singer, Pierre, Sessler, Daniel I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080177/
https://www.ncbi.nlm.nih.gov/pubmed/37027058
http://dx.doi.org/10.1007/s10877-023-00991-w
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author Fishman, Guy
Ram, Eilon
Gorfil, Dan
Kassif, Yigal
David, Rachel
Hershko, Tzlil
Malbrain, Manu L.N.G.
Singer, Pierre
Sessler, Daniel I.
author_facet Fishman, Guy
Ram, Eilon
Gorfil, Dan
Kassif, Yigal
David, Rachel
Hershko, Tzlil
Malbrain, Manu L.N.G.
Singer, Pierre
Sessler, Daniel I.
author_sort Fishman, Guy
collection PubMed
description Objectives: Urine output is used to evaluate fluid status and is an important marker for acute kidney injury (AKI). Our primary aim was to validate a new automatic urine output monitoring device by comparison to the current practice – the standard urometer. Methods: We conducted a prospective observational study in three ICUs. Urine flow measurements by Serenno Medical Automatic urine output measuring device (Serenno Medical, Yokneam, Israel) were compared to standard urometer readings taken automatically at 5-minutes intervals by a camera, and to hourly urometer readings by the nurses, both over 1 to 7 days. Our primary outcome was the difference between urine flow assessed by the Serenno device and reference camera-derived measurements (Camera). Our secondary outcome was the difference between urine flow assessed by the Serenno device and hourly nursing assessments (Nurse), and detection of oliguria. Results: Thirty-seven patients completed the study, with 1,306 h of recording and a median of 25 measurement hours per patient. Bland and Altman analysis comparing the study device to camera measurements demonstrated good agreement, with a bias of -0.4 ml/h and 95% confidence intervals ranging from − 28 to 27ml/h. Concordance was 92%. The correlation between Camera and hourly nursing assessment of urine output was distinctly worse with a bias of 7.2 ml and limits of agreement extending from − 75 to + 107 ml. Severe oliguria (urine output < 0.3 ml/kg/h) lasting 2 h or more was common and observed in 8 (21%) of patients. Among the severe oliguric events lasting more than 3 consecutive hours, 6 (41%) were not detected or documented by the nursing staff. There were no device-related complications. Conclusion: The Serenno Medical Automatic urine output measuring device required minimal supervision, little ICU nursing staff attention, and is sufficiently accurate and precise. In addition to providing continuous assessments of urine output, it was considerably more accurate than hourly nursing assessments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10877-023-00991-w.
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spelling pubmed-100801772023-04-07 Early detection of oliguric events in critically ill patients in the ICU with a novel continuous urine flow measurement device: results of an initial validation study Fishman, Guy Ram, Eilon Gorfil, Dan Kassif, Yigal David, Rachel Hershko, Tzlil Malbrain, Manu L.N.G. Singer, Pierre Sessler, Daniel I. J Clin Monit Comput Original Research Objectives: Urine output is used to evaluate fluid status and is an important marker for acute kidney injury (AKI). Our primary aim was to validate a new automatic urine output monitoring device by comparison to the current practice – the standard urometer. Methods: We conducted a prospective observational study in three ICUs. Urine flow measurements by Serenno Medical Automatic urine output measuring device (Serenno Medical, Yokneam, Israel) were compared to standard urometer readings taken automatically at 5-minutes intervals by a camera, and to hourly urometer readings by the nurses, both over 1 to 7 days. Our primary outcome was the difference between urine flow assessed by the Serenno device and reference camera-derived measurements (Camera). Our secondary outcome was the difference between urine flow assessed by the Serenno device and hourly nursing assessments (Nurse), and detection of oliguria. Results: Thirty-seven patients completed the study, with 1,306 h of recording and a median of 25 measurement hours per patient. Bland and Altman analysis comparing the study device to camera measurements demonstrated good agreement, with a bias of -0.4 ml/h and 95% confidence intervals ranging from − 28 to 27ml/h. Concordance was 92%. The correlation between Camera and hourly nursing assessment of urine output was distinctly worse with a bias of 7.2 ml and limits of agreement extending from − 75 to + 107 ml. Severe oliguria (urine output < 0.3 ml/kg/h) lasting 2 h or more was common and observed in 8 (21%) of patients. Among the severe oliguric events lasting more than 3 consecutive hours, 6 (41%) were not detected or documented by the nursing staff. There were no device-related complications. Conclusion: The Serenno Medical Automatic urine output measuring device required minimal supervision, little ICU nursing staff attention, and is sufficiently accurate and precise. In addition to providing continuous assessments of urine output, it was considerably more accurate than hourly nursing assessments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10877-023-00991-w. Springer Netherlands 2023-04-07 /pmc/articles/PMC10080177/ /pubmed/37027058 http://dx.doi.org/10.1007/s10877-023-00991-w Text en © The Author(s), under exclusive licence to Springer Nature B.V. 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Research
Fishman, Guy
Ram, Eilon
Gorfil, Dan
Kassif, Yigal
David, Rachel
Hershko, Tzlil
Malbrain, Manu L.N.G.
Singer, Pierre
Sessler, Daniel I.
Early detection of oliguric events in critically ill patients in the ICU with a novel continuous urine flow measurement device: results of an initial validation study
title Early detection of oliguric events in critically ill patients in the ICU with a novel continuous urine flow measurement device: results of an initial validation study
title_full Early detection of oliguric events in critically ill patients in the ICU with a novel continuous urine flow measurement device: results of an initial validation study
title_fullStr Early detection of oliguric events in critically ill patients in the ICU with a novel continuous urine flow measurement device: results of an initial validation study
title_full_unstemmed Early detection of oliguric events in critically ill patients in the ICU with a novel continuous urine flow measurement device: results of an initial validation study
title_short Early detection of oliguric events in critically ill patients in the ICU with a novel continuous urine flow measurement device: results of an initial validation study
title_sort early detection of oliguric events in critically ill patients in the icu with a novel continuous urine flow measurement device: results of an initial validation study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080177/
https://www.ncbi.nlm.nih.gov/pubmed/37027058
http://dx.doi.org/10.1007/s10877-023-00991-w
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