Cargando…

A Furosemide Excretion Stress Test Predicts Mortality in Mice After Sepsis and Outperforms the Furosemide Stress Test During Vasopressin Administration

OBJECTIVES: The furosemide stress test measures the volume of urine produced after a furosemide challenge. Furosemide stress test has previously demonstrated sensitive and specific prediction of progression to Kidney Disease: Improving Global Outcomes guideline defined acute kidney injury stage III...

Descripción completa

Detalles Bibliográficos
Autores principales: Street, Jonathan M., Bellomo, Tiffany R., Koritzinsky, Erik H., Kojima, Hiroshi, Yuen, Peter S. T., Star, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259566/
https://www.ncbi.nlm.nih.gov/pubmed/32671344
http://dx.doi.org/10.1097/CCE.0000000000000112
_version_ 1783540156378120192
author Street, Jonathan M.
Bellomo, Tiffany R.
Koritzinsky, Erik H.
Kojima, Hiroshi
Yuen, Peter S. T.
Star, Robert A.
author_facet Street, Jonathan M.
Bellomo, Tiffany R.
Koritzinsky, Erik H.
Kojima, Hiroshi
Yuen, Peter S. T.
Star, Robert A.
author_sort Street, Jonathan M.
collection PubMed
description OBJECTIVES: The furosemide stress test measures the volume of urine produced after a furosemide challenge. Furosemide stress test has previously demonstrated sensitive and specific prediction of progression to Kidney Disease: Improving Global Outcomes guideline defined acute kidney injury stage III in the ICU. Furosemide is actively excreted into the nephron lumen where it inhibits the sodium-potassium-chloride cotransporter, causing diuresis. We hypothesize that furosemide excretion is a more direct measure of tubule health than diuresis. DESIGN: We developed a furosemide excretion stress test to evaluate this hypothesis in a murine model of septic-acute kidney injury. SETTING: Basic science laboratory. SUBJECTS: Male and female 8-week old CD-1 mice. INTERVENTIONS: Sepsis was induced by cecal ligation and puncture in male and female mice. Furosemide stress test/furosemide excretion stress test started 42 hours post-cecal ligation and puncture with a 1 mg/kg furosemide bolus and urine was collected for 12 hours. The mice were then euthanized or monitored until 7 days post-cecal ligation and puncture. In another cohort, mice were treated with vasopressin, which decreases urine volume. Furosemide concentration was determined by high performance liquid chromatography. MEASUREMENTS AND MAIN RESULTS: Urine production during the 12-hour collection varied from 0.08 to 2.62 mL. Both urine production (furosemide stress test) and furosemide excretion (furosemide excretion stress test) predicted mortality (area under the receiver operating characteristic curve = 0.925 and 0.916) and time of death (R(2) = 0.26 and 0.74). Male and female mice demonstrated consistent results. Following vasopressin treatment, furosemide stress test specificity fell to 33% (p = 0.016) but furosemide excretion stress test specificity was maintained. CONCLUSIONS: The furosemide stress test and furosemide excretion stress test performed similarly in predicting mortality; however, furosemide excretion stress test was superior in predicting time to death and maintained performance when challenged with vasopressin treatment in a mouse sepsis model.
format Online
Article
Text
id pubmed-7259566
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Wolters Kluwer Health
record_format MEDLINE/PubMed
spelling pubmed-72595662020-07-14 A Furosemide Excretion Stress Test Predicts Mortality in Mice After Sepsis and Outperforms the Furosemide Stress Test During Vasopressin Administration Street, Jonathan M. Bellomo, Tiffany R. Koritzinsky, Erik H. Kojima, Hiroshi Yuen, Peter S. T. Star, Robert A. Crit Care Explor Original Basic Science Report OBJECTIVES: The furosemide stress test measures the volume of urine produced after a furosemide challenge. Furosemide stress test has previously demonstrated sensitive and specific prediction of progression to Kidney Disease: Improving Global Outcomes guideline defined acute kidney injury stage III in the ICU. Furosemide is actively excreted into the nephron lumen where it inhibits the sodium-potassium-chloride cotransporter, causing diuresis. We hypothesize that furosemide excretion is a more direct measure of tubule health than diuresis. DESIGN: We developed a furosemide excretion stress test to evaluate this hypothesis in a murine model of septic-acute kidney injury. SETTING: Basic science laboratory. SUBJECTS: Male and female 8-week old CD-1 mice. INTERVENTIONS: Sepsis was induced by cecal ligation and puncture in male and female mice. Furosemide stress test/furosemide excretion stress test started 42 hours post-cecal ligation and puncture with a 1 mg/kg furosemide bolus and urine was collected for 12 hours. The mice were then euthanized or monitored until 7 days post-cecal ligation and puncture. In another cohort, mice were treated with vasopressin, which decreases urine volume. Furosemide concentration was determined by high performance liquid chromatography. MEASUREMENTS AND MAIN RESULTS: Urine production during the 12-hour collection varied from 0.08 to 2.62 mL. Both urine production (furosemide stress test) and furosemide excretion (furosemide excretion stress test) predicted mortality (area under the receiver operating characteristic curve = 0.925 and 0.916) and time of death (R(2) = 0.26 and 0.74). Male and female mice demonstrated consistent results. Following vasopressin treatment, furosemide stress test specificity fell to 33% (p = 0.016) but furosemide excretion stress test specificity was maintained. CONCLUSIONS: The furosemide stress test and furosemide excretion stress test performed similarly in predicting mortality; however, furosemide excretion stress test was superior in predicting time to death and maintained performance when challenged with vasopressin treatment in a mouse sepsis model. Wolters Kluwer Health 2020-05-07 /pmc/articles/PMC7259566/ /pubmed/32671344 http://dx.doi.org/10.1097/CCE.0000000000000112 Text en Written work prepared by employees of the Federal Government as part of their official duties is, under the U.S. Copyright Act, a “work of the United States Government” for which copyright protection under Title 17 of the United States Code is not available. As such, copyright does not extend to the contributions of employees of the Federal Government.
spellingShingle Original Basic Science Report
Street, Jonathan M.
Bellomo, Tiffany R.
Koritzinsky, Erik H.
Kojima, Hiroshi
Yuen, Peter S. T.
Star, Robert A.
A Furosemide Excretion Stress Test Predicts Mortality in Mice After Sepsis and Outperforms the Furosemide Stress Test During Vasopressin Administration
title A Furosemide Excretion Stress Test Predicts Mortality in Mice After Sepsis and Outperforms the Furosemide Stress Test During Vasopressin Administration
title_full A Furosemide Excretion Stress Test Predicts Mortality in Mice After Sepsis and Outperforms the Furosemide Stress Test During Vasopressin Administration
title_fullStr A Furosemide Excretion Stress Test Predicts Mortality in Mice After Sepsis and Outperforms the Furosemide Stress Test During Vasopressin Administration
title_full_unstemmed A Furosemide Excretion Stress Test Predicts Mortality in Mice After Sepsis and Outperforms the Furosemide Stress Test During Vasopressin Administration
title_short A Furosemide Excretion Stress Test Predicts Mortality in Mice After Sepsis and Outperforms the Furosemide Stress Test During Vasopressin Administration
title_sort furosemide excretion stress test predicts mortality in mice after sepsis and outperforms the furosemide stress test during vasopressin administration
topic Original Basic Science Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259566/
https://www.ncbi.nlm.nih.gov/pubmed/32671344
http://dx.doi.org/10.1097/CCE.0000000000000112
work_keys_str_mv AT streetjonathanm afurosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT bellomotiffanyr afurosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT koritzinskyerikh afurosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT kojimahiroshi afurosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT yuenpeterst afurosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT starroberta afurosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT streetjonathanm furosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT bellomotiffanyr furosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT koritzinskyerikh furosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT kojimahiroshi furosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT yuenpeterst furosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration
AT starroberta furosemideexcretionstresstestpredictsmortalityinmiceaftersepsisandoutperformsthefurosemidestresstestduringvasopressinadministration