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Title: | Elevated serum urea-to-creatinine ratio is associated with adverse inpatient clinical outcomes in non-end stage chronic kidney disease. | Austin Authors: | Brookes, Elizabeth M;Power, David A | Affiliation: | Melbourne Medical School, The University of Melbourne, Parkville, VIC, Australia. Nephrology The Department of Medicine, The University of Melbourne, Victoria, Australia |
Issue Date: | 2-Dec-2022 | Date: | 2022 | Publication information: | Scientific Reports 2022; 12(1) | Abstract: | To better understand the role of the urea-to-creatinine ratio in chronic kidney disease patients, we assessed the epidemiology of the urea-to-creatinine ratio among hospitalised chronic kidney disease patients, and the association between the urea-to-creatinine ratio and inpatient clinical outcomes. This retrospective cohort study (n = 11,156) included patients with at least two eGFR values < 60 mL/min/1.73m2 measured greater than 90-days apart and admitted to a tertiary hospital between 2014 and 2019. Dialysis and renal transplant patients were excluded. Adjusted odds ratios for factors associated with an elevated urea-to-creatinine ratio were calculated. Multivariate regression was conducted to identify the relationship between elevated UCR and inpatient mortality, intensive care admission, hospital readmission and hospital length-of-stay. Urea-to-creatinine ratio > 100 was present in 27.67% of hospital admissions. Age ≥ 65 years, female gender, gastrointestinal tract bleeding, heart failure, acute kidney injury and lower serum albumin were associated with elevated urea-to-creatinine ratio. Higher urea-to-creatinine ratio level was associated with greater rates of inpatient mortality, hospital readmission within 30-days and longer hospital length-of-stay. Despite this, there was no statistically significant association between higher urea-to-creatinine ratio and intensive care unit admission. Elevated urea-to-creatinine ratio is associated with poor clinical outcomes in chronic kidney disease inpatients. This warrants further investigation to understand the pathophysiological basis for this relationship and to identify effective interventions. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/31814 | DOI: | 10.1038/s41598-022-25254-7 | ORCID: | Journal: | Scientific Reports | Start page: | 20827 | PubMed URL: | 36460694 | ISSN: | 2045-2322 | Type: | Journal Article |
Appears in Collections: | Journal articles |
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