Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/33081
Title: | Estimating baseline creatinine to detect acute kidney injury in patients with chronic kidney disease. | Austin Authors: | Larsen, Thomas;See, Emily J ;Holmes, Natasha E ;Bellomo, Rinaldo | Affiliation: | Data Analytics Research and Evaluation (DARE) Centre Department of Intensive Care, Royal Melbourne Hospital, Melbourne, Victoria, Australia Department of Critical Care, School of Medicine, University of Melbourne, Melbourne, Victoria, Australia. Australian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia. Department of Nephrology, Royal Melbourne Hospital, Melbourne, Victoria, Australia. Intensive Care |
Issue Date: | Aug-2023 | Date: | 2023 | Publication information: | Nephrology (Carlton, Vic.) 2023; 28(8) | Abstract: | Accurately estimating baseline kidney function is essential for diagnosing acute kidney injury (AKI) in patients with chronic kidney disease (CKD). We developed and evaluated novel equations to estimate baseline creatinine in patients with AKI on CKD. We retrospectively analysed 5649 adults with AKI out of 11 254 CKD patients, dividing them evenly into derivation and validation groups. Using quantiles regression, we created equations to estimate baseline creatinine, considering historical creatinine values, months since measurement, age, and sex from the derivation dataset. We assessed performance against back-estimation equations and unadjusted historical creatinine values using the validation dataset. The optimal equation adjusted the most recent creatinine value for time since measurement and sex. Estimates closely matched the actual baseline at AKI onset, with median (95% confidence interval) differences of just 0.9% (-0.8% to 2.1%) and 0.6% (-1.6% to 3.9%) when the most recent value was within 6 months to 30 days and 2 years to 6 months before AKI onset, respectively. The equation improved AKI event reclassification by an additional 2.5% (2.0% to 3.0%) compared to the unadjusted most recent creatinine value and 7.3% (6.2% to 8.4%) compared to the CKD-EPI 2021 back-estimation equation. Creatinine levels drift in patients with CKD, causing false positives in AKI detection without adjustment. Our novel equation adjusts the most recent creatinine value for drift over time. It provides more accurate baseline creatinine estimation in patients with suspected AKI on CKD, which reduces false-positive AKI detection, improving patient care and management. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/33081 | DOI: | 10.1111/nep.14191 | ORCID: | 0000-0002-6392-314X 0000-0003-4436-4319 0000-0001-8501-4054 0000-0002-1650-8939 |
Journal: | Nephrology | PubMed URL: | 37277898 | ISSN: | 1440-1797 | Type: | Journal Article | Subjects: | acute kidney injury/diagnosis acute kidney injury/epidemiology chronic kidney disease humans linear models quantile regression |
Appears in Collections: | Journal articles |
Show full item record
Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.