Risk factors for major adverse kidney events in the first year after acute kidney injury

Author:

See Emily J123,Toussaint Nigel D45,Bailey Michael16,Johnson David W78910,Polkinghorne Kevan R111213,Robbins Raymond14,Bellomo Rinaldo1314

Affiliation:

1. School of Medicine, University of Melbourne, Melbourne, Australia

2. Department for Continuing Education, University of Oxford, Oxford, UK

3. Department of Intensive Care, Austin Hospital, Heidelberg, Australia

4. Department of Medicine, University of Melbourne, Melbourne, Australia

5. Department of Nephrology, The Royal Melbourne Hospital, Parkville, Australia

6. Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Australia

7. Department of Nephrology, Princess Alexandra Hospital, Woolloongabba, Australia

8. Centre for Kidney Disease Research, University of Queensland, Brisbane, Australia

9. Australasian Kidney Trials Network, Brisbane, Australia

10. Translational Research Institute, Brisbane, Australia

11. School of Medicine, Monash University, Melbourne, Australia

12. Department of Nephrology, Monash Health, Clayton, Australia

13. Department of Epidemiology and Preventative Medicine, Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Australia

14. Data Analytics Research and Evaluation, The University of Melbourne and Austin Hospital, Melbourne, Australia

Abstract

Abstract Background Acute kidney injury (AKI) survivors are at increased risk of major adverse kidney events (MAKEs), including chronic kidney disease (CKD), end-stage kidney disease (ESKD) and death. High-risk AKI patients may benefit from specialist follow-up, but factors associated with increased risk have not been reported. Methods We conducted a retrospective study of AKI patients admitted to a single centre between 2012 and 2016 who had a baseline estimated glomerular filtration rate (eGFR) >30 mL/min/1.73 m2 and were alive and independent of renal replacement therapy (RRT) at 30 days following discharge. AKI was identified using International Classification of Diseases, Tenth Revision codes and staged according to the Kidney Disease: Improving Global Outcomes criteria. Patients were excluded if they were kidney transplant recipients or if AKI was attributed to intrinsic kidney disease. We performed Cox regression models to examine MAKEs in the first year, defined as the composite of CKD (sustained 25% drop in eGFR), ESKD (requirement for chronic RRT or sustained eGFR <15 mL/min/1.73 m2) or death. We examined secondary outcomes (CKD, ESKD and death) using Cox and competing risk regression analyses. Results We studied 2101 patients (mean ± SD age 69 ± 15 years, baseline eGFR 72 ± 23 mL/min/1.73 m2). Of these, 767 patients (37%) developed at least one MAKE (429 patients developed CKD, 21 patients developed ESKD, 375 patients died). MAKEs occurred more frequently with older age [hazard ratio (HR) 1.16 per decade, 95% confidence interval (CI) 1.10–1.24], greater severity of AKI (Stage 2 HR 1.38, 95% CI 1.16–1.64; Stage 3 HR 1.62, 95% CI 1.31–2.01), higher serum creatinine at discharge (HR 1.04 per 10 µmol/L, 95% CI 1.03–1.06), chronic heart failure (HR 1.41, 95% CI 1.19–1.67), liver disease (HR 1.68, 95% CI 1.39–2.03) and malignancy (non-metastatic HR 1.44, 95% CI 1.14–1.82; metastatic HR 2.26, 95% CI 1.80–2.83). Traditional risk factors (e.g. diabetes and cardiovascular disease) had limited predictive value. Conclusions More than a third of AKI patients develop MAKEs within the first year. Clinical variables available at the time of discharge can help identify patients at increased risk of such events.

Funder

National Health and Medical Research Council Postgraduate Scholarship

National Health and Medical Research Council Practitioner Fellowship

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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