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. Author manuscript; available in PMC: 2023 Mar 16.
Published in final edited form as: Am J Nephrol. 2022 Mar 16;53(4):273–281. doi: 10.1159/000522139

Table 2.

Association between nephrotoxin use and the development of study endpoints

De novo or progressive CKD by either diagnosis code or eGFR decline Composite of de novo or progressive CKD, readmission with AKI or death
Time Dependent covariates Hazard Ratio (95% CI) P value Hazard Ratio (95% CI) P value

Nephrotoxin (Y vs N) 1.38 (1.24–1.54) <0.001 1.41 (1.28–1.56) <0.001
Nephrotoxin count (continuous)a 1.23 (1.16–1.31) <0.001 1.25 (1.18–1.32) <0.001
Nephrotoxin count (categorical)
 0 Reference Reference
 1 1.34 (1.18–1.51) <0.001 1.39 (1.24–1.55) <0.001
 2 1.63 (1.35–1.96) <0.001 1.59 (1.34–1.88) <0.001
 3 1.60 (1.11–2.33) 0.013 1.84 (1.35–2.52) 0.001
 4+ 2.11 (1.25–3.59) 0.006 2.13 (1.32–3.45) 0.002

CKD: chronic kidney disease, eGFR: estimated glomerular filtration rate, AKI: acute kidney injury

a

Per 1 nephrotoxin prescribed