Predictive role of cystatin C and increased proteinuria in early assessment of acute renal toxicity in patient poisoned by nephrotoxic drugs and poisons

  • 0Forensic Medicine & Clinical Toxicology Department, Faculty of Medicine, Sohag University, Sohag, 82524, Egypt.

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Summary

This summary is machine-generated.

Proteinuria and serum cystatin C effectively predict early kidney damage in acutely poisoned patients. These biomarkers offer a more sensitive approach than traditional methods for detecting drug-induced nephrotoxicity.

Area Of Science

  • Nephrology
  • Clinical Toxicology
  • Biomarker Research

Background

  • Acute kidney injury (AKI) is a common complication in critical care, frequently caused by nephrotoxic medications.
  • Existing biomarkers like serum creatinine have limitations in the early detection of drug-induced kidney damage.

Purpose Of The Study

  • To evaluate the efficacy of proteinuria and serum cystatin C as early indicators of nephrotoxicity in patients with acute poisoning.
  • To compare the predictive value of these biomarkers against traditional markers.

Main Methods

  • A prospective study of 100 acutely poisoned patients at Sohag University Hospitals.
  • Inclusion of patients with symptomatic nephrotoxic effects, requiring at least four blood/urine samples.
  • Classification of AKI using Acute Kidney Injury Network (AKIN) criteria and measurement of serum creatinine, proteinuria (ACR), and serum cystatin C.

Main Results

  • Serum creatinine levels increased significantly from day 1 to day 2 post-ingestion.
  • Serum creatinine, proteinuria ACR, and serum cystatin C were significant predictors of acute renal toxicity.
  • Serum cystatin C demonstrated the highest predictive value (AUC = 0.993), followed by day 2 serum creatinine (AUC = 0.873) and proteinuria ACR (AUC = 0.805).

Conclusions

  • Proteinuria and serum cystatin C are reliable early predictors of nephrotoxicity in acutely poisoned individuals.
  • These biomarkers aid in the early identification and severity assessment of drug-induced kidney injury.
  • The findings support the use of cystatin C and proteinuria measurements for enhanced monitoring of kidney function in poisoned patients.

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