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Association of kidney function with posterior reversible encephalopathy syndrome in children
Insights
Kidney function markers like BUN and acute kidney injury (AKI) showed minimal association with posterior reversible encephalopathy syndrome (PRES) in children. Further research is needed to clarify the role of kidney function in PRES development.
Area of Science:
- Pediatric Nephrology
- Neurology
- Critical Care Medicine
Background:
- Posterior reversible encephalopathy syndrome (PRES) is a neurological condition with various potential causes.
- The role of kidney function as a predictor for PRES in pediatric populations requires further investigation.
Purpose of the Study:
- To determine if kidney function markers can predict the occurrence of PRES in high-risk children.
- To assess the association between blood urea nitrogen (BUN), serum creatinine, and acute kidney injury (AKI) with PRES development.
Main Methods:
- A case-control study compared 35 children with PRES to 14 controls.
- Data collected included BUN, serum creatinine, albumin, hemoglobin, estimated glomerular filtration rate, and AKI.
- Multivariable regression models and receiver operating characteristic (ROC) curves were utilized.
Main Results:
- While 29% of patients had AKI and 67% had nephrotoxic medication exposure, neither BUN nor AKI were statistically significant predictors of PRES.
- The best predictive threshold for BUN (21.6 mg/dL) demonstrated low predictive ability (AUC 0.664).
- Sensitivity and specificity for predicting PRES were 60.0% and 71.4%, respectively.
Conclusions:
- Kidney function appears to be a less significant risk factor for pediatric PRES than previously thought.
- Larger prospective studies with refined kidney function assessments are necessary to fully elucidate its role in PRES etiology.
Aims:
Investigate if kidney function markers predict posterior reversible encephalopathy syndrome (PRES) in children.
Materials And Methods:
In a case-control study of high-risk children with confirmed PRES (n = 35) compared to controls (n = 14), we recorded blood urea nitrogen (BUN), serum creatinine, serum albumin, hemoglobin concentrations, estimated glomerular filtration rate, and documentation of acute kidney injury (AKI). We applied multivariable regression models and determined receiver operating characteristic curves.
Results:
Mean age was 9.5 (SD 4.9) years, 51% were female, 29% had chronic kidney disease, 67% had nephrotoxic medication exposure, and 29% had AKI. A 1-mg/dL increase in BUN (adjusted OR 1.03, 95% CI 0.99 - 1.07) and AKI (adjusted OR 3.78, 0.68 - 21.13) were minimally, but not statistically significantly, associated with PRES. BUN = 21.6 mg/dL performed best but had low ability to predict PRES (area under the curve 0.664, 0.498 - 0.831), with 60.0% sensitivity, 71.4% specificity, and positive and negative predictive values of 84.0% and 41.7%, respectively.
Conclusion:
Kidney function may be a relatively more minor risk factor for PRES than previously believed. Further prospective studies with larger sample sizes and better kidney function assessments are warranted to evaluate the role of kidney function in the development of PRES.
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