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Evaluating Kidney Function Decline in Children with Chronic Kidney Disease Using a Multi-Institutional Electronic
Caroline A Gluck1, Christopher B Forrest2,3, Amy Goodwin Davies3
1Division of Pediatric Nephrology, Nemours Children's Health, Wilmington, Delaware.
Insights
In children with chronic kidney disease (CKD), factors like disease cause, proteinuria, hypertension, and younger age predict faster kidney function decline. Understanding these risks aids in managing pediatric CKD progression.
Area of Science:
- Pediatric Nephrology
- Real-world Evidence in Chronic Kidney Disease
- Clinical Epidemiology
Background:
- Chronic kidney disease (CKD) affects children, necessitating identification of progression factors.
- Electronic health records offer a valuable resource for studying pediatric CKD cohorts.
Purpose of the Study:
- To identify a large cohort of children with CKD using US national data.
- To evaluate CKD progression in this cohort.
- To examine clinical risk factors associated with kidney function decline.
Main Methods:
- Retrospective cohort study using PEDSnet data (2009-2022).
- Identified children (18 months-18 years) with CKD based on eGFR criteria.
- Defined CKD progression as a composite outcome including low eGFR, decline, dialysis, or transplant.
- Assessed associations of hypertension, proteinuria, and comorbidities with progression.
Main Results:
- 11,240 children with CKD identified from over 7 million.
- Key predictors of CKD progression included lower eGFR, glomerular disease, malignancy, proteinuria, hypertension, male sex, and younger age.
- Combined proteinuria and hypertension significantly increased progression risk.
Conclusions:
- Disease etiology, albuminuria, hypertension, age, sex, initial eGFR, and medical complexity are linked to faster kidney function decline in pediatric CKD.
- These findings highlight critical factors for monitoring and managing children with CKD.
Background:
The objectives of this study were to use electronic health record data from a US national multicenter pediatric network to identify a large cohort of children with CKD, evaluate CKD progression, and examine clinical risk factors for kidney function decline.
Methods:
This retrospective cohort study identified children seen between January 1, 2009, to February 28, 2022. Data were from six pediatric health systems in PEDSnet. We identified children aged 18 months to 18 years who met criteria for CKD: two eGFR values <90 and ≥15 ml/min per 1.73 m2 separated by ≥90 days without an intervening value ≥90. CKD progression was defined as a composite outcome: eGFR <15 ml/min per 1.73 m2, ≥50% eGFR decline, long-term dialysis, or kidney transplant. Subcohorts were defined based on CKD etiology: glomerular, nonglomerular, or malignancy. We assessed the association of hypertension (≥2 visits with hypertension diagnosis code) and proteinuria (≥1 urinalysis with ≥1+ protein) within 2 years of cohort entrance on the composite outcome.
Results:
Among 7,148,875 children, we identified 11,240 (15.7 per 10,000) with CKD (median age 11 years, 50% female). The median follow-up was 5.1 (interquartile range 2.8-8.3) years, the median initial eGFR was 75.3 (interquartile range 61-83) ml/min per 1.73 m2, 37% had proteinuria, and 35% had hypertension. The following were associated with CKD progression: lower eGFR category (adjusted hazard ratio [aHR] 1.44 [95% confidence interval (95% CI), 1.23 to 1.69], aHR 2.38 [95% CI, 2.02 to 2.79], aHR 5.75 [95% CI, 5.05 to 6.55] for eGFR 45-59 ml/min per 1.73 m2, 30-44 ml/min per 1.73 m2, 15-29 ml/min per 1.73 m2 at cohort entrance, respectively, when compared with eGFR 60-89 ml/min per 1.73 m2), glomerular disease (aHR 2.01 [95% CI, 1.78 to 2.28]), malignancy (aHR 1.79 [95% CI, 1.52 to 2.11]), proteinuria (aHR 2.23 [95% CI, 1.89 to 2.62]), hypertension (aHR 1.49 [95% CI, 1.22 to 1.82]), proteinuria and hypertension together (aHR 3.98 [95% CI, 3.40 to 4.68]), count of complex chronic comorbidities (aHR 1.07 [95% CI, 1.05 to 1.10] per additional comorbid body system), male sex (aHR 1.16 [95% CI, 1.05 to 1.28]), and younger age at cohort entrance (aHR 0.95 [95% CI, 0.94 to 0.96] per year older).
Conclusions:
In large-scale real-world data for children with CKD, disease etiology, albuminuria, hypertension, age, male sex, lower eGFR, and greater medical complexity at start of follow-up were associated with more rapid decline in kidney function.
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