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Noninvasive and Invasive Renal Hypoxia Monitoring in a Porcine Model of Hemorrhagic Shock
Published on: October 28, 2022
Serum renin and prorenin concentrations predict severe persistent acute kidney injury and mortality in pediatric
Natalja L Stanski1,2, Naomi Pode Shakked3,4, Bin Zhang5
1Cincinnati Children's Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH, 45229, USA. natalja.stanski@cchmc.org.
Insights
Elevated serum renin concentrations in children with septic shock predict severe acute kidney injury and mortality. Monitoring these levels and their trends can help identify high-risk pediatric patients.
Area of Science:
- Pediatric Critical Care Medicine
- Renal Physiology
- Sepsis Pathophysiology
Background:
- Renin-angiotensin-aldosterone system (RAAS) dysregulation is linked to poor outcomes in adult critical illness.
- Data on serum renin concentrations and their prognostic value in pediatric septic shock are limited.
- This study investigates serum renin + prorenin as a potential biomarker in critically ill children.
Purpose of the Study:
- To assess serum renin + prorenin concentrations in children with septic shock.
- To determine the predictive ability of these concentrations for severe persistent acute kidney injury (AKI) and mortality.
- To evaluate the prognostic value of renin + prorenin trends over the first 72 hours.
Main Methods:
- Secondary analysis of a multicenter observational study involving children (1 week to 18 years) with septic shock.
- Measurement of serum renin + prorenin concentrations on day 1 and day 3.
- Primary outcomes: severe persistent AKI (≥ KDIGO stage 2 for ≥ 48 hours) and 28-day mortality.
Main Results:
- Day 1 serum renin + prorenin predicted severe persistent AKI (AUROC 0.75) and mortality (AUROC 0.79).
- Elevated day 1 concentrations were independently associated with severe persistent AKI (aOR 6.8) and mortality (aOR 6.9).
- The day 3/day 1 renin + prorenin ratio also predicted mortality (AUROC 0.73; aOR 7.6).
Conclusions:
- Critically ill children with septic shock exhibit significantly elevated serum renin + prorenin levels.
- These concentrations and their trends are valuable predictors of severe persistent AKI and mortality.
- Serum renin + prorenin serves as a potential prognostic biomarker in pediatric septic shock.
Background:
Studies in critically ill adults demonstrate associations between serum renin concentrations (a proposed surrogate for renin-angiotensin-aldosterone system dysregulation) and poor outcomes, but data in critically ill children are lacking. We assessed serum renin + prorenin concentrations in children with septic shock to determine their predictive ability for acute kidney injury (AKI) and mortality.
Methods:
We conducted a secondary analysis of a multicenter observational study of children aged 1 week to 18 years admitted to 14 pediatric intensive care units (PICUs) with septic shock and residual serum available for renin + prorenin measurement. Primary outcomes were development of severe persistent AKI (≥ KDIGO stage 2 for ≥ 48 h) in the first week and 28-day mortality.
Results:
Among 233 patients, day 1 median renin + prorenin concentration was 3436 pg/ml (IQR 1452-6567). Forty-two (18%) developed severe persistent AKI and 32 (14%) died. Day 1 serum renin + prorenin predicted severe persistent AKI with an AUROC of 0.75 (95% CI 0.66-0.84, p < 0.0001; optimal cutoff 6769 pg/ml) and mortality with an AUROC of 0.79 (95% CI 0.69-0.89, p < 0.0001; optimal cutoff 6521 pg/ml). Day 3/day 1 (D3:D1) renin + prorenin ratio had an AUROC of 0.73 (95% CI 0.63-0.84, p < 0.001) for mortality. On multivariable regression, day 1 renin + prorenin > optimal cutoff retained associations with severe persistent AKI (aOR 6.8, 95% CI 3.0-15.8, p < 0.001) and mortality (aOR 6.9, 95% CI 2.2-20.9, p < 0.001). Similarly, D3:D1 renin + prorenin > optimal cutoff was associated with mortality (aOR 7.6, 95% CI 2.5-23.4, p < 0.001).
Conclusions:
Children with septic shock have very elevated serum renin + prorenin concentrations on PICU admission, and these concentrations, as well as their trend over the first 72 h, predict severe persistent AKI and mortality. A higher resolution version of the Graphical abstract is available as Supplementary information.
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