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Major Adverse Kidney Events in Pediatric Sepsis
Scott L Weiss1,2,3, Fran Balamuth4,2,5, Cary W Thurm6
1Departments of Anesthesiology and Critical Care and.
Insights
Major adverse kidney events (MAKEs) are common in pediatric sepsis, affecting 9.6% of patients within 30 days. These events are linked to higher mortality and costs, validating MAKEs as a key clinical trial endpoint.
Area of Science:
- Pediatric Nephrology
- Critical Care Medicine
- Clinical Trial Endpoints
Background:
- Sepsis-associated kidney injury (SAKI) poses significant risks to pediatric patients.
- Major adverse kidney events (MAKEs), a composite of death, kidney replacement therapy, or persistent kidney dysfunction, are a potential patient-centered outcome.
- Validating MAKEs as an endpoint in pediatric sepsis trials is crucial for advancing SAKI research.
Purpose of the Study:
- To determine the incidence of 30-day MAKEs in children with severe sepsis or septic shock.
- To validate 30-day MAKEs as a clinical endpoint by assessing its association with mortality, hospital costs, and long-term kidney function.
- To evaluate the feasibility of using MAKEs in future pediatric sepsis clinical trials.
Main Methods:
- Retrospective observational study using the Pediatric Health Information Systems Plus database (2007-2011).
- Inclusion criteria: patients aged >6 months to <18 years with severe sepsis/septic shock, specific orders, and known disposition.
- Primary outcome: incidence of 30-day MAKEs. Validation against mortality, hospital costs, length of stay, readmissions, and estimated glomerular filtration rate (eGFR) up to 1 year post-discharge.
Main Results:
- The incidence of 30-day MAKEs was 9.6% (95% CI, 8.1%–11.0%), comprising death (4.5%), kidney replacement therapy (1.7%), and persistent kidney dysfunction (5.8%).
- Patients with 30-day MAKEs experienced significantly higher all-cause mortality at discharge (28% vs. 1%, P<0.001) and increased total hospital costs ($61,188 vs. $28,107, P<0.001).
- A higher proportion of patients with 30-day MAKEs had eGFR <60 ml/min/1.73 m² between 3 months and 1 year post-discharge (19% vs. 4%, P=0.001).
Conclusions:
- Major adverse kidney events within 30 days are a common and significant outcome in pediatric sepsis.
- The 30-day MAKEs endpoint is feasible to measure and demonstrates strong associations with critical clinical outcomes.
- 30-day MAKEs represent a promising and validated endpoint for future clinical trials in pediatric sepsis-associated kidney injury.
Background And Objectives:
Major adverse kidney events, a composite of death, new kidney replacement therapy, or persistent kidney dysfunction, is a potential patient-centered outcome for clinical trials in sepsis-associated kidney injury. We sought to determine the incidence of major adverse kidney events within 30 days and validate this end point in pediatric sepsis.
Design, Setting, Participants, & Measurements:
We conducted a retrospective observational study using the Pediatric Health Information Systems Plus database of patients >6 months to <18 years old with a diagnosis of severe sepsis/septic shock; orders for bacterial blood culture, antibiotics, and at least one fluid bolus on hospital day 0/1; and known hospital disposition between January 2007 and December 2011. The primary outcome was incidence of major adverse kidney events within 30 days. Major adverse kidney events within 30 days were validated against all-cause mortality at hospital discharge, hospital length of stay, total hospital costs, hospital readmission within 30 days and 1 year, and lowest eGFR between 3 months and 1 year after discharge. We reported incidence of major adverse kidney events within 30 days with 95% confidence intervals using robust SEM and used multivariable logistic regression to test the association of major adverse kidney events within 30 days with hospital costs and mortality.
Results:
Of 1685 admissions, incidence of major adverse kidney events within 30 days was 9.6% (95% confidence interval, 8.1% to 11.0%), including 4.5% (95% confidence interval, 3.5% to 5.4%) death, 1.7% (95% confidence interval, 1.1% to 2.3%) kidney replacement therapy, and 5.8% (95% confidence interval, 4.7% to 6.9%) persistent kidney dysfunction. Patients with versus without major adverse kidney events within 30 days had higher all-cause mortality at hospital discharge (28% versus 1%; P<0.001), higher total hospital costs ($61,188; interquartile range, $21,272-140,356 versus $28,107; interquartile range, $13,056-72,697; P<0.001), and higher proportion with eGFR<60 ml/min per 1.73 m2 between 3 months and 1 year after discharge (19% versus 4%; P=0.001). Major adverse kidney events within 30 days was not associated with length of stay or readmissions.
Conclusions:
In children with sepsis, major adverse kidney events within 30 days are common, feasible to measure, and a promising end point for future clinical trials.
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