Organ support & nutrition

Cystatin C-derived measures of renal function as risk factors for mortality and renal replacement therapy in the critically ill – An analysis of the SWECRIT cohort

J Crit CarePublished Retrospective cohort study

Authors' conclusion

Our finding that SPS is more robustly associated with mortality in sepsis patients than in non-sepsis patients suggests that the association between SPS and mortality may depend on underlying pathophysiology. A cystatin C-based estimate of GFR is independently associated with RRT in sepsis and non-sepsis.

Study context

Population
Adults staying >24 h in four Swedish intensive care unit (ICUs), November 2015-December 2018 (SWECRIT cohort)32 % sepsis
Participants
4,455 adults
Exposure
Cystatin C-derived measures (eGFRcys, shrunken pore syndrome) as risk factors in sepsis and non-sepsis ICU patients
Outcome
Mortality and need for RRT due to AKI
Methodological detailsmulticentre, four ICUs
  • Multicentre
  • Four ICUs

Main finding

As reported in the abstract

Adjusted associations (Cox regression)
Hazard ratio (95 % CI)P value
SPS vs no SPS1-year mortality, sepsis patients, adjusted
1.4(1.1–1.9)
P = 0.021
eGFRcys <20 ml/min/1.73m2 vs eGFRcys ≥60 ml/min/1.73m2RRT, sepsis and non-sepsis patients, adjusted
3.1(1.6–6.0)
P < 0.001

Observational data: associations, not effects.

Further findings

Prevalence of shrunken pore syndrome (SPS) and 90-day mortality (cohort)

%

SPS present
7.4
90-day mortality
30.8

Original publication

Cystatin C-derived measures of renal function as risk factors for mortality and renal replacement therapy in the critically ill – An analysis of the SWECRIT cohort. J Crit Care. Published 14 May 2025. doi:10.1016/j.jcrc.2025.155116

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