Key result
Higher baseline eGFR in cardiogenic shock links to ~6% lower 30-day mortality per 10 ml/min.
Why the study?
In patients with cardiogenic shock without pre-existing chronic kidney disease, the prognostic value of baseline eGFR beyond serum lactate and across different shock aetiologies was unclear.
Does lower baseline eGFR predict increased 30-day mortality in patients with cardiogenic shock without pre-existing chronic kidney disease?
Cohort (n=935)
No
Does lower baseline eGFR predict increased 30-day mortality in patients with cardiogenic shock without pre-existing chronic kidney disease?
In patients with cardiogenic shock without prior CKD, low baseline eGFR is an independent predictor of 30-day mortality beyond lactate levels, particularly in those with heart failure-related cardiogenic shock.
Lower baseline eGFR was associated with higher 30-day mortality in cardiogenic shock without prior CKD, especially HF-CS; extends lactate prognostication but remains hypothesis-generating.
Background In patients with cardiogenic shock (CS) but without pre-existing chronic kidney disease (CKD), worsening kidney function may provide prognostic information beyond established biomarkers such as serum lactate. Purpose To determine the effect of baseline estimated glomerular filtration rate (eGFR) on short-term mortality across different aetiologies of cardiogenic shock and to evaluate whether kidney dysfunction carries prognostic relevance depending on the underlying cause of CS. Methods Consecutive patients presenting with CS without a prior history of CKD and treated between 2009 and 2019 at a large tertiary cardiovascular centre were retrospectively analysed. Multivariable regression models adjusted for clinically relevant confounders, including age, comorbidities, haemodynamic parameters, and lactate levels, were constructed to assess the association between baseline eGFR and 30-day mortality. Analyses were additionally stratified according to CS aetiology, particularly acute myocardial infarction–related CS (AMI-CS) and heart failure–related CS (HF-CS). Results Among 935 eligible patients (median age 69 years; 269 women [28.8%]; median lactate concentration 4.6 mmol/L; mean eGFR 46.2 ml/min; AMI-CS 50.7%), lower eGFR values were associated with increased 30-day mortality. The risk of death increased by 6% for every 10 ml/min decrease in eGFR (HR 0.94; 95% CI 0.90–0.99; p=0.016). In patients with eGFR at or below the cohort median (41.74 ml/min), this association remained significant only in HF-CS (HR 1.32; 95% CI 1.00–1.73; p=0.047), whereas no significant relationship was observed in AMI-CS (HR 1.03; 95% CI 0.77–1.37; p=0.86). Conclusions In patients with cardiogenic shock without pre-existing CKD, impaired renal function is an independent predictor of increased 30-day mortality even after adjustment for lactate levels. This prognostic effect appears to be primarily driven by patients with HF-CS, in whom myocardial recovery options are limited compared with revascularisation strategies such as PCI in AMI-CS. These findings underscore the importance of rapidly restoring and maintaining end-organ perfusion to prevent irreversible extracardiac organ damage, particularly in HF-CS patients, and suggest that assessment of renal function may aid risk stratification and therapeutic decision-making in this high-risk population.
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Kriz et al. (2026) conducted a cohort in Cardiogenic shock without pre-existing chronic kidney disease (n=935). Baseline estimated glomerular filtration rate (eGFR) vs. Higher baseline eGFR (per 10 ml/min increase) or eGFR above cohort median (41.74 ml/min) was evaluated on 30-day mortality (HR 0.94, 95% CI 0.90-0.99, p=0.016). Lower baseline eGFR in cardiogenic shock without prior CKD increased 30-day mortality by 6% per 10 ml/min decrease (HR 0.94; 95% CI 0.90-0.99; p=0.016), driven by heart failure-related CS.
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