Usefulness of serum creatinine-to-albumin ratio for 28-day all-cause mortality in critically ill patients with atrial fibrillation: A retrospective study based on the MIMIC-IV database.
Elevated creatinine-to-albumin ratio (CAR) was independently and consistently associated with an increased risk of short-term mortality in critically ill patients with AF, and a nomogram incorporating CAR demonstrated strong predictive performance.
Key Findings
Methods
The optimal CAR cutoff value for predicting 28-day mortality was 0.5, dividing patients into high (>0.5) and low (≤0.5) CAR groups.
Cutoff value determined using X-tile software
4501 critically ill patients with AF were identified from the MIMIC-IV database
The study was retrospective in design
Results
Kaplan-Meier analysis demonstrated significantly lower 28-day survival in patients with elevated CAR (>0.5) compared to those with low CAR (≤0.5).
Patients were stratified into high and low CAR groups based on the cutoff of 0.5
The survival difference between groups was statistically significant
28-day all-cause mortality was the primary endpoint
Results
CAR was independently associated with 28-day mortality as a continuous variable in multivariate Cox regression analysis.
Hazard ratio = 1.211 (95% CI = 1.061–1.381, P = .004)
Association remained after adjustment for confounders in multivariate analysis
CAR was analyzed both as a continuous and categorical variable
Results
CAR as a categorical variable (>0.5 vs ≤0.5) was independently associated with 28-day mortality in multivariate Cox regression analysis.
Hazard ratio = 1.377 (95% CI = 1.175–1.615, P < .001)
This represents a 37.7% increased hazard of 28-day mortality for patients with CAR >0.5 versus ≤0.5
Result remained significant after multivariate adjustment
Results
Restricted cubic spline analysis revealed a significant nonlinear dose-response relationship between CAR and 28-day mortality risk.
The relationship between CAR and mortality was nonlinear
Restricted cubic spline methodology was used to characterize the shape of the association
This finding suggests that risk does not increase at a constant rate across the range of CAR values
Results
CAR showed good discriminative ability for 28-day mortality in critically ill patients with AF.
Discriminative ability was assessed as part of the evaluation of CAR as a prognostic biomarker
CAR is calculated from routinely available laboratory values (serum creatinine and albumin)
The paper describes CAR as having 'good discriminative ability' for 28-day mortality
Results
Subgroup analyses showed consistent associations between elevated CAR and 28-day mortality across most prespecified subgroups.
Subgroup analyses were conducted across multiple prespecified subgroups
The association between CAR and mortality was described as consistent across most subgroups
This consistency supports the robustness of the finding
Results
A nomogram incorporating CAR demonstrated good discrimination, calibration, and clinical utility for predicting 28-day mortality.
The nomogram was built using a multivariate prediction model that included CAR
Performance was assessed by discrimination, calibration, and clinical utility metrics
The nomogram was designed for individualized prognostic assessment in critically ill AF patients
What This Means
This research suggests that a simple blood test ratio — creatinine divided by albumin (called CAR) — can help predict which critically ill patients with atrial fibrillation (an irregular heart rhythm) are most likely to die within 28 days of ICU admission. Using data from over 4,500 ICU patients recorded in a large U.S. hospital database (MIMIC-IV), researchers found that patients with a CAR above 0.5 had significantly worse survival odds than those with a CAR of 0.5 or below. Patients with higher CAR values had approximately 38% greater risk of dying within 28 days compared to those with lower values, even after accounting for other health factors.
The study also found that the relationship between CAR and death risk is not strictly linear — meaning the risk does not simply increase at a steady rate as CAR rises, but follows a more complex curve. The researchers used these findings to build a scoring tool (called a nomogram) that combines CAR with other clinical information to generate individualized risk predictions for patients. This tool showed strong performance in terms of both accuracy and practical usefulness.
This research suggests that CAR — which can be calculated from routine blood tests already performed in the ICU — may serve as a practical and readily available marker to help clinicians identify high-risk patients early and tailor their care accordingly. Because both creatinine (a kidney function marker) and albumin (a nutrition and inflammation marker) reflect different aspects of a patient's physiological stress, their ratio captures a combination of organ dysfunction and nutritional status that appears meaningful for predicting short-term outcomes in this vulnerable population.
Li W, Guo L, Huang H. (2026). Usefulness of serum creatinine-to-albumin ratio for 28-day all-cause mortality in critically ill patients with atrial fibrillation: A retrospective study based on the MIMIC-IV database.. Medicine. https://doi.org/10.1097/MD.0000000000048651