Key result
Regional citrate anticoagulation linked to ~18-hour longer CRRT filter lifespan versus nafamostat mesylate.
Why the study?
The optimal anticoagulation strategy for CRRT remains controversial, and real-world comparisons among regional citrate anticoagulation, nafamostat mesylate, and unfractionated heparin are limited.
Does regional citrate anticoagulation improve filter lifespan compared to nafamostat mesylate, unfractionated heparin, or no anticoagulation in critically ill adults undergoing continuous renal replacement therapy?
Cohort (n=420)
No
Does regional citrate anticoagulation improve filter lifespan compared to nafamostat mesylate, unfractionated heparin, or no anticoagulation in critically ill adults undergoing continuous renal replacement therapy?
Answers are grounded in this paper and cite their sources.
In real-world practice, regional citrate anticoagulation provides superior filter lifespan during CRRT compared to nafamostat mesylate and unfractionated heparin, though it requires vigilant metabolic monitoring.
Background The optimal anticoagulation strategy for continuous renal replacement therapy (CRRT) remains controversial. Real-world comparisons of contemporary agents—regional citrate anticoagulation (RCA), nafamostat mesylate (NM), and unfractionated heparin (UH)—are limited. Methods In this single-center retrospective cohort study, we analyzed 420 CRRT sessions (from 197 unique patients) conducted in four intensive care unit (ICU) wards at an academic medical center in China between September 2025 and November 2025. The primary efficacy outcome was filter lifespan, with Restricted Mean Survival Time (RMST) analysis adopted as the primary method (due to violation of the proportional hazards assumption). Propensity score matching (PSM) and mixed-effects Cox models were used as sensitivity analyses, adjusting for patient, treatment, ward, and machine factors. Multiplicity adjustment (Holm-Bonferroni) was applied for pairwise comparisons. Results Among 420 sessions, RCA was the most frequently used approach (59.0%), followed by NM (21.2%), UH (12.6%), and no anticoagulation (4.0%). Median filter lifespan was longest with RCA (65.5 h, IQR 48.0–72.0) compared to NM (32.0 h, IQR 15.5–52.5), UH (40.0 h, IQR 26.0–72.0), and no anticoagulation (12.5 h, IQR 6.0-19.5; P < 0.001). RMST analysis confirmed that RCA was associated with significantly longer mean filter survival time compared to NM (difference 18.2 h, 95% CI 10.5–25.9; adjusted P < 0.001) and UH (difference 14.6 h, 95% CI 5.8–23.4; adjusted P = 0.046). The NM vs. UH comparison showed no significant difference (difference − 3.6 h, 95% CI -12.1 to 4.9; adjusted P = 0.52). After PSM, results remained consistent. Major bleeding events were rare (n = 9, 2.1%), but the small number of events precludes meaningful between-group safety comparison. However, 20.9% of RCA sessions failed to achieve the protocol-specified post-filter ionized calcium target, reflecting a metabolic calcium monitoring challenge unique to citrate anticoagulation. Twenty-eight-day mortality (patient-level analysis, n = 197) did not differ significantly across groups after adjustment (overall 36.5%, 72/197). Conclusion In this retrospective data analysis of real-world practice, RCA provided superior filter lifespan compared to NM and UH for CRRT, while NM showed intermediate efficacy. Although major bleeding events were uncommon, the small number of events precludes definitive safety conclusions. Vigilant monitoring remains necessary regardless of the agent employed. The choice of anticoagulation should balance filter efficacy, bleeding risk, metabolic monitoring capabilities, and institutional resources.
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Ou et al. (2026) conducted a cohort in Acute kidney injury and fluid overload requiring continuous renal replacement therapy (n=420). Regional citrate anticoagulation (RCA) vs. Nafamostat mesylate (NM) and unfractionated heparin (UH) was evaluated on Filter lifespan (MD 18.2 hours, 95% CI 10.5-25.9, p=<0.001). Regional citrate anticoagulation provided superior filter lifespan compared to nafamostat mesylate (difference 18.2 hours) and unfractionated heparin (difference 14.6 hours) during continuous renal replacement therapy.
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