Mode
Text Size
Log in / Sign up

Nafamostat mesylate reduces bleeding risk compared to citrate for anticoagulation during continuous renal replacement therapyNafamostat mesylate may lower bleeding risks during kidney dialysis

AI-generated summary of the cited source, checked by automated accuracy review. How we work

Key Takeaway
Note that nafamostat mesylate is associated with a lower risk of bleeding than citrate in CRRT patients.

This systematic review and meta-analysis evaluated the efficacy and safety of nafamostat mesylate versus citrate for anticoagulation in patients receiving continuous renal replacement therapy (CRRT). The analysis included 2,247 CRRT patient episodes from 18 studies.

Nafamostat mesylate was associated with a lower risk of bleeding events compared to citrate (RR = 0.54; 95%CI: 0.36 to 0.82; p = 0.003). This reduction in bleeding risk was consistent across several subgroups, including high-risk bleeding patients (RR = 0.47; 95%CI: 0.25 to 0.88; p = 0.02), low-dose nafamostat mesylate users (RR = 0.39; 95%CI: 0.23 to 0.66; p < 0.001), and patients in randomized controlled trials (RR = 0.21; 95%CI: 0.07 to 0.66; p = 0.007). No significant differences were found between the two anticoagulants regarding filter lifespan, clotting events, platelet counts, activated partial thromboplastin time, or prothrombin time.

The authors note that the overall certainty of evidence is low to very low. They highlight a need for more multi-center, large-sample, high-quality randomized controlled trials. Nafamostat mesylate may serve as an alternative anticoagulant for CRRT patients with contraindications to citrate or those at high risk of bleeding.

When patients undergo continuous renal replacement therapy (CRRT), they need anticoagulants to keep the equipment running smoothly. Doctors often choose between citrate and nafamostat mesylate. Because some patients have a high risk of bleeding, finding a safe way to prevent blood from clotting in the machine is vital.

A large review of 2,247 patient episodes compared these two treatments. The results showed that both options were equally effective at keeping filters clear and preventing clots. However, the data suggested that nafamostat mesylate was associated with a lower risk of bleeding events overall. This trend was especially noticeable in patients who were already at high risk for bleeding or those receiving low doses of the medication.

While these findings are encouraging for patients who cannot safely use citrate, it is important to note that the quality of evidence is currently low to very low. Because the data comes from a collection of different studies rather than one large, high-quality trial, more research is needed to confirm these results before it can be used as a standard rule.

What this means for you:
Nafamostat mesylate may offer a safer alternative for patients at high risk of bleeding during certain types of dialysis.

Common questions

Is nafamostat mesylate safer than citrate?

The study found that nafamostat mesylate was associated with a lower risk of bleeding events compared to citrate. This was especially true for patients at high risk of bleeding and those receiving low doses. However, the overall certainty of this evidence is currently low to very low.

Does it work as well as citrate for keeping filters clear?

Yes. The analysis of 2,247 patient episodes showed no significant differences between nafamostat mesylate and citrate when it came to filter lifespan or the number of clotting events.

Who is this treatment for?

This finding is particularly relevant for patients undergoing continuous renal replacement therapy (CRRT) who have a high risk of bleeding or cannot safely use citrate as their anticoagulant.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedJul 2026
View Original Abstract ↓
BackgroundAnticoagulation is pivotal to the successful implementation of continuous renal replacement therapy (CRRT). Systematic comparative studies between nafamostat mesylate (NM) and citrate are scarce. There is currently a lack of evidence-based support for clinical practice.ObjectiveTo systematically compare the efficacy and safety of NM versus citrate for anticoagulation in CRRT.MethodsWe performed a comprehensive literature search in PubMed, Web of Science, Embase, Cochrane Library, China National Knowledge Infrastructure (CNKI), Wanfang Database (Wanfang), China Science and Technology Journal Database (VIP), and China Biological Medicine Database (CBM). Two researchers conducted literature screening, data extraction, and quality assessment using standardized procedures and double-blinded methods. Statistical analyses were performed using Review Manager V.5.4 and STATA 15.1. Statistical heterogeneity among studies was quantified using the Chi-square and I-square tests, and publication bias was evaluated using Egger’s test and funnel plots.ResultsA total of 18 studies involving 2,247 CRRT patient episodes were included. The meta-analysis showed no significant differences in filter lifespan or clotting events between NM and citrate (MD = −0.11, 95%CI: −1.87 to 1.65, p = 0.90; RR = 0.63, 95%CI: 0.25–1.59, p = 0.33). NM reduced the risk of bleeding events compared with citrate (RR = 0.54, 95%CI: 0.36–0.82, p = 0.003), subgroup analyses showed that NM was associated with a lower risk of bleeding events in high-risk bleeding, low-dose NM, and randomized controlled trials (RCTs) subgroups (RR = 0.47, 95%CI: 0.25–0.88, p = 0.02; RR = 0.39, 95%CI: 0.23–0.66, p < 0.001; RR = 0.21, 95%CI: 0.07–0.66, p = 0.007). No significant differences were found between NM and citrate in platelet (PLT), activated partial thromboplastin time (APTT), or prothrombin time (PT) (MD = 0.88, 95%CI: −5.83 to 7.59, p = 0.80; MD = −0.42, 95%CI: −2.74 to 1.91, p = 0.73; MD =-0.38, 95%CI: −1.45 to 0.68, p = 0.48).ConclusionNM suggests anticoagulant efficacy comparable to citrate in CRRT, with a lower risk of bleeding, particularly in high bleeding risk situations, among patients receiving low-dose NM. For CRRT patients with contraindications to citrate or high bleeding risk, NM may be an anticoagulant alternative that combines efficacy with safety. The overall certainty of the evidence from this study is low to very low; further multi-center, large-sample, high-quality RCTs are required to validate these findings.Systematic review registrationhttps://www.crd.york.ac.uk/PROSPERO/view/CRD420251182609, identifier CRD420251182609.
Free Newsletter

Clinical research that matters. Delivered to your inbox.

Join thousands of clinicians and researchers. No spam, unsubscribe anytime.