Abstract
Background
Continuous renal replacement therapy (CRRT) is the preferred extracorporeal renal support modality for haemodynamically unstable critically ill patients with acute kidney injury (AKI). Although regional citrate anticoagulation (RCA) is primarily used to maintain circuit patency, its biological effects may extend beyond anticoagulation itself. We hypothesized that different anticoagulation strategies are associated with distinct biological modulation across complementary pathophysiological domains during CRRT.
Methods
We conducted a prospective randomized pilot trial comparing RCA with systemic unfractionated heparin in critically ill adults with AKI requiring CRRT (1:1 allocation). Serial blood samples were obtained before CRRT initiation, at 1 hour and at 24 hours, with paired pre- and post-filter sampling at 1 and 24 hours. Biomarkers represented redox homeostasis (glutathione -GSH, GSSG- and their ratio), neutrophil activation (myeloperoxidase -MPO-), cellular injury (cell-free DNA -cfDNA-) and systemic inflammation (C-reactive protein -CRP-). Healthy reference participants established physiological reference values. Longitudinal analyses used linear mixed-effects models with fixed effects for time, anticoagulation strategy and their interaction. This trial was registered in the European Clinical Trials Database (EudraCT No. 2016-004361-12) and at ClinicalTrials.gov (NCT06646328).
Results
Twenty patients were randomized equally to RCA or systemic heparin; baseline characteristics were comparable between groups. Among six biomarkers spanning four pathophysiological domains, only MPO showed a significant systemic time × anticoagulation interaction (P = .008); although baseline-adjusted sensitivity analyses did not confirm a significant between-group difference. GSH and cfDNA changed significantly over time irrespective of anticoagulation strategy (both P = .016), while the GSSG/GSH ratio approached a treatment-level difference (P = .067). Across the extracorporeal circuit, CRP increased significantly post-filter at both timepoints, MPO increased at 1h, and GSH showed an anticoagulation-dependent pre-to-post change at 1h. No significant differences were observed in secondary clinical outcomes.
Conclusions
These pilot findings suggest that different anticoagulation strategies during CRRT may show domain-specific, rather than uniform, biological modulation, most evident within the neutrophil activation domain, with additional evidence of biomarker-specific kinetics across the extracorporeal circuit. These exploratory results are compatible with the concept that extracorporeal therapies may influence distinct domains differently, a hypothesis warranting confirmation in adequately powered, prospectively designed studies before implications for precision extracorporeal therapy can be drawn.