AI Article Synopsis

  • The study aimed to explore how sodium citrate is processed in critically ill patients, especially focusing on those with liver dysfunction.
  • The research involved a cohort of both cirrhotic and noncirrhotic patients receiving sodium citrate and calcium chloride infusions, with blood tests conducted to assess how the drug was metabolized.
  • Results indicated that cirrhotic patients had a significantly decreased ability to clear citrate compared to noncirrhotic patients, highlighting the importance of considering liver function in the clinical use of citrate, especially for anticoagulation in critically ill scenarios.

Article Abstract

Objectives: To investigate pharmacokinetics and metabolism of sodium citrate in critically ill patients. To determine the risk of citrate accumulation in the setting of liver dysfunction (cirrhosis, hepatorenal syndrome).

Design: Prospective cohort study.

Setting: Intensive Care Unit, Department of Medicine IV, University Hospital Vienna.

Patients: Consecutive critically ill cirrhotic (n = 16) and noncirrhotic patients (n = 16).

Interventions: Infusion of sodium citrate (0.5 mmol.kg-1.hr-1) and calcium chloride (0.17 mmol.kg-1.hr-1) for 2 hrs. Analysis of serial arterial blood samples.

Measurements And Main Results: Total body clearance of citrate was normal in noncirrhotic critically ill patients but significantly reduced in cirrhotic patients (710 vs. 340 mL/min, p =.008). Citrate peak concentrations and concentration over time were increased by 65% and 114% in cirrhotic patients (p <.001), respectively; volumes of distribution were similar. Net metabolic changes were quantitatively similar, with pH and plasma bicarbonate concentrations increasing more slowly in cirrhotic patients. No citrate-related side effects were noted. Citrate clearance could not be predicted by standard liver function tests and was not appreciably influenced by renal function and Acute Physiology and Chronic Health Evaluation II scores.

Conclusions: This first systematic study on citrate pharmacokinetics and metabolism in critically ill patients confirms a major role of hepatic citrate metabolism by demonstrating reduced citrate clearance in cirrhotic patients. Pharmacokinetic data could provide a basis for the clinical use of citrate anticoagulation in critically ill patients. Provided dose adaptation and monitoring of ionized calcium, citrate anticoagulation seems feasible even in patients with decompensated cirrhosis. Metabolic consequences of citrate infusion were not different between groups in this study but may be more pronounced in prolonged infusion.

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http://dx.doi.org/10.1097/01.CCM.0000084871.76568.E6DOI Listing

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