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Molecular Adsorbent Recirculating System and Single-pass Albumin Dialysis in Liver Failure--a Prospective, Randomised Crossover Study

Overview
Journal Crit Care
Specialty Critical Care
Date 2016 Jan 6
PMID 26728364
Citations 29
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Abstract

Background: The aim of extracorporeal albumin dialysis (ECAD) is to reduce endogenous toxins accumulating in liver failure. To date, ECAD is conducted mainly with the Molecular Adsorbents Recirculating System (MARS). However, single-pass albumin dialysis (SPAD) has been proposed as an alternative. The aim of this study was to compare the two devices with a prospective, single-centre, non-inferiority crossover study design with particular focus on reduction of bilirubin levels (primary endpoint) and influence on paraclinical and clinical parameters (secondary endpoints) associated with liver failure.

Methods: Patients presenting with liver failure were screened for eligibility and after inclusion were randomly assigned to be started on either conventional MARS or SPAD (with 4% albumin and a dialysis flow rate of 700 ml/h). Statistical analyses were based on a linear mixed-effects model.

Results: Sixty-nine crossover cycles of ECAD in 32 patients were completed. Both systems significantly reduced plasma bilirubin levels to a similar extent (MARS: median -68 μmol/L, interquartile range [IQR] -107.5 to -33.5, p = 0.001; SPAD: -59 μmol/L, -84.5 to +36.5, p = 0.001). However, bile acids (MARS: -39 μmol/L, -105.6 to -8.3, p < 0.001; SPAD: -9 μmol/L, -36.9 to +11.4, p = 0.131), creatinine (MARS: -24 μmol/L, -46.5 to -8.0, p < 0.001; SPAD: -2 μmol/L, -9.0 to +7.0/L, p = 0.314) and urea (MARS: -0.9 mmol/L, -1.93 to -0.10, p = 0.024; SPAD: -0.1 mmol/L, -1.0 to +0.68, p = 0.523) were reduced and albumin-binding capacity was increased (MARS: +10%, -0.8 to +20.9%, p < 0.001; SPAD: +7%, -7.5 to +15.5%, p = 0.137) only by MARS. Cytokine levels of interleukin (IL)-6 and IL-8 and hepatic encephalopathy were altered by neither MARS nor SPAD.

Conclusions: Both procedures were safe for temporary extracorporeal liver support. While in clinical practice routinely assessed plasma bilirubin levels were reduced by both systems, only MARS affected other paraclinical parameters (i.e., serum bile acids, albumin-binding capacity, and creatinine and urea levels). Caution should be taken with regard to metabolic derangements and electrolyte disturbances, particularly in SPAD using regional citrate anti-coagulation.

Trial Registration: German Clinical Trials Register ( www.drks.de) DRKS00000371. Registered 8 April 2010.

Citing Articles

Molecular Adsorbent Recirculating System in Acute Liver Failure.

Alsabbagh Alchirazi K, Bhavsar-Burke I, Syed H, Alkhayyat M, Bass S, Kapoor A ACG Case Rep J. 2024; 11(7):e01389.

PMID: 38988717 PMC: 11236392. DOI: 10.14309/crj.0000000000001389.


Safety and efficacy of Single-Pass Albumin Dialysis (SPAD), Prometheus, and Molecular Adsorbent Recycling System (MARS) liver haemodialysis vs. Standard Medical Therapy (SMT): meta-analysis and systematic review.

Gadour E, Kaballo M, Shrwani K, Hassan Z, Kotb A, Aljuraysan A Prz Gastroenterol. 2024; 19(2):101-111.

PMID: 38939063 PMC: 11200067. DOI: 10.5114/pg.2024.139297.


Immunosuppressive effects of circulating bile acids in human endotoxemia and septic shock: patients with liver failure are at risk.

Leonhardt J, Dorresteijn M, Neugebauer S, Mihaylov D, Kunze J, Rubio I Crit Care. 2023; 27(1):372.

PMID: 37759239 PMC: 10523742. DOI: 10.1186/s13054-023-04620-5.


Extracorporeal blood purification in patients with liver failure: Considerations for the low-and-middle income countries of Latin America.

Villanueva V, Barrera Amoros D, Castillo Echeverria E, Budar-Fernandez L, Salas Nolasco O, Juncos L Front Nephrol. 2023; 3:938710.

PMID: 37675369 PMC: 10479632. DOI: 10.3389/fneph.2023.938710.


Extracorporeal albumin dialysis in critically ill patients with liver failure: Comparison of four different devices-A retrospective analysis.

Sommerfeld O, Neumann C, Becker J, von Loeffelholz C, Roth J, Kortgen A Int J Artif Organs. 2023; 46(8-9):481-491.

PMID: 37609875 PMC: 10483887. DOI: 10.1177/03913988231191952.


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