Abstract | OBJECTIVES: The molecular adsorbent recirculating system removes water-soluble and albumin-bound toxins and may be beneficial for acute liver failure patients. We compared the rates of 21-day transplant-free survival in acute liver failure patients receiving molecular adsorbent recirculating system therapy and patients receiving standard medical therapy. DESIGN: Propensity score-matched retrospective cohort analysis. SETTING: PATIENTS: INTERVENTIONS: Molecular adsorbent recirculating system treatment versus standard medical therapy (control). MEASUREMENTS AND MAIN RESULTS: One-hundred four molecular adsorbent recirculating system patients were propensity score-matched (4:1) to 416 controls. Using multivariable conditional logistic regression adjusting for acute liver failure etiology ( acetaminophen: n = 248; vs nonacetaminophen: n = 272), age, vasopressor support, international normalized ratio, King's College Criteria, and propensity score (main model), molecular adsorbent recirculating system was significantly associated with increased 21-day transplant-free survival (odds ratio, 1.90; 95% CI, 1.07-3.39; p = 0.030). This association remained significant in several sensitivity analyses, including adjustment for acute liver failure etiology and propensity score alone ("model 2"; molecular adsorbent recirculating system odds ratio, 1.86; 95% CI, 1.05-3.31; p = 0.033), and further adjustment of the "main model" for mechanical ventilation, and grade 3/4 hepatic encephalopathy ("model 3"; molecular adsorbent recirculating system odds ratio, 1.91; 95% CI, 1.07-3.41; p = 0.029). In acetaminophen- acute liver failure (n = 51), molecular adsorbent recirculating system was associated with significant improvements (post vs pre) in mean arterial pressure (92.0 vs 78.0 mm Hg), creatinine (77.0 vs 128.2 µmol/L), lactate (2.3 vs 4.3 mmol/L), and ammonia (98.0 vs 136.0 µmol/L; p ≤ 0.002 for all). In nonacetaminophen acute liver failure (n = 53), molecular adsorbent recirculating system was associated with significant improvements in bilirubin (205.2 vs 251.4 µmol/L), creatinine (83.1 vs 133.5 µmol/L), and ammonia (111.5 vs 140.0 µmol/L; p ≤ 0.022 for all). CONCLUSIONS:
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Authors | Andrew J MacDonald, Ram M Subramanian, Jody C Olson, Jaime L Speiser, Valerie L Durkalski-Mauldin, Juan G Abraldes, David L Bigam, Mary M Flynn, Babusai Rapaka, Brianne M Shropshire, Ravi S Vora, Constantine J Karvellas, U.S. Acute Liver Failure Study Group |
Journal | Critical care medicine
(Crit Care Med)
Vol. 50
Issue 2
Pg. 286-295
(02 01 2022)
ISSN: 1530-0293 [Electronic] United States |
PMID | 34259656
(Publication Type: Journal Article)
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Copyright | Copyright © 2021 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved. |
Topics |
- Adult
- Alberta
(epidemiology)
- Cohort Studies
- Female
- Humans
- Liver Failure, Acute
(epidemiology, etiology, therapy)
- Liver Transplantation
(methods, statistics & numerical data)
- Logistic Models
- Male
- Middle Aged
- Models, Molecular
- Propensity Score
- Retrospective Studies
- Tertiary Care Centers
(organization & administration, statistics & numerical data)
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