1. Standard-Volume Plasma Exchange Improves Outcomes in Patients With Acute Liver Failure: A Randomized Controlled Trial.
- Author
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Maiwall, Rakhi, Bajpai, Meenu, Singh, Akanksha, Agarwal, Tanvi, Kumar, Guresh, Bharadwaj, Ankit, Nautiyal, Nidhi, Tevethia, Harsh, Jagdish, Rakesh Kumar, Vijayaraghavan, Rajan, Choudhury, Ashok, Mathur, Rajendra Prasad, Hidam, Ashini, Pati, Nirupama Trehan, Sharma, Manoj Kumar, Kumar, Anupam, and Sarin, Shiv Kumar
- Abstract
High volume plasma-exchange (HVPE) improves survival in patients with acute liver failure (ALF), but apprehension regarding volume overload and worsening of cerebral edema remain. In an open-label randomized controlled trial, 40 consecutive patients of ALF were randomized 1:1 to either standard medical treatment (SMT) or SMT with standard-volume plasma-exchange (SVPE). SVPE was performed using centrifugal apheresis [target volume of 1.5 to 2.0 plasma volumes per session] until desired response was achieved. Cerebral edema was assessed by brain imaging. Results were analyzed in an intention-to-treat analysis. Primary outcome was 21-day transplant-free survival. The levels of cytokines, damage-associated molecular patterns (DAMPs) and endotoxins were analyzed at baseline and day 5. ALF patients [aged 31.5 ± 12.2 years, 60% male, 78% viral, 83% hyperacute, 70% with SIRS were included. At day 5, SVPE [mean sessions 2.15 ± 1.42, median plasma volume replaced 5.049 L] compared to SMT alone, resulted in higher lactate clearance (p =.02), amelioration of SIRS (84% vs. 26%; P =.02), reduction in ammonia levels [(221.5 ± 96.9) vs.(439 ± 385.6) μg/dl, P =.02) and SOFA scores [9.9(±3.3) vs. 14.6(±4.8); P =.001]. There were no treatment related deaths. SVPE was associated with a higher 21-day transplant free-survival [75% vs. 45%; P =.04, HR 0.30, 95%CI 0.01-0.88]. A significant decrease in levels of pro-inflammatory cytokines and an increase in anti-inflammatory cytokines along with a decrease in endotoxin and DAMPs was seen with SVPE. In ALF patients with cerebral edema, SVPE is safe and effective and improves survival possibly by a reduction in cytokine storm and ammonia. ClinicalTrial.gov (identifier: NCT02718079) [Display omitted] [ABSTRACT FROM AUTHOR]
- Published
- 2022
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