Development and First Clinical Use of an Extracorporeal Artificial Multiorgan System in Acute-on-Chronic Liver Failure Patients.
Suhail AhmadAlexander NovokhodkoIris W LiouNancy Colobong SmithRobert L CarithersJorge ReyesRamasamy BakthavatsalamCarl MartinRenuka BhattacharyaNanye DuShaohang HaoDayong GaoPublished in: ASAIO journal (American Society for Artificial Internal Organs : 1992) (2024)
Multiple organ failure (MOF) is a common and deadly condition. Patients with liver cirrhosis with acute-on-chronic liver failure (AOCLF) are particularly susceptible. Excess fluid accumulation in tissues makes routine hemodialysis generally ineffective because of cardiovascular instability. Patients with three or more organ failures face a mortality rate of more than 90%. Many cannot survive liver transplantation. Extracorporeal support systems like MARS (Baxter, Deerfield, IL) and Prometheus (Bad Homburg, Germany) have shown promise but fall short in bridging patients to transplantation. A novel Artificial Multi-organ Replacement System (AMOR) was developed at the University of Washington Medical Center. AMOR removes protein-bound toxins through a combination of albumin dialysis, a charcoal sorbent column, and a novel rinsing method to prevent sorbent column saturation. It removes excess fluid through hemodialysis. Ten AOCLF patients with over three organ failures were treated by the AMOR system. All patients showed significant clinical improvement. Fifty percent of the cohort received liver transplants or recovered liver function. AMOR was successful in removing large amounts of excess body fluid, which regular hemodialysis could not. AMOR is cost-effective and user-friendly. It removes excess fluid, supporting the other vital organs such as liver, kidneys, lungs, and heart. This pilot study's results encourage further exploration of AMOR for treating MOF patients.
Keyphrases
- end stage renal disease
- liver failure
- chronic kidney disease
- peritoneal dialysis
- ejection fraction
- newly diagnosed
- hepatitis b virus
- gene expression
- intensive care unit
- heart failure
- stem cells
- cardiovascular disease
- risk factors
- small molecule
- deep learning
- binding protein
- cardiovascular events
- coronary artery disease
- acute respiratory distress syndrome
- mesenchymal stem cells
- extracorporeal membrane oxygenation
- clinical practice
- molecularly imprinted