Efficacy and Economic Evaluation of Nonbiological Artificial Liver Therapy in Acute-on-chronic Hepatitis B Liver Failure.
Chronic-on-acute Liver Failure
About this trial
This is an interventional treatment trial for Chronic-on-acute Liver Failure
Eligibility Criteria
Inclusion Criteria:
- aged 18-65 years old
- patients with ACLF caused by HBV infection
- meeting the diagnostic criteria for ACLF by the Asian Pacific Association for the Study of Liver.
Exclusion Criteria:
- pregnancy or lactation
- previous liver transplantation
- hepatocellular carcinoma or other malignancy
- human immunodeficiency virus(HIV) infection or other immunocompromised state
- complicated with underlying diseases such as severe heart, respiratory, and blood system diseases
Sites / Locations
- Xiangya Hospital of Central South University
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
comprehensive medical treatment
PE(plasma exchange)
DPMAS+half-dose sequential PE
All the 62 patients enrolled received comprehensive medical treatment after admission to the hospital, including anti-viral treatment, general supportive treatment, supplementation of blood products, such as albumin and plasma, and symptomatic treatment.
In addition to comprehensive medical treatment, the PE groups were treated with PE or PE plus half-dose sequential PE. In the current study, PE was carried out using the KM-8800 plasma exchange device (Kuraray, Tokyo, Japan). The device was pre-flushed with 2000 mL of normal saline and 20 U/mL heparin dilution. And the blood pump speed was 100 to 120 mL/min and the plasma exchange speed was 25 to 30 mL/min. Before PE, calcium gluconate and diphenhydramine were routinely administrated to prevent an allergic reaction. For each time of plasma exchange,2800 mL fresh frozen plasma was administrated.
DPMAS with half-dose sequential PE was applied using the EC-40W plasma separator (Asahi Kasei Medical, Tokyo, Japan), BS330 bilirubin adsorption column (Jianfan Biotechnology, Zhuhai, China), and the neutral microporous adsorption resin HA330-Ⅱ (Jianfan Biotechnology). After the bilirubin adsorption and hemoperfusion treatment, sequential half-dose PE treatment begins. 1400 mL plasma replacement was conducted each time.