Platelet Transfusion in Acute-on Chronic Liver Failure

Nanfang Hospital, Southern Medical University

Status: Unknown

Conditions: Acute-On-Chronic Liver Failure

Treatments: Other: platelet transfusion

Study type: Interventional

Funder types: Other

Identifiers

NCT04564651

013

Details and patient eligibility

About

Acute on-chronic liver failure (ACLF) is a severe liver disease with a 28-day mortality rate of up to 40%. When the patients get 3 or more organ failures, the 28-day mortality rate is up to 82.6%. Though the ACLF patients have high short-term mortality, and the only effective treatment method is liver transplantation. However, few patients can be treated due to the scarcity of liver source, rapid disease progression and short transplantation window.

Our team evaluated the platelet function of 100 patients with ACLF by using the thromboelastograghy (TEG 5000). It was found for the first time that the reactivity of platelets of ACLF patients decreased, and the platelet inhibition rate (especially the ADP pathway) was related to patients'short-term prognosis. When the ADP inhibition rate was 70%, the patients'28-day mortality was up to 100%. However, the mechanism of low platelet response to ADP in ACLF patients is still unclear. We found that the platelet function in patients with ACLF 2-3 grade and inhibition rate beyond 70% was improved and the 28-day mortality decreased after platelet transfusion. Whether platelet transfusion can prolong survival time needs to be determined in a prospective controlled study. Therefore, this study is expected to find a new therapeutic method to reduce the mortality of patients with ACLF.

Enrollment: 80 estimated patients

Sex: All

Ages: 16 to 60 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 18-60 years old;
• Patients with compensated cirrhosis conformed to the (ACLF) diagnostic criteria of chronic and acute liver failure defined by the European Association of Hepatology (EASL-CLIF), and met the ACLF-2 and 3 grades.

ADP inhibition rate ≥ 70%.

Exclusion criteria

• Patients with severe platelet allergy in the past;
• Coma caused by cerebral hemorrhage or primary diseases of the nervous system;
• Those who have taken anti-platelet drugs or anticoagulants within four weeks;
• Rupture and bleeding of EVB occurred within 1 week.
• Those who received platelet transfusion within 1 week;
• Patients with liver cancer or other malignant tumors;
• Pregnant and lactating women;
• Complicated with other serious chronic diseases;
• Not signing the informed consent form;
• Other researchers do not consider it appropriate to participate in the study.

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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80 participants in 2 patient groups

platelet transfusion treatment

Experimental group

Treatment:

Other: platelet transfusion

standard medical treatment

No Intervention group