Double Plasma Molecular Adsorption System with Sequential Low-dose Plasma Exchange in Patients with Hepatitis B Virus-related Acute-on-chronic Liver Failure: A Prospective Study

被引:2
|
作者
Wang, Lu [1 ,2 ,3 ]
Xu, Wenxiong [2 ,3 ]
Zhu, Shu [2 ,3 ]
Lin, Guoli [2 ,3 ]
Lai, Jing [2 ,3 ]
Zhang, Yufeng [2 ,3 ]
Liu, Ying [2 ,3 ]
Zheng, Lihua [2 ,3 ]
Luo, Qiumin [2 ,3 ]
Gao, Zhiliang [2 ,3 ]
Xie, Chan [2 ,3 ,4 ]
Peng, Liang [2 ,3 ,4 ]
机构
[1] Binzhou Med Univ, Sch Clin Med 2, Yantai, Shandong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Infect Dis, Guangzhou, Guangdong, Peoples R China
[3] Sun Yat sen Univ, Key Lab Trop Dis Control, Minist Educ, Guangzhou, Guangdong, Peoples R China
[4] Sun Yat sen Univ, Affiliated Hosp 3, Dept Infect Dis, Key Lab Trop Dis Control,Minist Educ, 600 Tianhe Rd, Guangzhou, Guangdong, Peoples R China
关键词
Plasma exchange; Double plasma molecular adsorption system; Acute-on-chronic liver failure; Prognosis;
D O I
10.14218/JCTH.2022.00254
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: To investigate the safety and effi cacy of double plasma molecular adsorption system (DPMAS) with sequential low-dose plasma exchange (LPE) in treating early hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF). Methods: Clinical data of patients with HBVACLF were prospectively collected, including patients in a DPMAS with sequential LPE (DPMAS+LPE) group and those in a standard medical treatment (SMT) group. The primary endpoint was death or liver transplantation (LT) at 12 weeks of follow-up. Propensity-score matching was performed to control the effects of confounding factors on prognosis between the two groups. Results: After 2 weeks, total bilirubin, alanine aminotransferase, blood urea nitrogen levels, and Chinese Group on the Study of Severe Hepatitis B score, were significantly lower in the DPMAS+LPE group than those in the SMT group (p<0.05). After 4 weeks, laboratory parameters of the two groups were similar. The cumulative survival rate of the DPMAS+LPE group was significantly higher than that of the SMT group at 4 weeks (97.9% vs. 85.4%, p=0.027), but not at 12 weeks (85.4% vs. 83.3%, p=0.687). Cytokine levels were significantly lower in 12-week survival group than in the death-or-LT group (p<0.05). Functional enrichment analysis showed that downregulated cytokines were mainly involved in positive regulation of proliferation and activation of lymphocytes and monocytes, regulation of immune effect response, regulation of endotoxin response, and glial cell proliferation. Conclusion: DPMAS+LPE significantly improved the 4-week cumulative survival rate, and ameliorated the inflammatory response in patients. DPMAS+LPE may be a promising modality for patients with early HBV-ACLF.
引用
收藏
页码:908 / 917
页数:10
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