Department of Gastroenterology, Nara Medical University, Kashihara, Japan.
Department of Gastroenterology, Nara Medical University, Kashihara, Japan;
In Vivo. 2023 May-Jun;37(3):1226-1235. doi: 10.21873/invivo.13199.
BACKGROUND/AIM: The management of refractory ascites is critical for the treatment of patients with decompensated cirrhosis. This study aimed to evaluate the feasibility and safety of cell-free and concentrated ascites reinfusion therapy (CART) in patients with cirrhosis and refractory ascites, with a focus on changes in coagulation and fibrinolytic factors in ascitic fluid following CART.
This was a retrospective cohort study including 23 patients with refractory ascites undergoing CART. Serum endotoxin activity (EA) before and after CART and the levels of coagulation and fibrinolytic factors and proinflammatory cytokines in original and processed ascitic fluid were measured. The Ascites Symptom Inventory-7 (ASI-7) scale was used for subjective symptom assessment before and after CART.
Body weight and waist circumference significantly decreased after CART, whereas serum EA did not significantly change after CART. Similar to the previous reports, ascitic fluid concentrations of total protein, albumin, high-density lipoprotein cholesterol, γ-globulin, and immunoglobulin G levels were significantly increased after CART; mild elevations in body temperature and interleukin 6 and tumor necrosis factor-alpha levels in ascitic fluid were also observed. Importantly, the levels of antithrombin-III, factor VII, and X, which are useful for patients with decompensated cirrhosis, were markedly increased in the reinfused fluid during CART. Finally, the total ASI-7 score was significantly lower following CART, compared with the pre-CART score.
CART is an effective and safe approach for the treatment of refractory ascites that allows the intravenous reinfusion of coagulation and fibrinolytic factors in the filtered and concentrated ascites.
背景/目的:失代偿期肝硬化患者腹水难消,管理棘手。本研究旨在评估无细胞浓缩腹水回输疗法(CART)治疗肝硬化合并难治性腹水的可行性和安全性,重点关注 CART 后腹水的凝血和纤溶因子变化。
这是一项回顾性队列研究,共纳入 23 例难治性腹水患者行 CART。测量 CART 前后血清内毒素活性(EA)以及原始和处理后腹水的凝血和纤溶因子及促炎细胞因子水平。采用腹水症状量表-7(ASI-7)在 CART 前后进行主观症状评估。
CART 后患者体重和腰围明显下降,而血清 EA 无明显变化。与既往报道一致,CART 后腹水总蛋白、白蛋白、高密度脂蛋白胆固醇、γ球蛋白和免疫球蛋白 G 浓度明显升高;腹水体温和白细胞介素 6、肿瘤坏死因子-α水平也轻度升高。重要的是,在 CART 过程中,用于治疗失代偿期肝硬化的抗凝血酶-III、VII 和 X 等凝血因子水平在回输液中明显升高。最后,CART 后腹水症状总评分(ASI-7)明显低于 CART 前。
CART 是治疗难治性腹水的有效且安全方法,可将过滤和浓缩腹水的凝血和纤溶因子静脉回输。