治疗急性慢性肝衰竭的三种人工肝模型。

IF 2.8 3区 医学 Q1 Pharmacology, Toxicology and Pharmaceutics Therapeutics and Clinical Risk Management Pub Date : 2024-10-25 eCollection Date: 2024-01-01 DOI:10.2147/TCRM.S485620
Yanping Xiang, Renhua Li, Jia Cai, Qian Jiang
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引用次数: 0

摘要

研究背景本研究旨在探讨血浆置换(PE)、血浆灌流联合PE(PP+PE)、双血浆分子吸附系统联合PE(DPMAS+PE)治疗急慢性肝衰竭(ACLF)的临床疗效、安全性和短期预后:方法:纳入本院收治的214例ACLF患者,分为PE组(72例)、PP+PE组(75例)和DPMAS+PE组(67例)。收集实验室指标和 MELD 评分,比较临床疗效。收集患者治疗期间和治疗后 24 小时的不良反应,比较安全性。对患者90天内的生存状况进行随访,分析预后情况:与治疗前相比,PE、PP+PE 和 DPMAS+PE 能明显降低 TBiL、DBiL、ALT、AST、SA、PT、INR、PCT 和 CRP 水平,提高 PA 和 PTA 水平(P < 0.05)。DPMAS+PE组的白细胞和SCR水平在治疗后明显下降(P < 0.05)。PE组和PP+PE组的Na+和Cl-水平在治疗后明显下降(P < 0.05)。PE组、PP+PE组、DPMAS+PE组不良反应总发生率分别为38.89%、22.70%、17.90%,三组间差异显著(P<0.05)。PE组、PP+PE组、DPMAS+PE组患者的90天死亡率分别为41.67%、34.67%、20.90%,三组间差异有学意义(P<0.05):结论:PE、PP+PE、DPMAS+PE三种人工肝治疗模式可有效改善ACLF患者的肝、肾及凝血功能。DPMAS+PE具有更好的清除内毒素和炎症介质的能力,在降低ACLF患者90天内死亡率方面表现出优势,且治疗后对电解质的影响最小。因此,DPMAS+PE 可作为临床治疗的更好选择。
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Three Artificial Liver Models of Treatment of Acute-on-Chronic Liver Failure.

Background: This study aimed to investigate clinical efficacy, safety and short-term prognosis of plasma exchange (PE), plasma perfusion combining PE (PP+PE), dual-plasma molecular adsorption system combining PE (DPMAS+PE) in treating acute-on-chronic liver failure (ACLF).

Methods: Two hundred and fourteen ACLF patients admitted to our hospital were included and divided into PE (n = 72), PP+PE (n = 75), DPMAS+PE group (n = 67). Laboratory indexes and MELD scores were collected, and clinical efficacy was compared. Patients' adverse reactions during and 24-h after treatment were collected, and safety was compared. Survival status of patients was followed-up within 90 days, and prognosis was analyzed.

Results: PE, PP+PE and DPMAS+PE significantly reduce TBiL, DBiL, ALT, AST, SA, PT, INR, PCT and CRP levels, and increase PA and PTA levels, compared with pre-treatments (P < 0.05). WBC and SCR levels in DPMAS+PE group decreased significantly post-treatment (P < 0.05). Na+ and Cl- levels in PE and PP+PE group decreased significantly post-treatment (P < 0.05). Total adverse reaction incidence in PE, PP+PE, DPMAS+PE group were 38.89%, 22.70%, 17.90%, respectively, with significant differences among three groups (P < 0.05). Ninety-day mortality rates of patients in PE, PP+PE, DPMAS+PE group were 41.67%, 34.67%, 20.90%, respectively, with significant differences among three groups (P < 0.05).

Conclusion: PE, PP+PE and DPMAS+PE three artificial liver treatment modes can effectively improve liver, kidney and coagulation function of ACLF patients. DPMAS+PE demonstrated better ability to remove endotoxin and inflammatory mediators, showed advantages in reducing ACLF patient mortality within 90 days, and had the least impact on electrolyte post-treatment. Therefore, DPMAS+PE can be used as a better choice for clinical treatment.

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来源期刊
Therapeutics and Clinical Risk Management
Therapeutics and Clinical Risk Management HEALTH CARE SCIENCES & SERVICES-
CiteScore
5.30
自引率
3.60%
发文量
139
审稿时长
16 weeks
期刊介绍: Therapeutics and Clinical Risk Management is an international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas. The journal welcomes submissions covering original research, clinical and epidemiological studies, reviews, guidelines, expert opinion and commentary. The journal will consider case reports but only if they make a valuable and original contribution to the literature. As of 18th March 2019, Therapeutics and Clinical Risk Management will no longer consider meta-analyses for publication. The journal does not accept study protocols, animal-based or cell line-based studies.
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