LT, liver transplantation

LT,肝移植
  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    终末期肝病(ESLD)是慢性肝病进展为肝硬化的高潮,代偿失调,慢性肝衰竭,以门静脉高压或肝细胞衰竭相关并发症为特征。肝移植为这些患者提供了改善的长期生存率,但受供体可用性的负面影响。发展中国家的财政紧张,活性物质滥用,等待名单上的疾病或恶性肿瘤的进展,败血症和肝外器官受累。在这种情况下,姑息治疗(PC),旨在预防和减轻痛苦的跨学科医学实践,提供最佳的生活质量,并且不仅限于临终护理。它还包括可实现的目标,如症状控制和积极的疾病改善治疗或干预措施,有益地改变疾病的自然进程,以提供治疗意图。在这篇叙述性评论中,我们讨论了定义ESLD病程的预后因素,基于循证最佳实践的晚期肝硬化PC的各种适应症和挑战以及ESLD患者主要症状负担的管理选择。
    End-stage liver disease (ESLD) is the culmination of progression of chronic liver disease to cirrhosis, decompensation, and chronic liver failure, featuring portal hypertension or hepatocellular failure-related complications. Liver transplantation offers improved long-term survival for these patients but is negatively influenced by donor availability, financial constraints in developing countries, active substance abuse, progression of disease or malignancy on wait-list, sepsis and extrahepatic organ involvement. In this context, palliative care (PC), an interdisciplinary medical practice that aim to prevent and relieve suffering, offers best possible quality of life and is not limited to end-of-life care. It also encompasses achievable goals such as symptom control and aggressive disease-modifying treatments or interventions that beneficially alter the natural course of the disease to offer curative intend. In this narrative review, we discuss the prognostic factors that define disease course in ESLD, various indications and challenges in PC for advanced cirrhosis and management options for major symptom burden in patients with ESLD based on evidence-based best practice.
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  • 文章类型: Journal Article
    基质金属蛋白酶7(MMP7)已被认为是诊断胆道闭锁(BA)的有希望的生物标志物。本研究旨在评估中东人群BA中血清MMP7的诊断准确性。
    在这项横断面研究中,纳马齐转诊医院收治的直接高胆红素血症新生儿和婴儿,设拉子,伊朗,被研究过。入院时获得基线人口统计学和临床特征以及血液样本。使用酶联免疫吸附测定法测量MMP7血清浓度(ZellBioGmbH,乌尔姆,德国)。
    研究了44名平均年龄为65.59天的婴儿。在这些病人中,13例确诊为BA,与其他病因有关的胆汁淤积31例。BA组血清MMP7浓度为2.13ng/mL,非BA组为1.85ng/mL。MMP7在那些有深色尿液或大便的人中明显更高。基于受试者工作特征曲线分析(曲线下面积:0.6,95%置信区间:0.45-0.75),MMP7的预测性能能力在BA与非BA组的区分中不显著。在1.9点的最佳切割中,灵敏度和特异度分别为84.6%和45.1%,分别。MMP7与γ-谷氨酰转移酶(GGT)的进一步组合,碱性磷酸酶,直接和总胆红素,深色尿液或下大便没有显着提高测试的诊断准确性。有趣的是,在230U/L的截止点下,GGT对BA的敏感性为84.6%,特异性为90.3%。
    我们的结果与以前关于该主题的研究不一致。考虑到更多的常规和可用的测试,如GGT,除了进行未来的研究与更大的样本和不同的地理区域建议。
    UNASSIGNED: Matrix metalloproteinase 7 (MMP7) has been suggested as a promising biomarker in diagnosing biliary atresia (BA). This study aimed to assess the diagnostic accuracy of serum MMP7 in BA in the Middle Eastern population.
    UNASSIGNED: In this cross-sectional study, neonates and infants with direct hyperbilirubinemia admitted to Namazi referral hospital, Shiraz, Iran, were studied. Baseline demographic and clinical characteristics and blood samples were obtained on admission. MMP7 serum concentration was measured using an enzyme-linked immunosorbent assay (ZellBio GmbH, Ulm, Germany).
    UNASSIGNED: 44 infants with a mean age of 65.59 days were studied. Of these patients, 13 cases were diagnosed with BA, and 31 cases\' cholestasis related to other etiologies. Serum MMP7 concertation was 2.13 ng/mL in the BA group and 1.85 ng/mL in the non-BA group. MMP7 was significantly higher in those presented with either dark urine or acholic stool. The predictive performance capability of the MMP7 was not significant in the discrimination of BA from the non-BA group based on receiver operating characteristic curve analysis (area under curve: 0.6, 95% confidence interval: 0.45-0.75). In the optimal cut of point 1.9, the sensitivity and specificity were 84.6% and 45.1%, respectively. Further combination of MMP7 with Gamma-glutamyl transferase (GGT), alkaline phosphatase, direct and total bilirubin, and dark urine or acholic stool was not remarkably boosted the diagnostic accuracy of the test. Interestingly, GGT at a cut-off point of 230 U/L was 84.6% sensitive and 90.3% specific for BA.
    UNASSIGNED: Our results are not consistent with previous studies on this subject. Considering more conventional and available tests like GGT besides conducting future studies with greater samples and different geographical areas is recommended.
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  • 文章类型: Journal Article
    自身免疫性肝病(AILD)是一组免疫介导的肝损伤可能导致需要移植的疾病。总的来说,它们几乎占所有肝移植手术的四分之一。几十年来,随着患者选择的改善,所有肝移植的移植物和患者存活率方面的结果都有了显着改善。手术技术和长期护理,这也见于AILDs患者。目前自身免疫性疾病移植后5年和10年生存率非常好,88%和78%,分别。在这些自身免疫性疾病的肝移植后保持良好结果的关键因素是免疫抑制策略。这些患者的排斥反应率增加,和自身免疫性疾病都可以在移植物中复发,范围为12%至60%,具体取决于所研究的人群。免疫抑制方案以钙调磷酸酶抑制剂为中心,经常与低剂量皮质类固醇联合使用,有或没有添加抗代谢药物治疗。对于这些情况,没有明确的基于证据的免疫抑制方案,并且经常使用量身定制的方法来平衡个体的免疫学特征与免疫抑制的风险。优化移植物功能需要考虑特定疾病,包括熊去氧胆酸在原发性胆汁性胆管炎和原发性硬化性胆管炎中的作用,以及结肠切除术在炎症性肠病患者原发性硬化性胆管炎中的作用和时机。然而,肝移植后AILDs的管理仍存在未满足的需求,特别是在建立最佳免疫抑制的证据基础以及降低疾病复发的风险方面.
    Autoimmune liver diseases (AILDs) are a group of conditions where immune-mediated liver damage can lead to the need for transplantation. Collectively, they account for almost a quarter of all liver transplants. Outcomes in terms of graft and patient survival for all liver transplants have improved markedly over decades with improvements in patient selection, surgical techniques and longer-term care and this is also seen in patients with AILDs. The current five- and ten-year survival rates post-transplant in autoimmune disease are excellent, at 88% and 78%, respectively. A key factor in maintaining good outcomes post liver transplant for these autoimmune conditions is the immunosuppression strategy. These patients have increased the rates of rejection, and autoimmune conditions can all recur in the graft ranging from 12 to 60% depending on the population studied. Immunosuppressive regimens are centred on calcineurin inhibitors, often combined with low dose corticosteroids, with or without the addition of antimetabolite therapy. There is no clear evidence-based immunosuppressive regimen for these conditions, and a tailored approach balancing the individuals\' immunological profile against the risks of immunosuppression is often used. There are disease-specific considerations to optimised graft function including the role of ursodeoxycholic acid in both primary biliary cholangitis and primary sclerosing cholangitis and the role and timing of colectomy in primary sclerosing cholangitis in inflammatory bowel disease patients. However, unmet needs still exist in the management of AILDs post liver transplantation particularly in building the evidence base for optimal immunosuppression as well as mitigating the risk of recurrent disease.
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  • 文章类型: Journal Article
    肝硬化的自然史通常是在从代偿性肝硬化发展到随后的代偿失调阶段的背景下概念化的。虽然这种单向概念是最常见的病理生理轨迹,对接受再补偿的患者亚组有了新的认识.虽然主要基于移植候补名单登记处的文献表明,对于这种经历疾病消退的人群,关于这个实体的整体文献仍然不明确。已尝试就定义补偿达成共识,这具有其自身的细微差别和局限性。我们总结了有关肝硬化中这种新兴但有争议的再补偿概念的现有文献,并深入研究了对现实生活实践的未来影响和影响。
    The natural history of cirrhosis has usually been conceptualized in the context of progression from compensated cirrhosis to subsequent stages of decompensation. While this unidirectional concept is the most common pathophysiological trajectory, there has been an emerging understanding of a subgroup of patients which undergo recompensation. While literature mostly based on transplant waitlist registries have indicated towards such a population who experience disease regression, the overall literature about this entity remains inexplicit. An effort to generate consensus on defining recompensation has been attempted which comes with its own nuances and limitations. We summarize the available literature on this emerging yet controversial concept of recompensation in cirrhosis and delve into future implications and impact on real-life practice.
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  • 文章类型: Journal Article
    死亡的供体肝移植(DDLT)在印度正在增加,现在占该国所有肝移植手术的近三分之一。目前没有统一的全国捐献者肝脏分配制度。
    在印度肝移植学会的主持下,成立了一个由来自全国各地的19名参与肝移植的临床医生组成的国家工作队,目的是使用改良的德尔菲共识制定过程来解决上述问题。
    国家肝脏分配政策共识文件包括46个声明,涵盖了DDLT的所有方面,包括最低上市标准,急性肝衰竭上市,DDLT等待列表管理,基于成人和儿童临床紧迫性的优先排序系统,儿科器官分配指南和从公共部门医院回收的肝移植物的分配优先级。
    该文件是建立全国一致的已故供体肝脏分配政策的第一步。
    UNASSIGNED: Deceased donor liver transplantation (DDLT) is increasing in India and now constitutes nearly one-third of all liver transplantation procedures performed in the country. There is currently no uniform national system of allocation of deceased donor livers.
    UNASSIGNED: A national task force consisting of 19 clinicians involved in liver transplantation from across the country was constituted under the aegis of the Liver Transplantation Society of India to develop a consensus document addressing the above issues using a modified Delphi process of consensus development.
    UNASSIGNED: The National Liver Allocation Policy consensus document includes 46 statements covering all aspects of DDLT, including minimum listing criteria, listing for acute liver failure, DDLT wait-list management, system of prioritisation based on clinical urgency for adults and children, guidelines for allocation of paediatric organs and allocation priorities for liver grafts recovered from public sector hospitals.
    UNASSIGNED: This document is the first step in the setting up of a nationally consistent policy of deceased donor liver allocation.
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  • 文章类型: Journal Article
    未经证实:肝硬化患者常出现贫血,并被确定为不良结局的预测因子。如死亡率增加和慢性急性肝衰竭的发生。迄今为止,补充铁对这些不良结局的可能影响没有很好的描述.因此,我们旨在评估铁补充剂在肝硬化患者中的作用及其改善预后的能力。
    UNASSIGNED:对2018年7月至2019年12月在埃森大学医院收治的肝硬化连续门诊患者进行了实验室诊断。在回归模型中评估与无移植存活的关联。
    UNASSIGNED:共纳入317名肝硬化门诊患者,其中61人接受了肝移植(n=19)或死亡(n=42)。在多元Cox回归分析中,男性(危险比[HR]=3.33,95%CI[1.59,6.99],p=0.001),终末期肝病评分模型(HR=1.19,95%CI[1.11,1.27],p<0.001)和6个月内血红蛋白水平的增加(ΔHb6)(HR=0.72,95%CI[0.63,0.83],p<0.001)与无移植生存率相关。关于血红蛋白增加的预测,利福昔明的摄入(β=0.50,SDβ=0.19,p=0.007)和铁补充剂(β=0.79,SDβ=0.26,p=0.003)是多变量分析中的显著预测因子.
    UASSIGNED:在肝硬化患者中,血红蛋白水平的升高与无移植生存率的改善有关。因为血红蛋白增加的预测显著依赖于利福昔明和铁的补充,这两种药物的应用会对这些患者的预后产生重要影响。
    UNASSIGNED:贫血在肝硬化患者中非常常见,已知是阴性结果的预测因子,但是对这些个体的铁替代作用知之甚少。在我们的队列中,血红蛋白水平升高可改善肝硬化患者的无移植生存率.血红蛋白水平的增加主要是由铁补充引起的,并且在同时使用铁和利福昔明的情况下甚至更强。
    未经评估:UME-ID-10042。
    UNASSIGNED: Anaemia is frequently observed in patients with cirrhosis and was identified as a predictor of adverse outcomes, such as increased mortality and occurrence of acute-on-chronic liver failure. To date, the possible effects of iron supplementation on these adverse outcomes are not well described. We therefore aimed to assess the role of iron supplementation in patients with cirrhosis and its capability to improve prognosis.
    UNASSIGNED: Laboratory diagnostics were performed in consecutive outpatients with cirrhosis admitted between July 2018 and December 2019 to the University Hospital Essen. Associations with transplant-free survival were assessed in regression models.
    UNASSIGNED: A total of 317 outpatients with cirrhosis were included, of whom 61 received a liver transplant (n = 19) or died (n = 42). In multivariate Cox regression analysis, male sex (hazard ratio [HR] = 3.33, 95% CI [1.59, 6.99], p = 0.001), model for end-stage liver disease score (HR = 1.19, 95% CI [1.11, 1.27], p <0.001) and the increase of haemoglobin levels within 6 months (ΔHb6) (HR = 0.72, 95% CI [0.63, 0.83], p <0.001) were associated with transplant-free survival. Regarding the prediction of haemoglobin increase, intake of rifaximin (beta = 0.50, SD beta = 0.19, p = 0.007) and iron supplementation (beta = 0.79, SD beta = 0.26, p = 0.003) were significant predictors in multivariate analysis.
    UNASSIGNED: An increase of haemoglobin levels is associated with improvement of transplant-free survival in patients with cirrhosis. Because the prediction of haemoglobin increase significantly depends on rifaximin and iron supplementation, application of these two medications can have an important impact on the outcome of these patients.
    UNASSIGNED: Anaemia is very common in patients with cirrhosis and is known to be a predictor of negative outcomes, but little is known about the effect of iron substitution in these individuals. In our cohort, increase of haemoglobin levels improved transplant-free survival of patients with cirrhosis. The increase of haemoglobin levels was mainly induced by iron supplementation and was even stronger in the case of concomitant use of iron and rifaximin.
    UNASSIGNED: UME-ID-10042.
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  • 文章类型: Journal Article
    UNASSIGNED:使用血清总胆红素和白蛋白水平作为评估肝功能的简单方法来计算白蛋白-胆红素(ALBI)评分。这项研究调查了基线ALBI评分/等级测量在日本全国大型队列中评估原发性胆汁性胆管炎(PBC)个体的组织学阶段和疾病进展的能力。
    UNASSIGNED:1980年至2016年期间,从469个机构中招募了8,768名日本PBC患者。其中83%只接受熊去氧胆酸(UDCA),9%接受了UDCA和苯扎贝特,8%的人没有服用任何药物。回顾性地从中央数据库检索和审查基线临床和实验室参数。ALBI评分/分级与组织学分期的关联,死亡率,使用Cox比例风险模型评估肝移植的需要。
    未经评估:在5.3年的中位随访期间,1,227例患者死亡(包括789例因肝脏相关原因死亡),113例接受LT。ALBI评分和ALBI分级与Scheuer分类显著相关(p均<0.0001)。根据Cox比例风险回归分析,ALBI2级或3级与全因死亡率或需要LT以及肝脏相关死亡率或需要LT显著相关(风险比3.453,95%CI2.942-4.052和风险比4.242,95%CI3.421-5.260;两者均p<0.0001)。ALBI1、2和3级组的5年累积无LT生存率为97.2%,82.4%,38.8%,分别,而各自的非肝脏相关生存率为98.1%,86.0%,和42.0%(均p<0.0001,对数秩检验)。
    UNASSIGNED:这项针对PBC患者的大型全国性研究表明,ALBI分级的基线测量是PBC预后的简单非侵入性预测指标。
    未经证实:原发性胆汁性胆管炎(PBC)是一种自身免疫性肝病,其特征是肝内胆管进行性破坏。这项研究通过日本的大规模全国性队列研究了白蛋白-胆红素(ALBI)评分/等级评估PBC组织学发现和疾病进展的能力。ALBI评分/等级与Scheuer分类阶段显著相关。基线ALBI等级测量可能是PBC预后的简单非侵入性预测指标。
    UNASSIGNED: The albumin-bilirubin (ALBI) score is calculated using serum levels of total bilirubin and albumin as a simple method to assess liver function. This study investigated the ability of baseline ALBI score/grade measurements to assess histological stage and disease progression in individuals with primary biliary cholangitis (PBC) in a large Japanese nationwide cohort.
    UNASSIGNED: A total of 8,768 Japanese patients with PBC were enrolled between 1980 and 2016 from 469 institutions, among whom 83% received ursodeoxycholic acid (UDCA) only, 9% received UDCA and bezafibrate, and 8% were given neither drug. Baseline clinical and laboratory parameters were retrospectively retrieved and reviewed from a central database. Associations of ALBI score/grade with histological stage, mortality, and need for liver transplantation (LT) were evaluated using Cox proportional hazards models.
    UNASSIGNED: During the median follow-up period of 5.3 years, 1,227 patients died (including 789 from liver-related causes) and 113 underwent LT. ALBI score and ALBI grade were significantly associated with Scheuer\'s classification (both p <0.0001). ALBI grade 2 or 3 had significant associations with all-cause mortality or need for LT as well as liver-related mortality or need for LT according to Cox proportional hazards regression analysis (hazard ratio 3.453, 95% CI 2.942-4.052 and hazard ratio 4.242, 95% CI 3.421-5.260, respectively; both p <0.0001). Cumulative LT-free survival rates at 5 years in the ALBI grade 1, 2, and 3 groups were 97.2%, 82.4%, and 38.8%, respectively, while respective non-liver-related survival rates were 98.1%, 86.0%, and 42.0% (both p <0.0001, log-rank test).
    UNASSIGNED: This large nationwide study of patients with PBC suggested that baseline measurements of ALBI grade were a simple non-invasive predictor of prognosis in PBC.
    UNASSIGNED: Primary biliary cholangitis (PBC) is an autoimmune liver disease characterized by progressive destruction of intrahepatic bile ducts. This study examined the ability of albumin-bilirubin (ALBI) score/grade to estimate histological findings and disease progression in PBC by means of a large-scale nationwide cohort in Japan. ALBI score/grade were significantly associated with Scheuer\'s classification stage. Baseline ALBI grade measurements may be a simple non-invasive predictor of prognosis in PBC.
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  • 文章类型: Journal Article
    未经证实:肝移植(LT)是治疗终末期非酒精性脂肪性肝病(NAFLD)(相关失代偿性肝硬化和/或肝细胞癌)的唯一方法。我们研究的目的是评估LT术后疾病复发的风险及其影响因素。
    UNASSIGNED:这项回顾性多中心研究包括2000年至2019年在20个参与的法语国家中心移植NAFLD肝硬化的成年人。疾病复发(脂肪变性,脂肪性肝炎和纤维化)是通过肝移植活检诊断的。
    UASSIGNED:我们分析了150例患者,在移植后≥6个月进行了至少一次移植肝活检,在361例NAFLD移植患者中。LT时的中位年龄(IQR)为61.3(54.4-64.6)岁。LT后的中位随访时间为4.7(2.8-8.1)年。5年脂肪变性和脂肪性肝炎的累计复发率分别为80.0%和60.3%,分别。多变量分析中脂肪性肝炎复发的重要危险因素是LT<65岁的接受者年龄(比值比[OR]4.214;p=0.044),LT后高密度脂蛋白-胆固醇<1.15mmol/L(OR3.463;p=0.013),LT后1年移植物脂肪变性≥2级(OR10.196;p=0.001)。晚期纤维化(F3-F4)的累积发生率在LT后5年为20.0%,多变量分析的显著危险因素是LT前的代谢综合征(OR8.550;p=0.038),长期使用环孢素(OR11.388;p=0.031)和LT后1年≥2级脂肪变性(OR10.720;p=0.049).未对NAFLD肝硬化复发进行再次LT。
    UNASSIGNED:我们的研究结果强烈表明,在大部分患者中,NAFLDLT术后初次疾病的复发是不可避免的和进行性的;预防其的手段仍有待进一步评估。
    UnASSIGNED:非酒精性脂肪性肝病(NAFLD)越来越成为肝移植的适应症,但是对疾病复发的分析,基于移植肝活检,研究得很差。脂肪变性的累积发生率,脂肪性肝炎和NAFLD相关的显著纤维化复发在5年为85.0%,60.3%和48.0%,分别。1年移植活检≥2级脂肪变性(25%的患者存在)高度预测脂肪性肝炎和晚期纤维化的复发:应特别讨论这些患者的减肥手术。
    UNASSIGNED: Liver transplantation (LT) is the only available treatment for end-stage non-alcoholic fatty liver disease (NAFLD) (related decompensated cirrhosis and/or hepatocellular carcinoma). The aim of our study was to evaluate the risk of disease recurrence after LT and the factors influencing it.
    UNASSIGNED: This retrospective multicenter study included adults transplanted for NAFLD cirrhosis between 2000 and 2019 in 20 participating French-speaking centers. Disease recurrence (steatosis, steatohepatitis and fibrosis) was diagnosed from liver graft biopsies.
    UNASSIGNED: We analyzed 150 patients with at least one graft liver biopsy available ≥6 months after transplantation, among 361 patients transplanted for NAFLD. The median (IQR) age at LT was 61.3 (54.4-64.6) years. The median follow-up after LT was 4.7 (2.8-8.1) years. The cumulative recurrence rates of steatosis and steatohepatitis at 5 years were 80.0% and 60.3%, respectively. Significant risk factors for steatohepatitis recurrence in multivariate analysis were recipient age at LT <65 years (odds ratio [OR] 4.214; p = 0.044), high-density lipoprotein-cholesterol <1.15 mmol/L after LT (OR 3.463; p = 0.013) and grade ≥2 steatosis on the graft at 1 year after LT (OR 10.196; p = 0.001). The cumulative incidence of advanced fibrosis (F3-F4) was 20.0% at 5 years after LT and significant risk factors from multivariate analysis were metabolic syndrome before LT (OR 8.550; p = 0.038), long-term use of cyclosporine (OR 11.388; p = 0.031) and grade ≥2 steatosis at 1 year after LT (OR 10.720; p = 0.049). No re-LT was performed for NAFLD cirrhosis recurrence.
    UNASSIGNED: Our results strongly suggest that recurrence of initial disease after LT for NAFLD is inevitable and progressive in a large proportion of patients; the means to prevent it remain to be further evaluated.
    UNASSIGNED: Non-alcoholic fatty liver disease (NAFLD) is a growing indication for liver transplantation, but the analysis of disease recurrence, based on graft liver biopsies, has been poorly studied. Cumulative incidences of steatosis, steatohepatitis and NAFLD-related significant fibrosis recurrence at 5 years were 85.0%, 60.3% and 48.0%, respectively. Grade ≥2 steatosis on graft biopsy at 1 year (present in 25% of patients) is highly predictive of recurrence of steatohepatitis and advanced fibrosis: bariatric surgery should be discussed in these patients specifically.
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  • 文章类型: Journal Article
    未经证实:肝移植(LT)是慢性急性肝衰竭(ACLF)的有效治疗方法,但受到器官短缺的限制。我们的目的是确定一个适当的评分来预测HBV相关ACLF患者LT的生存获益。
    UNASSIGNED:来自中国重型乙型肝炎(COSSH)开放队列研究小组的HBV相关慢性肝病急性恶化的住院患者(n=4577)被纳入评估五个常用评分预测预后和移植生存获益的表现。计算生存获益率,以反映预期寿命的延长率与没有LT
    未经批准:总共,368例HBV-ACLF患者接受LT。他们在整个HBV-ACLF队列中显示出比等待名单上的1年生存率显着提高(77.2%/52.3%,p<0.001)和倾向评分匹配队列(77.2%/27.6%,p<0.001)。受试者工作特征曲线下面积(AUROC)表明,COSSH-ACLFII评分在确定等待名单上的1年死亡风险方面表现最佳(AUROC0.849),在预测1年死亡风险方面表现最佳(AUROC0.864)。LT后的一年结局(COSSH-ACLFs/CLIF-CACLFs/MELDs/MELD-Nas:AUROC0.835/0.796C指数证实了COSSH-ACLFIIs的高预测价值。生存获益率分析显示,患有COSSH-ACLFIIs7-10的患者从LT获得的1年生存获益率(39.2%-64.3%)高于评分<7或>10的患者。这些结果得到了前瞻性验证。
    未经评估:COSSH-ACLFIIs确定了等待名单上的死亡风险,并准确预测了HBV-ACLF的LT后死亡率和生存获益。患有COSSH-ACLFII7-10的患者从LT获得了更高的净生存益处。
    UNASSIGNED:本研究得到了国家自然科学基金(编号:81830073,编号81771196)和国家高层次人才招聘特别支持计划(万人计划)。
    UNASSIGNED: Liver transplantation (LT) is an effective therapy for acute-on-chronic liver failure (ACLF) but is limited by organ shortages. We aimed to identify an appropriate score for predicting the survival benefit of LT in HBV-related ACLF patients.
    UNASSIGNED: Hospitalized patients with acute deterioration of HBV-related chronic liver disease (n = 4577) from the Chinese Group on the Study of Severe Hepatitis B (COSSH) open cohort were enrolled to evaluate the performance of five commonly used scores for predicting the prognosis and transplant survival benefit. The survival benefit rate was calculated to reflect the extended rate of the expected lifetime with vs. without LT.
    UNASSIGNED: In total, 368 HBV-ACLF patients received LT. They showed significantly higher 1-year survival than those on the waitlist in both the entire HBV-ACLF cohort (77.2%/52.3%, p < 0.001) and the propensity score matching cohort (77.2%/27.6%, p < 0.001). The area under the receiver operating characteristic curve (AUROC) showed that the COSSH-ACLF II score performed best (AUROC 0.849) at identifying the 1-year risk of death on the waitlist and best (AUROC 0.864) at predicting 1-year outcome post-LT (COSSH-ACLFs/CLIF-C ACLFs/MELDs/MELD-Nas: AUROC 0.835/0.825/0.796/0.781; all p < 0.05). The C-indexes confirmed the high predictive value of COSSH-ACLF IIs. Survival benefit rate analyses showed that patients with COSSH-ACLF IIs 7-10 had a higher 1-year survival benefit rate from LT (39.2%-64.3%) than those with score <7 or >10. These results were prospectively validated.
    UNASSIGNED: COSSH-ACLF IIs identified the risk of death on the waitlist and accurately predicted post-LT mortality and survival benefit for HBV-ACLF. Patients with COSSH-ACLF IIs 7-10 derived a higher net survival benefit from LT.
    UNASSIGNED: This study was supported by the National Natural Science Foundation of China (No. 81830073, No. 81771196) and the National Special Support Program for High-Level Personnel Recruitment (Ten-thousand Talents Program).
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