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肝衰竭决定慢加急性肝衰竭(ACLF)患者的结局:APASL ACLF 研究联盟(AARC)和 CLIF-SOFA 模型的比较。

Liver failure determines the outcome in patients of acute-on-chronic liver failure (ACLF): comparison of APASL ACLF research consortium (AARC) and CLIF-SOFA models.

机构信息

Department of Hepatology and Transplant, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.

Department of Hepatology, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.

出版信息

Hepatol Int. 2017 Sep;11(5):461-471. doi: 10.1007/s12072-017-9816-z. Epub 2017 Aug 30.

DOI:10.1007/s12072-017-9816-z
PMID:28856540
Abstract

BACKGROUND AND AIMS

Acute-on-chronic liver failure (ACLF) is a progressive disease associated with rapid clinical worsening and high mortality. Early prediction of mortality and intervention can improve patient outcomes. We aimed to develop a dynamic prognostic model and compare it with the existing models.

METHODS

A total of 1402 ACLF patients, enrolled in the APASL-ACLF Research Consortium (AARC) with 90-day follow-up, were analyzed. An ACLF score was developed in a derivation cohort (n = 480) and was validated (n = 922).

RESULTS

The overall survival of ACLF patients at 28 days was 51.7%, with a median of 26.3 days. Five baseline variables, total bilirubin, creatinine, serum lactate, INR and hepatic encephalopathy, were found to be independent predictors of mortality, with AUROC in derivation and validation cohorts being 0.80 and 0.78, respectively. AARC-ACLF score (range 5-15) was found to be superior to MELD and CLIF SOFA scores in predicting mortality with an AUROC of 0.80. The point scores were categorized into grades of liver failure (Gr I: 5-7; II: 8-10; and III: 11-15 points) with 28-day cumulative mortalities of 12.7, 44.5 and 85.9%, respectively. The mortality risk could be dynamically calculated as, with each unit increase in AARC-ACLF score above 10, the risk increased by 20%. A score of ≥11 at baseline or persisting in the first week was often seen among nonsurvivors (p = 0.001).

CONCLUSIONS

The AARC-ACLF score is easy to use, dynamic and reliable, and superior to the existing prediction models. It can reliably predict the need for interventions, such as liver transplant, within the first week.

摘要

背景与目的

慢加急性肝衰竭(ACLF)是一种进展性疾病,与快速临床恶化和高死亡率相关。对死亡率进行早期预测并采取干预措施可以改善患者的预后。本研究旨在建立一个动态预后模型,并与现有的模型进行比较。

方法

共纳入 1402 例接受 90 天随访的 ACLF 患者,这些患者均来自亚太肝脏研究学会慢加急性肝衰竭研究联盟(AARC)。在一个衍生队列(n=480)中建立 ACLF 评分,并进行验证(n=922)。

结果

ACLF 患者在 28 天时的总体生存率为 51.7%,中位生存时间为 26.3 天。总胆红素、肌酐、血清乳酸、INR 和肝性脑病这 5 个基线变量被发现是死亡率的独立预测因素,在衍生队列和验证队列中的 AUROC 分别为 0.80 和 0.78。AARC-ACLF 评分(范围为 5-15 分)在预测死亡率方面优于 MELD 和 CLIF-SOFA 评分,AUROC 为 0.80。点评分被分为肝功能衰竭等级(Gr I:5-7 分;Gr II:8-10 分;Gr III:11-15 分),28 天累积死亡率分别为 12.7%、44.5%和 85.9%。死亡率风险可以动态计算,AARC-ACLF 评分每增加 1 分,风险增加 20%。基线评分≥11 分或在第一周持续存在的患者通常是非幸存者(p=0.001)。

结论

AARC-ACLF 评分易于使用、动态且可靠,优于现有的预测模型。它可以可靠地预测在第一周内需要进行干预的情况,如肝移植。

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