已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Derivation and validation of prognostic models for predicting survival outcomes in Acute‐on‐chronic liver failure patients

医学 内科学 凝血酶原时间 逻辑回归 胃肠病学 肝性脑病 肝病 部分凝血活酶时间 肝肾综合征 糖尿病 肝硬化 凝结 内分泌学
作者
Fajuan Rui,Hongli Yang,Zhaoyang Guo,Zhengming Ge,Xinyu Hu,Lulu Zhang,Qi Xue,Haiping Chen,Yayun Xu,Meng H. Tan,Chengyong Qin,Zebao He,Jie Li
出处
期刊:Journal of Viral Hepatitis [Wiley]
卷期号:28 (12): 1719-1728 被引量:5
标识
DOI:10.1111/jvh.13611
摘要

Abstract Acute‐on‐chronic liver failure (ACLF) is a syndrome characterized by acute decompensation of chronic liver disease associated with high bacterial infection (BI) and short‐term mortality. However, many ACLF prognostic predictive modelsare complicated. The aim of this study is to develop prognostic models for ACLF patients to predict BI and mortality. We retrospective recruited 263 patients with ACLF from Shandong Provincial Hospital and Taizhou Enze Medical Center (Group) Enze Hospital. ACLF was defined according to the Asian Pacific Association for the Study of the Liver (APASL) criteria. Multivariable logistic regression was used to derive prediction models for occurring BI and 28‐day mortality in ACLF patients. Ninety seven of 263 patients (37%) occurred BI and 41 of 155 (26%) died within 28 days of admission. C‐reactive protein (CRP), glucose, and albumin were the independent predictors for occurring BI during the hospital stay. We also found that hepatic encephalopathy (HE), prothrombin time, activated partial thromboplastin time (APRI), and glucose were the independent predictors of 28‐day mortality of ACLF patients. Using logistic regression model, we generated a new modified MELD model (M‐MELD) by incorporating HE, APRI, and glucose. AUC of M‐MELD model was 0.871, which were significantly higher than MELD score (AUC:0.734), MELD‐Na score (AUC:0.742), and integrated MELD score (iMELD) (AUC:0.761). HE, MELD score, APRI, and blood glucose were independent risk factors for 28‐day mortality of ACLF patients. The modified MELD model (M‐MELD) by incorporating HE, APRI, and glucose has better discriminative performances compared with MELD in predicting 28‐day mortality.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Ava应助辣椒炒肉1采纳,获得10
1秒前
月关完成签到 ,获得积分10
3秒前
3秒前
5秒前
yang完成签到,获得积分10
7秒前
十六发布了新的文献求助10
9秒前
Milton_z完成签到 ,获得积分0
10秒前
zl完成签到 ,获得积分10
12秒前
13秒前
yang发布了新的文献求助10
13秒前
平常以云完成签到 ,获得积分10
13秒前
爱笑的鹿完成签到 ,获得积分10
15秒前
15秒前
小黄完成签到 ,获得积分10
16秒前
18秒前
21秒前
24秒前
所所应助十六采纳,获得10
27秒前
落叶捎来讯息完成签到 ,获得积分10
27秒前
风中小夏发布了新的文献求助10
29秒前
30秒前
虚心的铅笔完成签到 ,获得积分10
31秒前
31秒前
小蘑菇应助柯佳君采纳,获得10
32秒前
40秒前
耶耶粘豆包完成签到 ,获得积分10
43秒前
罗赛应助葛力采纳,获得30
43秒前
46秒前
柯佳君发布了新的文献求助10
47秒前
xxx关注了科研通微信公众号
49秒前
miki完成签到,获得积分10
50秒前
yjyy完成签到 ,获得积分10
51秒前
共享精神应助bb采纳,获得10
54秒前
潘啊潘完成签到 ,获得积分10
54秒前
55秒前
白小超人完成签到 ,获得积分10
58秒前
JYH12138完成签到,获得积分10
58秒前
bb完成签到,获得积分10
58秒前
vetzlk完成签到 ,获得积分10
59秒前
科研通AI6.1应助lxr采纳,获得10
59秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 3000
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 1100
3O - Innate resistance in EGFR mutant non-small cell lung cancer (NSCLC) patients by coactivation of receptor tyrosine kinases (RTKs) 1000
Signals, Systems, and Signal Processing 510
Discrete-Time Signals and Systems 510
Proceedings of the Fourth International Congress of Nematology, 8-13 June 2002, Tenerife, Spain 500
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5935323
求助须知:如何正确求助?哪些是违规求助? 7013645
关于积分的说明 15860907
捐赠科研通 5064113
什么是DOI,文献DOI怎么找? 2723902
邀请新用户注册赠送积分活动 1681432
关于科研通互助平台的介绍 1611207