肝肾综合征患者途径:电子健康记录的回顾性分析

IF 1.6 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Khurram Jamil MD , Xingyue Huang PhD , David Hayashida MSc , Kunal Lodaya MD
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引用次数: 2

摘要

背景:肝肾综合征(HRS)是慢性肝病患者住院和死亡的主要原因之一。目的评估HRS患者从入院前到出院后的病程,以了解患者特征、疾病进展、治疗模式和结局。方法采用来自全国电子健康记录数据库(Cerner health Facts, Kansas City, Missouri)的真实数据进行回顾性研究。我们使用ICD-9/10诊断代码对2009年1月1日至2018年1月31日期间因HRS住院的患者进行识别。我们评估了患者的特征和病史、临床表现、治疗和结果。在调整人口统计学和临床协变量的同时,进行回归分析以评估患者特征与生存率之间的关系。结果共纳入3563例患者,其中男性占62%。HRS的诱发因素包括胃肠道出血(18%)、利尿剂和感染(30%)、穿刺(26%)。虽然21%的患者肝损伤完全与饮酒相关,但20%患有丙型肝炎,8%患有非酒精性脂肪性肝炎,其余(51%)的病因要么是某些疾病的组合,要么是未知的。总共42%的患者接受了血管加压药物治疗,包括奥曲肽和米多宁(10%),其他血管加压药物联合(11%)或另一种血管加压药物(21%)。住院死亡率为34%,14%的患者出院至临终关怀。回归分析显示,急性慢性肝衰竭患者在急性慢性肝衰竭1级(优势比 = 1.59)、2级(优势比 = 2.49)和3级(优势比 = 4.53)的死亡率高于非急性慢性肝衰竭患者。在幸存者中,38%的患者在出院90天内再次入院;23%的再入院患者与hr相关。结论:本研究中呈现的HRS患者旅程突出了相关医院治疗策略的不一致性,并为相关医院治疗策略提供了见解。死亡率为34%,再入院率为23%,与rs相关的并发症需要更多的疾病意识和有效的治疗。需要进一步的研究来检查肝硬化病因、沉淀物、治疗和结果之间的相互作用。(中国临床医学杂志,2022;82: XXX-XXX)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Hepatorenal Syndrome Patient Pathway: Retrospective Analysis of Electronic Health Records

Background

Hepatorenal syndrome (HRS) is among the leading causes of hospitalization and mortality in patients with chronic liver disease.

Objective

To assess the HRS patient journey from preadmission to postdischarge to understand patient characteristics, disease progression, treatment patterns, and outcomes.

Methods

We conducted a retrospective study using real-world data from a nationwide electronic health record database (Cerner Health Facts, Kansas City, Missouri). We used ICD-9/10 diagnosis codes to identify patients hospitalized with HRS between January 1, 2009, and January 31, 2018. We assessed patient characteristics and history, clinical presentation, treatment, and outcomes. Regression analysis was conducted to assess the association between patient characteristics and survival while adjusting for demographic and clinical covariates.

Results

The study included 3563 patients (62% men). Precipitants of HRS included gastrointestinal bleeding (18%), diuretics and infections (30%), and paracentesis (26%). Although 21% of patients had liver injury exclusively associated with alcohol use, 20% had hepatitis C, 8% had nonalcoholic steatohepatitis, and the etiology of the remainder (51%) was either some combination of conditions or unknown. A total of 42% of patients received vasopressors, including octreotide and midodrine (10%), other combinations of vasopressors (11%), or another single vasopressor (21%). In-hospital mortality was 34%, and 14% of patients were discharged to hospice. Regression analysis showed patients with acute-on-chronic liver failure had higher mortality in acute-on-chronic liver failure grades 1 (odds ratio = 1.59), 2 (odds ratio = 2.49), and 3 (odds ratio = 4.53) versus no acute-on-chronic liver failure. Among survivor patients, 38% were readmitted within 90 days of discharge; 23% of readmissions were HRS-related.

Conclusions

The HRS patient journey presented in this study highlights inconsistencies in, and provides insight into, associated hospital-based treatment strategies. A mortality rate of 34% along with a readmission rate of 23% associated with HRS-related complications warrant more disease awareness and effective treatment. Further research is needed to examine the interactions between the etiology of cirrhosis, precipitants, treatment, and outcomes. (Curr Ther Res Clin Exp. 2022; 82:XXX–XXX)

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CiteScore
3.50
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31
审稿时长
3 months
期刊介绍: We also encourage the submission of manuscripts presenting preclinical and very preliminary research that may stimulate further investigation of potentially relevant findings, as well as in-depth review articles on specific therapies or disease states, and applied health delivery or pharmacoeconomics. CTR encourages and supports the submission of manuscripts describing: • Interventions designed to understand or improve human health, disease treatment or disease prevention; • Studies that focus on problems that are uncommon in resource-rich countries; • Research that is "under-published" because of limited access to monetary resources such as English language support and Open Access fees (CTR offers deeply discounted English language editing); • Republication of articles previously published in non-English journals (eg, evidence-based guidelines) which could be useful if translated into English; • Preclinical and clinical product development studies that are not pursued for further investigation based upon early phase results.
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