• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Hemophagocytic Lymphohistiocytosis in the Medical ICU: A Single-Institution Cohort Study on Acute Liver Failure and Mortality.医学重症监护病房中的噬血细胞性淋巴组织细胞增生症:一项关于急性肝衰竭和死亡率的单机构队列研究。
Crit Care Explor. 2021 Jan 8;3(1):e0318. doi: 10.1097/CCE.0000000000000318. eCollection 2021 Jan.
2
The Use of Ferritin to Identify Critically Ill Patients With Secondary Hemophagocytic Lymphohistiocytosis.铁蛋白在继发性噬血细胞性淋巴组织细胞增生症危重症患者中的应用。
Crit Care Med. 2016 Nov;44(11):e1045-e1053. doi: 10.1097/CCM.0000000000001878.
3
Hemophagocytic Lymphohistiocytosis in a PICU of a Developing Economy: Clinical Profile, Intensive Care Needs, Outcome, and Predictors of Mortality.发展中国家儿科重症监护病房噬血细胞性淋巴组织细胞增生症:临床特征、重症监护需求、结局和死亡预测因素。
Pediatr Crit Care Med. 2021 Jan 1;22(1):e44-e57. doi: 10.1097/PCC.0000000000002539.
4
Outcomes Analysis of Children Diagnosed With Hemophagocytic Lymphohistiocytosis in the PICU.儿童在 PICU 中被诊断为噬血细胞性淋巴组织细胞增生症的结果分析。
Pediatr Crit Care Med. 2019 Apr;20(4):e185-e190. doi: 10.1097/PCC.0000000000001827.
5
Bacteremia, acute physiology and chronic health evaluation II and modified end stage liver disease are independent predictors of mortality in critically ill nontransplanted patients with acute on chronic liver failure.菌血症、急性生理学与慢性健康状况评分系统 II 及改良终末期肝病模型评分是合并慢加急性肝衰竭的非移植危重症患者死亡的独立预测因子。
Crit Care Med. 2010 Jan;38(1):121-6. doi: 10.1097/CCM.0b013e3181b42a1c.
6
Acute circulatory failure in critically ill patients with hemophagocytic syndrome.危重症噬血细胞综合征患者的急性循环衰竭。
J Crit Care. 2022 Aug;70:154064. doi: 10.1016/j.jcrc.2022.154064. Epub 2022 May 19.
7
Hyperferritinemia in Critically Ill Patients.危重症患者的高血铁蛋白血症。
Crit Care Med. 2020 Apr;48(4):459-465. doi: 10.1097/CCM.0000000000004131.
8
Intensive care unit complications and outcomes of adult patients with hemophagocytic lymphohistiocytosis: A retrospective study of 16 cases.成人噬血细胞性淋巴组织细胞增生症患者在重症监护病房的并发症及预后:一项16例病例的回顾性研究
World J Crit Care Med. 2018 Nov 30;7(6):73-83. doi: 10.5492/wjccm.v7.i6.73.
9
Etiologies and Clinical Outcomes of Patients With Secondary Hemophagocytic Lymphohistiocytosis at a Tertiary PICU.三级儿童重症监护病房继发性噬血细胞性淋巴组织细胞增生症患者的病因和临床结局。
Pediatr Crit Care Med. 2019 Jul;20(7):e311-e318. doi: 10.1097/PCC.0000000000001980.
10
Hypofibrinogenemia Is Associated With Poor Outcome and Secondary Hemophagocytic Lymphohistiocytosis/Macrophage Activation Syndrome in Pediatric Severe Sepsis.低纤维蛋白原血症与儿科严重脓毒症不良预后及噬血细胞性淋巴组织细胞增多症/巨噬细胞活化综合征相关。
Pediatr Crit Care Med. 2018 May;19(5):397-405. doi: 10.1097/PCC.0000000000001507.

引用本文的文献

1
Cytokine Storm and Sepsis-Induced Multiple Organ Dysfunction Syndrome.细胞因子风暴与脓毒症致多器官功能障碍综合征
Adv Exp Med Biol. 2024;1448:441-457. doi: 10.1007/978-3-031-59815-9_30.
2
Patients with Hemophagocytic Lymphohistiocytosis Who Need Intensive Care Can Be Successfully Rescued by Timely Using Etoposide-Based HLH Regimens.需要重症监护的噬血细胞性淋巴组织细胞增生症患者通过及时使用依托泊苷为基础的HLH方案可成功获救。
Int J Gen Med. 2024 Feb 3;17:431-446. doi: 10.2147/IJGM.S443774. eCollection 2024.

本文引用的文献

1
Cytokine release syndrome in severe COVID-19: interleukin-6 receptor antagonist tocilizumab may be the key to reduce mortality.严重 COVID-19 中的细胞因子释放综合征:白细胞介素-6 受体拮抗剂托珠单抗可能是降低死亡率的关键。
Int J Antimicrob Agents. 2020 May;55(5):105954. doi: 10.1016/j.ijantimicag.2020.105954. Epub 2020 Mar 29.
2
Adult haemophagocytic lymphohistiocytosis: a Review.成人噬血细胞性淋巴组织细胞增生症:综述
QJM. 2020 Jan 14. doi: 10.1093/qjmed/hcaa011.
3
Hepatic sinusoidal hemophagocytosis with and without hemophagocytic lymphohistiocytosis.伴有和不伴有噬血细胞性淋巴组织细胞增生症的肝窦噬血细胞现象。
PLoS One. 2019 Dec 30;14(12):e0226899. doi: 10.1371/journal.pone.0226899. eCollection 2019.
4
Hemophagocytic Lymphohistiocytosis in Critically Ill Patients.危重症患者噬血细胞性淋巴组织细胞增生症
Shock. 2020 Jun;53(6):701-709. doi: 10.1097/SHK.0000000000001454.
5
Clinical characteristics of liver failure with hemophagocytic lymphohistiocytosis.噬血细胞性淋巴组织细胞增生症相关肝衰竭的临床特征。
Sci Rep. 2019 May 31;9(1):8125. doi: 10.1038/s41598-019-43909-w.
6
Patterns of necrosis in liver disease.肝脏疾病中的坏死模式。
Clin Liver Dis (Hoboken). 2017 Aug 30;10(2):53-56. doi: 10.1002/cld.653. eCollection 2017 Aug.
7
Recommendations for the management of hemophagocytic lymphohistiocytosis in adults.成人噬血细胞性淋巴组织细胞增生症的治疗建议。
Blood. 2019 Jun 6;133(23):2465-2477. doi: 10.1182/blood.2018894618. Epub 2019 Apr 16.
8
Hemophagocytic Lymphohistiocytosis: Potentially Underdiagnosed in Intensive Care Units.噬血细胞性淋巴组织细胞增生症:在重症监护病房中可能被漏诊。
Shock. 2018 Aug;50(2):149-155. doi: 10.1097/SHK.0000000000001048.
9
Predicting Mortality of Patients With Sepsis: A Comparison of APACHE II and APACHE III Scoring Systems.预测脓毒症患者的死亡率:急性生理与慢性健康状况评分系统Ⅱ(APACHE II)与急性生理与慢性健康状况评分系统Ⅲ(APACHE III)的比较
J Clin Med Res. 2017 Nov;9(11):907-910. doi: 10.14740/jocmr3083w. Epub 2017 Oct 2.
10
Confirmed efficacy of etoposide and dexamethasone in HLH treatment: long-term results of the cooperative HLH-2004 study.依托泊苷和地塞米松治疗噬血细胞性淋巴组织细胞增生症的确证疗效:HLH - 2004合作研究的长期结果
Blood. 2017 Dec 21;130(25):2728-2738. doi: 10.1182/blood-2017-06-788349. Epub 2017 Sep 21.

医学重症监护病房中的噬血细胞性淋巴组织细胞增生症:一项关于急性肝衰竭和死亡率的单机构队列研究。

Hemophagocytic Lymphohistiocytosis in the Medical ICU: A Single-Institution Cohort Study on Acute Liver Failure and Mortality.

作者信息

Al Nasrallah Nawar, Al-Hader Ahmad, Samala Niharika, Sears Catherine R

机构信息

Division of Pulmonary, Critical Care, Sleep & Occupational Medicine, Indiana University School of Medicine, Indianapolis, IN.

Division of Hematology/Oncology, Indiana University School of Medicine, Indianapolis, IN.

出版信息

Crit Care Explor. 2021 Jan 8;3(1):e0318. doi: 10.1097/CCE.0000000000000318. eCollection 2021 Jan.

DOI:10.1097/CCE.0000000000000318
PMID:33458685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7803668/
Abstract

UNLABELLED

Hemophagocytic lymphohistiocytosis is a life-threatening hyperinflammatory disorder that is associated with high morbidity and mortality in the ICU. It has also been associated with acute liver failure.

DESIGN

Retrospective observational study.

SETTING

Tertiary-care medical ICU.

PATIENTS

Thirty-one patients critically ill with hemophagocytic lymphohistiocytosis.

INTERVENTIONS

None.

MEASUREMENTS AND MAIN RESULTS

We performed a comprehensive review of critically ill hemophagocytic lymphohistiocytosis patients admitted to a tertiary-care medical ICU from January 2012 to December 2018. Most patients presented with constitutional symptoms and elevated liver enzymes and thrombocytopenia were common upon hospital admission. ICU admission laboratory and clinical variables were used to calculate Acute Physiology and Chronic Health Evaluation II, hemophagocytic syndrome diagnostic score, and model for end-stage liver disease. Mean age of the cohort was 48.1 years, and 45% were male. The mortality rate was 65% at 28 days and 77% at 1 year. About 28-day survivors were younger, had lower mean Acute Physiology and Chronic Health Evaluation II score (16.5 vs 23.0; = 0.004), and higher mean hemophagocytic syndrome diagnostic score (249.1 vs 226.0; = 0.032) compared with nonsurvivors. Survivors were less likely to receive mechanical ventilation, renal replacement therapy, or vasopressor support and were more likely to receive chemotherapy for hemophagocytic lymphohistiocytosis. In this ICU cohort, 29% were diagnosed with acute liver failure, of whom only 22% developed acute liver failure early during their hospital stay. Acute liver failure was associated with a higher model for end-stage liver disease score upon hospital admission. Available histology in those that developed acute liver failure showed massive hepatic necrosis, or histiocytic or lymphocytic infiltrates.

CONCLUSIONS

Patients admitted to the ICU with hemophagocytic lymphohistiocytosis have a high mortality. Those who survived had lower Acute Physiology and Chronic Health Evaluation scores, had higher hemophagocytic syndrome diagnostic scores, are more likely to receive hemophagocytic lymphohistiocytosis specific chemotherapy, and are less likely to have organ failure. Hemophagocytic lymphohistiocytosis can be associated with acute liver failure especially when model for end-stage liver disease score is elevated upon admission.

摘要

未标注

噬血细胞性淋巴组织细胞增生症是一种危及生命的高炎症性疾病,在重症监护病房(ICU)中具有较高的发病率和死亡率。它还与急性肝衰竭有关。

设计

回顾性观察研究。

地点

三级医疗ICU。

患者

31例患有噬血细胞性淋巴组织细胞增生症的危重症患者。

干预措施

无。

测量指标及主要结果

我们对2012年1月至2018年12月入住三级医疗ICU的噬血细胞性淋巴组织细胞增生症危重症患者进行了全面回顾。大多数患者出现全身症状,入院时肝酶升高和血小板减少很常见。ICU入院时的实验室和临床变量用于计算急性生理与慢性健康状况评分系统II(APACHE II)、噬血细胞综合征诊断评分和终末期肝病模型(MELD)。该队列的平均年龄为48.1岁,45%为男性。28天死亡率为65%,1年死亡率为77%。与非幸存者相比,28天幸存者更年轻,平均APACHE II评分更低(16.5对23.0;P = 0.ooo4),平均噬血细胞综合征诊断评分更高(249.1对226.0;P = 0.032)。幸存者接受机械通气、肾脏替代治疗或血管活性药物支持的可能性较小,接受噬血细胞性淋巴组织细胞增生症化疗的可能性更大。在这个ICU队列中,29%被诊断为急性肝衰竭,其中只有22%在住院早期发生急性肝衰竭。急性肝衰竭与入院时较高的MELD评分相关。发生急性肝衰竭患者的现有组织学检查显示广泛肝坏死,或组织细胞或淋巴细胞浸润。

结论

入住ICU的噬血细胞性淋巴组织细胞增生症患者死亡率很高。幸存者的APACHE评分较低,噬血细胞综合征诊断评分较高,更有可能接受噬血细胞性淋巴组织细胞增生症特异性化疗,且器官衰竭的可能性较小。噬血细胞性淋巴组织细胞增生症可能与急性肝衰竭有关,尤其是入院时MELD评分升高时。