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二十一世纪,通过转化研究改善创伤治疗。

Transforming research to improve therapies for trauma in the twenty-first century.

机构信息

Department of Intensive Care, Erasmus Medical Center, Rotterdam, The Netherlands.

Laboratory of Translational Intensive Care, Erasmus Medical Center, Rotterdam, The Netherlands.

出版信息

Crit Care. 2024 Feb 13;28(1):45. doi: 10.1186/s13054-024-04805-6.


DOI:10.1186/s13054-024-04805-6
PMID:38350971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10865682/
Abstract

Improvements have been made in optimizing initial care of trauma patients, both in prehospital systems as well as in the emergency department, and these have also favorably affected longer term outcomes. However, as specific treatments for bleeding are largely lacking, many patients continue to die from hemorrhage. Also, major knowledge gaps remain on the impact of tissue injury on the host immune and coagulation response, which hampers the development of interventions to treat or prevent organ failure, thrombosis, infections or other complications of trauma. Thereby, trauma remains a challenge for intensivists. This review describes the most pressing research questions in trauma, as well as new approaches to trauma research, with the aim to bring improved therapies to the bedside within the twenty-first century.

摘要

创伤患者的初始治疗已得到优化,无论是在院前系统还是在急诊科,这也对长期预后产生了有利影响。然而,由于缺乏针对出血的具体治疗方法,许多患者仍因出血而死亡。此外,组织损伤对宿主免疫和凝血反应的影响仍然存在重大知识空白,这阻碍了开发治疗或预防器官衰竭、血栓形成、感染或创伤其他并发症的干预措施。因此,创伤仍然是重症监护医生面临的挑战。本综述描述了创伤领域最紧迫的研究问题,以及创伤研究的新方法,旨在在 21 世纪将改进的治疗方法带到床边。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eabb/10865682/28a74fb6d725/13054_2024_4805_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eabb/10865682/28a74fb6d725/13054_2024_4805_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eabb/10865682/28a74fb6d725/13054_2024_4805_Fig1_HTML.jpg

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[1]
Transforming research to improve therapies for trauma in the twenty-first century.

Crit Care. 2024-2-13

[2]
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[4]
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[5]
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[7]
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引用本文的文献

[1]
Is Mechanism a Biological Variable?: A Secondary Analysis of the PROPPR Trial.

Ann Surg Open. 2025-5-6

[2]
From bedside to data and back to bedside: why do we need better data to perform trauma phenotyping and improve trauma care?

Intensive Care Med. 2025-6-4

[3]
Strengthening trauma resuscitation education and training in low-resource settings: A call for global inclusion.

Resusc Plus. 2025-3-20

[4]
Future directions in the treatment of pelvic fractures with abdominal organ injury: the potential of combined endovascular embolization and external fixation techniques.

Front Med (Lausanne). 2025-3-28

[5]
Adjuvant therapies for management of hemorrhagic shock: a narrative review.

Crit Care. 2025-3-29

[6]
Transforming research to improve therapies for trauma in the twenty-first century: an alternative perspective.

Crit Care. 2024-4-23

本文引用的文献

[1]
Early and Empirical High-Dose Cryoprecipitate for Hemorrhage After Traumatic Injury: The CRYOSTAT-2 Randomized Clinical Trial.

JAMA. 2023-11-21

[2]
Doing more with less: low-titer group O whole blood resulted in less total transfusions and an independent association with survival in adults with severe traumatic hemorrhage.

J Thromb Haemost. 2024-1

[3]
The effects of resuscitation with different plasma products on endothelial permeability and organ injury in a rat pneumosepsis model.

Intensive Care Med Exp. 2023-9-20

[4]
The persistent inflammation, immunosuppression, and catabolism syndrome 10 years later.

J Trauma Acute Care Surg. 2023-11-1

[5]
Safety and efficacy of artesunate treatment in severely injured patients with traumatic hemorrhage. The TOP-ART randomized clinical trial.

Intensive Care Med. 2023-8

[6]
Polymerized human hemoglobin with low and high oxygen affinity in trauma models.

Transl Res. 2023-10

[7]
Effect of P2Y12 Inhibitors on Organ Support-Free Survival in Critically Ill Patients Hospitalized for COVID-19: A Randomized Clinical Trial.

JAMA Netw Open. 2023-5-1

[8]
Predicting the Future in Trauma: Trauma and Injury Severity Score Loses Accuracy and Validity for Late Deaths After Injury.

Am Surg. 2023-10

[9]
A 3--sulfated heparan sulfate dodecasaccharide (12-mer) suppresses thromboinflammation and attenuates early organ injury following trauma and hemorrhagic shock.

Front Immunol. 2023

[10]
Association of Trauma Molecular Endotypes With Differential Response to Transfusion Resuscitation Strategies.

JAMA Surg. 2023-7-1

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