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本文引用的文献

1
Part I: Minimum Quality Threshold in Preclinical Sepsis Studies (MQTiPSS) for Study Design and Humane Modeling Endpoints.第一部分:临床前期脓毒症研究的最低质量阈值(MQTiPSS)用于研究设计和人道建模终点。
Shock. 2019 Jan;51(1):10-22. doi: 10.1097/SHK.0000000000001243.
2
Part II: Minimum Quality Threshold in Preclinical Sepsis Studies (MQTiPSS) for Types of Infections and Organ Dysfunction Endpoints.第二部分:感染类型和器官功能障碍终点的临床前期脓毒症研究(MQTiPSS)的最低质量阈值。
Shock. 2019 Jan;51(1):23-32. doi: 10.1097/SHK.0000000000001242.
3
Part III: Minimum Quality Threshold in Preclinical Sepsis Studies (MQTiPSS) for Fluid Resuscitation and Antimicrobial Therapy Endpoints.第三部分:临床前期脓毒症研究中液体复苏和抗菌治疗终点的最低质量阈值(MQTiPSS)。
Shock. 2019 Jan;51(1):33-43. doi: 10.1097/SHK.0000000000001209.
4
Premise for Standardized Sepsis Models.标准化脓毒症模型的前提条件。
Shock. 2019 Jan;51(1):4-9. doi: 10.1097/SHK.0000000000001164.
5
Preclinical efficacy studies in investigator brochures: Do they enable risk-benefit assessment?研究者手册中的临床前疗效研究:它们是否能进行风险获益评估?
PLoS Biol. 2018 Apr 5;16(4):e2004879. doi: 10.1371/journal.pbio.2004879. eCollection 2018 Apr.
6
An Official American Thoracic Society Workshop Report: Use of Animal Models for the Preclinical Assessment of Potential Therapies for Pulmonary Fibrosis.美国胸科学会官方研讨会报告:动物模型在肺纤维化潜在治疗方法临床前评估中的应用
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Sepsis-3 on the Block: What Does It Mean for Preclinical Sepsis Modeling?脓毒症-3登场:它对临床前脓毒症模型意味着什么?
Shock. 2017 May;47(5):658-660. doi: 10.1097/SHK.0000000000000775.
9
Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock: 2016.拯救脓毒症运动:脓毒症与脓毒性休克管理国际指南:2016版
Crit Care Med. 2017 Mar;45(3):486-552. doi: 10.1097/CCM.0000000000002255.
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Reporting Standards for Preclinical Studies of Stroke Therapy.中风治疗临床前研究报告标准。
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临床前期脓毒症研究的最低质量阈值 (MQTiPSS):改善脓毒症动物模型的国际专家共识倡议。

Minimum Quality Threshold in Pre-Clinical Sepsis Studies (MQTiPSS): an international expert consensus initiative for improvement of animal modeling in sepsis.

机构信息

Ludwig Boltzmann Institute for Experimental and Clinical Traumatology in the AUVA Research Center, Donaueschingenstrasse 13, 1200, Vienna, Austria.

Rhode Island Hospital and Alpert School of Medicine at Brown University, Providence, RI, USA.

出版信息

Infection. 2018 Oct;46(5):687-691. doi: 10.1007/s15010-018-1183-8.

DOI:
10.1007/s15010-018-1183-8
PMID:30105433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6182493/
Abstract

PURPOSE

Pre-clinical animal studies precede the majority of clinical trials. While the clinical sepsis definitions and recommended treatments are regularly updated, a systematic review of pre-clinical models of sepsis has not been done and clear modeling guidelines are lacking. To address this deficit, a Wiggers-Bernard Conference on pre-clinical sepsis modeling was held in Vienna in May, 2017. The conference goal was to identify limitations of pre-clinical sepsis models and to propose a set of guidelines, defined as the "Minimum Quality Threshold in Pre-Clinical Sepsis Studies" (MQTiPSS), to enhance translational value of these models.

METHODS

31 experts from 13 countries participated and were divided into 6 thematic Working Groups (WG): (1) Study Design, (2) Humane modeling, (3) Infection types, (4) Organ failure/dysfunction, (5) Fluid resuscitation and (6) Antimicrobial therapy endpoints. As basis for the MQTiPSS discussions, the participants conducted a literature review of the 260 most highly cited scientific articles on sepsis models (2002-2013).

RESULTS

Overall, the participants reached consensus on 29 points; 20 at "recommendation" (R) and 9 at "consideration" (C) strength. This Executive Summary provides a synopsis of the MQTiPSS consensus (Tables 1, 2 and 3).

CONCLUSIONS

We believe that these recommendations and considerations will serve to bring a level of standardization to pre-clinical models of sepsis and ultimately improve translation of pre-clinical findings. These guideline points are proposed as "best practices" that should be implemented for animal sepsis models. In order to encourage its wide dissemination, this article is freely accessible in Shock, Infection and Intensive Care Medicine Experimental.

摘要

目的

临床前动物研究先于大多数临床试验进行。虽然临床败血症的定义和推荐的治疗方法经常更新,但尚未对败血症的临床前模型进行系统审查,也缺乏明确的建模指南。为了解决这一不足,2017 年 5 月在维也纳举行了威格斯-伯纳德临床前败血症建模会议。会议的目的是确定临床前败血症模型的局限性,并提出一套准则,定义为“临床前败血症研究的最低质量阈值”(MQTiPSS),以提高这些模型的转化价值。

方法

来自 13 个国家的 31 名专家参加了会议,并分为 6 个专题工作组(WG):(1)研究设计,(2)人性化建模,(3)感染类型,(4)器官衰竭/功能障碍,(5)液体复苏和(6)抗菌治疗终点。作为 MQTiPSS 讨论的基础,参与者对 260 篇关于败血症模型的最具影响力的科学文章进行了文献回顾(2002-2013 年)。

结果

总体而言,与会者就 29 点达成共识;20 项为“建议”(R),9 项为“考虑”(C)强度。本执行摘要概述了 MQTiPSS 的共识(表 1、2 和 3)。

结论

我们相信,这些建议和考虑将有助于使临床前败血症模型标准化,并最终提高临床前研究结果的转化。这些指南要点被提议作为“最佳实践”,应在动物败血症模型中实施。为了鼓励广泛传播,本文在 Shock,Infection and Intensive Care Medicine Experimental 上免费提供。