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精准引导、个性化的胸膜内纤维蛋白溶解疗法治疗脓胸和复杂性肺炎旁胸腔积液:纤维蛋白溶解潜力的实例

Precision-guided, Personalized Intrapleural Fibrinolytic Therapy for Empyema and Complicated Parapneumonic Pleural Effusions: The Case for the Fibrinolytic Potential.

作者信息

Idell Steven, Florova Galina, Shetty Sreerama, Tucker Torry, Idell Richard, Koenig Kathy, Azghani Ali, Rahman Najib M, Komissarov Andrey

机构信息

Department of Cellular and Molecular Biology and Texas Lung Injury institute, The University of Texas Health Science Center.

Department of Behavioral Health, The University of Texas Health Science Center.

出版信息

Clin Pulm Med. 2017 Jul;24(4):163-169. doi: 10.1097/CPM.0000000000000216.

DOI:10.1097/CPM.0000000000000216
PMID:29081644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5654485/
Abstract

Complicated pleural effusions and empyema with loculation and failed drainage are common clinical problems. In adults, intrapleural fibrinolytic therapy is commonly used with variable results and therapy remains empiric. Despite the intrapleural use of various plasminogen activators; fibrinolysins, for about sixty years, there is no clear consensus about which agent is most effective. Emerging evidence demonstrates that intrapleural administration of plasminogen activators is subject to rapid inhibition by plasminogen activator inhibitor-1 and that processing of fibrinolysins is importantly influenced by other factors including the levels and quality of pleural fluid DNA. Current therapy for loculation that accompanies pleural infections also includes surgery, which is invasive and for which patient selection can be problematic. Most of the clinical literature published to date has used flat dosing of intrapleural fibrinolytic therapy in all subjects but little is known about how that strategy influences the processing of the administered fibrinolysin or how this influences outcomes. We developed a new test of pleural fluids , which is called the Fibrinolytic Potential or FP, in which a dose of a fibrinolysin is added to pleural fluids after which the fibrinolytic activity is measured and normalized to baseline levels. Testing in preclinical and clinical empyema fluids reveals a wide range of responses, indicating that individual patients will likely respond differently to flat dosing of fibrinolysins. The test remains under development but is envisioned as a guide for dosing of these agents, representing a novel candidate approach to personalization of intrapleural fibrinolytic therapy.

摘要

伴有分隔且引流失败的复杂性胸腔积液和脓胸是常见的临床问题。在成人中,胸膜腔内纤维蛋白溶解疗法常用但效果不一,治疗仍属经验性。尽管胸膜腔内使用各种纤溶酶原激活剂(纤维蛋白溶解素)已有约60年,但对于哪种药物最有效尚无明确共识。新出现的证据表明,胸膜腔内给予纤溶酶原激活剂会受到纤溶酶原激活剂抑制剂-1的快速抑制,并且纤维蛋白溶解素的加工受到其他因素的重要影响,包括胸腔积液DNA的水平和质量。目前针对胸膜感染伴发分隔的治疗方法还包括手术,手术具有侵入性,且患者选择可能存在问题。迄今为止发表的大多数临床文献在所有受试者中都采用了固定剂量的胸膜腔内纤维蛋白溶解疗法,但对于该策略如何影响所给予纤维蛋白溶解素的加工过程以及这如何影响治疗结果知之甚少。我们开发了一种新的胸腔积液检测方法,称为纤维蛋白溶解潜能(FP),即在胸腔积液中加入一定剂量的纤维蛋白溶解素,然后测量纤维蛋白溶解活性并将其标准化至基线水平。在临床前和临床脓胸积液中的检测显示出广泛的反应,表明个体患者对固定剂量的纤维蛋白溶解素可能有不同反应。该检测方法仍在开发中,但设想作为这些药物给药的指导,代表了胸膜腔内纤维蛋白溶解疗法个性化的一种新的候选方法。

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本文引用的文献

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The 21st Century Cures Act - A View from the NIH.《21世纪治愈法案》——国立卫生研究院的视角
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Translational Research in Pleural Infection and Beyond.胸膜感染及其他领域的转化研究
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Dose dependency of outcomes of intrapleural fibrinolytic therapy in new rabbit empyema models.新兔脓胸模型中胸膜内纤维蛋白溶解疗法疗效的剂量依赖性
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Targeting the PAI-1 Mechanism with a Small Peptide Increases the Efficacy of Alteplase in a Rabbit Model of Chronic Empyema.用一种小肽靶向纤溶酶原激活物抑制剂-1机制可提高阿替普酶在兔慢性脓胸模型中的疗效。
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DNase inhibits early biofilm formation in - or -induced empyema models.DNase 抑制 - 或 - 诱导的脓胸模型中的早期生物膜形成。
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PAI-1 Drives Septation and Clinical Outcomes in Pleural Infection.纤溶酶原激活物抑制剂-1驱动胸膜感染中的分隔形成及临床转归。
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The Biological Role of Pleural Fluid PAI-1 and Sonographic Septations in Pleural Infection: Analysis of a Prospectively Collected Clinical Outcome Study.胸腔液 PAI-1 和超声分隔在胸腔感染中的生物学作用:一项前瞻性临床结局研究分析。
Am J Respir Crit Care Med. 2023 Mar 15;207(6):731-739. doi: 10.1164/rccm.202206-1084OC.
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Update on Novel Targeted Therapy for Pleural Organization and Fibrosis.胸膜组织和纤维化的新型靶向治疗进展。
Int J Mol Sci. 2022 Jan 29;23(3):1587. doi: 10.3390/ijms23031587.
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From Bedside to the Bench-A Call for Novel Approaches to Prognostic Evaluation and Treatment of Empyema.从床边到实验室——呼吁采用新方法进行脓胸的预后评估和治疗
Front Pharmacol. 2022 Jan 20;12:806393. doi: 10.3389/fphar.2021.806393. eCollection 2021.
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Recent Insights into the Management of Pleural Infection.胸膜感染管理的最新见解
Int J Gen Med. 2021 Jul 14;14:3415-3429. doi: 10.2147/IJGM.S292705. eCollection 2021.
Am J Physiol Lung Cell Mol Physiol. 2016 Aug 1;311(2):L389-99. doi: 10.1152/ajplung.00171.2016. Epub 2016 Jun 24.
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Mesomesenchymal transition of pleural mesothelial cells is PI3K and NF-κB dependent.胸膜间皮细胞的间充质转化依赖于PI3K和NF-κB。
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Plasminogen activator inhibitor-1 suppresses profibrotic responses in fibroblasts from fibrotic lungs.纤溶酶原激活物抑制剂-1抑制纤维化肺成纤维细胞中的促纤维化反应。
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Thrombin down-regulates tissue factor pathway inhibitor expression in a PI3K/nuclear factor-κB-dependent manner in human pleural mesothelial cells.凝血酶以PI3K/核因子-κB依赖的方式下调人胸膜间皮细胞中组织因子途径抑制剂的表达。
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7
Response.回应。
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8
Targeting of plasminogen activator inhibitor 1 improves fibrinolytic therapy for tetracycline-induced pleural injury in rabbits.靶向纤溶酶原激活物抑制剂1可改善四环素诱导的兔胸膜损伤的纤溶治疗。
Am J Respir Cell Mol Biol. 2015 Apr;52(4):429-37. doi: 10.1165/rcmb.2014-0168OC.
9
Rebuttal from Drs Colice and Idell.科利斯博士和伊德尔博士的反驳。
Chest. 2014 Jan;145(1):21-23. doi: 10.1378/chest.13-2357.
10
Counterpoint: should fibrinolytics be routinely administered intrapleurally for management of a complicated parapneumonic effusion? No.反驳观点:对于复杂性类肺炎性胸腔积液的治疗,是否应常规胸膜腔内给予纤溶药物?不应常规给予。
Chest. 2014 Jan;145(1):17-20. doi: 10.1378/chest.13-2356.