达比加群逆转依达鲁珠单抗治疗大出血的超声参数。

IF 3.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Dorian Teissandier, Geoffroy Rousseau, Camille Lucchini, Boris Teulade, Camille Joly, Jeannot Schmidt, Bruno Pereira, Aurélien Lebreton, Farès Moustafa
{"title":"达比加群逆转依达鲁珠单抗治疗大出血的超声参数。","authors":"Dorian Teissandier, Geoffroy Rousseau, Camille Lucchini, Boris Teulade, Camille Joly, Jeannot Schmidt, Bruno Pereira, Aurélien Lebreton, Farès Moustafa","doi":"10.1016/j.jpet.2025.103605","DOIUrl":null,"url":null,"abstract":"<p><p>Bleeding during oral anticoagulant therapy is currently codified by expert guidelines. Monitoring coagulation during bleeding events remains challenging. This study aimed to assess viscoelastic hemostatic assays (VHAs) using the Quantra analyzer (HemoSonics) in dabigatran-treated patients with International Society on Thrombosis and Haemostasis major bleeding. We conducted a prospective, multicenter study at 2 university hospitals from January 2021 to December 2023. VHA were evaluated using whole blood sample collected upon emergency admission and 30 minutes after reversal therapy. Six dabigatran-treated patients with major bleeding were included in this study and received idarucizumab: 4 patients with an intracranial bleeding and 2 with gastrointestinal major bleeding. Prior to reversal therapy, clot time (CT) and clot time with heparinase coagulation time (CTH) were prolonged beyond normal range for all patients but clot stiffness (CS) was notably low, indicating a hypocoagulable state. After idarucizumab administration, both CT (median [interquartile range], 179.5 s [169.3-238.5 s] vs 126 s [96-135.5 s]; P = .002) and CTH (181.5 s [166.3-224.3 s] vs 118.5 s [99.5-121.3 s], P = .002) significantly decreased, whereas CS increased significantly (median [interquartile range], 18 hPa [12.3-24.3 hPa] vs 26.6 hPa [25.5-33.8 hPa]; P = .03), all values falling within the normal range. Median anti-IIa activity at emergency arrivals decreased under 30 ng/mL 30 minutes, 6 hours, and 24 hours after idarucizumab administration (P = .0008). No complications were reported during follow-up. After idarucizumab administration, VHA demonstrated significant reductions in CT and CTH, with a corresponding increase in CS within normal ranges. These findings suggest that VHA using the Quantra analyzer may be a valuable tool in assessing the presence of dabigatran and the efficacy of idarucizumab reversal in patients with major bleeding. SIGNIFICANCE STATEMENT: This study highlights viscoelastic hemostatic assays using the Quantra analyzer to monitor reversal therapy in dabigatran-treated patients with major bleeding. It demonstrates the efficacy of idarucizumab in restoring coagulation parameters, offering insights into clinical management.</p>","PeriodicalId":16798,"journal":{"name":"Journal of Pharmacology and Experimental Therapeutics","volume":"392 7","pages":"103605"},"PeriodicalIF":3.8000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sonorheometry parameters during dabigatran reversal with idarucizumab for major bleeding.\",\"authors\":\"Dorian Teissandier, Geoffroy Rousseau, Camille Lucchini, Boris Teulade, Camille Joly, Jeannot Schmidt, Bruno Pereira, Aurélien Lebreton, Farès Moustafa\",\"doi\":\"10.1016/j.jpet.2025.103605\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Bleeding during oral anticoagulant therapy is currently codified by expert guidelines. Monitoring coagulation during bleeding events remains challenging. This study aimed to assess viscoelastic hemostatic assays (VHAs) using the Quantra analyzer (HemoSonics) in dabigatran-treated patients with International Society on Thrombosis and Haemostasis major bleeding. We conducted a prospective, multicenter study at 2 university hospitals from January 2021 to December 2023. VHA were evaluated using whole blood sample collected upon emergency admission and 30 minutes after reversal therapy. Six dabigatran-treated patients with major bleeding were included in this study and received idarucizumab: 4 patients with an intracranial bleeding and 2 with gastrointestinal major bleeding. Prior to reversal therapy, clot time (CT) and clot time with heparinase coagulation time (CTH) were prolonged beyond normal range for all patients but clot stiffness (CS) was notably low, indicating a hypocoagulable state. After idarucizumab administration, both CT (median [interquartile range], 179.5 s [169.3-238.5 s] vs 126 s [96-135.5 s]; P = .002) and CTH (181.5 s [166.3-224.3 s] vs 118.5 s [99.5-121.3 s], P = .002) significantly decreased, whereas CS increased significantly (median [interquartile range], 18 hPa [12.3-24.3 hPa] vs 26.6 hPa [25.5-33.8 hPa]; P = .03), all values falling within the normal range. Median anti-IIa activity at emergency arrivals decreased under 30 ng/mL 30 minutes, 6 hours, and 24 hours after idarucizumab administration (P = .0008). No complications were reported during follow-up. After idarucizumab administration, VHA demonstrated significant reductions in CT and CTH, with a corresponding increase in CS within normal ranges. These findings suggest that VHA using the Quantra analyzer may be a valuable tool in assessing the presence of dabigatran and the efficacy of idarucizumab reversal in patients with major bleeding. SIGNIFICANCE STATEMENT: This study highlights viscoelastic hemostatic assays using the Quantra analyzer to monitor reversal therapy in dabigatran-treated patients with major bleeding. It demonstrates the efficacy of idarucizumab in restoring coagulation parameters, offering insights into clinical management.</p>\",\"PeriodicalId\":16798,\"journal\":{\"name\":\"Journal of Pharmacology and Experimental Therapeutics\",\"volume\":\"392 7\",\"pages\":\"103605\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pharmacology and Experimental Therapeutics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jpet.2025.103605\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/14 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmacology and Experimental Therapeutics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jpet.2025.103605","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/14 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

口服抗凝治疗期间出血目前已被专家指南编纂。在出血事件中监测凝血仍然具有挑战性。本研究旨在评估使用Quantra分析仪(HemoSonics)在达比加群治疗的国际血栓和止血学会大出血患者中的粘弹性止血试验(VHAs)。我们于2021年1月至2023年12月在2所大学医院进行了一项前瞻性多中心研究。采用急诊入院时和逆转治疗后30分钟采集的全血样本评估VHA。本研究纳入6例达比加群治疗的大出血患者,接受依达鲁珠单抗治疗:4例颅内出血,2例胃肠大出血。逆转治疗前,所有患者的凝块时间(CT)和凝块时间伴肝素酶凝块时间(CTH)均超出正常范围延长,但凝块硬度(CS)明显较低,提示低凝状态。idarucizumab给药后,两组CT(中位数[四分位数间距],179.5 s [169.3-238.5 s] vs 126 s [96-135.5 s];P = .002)和CTH (181.5 s [166.3-224.3 s] vs 118.5 s [99.5-121.3 s], P = .002)显著降低,而CS显著升高(中位数[四分位数范围],18 hPa [12.3-24.3 hPa] vs 26.6 hPa [25.5-33.8 hPa];P = .03),所有值都在正常范围内。依达鲁珠单抗给药后30分钟、6小时和24小时,急诊到达时抗iia活性中位数降至30 ng/mL以下(P = 0.0008)。随访期间无并发症发生。服用依达鲁珠单抗后,VHA显示CT和CTH显著降低,CS在正常范围内相应升高。这些发现表明,使用Quantra分析仪的VHA可能是评估达比加群存在和伊达鲁珠单抗逆转对大出血患者疗效的有价值的工具。意义声明:本研究强调了使用Quantra分析仪监测达比加群治疗的大出血患者的逆转治疗的粘弹性止血试验。它证明了idarucizumab在恢复凝血参数方面的功效,为临床管理提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sonorheometry parameters during dabigatran reversal with idarucizumab for major bleeding.

Bleeding during oral anticoagulant therapy is currently codified by expert guidelines. Monitoring coagulation during bleeding events remains challenging. This study aimed to assess viscoelastic hemostatic assays (VHAs) using the Quantra analyzer (HemoSonics) in dabigatran-treated patients with International Society on Thrombosis and Haemostasis major bleeding. We conducted a prospective, multicenter study at 2 university hospitals from January 2021 to December 2023. VHA were evaluated using whole blood sample collected upon emergency admission and 30 minutes after reversal therapy. Six dabigatran-treated patients with major bleeding were included in this study and received idarucizumab: 4 patients with an intracranial bleeding and 2 with gastrointestinal major bleeding. Prior to reversal therapy, clot time (CT) and clot time with heparinase coagulation time (CTH) were prolonged beyond normal range for all patients but clot stiffness (CS) was notably low, indicating a hypocoagulable state. After idarucizumab administration, both CT (median [interquartile range], 179.5 s [169.3-238.5 s] vs 126 s [96-135.5 s]; P = .002) and CTH (181.5 s [166.3-224.3 s] vs 118.5 s [99.5-121.3 s], P = .002) significantly decreased, whereas CS increased significantly (median [interquartile range], 18 hPa [12.3-24.3 hPa] vs 26.6 hPa [25.5-33.8 hPa]; P = .03), all values falling within the normal range. Median anti-IIa activity at emergency arrivals decreased under 30 ng/mL 30 minutes, 6 hours, and 24 hours after idarucizumab administration (P = .0008). No complications were reported during follow-up. After idarucizumab administration, VHA demonstrated significant reductions in CT and CTH, with a corresponding increase in CS within normal ranges. These findings suggest that VHA using the Quantra analyzer may be a valuable tool in assessing the presence of dabigatran and the efficacy of idarucizumab reversal in patients with major bleeding. SIGNIFICANCE STATEMENT: This study highlights viscoelastic hemostatic assays using the Quantra analyzer to monitor reversal therapy in dabigatran-treated patients with major bleeding. It demonstrates the efficacy of idarucizumab in restoring coagulation parameters, offering insights into clinical management.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信