超声辅助导管引导溶栓治疗肺栓塞:一家社区医院的单中心经验

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Jasmine Ventenilla, Todd Rushing, Becky Ngu, David Shavelle, Neepa Rai
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引用次数: 0

摘要

目前的指南建议低危肺栓塞(PE)患者只需进行抗凝治疗,高危肺栓塞患者则需进行全身溶栓治疗。然而,中危 PE 的治疗建议尚未明确。由于全身溶栓存在出血风险,超声辅助导管定向溶栓(USAT)已发展成为一种很有前景的治疗方式。超声辅助导管定向溶栓被认为可以通过局部给药和较低的溶栓剂量降低大出血的发生率。目前,在实际临床环境中实施 USAT 的指导很少。本研究旨在评估我们在一家新成立肺栓塞反应小组(PERT)的社区医院使用 USAT 的经验。研究纳入了 2021 年 1 月至 2023 年 1 月期间经计算机断层扫描(CT)确诊为急性肺栓塞的所有 PERT 识别患者。研究期间,PERT 共启动 89 次,40 名患者(1 名高风险 PE 患者和 37 名中度风险 PE 患者)接受了 USAT,阿替普酶以每根导管 1 毫克/小时的固定速率给药 6 小时。主要疗效指标是 USAT 后 48 小时内肺栓塞严重程度指数 (PESI) 评分的变化。主要安全性结果为 72 小时内的大出血。患者的平均年龄为 57.4 ± 17.4 岁,50%(n = 20)为男性,17.5%(n = 7)患有活动性恶性肿瘤,20%(n = 8)既往有深静脉血栓(DVT)或 PE 病史。从基线到USAT术后48小时,平均PESI评分有所下降(84.7 vs 74.9; p = 0.025),没有发生大出血事件。总住院时间为 7.5 ± 9.8 天,重症监护室住院时间为 2.2 ± 2.8 天。本研究概述了我们在这家社区医院的经验,结果显示,PESI 评分有所提高,且未观察到大出血事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultrasound-Assisted Catheter-Directed Thrombolysis for the Management of Pulmonary Embolism: A Single Center Experience in a Community Hospital.

Current guidelines recommend anticoagulation alone for low-risk pulmonary embolism (PE) with the addition of systemic thrombolysis for high-risk PE. However, treatment recommendations for intermediate-risk PE are not well-defined. Due to bleeding risks associated with systemic thrombolysis, ultrasound-assisted catheter-directed thrombolysis (USAT) has evolved as a promising treatment modality. USAT is thought to decrease the rate of major bleeding by using localized delivery with lower thrombolytic dosages. Currently, there is little guidance on the implementation of USAT in the real-world clinical setting. This study was designed to evaluate our experience with USAT at this single community hospital with a newly initiated Pulmonary Embolism Response Team (PERT). All patients identified by the PERT with an acute PE diagnosed by a computed tomography (CT) scan from January 2021 to January 2023 were included. During the study period, there were 89 PERT activations with 40 patients (1 high-risk and 37 intermediate-risk PE) receiving USAT with alteplase administered at a fixed rate of 1 mg/h per catheter for 6 h. The primary efficacy outcome was the change in Pulmonary Embolism Severity Index (PESI) score within 48 h after USAT. The primary safety outcome was major bleeding within 72 h. The mean age was 57.4 ± 17.4 years and 50% (n = 20) were male, 17.5% (n = 7) had active malignancy, and 20% (n = 8) had a history of prior deep vein thrombosis (DVT) or PE. The mean PESI score decreased from baseline to 48 h post-USAT (84.7 vs 74.9; p = 0.025) and there were no major bleeding events. The overall hospital length of stay was 7.5 ± 9.8 days and ICU length of stay was 2.2 ± 2.8 days. This study outlined our experience at this single community hospital which resulted in an improvement in PESI scores and no major bleeding events observed.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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