首页> 美国卫生研究院文献>Clinical and Applied Thrombosis/Hemostasis >SPOT GRADE II: Clinical Validation of a New Method for Reproducibly Quantifying Surgical Wound Bleeding: Prospective Multicenter Multispecialty Single-Arm Study
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SPOT GRADE II: Clinical Validation of a New Method for Reproducibly Quantifying Surgical Wound Bleeding: Prospective Multicenter Multispecialty Single-Arm Study

机译:II级:一种新方法可重复定量手术伤口出血的临床验证:前瞻性多中心多特点单臂研究

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摘要

The SPOT GRADE (SG), a Surface Bleeding Severity Scale, is a unique visual method for assessing bleeding severity based on quantitative determinations of blood flow. This study assessed the reliability of the SG scale in a clinical setting and collected initial data on the safety and efficacy of HEMOBLAST Bellows (HB), a hemostatic agent, in abdominal and orthopedic operations. Twenty-seven patients were enrolled across 3 centers and received the investigational device. Bleeding severity and hemostasis were independently assessed by 2 surgical investigators at baseline and at 3, 6, and 10 minutes after application of HB and compared for agreement. The mean paired κ statistic for assignment of SG scores was .7754. The mean paired κ statistics for determining eligibility for participation in the trial based on bleeding severity and the mean paired κ statistics determining the presence of hemostasis were .9301 and .9301, respectively. The proportion of patients achieving hemostasis within 3, 6, and 10 minutes of HB application were 50.0%, 79.2%, and 91.7%, respectively. There were no unanticipated adverse device effects and one possible serious adverse device effect, as determined by the Independent Data Monitoring Committee (IDMC). The reliability of the SG scale was validated in a clinical setting. Initial data on the safety and efficacy of HB in abdominal and orthopedic operations were collected, and there were no concerns raised by the investigators or the IDMC.
机译:斑点等级(SG),表面出血严重程度,是基于血流定量测定评估出血严重程度的独特视觉方法。该研究评估了SG标度在临床环境中的可靠性,并收集了血管壳波纹管(HB),止血剂,腹腔和整形外科操作的安全性和功效的初始数据。二十七名患者参加了3个中心并获得了调查装置。在施用HB的基线和3,6和10分钟内独立评估出血的严重程度和止血,并在3,6和3,6和10分钟内进行评估并与协议进行比较。用于分配SG分数的平均配对κ统计数是.7754。用于确定基于出血严重程度的参与试验和确定止血存在的平均配对κ统计的平均配对κ统计分别为.9301和.9301。在3,6和10分钟的HB申请中实现止血的患者的比例分别为50.0%,79.2%和91.7%。由独立数据监测委员会(IDMC)确定,没有意外的不利设备效应和一个可能的严重不良器件效应。 SG标度的可靠性在临床环境中验证。收集了腹部和矫形行动中HB安全性和疗效的初始数据,并由调查人员或IDMC提出了担忧。

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