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DUETT血管止血装置的安全性和有效性评估:安全有效的血管止血(SEAL)试验的最终结果。

Assessment of the safety and efficacy of the DUETT vascular hemostasis device: final results of the safe and effective vascular hemostasis (SEAL) trial.

出版信息

Am Heart J. 2002 Apr;143(4):612-9. doi: 10.1067/mhj.2002.121464.

Abstract

OBJECTIVE

We sought to determine the safety and efficacy of the novel DUETT vascular hemostasis device in comparison with standard manual compression after diagnostic and interventional coronary procedures.

BACKGROUND

Vascular hemostasis devices are increasingly used to improve patient comfort and speed mobilization after coronary and peripheral vascular procedures. Currently available devices have certain limitations, however.

METHODS

At 16 clinical sites, 630 patients who underwent diagnostic or interventional coronary procedures were randomized 5:3 to the DUETT sealing device or standard manual compression. The primary study end points were time to hemostasis and ambulation and the incidence of major vascular complications at 30 days.

RESULTS

Time to hemostasis from the completion of the procedure (catheter removal; median) was 14 minutes (interquartile range [IQR], 10, 17 minutes) in the DUETT group and 195 minutes (IQR, 46, 351 minutes) in the standard compression group (P <.001), and time from sheath removal (median) was 7 minutes (IQR, 6, 8 minutes) and 20 minutes (IQR, 15, 30 minutes) for the 2 groups, respectively (P <.001). Time to ambulation from catheter removal (median) was 338 minutes (IQR, 223, 526 minutes) in the DUETT group and 705 minutes (IQR, 400, 1120 minutes) in the standard compression group (P <.001). Major complications occurred in 3.6% of the DUETT group and 1.7% of the standard compression group (P =.22), with a diminishing risk of complications in the DUETT group as experience was accrued. Similar benefits from DUETT use were seen in patients who underwent both diagnostic and interventional procedures.

CONCLUSION

The DUETT sealing device allows immediate arterial sheath removal after both diagnostic and interventional procedures, dramatically reducing time to hemostasis and patient ambulation without compromising patient safety in comparison with standard compression techniques.

摘要

目的

我们试图确定新型DUETT血管止血装置与诊断性和介入性冠状动脉手术后的标准手动压迫法相比的安全性和有效性。

背景

血管止血装置越来越多地用于提高冠状动脉和外周血管手术后患者的舒适度并加快其活动能力。然而,目前可用的装置存在一定局限性。

方法

在16个临床地点,630例行诊断性或介入性冠状动脉手术的患者按5:3随机分为DUETT密封装置组或标准手动压迫组。主要研究终点为止血和下床活动时间以及30天时主要血管并发症的发生率。

结果

DUETT组从手术完成(拔出导管;中位数)到止血的时间为14分钟(四分位间距[IQR],10,17分钟),标准压迫组为195分钟(IQR,46,351分钟)(P<.001),两组从拔出鞘管(中位数)到止血的时间分别为7分钟(IQR,6,8分钟)和20分钟(IQR,15,30分钟)(P<.001)。DUETT组从拔出导管(中位数)到下床活动的时间为338分钟(IQR,223,526分钟),标准压迫组为705分钟(IQR,400,1120分钟)(P<.001)。DUETT组主要并发症发生率为3.6%,标准压迫组为1.7%(P = 0.22),随着经验积累,DUETT组并发症风险降低。在接受诊断性和介入性手术的患者中均观察到使用DUETT带来的类似益处。

结论

与标准压迫技术相比,DUETT密封装置可使诊断性和介入性手术后立即拔出动脉鞘管,显著缩短止血时间和患者下床活动时间,且不影响患者安全。

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