The Clinical Rationale for the Sentry Bioconvertible Inferior Vena Cava Filter for the Prevention of Pulmonary Embolism.

IF 2.5 Q2 PERIPHERAL VASCULAR DISEASE International Journal of Vascular Medicine Pub Date : 2019-05-26 eCollection Date: 2019-01-01 DOI:10.1155/2019/5795148
Michael D Dake, Gary M Ansel, Matthew S Johnson, Robert Mendes, H Bob Smouse
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引用次数: 8

Abstract

The Sentry inferior vena cava (IVC) filter is designed to provide temporary protection against pulmonary embolism (PE) during transient high-risk periods and then to bioconvert after 60 days after implantation. At the time of bioconversion, the device's nitinol arms retract from the filtering position into the caval wall. Subsequently, the stable stent-like nitinol frame is endothelialized. The Sentry bioconvertible IVC filter has been evaluated in a multicenter investigational-device-exemption pivotal trial (NCT01975090) of 129 patients with documented deep vein thrombosis (DVT) or PE, or at temporary risk of developing DVT or PE, and with contraindications to anticoagulation. Successful filter conversion was observed in 95.7% of patients at 6 months (110/115) and 96.4% at 12 months (106/110). Through 12 months, there were no cases of symptomatic PE. The rationale for development of the Sentry bioconvertible device includes the following considerations: (1) the period of highest risk of PE for the vast majority of patients occurs within the first 60 days after an index event, with most of the PEs occurring in the first 30 days; (2) the design of retrievable IVC filters to support their removal after a transitory high-PE-risk period has, in practice, been associated with insecure filter dynamics and time-dependent complications including tilting, fracture, embolization, migration, and IVC perforation; (3) most retrievable IVC filters are placed for temporary protection, but for a variety of reasons they are not removed in any more than half of implanted patients, and when removal is attempted, the procedure is not always successful even with advanced techniques; and (4) analysis of Medicare hospital data suggests that payment for the retrieval procedure does not routinely compensate for expense. The Sentry device is not intended for removal after bioconversion. In initial clinical use, complications have been limited. Long-term results for the Sentry bioconvertible IVC filter are anticipated soon.

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Sentry生物可转换下腔静脉滤器预防肺栓塞的临床依据。
Sentry下腔静脉(IVC)过滤器的设计目的是在短暂的高风险时期提供临时保护,防止肺栓塞(PE),然后在植入后60天进行生物转化。在生物转化时,装置的镍钛诺臂从过滤位置缩回到腔壁上。随后,将稳定的支架状镍钛合金框架进行内皮化。Sentry生物可转换IVC过滤器已在一项多中心试验性免器械关键试验(NCT01975090)中进行了评估,该试验纳入了129例有深静脉血栓形成(DVT)或PE,或有发生DVT或PE的暂时风险,且有抗凝禁忌证的患者。95.7%的患者在6个月(110/115)和96.4%的患者在12个月(106/110)时成功转换滤过器。在12个月的时间里,没有出现有症状的PE病例。开发Sentry生物可转换装置的理由包括以下考虑:(1)绝大多数患者PE风险最高的时期发生在指数事件后的前60天内,其中大部分PE发生在前30天;(2)在短暂的高pe风险期后,可回收的下腔静脉滤过器的设计支持其移除,在实践中,与不安全的滤过器动力学和时间依赖性并发症相关,包括倾斜、骨折、栓塞、迁移和下腔静脉穿孔;(3)大多数可回收的下腔静脉滤器是为了临时保护而放置的,但由于各种原因,超过一半的植入患者没有将其取出,并且当试图取出时,即使采用先进的技术,手术也不总是成功的;(4)对医疗保险医院数据的分析表明,为检索程序支付的费用通常不会补偿费用。Sentry装置不用于生物转化后的去除。在最初的临床应用中,并发症有限。Sentry生物可转换IVC过滤器的长期结果预计很快就会出来。
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来源期刊
International Journal of Vascular Medicine
International Journal of Vascular Medicine PERIPHERAL VASCULAR DISEASE-
CiteScore
3.50
自引率
0.00%
发文量
7
审稿时长
16 weeks
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