The Vascular Experts, Darien, Conn.
Vascular Breakthroughs, LLC, Darien, Conn.
J Vasc Surg Venous Lymphat Disord. 2019 Jan;7(1):45-55. doi: 10.1016/j.jvsv.2018.07.016. Epub 2018 Oct 24.
Factors affecting long-term clinical outcome and stent patency after iliofemoral venous stenting remain complex and ill-defined. Also, consensus is lacking among clinicians regarding the continuing role for the Wallstent (Boston Scientific, Marlborough, Mass) as dedicated nitinol-based venous stents become available. We undertook this study to review our long-term results using Wallstents and to evaluate the potential role of this stent in the future.
From 2007 to 2014, there were 77 limbs in 67 consecutive patients that received Wallstents for chronic iliofemoral vein obstruction. Intravascular ultrasound (IVUS) and venography were used to assess lesion type and extent. Baseline clinical severity was assessed with Venous Clinical Severity Score (VCSS) and Clinical, Etiology, Anatomy, and Pathophysiology (CEAP) classification. Clinical improvement was assessed with VCSS at 12, 24, and 36 months. VCSS change ≥4 points was considered significant improvement. Patency was assessed with duplex ultrasound. A retrospective review of patients' records and imaging was conducted to assess baseline and procedural factors associated with long-term clinical outcomes.
Lesions were nonthrombotic in 42 limbs (55%) and left-sided in 48 limbs (62%). Ten patients were treated for bilateral venous disease. Patients were predominantly male (55%); median age was 63 years (range, 47-83 years). Median baseline VCSS was 9 (range, 3-23). IVUS and venography estimated equal vessel compromise length in 37 limbs (48%). IVUS estimated a longer lesion in 32 limbs (42%). Stenting correlated with venography and IVUS in 37 limbs (48%) and more closely aligned with IVUS in 35 limbs (45%). Stents extended into the common femoral vein (CFV) in 17 limbs (22%) and into the inferior vena cava in 6 limbs (8%). Sixty-five (97%) patients had available imaging follow-up (median, 50 months). At 72 months, primary patency in the overall cohort was 87%; assisted primary patency and secondary patency were both 95%. In the nonthrombotic subset, assisted primary patency and secondary patency were 100%; primary patency was 97%. In the post-thrombotic subset, primary patency was 75%; assisted primary patency and secondary patency were 88%. Three early failures occurred. Eight patients required reintervention (range, 0.5-80 months); five interventions were to maintain patency. Cox multivariate regression identified that CFV disease predicted later complications. At last VCSS follow-up per patient (median, 26 months), 52 patients (68%) showed ≥4-point VCSS improvement. None had score worsening.
Venous stenting with Wallstents for iliofemoral post-thrombotic or compressive obstruction proved safe and effective through long-term follow-up, with excellent patency rates. The majority of patients exhibited significant clinical improvement. CFV occlusive disease predicts increased complications.
影响髂股静脉支架置入术后长期临床结局和支架通畅率的因素仍然复杂且不明确。此外,临床医生对于 Wallstent(波士顿科学公司,马萨诸塞州马尔伯勒)的持续作用存在分歧,因为专用的镍钛诺静脉支架已经问世。我们进行这项研究是为了回顾我们使用 Wallstent 的长期结果,并评估该支架在未来的潜在作用。
2007 年至 2014 年,连续 67 例患者的 77 条肢体因慢性髂股静脉阻塞接受 Wallstent 治疗。血管内超声(IVUS)和静脉造影用于评估病变类型和程度。基线临床严重程度采用静脉临床严重程度评分(VCSS)和临床、病因、解剖和病理生理学(CEAP)分类进行评估。采用 VCSS 在 12、24 和 36 个月时评估临床改善情况。VCSS 改善≥4 分被认为是显著改善。通过双功超声评估通畅率。对患者的病历和影像学资料进行回顾性分析,以评估与长期临床结局相关的基线和手术因素。
病变在 42 条肢体(55%)中为非血栓性,在 48 条肢体(62%)中为左侧。10 例患者因双侧静脉疾病接受治疗。患者主要为男性(55%);中位年龄为 63 岁(范围 47-83 岁)。中位基线 VCSS 为 9 分(范围 3-23 分)。IVUS 和静脉造影在 37 条肢体(48%)中估计等长的血管阻塞,在 32 条肢体(42%)中 IVUS 估计更长的病变。支架与静脉造影和 IVUS 相符在 37 条肢体(48%)中,与 IVUS 更相符在 35 条肢体(45%)中。支架延伸至股总静脉(CFV)的有 17 条肢体(22%),延伸至下腔静脉的有 6 条肢体(8%)。65 例(97%)患者有可用的影像学随访(中位随访时间为 50 个月)。72 个月时,总体队列的初始通畅率为 87%;辅助初始通畅率和二级通畅率均为 95%。在非血栓性亚组中,辅助初始通畅率和二级通畅率均为 100%;初始通畅率为 97%。在血栓后亚组中,初始通畅率为 75%;辅助初始通畅率和二级通畅率为 88%。有 3 例早期失败。8 例患者需要再次干预(范围 0.5-80 个月);5 次干预是为了维持通畅率。Cox 多变量回归分析发现 CFV 疾病预测后期并发症。在最后一次每位患者的 VCSS 随访(中位随访时间 26 个月)中,52 例患者(68%)的 VCSS 改善≥4 分。无一例患者的评分恶化。
髂股静脉支架置入术治疗血栓后或压迫性阻塞安全有效,通过长期随访,通畅率高,效果良好。大多数患者都表现出明显的临床改善。CFV 闭塞性疾病预测并发症增加。