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接受监测静脉造影和介入治疗的中心静脉阻塞性疾病患者的中期结果。

Mid-Term Outcomes of Patients with Central Venous Occlusive Disease Undergoing Surveillance Venography and Intervention.

机构信息

Department of Vascular and Interventional Radiology, Singapore General Hospital, Singapore.

出版信息

Ann Acad Med Singap. 2020 Jun;49(6):360-366.

Abstract

INTRODUCTION

To evaluate the mid-term outcomes of regular surveillance venography with or without percutaneous transluminal angioplasty (PTA) in haemodialysis patients presenting with central venous occlusive disease.

MATERIALS AND METHODS

A single-centre retrospective analysis of haemodialysis patients who presented with central vein occlusion (CVO) and central vein stenosis (CVS) between January 2008 and December 2011 was performed. CVO and significant CVS were defined as 100% and >50% luminal narrowing, respectively. Upon successful angioplasty on first presentation, patients were followed up with regular surveillance venography within 3-6 months of the intervention and were re-treated when a significant stenosis or occlusion was demonstrated. Data on patient's demographics, comorbidities, presenting symptoms, type of upper limb dialysis access, lesion characteristics and complications were collected. Technical success, primary patency and primary assisted patency were analysed.

RESULTS

Thirty-five patients with CVO and 77 patients with CVS were enrolled. The technical success of initial PTA was 77% and 73% for the CVO and CVS groups, respectively. The primary patency at 3 months was 65% and 55% for the CVO group and CVS group, respectively ( = 0.32). The primary assisted patency at 1 year was 88% and 99% for the CVO group and CVS group, respectively ( = 0.009). At 2 years, the primary assisted patency were 77% and 90%, respectively ( = 0.07). There was significant difference in the overall primary assisted patency ( = 0.048) between the CVO and CVS groups.

CONCLUSION

CVOs are more difficult to treat than CVS. High primary assisted patency rates can be achieved with surveillance venography, albeit at the expense of increased number of interventions. Further cost effectiveness studies need to be performed to study the true benefit of our surveillance programme.

摘要

简介

评估常规监测静脉造影术联合或不联合经皮腔内血管成形术(PTA)治疗血液透析患者中心静脉阻塞(CVO)和中心静脉狭窄(CVS)的中期疗效。

材料与方法

对 2008 年 1 月至 2011 年 12 月期间出现中心静脉阻塞(CVO)和中心静脉狭窄(CVS)的血液透析患者进行单中心回顾性分析。CVO 和明显 CVS 定义为管腔狭窄分别为 100%和>50%。初次血管成形术成功后,患者在干预后 3-6 个月内进行常规监测静脉造影,并在出现明显狭窄或阻塞时再次治疗。收集患者的人口统计学、合并症、临床表现、上肢透析通路类型、病变特征和并发症等数据。分析技术成功率、初始通畅率和初始辅助通畅率。

结果

共纳入 35 例 CVO 患者和 77 例 CVS 患者。初次 PTA 的技术成功率分别为 CVO 组 77%和 CVS 组 73%。CVO 组和 CVS 组的 3 个月初始通畅率分别为 65%和 55%( = 0.32)。CVO 组和 CVS 组的 1 年初始辅助通畅率分别为 88%和 99%( = 0.009)。2 年时,CVO 组和 CVS 组的初始辅助通畅率分别为 77%和 90%( = 0.07)。CVO 组和 CVS 组的总体初始辅助通畅率有显著差异( = 0.048)。

结论

CVO 比 CVS 更难治疗。尽管增加了干预次数,但通过监测静脉造影术可以获得较高的初始辅助通畅率。需要进行进一步的成本效益研究,以研究我们的监测方案的真正收益。

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