首页> 外文期刊>Journal of vascular surgery >Outcomes of endoluminal reintervention for restenosis after percutaneous renal angioplasty and stenting.
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Outcomes of endoluminal reintervention for restenosis after percutaneous renal angioplasty and stenting.

机译:经皮肾血管成形术和支架置入后再狭窄的腔内再介入治疗结果。

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BACKGROUND: Endovascular therapy for symptomatic atherosclerotic renal artery stenosis (ARAS) is common but is associated with a significant restenosis rate. This study evaluates the outcomes of percutaneous endoluminal therapy for symptomatic restenosis (>50% on angiography) after renal intervention. METHODS: We performed a retrospective analysis of records from patients who underwent endovascular intervention for ARAS and were followed by duplex ultrasound scan between January 1990 and January 2008. Clinical benefit defined as freedom from recurrent hypertension or renal-related morbidity (increase in persistent creatinine >20% of baseline, progression to hemodialysis, death from renal-related causes), anatomic patency, restenosis, and patient survival were measured. RESULTS: A total of 447 patients underwent 619 renal artery interventions. A total of 80 vessels restenosed with an actuarial restenosis rate of 19% at 5 years. Of these restenoses, 65 (81%) were associated with recurrent symptoms (recurrent hypertension 84%, or continuing deterioration in renal function 16%). Fifty-five (85%) underwent repeat angioplasty and 10 underwent bypass surgery. The remainder was observed. The 55 percutaneous interventions were performed in 51 patients (61% female, average age 62 years, range, 51-85). A total of 73% had metabolic syndrome, 58% had hyperlipidemia, and 51% were considered diabetic; all of them had primary stenting during their first procedure. There was a 4% technical failure rate in both groups. In the restenosis group, the presence of stent was associated with a 9% technical failure rate, while in the absence of a stent the technical failure rate was only 3% (P < .05). At 5 years, outcomes were equivalent between the primary and recurrent groups for survival (76 +/- 2% vs 75 +/- 8%, primary vs recurrent), cumulative patency (82 +/- 3% vs 70 +/- 10%), freedom from restenosis (81 +/- 3% vs 81 +/- 9%), and retained clinical benefit (44 +/- 4% vs 46 +/- 10%). By Cox proportional hazards and multivariate analysis, administration of statins were associated with freedom from restenosis in the recurrent lesions. Statins, contralateral kidney size (>9 cm) and a >/=20% improvement in baseline creatinine with 3 months were associated with freedom from recurrent symptoms. Restenosis after therapy in recurrent lesions was significantly correlated with recurrent symptoms (Spearman r = 0.4614, P < .0004). CONCLUSION: Percutaneous reintervention for renal artery restenosis is safe and effective with equivalent outcomes to primary intervention. The patients are more likely to present with recurrent hypertension and be younger and of female gender than patients presenting for primary intervention. Functional outcomes after reintervention are equivalent to primary intervention.
机译:背景:有症状的动脉粥样硬化性肾动脉狭窄(ARAS)的血管内治疗很普遍,但与明显的再狭窄率相关。这项研究评估了经肾脏介入治疗后症状性再狭窄(血管造影> 50%)的经皮腔内治疗的效果。方法:我们对1990年1月至2008年1月间接受ARAS血管内介入治疗的患者的记录进行了回顾性分析,随后进行了双路超声扫描。临床获益定义为无复发性高血压或肾脏相关疾病(持续性肌酐增加>测量基线的20%,进展为血液透析,肾相关原因导致的死亡),解剖通畅性,再狭窄和患者生存率。结果:总共447例患者接受了619例肾动脉干预。在5年的时间里,共有80艘血管被精算,精算再狭窄率为19%。在这些再狭窄中,有65个(81%)与复发症状相关(复发性高血压84%,或肾功能持续恶化16%)。 55例(85%)进行了重复血管成形术,其中10例进行了旁路手术。观察到其余的。 55例经皮介入治疗在51例患者中进行(女性占61%,平均年龄62岁,范围51-85)。共有73%的人患有代谢综合征,58%的人患有高血脂症,51%的人认为是糖尿病;他们都在他们的第一个过程中进行了主要的支架置入术。两组的技术故障率均为4%。在再狭窄组,支架的存在使技术失败率达到9%,而在没有支架的情况下,技术失败率仅为3%(P <.05)。在5年时,主要组和复发组的生存期(76 +/- 2%vs 75 +/- 8%,原发与复发),累积通畅率(82 +/- 3%vs 70 +/- 10)相等。 %),无再狭窄的发生率(81 +/- 3%vs 81 +/- 9%)和保留的临床获益(44 +/- 4%vs 46 +/- 10%)。通过Cox比例风险和多变量分析,他汀类药物的给药与复发性病变中无再狭窄有关。他汀类药物,对侧肾脏大小(> 9厘米)和3个月基线肌酐改善> / = 20%与无复发症状相关。复发性病变治疗后的再狭窄与复发症状显着相关(Spearman r = 0.4614,P <.0004)。结论:经皮再次介入治疗肾动脉再狭窄是安全有效的,其效果与主要干预措施相同。与主要进行干预的患者相比,患者更容易出现复发性高血压,并且年龄更小且具有性别。再干预后的功能预后等同于主要干预。

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