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ASTRAL 试验中动脉粥样硬化性肾血管疾病的肾血管重建后的长期结果。

Long Term Outcomes After Renal Revascularization for Atherosclerotic Renovascular Disease in the ASTRAL Trial.

机构信息

Renal Medicine, Salford Royal Hospital, United Kingdom (H.O.K., D.G., A.d.B., R.C., P.A.K.).

Faculty of Biology, Medicine and Health, University of Manchester, United Kingdom (H.O.K., D.G., R.C., P.A.K.).

出版信息

Circ Cardiovasc Interv. 2024 Sep;17(9):e013979. doi: 10.1161/CIRCINTERVENTIONS.123.013979. Epub 2024 Aug 15.

Abstract

BACKGROUND

The ASTRAL trial (Angioplasty and Stenting for Renal Artery Lesions) recruited 806 patients between 2000 and 2007. Patients with atherosclerotic renal artery stenosis (RAS) and clinician uncertainty about the benefit of revascularization were randomized 1:1 to medical therapy with or without renal artery stenting. The initial results were presented in 2009 at a median 33.6-month follow-up, with no benefit of revascularization on renal or cardiovascular outcomes. Surviving patients remained under follow-up until the end of 2013, and the long-term results are presented in this study.

METHODS

Data were analyzed to assess whether there was a later impact of revascularization on renal function, cardiovascular events, and survival, including a composite outcome of renal and cardiovascular outcomes and death (as in the CORAL trial [Cardiovascular Outcomes in Renal Atherosclerotic Lesions]). Prespecified subgroup analyses included different categories of renal function, rapid deterioration in kidney function, and degree of RAS. Post hoc analyses of patients with severe RAS (bilateral 70% or >70% in a solitary kidney), those with or without proteinuria, and a per-protocol analysis were performed.

RESULTS

The mean age of the entry population was 70.5 years, the mean estimated glomerular filtration rate was 40 mL/min/1.73 m, the mean RAS was 76%, and the mean blood pressure was 150/76 mm Hg; 83% of the revascularization group underwent attempted stenting. The median follow-up was 56.4 months, with 108 patients lost to follow-up. By the end of follow-up, 50% of the evaluable population had died, 18% had suffered a first renal event, and 40% had suffered a first cardiovascular event. No statistical difference was observed for any outcome in the intention-to-treat and per-protocol analyses.

CONCLUSIONS

The long-term follow-up of the ASTRAL trial showed no overall benefit of renal revascularization to renal and cardiovascular outcomes. It has been highlighted that a proportion of the population had lower-risk RAS, and there is likely to be merit in further study in a higher-risk population.

REGISTRATION

URL: https://www.isrctn.com; Unique identifier: ISRCTN59586944.

摘要

背景

ASTRAL 试验(肾动脉病变的血管成形术和支架置入术)于 2000 年至 2007 年间招募了 806 名患者。患有动脉粥样硬化性肾动脉狭窄(RAS)且临床医生对血运重建益处存在疑虑的患者被随机分为 1:1 接受药物治疗加或不加肾动脉支架置入术。最初的结果于 2009 年在中位随访 33.6 个月时呈现,血运重建对肾脏或心血管结局没有益处。存活的患者继续接受随访直至 2013 年底,本研究呈现了长期结果。

方法

对数据进行分析,以评估血运重建对肾功能、心血管事件和生存的影响是否存在滞后,包括肾脏和心血管结局及死亡的复合结局(如 CORAL 试验[肾动脉粥样硬化病变的心血管结局])。预设的亚组分析包括不同类别的肾功能、肾功能快速恶化以及 RAS 的严重程度。对严重 RAS(孤立肾中双侧 70%或>70%)患者、有或无蛋白尿患者进行了事后分析,并进行了意向治疗和符合方案分析。

结果

入选人群的平均年龄为 70.5 岁,平均估算肾小球滤过率为 40ml/min/1.73m,平均 RAS 为 76%,平均血压为 150/76mmHg;血管重建组中 83%的患者进行了支架置入术尝试。中位随访时间为 56.4 个月,有 108 例患者失访。随访结束时,50%的可评估人群死亡,18%发生首次肾脏事件,40%发生首次心血管事件。意向治疗和符合方案分析中,任何结局均无统计学差异。

结论

ASTRAL 试验的长期随访结果显示,肾血管重建对肾脏和心血管结局没有总体益处。研究结果强调,一部分人群的 RAS 风险较低,对高危人群进一步研究可能具有价值。

注册

网址:https://www.isrctn.com;唯一标识符:ISRCTN59586944。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d29/11404757/55cea21cd268/hcv-17-e013979-g002.jpg

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