Bax Liesbeth, Mali Willem P Th M, Buskens Erik, Koomans Hein A, Beutler J J, Braam B, Beek F J A, Rabelink T J, Postma C T, Huysmans F T M, Deinum J, Thien Th, Schultze Kool L J, Woittiez A J J, Kouwenberg J J, van den Meiracker A H, Pattynama P M T, van de Ven P J G, Vroegindeweij D, Doorenbos C J, Aarts J C N M, Kroon A A, de Leeuw P W, de Haan M W, van Engelshoven J M A, Rutten M J C M, van Montfrans G A, Reekers J A, Plouin P F, La Batide Alanore A, Azizi M, Raynaud A, Harden P N, Cowling M
University Medical Centre Utrecht, The Netherlands.
J Nephrol. 2003 Nov-Dec;16(6):807-12.
Atherosclerotic renal artery stenosis (ARAS) is associated with progressive loss of renal function and is one of the most important causes of renal failure in the elderly. Current treatment includes restoration of the renal arterial lumen by endovascular stent placement. However, this treatment only affects damage caused by ARAS due to the stenosis and ensuing post-stenotic ischemia. ARAS patients have severe general vascular disease. Atherosclerosis and hypertension can also damage the kidney parenchyma causing renal failure. Medical treatment focuses on the latter. Lipid-lowering drugs (statins) could reduce renal failure progression and could reduce the overall high cardiovascular risk. The additional effect on preserving renal function of stent placement as compared to medical therapy alone is unknown. Therefore, the STAR-study aims to compare the effects of renal artery stent placement together with medication vs. medication alone on renal function in ARAS patients.
Patients with an ARAS of > or = 50% and renal failure (creatinine (Cr) clearance < 80 mL/min/1.73 m2) are randomly assigned to stent placement with medication or to medication alone. Medication consists of statins, anti-hypertensive drugs and antiplatelet therapy. Patients are followed for 2 yrs with extended follow-up to 5 yrs. The primary outcome of this study is a reduction in Cr clearance > 20% compared to baseline. This trial will include 140 patients.
动脉粥样硬化性肾动脉狭窄(ARAS)与肾功能的渐进性丧失相关,是老年人肾衰竭的最重要原因之一。目前的治疗方法包括通过血管内支架置入术恢复肾动脉管腔。然而,这种治疗仅影响由ARAS的狭窄及随后的狭窄后缺血所造成的损害。ARAS患者存在严重的全身性血管疾病。动脉粥样硬化和高血压也会损害肾实质,导致肾衰竭。药物治疗主要针对后者。降脂药物(他汀类药物)可以减缓肾衰竭的进展,并可降低总体较高的心血管疾病风险。与单纯药物治疗相比,支架置入术对肾功能的额外保护作用尚不清楚。因此,STAR研究旨在比较肾动脉支架置入术联合药物治疗与单纯药物治疗对ARAS患者肾功能的影响。
肾动脉狭窄≥50%且伴有肾衰竭(肌酐(Cr)清除率<80 mL/min/1.73 m2)的患者被随机分配至接受支架置入术联合药物治疗组或单纯药物治疗组。药物治疗包括他汀类药物、抗高血压药物和抗血小板治疗。对患者进行为期2年的随访,并延长至5年。本研究的主要结局是与基线相比,Cr清除率降低>20%。该试验将纳入140例患者。