Zeller Thomas
Abteilung Angiologie, Herz-Zentrum Bad Krozingen, Südring 15, D-79189 Bad Krozingen, Germany.
Curr Treat Options Cardiovasc Med. 2007 Apr;9(2):90-8. doi: 10.1007/s11936-007-0002-9.
Fibromuscular dysplasia (FMD) and aortoarteritis are the most frequent causes of secondary hypertension induced by renal artery stenosis (RAS). Revascularization of this disease entity usually cures arterial hypertension. Demographic evolution leads to an increasing incidence of atherosclerotic RAS, one of the major causes of end-stage renal failure. Furthermore, atherosclerotic RAS leads to deterioration of primary hypertension, progression of atherosclerosis manifestation such as occlusive and aneurysmatic peripheral artery disease, and chronic or acute organ damage such as left ventricular hypertrophy and recurrent flash pulmonary edema. Despite the lack of sufficiently powered randomized controlled trials, each hemodynamically relevant RAS (eg, > or = 70%) should be considered for stent angioplasty in patients without end-stage ischemic nephropathy or limited life expectancy due to concomitant disease (eg, cancer). Drug-eluting stents will probably reduce the overall low in-stent restenosis rate of 10% to 20%. Interventions in patients with dialysis-dependent end-stage nephropathy are left to appropriate clinical study protocols.
纤维肌发育不良(FMD)和大动脉炎是肾动脉狭窄(RAS)所致继发性高血压最常见的病因。对这一疾病实体进行血运重建通常可治愈动脉性高血压。人口结构的演变导致动脉粥样硬化性RAS的发病率不断上升,而动脉粥样硬化性RAS是终末期肾衰竭的主要病因之一。此外,动脉粥样硬化性RAS会导致原发性高血压恶化、动脉粥样硬化表现进展,如闭塞性和动脉瘤性外周动脉疾病,以及慢性或急性器官损害,如左心室肥厚和反复性急性肺水肿。尽管缺乏足够大样本量的随机对照试验,但对于没有终末期缺血性肾病或因伴发疾病(如癌症)而预期寿命有限的患者,每一例具有血流动力学意义的RAS(如≥70%)均应考虑行支架血管成形术。药物洗脱支架可能会降低总体10%至20%的支架内再狭窄率。对于依赖透析的终末期肾病患者的干预措施则留待适当的临床研究方案来确定。