Thatipelli Mallik R, Misra Sanjay, Sanikommu Srinivas R, Schainfeld Robert M, Sharma Sandeep K, Soukas Peter A
St. Elizabeth's Medical Center, Boston, Massachusetts, USA.
J Vasc Interv Radiol. 2009 May;20(5):580-6. doi: 10.1016/j.jvir.2009.01.025. Epub 2009 Mar 27.
The purpose of the present study was to report safety, efficacy, and renal function outcomes with use of the GuardWire embolic protection device (EPD) in renal artery stent placement for patients with renal artery stenosis (RAS) and chronic renal insufficiency (CRI).
This was a retrospective study of all patients with RAS and CRI treated concomitantly with a GuardWire EPD and renal artery stents from December 2002 through June 2006. Renal function was determined by calculating the estimated glomerular filtration rate (eGFR) according to the Modification of Diet in Renal Disease formula, and subjects were divided into Kidney Disease Outcomes and Quality Initiative (K-DOQI) classes based on baseline eGFR. After revascularization, an improvement from baseline of at least one K-DOQI class was defined as improvement, unchanged K-DOQI class as stabilization, and worsening of at least one K-DOQI class as deterioration.
There were 63 patients (54% men) with a mean age of 75.2 years +/- 7.7. The mean baseline serum creatinine level and eGFR were 1.87 mg/dL +/- 0.6 (range, 1-3.8 mg/dL) and 36.63 mL/min per 1.73 m(2) +/- 11.42 (range, 13.85-59.99 mL/min per 1.73 m(2)), respectively, and at the last clinical follow-up, the respective measurements were 1.96 mg/dL +/- 0.72 and 38.75 mL/min per 1.73 m(2) +/- 13.25 (P = not significant). Over a mean follow-up period of 16 months +/- 12, 14 patients (25%) showed improvement, 33 (58%) had stable renal function, and 10 (18%) showed deterioration. There was one GuardWire-related dissection, which was successfully treated with a stent.
The GuardWire EPD, used during renal artery stent placement, is safe and was associated with stabilization or improvement in kidney function in 83% of patients with RAS and CRI.
本研究旨在报告在肾动脉狭窄(RAS)和慢性肾功能不全(CRI)患者的肾动脉支架置入术中使用GuardWire栓子保护装置(EPD)的安全性、有效性及肾功能结果。
这是一项对2002年12月至2006年6月期间同时接受GuardWire EPD和肾动脉支架治疗的所有RAS和CRI患者的回顾性研究。根据肾脏病饮食改良公式计算估算肾小球滤过率(eGFR)来确定肾功能,并根据基线eGFR将受试者分为肾脏病预后质量倡议(K-DOQI)分级。血管重建后,K-DOQI分级较基线至少改善一级定义为改善,K-DOQI分级不变定义为稳定,K-DOQI分级至少恶化一级定义为恶化。
共有63例患者(54%为男性),平均年龄75.2岁±7.7岁。平均基线血清肌酐水平和eGFR分别为1.87mg/dL±0.6(范围1 - 3.8mg/dL)和36.63mL/min per 1.73m²±11.42(范围13.85 - 59.99mL/min per 1.73m²),在最后一次临床随访时,相应测量值分别为1.96mg/dL±0.72和38.75mL/min per 1.73m²±13.25(P值无统计学意义)。在平均16个月±12的随访期内,14例患者(25%)显示改善,33例(58%)肾功能稳定,10例(18%)显示恶化。发生1例与GuardWire相关的夹层,经支架成功治疗。
在肾动脉支架置入术中使用的GuardWire EPD是安全的,并且在83%的RAS和CRI患者中与肾功能稳定或改善相关。