Miller Andrew J, Takahashi Edwin A, Harmsen William S, Mara Kristin C, Misra Sanjay
Department of Radiology, Mayo Clinic, Rochester, Minnesota; Division of Vascular and Interventional Radiology, Mayo Clinic, Rochester, Minnesota.
Department of Radiology, Mayo Clinic, Rochester, Minnesota.
J Vasc Interv Radiol. 2017 Dec;28(12):1681-1686. doi: 10.1016/j.jvir.2017.07.032. Epub 2017 Sep 19.
To determine the predictors of restenosis, major adverse limb events (MALEs), postoperative death (POD), and all-cause mortality after repeat endovascular treatment of superficial femoral artery (SFA) restenosis.
This was a retrospective review of 440 patients with 518 SFA lesions who were treated between January 2002 and October 2011. Ninety-six limbs were treated for restenosis with bare metal stents (BMSs) or percutaneous transluminal angioplasty (PTA), of which 28 limbs developed another restenosis requiring a third procedure. The interaction measured in this study was between the second and third intervention. Predictors of SFA patency, MALEs, POD, and all-cause mortality after SFA restenosis treatment were identified.
Patients who were treated with BMSs (n = 51) had similar rates of restenosis compared with patients who were treated with PTA (n = 45) (hazard ratio [HR] 1.40; 95% confidence interval [CI] 0.68-2.90; P = .37). Patients in the BMS group who took statins had a significantly lower risk of restenosis than patients who did not take statins (HR 0.13; 95% CI 0.04-0.41; P < .001). Stage 4-5 chronic kidney disease (CKD) (n = 12) was associated with a significantly higher risk of MALE + POD (HR 6.17; 95% CI 1.45-26.18; P = .014) and all-cause mortality (HR 2.83; 95% CI 1.27-6.33; P = .01). Clopidogrel was protective against all-cause mortality (HR 0.41; 95% CI 0.20-0.80; P = .01).
Patients in the BMS group who took statins at the time of intervention had a significantly lower risk of developing restenosis. Stage 4-5 CKD was a risk factor for MALE + POD and all-cause mortality, while clopidogrel decreased all-cause mortality risk.
确定股浅动脉(SFA)再狭窄重复血管腔内治疗后再狭窄、主要不良肢体事件(MALE)、术后死亡(POD)及全因死亡率的预测因素。
对2002年1月至2011年10月间接受治疗的440例患者的518处SFA病变进行回顾性分析。96条肢体接受了裸金属支架(BMS)或经皮腔内血管成形术(PTA)治疗再狭窄,其中28条肢体发生了再次狭窄,需要进行第三次手术。本研究测量的相互作用发生在第二次和第三次干预之间。确定了SFA再狭窄治疗后SFA通畅、MALE、POD及全因死亡率的预测因素。
接受BMS治疗的患者(n = 51)与接受PTA治疗的患者(n = 45)再狭窄发生率相似(风险比[HR] 1.40;95%置信区间[CI] 0.68 - 2.90;P = 0.37)。BMS组中服用他汀类药物的患者再狭窄风险显著低于未服用他汀类药物的患者(HR 0.13;95% CI 0.04 - 0.41;P < 0.001)。4 - 5期慢性肾脏病(CKD)(n = 12)与MALE + POD风险显著升高(HR 6.17;95% CI 1.45 - 26.18;P = 0.014)及全因死亡率升高(HR 2.83;95% CI 1.27 - 6.33;P = 0.01)相关。氯吡格雷可预防全因死亡率(HR 0.41;95% CI 0.20 - 0.80;P = 从0.01)。
BMS组中干预时服用他汀类药物的患者发生再狭窄的风险显著降低。4 - 5期CKD是MALE + POD及全因死亡率的危险因素,而氯吡格雷可降低全因死亡风险。