Department of Vascular Surgery, St. Franziskus Hospital GmbH, Muenster, Germany; Department of Vascular Surgery, University Clinic of Muenster, Muenster, Germany.
Institute of Biostatistics and Clinical Research, University of Muenster, Muenster, Germany.
JACC Cardiovasc Interv. 2016 Dec 26;9(24):2557-2565. doi: 10.1016/j.jcin.2016.09.039.
The most effective first-line treatment between endovascular therapy and bypass surgery for patients with critical limb ischemia (CLI) is still not well defined. The primary aim of the interim analysis of CRITISCH (Registry of First-Line Treatments in Patients With Critical Limb Ischemia) was to compare both treatment options in a prospective confirmatory manner.
Only 1 randomized controlled trial between endovascular therapy and bypass surgery has been published yet. Several retrospective studies showed comparable outcomes between the 2 treatment strategies, but in the majority of them, current endovascular technologies have not been included.
Between January 2013 and September 2014, 1,200 CLI patients (Rutherford 4 to 6) from 27 vascular centers were enrolled. The selection of the first-line treatment was left completely to the discretion of the responsible physician. The primary composite endpoint was amputation-free survival (AFS), that is, time to major amputation and/or death from any cause. A pre-specified interim analysis aimed at showing noninferiority of the endovascular therapy versus bypass surgery as to the hazard ratio (HR) of AFS (noninferiority bound = 1.33; interim α = 0.0058). Time-to-event analyses of major amputation, death, and the composite endpoint of reintervention and/or above-ankle amputation were also conducted.
Endovascular therapy was applied to 642 (54%) and bypass surgery to 284 (24%) patients. Median follow-up time was 12 months in both groups. One-year AFS was 75% and 72%, respectively. The noninferiority of endovascular therapy versus bypass surgery for AFS was confirmed (HR: 0.91; upper bound of 1-sided (1 - 0.0058) confidence interval [CI]: 1.29; p = 0.003). An impact of the treatment strategy on time until death (HR: 1.14; 95% CI: 0.80 to 1.63; p = 0.453), major amputation (HR: 0.86; 95% CI:0.56 to 1.30; p = 0.463), and reintervention and/or above-ankle amputation (HR: 0.89; 95% CI: 0.70 to 1.14; p = 0.348) was not observed.
The interim analysis confirmed that when physicians are free to individualize therapy to CLI patients, the endovascular-first approach achieved a noninferior AFS rate compared with bypass surgery. (Registry of First-Line Treatments in Patients With Critical Limb Ischemia [CRITISCH]; NCT01877252).
对于重症肢体缺血(CLI)患者,血管内治疗与旁路手术之间的一线治疗方法仍未得到很好的定义。CRITISCH(重症肢体缺血患者一线治疗登记研究)的中期分析的主要目的是前瞻性地比较这两种治疗方案。
目前仅有一项血管内治疗与旁路手术的随机对照试验发表。几项回顾性研究表明,这两种治疗策略的结果相当,但在大多数研究中,并未纳入目前的血管内技术。
2013 年 1 月至 2014 年 9 月,来自 27 个血管中心的 1200 例 CLI 患者(Rutherford 4 至 6 级)入组。一线治疗的选择完全由负责医生决定。主要复合终点是免于截肢的生存率(AFS),即主要截肢和/或任何原因导致的死亡时间。中期分析旨在显示血管内治疗与旁路手术相比,在 AFS 的风险比(HR)方面非劣效性(非劣效性边界=1.33;中期α=0.0058)。主要截肢、死亡和再干预及/或踝关节以上截肢的复合终点的时间至事件分析也进行了评估。
血管内治疗应用于 642 例(54%)患者,旁路手术应用于 284 例(24%)患者。两组的中位随访时间均为 12 个月。一年时 AFS 分别为 75%和 72%。血管内治疗与旁路手术的 AFS 非劣效性得到证实(HR:0.91;单侧(1-0.0058)置信区间上限:1.29;p=0.003)。治疗策略对死亡时间(HR:1.14;95%CI:0.80 至 1.63;p=0.453)、主要截肢(HR:0.86;95%CI:0.56 至 1.30;p=0.463)和再干预及/或踝关节以上截肢(HR:0.89;95%CI:0.70 至 1.14;p=0.348)的影响无统计学意义。
中期分析证实,当医生可以自由地为 CLI 患者个体化治疗时,血管内优先治疗与旁路手术相比,达到了非劣效的 AFS 率。(重症肢体缺血患者一线治疗登记研究[CRITISCH];NCT01877252)。