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在接受初次搭桥或血管成形术(无论是否置入支架)治疗慢性肢体威胁性缺血的患者中对BEST-CLI进行验证。

Validation of BEST-CLI among patients undergoing primary bypass or angioplasty with or without stenting for chronic limb-threatening ischemia.

作者信息

Darling Jeremy D, Guetter Camila R, Park Jemin, Caron Elisa, van Galen Isa, Liang Patric, Lee Andy, Stangenberg Lars, Wyers Mark C, Hamdan Allen D, Schermerhorn Marc L

机构信息

Division of Vascular and Endovascular Surgery, Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.

Division of Vascular and Endovascular Surgery, Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.

出版信息

J Vasc Surg. 2025 May;81(5):1138-1147.e2. doi: 10.1016/j.jvs.2025.01.009. Epub 2025 Jan 16.

DOI:10.1016/j.jvs.2025.01.009
PMID:39826656
Abstract

OBJECTIVE

BEST-CLI established the superiority of single-segment great saphenous vein (ssGSV) conduits for revascularization in patients with chronic limb-threatening ischemia (CLTI); however, the generalizability of these data is unknown. Thus, we aimed to validate the long-term results of open surgical bypass (BPG) vs percutaneous transluminal angioplasty with or without stenting (PTA/S) using the BEST-CLI inclusion and randomization criteria.

METHODS

All patients undergoing a first-time lower extremity revascularization for CLTI at our institution from 2005 to 2022 were retrospectively reviewed. To approximate BEST-CLI, one-to-one propensity score matching was used. Cohort 1 included BPG with ssGSV vs PTA/S; Cohort 2 included BPG without ssGSV vs PTA/S. Primary outcomes included wound healing, major amputation, major reintervention, major amputation/death (amputation/death), and major adverse limb events (MALE) or death (MALE/death) and were evaluated using Kaplan-Meier estimates and log-rank tests.

RESULTS

Of 1946 limbs undergoing a first-time intervention for CLTI between 2005 and 2022, 765 underwent BPG and 1181 underwent PTA/S. After matching, 862 fit Cohort 1 (431 BPG and 431 PTA/S), and 274 fit Cohort 2 (137 BPG and 137 PTA/S). Both cohorts exhibited a median follow-up of 2.7 years. In Cohort 1, major reintervention and MALE/death were both noted to be significantly lower following ssGSV BPG, as compared with PTA/S (at 7 years: 11% vs 24%; P = .001 and 72% vs 78%; P = .03, respectively). These findings correlated with a 53% and 28% reduction in the aforementioned adjusted events (hazard ratio, 0.47; 95% confidence interval, 0.30-0.74 and hazard ratio, 0.82; 95% confidence interval, 0.69-0.98, respectively). These significant differences in major reintervention and MALE/death were not noted in Cohort 2 (at 7 years: 25% vs 24%; P = .92 and 82% vs 80%; P = .31, respectively). Further, neither cohort demonstrated significant differences in complete wound healing (at 6 months, Cohort 1: 47% vs 40%; P = .32; Cohort 2: 40% vs 38%; P = .12), major amputation (at 7 years: Cohort 1: 15% vs 15%; P = .89; Cohort 2: 35% vs 25%; P = .86), or amputation/death (at 7 years, Cohort 1: 70% vs 66%; P = .99; Cohort 2: 78% vs 76%; P = .45).

CONCLUSIONS

Patients undergoing revascularization using ssGSV demonstrate significantly lower rates of major reintervention and MALE/death compared with those undergoing endovascular interventions for CLTI. However, similar outcomes are not seen among patients undergoing revascularization without a suitable ssGSV. These findings correlate with those demonstrated in BEST-CLI, suggesting generalizability.

摘要

目的

“最佳慢性肢体威胁性缺血(BEST-CLI)”研究证实了单段大隐静脉(ssGSV)血管移植术在慢性肢体威胁性缺血(CLTI)患者血管重建中的优势;然而,这些数据的可推广性尚不清楚。因此,我们旨在使用BEST-CLI的纳入和随机标准,验证开放手术旁路移植术(BPG)与经皮腔内血管成形术(无论是否置入支架,即PTA/S)的长期结果。

方法

回顾性分析2005年至2022年在我院首次接受CLTI下肢血管重建术的所有患者。为了近似于BEST-CLI,采用一对一倾向评分匹配法。队列1包括使用ssGSV的BPG与PTA/S;队列2包括未使用ssGSV的BPG与PTA/S。主要结局包括伤口愈合、大截肢、再次大干预、大截肢/死亡(截肢/死亡)以及主要不良肢体事件(MALE)或死亡(MALE/死亡),并使用Kaplan-Meier估计法和对数秩检验进行评估。

结果

在2005年至2022年间首次接受CLTI干预的1946条肢体中,765条接受了BPG,1181条接受了PTA/S。匹配后,862条符合队列1(431条BPG和431条PTA/S),274条符合队列2(137条BPG和137条PTA/S)。两个队列的中位随访时间均为2.7年。在队列1中,与PTA/S相比,使用ssGSV的BPG术后再次大干预和MALE/死亡的发生率均显著降低(7年时:分别为11%对24%;P = 0.001和72%对78%;P = 0.03)。这些结果与上述调整后事件减少53%和28%相关(风险比分别为0.47;95%置信区间为0.30 - 0.74和风险比为0.82;95%置信区间为0.69 - 0.98)。队列2中未观察到再次大干预和MALE/死亡的这些显著差异(7年时:分别为25%对24%;P = 0.92和82%对80%;P = 0.31)。此外,两个队列在完全伤口愈合(6个月时,队列1:47%对40%;P = 0.32;队列2:40%对38%;P = 0.12)、大截肢(7年时:队列1:15%对15%;P = 0.89;队列2:35%对25%;P = 0.86)或截肢/死亡(7年时,队列1:70%对66%;P = 0.99;队列2:78%对76%;P = 0.45)方面均未显示出显著差异。

结论

与接受CLTI血管腔内介入治疗的患者相比,使用ssGSV进行血管重建的患者再次大干预和MALE/死亡的发生率显著降低。然而,在没有合适的ssGSV进行血管重建的患者中未观察到类似结果。这些结果与BEST-CLI研究结果相关,提示具有可推广性。

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