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November 7, 2022New England Journal of Medicine876 citationsOpen Access

Surgery or Endovascular Therapy for Chronic Limb-Threatening Ischemia

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AFAlik FarberMMMatthew T. MenardMCMichael S. Conte

Key Points

  • To determine whether an initial strategy of endovascular therapy or surgical revascularization provides superior limb outcomes and survival in patients with chronic limb-threatening ischemia.
  • International, parallel-cohort randomized trial (BEST-CLI, NCT02060630) enrolling 1830 patients with chronic limb-threatening ischemia and infrainguinal peripheral artery disease.
  • Patients with an adequate single segment of great saphenous vein were assigned to cohort 1, while those requiring an alternative bypass conduit were assigned to cohort 2.
  • The primary composite outcome was a major adverse limb event (above-ankle amputation or major limb reintervention including new bypass graft, revision, thrombectomy, or thrombolysis) or death from any cause.
  • In cohort 1 (median follow-up 2.7 years), primary-outcome events occurred in 302 of 709 patients (42.6%) in the surgical group versus 408 of 711 patients (57.4%) in the endovascular group (HR, 0.68; 95% CI, 0.59 to 0.79; P<0.001).
  • In cohort 2 (median follow-up 1.6 years), primary-outcome events occurred in 83 of 194 patients (42.8%) in the surgical group versus 95 of 199 patients (47.7%) in the endovascular group (HR, 0.79; 95% CI, 0.58 to 1.06; P=0.12).
  • The incidence of general adverse events was similar between surgical and endovascular groups across both cohorts.

Abstract

BACKGROUND: Patients with chronic limb-threatening ischemia (CLTI) require revascularization to improve limb perfusion and thereby limit the risk of amputation. It is uncertain whether an initial strategy of endovascular therapy or surgical revascularization for CLTI is superior for improving limb outcomes. METHODS: In this international, randomized trial, we enrolled 1830 patients with CLTI and infrainguinal peripheral artery disease in two parallel-cohort trials. Patients who had a single segment of great saphenous vein that could be used for surgery were assigned to cohort 1. Patients who needed an alternative bypass conduit were assigned to cohort 2. The primary outcome was a composite of a major adverse limb event - which was defined as amputation above the ankle or a major limb reintervention (a new bypass graft or graft revision, thrombectomy, or thrombolysis) - or death from any cause. RESULTS: In cohort 1, after a median follow-up of 2.7 years, a primary-outcome event occurred in 302 of 709 patients (42.6%) in the surgical group and in 408 of 711 patients (57.4%) in the endovascular group (hazard ratio, 0.68; 95% confidence interval CI, 0.59 to 0.79; P<0.001). In cohort 2, a primary-outcome event occurred in 83 of 194 patients (42.8%) in the surgical group and in 95 of 199 patients (47.7%) in the endovascular group (hazard ratio, 0.79; 95% CI, 0.58 to 1.06; P = 0.12) after a median follow-up of 1.6 years. The incidence of adverse events was similar in the two groups in the two cohorts. CONCLUSIONS: Among patients with CLTI who had an adequate great saphenous vein for surgical revascularization (cohort 1), the incidence of a major adverse limb event or death was significantly lower in the surgical group than in the endovascular group. Among the patients who lacked an adequate saphenous vein conduit (cohort 2), the outcomes in the two groups were similar. (Funded by the National Heart, Lung, and Blood Institute; BEST-CLI ClinicalTrials.gov number, NCT02060630.).

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Cite This Study

Farber et al. (2022) studied this question.

synapsesocial.com/papers/6a0ec4a5a14f152feaf9d0e0https://doi.org/10.1056/nejmoa2207899
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