A Review of Antithrombotic Treatment in Critical Limb Ischemia After Endovascular Intervention

Amol Gupta1, Michael S Lee2, Kush Gupta3

  • 1Heart, Vascular & Leg Center, Bakersfield, CA, USA. amol@vippllc.com.

Cardiology and Therapy
|October 21, 2019
PubMed

Insights

Dual antiplatelet therapy (DAPT) and antiplatelet plus anticoagulant (AP+AC) therapy may improve outcomes for critical limb ischemia (CLI) patients after endovascular procedures, reducing restenosis and amputation risks compared to mono-antiplatelet therapy (MAPT).

Area of Science:

  • Vascular Surgery
  • Pharmacology
  • Cardiovascular Medicine

Background:

  • Endovascular intervention is a common treatment for critical limb ischemia (CLI).
  • Post-intervention antithrombotic therapy is crucial for managing cardiovascular complications in CLI patients.

Purpose of the Study:

  • To review and compare pharmacologic treatment protocols for CLI following endovascular procedures.
  • To analyze outcomes of different antithrombotic therapies: mono-antiplatelet therapy (MAPT), dual antiplatelet therapy (DAPT), and antiplatelet plus anticoagulant (AP+AC) therapy.

Main Methods:

  • Literature review comparing antithrombotic treatment outcomes in CLI patients.
  • Categorization of therapies into MAPT vs. DAPT, MAPT vs. AP+AC, and AC vs. AP+AC.
  • Extraction of data on re-stenosis, occlusion, target limb revascularization (TLR), amputation, major adverse cardiac events, all-cause death, and bleeding.

Main Results:

  • DAPT may reduce restenosis, TLR, and amputation in diabetic CLI patients compared to MAPT.
  • AP+AC therapy shows superior efficacy over antiplatelet monotherapy for restenosis, limb salvage, and survival.
  • No significant increase in bleeding incidence was observed for DAPT or AP+AC compared to MAPT or antiplatelet monotherapy, respectively.

Conclusions:

  • DAPT and AP+AC therapy appear to offer better outcomes than MAPT for CLI patients post-endovascular intervention.
  • Individual patient condition should guide the choice of optimal antithrombotic therapy.
  • Further large-scale, controlled studies are needed due to the heterogeneity and small sample sizes of existing research.

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