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January 22, 2026Annals of The Royal College of Surgeons of England0 citationsOpen Access

Thromboelastography and clinical outcomes in peripheral arterial disease: a systematic review and narrative synthesis

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JBJ-A BroomfieldAAAhmed AbidiaJGJP Gopal

Key Result

TEG-PM was able to predict thrombotic events and guide individualized thromboprophylaxis in patients with peripheral arterial disease.

Key Points

  • This study aims to determine how thromboelastography (TEG) can guide individualized thromboprophylaxis and predict thrombotic events in patients with peripheral arterial disease (PAD).
  • Conducted a systematic review following PRISMA guidelines.
  • Searched PubMed and Embase databases for relevant studies.
  • Included only full-text English articles reporting on TEG in PAD.
  • Registered the study protocol with PROSPERO.
  • Included 14 studies in the analysis.
  • TEG-PM effectively quantified response to antiplatelet therapy and guided thromboprophylaxis.
  • Maximum amplitude, platelet aggregation, and inhibition predicted thrombotic events.
  • Observed substantial heterogeneity in thromboprophylaxis methods and patient populations.

Structured PICO

Does Thromboelastography (TEG) or TEG with platelet mapping (TEG-PM) predict thrombotic events and inform individualised thromboprophylaxis in patients with peripheral arterial disease?

P
Population
Patients with peripheral arterial disease (PAD) (based on 14 included studies)
I
Intervention
Thromboelastography (TEG) or TEG with platelet mapping (TEG-PM)
O
Outcome
Prediction of thrombotic events following re-vascularisation and informing individualised thromboprophylaxissurrogate

TEG-PM may serve as a valuable point-of-care tool for tailoring antiplatelet therapy and predicting thrombotic outcomes in patients with peripheral arterial disease.

Limitations

  • Substantial heterogeneity in thromboprophylaxis
  • Substantial heterogeneity in surgical procedures
  • Substantial heterogeneity in comorbidities

Abstract

Introduction Thromboelastography (TEG) is a point-of-care test that provides a quantitative of measure of the dynamic changes in clot strength and viscoelastic properties of a whole blood sample. Although conventional coagulation tests are well established in vascular surgery, they do not identify the hypercoagulable state and response to antiplatelet therapy. The role of TEG in peripheral arterial disease (PAD) is unclear and its application as demonstrated in the literature has undergone limited appraisal. The objectives of our study were to identify whether TEG can inform individualised thromboprophylaxis and predict thrombotic events following re-vascularisation in PAD. Methods We adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and a PRISMA checklist was completed. PubMed and Embase databases were searched from inception until October 2024 using the relevant Medical Subject Headings terms. Only full-text articles published in the English language reporting the outcomes in PAD with TEG or TEG with platelet mapping (TEG-PM) were analysed. The protocol was registered on the PROSPERO database (ID:CRD42024580627). Findings The analysis included 14 studies. TEG-PM was able to quantify the response to antiplatelet therapy and potentially guide individualised thromboprophylaxis. The parameters maximum amplitude, platelet aggregation and platelet inhibition were able to predict thrombotic events. However, substantial heterogeneity in thromboprophylaxis, surgical procedures and comorbidities was observed in the studies. Conclusions TEG-PM could serve as a valuable tool for tailoring antiplatelet therapy and predicting outcomes in patients with PAD. Further studies including randomised controlled trials are needed to validate the findings.

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Cite This Study

Broomfield et al. (2026) studied this question. TEG-PM was able to predict thrombotic events and guide individualized thromboprophylaxis in patients with peripheral arterial disease.

synapsesocial.com/papers/6971bdad642b1836717e2505https://doi.org/10.1308/rcsann.2025.0091
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