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Reducing the risk of venous thromboembolism following superficial endovenous treatment: A UK and Republic of Ireland consensus study

  • The Vascular and Endovascular Research Network (VERN) collaborators
  • Worcestershire Acute Hospitals NHS Trust
  • Imperial College Healthcare NHS Trust
  • Newcastle University
  • Imperial College London
  • Ipswich Hospital NHS Trust
  • Frimley Health NHS Foundation Trust
  • Royal Cornwall Hospitals NHS Trust
  • University Hospitals of Leicester NHS Trust
  • The Royal Wolverhampton NHS Trust
  • University Hospital Trust
  • Norfolk and Norwich University Hospitals NHS Foundation Trust
  • The Dudley Group NHS Foundation Trust
  • Lancashire Teaching Hospitals NHS Foundation Trust
  • Sunderland Royal Hospital
  • Newcastle upon Tyne NHS Hospitals Foundation Trust
  • Hull Royal Infirmary
  • Southmead Hospital NHS Foundation Trust
  • University of Limerick Hospitals Group
  • University of Limerick School of Medicine
  • East Birmingham Hospital
  • University Hospital Waterford
  • Royal Gwent Hospital
  • Regional Hospital
  • Guy's Hospital
  • Musgrove Park Hospital
  • Mater Misericordiae University Hospital
  • University Hospitals Coventry and Warwickshire NHS Trust
  • Beaumont Hospital
  • Basildon and Thurrock Hospital
  • Royal Infirmary of Edinburgh
  • St. Georges Hospital
  • Addenbrookes Hospital
  • Royal Free NHS Trust
  • University of Birmingham
  • Gloucestershire Hospitals NHS Foundation Trust
  • Brighton and Sussex University Hospitals
  • Liverpool University Hospitals NHS Foundation Trust
  • Erne Hospital

Research output: Contribution to a Journal (Peer & Non Peer) › Article › peer-review

16 Citations (Scopus)

Abstract

Objectives: Venous thromboembolism is a potentially fatal complication of superficial endovenous treatment. Proper risk assessment and thromboprophylaxis could mitigate this hazard; however, there are currently no evidence-based or consensus guidelines. This study surveyed UK and Republic of Ireland vascular consultants to determine areas of consensus. Methods: A 32-item survey was sent to vascular consultants via the Vascular and Endovascular Research Network (phase 1). These results generated 10 consensus statements which were redistributed (phase 2). ‘Good’ and ‘very good’ consensus were defined as endorsement/rejection of statements by '67% and '85% of respondents, respectively. Results: Forty-two consultants completed phase 1. This generated seven statements regarding risk factors mandating peri-procedural pharmacoprophylaxis and three statements regarding specific pharmacoprophylaxis regimes. Forty-seven consultants completed phase 2. Regarding venous thromboembolism risk factors mandating pharmacoprophylaxis, ‘good’ and ‘very good’ consensus was achieved for 5/7 and 2/7 statements, respectively. Regarding specific regimens, ‘very good’ consensus was achieved for 3/3 statements. Conclusions: The main findings from this study were that there was ‘good’ or ‘very good’ consensus that patients with any of the seven surveyed risk factors should be given pharmacoprophylaxis with low-molecular-weight heparin. High-risk patients should receive one to two weeks of pharmacoprophylaxis rather than a single dose.

Original languageEnglish
Pages (from-to)706-714
Number of pages9
JournalPhlebology
Volume35
Issue number9
DOIs
Publication statusPublished - 1 Oct 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Deep vein thrombosis
  • varicose veins
  • venous thromboembolism
  • VTE management

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