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Editorial selection
Vascular surgery
Week of 13 April 2026
1 regulatory item · 2 guidelines · 2 innovations ·HAS · SVS · JVS · Vascular News · SOFMER

Regulation, clinical guidelines, innovation: every week MedNews selects the publications with the greatest practical impact for your specialty. This edition brings together 5 articles from the April 2026 issues and the month before, sorted by dimension and by clinical relevance.

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Regulation
26 mars 2026 Medicines & devices HAS — CNEDiMTS
ENDURANT II/IIS (Medtronic) · CNEDiMTS reassessment of the aorto-iliac stent graft for EVAR

Reassessment of the bifurcated aorto-iliac ENDURANT II/IIS stent graft, a mainstay of endovascular repair of abdominal aortic aneurysms. The opinion sets out the updated conditions for reimbursement, the anatomical indications retained (diameter above 5.5 cm in men, above 5 cm in women, or rapid growth) and the added benefit against the alternatives listed on the LPPR: sufficient benefit, added benefit level V.

Updated reimbursement conditions for the EVAR stent graft most used in France, with direct bearing on practice. Check that your indications and your anatomical documentation, neck, angulation and diameter, meet the criteria the CNEDiMTS has retained.
Lire l'avis HAS →
Clinical guidelines
9 avr. 2026 Guideline SVS
SVS 2026 · New guidelines on blunt thoracic aortic injury, a full update after 15 years

The Society for Vascular Surgery publishes new clinical practice guidelines on the management of blunt thoracic aortic injury, superseding the 2011 recommendations. The document confirms TEVAR as the treatment of reference, introduces a new classification of injury grades and sets out the timing of intervention according to haemodynamic instability and anatomical grade.

Adopt the 2026 SVS injury grade definitions and the TEVAR timing recommendations as your institutional reference. Applicable immediately in vascular trauma, and worth circulating at meetings with the orthopaedic surgery and intensive care teams.
Read the guidelines →
12 avr. 2026 Clinique SOFMER
SOFMER · Good practice guidance on medical compression in venous thromboembolism (DVT, PE)

SOFMER publishes good practice guidance setting out the use of medical compression in the management of venous thromboembolism. It specifies the choice of device, class and length, according to the clinical stage and the type of event, deep vein thrombosis or pulmonary embolism, the optimal duration, and coordination with anticoagulation to prevent post-thrombotic syndrome.

Prescribe medical compression matched to the stage, class and length, following the SOFMER criteria. Coordinate with nursing staff to check that it is worn. A reminder: early compression markedly reduces the risk of post-thrombotic syndrome.
Read the guidance →
Innovation
9 avr. 2026 Innovation JVS
JVS · TADV meta-analysis: transcatheter arterialisation of the deep veins establishes itself in no-option CLTI

A systematic review and meta-analysis published in the Journal of Vascular Surgery (Anahita Dua, Boston) shows that transcatheter arterialisation of the deep veins achieves higher rates of limb salvage, amputation-free survival and wound healing than standard treatment in patients with chronic limb-threatening ischaemia and no conventional arterial revascularisation option.

Transcatheter arterialisation of the deep veins becomes the standard of care in no-option CLTI: the JVS meta-analysis is evidence enough to write the technique into institutional protocols. Worth discussing at the multidisciplinary meeting for CLTI patients otherwise facing amputation.
See the study →
7 avr. 2026 Innovation Vascular News
Nexus (Endospan) approved by the FDA · the first total endovascular aortic arch stent graft covering chronic dissection

Endospan announces FDA approval of the Nexus stent graft for treatment of the aortic arch, including chronic aortic dissection. The approval is supported by the one-year results of the TRIOMPHE IDE study. Nexus allows total endovascular treatment of the arch without deep hypothermia or cardiopulmonary bypass, in patients at high surgical risk.

An FDA approval to bring into the discussion at aortic reference centres for patients at high surgical risk. Access in Europe still depends on CE marking: watch the EMA procedure over the coming months.
See the approval →