The NeVa Net stent-retriever – initial report of 20 cases from two high volume centres - Scorecard - MDSpire

The NeVa Net stent-retriever – initial report of 20 cases from two high volume centres

  • By

  • Pervinder Bhogal

  • Marco Mancuso-Marcello

  • Rory Fairhead

  • Nadia Shah

  • Keng Siang Lee

  • Christos Nikola

  • Katherine Parkin

  • Giovanna Klefti

  • Levansri Makalanda

  • Ken Wong

  • Joe Lansley

  • Michael Przyszlak

  • Oliver Spooner

  • Branimir Čulo

  • Vladimir Kalousek

  • July 15, 2025

  • 0 min

Share

Clinical Scorecard: Initial Findings from 20 Cases Utilizing the NeVa Net Stent-Retriever in Two High-Volume Centers

At a Glance

CategoryDetail
ConditionLarge Vessel Occlusion (LVO) Stroke
Key MechanismsMechanical thrombectomy using the NeVa NET stent-retriever with distal clot capture technology to prevent microembolisation and improve recanalization and reperfusion
Target PopulationPatients with acute ischemic stroke due to LVO, NIHSS > 5, ASPECT score ≥ 3, life expectancy > 6 months
Care SettingComprehensive stroke centers performing endovascular mechanical thrombectomy

Key Highlights

  • NeVa NET incorporates a dual-layered nitinol braid 'NET' designed to capture microemboli <400 microns, aiming to reduce distal embolisation during thrombectomy.
  • Initial retrospective analysis of 20 patients showed use of NeVa NET as first-line device with median NIHSS 18 and 30% receiving IV tPA prior to thrombectomy.
  • Device available in two sizes (5.5 × 37 mm and 4 × 30 mm) compatible with standard microcatheters, with radial force comparable to Solitaire 6 × 30 mm device.

Guideline-Based Recommendations

Diagnosis

  • Confirm LVO via CT angiography from arch to vertex prior to thrombectomy.
  • Assess ASPECT score ≥ 3 to determine eligibility for mechanical thrombectomy.
  • Evaluate NIHSS score > 5 and life expectancy > 6 months for patient selection.

Management

  • Perform mechanical thrombectomy using NeVa NET as first-line stent-retriever device.
  • Administer IV tPA if patient meets criteria prior to thrombectomy.
  • Use local or general anesthesia based on operator discretion.
  • Employ ancillary devices such as balloon guide catheters and distal aspiration catheters as per operator preference.

Monitoring & Follow-up

  • Perform post-procedural imaging at 24 ± 6 hours or earlier if neurological deterioration occurs.
  • Record eTICI score after first pass and at procedure end to assess recanalization success.
  • Assess 90-day modified Rankin Scale (mRS) via telephone or clinic follow-up.

Risks

  • Potential for distal embolisation minimized by NeVa NET design but procedural complications should be monitored.
  • Incomplete data sets or use of alternative initial devices excluded from analysis.

Patient & Prescribing Data

20 patients with acute ischemic stroke due to LVO treated with NeVa NET as first-line device

Median NIHSS 18, 30% received IV tPA prior to thrombectomy, majority had mRS 0 or 1 pre-stroke, left-sided occlusions more common (60%), cardioembolic cause predominant

Clinical Best Practices

  • Select patients with NIHSS > 5, ASPECT score ≥ 3, and life expectancy > 6 months for NeVa NET thrombectomy.
  • Use CT angiography for precise occlusion localization and procedural planning.
  • Consider use of balloon guide catheters and distal aspiration catheters to optimize thrombectomy outcomes.
  • Monitor recanalization success with eTICI scoring and follow neurological status closely post-procedure.
  • Record functional outcomes at 90 days to evaluate long-term efficacy.

References

Original Source(s)

Related Content