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Extra-anatomical Cephalic to Internal Jugular Vein Bypass for Central Venous Occlusion
1Department of Surgery, The Aga Khan University Hospital, Karachi, Pakistan.
Insights
Extra-anatomical bypass offers a durable solution for central venous stenosis (CVS) when venoplasty fails. This surgical technique can improve arteriovenous access patency and salvage failing fistulas.
Area of Science:
- Vascular Surgery
- Interventional Nephrology
Background:
- Central venous stenosis (CVS) can compromise arteriovenous access for hemodialysis.
- Percutaneous venoplasty is a common treatment, but recurrence is frequent.
Observation:
- A 60-year-old male with recurrent subclavian vein stenosis post-brachiocephalic arteriovenous fistula underwent two venoplasty sessions with recurrence.
- The patient's CVS lesion became refractory to venoplasty.
Findings:
- Cephalic to internal jugular venovenous bypass using a PTFE graft successfully treated the refractory CVS.
- The bypass provided immediate symptomatic relief and maintained fistula patency at six months.
Implications:
- Extra-anatomical venovenous bypass is a viable and durable alternative for complex CVS.
- Consideration of bypass earlier in selected patients may prevent fistula loss.
Abstract:
Extra-anatomical cephalic to internal jugular venovenous bypass is a surgical method of improving the patency of arteriovenous access in patients with central venous stenosis (CVS), which is infrequently performed. It can be more durable compared to percutaneous venoplasty for CVS. We present a 60-year male who developed right subclavian vein stenosis after brachiocephalic arteriovenous fistula. He had two sessions of venoplasty, but had recurrence. Later, his CVS lesion was not amenable to venoplasty. He underwent cephalic to internal jugular venovenous bypass with externally supported polytetrafluoroethylene (PTFE) graft. This provided immediate symptomatic relief and also salvaged his fistula, which was patent at his last follow-up visit at six months. Venovenous bypass can be considered earlier in 'selected' patients to deal CVS not amenable to percutaneous interventions.
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