Effectiveness of haemodialysis access with an autologous tissue-engineered vascular graft: a multicentre cohort study
- PMID: 19394535
- DOI: 10.1016/S0140-6736(09)60248-8
Effectiveness of haemodialysis access with an autologous tissue-engineered vascular graft: a multicentre cohort study
Abstract
Background: Application of a tissue-engineered vascular graft for small-diameter vascular reconstruction has been a long awaited and much anticipated advance for vascular surgery. We report results after a minimum of 6 months of follow-up for the first ten patients implanted with a completely biological and autologous tissue-engineered vascular graft.
Methods: Ten patients with end-stage renal disease who had been receiving haemodialysis through an access graft that had a high probability of failure, and had had at least one previous access failure, were enrolled from centres in Argentina and Poland between September, 2004, and April, 2007. Completely autologous tissue-engineered vascular grafts were grown in culture supplemented with bovine serum, implanted as arteriovenous shunts, and assessed for both mechanical stability during the safety phase (0-3 months) and effectiveness after haemodialysis was started.
Findings: Three grafts failed within the safety phase, which is consistent with failure rates expected for this high-risk patient population. One patient was withdrawn from the study because of severe gastrointestinal bleeding shortly before implantation, and another died of unrelated causes during the safety period with a patent graft. The remaining five patients had grafts functioning for haemodialysis 6-20 months after implantation, and a total of 68 patient-months of patency. In these five patients, only one intervention (surgical correction) was needed to maintain secondary patency. Overall, primary patency was maintained in seven (78%) of the remaining nine patients 1 month after implantation and five (60%) of the remaining eight patients 6 months after implantation.
Interpretation: Our proportion of primary patency in this high-risk cohort approaches Dialysis Outcomes Quality Initiative objectives (76% of patients 3 months after implantation) for arteriovenous fistulas, averaged across all patient populations.
Comment in
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Emergence of clinical vascular tissue engineering.Lancet. 2009 Apr 25;373(9673):1402-4. doi: 10.1016/S0140-6736(09)60799-6. Lancet. 2009. PMID: 19394518 No abstract available.
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Haemodialysis access via tissue-engineered vascular graft.Lancet. 2009 Jul 18;374(9685):199-200; author reply 201. doi: 10.1016/S0140-6736(09)61326-X. Lancet. 2009. PMID: 19616713 No abstract available.
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Haemodialysis access via tissue-engineered vascular graft.Lancet. 2009 Jul 18;374(9685):200; author reply 201. doi: 10.1016/S0140-6736(09)61328-3. Lancet. 2009. PMID: 19616714 No abstract available.
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Haemodialysis access via tissue-engineered vascular graft.Lancet. 2009 Jul 18;374(9685):200-1; author reply 201. doi: 10.1016/S0140-6736(09)61329-5. Lancet. 2009. PMID: 19616715 No abstract available.
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Haemodialysis access via tissue-engineered vascular graft.Lancet. 2009 Jul 18;374(9685):200; author reply 201. doi: 10.1016/S0140-6736(09)61327-1. Lancet. 2009. PMID: 19616716 No abstract available.
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