Biological Materials in Vascular Surgery: Clinical Applications, Benefits, and Limitations
Vascular grafting has progressed significantly in the pursuit of materials capable of achieving seamless biological integration with host tissue; however, an ideal graft that combines availability, durability, and biocompatibility remains elusive. This review provides a comprehensive overview of currently available biomaterials in vascular surgery, highlighting their clinical applications, benefits, and limitations. While autologous material (e.g., veins) remains the gold standard, its limited availability and harvesting-related morbidity, such as infection and thrombosis, have prompted the search for alternative biological grafts. Xenografts, derived from non-human donors (e.g., bovine, ovine, & porcine tissues), have demonstrated favorable patency rates and relatively low infection rates in vascular access, extremity revascularization, and aortic surgery. Human allografts have shown excellent performance in infected fields; however, their use is constrained by logistical challenges, including limited donor availability and labor-intensive preparation. Emerging tissue-engineered vascular grafts (TEVGs), often composed of biodegradable scaffolds seeded with biologically active cells, aim to replicate the structure and function of native vessels. Some TEVGs are designed to transform into native vasculature following biodegradation of the scaffold. However, further technical refinement and cost reduction are essential before TEVGs can be widely adopted as off-the-shelf solutions.
- Spadaccio C, Rainer A, Barbato R, Trombetta M, Chello M, Meyns B. The long-term follow-up of large-diameter Dacron® vascular grafts in surgical practice: a review. J Cardiovasc Surg (Torino). 2019;60(4):501-513. doi: 10.23736/S0021-9509.16.08061-7
- Hastings OM, Jain KM, Hobson RW II, Swan KG. A prospective randomized study of three expanded polytetrafluoroethylene (PTFE) grafts as small arterial substitutes. Ann Surg. 1978;188(6):743-747. doi: 10.1097/00000658-197812000-00005
- LeVeen HH, Rarberio JR. Tissue reaction to plastics used in surgery with special reference to teflon. Ann Surg. 1949;129(1):74-84. doi: 10.1097/00000658-194901000-00008
- Criado E, Giron F. José Goyanes Capdevila, unsung pioneer of vascular surgery. Ann Vasc Surg. 2006;20(3):422-425. doi: 10.1007/s10016-006-9042-y
- Klinkert P, Post PN, Breslau PJ. Saphenous vein versus PTFE for above-knee femoropopliteal bypass. A review of the literature. Eur J Vasc Endovasc Surg. 2004;27(4):357-362. doi: 10.1016/j.ejvs.2003.12.027
- Dorweiler B, Neufang A, Chaban R, Reinstadler J, Duenschede F, Vahl CF. Use and durability of femoral vein for autologous reconstruction with infection of the aortoiliofemoral axis. J Vasc Surg. 2014;59(3):675-683. doi: 10.1016/j.jvs.2013.09.029
- Ali AT, Modrall JG, Hocking J, et al. Long-term results of the treatment of aortic graft infection by in situ replacement with femoral popliteal vein grafts. J Vasc Surg. 2009;50(1):30-39. doi: 10.1016/j.jvs.2009.01.008
- Heinola I, Kantonen I, Jaroma M, et al. Editor's choice – treatment of aortic prosthesis infections by graft removal and in situ replacement with autologous femoral veins and fascial strengthening. Eur J Vasc Endovasc Surg. 2016;51(2):232-239. doi: 10.1016/j.ejvs.2015.09.015
- Hicks CW, Wang P, Kernodle A, Lum YW, Black JH, Makary MA. Assessment of use of arteriovenous graft vs arteriovenous fistula for first-time permanent hemodialysis access. JAMA Surg. 2019;154(9):844-851. doi: 10.1001/jamasurg.2019.1736
- Chew DKW, Owens CD, Belkin M, et al. Bypass in the absence of ipsilateral greater saphenous vein: safety and superiority of the contralateral greater saphenous vein. J Vasc Surg. 2002;35(6):1085-1092. doi: 10.1067/mva.2002.124628
- Labropoulos N, Bishawi M, Gasparis A, Tassiopoulos A, Gupta S. Great saphenous vein stump thrombosis after harvesting for coronary artery bypass graft surgery. Phlebology. 2014;29(4):215-219. doi: 10.1258/phleb.2012.012094
- Modrall JG, Hocking JA, Timaran CH, et al. Late incidence of chronic venous insufficiency after deep vein harvest. J Vasc Surg. 2007;46(3):520-525. doi: 10.1016/j.jvs.2007.04.061
- Swenne CL, Borowiec J, Carlsson M, Lindholm C. Prediction of and risk factors for surgical wound infection in the saphenous vein harvesting leg in patients undergoing coronary artery bypass. Thorac Cardiovasc Surg. 2006;54(3):300-306. doi: 10.1055/s-2006-924093
- Zenati MA, Bhatt DL, Bakaeen FG, et al. Randomized trial of endoscopic or open vein-graft harvesting for coronary-artery bypass. N Engl J Med. 2019;380(2):132-141. doi: 10.1056/NEJMoa1812390
- Cervantes J. Reflections on the 50th anniversary of the first abdominal aortic aneurysm resection. World J Surg. 2003;27(2):246-248. doi: 10.1007/s00268-002-6413-6
- Stephen M, Sheil AG, Wong J. Allograft vein arterial bypass. Arch Surg. 1978;113(5):591-593. doi: 10.1001/archsurg.1978.01370170053009
- Perloff LJ, Rowlands DT, Barker CF. Studies of the modified venous allograft. Ann Surg. 1977;186(2):227-232. doi: 10.1097/00000658-197708000-00018
- Callow AD. Arterial homografts. Eur J Vasc Endovasc Surg. 1996;12(3):272-281. doi: 10.1016/s1078-5884(96)80244-9
- Lesèche G, Castier Y, Petit M-D, et al. Long-term results of cryopreserved arterial allograft reconstruction in infected prosthetic grafts and mycotic aneurysms of the abdominal aorta. J Vasc Surg. 2001;34(4):616-622. doi: 10.1067/mva.2001.116107
- Antonopoulos CN, Papakonstantinou NA, Hardy D, Lyden SP. Editor's choice – cryopreserved allografts for arterial reconstruction after aorto-iliac infection: a systematic review and meta-analysis. Eur J Vasc Endovasc Surg. 2019;58(1):120-128. doi: 10.1016/j.ejvs.2019.03.003
- Fahner PJ, Idu MM, van Gulik TM, Legemate DA. Systematic review of preservation methods and clinical outcome of infrainguinal vascular allografts. J Vasc Surg. 2006;44(3):518-524. doi: 10.1016/j.jvs.2006.05.037
- Vyas KS, Burns C, Ryan DT, Wong L. Prolonged allograft survival in a patient with chronic immunosuppression: a case report and systematic review. Wounds. 2017;29(6):159-162.
- Guevara-Noriega KA, Villamizar MA, Castro-Rios JG, Pomar JL. Outcomes of vascular allograft transplants in the autonomous community of Catalonia, Spain. Cir Cir. 2021;89(6):797-805. doi: 10.24875/CIRU.20001069
- Chakfé N, Diener H, Lejay A, et al. Editor's choice – European Society for Vascular Surgery (ESVS) 2020 clinical practice guidelines on the management of vascular graft and endograft infections. Eur J Vasc Endovasc Surg. 2020;59(3):339-384. doi: 10.1016/j.ejvs.2019.10.016
- Smeds MR, Duncan AA, Harlander-Locke MP, et al. Treatment and outcomes of aortic endograft infection. J Vasc Surg. 2016;63(2):332-340. doi: 10.1016/j.jvs.2015.08.113
- Lejay A, Delay C, Girsowicz E, et al. Cryopreserved cadaveric arterial allograft for arterial reconstruction in patients with prosthetic infection. Eur J Vasc Endovasc Surg. 2017;54(5):636-644. doi: 10.1016/j.ejvs.2017.07.016
- Harlander-Locke MP, Harmon LK, Lawrence PF, et al. The use of cryopreserved aortoiliac allograft for aortic reconstruction in the United States. J Vasc Surg. 2014;59(3):669-674.e1. doi: 10.1016/j.jvs.2013.09.009
- McCready RA, Bryant MA, Fehrenbacher JW, et al. Long-term results with cryopreserved arterial allografts (CPAs) in the treatment of graft or primary arterial infections. J Surg Res. 2011;168(1):e149-e153. doi: 10.1016/j.jss.2010.09.026
- Randon C, Jacobs B, De Ryck F, Beele H, Vermassen F. Fifteen years of infrapopliteal arterial reconstructions with cryopreserved venous allografts for limb salvage. J Vasc Surg. 2010;51(4):869-877. doi: 10.1016/j.jvs.2009.11.062
- Touma J, Cochennec F, Parisot J, Fialaire Legendre A, Becquemin J-P, Desgranges P. In situ reconstruction in native and prosthetic aortic infections using cryopreserved arterial allografts. Eur J Vasc Endovasc Surg. 2014;48(3):292-299. doi: 10.1016/j.ejvs.2014.04.023
- Whaley D, Damyar K, Witek RP, Mendoza A, Alexander M, Lakey JR. Cryopreservation: an overview of principles and cell-specific considerations. Cell Transplant. 2021;30:963689721999617. doi: 10.1177/0963689721999617
- Darby CR, Roy D, Deardon D, Cornall A. Depopulated bovine ureteric xenograft for complex haemodialysis vascular access. Eur J Vasc Endovasc Surg. 2006;31(2):181-186. doi: 10.1016/j.ejvs.2005.07.006
- Lantz GC, Badylak SF, Hiles MC, et al. Small intestinal submucosa as a vascular graft: a review. J Invest Surg. 1993;6(3):297-310. doi: 10.3109/08941939309141619
- Tolva V, Bertoni GB, Trimarchi S, Grassi, V, Fusari M, Rampoldi V. Unreliability of depopulated bovine ureteric xenograft for infrainguinal bypass surgery: mid-term results from two vascular centres. Eur J Vasc Endovasc Surg. 2007;33(2):214-216. doi: 10.1016/j.ejvs.2006.10.007
- Manduz S, Katrancioglu N, Ozker E, Dogan K. Early thrombosis in bovine mesenteric vein grafts after infrainguinal reconstruction. Int J Angiol. 2008;17(1):37-39. doi: 10.1055/s-0031-1278278
- Spark JI, Yeluri S, Derham C, Wong YT, Leitch D. Incomplete cellular depopulation may explain the high failure rate of bovine ureteric grafts. Br J Surg. 2008;95(5):582-585. doi: 10.1002/bjs.6052
- Grills S, El-Diaz N, Walker-Jacobs A, Borucki J, Stather P. Outcomes following use of bovine pericardium (xenoprosthetic) grafts for reconstruction of mycotic aortic aneurysms and infected aortic grafts: a systematic review and meta-analysis. Ann Vasc Surg. 2024;102:181-191. doi: 10.1016/j.avsg.2023.11.037
- Orrapin S, Benyakorn T, Howard DP, Siribumrungwong B, Rerkasem K. Patches of different types for carotid patch angioplasty. Cochrane Database Syst Rev. 2021;2:CD000071. doi: 10.1002/14651858.CD000071.pub4
- Liesker DJ, Gareb B, Looman RS, et al. Patch angioplasty during carotid endarterectomy using different materials has similar clinical outcomes. J Vasc Surg. 2023;77(2):559-566.e1. doi: 10.1016/j.jvs.2022.09.027
- Chaney M, Joshi G, Serrato JC, et al. Morbidity and mortality of common femoral endarterectomy. J Vasc Surg. 2024;80(1):199-203. doi: 10.1016/j.jvs.2024.01.211
- Song L, Wang X, Tao C, et al. Trileaflet aortic valve reconstruction using bovine pericardium. Heart Lung Circ. 2021;30(10):1570-1577. doi: 10.1016/j.hlc.2021.03.278
- Donato F, Donati T, Minelli F, et al. Treatment of aorto-iliac and infrainguinal vascular infections with a prefabricated bovine pericardial graft. Ann Vasc Surg. 2024;105:177-188. doi: 10.1016/j.avsg.2024.01.015
- Jara M, Malinowski M, Bahra M, et al. Bovine pericardium for portal vein reconstruction in abdominal surgery: a surgical guide and first experiences in a single center. Dig Surg. 2015;32(2):135-141. doi: 10.1159/000370008
- De Vita R, Mangialardi ML, Pozzi M, et al. A pericardium bovine matrix pocket in DTI prepectoral breast reconstruction. Clin Breast Cancer. 2024;24(7):e613-e621. doi: 10.1016/j.clbc.2024.06.004
- Eslahi A, Ahmed F, Askarpour MR, et al. Outcomes of surgical correction of Peyronie's disease with plaque excision and grafting: comparison of testicular tunica vaginalis graft versus bovine pericardium graft. Asian J Urol. 2024;11(3):497-503. doi: 10.1016/j.ajur.2023.03.005
- van Hoefen Wijsard M, Haan M, Rietveld E, van Rijn LJ. Donor sclera versus bovine pericardium as patch graft material in glaucoma implant surgery and the impact of a drainage suture. Acta Ophthalmol. 2018;96(7):692-698. doi: 10.1111/aos.13721
- Anderson CB, Sicard GA, Etheredge EE. Bovine carotid artery and expanded polytetrafluoroethylene grafts for hemodialysis vascular access. J Surg Res. 1980;29(2):184-188. doi: 10.1016/0022-4804(80)90036-0
- Kostakis ID, Loukopoulos I. Comparison between bovine carotid artery graft and polytetrafluoroethylene graft for haemodialysis vascular access: a systematic review and meta-analysis. J Vasc Access. 2021;22(1):26-33. doi: 10.1177/1129729820926088
- Lindsey P, Echeverria A, Cheung M, Kfoury E, Bechara CF, Lin PH. Lower extremity bypass using bovine carotid artery graft (Artegraft): an analysis of 124 cases with long-term results. World J Surg. 2018;42(1):295-301. doi: 10.1007/s00268-017-4161-x
- Reilly B, Khan S, Dosluoglu H, et al. Comparison of autologous vein and bovine carotid artery graft as a bypass conduit in arterial trauma. Ann Vasc Surg. 2019;61:246-253. doi: 10.1016/j.avsg.2019.05.017
- Wang J-N, Kan C-D, Lin S-H, Chang K-C, Tsao S, Wong T-W. Potential of autologous progenitor cells and decellularized porcine artery matrix in construction of tissue-engineered vascular grafts. Organogenesis. 2021;17(3-4):72–84. doi: 10.1080/15476278.2021.1963603
- Jaramillo J, Valencia-Rivero KT, Cedano-Serrano FJ, López R, Sandoval N, Briceño JC. Design and evaluation of a structural reinforced small intestinal submucosa vascular graft for hemodialysis access in a porcine model. ASAIO J. 2018;64(2):270-7. doi: 10.1097/MAT.0000000000000618
- Palumbo R, Niscola P, Calabria S, et al. Long-term favorable results by arteriovenous graft with Omniflow II prosthesis for hemodialysis. Nephron Clin Pract. 2009;113(2):c76-80. doi: 10.1159/000228538
- Shakarchi JA, McGrogan D, Yates PJ, Inston N. Use of biosynthetic grafts (Omniflow II) for high infection risk haemodialysis vascular access. J Vasc Access. 2016;17(2):151-154. doi: 10.5301/jva.5000462
- El-Diaz N, Walker-Jacobs A, Althaher A, Alalwani Z, Borucki J, Stather PW. The Omniflow II biosynthetic graft for aortic reconstruction: a systematic review and meta-analysis. J Vasc Surg. 2023;77(3):964-970.e4. doi: 10.1016/j.jvs.2022.09.009
- Van de Laar BC, van Heusden HC, Pasker-de Jong PC, van Weel V. Omniflow II biosynthetic grafts versus expanded polytetrafluoroethylene grafts for infrainguinal bypass surgery: a single-center retrospective analysis. Vascular. 2022;30(4):749-758. doi: 10.1177/17085381211029815
- Liesker DJ, Gareb B, Speijers MJ, et al. Outcomes of Omniflow® II prosthesis used for revascularization in the femoral tract both in infected and non-infected setting. J Cardiovasc Surg (Torino). 2023;64:634-644. doi: 10.23736/S0021-9509.23.12692-9
- Caradu C, Brunet C, Spampinato B, et al. Contemporary results with the biosynthetic glutaraldehyde-denatured ovine collagen graft (Omniflow II) in lower extremity arterial revascularization in a septic context. Ann Vasc Surg. 2022;85:22-31. doi: 10.1016/j.avsg.2022.04.011
- Hodge S, Greaves N, Murray D. The use of bovine pericardial patches in vascular surgery: where do we draw the line in obtaining informed consent? Ann Vasc Surg. 2021;76:536-541. doi: 10.1016/j.avsg.2021.03.033
- West-Livingston L, Lim JW, Lee SJ. Translational tissue-engineered vascular grafts: from bench to bedside. Biomaterials. 2023;302:122322. doi: 10.1016/j.biomaterials.2023.122322
- Antonyshyn JA, D'Costa KA, Santerre JP. Advancing tissue-engineered vascular grafts via their endothelialization and mechanical conditioning. J Cardiovasc Surg (Torino). 2020;61(5):555-576. doi: 10.23736/S0021-9509.20.11582-9
- Blum KM, Zbinden JC, Ramachandra AB, et al. Tissue-engineered vascular grafts transform into autologous neovessels capable of native function and growth. Commun Med (Lond). 2022;2:3. doi: 10.1038/s43856-021-00063-7
- Shoji T, Shinoka T. Tissue engineered vascular grafts for pediatric cardiac surgery. Transl Pediatr. 2018;7(2):188-195. doi: 10.21037/tp.2018.02.01
- Weinberg CB, Bell E. A blood vessel model constructed from collagen and cultured vascular cells. Science. 1986;231(4736):397-400. doi: 10.1126/science.2934816
- Durán-Rey D, Crisóstomo V, Sánchez-Margallo JA, Sánchez-Margallo FM. Systematic review of tissue-engineered vascular grafts. Front Bioeng Biotechnol. 2021;9:771400. doi: 10.3389/fbioe.2021.771400
- Cifuentes S, Sen I, Shuja F, et al. Outcomes of lower extremity arterial bypass using the human acellular vessel in patients with chronic limb-threatening ischemia. J Vasc Surg. 2024;79(2):348-357.e2. doi: 10.1016/j.jvs.2023.10.040
- Gutowski P, Guziewicz M, Ilzecki M, et al. Six-year outcomes of a phase II study of human-tissue engineered blood vessels for peripheral arterial bypass. JVS Vasc Sci. 2023;4:100092. doi: 10.1016/j.jvssci.2022.11.001
- Lawson JH, Glickman MH, Ilzecki M, et al. Bioengineered human acellular vessels for dialysis access in patients with end-stage renal disease: two phase 2 single-arm trials. Lancet. 2016;387(10032):2026-2034. doi: 10.1016/S0140-6736(16)00557-2
- Nakayama Y, Higashita R, Shiraishi Y, et al. iBTA-induced Biotube® blood vessels: 2020 update. Kidney Dial. 2021;1(1):3-13. doi: 10.3390/kidneydial1010002
- Nakayama Y, Iwai R, Terazawa T, et al. Pre-implantation evaluation of a small-diameter, long vascular graft (Biotube®) for below-knee bypass surgery in goats. J Biomed Mater Res B Appl Biomater. 2022;110(11):2387-2398. doi: 10.1002/jbm.b.35084
- Mori K, Umeno T, Kawashima T, et al. Breaking the limit of cardiovascular regenerative medicine: successful 6-month goat implant in the world's first ascending aortic replacement using Biotube blood vessels. Bioengineering. 2024;11(4):405. doi: 10.3390/bioengineering11040405
- Higashita R, Miyazaki M, Oi M, Ishikawa N. First-in-human results of an in-body tissue architecture-induced tissue-engineered vascular graft "Biotube" for distal bypass in chronic limb-threatening ischemia. J Vasc Surg Cases Innov Tech. 2022;8(3):488-493. doi: 10.1016/j.jvscit.2022.07.007
- Nakayama Y, Kaneko Y, Okumura N, Terazawa T. Initial 3-year results of first human use of an in-body tissue-engineered autologous "Biotube" vascular graft for hemodialysis. J Vasc Access. 2020;21(1):110-115. doi: 10.1177/1129729819852550
- Brugmans M, Serrero A, Cox M, Svanidze O, Schoen FJ. Morphology and mechanisms of a novel absorbable polymeric conduit in the pulmonary circulation of sheep. Cardiovasc Pathol. 2019;38:31-38. doi: 10.1016/j.carpath.2018.10.008
- Tozzi M, De Letter J, Krievins D, et al. First-in-human feasibility study of the aXess graft (aXess-FIH): 6-month results. J Vasc Access. 2025;26(2):502-509. doi: 10.1177/11297298231220967
- Rodriguez-Soto MA, Riveros A, Suarez Vargas N, et al. Failure analysis of TEVG's II: late failure and entering the regeneration pathway. Cells. 2022;11(6):939. doi: 10.3390/cells11060939
- de la Puente P, Ludeña D. Cell culture in autologous fibrin scaffolds for applications in tissue engineering. Exp Cell Res. 2014;322(1):1-11. doi: 10.1016/j.yexcr.2013.12.017
- Thottappillil N, Nair PD. Scaffolds in vascular regeneration: current status. Vasc Health Risk Manag. 2015;11:79-91. doi: 10.2147/VHRM.S50536
- Sanz-Horta R, Matesanz A, Gallardo A, et al. Technological advances in fibrin for tissue engineering. J Tissue Eng. 2023;14:20417314231190288. doi: 10.1177/20417314231190288
- Kyriakides TR, Raj A, Tseng TH, et al. Biocompatibility of nanomaterials and their immunological properties. Biomed Mater (Bristol). 2021;16(4):10.1088/1748-605X/abe5fa. doi: 10.1088/1748-605X/abe5fa
- Badylak S, Freytes D, Gilbert T. Extracellular matrix as a biological scaffold material: structure and function. Acta Biomater. 2009;5(1):1-13. doi: 10.1016/j.actbio.2008.09.013
- Rizzi S, Mantero S, Boschetti F, Pesce M. Luminal endothelialization of small-caliber silk tubular graft for vascular constructs engineering. Front Cardiovasc Med. 2022;9:1013183. doi: 10.3389/fcvm.2022.1013183
- Zhu J, Ma H, Du J, et al. A coaxial 3D-bioprinted hybrid vascular scaffold based on decellularized extracellular matrix/nano clay/sodium alginate bioink. Int J Biol Macromol. 2025;290:139056. doi: 10.1016/j.ijbiomac.2024.139056
- Marcus P, Echeverria A, Cheung M, Kfoury E, Shim K, Lin PH. Early cannulation of bovine carotid artery graft reduces tunneled dialysis catheter-related complications: comparison of bovine carotid artery vs expanded polytetrafluoroethylene grafts in hemodialysis access. Vasc Endovascular Surg. 2019;53(2):104-111. doi: 10.1177/1538574418813595
- Hofstra L, Bergmans DC, Hoeks AP, Kitslaar PJ, Leunissen KM, Tordoir JH. Mismatch in elastic properties around anastomoses of interposition grafts for hemodialysis access. J Am Soc Nephrol. 1994;5(5):1243-1250. doi: 10.1681/ASN.V551243
- Hao D, Lin J, Liu R, et al. A bio-instructive parylene-based conformal coating suppresses thrombosis and intimal hyperplasia of implantable vascular devices. Bioact Mater. 2023;28:467-479. doi: 10.1016/j.bioactmat.2023.06.014
- Bello AK, Okpechi IG, Osman MA, et al. Epidemiology of haemodialysis outcomes. Nat Rev Nephrol. 2022;18(6):378-395. doi: 10.1038/s41581-022-00542-7
- Beckman JA, Creager MA. Critical limb ischemia and intermediate-term survival. JACC Cardiovasc Interv. 2014;7(12):1450-1452. doi: 10.1016/j.jcin.2014.07.012
- Kirkton RD, Santiago-Maysonet M, Lawson JH, et al. Bioengineered human acellular vessels recellularize and evolve into living blood vessels after human implantation. Sci Transl Med. 2019;11(485):eaau6934. doi: 10.1126/scitranslmed.aau6934
