Local tissue reactions after nerve repair with ethyl-cyanoacrylate compared with epineural sutures

References

• Millesi H. Peripheral nerve surgery today: turning point or continuous development?. J Hand Surg 1990; 15B: 281–7
   Google Scholar
• Smahel J, Meyer VE, Bachem U. Glueing of peripheral nerves with fibrin: experimental studies. J Reconstr Microsurg 1987; 3: 211–20
   Google Scholar
• Suri A, Mehta VS, Sarkar C. Microneural anastomosis with fibrin glue: an experimental study. Neurol India 2002; 50: 23–6
   PubMedGoogle Scholar
• Povlsen B. A new fibrin seal in primary repair of peripheral nerves. J Hand Surg 1994; 19B: 43–7
   Google Scholar
• Tetik C, Ozer K, Ayhan S, Siemionow K, Browne E, Siemionow M. Conventional versus epineural sleeve neurorrhaphy technique: functional and histomorphometric analysis. Ann Plast Surg 2002; 49: 397–403
   PubMed Web of Science ®Google Scholar
• Wieken K, Angioi-Duprez K, Lim A, Marchal L, Merle M. Nerve anastomosis with glue: comparative histologic study of fibrin and cyanoacrylate glue. J Reconstr Microsurg 2003; 19: 17–20
   PubMed Web of Science ®Google Scholar
• Jackson MR. Fibrin sealants in surgical practice: an overview. Am J Surg 2001; 182(suppl 2)1S–7S
   PubMedGoogle Scholar
• Ang ES, Tan KC, Tan LH, Ng RT, Song IC. 2-octylcyanoacrylate-assisted microvascular anastomosis: comparison with a conventional suture technique in rat femoral arteries. J Reconstr Microsurg 2001; 17: 193–201
   Google Scholar
• Landegren T, Risling M, Brage A, Persson JK. Long-term results of peripheral nerve repair: a comparison of nerve anastomosis with ethyl-cyanoacrylate and epineural sutures. Scand J Plast Reconstr Surg Hand Surg 2006; 40: 65–72
   PubMed Web of Science ®Google Scholar
• Pineros-Fernandez A, Rodeheaver PF, Rodeheaver GT. Octyl 2-cyanoacrylate for repair of peripheral nerve. Ann Plast Surg 2005; 55: 188–95
   Google Scholar
• Choi BH, Kim BY, Huh JY, et al. Microneural anastomosis using cyanoacrylate adhesives. Int J Oral Maxillofac Surg 2004; 33: 777–80
   Google Scholar
• Javelet J, Torabinejad M, Danforth R. Isobutyl cyanoacrylate: a clinical and histologic comparison with sutures in closing mucosal incisions in monkeys. Oral Surg Oral Med Oral Pathol 1985; 59: 91–4
   Google Scholar
• Forseth M, O'Grady K, Toriumi DM. The current status of cyanoacrylate and fibrin tissue adhesives. J Long Term Eff Med Implants 1992; 2: 221–33
   PubMedGoogle Scholar
• Hurwitz PJ, Magora A, Gonen B, Appelboim J, Ben-Hur N. Microsurgical techniques and the use of tissue adhesive in the repair of peripheral nerves. J Surg Res 1974; 17: 245–52
   Google Scholar
• Brown MC, Perry VH, Lunn ER, Gordon S, Heumann R. Macrophage dependence of peripheral sensory nerve regeneration: possible involvement of nerve growth factor. Neuron 1991; 6: 359–70
   PubMed Web of Science ®Google Scholar
• Perry VH, Brown MC. Role of macrophages in peripheral nerve degeneration and repair. Bioessays 1992; 14: 401–6
   PubMed Web of Science ®Google Scholar
• Miyauchi A, Kanje M, Danielsen N, Dahlin LB. Role of macrophages in the stimulation and regeneration of sensory nerves by transposed granulation tissue and temporal aspects of the response. Scand J Plast Reconstr Surg Hand Surg 1997; 31: 17–23
   PubMed Web of Science ®Google Scholar
• Skene JH. Axonal growth-associated proteins. Annu Rev Neurosci 1989; 12: 127–56
   PubMed Web of Science ®Google Scholar
• Stark B, Carlstedt T, Cullheim S, Risling M. Developmental and lesion-induced changes in the distribution of the glucose transporter Glut-1 in the central and peripheral nervous system. Exp Brain Res 2000; 131: 74–84
   Google Scholar
• Gundersen HJ, Bendtsen TF, Korbo L, et al. Some new, simple and efficient stereological methods and their use in pathological research and diagnosis. APMIS 1988; 96: 379–94
   PubMed Web of Science ®Google Scholar
• Vote BJ, Elder MJ. Cyanoacrylate glue for corneal perforations: a description of a surgical technique and a review of the literature. Clin Experiment Ophthalmol 2000; 28: 437–42
   PubMedGoogle Scholar
• Howell K, Hopkins N, McLoughlin P. Combined confocal microscopy and stereology: a highly efficient and unbiased approach to quantitative structural measurement in tissues. Exp Physiol 2002; 87: 747–56
   PubMed Web of Science ®Google Scholar
• Harik SI, Kalaria RN, Andersson L, Lundahl P, Perry G. Immunocytochemical localization of the erythroid glucose transporter: abundance in tissues with barrier functions. J Neurosci 1990; 10: 3862–72
   Google Scholar
• Kiernan JA. Hypotheses concerned with axonal regeneration in the mammalian nervous system. Biol Rev Camb Philos Soc 1979; 54: 155–97
   PubMed Web of Science ®Google Scholar
• Magnani P, Cherian PV, Gould GW, Greene DA, Sima AA, Brosius FC III. Glucose transporters in rat peripheral nerve: paranodal expression of GLUT-1 and GLUT-3. Metabolism 1996; 45: 1466–73
   PubMed Web of Science ®Google Scholar
• Stoll G, Griffin JW, Li CY, Trapp BD. Wallerian degeneration in the peripheral nervous system: participation of both Schwann cells and macrophages in myelin degradation. J Neurocytol 1989; 18: 671–83
   PubMedGoogle Scholar
• Stoll G, Muller HW. Nerve injury, axonal degeneration and neural regeneration: basic insights. Brain Pathol 1999; 9: 313–25
   PubMed Web of Science ®Google Scholar
• Dahlin LB. Stimulation of regeneration of the sciatic nerve by experimentally induced inflammation in rats. Scand J Plast Reconstr Surg Hand Surg 1992; 26: 121–5
   PubMed Web of Science ®Google Scholar
• Dahlin LB. Prevention of macrophage invasion impairs regeneration in nerve grafts. Brain Res 1995; 679: 274–80
   PubMed Web of Science ®Google Scholar
• McGee JOD, Isaacson PG, Wright NA. In: Oxford textbook of pathology. Oxford: Oxford University Press; 1992. p 236–57, 394–406.
   Google Scholar