The effect of mitomycin C as fibrosis preventive agent during craniectomies

References

• Kawaguchi T, Hosoda K, Shibata Y, Koyama J. Expaneded polytetrafluoroethylene membrane for prevention of adhesion in patientsundergoing external decompression and subsequent cranioplasty. Neurol Med Chir (Tokyo) 2003; 43: 320–323
   PubMed Web of Science ®Google Scholar
• Abitbol J J, Lincoln T L, Lind B I, et al. Preventing postlaminectomy adhesion. A new experimental model. Spine 1994; 19: 1809–1814
   PubMed Web of Science ®Google Scholar
• Barberá J, Gonzalez J, Esquerdo J, et al. Prophylaxis of the laminectomy membrane. An experimental study in dogs. J Neurosurg 1978; 49: 419–424
   PubMed Web of Science ®Google Scholar
• Boot D A, Hughes S PF. The prevention of adhesions after laminectomy. Adverse results of Zenoderm implantations into laminectomy sites in rabbits. Clin Orthop 1987; 215: 296–302
   PubMed Web of Science ®Google Scholar
• Colak A, Bavbek M, Aydin N E, et al. Effect of CO2 laser on spinal epidural fibrosis. Acta Neurochir 1996; 138: 162–166
   PubMed Web of Science ®Google Scholar
• Cook S D, Prewett A B, Dalton J E, et al. Reduction in perineural scar formation after laminectomy with Polyactive membrane sheets. Spine 1994; 19: 1815–1825
   PubMed Web of Science ®Google Scholar
• Foulkes G D, Robinson J S, Jr. Intraoperative dexamethasone irrigation in lumbar microdiskectomy. Clin Orthop 1990; 261: 224–228
   PubMed Web of Science ®Google Scholar
• Gill G G, Sakovich L, Thompson E. Pedicle fat grafts for the prevention of scar formation after laminectomy. An experimental study in dogs. Spine 1979; 4: 176–186
   PubMedGoogle Scholar
• Hadani M, Ram Z, Horowitz A, et al. Silicon prevents postlaminectomy epidural root adhesions. An experimental study in rats. Acta Neurochir 1993; 123: 153–162
   PubMed Web of Science ®Google Scholar
• Jacobs R R, McClain O, Neff J. Control of postlaminectomy scar formation: an experimental and clinical study. Spine 1980; 5: 223–229
   PubMed Web of Science ®Google Scholar
• Keller J T, Dunsker S B, McWhorter J M, et al. The fate of autogenous grafts to the spinal dura. An experimental study. J Neurosurg 1978; 49: 412–418
   PubMed Web of Science ®Google Scholar
• Kitano T, Zerwekh J E, Edwards M L, et al. Viscous carboxymethylcellulose in the prevention of epidural scar formation. Spine 1991; 16: 820–823
   PubMed Web of Science ®Google Scholar
• Kiviluoto O. Use of free fat transplants to prevent epidural scar formation. An experimental study. Acta Orthop Scand 1976; 164: 73–75
   Google Scholar
• Langenskiöld A, Kiviluoto O. Prevention of epidural scar formation after operations on the lumbar spine by means of free fat transplants. A preliminary report. Clin Orthop 1976; 115: 92–95
   PubMed Web of Science ®Google Scholar
• LaRocca H, Macnab I. The laminectomy membrane. Studies in its evolution, characteristics, effects and prophylaxis in dogs. J Bone Joint Surg Br 1974; 46: 545–550
   Google Scholar
• MacMillan M, Stauffer E. The effect of omental pedicle graft transfer on spinal microcirculation and laminectomy membrane formation. Spine 1991; 16: 176–180
   PubMed Web of Science ®Google Scholar
• Lo H, Frederickson R CA. Use of ADCON(r) in neurosurgery: Preclinical review. Neurol Res 1999; 21: 27–32
   PubMed Web of Science ®Google Scholar
• Lee J Y, Stenzel W, Ebel H, et al. Mitomycin C in preventing spinal epidural fibrosis in a laminectomy model in rats. J Neurosurg 2004; 100: 52–55
   PubMed Web of Science ®Google Scholar
• Majmudar P A, Forstot S L, Dennis R F, et al. Topical mitomycin-C for subepithelial fibrosis after refractive corneal surgery. Ophthalmology 2000; 107: 89–94
   PubMed Web of Science ®Google Scholar
• Esme A, Yildirim C, Tatlipinar S, et al. Effects of intraoperative sponge mitomycin C and 5-fluorouracil on scar formation following strabismus surgery in rabbits. Strabismus 2004; 12: 141–148
   PubMedGoogle Scholar
• Araf D, Moura Eda M, Rodrigues C J, Figueiredo L A. Homologous scleral and dura mater grafts in rabbit eyes: a comparative histopathological analysis. Arq Bras Oftalmol 2007; 70: 981–987
   PubMedGoogle Scholar
• He Y, Revel M, Loty B. A quantitative model of post-laminectomy scar formation. Effects of a nonsteroidal anti-inflammatory drug. Spine 1995; 20: 557–563
   PubMed Web of Science ®Google Scholar
• Gill K, Frymoyer J W. The management of treatment failures after decompressive surgery. The Adult Spine: Principles and Practice, Vol 2, J W Frymoyer, T B Ducker, N M Hadler, et al. Raven Press, New York 1991; 1848–1870
   Google Scholar
• North R B, Campbell J N, James C S, et al. Failed back surgery syndrome: 5-year follow-up in 102 patients undergoing repeated operation. Neurosurgery 1991; 28: 685–691
   PubMed Web of Science ®Google Scholar
• Silvers H R, Lewis P J, Asch H L, Clabeaux D E. Lumbar diskectomy for recurrent disc herniation. J Spinal Disord 1994; 7: 408–419
   PubMedGoogle Scholar
• Benoist M, Ficat C, Baraf P, Cauchoix J. Postoperative lumbar epiduro-arachnoiditis. Diagnostic and therapeutic aspects. Spine 1980; 5: 432–436
   PubMed Web of Science ®Google Scholar
• Lee J Y, Ebel H, Friese M, et al. Influence of TachoComb in comparison to local hemostyptic agents on epidural fibrosis in a rat laminectomy model. Minim Invasive Neurosurg 2003; 46: 106–109
   PubMed Web of Science ®Google Scholar
• Cooper R G, Mitchel W S, Illingworth K J, et al. The role of epidural fibrosis and defective fibrinolysis in the persistence of postlaminectomy back pain. Spine 1991; 16: 1044–1048
   PubMed Web of Science ®Google Scholar
• Hoyland J A, Freemont A J, Denton J, et al. Retained surgical swab debris in post-laminectomy arachnoiditis and peridural fibrosis. J Bone Joint Surg Br 1988; 70: 659–662
   PubMedGoogle Scholar
• Vakis A, Koutentakis D, Karabetsos D, Kalostos G. Use of polytetrafluoroethylene dural substitute as adhesion preventive material during craniectomies. Clin Neurol Neurosurg 2006; 108: 798–802
   PubMed Web of Science ®Google Scholar
• Chen C W, Huang H T, Bair J S, et al. Trabeculectomy with simultaneous topical application of mitomycin-C in refractory glaucoma. J Ocul Pharmacol 1990; 6: 175–182
   PubMedGoogle Scholar
• Palmer S S. Mitomycin as adjunct chemotherapy with trabeculectomy. Ophthalmology 1991; 98: 317–321
   PubMed Web of Science ®Google Scholar
• Lee J Y, Stenzel W, Löhr M, et al. The role of mitomycin C in reducing recurrence of epidural fibrosis after repeated operation in a laminectomy model in rats. J Neurosurg Spine 2006; 4: 329–333
   PubMed Web of Science ®Google Scholar
• Costa V P, Spaeth G L, Eiferman P A, et al. Wound healing modulation in glaucoma filtration surgery. Ophthalmic Surg 1993; 24: 152–170
   PubMedGoogle Scholar
• Tahery M M, Lee D A. Review. Pharmacologic control of wound healing in glaucoma filtration surgery. J Ocul Pharmacol 1989; 5: 155–179
   PubMedGoogle Scholar
• Skuta F L, Beeson C C, Higginbotham E J, et al. Intraoperative mitomycin versus postoperative 5-fluorouracil in high-risk glaucoma filtering surgery. Ophthalmology 1992; 99: 438–444
   PubMed Web of Science ®Google Scholar
• Broom W J, Ay I, Pasinelli P, Brown R H, Jr. Inhibition of SOD1 expression by mitomycin C is a non-specific consequence of cellular toxicity. Neurosci Lett 2006; 393: 184–188
   PubMed Web of Science ®Google Scholar
• Kooistra K L, Rodriguez M, Powis G. Toxicity of intrathecally administered cytotoxic drugs and their antitumor activity against an intrathecal Walker 256 carcinosarcoma model for meningeal carcinomatosis in the rat. Cancer Res 1989; 49: 977–982
   PubMed Web of Science ®Google Scholar
• Ashizawa T, Okabe M, Gomi K, Hirata T. Reduced bone marrow toxicity of KW-2149, a mitomycin C derivative, in mice. Anticancer Drugs 1993; 4: 181–188
   PubMed Web of Science ®Google Scholar