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兔眼滤过性手术中植入硅凝胶膜的实验研究

http://www.cnophol.com 2009-8-25 14:37:21 中华眼科在线

  DISCUSSION

  Histomorphological Change in the Implanted Silicone Membrane and Clinical Implication  In our study fibrosis occurred around silicone membrane and resulted in a sac,which is similar to that observed in the study of Rubin et al[6]. Minckler found that the pressure inside the sac was the same as IOP[7]. This implied that IOP achieved after the operation was determined by the size and permeability of the sac around the implant, which in turn, was related to the material, shape and size of the implant[8,9]. Silicone seems to be an ideal material at present because it causes slighter inflammation and has better biocompatibility. Silicone membrane in rectangle helps to form bigger drainage area, facilitate outflow of aqueous humor and form filtering blebs. In our study, the sac wall was formed of 45 layers of collagen fibers, which communicated with blebs.

  Fibrosis around silicone membrane is similar in mechanism to that in retinal detachment model[10]. The sac formed is the foundation of filtering blebs. Under microscope, the outer layer of bleb wall was constructed by collagen fibers and small
Figure 1 Bleb ranks of the implant group and control group at different timepoints

  blood vessels; in the inner layer, loose connective tissue and capillary vessels can be seen; between the inner and outer layer, debris of inflammatory cells can be seen. Such structure is very important for aqueous humor filtration.

  The slender void between the sac and silicone membrane ensures aqueous humor flow, but the speed and amount of the aqueous humor outflow is related to fibroblast proliferation. That is to say, silicone membrane stimulates inflammation to produce adequate collagen to fix silicon membrane; the amount of collagen produced is controlled to allow for the adequate aqueous humor flow to filter blebs. Fibrous tissue grows to the point that it can encapsulate the drainage implant but not result in adhesion or overproliferation. There might be two explanations for this: first, silicone membrane does not support adherence of fibrocytes; second, aqueous humor is inhibitory to fibroblasts[11].

  Implant drainage surgery is a special filtering surgery. IOP is the major evaluating index. In the present study, IOP changes were found to be in positive correlation with fibroblast proliferation in the control group, but no such linear correlation was found in the implant group. IOP control in the implant group was much better than that in the control group. However, on the 30th day, IOP ran out of control in 20% eyes in the implant group. This could be the result of subconjunctival fibrosis or shift of silicone membrane so that drainage tract was blocked by fibrous tissue.

  AgNoRs Expression in Fibroblast Proliferation  The number and shape of AgNors particles indicate activity of fibroblast proliferation. The more AgNors particles there are, the more active proliferation is. In our study, according to the number and shape of AgNoRs particles, fibroblasts in the control group began to proliferate from the 2nd3rdday after operation, reached the peak on the 5th 7th day and then gradually transformed into fibrocytes. This was agreed with Jampels findings[12]. So it can be concluded that silicone membrane does not stimulate constant or excessive proliferation of fibroblasts.
Comparison of Silicone Membrane with Other Implants  The silicone membrane used in this study has dual functions of drainage and aqueous diffusion, which avoids postoperative fibrosis in the connection of tube and disk in other implants. In addition, silicone membrane, being soft, can achieve moreadequate anastomosis than other implants and thus avoids diplopia and strabismus resulting from unfit implantation. In the filtering surgery with implants of all other types, the incidence of complications is approximately 50%70% with more than 20 complications. Most of the complications can be avoided because silicone membrane is soft, its fixing site is away from rectus muscle and it does not enter the anterior chamber.

  【参考文献】

  1 Meng N,Ren BC.Progress in glaucoma drainage devices. Int J Ophthalmol(Guoji Yanke Zazhi)2005;5(4):715718

  2 Xu H,Xu L.Treatment of refractory glaucoma with Ahmed glaucoma valve implant and its combination surgery. Int J Ophthalmol(Guoji Yanke Zazhi)2007;7(2):563565

  3 Hong CH, Arosemena A, Zurakowski D, Ayyala RS. Glaucoma drainage devices: a systematic literature review and current controversies. Surv Ophthalmol2005;50:4860

  4 Doyle JW, Sherwood MB, Khaw PT, McGrory S, Smith MF. Intraoperative 5fluorouracil for filtration surgery in the rabbit. Invest Ophthalmol Vis Sci1993;34(12):33133319

  5 Khaw PT, Doyle JW, Sherwood MB, Smith MF, McGorray S. Effects of intraoperative 5fluorouracil or mitomycin C on glaucoma filtration surgery in the rabbit. Ophthalmology1993;100(3):367372

  6 Rubin B, Chan CC, Burnier M, Munion L, Freedman J. Histopathologic study of the Molteno glaucoma implant in three patients. Am J Ophthalmol2000;110(4):371379

  7 Minckler DS,Shammas A,Wilcox M,Ogden TE.Experimental studies of aqueous filtration using the Molteno implant. Trans Am Ophthalmol Soc1987;85:368392

  8 Guo WY. Some operational skills in drainage implant surgery for refractory glaucoma. Int J Ophthalmol(Guoji Yanke Zazhi)2002;2(4):2023

  9 Prabhasawat P, Tesavibul N, Leelapatranura K, Phonjan T. Efficacy of subconjunctival 5fluorouracil and triamcinolone injection in impending recurrent terygium. Ophthalmology2006;113:11021109

  10 Jacob JT, Lacour OJ, Burgoyne CF. Slow release of the antimetabolite 5fluorouracil (5FU) from modified Baerveldt glaucoma drains to prolong drainfunction. Biomaterials2001;22:33293335

  11 Singh K, Mehta K, Shaikh NM, Tsai JC, Moster MR, Budenz DL, Greenfield DS, Chen PP, Cohen JS, Baerveldt GS, Shaikh S. Trabeculectomy with intraoperative mitomycin C versus 5fluorouracil. Prospective randomized clinical trial. Ophthalmology2000;107:23052309

  12 Jampel HD, McGuigan LJ, Dunkelberger GR, LHernault NL, Quigley HA. Cellular proliferation after experimental glaucoma filtration surgery. Arch Ophthalmol1988;106(1):8994 

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