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B超评估凝胶和多孔聚乙烯义眼台重建无眼眼眶

http://www.cnophol.com 2009-5-22 10:27:36 中华眼科在线

  Porous Polyethylene Spheres

  Clinical evaluation  Five animals (27.8%) with porous polyethylene spheres presented implant extrusion after 30 days of surgery. Conjunctival dehiscence occurred in two animals (11.1%) and one of them was excluded due to systemic infection not related to the surgical procedure.

  Ultrasound evaluation  Spheres vascularization was observed though neovessels filling theirs porous, indicating spherehosted integration. Porous polyethylene showed medium reflectivity (40%60%) until 90 days after surgery, although the image was more echodense at the time. An irregular internal structure indicating heterogeneous architecture was also present, despite of the sound attenuation observed during the examination (Figure 2).

  DISCUSSION

  This study compared the porous polyethylene, already commercially available, and the polyethylene sphere in the gel form.
  Both spheres were made by the same professional and consisted basically of the same chemical substance. However, the porous polyethylene sphere presented a rough external surface and the gel polyethylene, a smooth surface because of its membranelike wrapper material, employed to contain the gel or semiliquid polyethylene.

  The main cause of gel implant extrusion seemed to be the sphere volume increase after implantation. The spheres showed an increase in size which caused suture dehiscence due to mechanical forces and elicited their extrusion. The extrusion was probably a combination of factors: the increase of the spheres size which hydrated and became bigger than the orbital volume and the lack of implants integration to the host tissues,observed by the high early expulsion rate after surgeries.

  The integration rate of a biomaterial is measured by the pattern of vascularization between the implant and the host tissues. Many studies described the vascularization pattern using histological methods[79]. Others used the computerized tomography and/or the magnetic resonance imaging[35].

  Figure 1  B scan ultrasound of a gel polyethylene sphere 90 days after surgery(略)

  Figure 2  B scan ultrasound of a porous polyethylene sphere 90 days after surgery(略)

  However, there are only few studies using conventional ultrasound scan to evaluate the vascularization pattern inside the sphere implants[10].

  A previous reports showed that the porous polyethylene implant vascularization occurred during the first month after surgeries[9,11], we decided to start the B ultrasound evaluation around this time. This method provided useful information for further studies in vivo. The vascularized porous polyethylene implants showed low reflective peaks similar to blood pattern[12]. So, the B ultrasound evaluation showed us that the Polietigel implants did not vascularize, in contrast to the Polipore implants which presented increased neovessels colonization inside.

  The polyethylene spheres in the gel form hydrated and increased in volume after orbital implantation procedure. More studies need to be performed to determine the ideal biomaterial size necessary to replace the orbital volume deficiency in the anophthalmic cavity reconstruction.

  The B scan ultrasound technique is an alternative method to substitute the more expensive methods employed to evaluate the spheres vascularization pattern.

  Acknowledgements: The authors thank Romualdo Rossa, MD (in memorian) for providing the polyethylene spheres.

【参考文献】
    1 Karesh JW, Dresner SC. Highdensity porous polyethylene (Medpore) as a successful anophthalmic socket implant. Ophthalmology 1994;101(10):16881696

  2 Schellini SA, Xavier AP, Hoyama E, Rossa R, Pellizon C, Marques ME, Padovani CR. Gelatinous polyethylene in the treatment of the anophthalmic cavity. Orbit 2002;21(3):189193

  3 Ainbinder DJ, Haik BG, Mazzoli RA. Anophthalmic socket and orbital implants. Role of CT and MR imaging. Radiol Clin North Am 1998;36(6): 11331147

  4 De Potter P, Duprez T, Cosnard G. Postcontrast magnetic resonance imaging assessment of porous polyethylene orbital implant (Medpor). Ophthalmology 2000;107(9):16561660

  5 Flanders AE, De Potter P, Rao VM, Tom BM, Shields CL, Shields JA. MRI of orbital hydroxyapatite implants. Neuroradiology 1996;38(3):273277

  6 Norman GR, Streiner DL. Biostatistics: the bare essentials. St. Louis: Mosby; 1994.260p.

  7 Mawn LA, Jordan DR, Gilberg S. Proliferation of human fibroblasts in vitro after exposure to orbital implants. Can J Ophthalmol 2001;36(5):245251

  8 Rubin PA, Popham JK, Bilyk JR, Shore JW. Comparison of fibrovascular ingrowth into hydroxyapatite and porous polyethylene orbital implants. Ophthal Plast Reconstr Surg 1994;10(2):96103

  9 Schellini SA, Marques ME, Padovani CR, Taga EM, Rossa R. Comparison of synthetic hydroxyapatite and porous polyethylene implants in evsicerated rabbit eyes. Ophthal Plast Reconstr Surg 2003;19(2):136139

  10 Yamamoto ES, Hoyama E, Schellini SA, Padovani CR. Avalia o ultrassonogr fica do implante orbit rio em cavidade anoftalmica. Rev Bras Oftalmol 2001;60:637642

  11 Murray TG,Cicciarelli NL,Croft BH,Garonzik S,Voigt M,Hernandez E.Design of a magnetically integrated microporous implant. Arch Ophthalmol 2000;118(9):12591262

  12 Byrne SF, Green Ronald. Examination techniques for the orbit. In: Ultrasound of the eye and the orbit. St. Louis: Mosby; 2002:1545,273289

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