Pad. Rubin et al., COMPARISON OF FIBROVASCULAR INGROWTH INTO HYDROXYAPATITE AND POROUS POLYETHYLENE ORBITAL IMPLANTS, Ophthalmic plastic and reconstructive surgery, 10(2), 1994, pp. 96-103
Two porous orbital implants available for clinical use in the anophtha
lmic socket are hydroxyapatite (HA) and porous polyethylene (PP). We e
xamined the rate and the extent of fibrovascular ingrowth into these i
mplants using histopathologic criteria in a rabbit model. Thirty-two N
ew Zealand white rabbits underwent a unilateral enucleation with place
ment of a 14-mm spherical orbital implant. Twelve rabbits received HA,
12 small-pore PP, and 8 large-pore PP. The implants inserted were wra
pped either in autologous sclera with and without anterior fenestratio
ns or as unwrapped spheres. The implants were harvested at 6 and 12 we
eks. The extent of fibrovascular ingrowth was assessed by determining
the percentage of the cross-sectional area penetrated by fibrovascular
tissue. On gross inspection, 12 implants (37.5%) were found to be exp
osed at harvesting; however, only two were grossly infected. The highe
st- rate of exposure was found among the unwrapped implants. Wrapped v
ersus unwrapped and fenestrated versus unfenestrated implants did not
result in significant differences in the extent of vascularization. Hy
droxyapatite implants were vascularized most rapidly. The small-pore P
P implants did not become fully vascularized during the study, and yet
complete vascularization was found in the large-pore PP at 12 weeks.
The most intense areas of microscopic fibrovascular ingrowth were in t
he region where the extraocular muscles were in direct contact with th
e implant and at the posterior opening. Exposure of the implant was ac
companied by chronic and acute inflammation. Both HA and large-pore PP
spherical implants are capable of complete vascularization in this an
imal model. Increasing the interstitial pore size resulted in more com
plete vascularization of the PP. Vascularization of the implants is li
mited by exposure, secondary inflammation, and infection.