We aimed to compare clinical and pathological reactions towards locally synthesized bovine bone derived from hydroxyapatite (bone docosahexaenoic acid (dHA)) and commercially available porous polyethylene (Medpor®, Porex Surgical Incorporation, Georgia, USA) orbital implants in animal models. An experimental study was performed on 14 New Zealand white rabbits. Group A (n=7) was implanted with bovine bone dHA and group B (n=7) was implanted with Medpor®. Clinical examinations were performed on Days 1, 7, 14, 28, and 42 post-implantation. The implanted eyes were enucleated on Day 42 and were sent for pathological evaluation. Serial clinical examinations included urine color and odor; feeding and physical activity demonstrated normal wellbeing in all the subjects. Localized minimal infection was observed in both groups during the first two weeks following implantation, and the subjects responded well to topical moxifloxacin. Both groups exhibited evidence of wound breakdown. No signs of implant migration or extrusion were observed in either group. The histopathological examination revealed no statistically significant difference in inflammatory cell reactions and fibrovascular tissue maturation between both types of implants. However, all (100%) of the bovine bone dHA implants displayed complete fibrovascular ingrowth compared to Medpor® implants (57.1%) at six weeks post-implantation (p=0.001). In conclusion, bovine bone dHA and Medpor® orbital implants were well-tolerated clinically and displayed similar inflammatory reactions and fibrovascular tissue maturation. Locally synthesized bovine bone dHA orbital implants displayed significantly greater complete fibrovascular ingrowth in comparison with Medpor® implants.
The use of orbital implants to replace lost volume was a major breakthrough in anophthalmic socket surgery. The implant aims to reduce frequent incidences and severity of infection due to the availability of immune responses, allowing soft tissue connection between the extraocular muscles and resulting in better motility and reduced implant migration and extrusion . The most common porous orbital implants used today include hydroxyapatite, porous polyethylene, and aluminum oxide.
Bone derived from hydroxyapatite (bone dHA) orbital implants was first introduced by Schmidt in 1899. Jordan et al. documented that this implant had pore sizes that varied from 300 to 600 µm . Pore size appears to have an effect on the rate of fibrovascular ingrowth, which occurs more rapidly in implants with a 200 µm pore size than in implants with a 500 µm pore size . Porous polyethylene implants were introduced over a decade ago and have been available for orbital implantation (Medpor®, Porex Surgical Incorporation, Georgia, USA) since 1991. They have pores similar to hydroxyapatite but are less uniform in size and more irregular in shape. Commercially available Medpor® has pore sizes of 100-500 μm and 125-1000 μm.
In current practice, Medpor® has been accepted as the preferred option of orbital implant in Malaysia. However, its cost is still the most concerning drawback. The National Tissue Bank of Universiti Sains Malaysia has invented and prepared biocompatible bovine bone dHA orbital implants at a lower cost . We conducted this study in order to compare clinical and pathological reactions toward locally synthesized bovine bone dHA and Medpor® orbital implants in animal models.
Materials & Methods
This experimental study was conducted at the Laboratory of Animal Research and the Laboratory of Histopathology, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia. Approval was obtained from the Research and Ethical Committee, School of Medical Sciences, and Animal Ethics Committee, Health Campus, Universiti Sains Malaysia. The study’s protocol adhered to the Association for Research and Vision in Ophthalmology Statement for the Use of Animals in Ophthalmic and Vision Research.
Fourteen healthy New Zealand white rabbits weighing between two and three kg were included in this study. All animals were free from any eye disease and were kept, fed, and cared for in the Laboratory Animal Research, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
These rabbits were randomly divided into two groups (A and B) using single block randomization. Group A subjects (n=seven) were implanted with the bovine bone docosahexaenoic acid (dHA) while group B subjects (n=seven) were implanted with Medpor®. The implantation was performed in the right eye of each rabbit. All the rabbits that had successful implantation were included in the study. Rabbits were excluded if the implantation failed or if severe systemic infection developed following the implantation phase.
The bovine dHA implants were synthesized from local bovine femoral heads and prepared at the National Tissue Bank, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia . Medpor® implants were supplied by the manufacturer. They were implanted after evisceration was performed on the right eye by an identified investigator (Figure 1).
Serial clinical examinations were performed on Days 1, 7, 14, 28, and 42 post-implantation by another masked investigator. The general wellbeing of the animals was assessed based on the presence of eye discharge, urine color and odor, feeding, and physical activity. The wounds were examined using a portable slit lamp for integrity, implant migration, or extrusion. On Day 42, the rabbits underwent euthanasia and the eyes with the implants were enucleated.
The orbital implants together with scleral coating were dissected and maintained in a 4% neutral formalin buffered solution. The gross appearances of the bisected implants were examined by an assigned independent examiner. The specimens were then prepared using the undecalcified method. After the fixation process, the samples were dehydrated and then embedded in a methacrylate solution (Technovit 720 Virus Creation Laboratory, Kulzer, Wehrheim, Germany).
After polymerization, they were processed according to the cutting-grinding technique and sliced between 0.1 and 0.3 mm thick . The sections were stained with hematoxylin and eosin and examined using light microscopy. They were evaluated for the grade of cellular inflammation and fibrovascular ingrowth according to standardized histopathological grading as described by Tienen et al. and Chung et al. [6-7]. The findings are summarized in Tables 1-2.
Statistical analysis was performed with the Statistical Package for the Social Sciences (SPSS) version 11.0 (IBM Corp, Armonk, NY, US). Data were analyzed by a statistical test with statistical significance set at p<0.05.
In both groups, eye discharge was observed as early as Day 1 post-implantation. Three subjects (42.9%) emanated from the bovine bone dHA group and two subjects (28.6%) were derived from the Medpor® group. Conjunctival swab culture and sensitivity proved negative in all the involved subjects. They were treated with topical moxifloxacin four times per day in the affected eyes. All subjects had normal urine color, urine odor, and physical and feeding activity throughout the study period. The results are shown in Table 3.
All subjects from both groups displayed no implant migration or extrusion. The bovine bone dHA group demonstrated partial wound integrity earlier than the Medpor® group. One subject from the bovine bone dHA group exhibited changes on Day 7 while two subjects from the Medpor® group displayed partial wound integrity during Day 14 of observation. These three subjects demonstrated partial wound integrity until the last observation day.
Gross and microscopic histopathological examination
All specimens displayed visible tissue ingrowth in between interconnecting channels from the peripheral towards the center of the implant. Specimens from the Medpor® group demonstrated a relatively smooth implant surface. Their interconnecting channels were more uniform and noticeably smaller in size than the bovine bone dHA implants. Tissue ingrowth was observed in the entire bovine bone dHA implant, whilst the central-most area was spared in the Medpor® implant (Figure 2).
Grade 1 inflammatory cell reaction was observed in two (28.6%) specimens with bovine bone dHA implants but none in the specimens with the Medpore® implant. Four (57.1%) specimens demonstrated Grade 2 inflammatory reactions in both groups. The remaining specimens exhibited a Grade 3 inflammatory reaction. No specimen disclosed Grade 4 or Grade 5 inflammatory reactions. However, there occurred no significant differences between both groups (p=0.560, Chi-square test). The results are shown in Tables 4-5.
Grade 4 maturation was observed in two (28.6%) specimens from the bovine bone dHA and Medpore® groups, respectively. Grade 5 maturation was displayed by five (71.4%) specimens from the bovine bone dHA group and three (42.9%) from the Medpore® group. However, there was no statistically significant difference between the groups (p>0.950). Figures 3-4 demonstrate evidence of fibrovascular tissue maturation in both groups.
All specimens from the bovine bone dHA group achieved 100% depth of fibrovascular ingrowth while none from the Medpor® group displayed similar features. One specimen from the Medpor® group demonstrated evidence of ingrowth less than 50% in depth. Statistical analysis exemplified a significant difference between both groups (p=0.001).
Our study demonstrated that all subjects from the bovine bone dHA group had similar clinical reactions as those in the Medpor® group. No cross-infection was demonstrated in either group. Subclinical infection, as evidenced by the presence of eye discharge that responded to a topical antibiotic, was demonstrated in five (35.7%) subjects.
The above observation is consistent with an animal study reported by Sclafani et al. . They implanted expanded polytetrafluoroethylene and Medpor® in Sprague-Dawley rats. Staphylococcus aureus was inoculated 14 days after implantation to induce infection, and 75.0% of the implants remained clinically uninfected. They suggested that the presence of vascularized host tissue in and around the implant lends resistance to experimentally induced infection. Recently, Fernandez-Bueno et al. reported a similar outcome between Medpor® and a new porous implant (Oculfit I and II) .
Our study showed that bovine bone dHA implants developed early wound dehiscence. We postulated that the rough surface of the bovine bone dHA contributed to this early complication. In contrast, two subjects from the Medpor® group developed wound dehiscence much later on Day 14 post-implantation. The smoother surface of the Medpor® implant caused less friction, thereby reducing the rate of wound dehiscence. This suggests that the Medpor® implant has better wound integrity than the bovine bone dHA implant. However, we are unable to proceed with appropriate statistical tests.
Our results are consistent with findings reported by Goldberg et al. They described six cases of conjunctival dehiscence with a hydroxyapatite implant at a mean of 4.5 weeks post-implantation . They hypothesized that spicules of the implant inhibited epithelialization, which subsequently led to wound dehiscence.
Kim et al. also reported a similar observation . They compared 32 subjects with orbital implants and reported three cases of wound dehiscence that included two cases of hydroxyapatite implants and one case of a Medpor® implant. The low rate of wound dehiscence with Medpor® implants is consistent with other previously reported studies [12-14].
We noted that the bovine bone dHA group demonstrated a higher trend of tissue maturation. Grade 5 fibrovascular maturation was seen in 71.4% compared to 42.9% of subjects in the Medpor® group. However, these data were not statistically significant.
We observed that fibrovascular ingrowth developed in the centripetal progression toward the center of the implants. All of the bovine bone dHA groups showed complete fibrovascular ingrowth while only 57.1% from the Medpor® group demonstrated more than 80% depth of ingrowth towards the end of the six-week period. Our observation is parallel with a few other published studies, which reported that complete fibrovascularization occurred after the Medpor® implant was observed at 12 weeks [15-19].
Hsu et al. implanted the Medpor® implant into 12 rabbits and reported that the extent of fibrovascular ingrowth at six weeks was at an average of 76.3%. This is lower than our findings of an average of 82.9% . Rubin et al. compared the extent of fibrovascular ingrowth in porous polyethylene versus hydroxyapatite . They reported complete fibrovascularization at six weeks in hydroxyapatite and 12 weeks in porous polyethylene.
The size and distribution of the pores in the porous implant determined the rapidity of fibrovascular ingrowth. Generally, larger pore size will allow more rapid fibrovascularization. Our study demonstrated how the bovine bone dHA implant achieved complete fibrovascularization after six weeks. This is in keeping with gross specimen observation, which displays larger pore sizes (300-600μm) in bone dHA than in Medpor® (100-500μm). However, previous studies reported that fibrovascular ingrowth was sluggish when pore sizes were larger than 700 μm [17-18,20]. These were attributed to an insufficient supporting structure, increased fragility, decreased intensity, and higher risk of infection [17-18,20].
We confirmed fibrovascular ingrowth with histopathological examinations in our study. In clinical practice, this method would be impossible. There were reported studies that advocated the use of post-contrast magnetic resonance imaging (MRI) in assessing fibrovascular ingrowth in porous orbital implants [21-22]. They reported that the MRI study was identical to the histological fibrovascular ingrowth pattern [21-22].
There are two main drawbacks in our experimental animal study. We were limited to a small sample size and a short observation period. Perhaps a bigger sample size and a longer observational period would have more advantages and describe a better picture.
Locally synthesized bovine bone dHA orbital implants were as well-tolerated clinically as commercially prepared Medpor® implants in our animal models. All bovine bone dHA displays complete fibrovascular ingrowth as compared to 57.1% of Medpor® implants at six weeks post-implantation. However, both implants demonstrated a similar degree of inflammatory cell reaction and fibrovascular tissue maturation.
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Comparison of Clinical Results and Pathological Examinations Between Locally Synthesized Bone-derived Hydroxyapatite and Medpor® Orbital Implants in Animal Models
Ethics Statement and Conflict of Interest Disclosures
Human subjects: All authors have confirmed that this study did not involve human participants or tissue. Animal subjects: Research and Ethical Committee, School of Medical Sciences and Animal Ethics Committee, Health Campus, Universiti Sains Malaysia Issued protocol number 304/PPSP/6139048. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
The authors would like to acknowledge the Universiti Sains Malaysia for providing financial support (short-term grant).
Cite this article as:
Roslinah M, Wan Hitam W, Md Salleh M, et al. (January 25, 2019) Comparison of Clinical Results and Pathological Examinations Between Locally Synthesized Bone-derived Hydroxyapatite and Medpor® Orbital Implants in Animal Models. Cureus 11(1): e3954. doi:10.7759/cureus.3954
Received by Cureus: January 04, 2019
Peer review began: January 13, 2019
Peer review concluded: January 19, 2019
Published: January 25, 2019
© Copyright 2019
Roslinah et al. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 3.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.