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Original

Adjuvant therapies of bone graft around non-cemented experimental orthopedic implants stereological methods and experiments in dogs

, MD
Pages 2-43 | Published online: 08 Jul 2009

Figures & data

Figure 1. Observation time

Figure 1. Observation time

Figure 2. Non‐coated and HA‐coated plasma spray porous Ti implants with a 2.5 mm gap

Figure 2. Non‐coated and HA‐coated plasma spray porous Ti implants with a 2.5 mm gap

Figure 3. Implant sites

Figure 3. Implant sites

Table 1.  Mechanical specimens' diameter and height

Figure 4. Transverse section for mechanical testing

Figure 4. Transverse section for mechanical testing

Figure 5. Force‐displacement curve (normalized)

Figure 5. Force‐displacement curve (normalized)

Figure 6. Force‐displacement curve with two peaks

Figure 6. Force‐displacement curve with two peaks

Figure 7. Force and material stress multiplicity at the bone‐implant interface at axial push‐out test

Figure 7. Force and material stress multiplicity at the bone‐implant interface at axial push‐out test

Figure 8. Schematics of cyclic test and push‐out

Figure 8. Schematics of cyclic test and push‐out

Figure 9. Vertical sectioning technique

Figure 9. Vertical sectioning technique

Figure 10. Exhaustive vertical sections (above) and central vertical sections (below)

Figure 10. Exhaustive vertical sections (above) and central vertical sections (below)

Figure 11. ROI reference line (”approximated surface line”) for placement of Zones 1 and 2

Figure 11. ROI reference line (”approximated surface line”) for placement of Zones 1 and 2

Figure 12. Section offset

Figure 12. Section offset

Figure 13. Central section point representation of coaxial volumes

Figure 13. Central section point representation of coaxial volumes

Figure 15. Transverse section of implant (left) and objects with increasing distance to vertical axis

Figure 15. Transverse section of implant (left) and objects with increasing distance to vertical axis

Figure 14. FAVER sections

Figure 14. FAVER sections

Table 2.  Influence of central section bias on sample tissue volume fraction estimates in Zones B+C+D = Zone 2 (3.5–5 mm). VVUR: Non‐weighted tissue fraction. VFAV: distance‐weighted tissue fraction. V/V= VVUR/ VFAV

Figure 16. Relative tissue representation as a function of distance from the vertical axis, fT (r)

Figure 16. Relative tissue representation as a function of distance from the vertical axis, fT (r)

Figure 17. Relative total tissue representation as a function of distance from the vertical axis, fTOT (r)

Figure 17. Relative total tissue representation as a function of distance from the vertical axis, fTOT (r)

Figure 18. Different geometric centroid for all tissues TOT and a specific tissue T. The area ATOT, has a gravitational centre in the symmetry line of the ROI; r = ½(t + s). Because of the skew tissue distribution of T, the area AT, has a gravitational centre to the right of r = ½(t + s.

Figure 18. Different geometric centroid for all tissues TOT and a specific tissue T. The area ATOT, has a gravitational centre in the symmetry line of the ROI; r = ½(t + s). Because of the skew tissue distribution of T, the area AT, has a gravitational centre to the right of r = ½(t + s.

Figure 19. Volume of torus: A×2πr

Figure 19. Volume of torus: A×2πr

Figure 20. Example of distance‐dependent tissue representation symmetrical around r = ½(t + s)

Figure 20. Example of distance‐dependent tissue representation symmetrical around r = ½(t + s)

Figure 21. Relative tissue representation as a function of distance from the vertical axis, fT(r).

Figure 21. Relative tissue representation as a function of distance from the vertical axis, fT(r).

Figure 22. Graphic representation of the VT(VUR)/VT(FAVER) ratio in Zone 1 and Zone 2 as a function of A and B (Eq 19 and Eq 20) under the assumptions of linearity and tissue representation throughout the ROI.

Figure 22. Graphic representation of the VT(VUR)/VT(FAVER) ratio in Zone 1 and Zone 2 as a function of A and B (Eq 19 and Eq 20) under the assumptions of linearity and tissue representation throughout the ROI.

Figure 23. ROI Zones 1 (inner) and 2 (outer)

Figure 23. ROI Zones 1 (inner) and 2 (outer)

Figure 24. ROI Zones A, B, C, D and E

Figure 24. ROI Zones A, B, C, D and E

Figure 25. Tissue fractions (not weighted by distance to vertical axis) of the 0.5 mm Zones A‐E of the recount of four implants in study III.

Figure 25. Tissue fractions (not weighted by distance to vertical axis) of the 0.5 mm Zones A‐E of the recount of four implants in study III.

Figure 26. Shadow effect

Figure 26. Shadow effect

Figure 27. Reducing the amount of sections

Figure 27. Reducing the amount of sections

Figure 28. Double counts of four implants

Figure 28. Double counts of four implants

Table 3.  Histomorphometrical reproducibility (CV in percent)

Figure 29. Overview of studies I‐III

Figure 29. Overview of studies I‐III

Table 4.  Change relative to control. “0”: no change. “+”: improvement. “−”: deterioration. The double signs “+ +” and “− −” indicate a group best or group worst

Figure 30. Study I; representative histology. All four implant sections are from the same dog (Ti implants). Upper left: Control implant with allograft only. Upper right: Allograft added rhBMP‐2. Lower right: Allograft added pamidronate. Lower left: Allograft added rhBMP‐2 and pamidronate in combination.

Figure 30. Study I; representative histology. All four implant sections are from the same dog (Ti implants). Upper left: Control implant with allograft only. Upper right: Allograft added rhBMP‐2. Lower right: Allograft added pamidronate. Lower left: Allograft added rhBMP‐2 and pamidronate in combination.

Table 5.  Change relative to control. “0”: no change. “+”: improvement. “−”: deterioration. The double signs “+ +” and “− −” indicate a group best or group worst

Table 6.  Change relative to control. “0”: no change. “+”: improvement. “−”: deterioration

Figure 31. Study III; histology from two implants grafted with β‐TCP granules with Colloss E (left side) and without Colloss E (right side). Implants are not representative of group means and are from different animals.

Figure 31. Study III; histology from two implants grafted with β‐TCP granules with Colloss E (left side) and without Colloss E (right side). Implants are not representative of group means and are from different animals.

Figure 32. Study III; new bone formation on surface and in gap. Implant pairs interconnected +/− Colloss E (signal).

Figure 32. Study III; new bone formation on surface and in gap. Implant pairs interconnected +/− Colloss E (signal).

Figure 33. Study III; fibrous tissue on surface and in gap. Implant pairs interconnected +/− Colloss E (signal).

Figure 33. Study III; fibrous tissue on surface and in gap. Implant pairs interconnected +/− Colloss E (signal).

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