This study addresses the clinical problems regarding access of wear debris
to the bone-implant interface and the possible dissemination of polyethylen
e (PE) particles to distant organs. We inserted two implants into each knee
of 7 dogs allowing access of joint fluid to the bone-implant interface wit
h a 0.75 mm initial gap around the implant. Hydroxyapatite (HA)-coated and
non-coated (Ti) titanium alloy implants were randomly allocated to each dis
tal femoral condyle. PE particles were repeatedly injected into the right k
nee joint 3 weeks after surgery for a period of 49 weeks, while only vehicl
e was injected into the left knee joint.
We found huge amounts of RE particles mainly in the bone-implant interface
around Ti implants. Infiltration of mononuclear inflammatory cells was pres
ent around 3 of 7 Ti implants in relation to PE particles. HA implants had
approximately 70% bone ongrowth. In contrast, no bone ongrowth was seen on
any Ti implants, all being surrounded by a fibrous membrane. The number of
RE particles was evaluated semi quantitatively. More PE particles were foun
d around Ti implants than with HA implants (p < 0.002).
Specimens from iliac lymph nodes, liver, spleen and lung mere examined and
showed dissemination of PE particles only in regional lymph nodes.