J Korean Orthop Assoc.  1996 Apr;31(2):319-327. 10.4055/jkoa.1996.31.2.319.

Hydroxyapatite-Coated Primary Total Hip Arthroplasty: Minimum two year clinical and roentgenographic analysis

Abstract

Plasma sprayed coating of the hydroxyapatite(HA) are biocompatible and may contribute to the early fixation of total joint prosthesis. We studied 64 hips(58 patients) who had hydroxyapatite coated primary total hip arthroplasty during the period from January 1992 to June 1993 about clinical and radiological result prospectively. The components have been followed for a minimum of 26 months and an average 31 months. Harris hip score averaged 92 at most recent follow up intervals. At the last follow up, the pain in 7 cases(11%) respectively and only slightly to mild in mostly. Although thigh pain has been occurred in 7 cases(11%), all patients had not trouble in daily activity. In radiological evaluation, there was a rapid and good endosteal bone formation of implants with bone apposition on the Gruen zone 2 and 6 of HA coating area. No radiolucent line formation was detected around HA coated area. In acetabular component, the endosteal bone formation was found in 12 cases and the radiolucent line was occurred in 4 cases. No revision were done for the femoral and acetabular component. The result of the study indicate that this hydroxyapatite coated component can provide satisfactory clinical and radiological result. Further prospective follow up is necessary to determine whether the favorable early result of this implant are maintained over longer period.

Keyword

Hydroxyapatite; Total hip arthroplasty

MeSH Terms

Acetabulum
Arthroplasty, Replacement, Hip*
Durapatite
Follow-Up Studies
Hip
Humans
Joint Prosthesis
Osteogenesis
Plasma
Prospective Studies
Thigh
Durapatite
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