TY - JOUR
T1 - The origin of osteoprogenitor cells responsible for heterotopic ossification following hip surgery
T2 - An animal model in the rabbit
AU - Rumi, Mustasim N.
AU - Deol, Gurvinder S.
AU - Singapuri, Kishor P.
AU - Pellegrini, Vincent D.
N1 - Funding Information:
This work was supported in part by Orthopaedic Research and Education Foundation Research Grant # 95-027. The authors express special appreciation to C. McCollister Evarts M.D. for his pioneering investigation in the field of heterotopic ossification and his invaluable mentoring. The authors also gratefully acknowledge Ronald Wilson D.V.M., Joy Ellwanger, and Doug Ednie for their assistance in animal care and surgery, and the statistical assistance of Erik B. Lehman MS.
PY - 2005/1
Y1 - 2005/1
N2 - Purpose. To investigate the source of osteoprogenitor cells responsible for heterotopic ossification (HO) following total hip arthroplasty in an animal model. Methods. New Zealand White (NZW) rabbits (n=20) received a radiation treatment 24 h preoperatively to the hip joint of one hindquarter and to the femoral shaft of the contralateral side. Subjects underwent bilateral hip surgery 24 h after treatment. Subjects were euthanized and radiographed 4 months postoperatively. Heterotopic ossification was graded according to a modified Brooker scale. Mean grade, intra-observer reliability, and statistical significance (p<0.05) were evaluated to compare the severity of heterotopic ossification between hindquarters treated with hip irradiation versus those treated with femoral shaft irradiation. Results. The Fleiss Weighted Kappa Statistic indicated "almost perfect" (0.872) intra-rater reliability of radiographic heterotopic ossification grading. The average heterotopic ossification grade for the group receiving radiation to the hip was significantly greater than that for the group receiving radiation to the femoral shaft (2.575 versus 2.0, p<0.02). Conclusion. Although both have some beneficial effect, our results demonstrate that irradiation of the femoral canal is significantly more effective than irradiation of the hip joint and abductor musculature for heterotopic ossification prophylaxis. This suggests that osteoprogenitor cells responsible for heterotopic ossification originate from both the hip abductors and the femoral canal, but the data provide indirect evidence that the femoral canal may be a more dominant source of these cells in the rabbit model.
AB - Purpose. To investigate the source of osteoprogenitor cells responsible for heterotopic ossification (HO) following total hip arthroplasty in an animal model. Methods. New Zealand White (NZW) rabbits (n=20) received a radiation treatment 24 h preoperatively to the hip joint of one hindquarter and to the femoral shaft of the contralateral side. Subjects underwent bilateral hip surgery 24 h after treatment. Subjects were euthanized and radiographed 4 months postoperatively. Heterotopic ossification was graded according to a modified Brooker scale. Mean grade, intra-observer reliability, and statistical significance (p<0.05) were evaluated to compare the severity of heterotopic ossification between hindquarters treated with hip irradiation versus those treated with femoral shaft irradiation. Results. The Fleiss Weighted Kappa Statistic indicated "almost perfect" (0.872) intra-rater reliability of radiographic heterotopic ossification grading. The average heterotopic ossification grade for the group receiving radiation to the hip was significantly greater than that for the group receiving radiation to the femoral shaft (2.575 versus 2.0, p<0.02). Conclusion. Although both have some beneficial effect, our results demonstrate that irradiation of the femoral canal is significantly more effective than irradiation of the hip joint and abductor musculature for heterotopic ossification prophylaxis. This suggests that osteoprogenitor cells responsible for heterotopic ossification originate from both the hip abductors and the femoral canal, but the data provide indirect evidence that the femoral canal may be a more dominant source of these cells in the rabbit model.
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U2 - 10.1016/j.orthres.2004.05.003
DO - 10.1016/j.orthres.2004.05.003
M3 - Article
C2 - 15607872
AN - SCOPUS:11044225693
SN - 0736-0266
VL - 23
SP - 34
EP - 40
JO - Journal of Orthopaedic Research
JF - Journal of Orthopaedic Research
IS - 1
ER -