The Journal of Bone and Joint Surgery (American). 2005;87:550-557.
doi:10.2106/JBJS.D.02192
© 2005 The Journal of Bone and Joint Surgery, Inc.
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Ibandronate for Prevention of Femoral Head Deformity After Ischemic Necrosis of the Capital Femoral Epiphysis in Immature Pigs

Harry K.W. Kim, MD, MSC, FRCSC1, Timothy S. Randall, BS1, Haikuo Bian, MD1, Joe Jenkins, BS1, Amanda Garces1 and Frieder Bauss, PhD2

1 Shriners Hospitals for Children, 12502 Pine Drive, Tampa, FL 33612. E-mail address for H.K.W. Kim: hkim{at}shrinenet.org
2 Roche Diagnostics, GmbH, Pharma Research, Bone Metabolism, Nonnenwald 2, Building 231, Room 321, D-82377 Penzberg, Germany

Investigation performed at the Center for Research in Skeletal Development and Pediatric Orthopaedics, Shriners Hospitals for Children, Tampa, Florida

In support of their research or preparation of this manuscript, one or more of the authors received grants or outside funding from Shriners Hospitals for Children and F. Hoffmann-La Roche, Ltd., Basel, Switzerland. None of the authors received payments or other benefits or a commitment or agreement to provide such benefits from a commercial entity. A commercial entity (F. Hoffmann-La Roche) sponsored the study.


Background: Femoral head deformity is the most serious sequela of ischemic necrosis of the immature femoral head. The purpose of this study was to determine if a highly potent antiresorptive agent, ibandronate, can inhibit bone resorption during the repair of the infarcted femoral head and thus alter the repair process. We hypothesized that preservation of the trabecular framework by inhibiting osteoclastic bone resorption would minimize the development of deformity in a piglet model of ischemic necrosis. The effect of ibandronate on long-bone growth was also assessed.

Methods: Ischemic necrosis of the right femoral head was produced in twenty-four piglets by placing a ligature tightly around the femoral neck. The animals were divided into three groups according to whether they received saline solution, prophylactic treatment, or post-ischemia treatment. The contralateral, untreated femoral heads from the animals that had received saline solution served as the normal control group. At eight weeks, the femoral heads were assessed for deformity with radiography and for trabecular bone indices with histomorphometry. Also, the length of femur from the untreated side was measured on the radiographs and compared among the groups.

Results: Radiographic assessment showed that the epiphyseal quotient, determined by dividing the maximum height of the osseous epiphysis by the maximum diameter, was better preserved in the prophylactic (p < 0.001) and post-ischemia (p = 0.02) treatment groups than in the group treated with saline solution. Histomorphometric assessment also showed that the trabecular bone indices were better preserved in the prophylactic and the post-ischemia treatment groups than in the group treated with saline solution (p < 0.01). The mean femoral length on the untreated side of the animals treated with ibandronate was reduced compared with the length on the untreated side of the animals that had received saline solution (p ≤ 0.01).

Conclusions: Ibandronate preserves the trabecular structure of the osseous epiphysis and prevents femoral head deformity during the early phase of repair of ischemic necrosis in the piglet model.

Clinical Relevance: Administration of an anti-osteolytic agent, ibandronate, during the fragmentation stage of Legg-Calvé-Perthes disease may prevent early flattening of the osseous epiphysis. Additional preclinical studies are needed to determine the optimum dose and delivery of the drug to prevent the deformity while minimizing its effect on long-bone growth. Studies are also needed to determine the long-term effects of ibandronate in terms of preventing deformity.


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Letters to the Editor:

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Drug Treatment for Prevention of Femoral Head Deformity after Necrosis of the Femoral Epiphysis
David H. Gershuni
JBJS Online, 24 May 2005 [Full text]