Objective: Facial osseous defects are a common and challenging problem
for the otolaryngologist-head and neck surgeon. Current methods of re
pair including synthetic grafts, cadaveric material, and autologous ti
ssue have drawbacks of foreign body reaction, infectious agent transmi
ssion, and the morbidity of a second surgical site. In the effort to d
evelop an ideal technique for osseous reconstruction, a critical-size
facial defect has previously been developed in the Sprague-Dawley rat.
This model exhibits less than 10% healing by surface area over 6 mont
hs. A novel approach to osseous reconstruction is attempted using this
model with type I collagen gel augmented with insulin-like growth fac
tor 1 (IGF-1). Study Design: Randomized controlled trial using a roden
t model. Methods: Twelve adult male Sprague-Dawley rats underwent a su
rgical procedure to produce a critical-size nasal defect by removing t
he nasal bones with a cutting burr. Six animals were repaired with 300
mu g of type I collagen gel. Six animals were repaired with 300 mu g
of type I collagen gel augmented with 3.0 mu g of IGF-1. Thirty days l
ater, the animals were examined after necropsy. Precise planimetry, ra
diodensitometric analysis, and histologic sectioning were performed. R
esults: All animals had a complete coverage of this defect with a thin
layer of bone. Radiodensitometric analysis indicated that there was a
statistically significant (P < .037) increase in bone density in the
collagen plus IGF-1 group compared with that of collagen only. In addi
tion, histologic evaluation revealed increased bone density and thickn
ess in the IGF-1 group. Conclusion: Type I collagen gel augmented with
IGF-1 results in a significant increase in healing of a nasal critica
l-size defect in a rodent model.