In order to evaluate a new method for the direct application of a polypepti
de growth factor to injured tracheal epithelium and to determine the effect
of topical platelet-derived growth factor (PDGF) on tracheal wound healing
, a controlled animal study was designed using six adult beagle dogs. Four
2 x 1 cm mucosal defects were created in the tracheal lumen of each dog for
a total of 24 experimental sites. Twelve wounds were treated with PDGF in
a collagen-fibrin composite tissue adhesive (CTA) carrier. Eight sites rece
ived CTA alone and four were left untreated. Healing was assessed by endosc
opic exam on post-operative days 4, 7, 10, 14, 17 and 21. The animals were
sacrificed on day 21 and the tracheas were harvested for histological exami
nation of the experimental sites and adjacent unwounded trachea. By 21 days
, complete healing of all sites was observed endoscopically. Wounds treated
with CTA or PDGF-CTA healed at a faster rate than control sites. The PDGF-
CTA treated wounds demonstrated excessive granulation tissue formation. His
tological examination demonstrated a higher percentage of wound coverage wi
th ciliated epithelium most similar to normal trachea in the PDGF treated w
ounds. CTA is effective as a carrier for the direct delivery of a growth fa
ctor to injured tracheal epithelium. The application of CTA or PDGF-CTA res
ults in a more rapid rate of tracheal wound healing as compared with contro
l wounds. PDGF-CTA led to increased acute local inflammatory changes but wa
s associated with a structurally more normal respiratory epithelium after h
ealing. Physiological studies are necessary to determine the functional sig
nificance of these findings. (C) 1998 Elsevier Science Ireland Ltd. All rig
hts reserved.