Jm. Burns et al., PREVENTION OF TISSUE-INJURY AND POSTSURGICAL ADHESIONS BY PRECOATING TISSUES WITH HYALURONIC-ACID SOLUTIONS, The Journal of surgical research, 59(6), 1995, pp. 644-652
The effectiveness of inhibiting serosal tissue damage and preventing s
urgical adhesions by precoating tissues with dilute solutions of hyalu
ronic acid (I was evaluated in a rat cecal abrasion model. This study
was performed at three independent laboratories using the same protoco
l. Three hundred and seventy-five adult rats were divided into five tr
eatment groups (125 animals at each study site): 0.1% HA, 0.25% HA, 0.
4% HA, phosphate-buffered saline solution (PBS), and no solution. The
abdominal cavity of each animal was precoated with 4 ml of test soluti
on or no solution, prior to a controlled abrasion of the cecum. One we
ek later, the animals were sacrificed and adhesions were scored on a 0
-4 scale. The data were pooled because no statistical difference was f
ound in the trends at the three study sites. The PBS precoating and no
tissue precoating treatment groups had the same high incidence of cec
al adhesions, which was significantly higher than the incidence of adh
esions in the HA treatment groups. As the HA concentration in the prec
oating solution increased from 0% (PBS group) to 0.4% HA, the mean inc
idence of cecal adhesions decreased in a concentration-dependent manne
r from 1.6 +/- 0.11 to 0.7 +/- 0.09 (P < 0.001). The percentage of ani
mals with no cecal adhesions increased from 11% in the PBS group to 50
% in the 0.4% HA treatment group (P < 0.001). In a separate histologic
al study employing 150 rats, HA solutions significantly inhibited sero
sal tissue damage and ameliorated the inflammatory response due to abr
asion and desiccation compared to that with no coating or precoating w
ith buffered saline. Together, these studies demonstrate that tissue p
recoating with dilute HA solutions reduces damage to serosal tissues d
uring surgery and thereby limits formation of postsurgical adhesions.
(C) 1995 Academic Press, Inc.