A preliminary single-animal study of in vivo argon laser vascular weld
ing was conducted using a canine model. The effects of temperature fee
dback control and saline drip cooling on patency and collagen cross-li
nking were investigated. The surface temperature at the centre of the
laser spot was monitored using a two-colour infrared thermometer. The
surface temperature was limited by either a saline drip or feedback co
ntrol of the laser. Acute patency was evaluated and collagen cross-lin
k assays were performed. Though both protocols yielded successful tiss
ue fusion, welds maintained at a surface temperature of 50 degrees C u
sing feedback control had an elevated cross-link count compared to con
trols, whereas tissues irradiated without feedback control experienced
a cross-link decrease. Simulations using the LATIS (LAser-TISsue) com
puter code suggest that drip-cooled procedures achieve significantly h
igher temperatures beneath the tissue surface than temperature feedbac
k-controlled procedures. Differences between the volumetric heating as
sociated with drip-cooled and feedback-controlled protocols may accoun
t for the different effects on collagen cross-links. Covalent mechanis
ms may play a role in argon laser vascular fusion.