Rj. Baskett et al., FACTORS IN THE EARLY FAILURE OF CRYOPRESERVED HOMOGRAFT PULMONARY VALVES IN CHILDREN - PRESERVED IMMUNOGENICITY, Journal of thoracic and cardiovascular surgery, 112(5), 1996, pp. 1170-1178
Methods: Between 1990 and 1995, 48 homograft valves (15 aortic and 33
pulmonary), cryopreserved on-site, were implanted to reconstruct the r
ight ventricular outflow tracts in 44 children (mean age 6.2 +/- 6.0 y
ears; range 3 days to 20.2 years), Blinded serial echocardiographic fo
llow-up evaluation was performed for ail 45 valves in the 41 survivors
, Results: Four homograft valves were replaced because of pulmonary in
sufficiency (3) or stenosis and insufficiency (1). freedom from reoper
ation was 90% (70% interval, 84% to 97%) at 50 months, During the foll
ow-up period 15 valves developed progressive pulmonary insufficiency o
f at least two grades, Three valves developed transvalvular gradients
of greater than or equal to 50 mm Hg, and one of these valves was also
insufficient, The freedom from echocardiographic failure (two or more
grades of pulmonary regurgitation or greater than or equal to 50 mm H
g gradient) was 44% at 50 months (70% confidence interval, 32% to 55%)
, Young age (p = 0.03), low operative weight (p = 0.04), small graft s
ize (p = 0.04), and homograft retrieval-to-cryopreservation time of le
ss than 24 hours (p = 0.02) were significantly associated with failure
, The type of donor valve (pulmonic or aortic), donor age, and blood g
roup mismatch were not associated with failure, although blood group m
ismatch approached significance (p = 0.05), Conclusions: Homografts fu
nction well as conduits between the pulmonary ventricle and pulmonary
arteries if long-term valve competency is not crucial, However, many r
apidly become insufficient. This has important implications for the ch
oice of a valve if the indication for valve replacement is to protect
a ventricle failing due to pulmonary insufficiency. Short periods betw
een homograft retrieval and cryopreservation enhance viability and ant
igenicity. This may suggest an immunologic basis for the failure.