Progress in the field of ventricular assist devices requires a more rigorou
s and systematic method of collecting outcomes data. A worldwide registry o
f device implants and results is proposed. With widespread participation, d
ata from this registry would improve the identification of risk factors and
complications, and allow for the creation of predictive models that would
enhance patient selection. Professional societies should lead the developme
nt of a registry in close partnership with government and industry. Data co
llection using the Web, with rigorous security measures to protect patient
privacy, would offer numerous advantages in efficiency and immediacy of com
munication for all participants. (C) 2001 by The Society of Thoracic Surgeo
ns.