I am running a multicentre study on portal vein obstruction after pediatric liver transplantation in which numerous data will be collected from different centres.
But, honestly, I think that the data will be too heterogeneous because the way to diagnose a portal vein obstruction (stenosis and/or thrombosis after LT in children; and the therapeutic approach are very different between centers.
Any ideas how to deal with such? regarding future ata collection/analysis?can we overcome this by any means?d
Thanks,bader.