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.

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