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Patients are willing to allow personal information from their medical
records to be used for research purposes but want to be consulted
first. Willison and colleagues (p 373) investigated the concerns
of Canadian patients whose doctors used electronic medical records.
Three quarters of those surveyed wanted the chance to consent before
their deidentified data were used for research. This presents
logistical challenges that call for new approaches to consent, taking
into account the varying needs of the public and the evolving uses of
individuals' information in a broader context.

(Credit: KOBAL COLLECTION)