You should contribute at least three times to the discussion. Post your brief initial entry on the FIRST DAY so that everyone can respond to others' ideas throughout the discussion. We expect a lively discussion, not an essay, and it is OKAY to change your views more than once during the discussion or to stick to your views throughout the discussion. Discuss the ethical issues raised by each design. In this discussion forum, create a thread telling your classmates which design (opt-out or opt-in) you would choose and why. In both cases, each patient’s data will be anonymized as much as possible and then stored in a database of other patients’ genetic data. Under the opt-in design, patients’ data would only be used by doctors in their own healthcare system unless patients explicitly ask to have their data included in a large international database. Patients would have to explicitly ask for their data to be removed from this database, in which case their data would only be used by doctors in their healthcare system. Under the opt-out design, patients’ data would automatically be included in a large international database, accessible by a wide range of researchers, and those researchers would determine how the data is used. Suppose the committee has been asked to choose between an “opt-out” and an “opt-in” design.
Imagine you are a researcher conducting gene therapy research and you have been appointed to a committee that is charged with creating a standardized consent form for patients to decide how their genetic data will be used in the future.
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