Human Genome Editing is Here. How Should It Be Governed?
[from the AMA Morning Rounds]
Gene editing is inexpensive, simple and becoming more widely used
in clinical applications. One example is clustered regularly interspaced
short palindromic repeats (CRISPR) genome editing, which is an
efficient tool to introduce changes in DNA. Germline editing promises
efficiency in eradicating many diseases, but ethical and legal questions
persist about unknown, transgenerational and global consequences.
The December issue of the AMA Journal of Ethics® (@JournalofEthics) features numerous perspectives on governing human genome editing and gives you an opportunity to earn CME credit.
Articles include:
“How Should Physicians Respond When They Learn Patients Are Using Unapproved Gene Editing Interventions?” Responding
to patients violating U.S. health commerce regulations can be critical
when they buy and use unproven interventions.
“Using the 4-S Framework to Guide Conversations With Patients About CRISPR.” Empathic
communication skills help motivate understanding of safety,
significance of harms, impact on succeeding generations, and social
consequences.
“What Should Clinicians Do to Engage the Public About Gene Editing?” Clinicians
should have a working understanding of gene editing, controversy
surrounding its use, and its far-reaching clinical and ethical
implications.
“How Should ‘CRISPRed’ Babies Be Monitored Over Their Life Course to Promote Health Equity?” Transnational monitoring efforts should focus on safety, defining standard of care, and promoting just access to innovation.
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