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AGA’s first guideline on AI open for public comment

Review our draft recommendations on the use of computer-aided detection (CADe) systems for the detection of colorectal polyps during colonoscopy.
Medical technology, doctor use AI robots for diagnosis, care, and increasing accuracy patient treatment in future. Medical research and development innovation technology to improve patient health.
Medical technology, doctor use AI robots for diagnosis, care, and increasing accuracy patient treatment in future. Medical research and development innovation technology to improve patient health.

The draft AGA Clinical Practice Guideline on Computer-Aided-Detection Assisted Colonoscopy is now open for public comment.

To be published in March 2024, this is AGA’s first guideline to critically evaluate the role of artificial intelligence in GI care. The guideline provides an overview of the evidence and guides endoscopists and patients on the use of computer-aided detection (CADe) systems for the detection of colorectal polyps during colonoscopy.

As part of our guideline development process, we invite you to review this draft guideline and share feedback during the public comment period.  

Submit your comments by Oct. 28, 2024.

Guideline documents for review

About the public comment period

AGA develops clinical practice guidelines using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) methodology, which provides a common, sensible and transparent approach to grading the quality of evidence and strength of recommendations, and uses the best practices outlined by the Institute of Medicine.

The public comment period is an integral part of AGA’s guideline development process. It allows AGA members and key stakeholders to review and comment on upcoming guidelines and their accompanying technical reviews.

Once an AGA guideline panel releases the drafts for public comment, identified stakeholders are alerted and submit their comments through an online survey. After the period ends, the guideline panel reviews and responds to the comments within two weeks. Revisions to the draft documents are at the discretion of the panel, but all comments will be considered and responses internally documented.

To see previously published guidelines, visit AGA’s clinical guidance library.

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