Welcome to the October edition of AOE Compliance Connection, AOE’s monthly newsletter! We are excited to share our monthly ACCME, ACPE and ANCC board updates along with news from the world of CME/CE. This newsletter is one of the many ways we stay in touch with our clients, providing educational resources to help you achieve compliance and success in your CME/CE endeavors.
This month, AOE is thrilled to welcome its newest member to our Managing Director, Annika, and her husband, Justin – it’s a boy! Soren Blair Borvansky was born Saturday, October 7th at 11:03am weighing in at 6lbs 11oz and 20 inches. Annika and baby are doing very well!
We hope you enjoy this month’s edition of AOE Compliance Connection! Visit www.aoeconsulting.com for additional information, weekly compliance tips, guideline updates and more!
Accreditation Board Bulletin
ACCME
Accredited CME providers are accountable to the CME community and to the public to present content that promotes safe and effective patient care. The ACCME created the Clinical Content Validation Policy to help protect the integrity of accredited CME as well as ensure that recommendations on patient care made during a CME activity are accurate, reliable and based on scientific evidence. The policy states:
- All the recommendations involving clinical medicine in a CME activity must be based on evidence that is accepted within the profession of medicine as adequate justification for their indications and contraindications in the care of patients.
- All scientific research referred to, reported, or used in CME in support or justification of a patient care recommendation must conform to the generally accepted standards of experimental design, data collection and analysis.
- Activities that promote recommendations, treatment, or manners of practicing medicine that are not within the definition of CME, or known to have risks or dangers that outweigh the benefits or known to be ineffective in the treatment of patients are not eligible for accreditation.
Criterion 10 and Standard 5 of the Standards for Commercial Support provide further information about the validity of CME content, stating that CME activities must promote improvements or quality in healthcare and not a specific proprietary business interest of a commercial interest and that presentations must give a balanced view of therapeutic options.
If a provider’s CME activity is found to be noncompliant with the Clinical Content Validation Policy the accredited provider is required to provide corrective information to the learners, faculty and planners. The provider will also submit a report to the ACCME that describes the action taken and the information that was communicated.
ACPE
The ACPE and the National Association of Boards of Pharmacy (NABP) collaborated to create the CPE Monitor, a CPE tracking service to process and authenticate data for CPE units received by learners from ACPE-accredited providers.
There are three methods of data transfer possible when using CPE Monitor: Manual, Automated, or Web-Service.
Manual transmission is intended for smaller organizations with limited and/or no support staff in this area. Record count for one transmission cannot exceed 10,000, and data is uploaded by one authorized user and monitored through a personal dashboard.
Automated transmission is designed for larger organizations that are equipped with information system staff who can transmit via an automated batch process. This is the recommended method for those providers who need to transmit files of 10,000 records (or more).
Web-Service transmission is for those organizations who require real-time validation of provider education and who specifically want to integrate the participant submission into custom application that are managed by their support staff.
For more information about these three modes of transmission, and to find which is the best fit for your organization, please visit this ACPE website.
ANCC
An important part of the educational design process for ANCC Accredited Providers is the determination of the criteria that learners must meet to earn contact hours as well as correctly calculating the amount to award for an accredited CNE activity.
Criteria for awarding contact hours should be based on the desired learning outcomes (i.e. knowledge, skills, and/or performance) and determined in a logical and defensible manner. Examples of criteria often includes, but are not limited to:
- Participation in the activity
- Attendance for a specified period of time
- Successful completion of a post-test
- Completion of an evaluation form
- Successful completion of a return demonstration
Contact hours are awarded to learners for the portions of a CNE activity that are devoted to the learning experience and evaluation/assessment time spent at an activity. If an activity lasts sixty minutes, and meets the standards, then one contact hour may be approved. The ANCC does allow contact hours to be rounded, but only to the nearest 0.1 or 0.01.
For a live CNE activity, the timeframes must support the contact hour calculation. Examples of evidence to document the timeframes may be shown via the agenda for the activity, outline of content to be delivered in the activity and/or other marketing materials as appropriate. When breaks and meals occur, there should be a clear allocation and this time is not to be included in the total contact hours awarded.
Enduring CNE activities should have a clear method for calculating contact hours identified prior to activity launch. Methods implemented for calculating contact hours for enduring material may include a pilot study or historical data.
CME in the News: New AMA PRA Booklet
The AMA and ACCME have released additional resources to support the recent alignment of their expectations for CME certified for AMA PRA Category 1 Credit™. The two new resources include a FAQ about the alignment and a revised AMA PRA booklet. The revised section of the booklet is specific to the “Requirements for educational activities eligible for AMA PRA Category 1 Credit™”.
The FAQ about the AMA/ACCME alignment webpage addresses frequently asked questions in the categories of:
- Core Requirements
- Enduring Materials
- Journal-based CME
- Test-item Writing
- Manuscript Review
- PI CME
- Internet point-of-care
It includes a designated section for additional questions, along with a summary table tool for calculating and designating credit.
The AMA PRA booklet includes the recent updates, in addition to AMA core requirements, format-specific requirements, requirements for designating and awarding credit, and instructions about the credit designation statement.
The ACCME and AMA have long been vocal about this simplification and alignment reflecting a desire for increased innovation and flexibility. Providers can now use the designation “other” for activities that reflect a blended approach and do not fit into an established learning format. The ACCME has explained that they are, “using the label “other” because we do not want to imply any restrictions on this category and to encourage providers to develop new, creative, and blended educational approaches. As providers design and describe innovative approaches to education, we expect to identify a descriptor that better represents the evolution of CME.”
For more information, please visit the AMA/ACCME Alignment webpage.
Clinical Content Review – Is Reviewing Content Enough?
When it comes to resolving conflicts-of-interest for faculty and presenters, the most common mechanism of resolution is a clinical content review. Most providers utilize a standard form for reviewing content and rely upon the expertise of individuals with a clinical background. This typically includes members of a CME or Education Committee or healthcare providers within an organization.
But is completion of a clinical content review sufficient to demonstrate resolution for a conflicted presenter?
It depends on a few variables:
- Did the clinical content reviewer indicate that the content was fair and balanced, free from commercial bias, evidence-based and did not require any changes to the content? Then completion of the form is sufficient documentation to show resolution.
- If, however, the clinical content reviewer indicated that there were concerns regarding fair balance, commercial bias, evidence-based recommendations and/or required changes to the content, then, no, completion of the form is not sufficient documentation. It is incumbent upon the CME provider to take the following next steps:
- Correspond with the presenter regarding required content changes.
- Request resubmission of the updated content and complete a re-review to ensure that required changes were implemented. In some cases, a presenter might provide justification for not implementing a required change. If the CME provider is in agreement, it should be documented on the review form and saved to the activity file.
Remember: The key to resolution with a clinical content review is to fully close the loop.
- Getting Started with Joint Accreditation
October 17, 2017, Chicago, IL
Read More >> - “CME for MOC: Ask Your Questions” Webinar
November 15, 2017, Online
Read More >> - MAACME 7th Annual Conference
November 16, 2017, Hunt Valley, MD
Read More >> - Professional Nurse Educators Group Conference
November 9-12, 2017, Pittsburgh, PA
Read More >> - Self-Study for ACCME Accreditation Webinar
December 8, 2017, Online
Read More >> - Alliance 2018 Annual Conference
January 20-23, 2018, Orlando, FL
Read More >>