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CME Evaluation & Post Test: December 10, 2020 Craniofacial Anomalies for the PCP, Rohit Khosla, MD

Evaluation

December 10, 2020 Craniofacial Anomalies for the PCP, Rohit Khosla, MD
ESTIMATED TIME TO COMPLETE: 1.00 HOUR. Activity and content expires: December 10, 2021
STATEMENT OF DISCLOSURE: THE PLANNERS AND FACULTY FOR THIS ACTIVITY HAVE NO RELEVANT FINANCIAL RELATIONSHIPS WITH COMMERCIAL INTERESTS. NO OTHERS INDIVIDUALS INVOLVED IN THE PLANNING OR PRESENTATION OF THIS ACTIVITY HAVE ANY RELEVANT FINANCIAL RELATIONSHIPS WITH COMMERCIAL INTERESTS TO DISCLOSE.
ACCREDITATION STATEMENT: JOHN MUIR HEALTH IS ACCREDITED BY THE ACCREDITATION COUNCIL FOR CONTINUING MEDICAL EDUCATION/CALIFORNIA MEDICAL ASSOCIATION (ACCME/CMA) TO PROVIDE CONTINUING MEDICAL EDUCATION FOR PHYSICIANS.
CREDIT DESIGNATION STATEMENT: JOHN MUIR HEALTH DESIGNATES THIS ENDURING MATERIAL FOR A MAXIMUM OF ONE (1.00) AMA PRA CATEGORY 1 CREDITS™.  PHYSICIANS SHOULD CLAIM ONLY THE CREDIT COMMENSURATE WITH THE EXTENT OF THEIR PARTICIPATION IN THE ACTIVITY. 
Please complete and return this evaluation form in order to receive a maximum of .75 AMA PRA Category 1 Credit™ for this session
2. Physician Info
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4. Member ABP
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6. As a result of attending this CME activity, which of these do you plan to implement and/or change in your practice?
Space Cell DefinitelyMaybeNo Change
Formulate and communicate treatment plans for the management of medically and socially complex patients
Apply best practice strategies to overcome co-morbidities in medically and socially complex patients become better informed and more involved in health care decisions.
Utilize EBM Guidelines for a multitude of conditions that are encountered in primary care
Utilize Patient Centered Care skill to help patients become better informed and more involved in their health care decisions.
12.
TWIST gene mutations can result in craniosynostosis.  This is seen in which syndrome?
13.
A Full-term baby boy is born with Robin Sequence.  The baby is now 3 weeks old and is at home with intermittent signs of OSA.  What is the appropriate first step in managing the OSA?
14.
A 8 yo F with Crouzon Syndrome presents with Severe OSA.  Her AHI is 45.  She does not tolerate CPAP.  Optimal surgical management would be?
15.
A 5 yo boy presents to your office with a diagnosis of Treacher Collins Syndrome.  He is stable with a trach and has had a soft palate cleft repair in the past.  There is bilateral grade 3 microtia.  In which structures dida an embryonic derangement during gestational development?
16.
A 10 yo girl with history of unilateral cleft lip and palate has completed phase 1 orthodontics.  She is now ready for an Alveolar bone graft operation.  The best source for bone is?