Impact of Continuing Medical Education on Primary Care Providers Knowledge and Confidence in Caring for Patients with Congenital Hypothyroidism

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Impact of Continuing Medical Education on Primary Care Providers Knowledge and Confidence in Caring for Patients with Congenital Hypothyroidism Emily Bezar, MA 1, Ning Rosenthal, MD, PhD 2, Lisa Feuchtbaum Dr.PH, MPH 2 1 Public Health Foundation Enterprises 2 Genetic Disease Screening Program, California Department of Public Health Supported by HRSA Grant # D93MC26187: Demonstration projects for integrating newborn screening long term follow-up into primary care practice

Long Term Follow-Up of Patients with Primary Congenital Hypothyroidism (PCH) by Primary Care Providers (PCPs) A three-year grant funded by the Health Resources and Services Administration (HRSA) from August 1 st, 2013 through July 31 st, 2016 Participating states: California and Hawaii Target populations: PCPs and their patients with PCH

PCH Project: Overall Objectives 1) Assess the willingness and capability of PCPs to provide long-term care for patients with PCH and their needs for PCH-related continuing medical education 2) Evaluate the current case management patterns and clinical outcomes 3) Determine PCPs willingness to obtain informed consent and provide data to the PCH long-term follow-up (LTFU) database 4) Investigate the practicality of providing real time LTFU data by PCPs and identify barriers incurred 5) Improve PCPs knowledge about PCH and increase their capability of providing care for patients with PCH

Why develop a CME course for PCPs? Clinical Knowledge Gaps Our 2014 cross-sectional survey (N=226) revealed gaps in PCPs knowledge on treating patients with PCH: Only 49% knew the recommended frequency of blood tests to monitor PCH over a patient s lifespan Only 23% knew when to try a patient off levothyroxine treatment to determine if PCH is transient Interest 84% of surveyed PCPs reported that they are likely or very likely to participate in CME on PCH if available

High incidence rate: PCH is the most common disorder identified in blood spot screening and affects 1 in 1,706 live births in CA Geographic distribution of cases: Need to increase number of PCPs who can provide PCH case-management in rural areas of CA with very few pediatric endocrinologists More good reasons for a PCH course. Relatively simple to treat: Patients with PCH can potentially be managed well by PCPs with support from endocrinologists To improve access to quality care: CME for PCPs may reduce barriers to quality follow-up care for families for whom specialty care is difficult to obtain

Course was developed with the PCH Project s Advisory Committee of CA pediatric endocrinologists Continuing Medical Education (CME) can be a key element in a PCP-centered follow-up model

Course Format and Content Summary 50 minute lecture, followed by a 10 minute Q & A Begin by presenting 5 Case Studies in question format Review of California s PCH newborn screening methodology Review of thyroid pathophysiology and clinical presentation of PCH symptoms Focus on the functional priorities of PCH diagnosis, treatment and follow-up in the pediatric primary care context Recommend consultation with endocrinologist when needed Conclude with the same 5 Case Studies, with opportunity for audience self-assessment and discussion

Learning Objectives At the end of this course, participants will be able to: 1 2 3 4 Perform confirmatory testing and initiate treatment if newborn thyroid function screening is abnormal Assess treatment needs and monitor clinical outcomes for infants, children, and adolescents with congenital hypothyroidism Describe the diagnostic process for determining whether a patient has transient or permanent hypothyroidism Educate families about the importance of adherence to treatment for congenital hypothyroidism

5 Handouts

PCPs and PCH?? CME Evaluation Questions Medical Specialty of participant? Paired Pre- and Post- Course Questions: CONFIDENCE? 3 questions assessing PCP s confidence with PCH Diagnosis, Treatment and Follow-up KNOWLEDGE? 8 True/False PCH clinical knowledge questions Intending to make changes to practice? Course Ratings? Comments and suggestions?

Medical Specialties of Course Participants (N=171) 10% 21% 7% 6% 56% Pediatrics Nurse Pract. / Physician Asst. Other (Resident, Student etc.) Family Medicine Nurse 6 Events / Total attendance: ~ 300 / Evaluations Returned: 195

Confidence with CONFIRMING a PCH Diagnosis 100% 80% 15 21 48 70 % improved their confidence 60% Very Confident 40% 39 34 Confident 20% 0% 25 15 3 Pre-Course Post-Course N=144 Somewhat confident Not confident at all

Confidence with INITIATING TREATMENT for PCH 100% 80% 9 14 39 80 % improved their confidence 60% 39 Very Confident 40% 42 Confident 20% 0% 38 16 3 Pre-Course Post-Course N=140 Somewhat confident Not confident at all

Confidence with PROVIDING FOLLOW-UP for PCH 100% 80% 12 18 42 69 % improved their confidence 60% 40% 39 38 Very Confident Confident 20% 0% 31 17 3 Pre-Course Post-Course N=143 Somewhat confident Not confident at all

Improvements in Knowledge: True/False Questions Question 1: The recommended frequency of blood tests to monitor PCH patients in first 6 months of life is every 1-2 months (N=167) Question 2: When transient PCH is suspected, it is safe to do a trial off levothyroxine for 4 6 weeks after 1 year of age (N=164) False! 100% True! After 3 years of age % of Course participants 80% 60% 40% 20% 80% 88% 41% 79% Pre-Course Correct Post-Course Correct 0% Question 1 Question 2 Correct Answers

Question 3: The American Academy of Pediatrics (AAP) False! recommended initial treatment dose of LT4 for babies with confirmed PCH is 15 20 μg/kg (N=162) 10-15 μg/kg Question 4: Thyroid stimulating hormone (TSH) surges by 30 minutes after birth and returns to <10 μiu/ml within 3 days (N=159) False! 100% Within 5-7 days % of Course participants 80% 60% 40% 20% 40% 68% 26% 46% Pre-Course Correct Post-Course Correct 0% Question 3 Question 4 Correct Answers

Overall Improvement in True/False Total Score 135 respondents answered all 8 pre-course and post-course true/false questions Improvement on T/F Test Score (N=135) Percentage Improved their score 72% Unchanged score 22% Lower score 6%

Pre- and Post- Test Score Distributions For 8 True/False Knowledge Questions (N=135) % of Course participants Pre-Test: 40 35 30 25 20 15 10 5 0 Post-Test: Pre-test median score: 63% te 25% 38% 50% 63% 75% 88% 100% Test Scores Post-test median score: 88%

Key Conclusions from True/False Results Results suggest largest knowledge gaps among PCPs about the following issues: Timing of post-natal TSH surge and return to normal Initial treatment dosage When and how to assess patients for transient PCH

Speaker covered practical, useful information. Very applicable to general providers. I will be more conscious of following the monitoring of CH in newborns with guidelines discussed. I like the simple explanation of the process. 88% rated the course as Outstanding 75% said they plan to make changes to practice

Summary The course was shown to be effective in improving PCPs knowledge and confidence in providing follow-up care for patients with PCH PCPs were especially enthusiastic about the simplicity of the course format and the practical instructions provided Participants indicated willingness and intention to make changes to their clinical practice in treating PCH Newborn screening programs may consider offering CME courses to PCPs who care for patients with PCH

Research Team Lisa Feuchtbaum, Dr. P.H., M.P.H. Principal Investigator Genetic Disease Screening Program, CDPH Co-Investigators: Ning Rosenthal, M.D., Ph.D. Principal Research Scientist Premier Inc. Los Angeles, CA Sylvia Mann Au, M.S., CGC Hawaii Department of Health, Genetic Section Laura Bachrach, M.D. Professor of Pediatrics Division of Endocrinology Stanford University Medical Center Study Manager: Emily Bezar, M.A. Public Health Foundation Enterprises Advisory Committee Swati Banerjee, M.D. Division of Pediatric Endocrinology Valley Children s Hospital, Madera, CA Mitchell E. Geffner, M.D. Chief, Center for Endocrinology, Diabetes and Metabolism, Children s Hospital Los Angeles, CA Michael Gottschalk, M.D., Ph.D. Chief, Pediatric Endocrinology UC San Diego/Rady Children s Hospital, CA Mary Rutherford, M.D. Pediatrician Children s Hospital Oakland, CA Stuart K. Shapira, M.D., Ph.D. Chief Medical Officer and Associate Director for Science National Center on Birth Defects and Developmental Disabilities (NCBDDD) CDC, Atlanta, GA

The contents, including all opinions and views expressed or implied, are entirely personal and do not necessarily represent the opinions or views of any person or organization, including the California Department of Public Health.