The UTHealth Houston Adult Cardiovascular Genomics Certificate Program: Efficacy and Impact on Healthcare Professionals

Author:

Garner Melyssa1,Rajani Bansari2,Vaidya Priyanka2,Dayeh Samer Abu2,Cecchi Alana C.2,Miyake Christina C.3,Huff Vicki4,Wanat Matthew5,Wang Elisabeth5,Kurzlechner Leonie M.6,Landstrom Andrew P.6,An Daniel2,Liang Yafen2,Moulik Mousumi7,Wong Timothy C.7,Cunha Shane R.2,Cannon Ashley1,Holt R. Lynn1,Milewicz Dianna M.2,Prakash Siddharth K.2

Affiliation:

1. University of Alabama at Birmingham

2. University of Texas Health Science Center at Houston

3. Baylor College of Medicine

4. University of Texas MD Anderson Cancer Center

5. University of Houston College of Pharmacy

6. Duke University School of Medicine

7. University of Pittsburgh School of Medicine

Abstract

Abstract

Background The demand for genetic services has outpaced the availability of resources, challenging clinicians untrained in genetic integration into clinical decision-making. The UTHealth Adult Cardiovascular Genomics Certificate (CGC) program trains non-genetic healthcare professionals to recognize, assess, and refer patients with heritable cardiovascular diseases. This asynchronous online course includes 24 modules in three tiers of increasing complexity, using realistic clinical scenarios, interactive dialogues, quizzes, and tests to reinforce learning. We hypothesized that the CGC will increase genomic competencies in this underserved audience and encourage applying genomic concepts in clinical practice. Methods Required course evaluations include pre- and post- assessments, knowledge checks in each module, and surveys for module-specific feedback. After 6 months, longitudinal feedback surveys gathered data on the long-term impact of the course on clinical practice and conducted focused interviews with learners. Results The CGC was accredited in September 2022. Principal learners were nurses (24%), nurse practitioners (21%), physicians (16%), and physician assistants. Scores of 283 learners in paired pre- and post-assessments increased specific skills related to recognizing heritable diseases, understanding inheritance patterns, and interpreting genetic tests. Interviews highlighted the CGC's modular structure and linked resources as key strengths. Learners endorsed confidence to use genetic information in clinical practice, such as discussing genetic concepts and risks with patients and referring patients for genetic testing. Learners were highly likely to recommend the CGC to colleagues, citing its role in enhancing heritable disease awareness. Conclusions The CGC program effectively empowers non-genetic clinicians to master genomic competencies, fostering collaboration to prevent deaths from heritable cardiovascular diseases, and potentially transforming healthcare education and clinical practice.

Publisher

Springer Science and Business Media LLC

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