(405) 271-8001, ext. 43414
Education:
- Bachelor of Science in Pharmacy, Auburn University, Auburn, Alabama, 1981
- Doctor of Pharmacy, University of Texas Health Sciences Center, San Antonio, Texas and the University of Texas, Austin, Texas, 1983
- Ambulatory Care Pharmacy Practice Residency, Brackenridge Hospital and the University of Texas, Austin, Texas, 1984
- Master of Divinity, Western Theological Seminary, Holland, Michigan, 2012
Teaching:
- AHS 1400 Orientation to the Health Professions (course director)
- NS 7244: Medical Nutrition Therapy I
- NS 7542: Medical Nutrition Therapy Practicum
- OCTH 7012: Clinical Management for Health
- OCTH-PHTH 9391 Interprofessional Case Management
- PA 7831 Focuses in PA Practice III
Clinical:
- Pharmacotherapy and management of diabetes, dyslipidemia, and hypertension
- Pharmacotherapy for health issues commonly encountered in primary care practice
Societies and Organizations:
- American Society of Health-System Pharmacists
- Association of Diabetes Care and Education Specialists
- Oklahoma Pharmacists Association
Clinical/Research Interests:
- Curriculum development, delivery, and assessment
- Interprofessional collaboration in practice and teaching
- Diabetes management
- Cost-effective clinical care models
Funding:
- Britton ML, Letassy NA. Development of Team-Based Experiential Education Rotations for Foot Care and Dental care of Patients with Diabetes at a Primary Care Practice Site, funded by the Wisdom Family Foundation, $164,500, February 2015-August 2016
- Britton ML, Letassy NA, Carter SM. Evaluation of an Assessment Method for Health Professional Students Completing an Inter-Professional Curriculum Focused on Team-Based Care of Patients with Diabetes Mellitus, funded by the Wisdom Family Foundation, $139,000, January 2013-June 2015
- Fisher MJ, Thompson B, Sparks R, Britton ML, Dennis V, Letassy NL, Blevins S, Reinhardt L, Ferretti M, Turner P, Loving G, Bratzler D, Dmytryk J, Jones R, Miller C, Fritz T, Johnson C. Empowering Patients through Interprofessional Collaboration (EPIC), Wisdom Family Foundation, $150,000, August 2012-June 2015
- Britton ML, Letassy NA, Armor BL, Dennis VC, Marcy TR, Barud S, Hall M, Chonlahan J, Beach P. Educational Grant to Develop a Diabetes Traineeship, funded by the American Society of Health-System Pharmacists Foundation, $20,000, June 2002, June 2003, June 2004, June 2005, June 2006
- Whitsett T (principal investigator), Havrda D, Hawk T, Letassy N, Dennis V, Britton ML (sub-investigator), “Efficacy and Safety Study of the Oral Direct Thrombin Inhibitor H 376/95 Compared with Dose-Adjusted Warfarin (Coumadin®) in the Prevention of Stroke and Systemic Embolic Events in Patients in Patients with Atrial Fibrillation (SPORTIF V), Protocol #233 (SH-TPA-0005), April 2001-February 2002
- Kem DC (principal investigator), Britton ML (co-principal investigator), Havrda D, Letassy NA, Counts S, Feuge R, Halloran M, Dennis J, Hawk T. Participating as a site in the study entitled “Clinical protocol for a double-blind, randomized comparison of eplerenone and losartan in patients with low rennin hypertension,” G.D. Searle & Co. Study IE3-99-02-019, $3460 per patient enrolled, July 2000-October 2000 (study closed as a cost efficiency by Searle before patients could be enrolled)
- Kem DC (principal investigator), Britton ML (co-principal investigator), Havrda D, Letassy NA, Counts S, Feuge R, Halloran M, Dennis J, Hawk T. Participating as a site in the study entitled “Clinical protocol for a double-blind, controlled, randomized comparison study of the antihypertensive effect of eplerenone and spironolactone in patients with hypertension secondary to primary aldosteronism,” G.D. Searle & Co. Study IE3-99-02-018, $2815 per patient enrolled, July 2000-October 2000 (study closed as a cost efficiency by Searle before patients could be enrolled)
- Comp P (principal investigator), Havrda D, Letassy N, Counts S, Feuge R, Halloran M, Britton ML (sub-investigator), “PREVENT: Prevention of Recurrent Venous Thromboembolism,” National Heart Lung and Blood Institute Protocol #HL58036, $1100 per patient enrolled, November 1999-September 2004
- Kem DC (principal investigator), Britton ML (co-principal investigator), Havrda D, Letassy NA, Counts S, Feuge R, Halloran M, Beck J. Participating as a site in the study entitled “A 20-week, double-blind, randomized, active-controlled, multicenter study comparing efficacy and safety of troglitazone plus metformin or rosiglitazone plus metformin to metformin plus placebo in type 2 diabetic patients not optimally controlled on metformin,” Parke-Davis protocol 991-241, $2,670 per patient enrolled, October 1999-March 2000 (study closed before patients were enrolled due to troglitazone’s withdrawal from the market)