Faculty

George
L. Bakris, MD, F.A.S.N.
Professor and Vice-Chairman Dept. of Preventive Medicine
Rush University Medical Center
Medical Writer

Diep
Koly, MD
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Release Date:
October 15, 2005 Available for Credit Through:(Accreditation Expired) |
Program Description
Micro- and macrovascular complications affecting the heart and kidneys are a
major cause of morbidity and mortality in patients with diabetes and the
metabolic syndrome. Aggressive blood pressure (BP) management, in addition to
glycemic and lipid management, can provide significant cardiovascular and renal
protection in this high-risk patient population. Controlling blood pressure has
been shown to reduce cardiovascular disease (CVD) (heart disease and stroke) by
approximately 33% to 50%, and microvascular disease (eye, kidney, and nerve
disease) by approximately 33%. [National Diabetes Fact Sheet] However, only one
third of patients with hypertension (HTN) reach recommended BP goals and many
receive no or suboptimal treatment. [Saydah et al, 2004; Schaars et al, 2004;
Donnelly et al, 1997; Geiss et al, 2001] This program addresses the challenges
faced by clinicians who treat HTN and provides evidence-based strategies for
optimizing BP control to prevent cardiovascular and renal complications in
patients with diabetes and the metabolic syndrome.
Target Audience
This educational initiative is intended for primary care physicians, cardiologists, endocrinologists, nephrologists, and all health care providers caring for patients with hypertension. |
Learning Objectives
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Apply the seventh report of the
Joint National Committee (JNC-7) guidelines, American Diabetes Association
(ADA) guidelines, and other evidence-based treatment strategies to optimize HTN
management and improve outcomes in individuals with diabetes and the metabolic
syndrome
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Understand the role
of combination therapy in achieving blood pressure control and preventing
cardiovascular and renal complications
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Summarize clinical trials data
supporting the use of angiotensin converting enzyme inhibitors (ACEIs) and
angiotensin receptor blockers (ARBs) in high-risk patients
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