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michigan hypertension core curriculum - State of Michigan

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clonidine (Catapres†) 0.1–0.8 mg PO BID<br />

clonidine patch (Catapres-TTS) 0.1–0.3 mg TD weekly<br />

methyldopa (Aldomet†) 250–1,000 mg PO BID<br />

reserpine (generic) 0.1–0.25 mg PO daily<br />

guanfacine (Tenex†) 0.5–2 mg PO daily<br />

In summary, there are a number <strong>of</strong> drug classes for clinicians to choose from to treat patients.<br />

Which class or classes <strong>of</strong> medications are used depends on what compelling indications the patient<br />

has for a specific class and which side effects are likely to be well tolerated and also, quite importantly,<br />

which drug classes work most effectively with each other. There has been a progressive appearance<br />

<strong>of</strong> new drug classes over the last sixty years and we are likely to continue to see additional medications<br />

added to the anti-hypertensive regimen as drug development continues.<br />

1. Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting<br />

enzyme inhibitor or calcium channel blocker vs diuretic: The Antihypertensive and Lipid-<br />

Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). JAMA. Dec 18 2002;288(23):2981-<br />

2997.<br />

2. Chobanian AV, Bakris GL, Black HR, et al. The Seventh Report <strong>of</strong> the Joint National Committee<br />

on Prevention, Detection, Evaluation, and Treatment <strong>of</strong> High Blood Pressure: the JNC 7<br />

report.[see comment][erratum appears in JAMA. 2003 Jul 9;290(2):197]. JAMA. May 21<br />

2003;289(19):2560-2572.<br />

3. Cushman WC, Ford CE, Cutler JA, et al. Success and predictors <strong>of</strong> blood pressure control in<br />

diverse North American settings: the antihypertensive and lipid-lowering treatment to prevent<br />

heart attack trial (ALLHAT). J Clin Hypertens (Greenwich). Nov-Dec 2002;4(6):393-404.<br />

4. Salpeter S, Ormiston T, Salpeter E. Cardioselective beta-blockers for chronic obstructive<br />

pulmonary disease. Cochrane Database Syst Rev. 2005(4):CD003566.<br />

5. Elliott WJ, Meyer PM. Incident diabetes in clinical trials <strong>of</strong> antihypertensive drugs: a network<br />

meta-analysis. Lancet. Jan 20 2007;369(9557):201-207.<br />

6. Materson BJ, Reda DJ, Cushman WC, et al. Single-drug therapy for <strong>hypertension</strong> in men. A<br />

comparison <strong>of</strong> six antihypertensive agents with placebo. The Department <strong>of</strong> Veterans Affairs<br />

Cooperative Study Group on Antihypertensive Agents. N Engl J Med. Apr 1 1993;328(13):914-<br />

921.<br />

7. Neaton JD, Grimm RH, Jr., Prineas RJ, et al. Treatment <strong>of</strong> Mild Hypertension Study.<br />

Final results. Treatment <strong>of</strong> Mild Hypertension Study Research Group. JAMA. Aug 11<br />

1993;270(6):713-724.<br />

8. Philipp T, Anlauf M, Distler A, Holzgreve H, Michaelis J, Wellek S. Randomised, double<br />

blind, multicentre comparison <strong>of</strong> hydrochlorothiazide, atenolol, nitrendipine, and enalapril in<br />

antihypertensive treatment: results <strong>of</strong> the HANE study. HANE Trial Research Group. BMJ. Jul<br />

19 1997;315(7101):154-159.<br />

9. Turnbull F, Neal B, Algert C, et al. Effects <strong>of</strong> different blood pressure-lowering regimens on major<br />

cardiovascular events in individuals with and without diabetes mellitus: results <strong>of</strong> prospectively<br />

designed overviews <strong>of</strong> randomized trials. Arch Intern Med. Jun 27 2005;165(12):1410-1419.<br />

10. Major cardiovascular events in hypertensive patients randomized to doxazosin vs<br />

202 Hypertension Core Curriculum

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