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Stroke. 2006;37:1967
Published online before print June 22, 2006, doi: 10.1161/01.STR.0000231850.73983.cc
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(Stroke. 2006;37:1967.)
© 2006 American Heart Association, Inc.


Letters to the Editor

Addressing the Guidelines

Tania Mysak, BSP, PharmD

University of Alberta Hospital, Edmonton, Alberta, Canada

Karen Tulloch, BSc (Pharm), PharmD, ACPR

Vancouver General Hospital, Vancouver, British Columbia, Canada

To the Editor:

We commend you on the publication of these timely guidelines.1 Increasingly, those who are involved in the care of stroke patients are heightening their focus toward prevention strategies because there are many modifiable risk factors we can tackle. There are, however, a few areas in the guidelines we would like to address.

First, in the hypertension segment, the recommendation states "Because this benefit (of antihypertensive treatment) extends to persons with and without a history of hypertension, this recommendation should be considered for all ischemic stroke and TIA patients." This recommendation is based on Class IIa, Level B evidence, presumably the PROGRESS study.2 However, an important consideration is the definition of hypertension that was used in the PROGRESS study. As stated within the text of the guidelines, patients were classified as hypertensive if their baseline blood pressure was >160 mm Hg systolic or 90 mm Hg diastolic. The mean baseline blood pressure in the nonhypertensive group was 139/79, which according to the JNC VII, is considered prehypertension.3 The JNC VII thereby recommends that patients who have had a stroke and maintain blood pressures above 120/80 should be considered for antihypertensive therapy, and references the PROGRESS study for this recommendation. However, the 2006 stroke guidelines advocate antihypertensive therapy in patients "without a history of hypertension," which could be erroneously interpreted as applying to patients with normal blood pressure (ie, <120/80) and is not supported by the current evidence. Perhaps the authors did not intend to suggest this; however, the busy clinician scanning the recommendation sections and not closely reviewing the text may be led to believe otherwise.

Second, recommendations in the diabetes segment state "ACEIs and ARBs are more effective in reducing the progression of renal disease and are recommended as first-choice medications for patients with DM". The supporting reference for this recommendation is the 2004 ADA guidelines, the text of which actually states "Because many studies demonstrate the benefits of ACE inhibitors on multiple adverse outcomes in patients with diabetes... the established practice of choosing an ACE inhibitor as the first-line agent (for the management of hypertension) in most patients with diabetes is reasonable."4 The ADA guidelines later summarize "All patients with diabetes and hypertension should be treated with a regimen that includes either an ACE inhibitor or ARB"; however, this is appropriately given a Level E class of evidence (ie, expert opinion). The results of the ALLHAT study, which demonstrated equivalent macrovascular protection and prevention of end stage renal disease in diabetic patients in the thiazide, ACEI and CCB subgroups support the use of any of these classes in the hypertensive diabetic patient.5,6 In fact, the "renal protective" effects of ACEIs and ARBs independent of their blood pressure–lowering activities have been called into question in a recent meta-analysis.7 When considering that thiazides cost pennies a day, and ACEIs/ARBs considerably more, it is unclear why clinical practice guidelines continue to use consensus level recommendations to encourage ACEI/ARB use first-line. A more appropriate emphasis would be on ensuring target blood pressures are met.

Finally, it is imperative that guidelines produced by national bodies such as the American Stroke Association remain unbiased toward any manufacturer of any drug, therapeutic or diagnostic product. Despite the fact that several versions of the drug warfarin are available on both the American and Canadian markets, we identified the word "Coumadin" several times within the text of the document. Considering the much more cumbersome "extended-release dipyridamole" was consistently used over the branded name of this product (we cannot however commend you on using the term "aspirin", which is also a brand name), we can only assume that the use of the brand name version of warfarin was an unintentional editing error. We trust that it will be corrected for future updates or revisions to these guidelines.

Acknowledgments

Disclosures

None.

References

  1. Sacco RL, Adams R, Albers G, Alberts MJ, Benavente O, Furie K, Goldstein LB, Gorelick P, Halperin J, Harbaugh R, Johnston SC, Katzan I, Kelly-Hayes M, Kenton EJ, Marks M, Schwamm LH, Tomsick T. Guidelines for prevention of stroke in patients with ischemic stroke or transient ischemic attack: a statement for healthcare professionals from the American Heart Association/American Stroke Association council on stroke: co-sponsored by the council on cardiovascular radiology and intervention: the American academy of neurology affirms the value of this guideline. Stroke. 2006; 37: 577–617.[Abstract/Free Full Text]
  2. PROGRESS Collaborative Group. Randomised trial of a perindopril-based blood-pressure-lowering regimen among 6105 individuals with previous stroke or transient ischaemic attack. Lancet. 2001; 358: 1033–1041.[CrossRef][Medline] [Order article via Infotrieve]
  3. Chobanian AV, Bakris GL, Black HR, Cushman WC, Green LA, Izzo JL, Jones DW, Materson BJ, Oparil S, Wright JT Jr, Roccella EJ; the National High Blood Pressure Education Program Coordinating Committee. The seventh report of the joint national committee on prevention, detection, evaluation, and treatment of high blood pressure: the JNC 7 report. JAMA. 2003; 289: 2560–2572.[Abstract/Free Full Text]
  4. American Diabetes Association. ADA clinical practice recommendations. Diabetes Care. 2004; 27: S1–143.[CrossRef]
  5. The ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group. Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic: the antihypertensive and lipid-lowering treatment to prevent heart attack trial (ALLHAT). JAMA. 2002; 288: 2981–2997.[Abstract/Free Full Text]
  6. Whelton PK, Barzilay J, Cushman WC, Davis BR, Ilamathi E, Kostis JB, Leenen FHH, Louis GT, Margolis KL, Mathis DE, Moloo J, Nwachuku C, Panebianco D, Parish DC, Pressel S, Simmons DL, Thadani U; for the ALLHAT Collaborative Research Group. Clinical outcomes in antihypertensive treatment of type 2 diabetes, impaired fasting glucose concentration, and normoglycemia: antihypertensive and lipid-lowering treatment to prevent heart attack trial (ALLHAT). Arch Intern Med. 2005; 165: 1401–1409.[Abstract/Free Full Text]
  7. Casas JP, Chua W, Loukogeorgakis S, Vallance P, Smeeth L, Hingorani AD, MacAllister RJ. Effect of inhibitors of the renin-angiotensin system and other antihypertensive drugs on renal outcomes: systematic review and meta-analysis. Lancet. 2005; 366: 2026–2033.[CrossRef][Medline] [Order article via Infotrieve]

Related Article:

Response to Letter by Mysak et al
Ralph L. Sacco and Larry B. Goldstein
Stroke 2006 37: 1968. [Full Text] [PDF]




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