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The Pharmaceutical Journal
Vol 271 No 7275 p666
15 November 2003

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Treat normotensive patients after MI or stroke with antihypertensives, too

People with normal blood pressure should be given antihypertensives as part of a secondary prevention regimen in cardiovascular disease, according to Professor Richard Peto, University of Oxford.

“The key determinant is to treat high risk rather than high blood pressure,” he stated. If a patient has already had a heart attack or stroke then, without any long-term medication, there is a one in two risk of another event occurring within the next five to 10 years, regardless of whether they have high blood pressure. When a multi-drug regimen, including aspirin and drugs to lower blood pressure and cholesterol, is introduced this risk is reduced to one in six.

“Once someone has had a heart attack or stroke, the recurrence rate is substantial,” he explained. Patients with a systolic blood pressure of 130mmHg and previous stroke or myocardial infarction are at higher annual risk than patients with a systolic blood pressure of 150mmHg and no relevant disease. Professor Peto emphasised that it was a combination of drugs that was important rather than which drugs, but he suggested that all patients at high risk of events, even those with normal blood pressure, should be treated with aspirin, a statin, a diuretic and an angiotensin converting enzyme (ACE) inhibitor.

However, he was more cautious about primary prevention and stressed that his recommendation differed from recent suggestions for this type of polypharmacy approach for everyone aged over 55 years (PJ, 28 June, p881).

Professor Peto was speaking during a debate about influential hypertension trials at this year’s American Heart Association conference in Orlando, Florida, on 10 November. During the debate, Professor John Reid, University of Glasgow, said that there had been much discussion over a lack of efficacy of beta-blockers in stroke prevention. However, as yet unpublished data from an analysis conducted by the National Institute for Clinical Excellence shows that beta-blockers are better than placebo and not different from diuretics in stroke prevention, he said. “The meta-analysis of beta-blockers in fatal and non-fatal stroke prevention found a 28 per cent significant reduction in favour of beta-blockers compared with placebo.”

Dr Bryan Williams, University of Leicester, said the question raised by the HOPE (heart outcomes prevention evaluation) trial was whether or not cardiovascular and stroke prevention were solely an effect of lowering blood pressure in high risk patients or if they were specific benefits of ACE inhibitors. He explained that HOPE was designed as a trial of normotensive patients but that almost half had what would be considered high blood pressure. The results for these patients influenced the trial outcome, he said.

Head-to-head trials, including a report of the Blood Pressure Lowering Treatment Trialists’ Collaboration published in The Lancet last week (see p671), led Dr Williams to conclude that there is no evidence to show that ACE inhibitors offer further advantage than lowering blood pressure alone. “However, there are consistent findings that ACE inhibitors are associated with less new-onset diabetes,” he said.

The Journal’s attendance at the AHA conference was made possible by Pfizer. Coverage of the conference continues next week.

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