Hypertension. 2006;47:10-13
Published online before print December 12, 2005,
doi: 10.1161/01.HYP.0000196271.03526.50
(Hypertension. 2006;47:10.)
© 2006 American Heart Association, Inc.
Treatment of Hypertension
Remaining Issues After the Anglo-Scandinavian Cardiac Outcomes Trial
Norman M. Kaplan
From the University of Texas Southwestern Medical Center, Dallas.
Correspondence to Norman M. Kaplan, UT Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390. E-mail norman. kaplan@utsouthwestern.edu
An extract of the first 250 words of the full text is provided, because this article has no abstract.
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Introduction
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At least in hypertension, there has never been a perfect clinical
trial. By its nature, hypertension poses several barriers to
the performance and interpretation of even the most carefully
planned and conducted therapeutic trial. First and perhaps foremost,
blood pressure is a constantly moving target so that both the
initial recognition of hypertension and its subsequent response
to therapy are often difficult to validate. Certainly, the performance
of only a few blood pressure measurements in an office setting
usually provides blood pressure levels that are higher than
multiple blood pressures taken out of the office.
1 Both automatic
ambulatory measurements
2 and self-recorded home measurements
3 have been found to be more predictive of future morbidity and
mortality than office readings, but until now, all clinical
trials have used a few office readings for identification of
hypertension and quantification of therapeutic benefits. The
inclusion of even many thousands of patients in a given trial
does not erase the potential errors of the inherent variability
in blood pressure that is often accentuated by the alerting
reaction to office measurements. Moreover, even carefully selected
meta-analyses may not cover the faults of incorrect data.
4
A second barrier to the interpretation of trials that last 3 to 5 years, as most do, is the usual long duration of hypertension before overt target organ damage develops. It is obvious that the results of trials of limited duration may not provide a valid indication of the effects of therapy over the longer duration of the disease. Moreover, only mortality . . . [Full Text of this Article]