Hypertension. 1996;28:1-2
(Hypertension. 1996;28:1-2.)
© 1996 American Heart Association, Inc.
Intervention Trials
Concerns and Publishing Pitfalls
Edward D. Frohlich, Editor of Hypertension
Correspondence to Edward D. Frohlich, MD, Alton Ochsner Medical Foundation, 1516 Jefferson Highway, New Orleans, LA 70124.
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Introduction
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I have just attended a small meeting on intervention trials
in hypertension organized by the International and European
Societies of Hypertension, the proceedings of which will be
published soon in the
Journal of Hypertension. I am delighted
to see the continued and warm cooperation of our two journals.
More specifically, I am continually impressed with how far we
have come since our early Veterans Administration Cooperative
Studies organized by Edward D. Freis over 30 years ago. During
these years we have seen the established efficacy of antihypertensive
agents in reducing arterial pressure and controlling outcomes
of hypertensive cardiac and vascular diseases. We have seen
a reversal of cardiovascular morbidity and mortality that is
associated with marked reductions in the prevalence of hypertensive
emergencies and accelerated and malignant hypertension and,
of course, dramatic reductions in deaths from stroke and coronary
heart disease (CHD).
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Data Analyses
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As we have become well aware, we have been served well by the
relatively recent developments in "post hoc analyses" of studies
and trials. Nevertheless, cautions were raised at this symposium
on the conduct of meta-analysis and the use of drug study databases.
One presentation was concerned with the "pros and cons" of meta-analysis,
suggesting that perhaps a better term would be "pros and cautions."
However, the subject of these analyses might be more appropriately
termed "cautions and cons." With the recent plethora of publications
employing these and other sophisticated epidemiological and
biostatistical techniques, another presentation emphasized the
need for more rigorous and careful review, analysis, and inclusion
of the extant, but peer-reviewed only, published literature.
We must keep in mind that by publishing a meta-analysis, we
do not necessarily confer truth to that analysis. Inclusion
of studies in a meta-analysis requires a meticulous and highly
discriminating literature search and review.
We emphasize again that such references must be restricted only to peer-reviewed publications, and editors of major hypertension journals must insist that the literature review not be restricted exclusively to a Medline or Medlars search. Although these indexes are most serviceable, the world literature is not restricted to the 3- to 6-year retrospective data storage that are instantly available on our desktop computers. The selection of a handful of key words and phrases provided by a thoughtful author by no means satisfies the necessity of a more-comprehensive literature review. Too often in submitted manuscripts the author believes that such a search of the extant published data and analysis is satisfied. Clearly, this is an inadequate aspect of the overall research work, and it ill serves the overall needs and purposes of a comprehensive manuscript, the author, and, most of all, the readers. We recently heard one critic of poorly done meta-analyses say that the relationship of "analysis to meta-analysis is analogous to physics to metaphysics." We all must be aware of the adage of which we were reminded at the symposium: "If garbage is included in any analysis, for sure, garbage will come out."
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Conclusions of Study Findings
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Most participants at this symposium, I believe, had been convinced
from the analysis of the first 14 multicenter trials of antihypertensive
therapy by Collins et al
1 that the antihypertensive drugs that
had reduced arterial pressure reduced deaths from stroke. Some
had been less convinced (at the time) that the deaths from CHD
were as dramatically reduced; certainly, they were less than
predicted. Few who attended the symposium ever believed that
lipid elevations that may have been produced by the diuretics
accounted for this "less than predicted significant reduction
in CHD." Since subsequent meta-analysis of subsequent studies
employing lower doses of diuretics satisfied the original predictions,
a more reasonable conclusion seems that hypokalemia contributing
to sudden cardiac death and, hence, deaths from CHD seems more
reasonable.
2 The obvious lesson from this standing issue is
that whatever conclusions are drawn from those trials, readers
and other scientists must be extremely cautious in making inferences
and conclusions. The consequence of making erroneous conclusions
may be extremely costly in falsely justifying new, additional,
and confirmatory studies.
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Definitions
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There is always a great need for us to be certain of the terminology
we use. In the initial 14-study meta-analysis referred to above,
the planning groups for each of these studies defined CHD to
include deaths from myocardial infarction; angina pectoris without
pathologically demonstrable myocardial infarction, lethal congestive
heart failure, or pulmonary edema; lethal cardiac arrhythmias;
or otherwise unexplainable sudden cardiac deaths. However, it
does not appear to be certain that recently designed multicenter
trials have made clear-cut definitions of deaths from CHD. Thus,
many of the deaths from CHD in the early 14 multicenter trials
may have been produced by myocardial infarction or occlusive
epicardial coronary artery disease; however, they may also have
resulted from hypertensive coronary arteriolar (microvascular)
disease or even from antihypertensive treatment (eg, hypokalemia).
It would be of immense value to have such outcomes defined to
obviate post hoc problems. And, it was of great interest to
note that most participants at this symposium were unable to
define the current criteria of ongoing studies for CHD.
Another definition problem relates to just what is meant by hypertension. There are major differences in this definition among the many studies in the United States and Europe. In the United States, hypertension is defined and classified (ie, "staged") according to the heights of systolic and diastolic pressures. Thus, a patient has hypertension if systolic and diastolic pressures exceed 140 and 90 mm Hg, respectively. In Europe, however, even though systolic hypertension is now considered treatable, the existence of hypertension is usually defined by diastolic pressure, with a minimal level of 95 mm Hg (based on the World Health Organization criteria). Thus, studies from the United States and elsewhere must be qualified accordingly because many of our current, ongoing studies involve patients with lower levels of diastolic pressure and with systolic hypertension. Again, when retrospective analyses of studies are pursued, investigators should consider these differences in definition.
It seems clear that we have learned and benefited much from the past intervention trials in hypertension. Although we no doubt will continue to learn much from ongoing and future trials, there is one lesson we may not have learned: We must analyze the data and define our terms, goals, and end points more precisely, or, for certain, new and avoidable controversies will arise.
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References
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1.
Collins R, Peto R, MacMahon S, Hebert P, Fiebach NH, Eberlein KA, Godwin J, Qizilbash N, Taylor JO, Hennekens CH. Blood pressure, stroke, and coronary heart disease. Part 2, Short-term reductions in blood pressure: overview of randomised drug trials in their epidemiological context.
Lancet. 1990;335:827-838.
[Medline]
[Order article via Infotrieve]
2.
Thijs L, Fagard R, Lijnen P, Staessen J, Van Hoof R, Amery A. A meta-analysis of outcome trials in elderly hypertensives. J Hypertens.. 1992;10:1103-1109.[Medline]
[Order article via Infotrieve]
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