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血压变异性在临床研究中导致高血压的误判:一项计算机模拟研究。

Blood pressure variability causes spurious identification of hypertension in clinical studies: a computer simulation study.

作者信息

Turner Martin J, van Schalkwyk Johan M

机构信息

Department of Anaesthesia, University of Sydney, New South Wales, Australia.

出版信息

Am J Hypertens. 2008 Jan;21(1):85-91. doi: 10.1038/ajh.2007.25.

Abstract

BACKGROUND

The blood pressure (BP) of an individual varies considerably from day to day. Hypertension is commonly identified based on the average of two BPs taken at each of two visits, a practice consistent with current guidelines. We hypothesized that (i) in the setting of high-normal BP ("prehypertension"), this practice results in frequent spurious detection of hypertension, and (ii) that random, spurious detection of hypertension and flawed study design together explain why in the Trial of Preventing Hypertension (TROPHY) study candesartan appeared to suppress the development of hypertension for 2 years after cessation of therapy.

METHODS

We used Monte Carlo simulation to quantify spurious detection of hypertension at repeated clinic visits in one million subjects with unchanging usual systolic BPs (SBPs) between 130 and 139 mm Hg and normal BP variability. Criteria for identifying hypertension derived from Rosner and Polk, Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC 7), and the Trials of Hypertension Prevention (TOHP), TROPHY, and Framingham studies were applied to Canadian Heart Health Survey data. On the basis of these simulations, we created a three-parameter model of Kaplan-Meier curves recorded in the TROPHY study. We used the model to analyze the rates at which hypertension was identified in the TROPHY study.

RESULTS

TROPHY criteria spuriously identify hypertension in 76% of subjects over 18 clinic visits. Higher rates of spurious detection of hypertension are seen with JNC 7, TOHP and Framingham study criteria. Even highly conservative criteria falsely identify hypertension in 27% of subjects over 18 visits. Our three-parameter model suggests no postdiscontinuation benefit of candesartan.

CONCLUSIONS

When applied over multiple visits, current criteria for detecting hypertension are intolerant of normal BP variation. The use of conservative criteria would reduce spurious identification of hypertension. The apparent long-term beneficial effect of candesartan seen in the TROPHY study can be explained by an inadequate method for detecting hypertension, and flawed study design.

摘要

背景

个体的血压在一天内会有很大变化。高血压通常是根据在两次就诊时每次测量的两个血压值的平均值来确定的,这种做法符合当前指南。我们假设:(i)在血压处于高正常范围(“高血压前期”)的情况下,这种做法会导致频繁地错误检测出高血压;(ii)高血压的随机错误检测和有缺陷的研究设计共同解释了为什么在预防高血压试验(TROPHY)中,坎地沙坦在治疗停止后2年似乎抑制了高血压的发展。

方法

我们使用蒙特卡洛模拟来量化在100万名受试者中,重复门诊就诊时高血压的错误检测情况,这些受试者的日常收缩压(SBP)在130至139毫米汞柱之间且保持不变,血压变异性正常。将源自罗斯纳和波尔克、美国预防、检测、评估与治疗高血压联合委员会第七次报告(JNC 7)以及高血压预防试验(TOHP)、TROPHY和弗雷明汉姆研究的高血压识别标准应用于加拿大心脏健康调查数据。基于这些模拟,我们创建了一个在TROPHY研究中记录的Kaplan-Meier曲线的三参数模型。我们使用该模型分析TROPHY研究中高血压的识别率。

结果

按照TROPHY标准,在18次门诊就诊中,76%的受试者被错误地判定为高血压。采用JNC 7、TOHP和弗雷明汉姆研究标准时,高血压的错误检测率更高。即使是高度保守的标准,在18次就诊中也会有27%的受试者被错误地判定为高血压。我们的三参数模型表明坎地沙坦在停药后没有益处。

结论

当应用于多次就诊时,当前的高血压检测标准无法容忍正常的血压变化。使用保守标准会减少高血压的错误识别。TROPHY研究中观察到的坎地沙坦明显的长期有益效果,可以通过检测高血压的方法不充分以及研究设计有缺陷来解释。

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