OBJECTIVE:To estimate the contribution of inadequate sphygmomanometer calibration to over- and under-detection of hypertension. DESIGN:Monte Carlo simulation of the measurement of blood pressure (BP) of a population with calibrated and uncalibrated sphygmomanometers. Simulated BP measurements included systematic sphygmomanometer error and random variability. MAIN OUTCOME MEASURES:The percentage of hypertensive adults (BP > 140/90 mmHg) not detected and the percentage of adults incorrectly classified hypertensive due to sphygmomanometer error. The percentage of the false positives and false negatives attributable to sphygmomanometer error. The number of additional visits patients need to make to obtain the same improvement in hypertension detection as is obtained by sphygmomanometer calibration. RESULTS:After three visits, uncalibrated sphygmomanometer error causes 20 and 28% of all undetected adult systolic and diastolic hypertension, respectively, and 15 and 31% of all falsely detected adult systolic and diastolic hypertension. In some groups, under-detection is worse; for example, sphygmomanometer error causes 27% of all missed systolic hypertension in 35-44-year-old females. In some age groups, over-detection is worse; for example, after three visits, sphygmomanometer error causes 63 and 50% of falsely detected systolic and diastolic hypertension in 18-24-year-old females, respectively. In-service sphygmomanometer calibration achieves the same or greater improvement in hypertension detection as an additional two visits. CONCLUSIONS:Uncalibrated sphygmomanometers are a preventable cause of clinically significant over- and under-detection of hypertension. Sphygmomanometers should be calibrated regularly by accredited organizations or technicians. Standards and guidelines governing sphygmomanometers in service should be revised. Sphygmomanometer calibration is a cost-effective way of improving hypertension detection.

译文

目的:评估血压计校准不足对高血压检测过度和检测不足的影响。
设计:蒙特卡洛模拟使用校准和未校准的血压计测量人群的血压(BP)。模拟的BP测量包括系统血压计误差和随机变异性。
主要观察指标:未检测到高血压成年人(BP> 140/90 mmHg)的百分比,以及由于血压计误差而错误归为高血压的成年人百分比。归因于血压计误差的误报和误报的百分比。为了获得与血压计校准获得的高血压检测相同的改善,患者需要进行的其他就诊次数。
结果:三次就诊后,未经校准的血压计误差分别导致所有未检测到的成人收缩压和舒张压高血压分别占20%和28%,以及所有错误检测到的成人收缩压和舒张压高血压分别占15%和31%。在某些人群中,检测不足的情况更加严重。例如,血压计误差导致35-44岁女性的所有收缩压漏诊占27%。在某些年龄段,过度检测的情况更严重;例如,在3次就诊后,血压计误差分别导致18-24岁女性的63%和50%错误检测出的收缩压和舒张压高血压。使用中的血压计校准与另外两次就诊相比,在高血压检测中达到了相同或更大的改善。
结论:未经校准的血压计是可预防的临床上显着过高和过低检测到高血压的原因。血压计应由经认可的组织或技术人员定期校准。应修订有关使用中的血压计的标准和指南。血压计校准是改善高血压检测的一种经济有效的方法。

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