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Validity and reliability of central blood pressure estimated by upper arm oscillometric cuff pressure

机译:通过上臂示波法袖带压估计的中心血压的有效性和可靠性

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Background: Noninvasive central blood pressure (BP) independently predicts mortality, but current methods are operator-dependent, requiring skill to obtain quality recordings. The aims of this study were first, to determine the validity of an automatic, upper arm oscillometric cuff method for estimating central BP (O CBP) by comparison with the noninvasive reference standard of radial tonometry (T CBP). Second, we determined the intratest and intertest reliability of O CBP. Methods: To assess validity, central BP was estimated by O CBP (Pulsecor R6.5B monitor) and compared with T CBP (SphygmoCor) in 47 participants free from cardiovascular disease (aged 57 ± 9 years) in supine, seated, and standing positions. Brachial mean arterial pressure (MAP) and diastolic BP (DBP) from the O CBP device were used to calibrate in both devices. Duplicate measures were recorded in each position on the same day to assess intratest reliability, and participants returned within 10 ± 7 days for repeat measurements to assess intertest reliability. Results: There was a strong intraclass correlation (ICC = 0.987, P 0.001) and small mean difference (1.2 ± 2.2 mm Hg) for central systolic BP (SBP) determined by O CBP compared with T CBP. Ninety-six percent of all comparisons (n = 495 acceptable recordings) were within 5 mm Hg. With respect to reliability, there were strong correlations but higher limits of agreement for the intratest (ICC = 0.975, P 0.001, mean difference 0.6 ± 4.5 mm Hg) and intertest (ICC = 0.895, P 0.001, mean difference 4.3 ± 8.0 mm Hg) comparisons. Conclusions: Estimation of central SBP using cuff oscillometry is comparable to radial tonometry and has good reproducibility. As a noninvasive, relatively operator-independent method, O CBP may be as useful as T CBP for estimating central BP in clinical practice.
机译:背景:无创中央血压(BP)可以独立预测死亡率,但当前的方法取决于操作员,需要获得高质量记录的技能。这项研究的目的首先是,通过与径向眼压测量的非侵入性参考标准(T CBP)进行比较,确定一种自动的上臂示波法袖套法估算中心血压(O CBP)的有效性。其次,我们确定了O CBP的内部测试和内部测试的可靠性。方法:为评估有效性,通过O CBP(Pulsecor R6.5B监护仪)评估了中心血压,并与47位无心血管疾病(57±9岁)仰卧位,坐位和站立位的参与者进行了T CBP(SphygmoCor)比较。使用O CBP装置的肱平均动脉压(MAP)和舒张压BP(DBP)在两个装置中进行校准。在同一天在每个位置记录重复的测量值以评估测试内可靠性,参与者在10±7天内返回以进行重复测量以评估测试间的可靠性。结果:与T CBP相比,O CBP测定的中心收缩压(SBP)的组内相关性强(ICC = 0.987,P <0.001),均值差小(1.2±2.2 mm Hg)。所有比较的百分之九十六(n = 495个可接受的记录)在5毫米汞柱以内。关于可靠性,内部测试(ICC = 0.975,P <0.001,平均差异为0.6±4.5 mm Hg)和中间测试(ICC = 0.895,P <0.001,平均差异为4.3±8.0)之间存在很强的相关性,但一致性较高。毫米汞柱)比较。结论:袖带示波法估算中枢性SBP与放射线眼压法相当,并且具有良好的重现性。作为一种非侵入性的,相对独立于操作员的方法,在临床实践中,O CBP可能与T CBP一样有用。

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