Robert B. Schonberger MD, MHS , Adambeke Nwozuzu MD, MHS , Jill Zafar MD , Eric Chen BS , Simon Kigwana BA , Miriam M. Monteiro BA , Jean Charchaflieh MD, MPH , Sophisa Sophanphattana MD , Feng Dai PhD , Matthew M. Burg PhD
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We prospectively enrolled 200 patients at a presurgical evaluation clinic with clinic blood pressures (CBPs) ≥130/85 mm Hg, as measured using a previously validated automated upper-arm device (Welch Allyn Vital Sign Monitor 6000 Series), to undergo daily </span>HBP monitoring<span><span> (Omron Model BP742N) between the index clinic visit and their day of surgery<span>. Elevated HBP was defined, per American Heart Association guidelines, as mean systolic HBP ≥135 mm Hg or mean diastolic HBP ≥85 mm Hg. Of the 200 participants, 188 (94%) returned their home blood pressure monitors with valid data. The median number of HBP recordings was 10 (interquartile range, 7–14). Presurgical CBP thresholds of 140/90, 150/95, and 160/100 mm Hg yielded positive predictive values (95% confidence interval) for elevated HBP of 84.1% (0.78–0.89), 87.5% (0.81–0.92), and 94.6% (0.87–0.99), respectively. 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引用次数: 9
摘要
术前评估时测量血压(BP)已被认为是改善高血压纵向检测和治疗的一种方法。在这项评估中测量的血压与家庭血压(HBP)之间的关系尚不清楚,HBP是高血压的一个更好的指标。本研究的目的是确定术前血压对预测HBP升高的阳性预测值。我们前瞻性地在术前评估诊所招募了200名临床血压(CBPs)≥130/85 mm Hg的患者,使用先前验证的自动上臂设备(Welch Allyn生命体征监测仪6000系列)进行测量,在指标门诊就诊和手术当天之间进行每日血压监测(欧姆龙BP742N型)。根据美国心脏协会指南,HBP升高被定义为平均收缩压≥135毫米汞柱或平均舒张压≥85毫米汞柱。在200名参与者中,188名(94%)返回了带有有效数据的家庭血压计。HBP记录的中位数为10次(四分位数范围为7-14)。术前CBP阈值为140/90、150/95和160/100 mm Hg,对HBP升高的阳性预测值(95%置信区间)分别为84.1%(0.78-0.89)、87.5%(0.81-0.92)和94.6%(0.87-0.99)。相比之下,自我报告的血压控制、降压治疗、初级保健的可用性和术前疼痛评分显示与HBP升高不一致。术前CBP升高是纵向HBP升高的高度预测指标。术前评估时的血压测量可能为改善高血压的纵向检测和治疗提供了一种方法。
Elevated preoperative blood pressures in adult surgical patients are highly predictive of elevated home blood pressures
Blood pressure (BP) measurement during the presurgical assessment has been suggested as a way to improve longitudinal detection and treatment of hypertension. The relationship between BP measured during this assessment and home blood pressure (HBP), a better indicator of hypertension, is unknown. The purpose of the present study was to determine the positive predictive value of presurgical BP for predicting elevated HBP. We prospectively enrolled 200 patients at a presurgical evaluation clinic with clinic blood pressures (CBPs) ≥130/85 mm Hg, as measured using a previously validated automated upper-arm device (Welch Allyn Vital Sign Monitor 6000 Series), to undergo daily HBP monitoring (Omron Model BP742N) between the index clinic visit and their day of surgery. Elevated HBP was defined, per American Heart Association guidelines, as mean systolic HBP ≥135 mm Hg or mean diastolic HBP ≥85 mm Hg. Of the 200 participants, 188 (94%) returned their home blood pressure monitors with valid data. The median number of HBP recordings was 10 (interquartile range, 7–14). Presurgical CBP thresholds of 140/90, 150/95, and 160/100 mm Hg yielded positive predictive values (95% confidence interval) for elevated HBP of 84.1% (0.78–0.89), 87.5% (0.81–0.92), and 94.6% (0.87–0.99), respectively. In contrast, self-reported BP control, antihypertensive treatment, availability of primary care, and preoperative pain scores demonstrated poor agreement with elevated HBP. Elevated preoperative CBP is highly predictive of longitudinally elevated HBP. BP measurement during presurgical assessment may provide a way to improve longitudinal detection and treatment of hypertension.
期刊介绍:
Cessation.
The Journal of the American Society of Hypertension (JASH) publishes peer-reviewed articles on the topics of basic, applied and translational research on blood pressure, hypertension and related cardiovascular disorders and factors; as well as clinical research and clinical trials in hypertension. Original research studies, reviews, hypotheses, editorial commentary and special reports spanning the spectrum of human and experimental animal and tissue research will be considered. All research studies must have been conducted following animal welfare guidelines. Studies involving human subjects or tissues must have received approval of the appropriate institutional committee charged with oversight of human studies and informed consent must be obtained.