Mazze R S, Simonson G D, Robinson R L, Kendall D M, Idrogo M A, Adlis S A, Boyce K S, Dunne C J, Anderson R L, Bergenstal R M
International Diabetes Center and the University of Minnesota Medical School, Minneapolis, MN 55416, USA.
Diabet Med. 2003 Sep;20(9):752-7.
To determine the relationship between blood pressure (BP) measurement in the clinic and self-monitored blood pressure (SMBP); and to evaluate the accuracy of self-reported data in patients with Type 2 diabetes treated intensively for hypertension.
Seventy subjects had baseline and 1-week follow-up clinic BP measured using an Omron 907 automated device. During a contemporaneous 14-day period these subjects measured their BP at least four times each day using an Omron IC semiautomatic portable monitor which, unknown to them, contained an onboard memory capable of storing BP with corresponding time and date.
There was no significant difference between mean clinic and mean self-monitored BP. Correlations between clinic BP and SMBP were r=0.61 (P<0.0001) for systolic BP and r=0.69 (P<0.0001) for diastolic BP. Clinic BP classified 56 subjects as uncontrolled hypertension (BP > or = 130/80 mmHg, adjusted for diabetes) and 14 subjects as controlled hypertension. Using World Health Organization-International Society of Hypertension criteria for SMBP (> or = 125/75 mmHg), 55 cases of clinic classified uncontrolled hypertension were confirmed, resulting in 98% sensitivity. Clinic and SMBP agreed in one case of controlled hypertension, resulting in 7% specificity. For all subjects, the median percent of values exceeding SMBP criteria for controlled hypertension was systolic 92% and diastolic 70%. Self-reporting precision averaged 89+/-10% (range 45-100%); under-reporting was 25+/-16% (ranging from 0 to 56%) and over-reporting was 12+/-15% (ranging from 0 to 46%). The overall logbook mean was not significantly different from the downloaded data from the Omron IC(R) monitors.
SMBP was able to identify 13 patients with uncontrolled hypertension who, by clinic BP measurement, had been classified as controlled.
确定诊室血压(BP)测量与自我监测血压(SMBP)之间的关系;并评估强化治疗高血压的2型糖尿病患者自我报告数据的准确性。
70名受试者使用欧姆龙907自动设备测量基线血压和1周随访时的诊室血压。在同期的14天内,这些受试者使用欧姆龙IC半自动便携式监测仪每天至少测量4次血压,他们并不知道该监测仪内置有能够存储血压及相应时间和日期的存储器。
诊室平均血压与自我监测平均血压之间无显著差异。诊室收缩压与SMBP之间的相关性为r = 0.61(P < 0.0001),舒张压与SMBP之间的相关性为r = 0.69(P < 0.0001)。根据诊室血压,56名受试者被归类为高血压未控制(血压≥130/80 mmHg,根据糖尿病情况进行调整),14名受试者被归类为高血压已控制。使用世界卫生组织 - 国际高血压学会的SMBP标准(≥125/75 mmHg),55例诊室分类为高血压未控制的病例得到确认,灵敏度为98%。诊室血压与SMBP在1例高血压已控制病例中一致,特异性为7%。对于所有受试者,超过高血压已控制SMBP标准值的中位数百分比,收缩压为92%,舒张压为70%。自我报告的精确度平均为89±10%(范围45 - 100%);少报为25±16%(范围0至56%),多报为12±15%(范围0至46%)。日志总体平均值与从欧姆龙IC监测仪下载的数据无显著差异。
SMBP能够识别出13名高血压未控制患者,而根据诊室血压测量,这些患者被归类为高血压已控制。