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根据ANSI/AAMI SP10: 2002标准对Welch Allyn Spot生命体征血压测量仪进行验证。成功实现了准确性与成本效益的结合。

Validation of the Welch Allyn Spot Vital Signs blood pressure device according to the ANSI/AAMI SP10: 2002. Accuracy and cost-efficiency successfully combined.

作者信息

Alpert Bruce S

机构信息

University of Tennessee Health Science Center, Memphis, Tennessee 38105, USA.

出版信息

Blood Press Monit. 2007 Oct;12(5):345-7. doi: 10.1097/MBP.0b013e3282c9abf7.

Abstract

OBJECTIVES

To validate a significantly lower priced, new-generation blood pressure device by using the ANSI/AAMI SP10:2002 Standard evaluation.

METHODS

The Spot Vital Signs device evaluation was performed using the procedure specified in the SP10: 2002 American National Standard. Both obese and hypertensive participants were overrepresented in the study population.

RESULTS

The mean+/-standard deviation for the device readings compared with auscultation by paired, trained, blinded observers for systolic blood pressure was -1.0+/-4.1 mmHg; for diastolic blood pressure it was -0.4+/-6.1 mmHg. These passed AAMI criteria. The device, at a cost well below those of comparable professional-quality (vs. self measurement) electronic blood pressure devices, was extremely accurate.

CONCLUSIONS

The Welch Allyn Spot Vital Signs device provides a cost-effective alternative for medical-care delivery sites where accuracy and cost are both high priorities. The study population was oversampled for obese and hypertensive patients, the major target groups in whom blood pressure must be able to be recorded accurately to optimize diagnosis and management of cardiovascular disease.

摘要

目的

通过使用ANSI/AAMI SP10:2002标准评估来验证一款价格显著更低的新一代血压测量设备。

方法

使用SP10:2002美国国家标准中规定的程序对Spot Vital Signs设备进行评估。肥胖和高血压参与者在研究人群中占比过高。

结果

与经过配对、培训且不知情的观察者进行听诊相比,该设备测量的收缩压读数的均值±标准差为-1.0±4.1 mmHg;舒张压读数的均值±标准差为-0.4±6.1 mmHg。这些结果符合AAMI标准。该设备的成本远低于同类专业品质(与自我测量相比)的电子血压设备,且极其准确。

结论

Welch Allyn Spot Vital Signs设备为那些将准确性和成本都列为高度优先事项的医疗服务提供场所提供了一种经济高效的选择。该研究人群中肥胖和高血压患者的样本过多,而这两类人群是主要目标群体,在他们当中必须能够准确记录血压,以优化心血管疾病的诊断和管理。

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