通用标准是否接受之前经过验证的血压自我测量设备?系统回顾。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Estefanie Siqueira Vigato de Oliveira, Nila Larisse Silva de Albuquerque, Priscila Rangel Dordetto, José Luiz Tatagiba Lamas
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引用次数: 0

摘要

本研究旨在分析针对普通人群验证的示波测量血压装置是否可被视为符合《通用标准》标准。研究人员对截至 2023 年 9 月的 9 个数据库进行了系统性检索,其中包括 32 项关于用于自我测量的无创臂带式血压计的验证研究。最常见的是英国高血压学会协议(68%),其次是医学仪器促进协会协议(40%)。大多数设备符合通用标准准则 1,但只有 17 台(53%)符合准则 2。很少有研究详细说明袖带的选择、按臂围划分的参与者人数或按袖带分组划分的方法之间的差异。由于验证方案之间存在很大差异,53% 的分析设备是根据通用标准批准的。这项研究有助于扩大通用标准下的自我测量设备验证库。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Are previously validated blood pressure self-measurement devices accepted under the Universal Standard? A systematic review.

This study aimed to analyze whether oscillometric blood pressure devices validated for the general population may be considered approved under Universal Standard criteria. A systematic review was conducted, with searches in nine databases, up to September 2023, including 32 validation studies of noninvasive arm cuff devices for self-measurement. The British Hypertension Society protocol was most common (68%), followed by the Association for the Advancement of Medical Instrumentation (40%). Most devices met Universal Standard criterion 1, but only 17 (53%) met criterion 2. Few studies contained details about the choice of cuffs, the number of participants by arm circumference, or the differences between methods by cuff subgroup. Due to the considerable differences between validation protocols, 53% of the devices analyzed were approved under the Universal Standard. The study contributes to expanding the validated pool of self-measurement devices under the Universal Standard.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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