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Accuracy of Blood Pressure Measurement Devices in Pregnancy: A Systematic Review of Validation Studies

机译:妊娠期血压测量设备的准确性:对验证研究的系统评价

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摘要

The accurate measurement of blood pressure in pregnancy is essential to guide medical decision making that affects both mother and fetus. The aim of this systematic review was to determine the accuracy of ambulatory, home, and clinic blood pressure measurement devices in pregnant women. We searched Ovid MEDLINE, The Cochrane Library, EMBASE, CINAHL EBSCO, Clinicaltrials.gov, International Clinical Trials Registry Platform, and dabl from inception through August 3, 2017 for articles that assessed the validity of an upper arm blood pressure measurement device against a mercury sphygmomanometer in pregnant women. Two independent investigators determined eligibility, extracted data, and adjudicated protocol violations. From 1,798 potential articles identified, 41, that assessed 28 devices, met the inclusion criteria. Most articles (N= 32) followed a standard or modified American National Standards Institute/Association for the Advancement of Medical Instrumentation/International Organization for Standardization, British Hypertension Society, or European Society of Hypertension validation protocol. Several articles described the results of validation studies performed on more than one device (N=7) and/or in more than one population of pregnant women (N=12), comprising 64 pairwise validity assessments. The device was validated in 61% (32 of 52) of studies which used a standard or modified protocol. Only 34% (11 of 32) of the studies wherein the device was successfully validated were performed without a protocol violation. Given the implications of inaccurate blood pressure measurement in pregnant women, healthcare providers should be aware of and try to use the blood pressure measurement devices which have been properly validated in this population.
机译:怀孕期间血压的准确测量对于指导影响母亲和胎儿的医学决策至关重要。该系统评价的目的是确定孕妇的门诊,家庭和诊所血压测量设备的准确性。从开始到2017年8月3日,我们搜索了Ovid MEDLINE,Cochrane图书馆,EMBASE,CINAHL EBSCO,Clinicaltrials.gov,International Clinical Trials Registry Platform和dabl,以评估评估上臂血压测量装置对汞的有效性的文章。孕妇血压计。两名独立调查员确定了资格,提取了数据并裁定违反协议。在确定的1,798篇潜在文章中,有41篇评估了28项设备,符合纳入标准。大多数文章(N = 32)遵循标准或经修改的美国国家标准协会/医疗仪器发展协会/国际标准化组织,英国高血压学会或欧洲高血压学会的验证协议。几篇文章描述了对不止一种设备(N = 7)和/或不止一种孕妇(N = 12)进行的验证研究的结果,包括64个成对有效性评估。使用标准或经过修改的协议的61%(52项中的32项)研究对该设备进行了验证。在不违反协议的情况下,仅进行了34%(32个中的11个)成功验证了设备的研究。考虑到孕妇血压测量不准确的含义,医疗保健提供者应意识到并尝试使用已在该人群中正确验证的血压测量设备。

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