Why the study?
Does a handheld ultrasound device accurately evaluate aortic stenosis severity compared to standard echocardiography in patients with suspected severe aortic stenosis?
Does a handheld ultrasound device accurately evaluate aortic stenosis severity compared to standard echocardiography in patients with suspected severe aortic stenosis?
Handheld echocardiography provides comparable diagnostic accuracy to standard echocardiography for evaluating the severity of aortic stenosis.
Handheld devices yield comparable aortic stenosis metrics; supports validation studies but should not yet alter clinical decision-making.
BACKGROUND: Symptomatic severe aortic stenosis is associated with increased mortality and morbidity. Early identification of these patients by echocardiography is crucial. We conducted this study to evaluate a handheld ultrasound device (HCU) in patients with suspected severe aortic stenosis (AS) in comparison to a standard echocardiography device (SE). METHODS: A HCU (Vivid I; GE Healthcare) and a SE device (Philips iE 33) were used to evaluate 50 consecutive patients with suspected severe AS. Two consecutive echocardiographic studies were performed by two experienced and blinded examiners using HCU and SE device. AS was graded by mean transaortic pressure, aortic valve area (AVA), and indexed AVA (AVA adjusted for body surface area). RESULTS: Mean difference for mean transaortic gradient, AVA and indexed AVA for the SE and HCU device were 1.28 mmHg (-0.70 to 3.26 mmHg), -0.02 cm(2) (-0.06 to 0.01 cm(2)), and -0.01 cm(2)/m(2) (-0.03 to 0.01 cm(2)/m(2)), respectively. Discrepancies between both devices were not associated with misinterpretation of the degree of AS. CONCLUSION: Our study demonstrates that HCU can be used to evaluate patients with suspected AS. (ECHOCARDIOGRAPHY 2010;27:481-486).
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Schaefer et al. (2010) studied this question.
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