How Important is the Impact of Pressure Recovery on Routine Evaluation of Aortic Stenosis? A Clinical Study in 91 Patients Karl Isaaz, Olivier Gaillard, Alexis Cerisier, Antoine Da Costa,
Emmanuel Faure, Michel Lamaud, Claude Gerenton |
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Background and aim of the study: Experimental
investigations and invasive studies conducted in small series of patients
using specially designed high-fidelity micromanometer tip catheters have
suggested that downstream pressure recovery (PR) within the aorta may
significantly affect transvalvular pressure gradient (PG) measurement.
The study aims were to evaluate in a large cohort of patients the extent
of PR when transvalvular PGs are routinely measured by fluid-filled pigtail
side-hole catheters (FPC) using pullback from the left ventricle to the
ascending aorta (AO), and to analyze factors influencing PR. The influence
of PR on the correlation between catheter and Doppler PG measurements
was also assessed in a subset of patients. |
Results: Mean PR ranged from 0 to 20 mmHg, corresponding
to a PR index (percent of maximal PG) ranging from 0 to 31%. PG was <50
mmHg in nine of 61 patients (15%) with a PG >50 mmHg at the origin of
the aorta when further measurements were conducted with the catheter positioned
more distally in the ascending aorta. PR index better correlated with the
ratio of valve area to ascending AO cross-sectional area (r = 0.61, p =
0.001) than with valve area (r = 0.37, p = 0.001) and ascending AO cross-sectional
area (0.27, p = 0.02) alone. Differences between Doppler- and catheter-predicted
PG were minimized when correcting Doppler by non-invasively calculated
PR (p <0.0001). Conclusion: The magnitude of PR recorded in aortic stenosis by FPC, as used in most clinical catheterization laboratories, is low in the vast majority of patients. As predicted from fluid mechanics theory, the ratio of valve area to ascending AO cross-sectional area is the central determinant of PR. PR may affect the Doppler-catheter correlation in some patients. The Journal of Heart Valve Disease 2004;13:347-356 |
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