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Fractional Flow Reserve in End-Stage Liver Disease

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Journal Am J Cardiol
Date 2021 Dec 24
PMID 34949471
Citations 1
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Abstract

Fractional flow reserve (FFR) determines the functional significance of epicardial stenoses assuming negligible venous pressure (P) and microvascular resistance. However, these assumptions may be invalid in end-stage liver disease (ESLD) because of fluctuating P and vasodilation. Accordingly, all patients with ESLD who underwent right-sided cardiac catheterization and coronary angiography with FFR as part of their orthotopic liver transplantation evaluation between 2013 and 2018 were included in the present study. Resting mean distal coronary pressure (P)/mean aortic pressure (P), FFR, and P were measured. FFR accounting for P (FFR - P) was defined as (P - P)/(P - P). The hyperemic effect of adenosine was defined as resting P/P - FFR. The primary outcome was all-cause mortality at 1 year. In 42 patients with ESLD, 49 stenoses were interrogated by FFR (90% were <70% diameter stenosis). Overall, the median model for ESLD score was 16.5 (10.8 to 25.5), FFR was 0.87 (0.81 to 0.94), P was 8 mm Hg (4 to 14), FFR-P was 0.86 (0.80 to 0.94), and hyperemic effect of adenosine was 0.06 (0.02 to 0.08). FFR-P led to the reclassification of 1 stenosis as functionally significant. There was no significant correlation between the median model for ESLD score and the hyperemic effect of adenosine (R = 0.10). At 1 year, 13 patients had died (92% noncardiac in etiology), and patients with FFR ≤0.80 had significantly higher all-cause mortality (73% vs 17%, p = 0.001. In conclusion, in patients with ESLD who underwent orthotopic liver transplantation evaluation, P has minimal impact on FFR, and the hyperemic effect of adenosine is preserved. Furthermore, even in patients with the predominantly angiographically-intermediate disease, FFR ≤0.80 was an independent predictor of all-cause mortality.

Citing Articles

[Abdominal organ transplantation in multimorbid patients].

Bauschke A, Ali-Deeb A, Dondorf F, Rauchfuss F, Rohland O, Settmacher U Chirurgie (Heidelb). 2024; 96(2):124-129.

PMID: 39643669 DOI: 10.1007/s00104-024-02201-y.