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    In: Catheterization and Cardiovascular Interventions, Wiley, Vol. 92, No. 6 ( 2018-11-15), p. 1063-1074
    Kurzfassung: The prognostic value of physiological indices in non‐ST‐segment elevation acute coronary syndrome (NSTE‐ACS) patients undergoing percutaneous coronary intervention (PCI) is unknown. We investigated the prognostic efficacy of physiological indices obtained after PCI in patients with NSTE‐ACS. Methods Eighty‐three patients (men: n  = 70, age: 63.7 ± 9.7 years) undergoing PCI for NSTE‐ACS within 48 hr postadmission were investigated. Fractional flow reserve (FFR), coronary flow reserve (CFR), and the index of microcirculatory resistance (IMR) of the culprit vessels were measured after the completion of PCI. The patients were clinically followed up to determine major cardiac adverse events (MACE), including death, congestive heart failure requiring hospitalization, and remote coronary revascularization. Results The median FFR, CFR, and IMR values were 0.90 (interquartile range [IQR] 0.86–0.95), 2.38 (IQR 1.75–4.17), and 22.9 (IQR 11.2–31.5), respectively. During a median follow‐up of 20.7 months, 19 MACEs (22.9%) were documented. No significant difference in baseline patient characteristics, except for age, was detected between patients with and without MACE. Patients with MACE showed higher IMR and lower CFR than those without (IMR: 27.2 vs. 16.3; P  = 0.001, CFR: 1.82 vs. 2.55; P  = 0.04), whereas FFR was not significantly different (0.92 vs. 0.89; P  = 0.72), irrespective of the MACE occurrence. Post‐PCI IMR was the only independent predictor of MACE (hazard ratio 1.033, 95% confidence interval 1.013–1.052, P  = 0.001). The MACE‐free survival was significantly worse in patients with high post‐PCI IMR (χ 2 7.12; P  = 0.008). Conclusion Post‐PCI IMR may help identify patients at high risk for subsequent adverse coronary events who require adjunctive therapeutic strategies.
    Materialart: Online-Ressource
    ISSN: 1522-1946 , 1522-726X
    URL: Issue
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2018
    ZDB Id: 2001555-0
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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