Key result
Rapid post-transplant vasculopathy on IVUS is linked to ~2.4-fold higher all-cause mortality.
Why the study?
Does rapidly progressive vasculopathy detected by IVUS predict all-cause mortality and MI in cardiac transplant patients?
Cohort (n=143)
Does rapidly progressive vasculopathy detected by IVUS predict all-cause mortality and MI in cardiac transplant patients?
Absolute Event Rate: 26% vs 11%
p-value: p=0.03
Rapidly progressive vasculopathy detected by IVUS within the first year after cardiac transplantation is a powerful predictor of long-term all-cause mortality and myocardial infarction.
OBJECTIVES: The aim of this study was to determine whether angiographically silent early coronary intimal thickening could predict long-term morbidity and mortality. BACKGROUND: Although intravascular ultrasound (IVUS) is widely used to detect early transplant coronary disease, its prognostic significance has not been well defined. METHODS: The study cohort consisted of 143 patients who underwent early multivessel (2.1 +/- 0.7 arteries/patient) IVUS examination 1.0 +/- 0.5 month and 12.0 +/- 1.0 month after transplantation. The change in intimal thickness was evaluated using paired analysis of 1,069 matched sites. Rapidly progressive vasculopathy was defined as the change in intimal thickness >/=0.5 mm. Patients were followed for a primary end point of all-cause mortality and a secondary composite end point of mortality and nonfatal myocardial infarction (MI). Angiographic disease, defined as any >/=50% diameter stenosis, was assessed in 126 patients. RESULTS: Intravascular ultrasound at one year demonstrated rapid progression in 54 (37%) of 143 patients and new lesions in 67 (47%) of 143 of patients. At a mean clinical follow-up of 5.9 years, more patients with rapidly progressive vasculopathy died, as compared with those without (26% vs. 11%, p = 0.03). Death and MI also occurred more frequently among those with rapid progression than in those without it (51% vs. 16%, p < 0.0001). There was no significant difference in outcome in patients with and without donor-transmitted lesions. Angiographic disease was found in 11 (22%) of 50 patients with and in 2 (2.1%) of 76 patients without (p = 0.003) rapidly progressive vasculopathy. The IVUS-defined rapid progression correlated highly with future development of angiographic disease (p = 0.0005). CONCLUSIONS: Rapidly progressive vasculopathy by IVUS, defined as an increase of >/=0.5 mm in intimal thickness within the first year after transplantation, is a powerful predictor of all-cause mortality, MI, and angiographic abnormalities. Accordingly, such patients may be candidates for more aggressive anti-atherosclerotic and/or immunosuppressive therapy.
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Tuzcu et al. (2005) conducted a cohort in Cardiac transplantation (n=143). Rapidly progressive vasculopathy (≥0.5 mm intimal thickening by IVUS) vs. No rapidly progressive vasculopathy was evaluated on All-cause mortality (p=0.03). Rapidly progressive vasculopathy (≥0.5 mm intimal thickening by IVUS at 1 year) after cardiac transplantation predicted higher all-cause mortality compared to no rapid progression (26% vs. 11%, p=0.03).
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