Key result
Baseline RV dysfunction during Impella-supported high-risk PCI predicts higher 90-day MACCE and 1-year mortality.
Why the study?
The impact of baseline right ventricular dysfunction on clinical outcomes of patients undergoing high-risk percutaneous coronary intervention supported by Impella was unknown.
Does baseline right ventricular dysfunction worsen clinical outcomes in patients undergoing high-risk PCI supported by Impella?
Observational (n=239)
Yes
Does baseline right ventricular dysfunction worsen clinical outcomes in patients undergoing high-risk PCI supported by Impella?
Baseline right ventricular dysfunction is associated with higher 90-day MACCE and 1-year mortality in patients undergoing Impella-supported high-risk PCI, despite similar procedural success.
May warrant enhanced pre-Impella RV assessment; leaves open whether RV-targeted strategies improve outcomes in prospective trials.
BACKGROUND: Right ventricular dysfunction (RVD) is an important prognostic factor in several cardiac conditions, including acute and chronic heart failure. The impact of baseline RVD on clinical outcomes of patients undergoing high-risk percutaneous coronary intervention (HRPCI) supported by Impella is unknown. METHODS: Patients from the single-arm, multicenter PROTECT III study of Impella-supported HRPCI were stratified based on the presence or absence of RVD. RVD was quantitatively assessed by an echocardiography core laboratory and was defined as fractional area change < 35%, tricuspid annular plane systolic excursion < 17 mm or pulsed-wave Doppler S-wave of the lateral tricuspid annulus < 9.5 cm/s. Procedural outcomes, 90-day major adverse cardiac and cerebrovascular events (MACCE: the composite of all-cause mortality, myocardial infarction, stroke/TIA, and repeat revascularization), and 1-year mortality were assessed. RESULTS: Of the 239 patients who underwent RV function assessment, 124 were found to have RVD. Lower left ventricular ejection fraction, higher blood urea nitrogen levels, and more severe RV dilation were independently associated with RVD. The incidence of hypotensive episodes during PCI, the proportion of patients requiring prolonged Impella support, the completeness of revascularization, and the rate of in-hospital mortality did not differ significantly between patients with vs without RVD. However, 90-day MACCE rates were higher in those with RVD, and RVD was a robust predictor of 1-year mortality in multivariable Cox-regression analyses. CONCLUSION: In patients undergoing HRPCI with Impella, RVD was associated with more advanced biventricular failure. The use of Impella support during HRPCI facilitated effective revascularization, even in those with concomitant RVD. Nevertheless, RVD was associated with unfavorable long-term prognoses.
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Rommel et al. (2024) conducted an observational in High-risk percutaneous coronary intervention (n=239). Right ventricular dysfunction vs. No right ventricular dysfunction was evaluated on 90-day major adverse cardiac and cerebrovascular events (MACCE) and 1-year mortality. Baseline right ventricular dysfunction (n=124) in patients undergoing Impella-supported high-risk PCI was associated with higher 90-day MACCE rates and predicted 1-year mortality.
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