Percutaneous coronary intervention in patients with cardiac allograft vasculopathy: a Nationwide Inpatient Sample (NIS) database analysis.
Waqas UllahNishant ThalambeduSalman ZahidMuhammad Zia KhanTanveer MirSohaib Sanan RoomiDavid L FischmanSalim S ViraniMahboob AlamPublished in: Expert review of cardiovascular therapy (2021)
Cardiac allograft vasculopathy (CAV) is a major cause of heart transplant failure and mortality. The role of percutaneous coronary intervention (PCI) in these patients remains unknown.Methods: The National Inpatient Sample (NIS) (2015-2017) was queried to identify all cases of CAV. The merits of PCI were determined using a propensity-matched multivariate logistic regression model. Adjusted odds ratios (aOR) for in-hospital complications were calculated.Results: A total of 2,380 patients (PCI 185, no-PCI 21,95) with CAV were included in the analysis. There was no significant difference in the odds of major bleeding (OR 1.87, 95% CI 0.94-3.7, P = 0.11), post-procedure bleeding (P = 0.37), cardiogenic shock (OR 0.87, 95% CI 0.45-1.69, P = 0.80), acute kidney injury (uOR 0.92, 95% CI 0.68-1.24, P = 0.64), cardiopulmonary arrest (OR 0.84, 95% CI 0.34-2.11, P = 0.88), and in-hospital mortality (OR 1.59, 95% CI 0.91-2.79, P = 0.14) between patients undergoing PCI compared to those treated conservatively. A propensity-matched analysis closely followed the results of unadjusted crude analysis.Conclusion: PCI in CAV may be associated with increased in-hospital complications and higher resource utilization.
Keyphrases
- percutaneous coronary intervention
- acute coronary syndrome
- coronary artery disease
- acute myocardial infarction
- st segment elevation myocardial infarction
- st elevation myocardial infarction
- atrial fibrillation
- antiplatelet therapy
- acute kidney injury
- coronary artery bypass grafting
- ejection fraction
- end stage renal disease
- patients undergoing
- risk factors
- healthcare
- type diabetes
- heart failure
- prognostic factors
- cardiac surgery
- cross sectional
- adverse drug
- cell cycle