Background: Infiltrative diseases (IDs), including amyloidosis, sarcoidosis, and hemochromatosis, are characterized by abnormal cellular infiltration in multiple organs, including the heart. The prognosis of percutaneous coronary intervention (PCI) patients with underlying IDs has not been well-studied. We evaluated the prevalence of IDs in patients undergoing PCI and their association with post-PCI outcomes.
Methods: The National Inpatient Sample (NIS) 2016-2020 database was used to identify PCI patients with ICD-10 codes for a retrospective analysis. PCI patients were then divided into those with and without underlying IDs, which included amyloidosis, sarcoidosis, and hemochromatosis. Multivariable logistic regression was performed for composite post-PCI outcomes analyses.
Results: Among 2,360,860 patients admitted to undergo PCI, 7855 patients had underlying IDs. The highest prevalence was observed for sarcoidosis (0.2%) followed by hemochromatosis (0.07%) and amyloidosis (0.04%). Underlying amyloidosis was associated with worse composite post-PCI outcomes (odds ratio [OR], 1.6; 95% CI, 1.1-2.44; = .02), including higher in-hospital mortality (OR, 1.9; 95% CI, 1.1-3.4; = .04), higher risk of intra/post-PCI stroke (OR, 4.0; 95% CI, 1.1-16.0; = .04), but not major bleeding (OR, 2.2; 95% CI, 0.97-5.03; = .058). In contrast, underlying sarcoidosis (OR, 1.1; 95% CI, 0.87-1.41; = .4), and hemochromatosis (OR, 1.18; 95% CI, 0.77-1.8; = .44) were not associated with composite post-PCI outcomes. Amyloidosis patients undergoing PCI also had higher hospitalization charges ($212,123 vs $141,137; = .03) and longer length of stay (8.2 vs 3.9 days; < .001).
Conclusions: Underlying amyloidosis was associated with worse post-PCI outcomes including higher in-hospital mortality, intra/post-PCI stroke, and socioeconomic burden. A multidisciplinary approach and future studies are needed to investigate the screening and treatment strategies in these patients.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11308414 | PMC |
http://dx.doi.org/10.1016/j.jscai.2023.101267 | DOI Listing |
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