Key result
Rheumatologic disease is linked to ~7% higher all-cause mortality in patients undergoing TAVR.
Why the study?
Patients with rheumatologic diseases present unique cardiovascular challenges due to systemic inflammation, but TAVR outcomes in this population remain poorly characterized.
Does transcatheter aortic valve replacement (TAVR) in patients with rheumatologic diseases increase all-cause mortality and cardiovascular complications compared to patients without rheumatologic diseases?
Cohort (n=8,894)
Yes
Does transcatheter aortic valve replacement (TAVR) in patients with rheumatologic diseases increase all-cause mortality and cardiovascular complications compared to patients without rheumatologic diseases?
TAVR in patients with rheumatologic diseases is associated with modestly higher all-cause mortality and significantly increased cardiovascular complications compared to matched non-RD patients.
Answers are grounded in this paper and cite their sources.
May warrant closer post-TAVR monitoring in rheumatologic disease; leaves open whether steroids or disease activity drive excess risk.
BACKGROUND Patients with rheumatologic diseases (RD) present unique challenges in cardiovascular care due to systemic inflammation and complex medical management. However, transcatheter aortic valve replacement (TAVR) outcomes in this population remain poorly characterized. METHODS Using the TriNetX database, we conducted a retrospective cohort study of patients undergoing TAVR between 2015 and 2023. Patients with RD (systemic lupus erythematosus, rheumatoid arthritis, or ankylosing spondylitis; n=4,447) were compared with non-RD patients (n=4,447) using 1:1 propensity score matching. The primary outcome was all-cause mortality. Secondary outcomes included major adverse cardiovascular and cerebrovascular events (MACCE), acute kidney injury, and other clinical endpoints. RESULTS After propensity matching, baseline characteristics were well-balanced. During follow-up, RD patients demonstrated higher all-cause mortality compared to non-RD patients (25.4% vs 23.2%; hazard ratio [HR] 1.069; [1.002-1.139]; P=0.043). Kaplan-Meier survival analysis showed gradual curve separation over time. RD patients experienced significantly higher rates of MACCE (41.9% vs 32.3%; HR 1.266; [1.062-1.511]; P=0.008), acute kidney injury (20.5% vs 18.0%; HR 1.140; [1.016-1.279]; P=0.025), myocardial infarction (11.9% vs 9.6%; HR 1.236; [1.083-1.410; P=0.004), and heart failure events (7.3% vs 6.1%; HR 1.195; [1.002-1.424]; P=0.047). In multivariable Cox regression of the entire matched cohort, prednisone use was associated with increased mortality (HR 1.215; [1.167-1.264]; P<0.001), while lipid-modifying agents showed protective effects (HR 0.947; [0.905-0.990]; P=0.016). CONCLUSIONS TAVR in RD patients was associated with modestly higher all-cause mortality and significantly increased cardiovascular complications compared to non-RD patients. Optimized medication management, particularly regarding corticosteroid use and lipid modification, may improve outcomes in this high-risk population.
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Bolaji et al. (2026) conducted a cohort in Rheumatologic diseases in patients undergoing transcatheter aortic valve replacement (n=8,894). Rheumatologic diseases (exposure) vs. Non-rheumatologic diseases was evaluated on All-cause mortality (HR 1.069, 95% CI 1.002-1.139, p=0.043). Patients with rheumatologic diseases undergoing TAVR had higher all-cause mortality compared to non-RD patients (25.4% vs 23.2%; HR 1.069; 95% CI 1.002-1.139; P=0.043).
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