Rheumatoid arthritis

Outcomes with transcatheter aortic valve replacement for aortic stenosis in rheumatoid arthritis: an observational study

Rheumatology (Oxford)Published Retrospective cohort study

Main finding · All-cause mortalityResult — go to the resultOdds ratio 1.29 95% CI 0.73–2.29

Authors' conclusion

In this large observational study, TAVR was not associated with excess short- or long-term risk in patients with RA.

Study context

Population
Participants with aortic stenosis undergoing transcatheter aortic valve replacement (TAVR), TriNetX Research Network1,374 per cohort after matching
Participants
1,374 vs 1,374
Exposure
TAVR in RA vs without RA
  • RA+n = 1,374
  • RA-n = 1,374reference
Outcome
30-day all-cause mortality
Follow-up
30 days
Methodological detailsmulticentre registry (TriNetX Research Network), matched, Cox regression, Before matching: 1414 RA+ (4.3%) and 39 004 RA- eligible
  • Multicentre registry (TriNetX Research Network)
  • Matched
  • Cox regression
  • Before matching: 1414 RA+ (4.3%) and 39 004 RA- eligible

Main finding

All-cause mortality

Odds ratio

1.29

95% CI 0.73–2.29

By group

RA+vs RA-
OR 1.29 (95% CI 0.73–2.29)

As reported in the abstract

Observational data: associations, not effects.

Further findings

Other 30-day endpoints (permanent pacemaker implantation, ischaemic stroke, acute kidney injury, MI, cardiogenic shock, major vascular complications, major or life-threatening bleeding)

No significant differences in other endpoints
  • Matched cohort

Stroke, MI and hospitalization · 5 years

Similar between RA+ and RA-; Hazard ratios (HRs) concordant with OR estimates
  • Matched cohort

Outcomes by sex (RA patients, sex-based analyses)

Outcomes did not differ by sex

Parts of this Brief are withheld: the automatic checks could not confirm them against the abstract.

Original publication

Outcomes with transcatheter aortic valve replacement for aortic stenosis in rheumatoid arthritis: an observational study. Rheumatology (Oxford). Published 28 April 2026. doi:10.1093/rheumatology/keag234

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