Transcatheter Aortic Valve Replacement in Patients With or Without Active Cancer

Author:

Aikawa Tadao12ORCID,Kuno Toshiki34ORCID,Malik Aaqib H.5,Briasoulis Alexandros6ORCID,Kolte Dhaval7ORCID,Kampaktsis Polydoros N.8,Latib Azeem3ORCID

Affiliation:

1. Department of Cardiology Juntendo University Urayasu Hospital Urayasu Japan

2. Department of Radiology Jichi Medical University Saitama Medical Center Saitama Japan

3. Division of Cardiology, Montefiore Medical Center Albert Einstein College of Medicine New York NY USA

4. Division of Cardiology, Jacobi Medical Center Albert Einstein College of Medicine New York NY USA

5. Department of Cardiology Westchester Medical Center Valhalla NY USA

6. Division of Cardiovascular Medicine, Section of Heart Failure and Transplantation University of Iowa Iowa City IA USA

7. Division of Cardiology Massachusetts General Hospital and Harvard Medical School Boston MA USA

8. Division of Cardiology Columbia University Irving Medical Center New York NY USA

Abstract

Background Data on clinical outcomes after transcatheter aortic valve replacement (TAVR) in specific cancer types or the presence of metastatic disease remain sparse. This study aimed to investigate the impact of active cancer on short‐term mortality, complications, and readmission rates after TAVR across different cancer types. Methods and Results The authors assessed the Nationwide Readmissions Database for TAVR cases from 2012 to 2019. Patients were stratified by specific cancer types. Primary outcome was in‐hospital mortality. Secondary outcomes included bleeding requiring blood transfusion and readmissions at 30, 90, and 180 days after TAVR. Overall, 122 573 patients undergoing TAVR were included in the analysis, of whom 8013 (6.5%) had active cancer. After adjusting for potential confounders, the presence of active cancer was not associated with increased in‐hospital mortality (adjusted odds ratio [aOR], 1.06 [95% CI, 0.89–1.27]; P =0.523). However, active cancer was associated with an increased risk of readmission at 30, 90, and 180 days after TAVR and increased risk of bleeding requiring transfusion at 30 days. Active colon and any type of metastatic cancer were individually associated with readmissions at 30, 90, and 180 days after TAVR. At 30 days after TAVR, colon (aOR, 2.51 [95% CI, 1.68–3.76]; P <0.001), prostate (aOR, 1.40 [95% CI, 1.05–1.86]; P =0.021), and any type of metastatic cancer (aOR, 1.65 [95% CI, 1.23–2.22]; P =0.001) were individually associated with an increased risk of bleeding requiring transfusion. Conclusions Patients with active cancer had similar in‐hospital mortality after TAVR but higher risk of readmission and bleeding requiring transfusion, the latter depending on certain types of cancer.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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