학술논문
Systemic inflammatory response syndrome in patients undergoing transcatheter aortic valve implantation.
Document Type
Academic Journal
Author
Syryca F; Department of Cardiology, German Heart Center Munich, Technical University of Munich, Munich, Germany.; Pellegrini C; Department of Cardiology, German Heart Center Munich, Technical University of Munich, Munich, Germany.; Rheude T; Department of Cardiology, German Heart Center Munich, Technical University of Munich, Munich, Germany.; Zobel F; Department of Cardiology, German Heart Center Munich, Technical University of Munich, Munich, Germany.; Kornhuber K; Department of Cardiology, German Heart Center Munich, Technical University of Munich, Munich, Germany.; Xhepa E; Department of Cardiology, German Heart Center Munich, Technical University of Munich, Munich, Germany.; Mayr NP; Institute of Anaesthesiology, German Heart Center Munich, Technical University of Munich, Germany.; Alvarez-Covarrubias HA; Department of Cardiology, German Heart Center Munich, Technical University of Munich, Munich, Germany; Hospital de Cardiología, Centro Médico Nacional Siglo XXI, IMSS, Ciudad de México, Mexico.; Holdenrieder S; Institute of Laboratory Medicine, German Heart Center Munich, Technical University of Munich, Germany.; Schunkert H; Department of Cardiology, German Heart Center Munich, Technical University of Munich, Munich, Germany; DZHK (German Center for Cardiovascular Research), Partner Site Munich Heart Alliance, Munich, Germany.; Thilo C; Department of Cardiology, RoMed Klinikum, Rosenheim, Germany.; Kastrati A; Department of Cardiology, German Heart Center Munich, Technical University of Munich, Munich, Germany; DZHK (German Center for Cardiovascular Research), Partner Site Munich Heart Alliance, Munich, Germany.; Joner M; Department of Cardiology, German Heart Center Munich, Technical University of Munich, Munich, Germany; DZHK (German Center for Cardiovascular Research), Partner Site Munich Heart Alliance, Munich, Germany. Electronic address: joner@dhm.mhn.de.
Source
Publisher: Elsevier Country of Publication: United States NLM ID: 101238551 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0938 (Electronic) Linking ISSN: 18780938 NLM ISO Abbreviation: Cardiovasc Revasc Med Subsets: MEDLINE
Subject
Language
English
Abstract
Background: Data on systemic inflammatory response syndrome (SIRS) after transcatheter aortic valve implantation (TAVI) are scarce and limited to small cohorts. We aimed to investigate its incidence and mid-term impact in a large cohort of TAVI patients.
Methods: From January 2018 to December 2020, 717 patients with severe aortic valve stenosis undergoing TAVI were included. SIRS was defined as fulfilling at least two of the following criteria within 48 h from the procedure: leucocyte count >12.0 or <4.0 × 109 /l, respiratory rate > 20 breaths per minute or PaCO 2 ≤ 4.3 kPa/32 mmHg, heart rate > 90 beats per minute and temperature > 38.0 °C or <36.0 °C. Clinical endpoints were 1-year rehospitalization for chronic heart failure (CHF) and 2-years all-cause mortality. Event rates during follow-up were calculated as Kaplan-Meier estimates.
Results: SIRS developed in 56.3 % (404/717) of patients after TAVI. SIRS occurred more frequently in patients with post-dilatation (SIRS 34.7 % (140/404) vs. no SIRS 23.3 % (73/313); p < 0.001) and major vascular complications (SIRS 16.1 % (65/404) vs. no SIRS 8.6 % (27/313); p = 0.004). Further, ICU days were more in patients who developed SIRS (SIRS 1.56 ± 1.50 days vs. no SIRS 1.22 ± 1.02 days; p = 0.001). At 2-years, all-cause mortality in the entire population was 23.9 %. However, there was no difference in CHF at 1-year (5.9 % vs. 4.1 %; log-rank = 0.347) nor in all-cause mortality at 2-years (22.0 % vs. 26.2 %; log-rank = 0.690) between the groups.
Conclusions: SIRS is a common finding after TAVI, which may prolong hospital stay but is without effect on mortality during 2-years follow-up.
Competing Interests: Declaration of competing interest Costanza Pellegrini reports receiving a personal research grant from Else Kröner Fresenius not related to the current work. Stiftung. Tobias Rheude received lecture fees from SIS Medical AG and AstraZeneca and travel support from SIS Medical AG (not related to the current work). Stefan Holdenrieder reports receiving research funding or honoraria from Roche Diagnostics, Bristol Myers Squibb, Merck KgaA, Sysmex Inostics and Volition SPRL. Michael Joner reports lecture fees and research grants from Edwards Lifesciences, Cardiac Dimensions, Infraredx, and Boston Scientific; is a consultant for Biotronik, Boston Scientific, Cardiac Dimensions, and Shockwave Medical; has received honoraria from Abbott, AstraZeneca, Biotronik, Boston Scientific, Edwards Lifesciences, Recor, Shockwave Medical, and Orbus Neich; and is a Member of the Board of Biotronik and Shockwave Medical. The other authors report no conflict of interest.
(Copyright © 2023 Elsevier Inc. All rights reserved.)
Methods: From January 2018 to December 2020, 717 patients with severe aortic valve stenosis undergoing TAVI were included. SIRS was defined as fulfilling at least two of the following criteria within 48 h from the procedure: leucocyte count >12.0 or <4.0 × 10
Results: SIRS developed in 56.3 % (404/717) of patients after TAVI. SIRS occurred more frequently in patients with post-dilatation (SIRS 34.7 % (140/404) vs. no SIRS 23.3 % (73/313); p < 0.001) and major vascular complications (SIRS 16.1 % (65/404) vs. no SIRS 8.6 % (27/313); p = 0.004). Further, ICU days were more in patients who developed SIRS (SIRS 1.56 ± 1.50 days vs. no SIRS 1.22 ± 1.02 days; p = 0.001). At 2-years, all-cause mortality in the entire population was 23.9 %. However, there was no difference in CHF at 1-year (5.9 % vs. 4.1 %; log-rank = 0.347) nor in all-cause mortality at 2-years (22.0 % vs. 26.2 %; log-rank = 0.690) between the groups.
Conclusions: SIRS is a common finding after TAVI, which may prolong hospital stay but is without effect on mortality during 2-years follow-up.
Competing Interests: Declaration of competing interest Costanza Pellegrini reports receiving a personal research grant from Else Kröner Fresenius not related to the current work. Stiftung. Tobias Rheude received lecture fees from SIS Medical AG and AstraZeneca and travel support from SIS Medical AG (not related to the current work). Stefan Holdenrieder reports receiving research funding or honoraria from Roche Diagnostics, Bristol Myers Squibb, Merck KgaA, Sysmex Inostics and Volition SPRL. Michael Joner reports lecture fees and research grants from Edwards Lifesciences, Cardiac Dimensions, Infraredx, and Boston Scientific; is a consultant for Biotronik, Boston Scientific, Cardiac Dimensions, and Shockwave Medical; has received honoraria from Abbott, AstraZeneca, Biotronik, Boston Scientific, Edwards Lifesciences, Recor, Shockwave Medical, and Orbus Neich; and is a Member of the Board of Biotronik and Shockwave Medical. The other authors report no conflict of interest.
(Copyright © 2023 Elsevier Inc. All rights reserved.)