TY - JOUR
T1 - Infective Endocarditis Caused by Staphylococcus aureus After Transcatheter Aortic Valve Replacement
AU - del Val, David
AU - Abdel-Wahab, Mohamed
AU - Mangner, Norman
AU - Durand, Eric
AU - Ihlemann, Nikolaj
AU - Urena, Marina
AU - Pellegrini, Costanza
AU - Giannini, Francesco
AU - Gasior, Tomasz
AU - Wojakowski, Wojtek
AU - Landt, Martin
AU - Auffret, Vincent
AU - Sinning, Jan Malte
AU - Cheema, Asim N.
AU - Nombela-Franco, Luis
AU - Chamandi, Chekrallah
AU - Campelo-Parada, Francisco
AU - Munoz-Garcia, Erika
AU - Herrmann, Howard C.
AU - Testa, Luca
AU - Won-Keun, Kim
AU - Castillo, Juan Carlos
AU - Alperi, Alberto
AU - Tchetche, Didier
AU - Bartorelli, Antonio L.
AU - Kapadia, Samir
AU - Stortecky, Stefan
AU - Amat-Santos, Ignacio
AU - Wijeysundera, Harindra C.
AU - Lisko, John
AU - Gutiérrez-Ibanes, Enrique
AU - Serra, Vicenç
AU - Salido, Luisa
AU - Alkhodair, Abdullah
AU - Vendramin, Igor
AU - Chakravarty, Tarun
AU - Lerakis, Stamatios
AU - Vilalta, Victoria
AU - Regueiro, Ander
AU - Romaguera, Rafael
AU - Kappert, Utz
AU - Barbanti, Marco
AU - Masson, Jean Bernard
AU - Maes, Frédéric
AU - Fiorina, Claudia
AU - Miceli, Antonio
AU - Kodali, Susheel
AU - Ribeiro, Henrique B.
AU - Mangione, Jose Armando
AU - Sandoli de Brito, Fabio
AU - Actis Dato, Guglielmo Mario
AU - Rosato, Francesco
AU - Ferreira, Maria Cristina
AU - Corriea de Lima, Valter
AU - Colafranceschi, Alexandre Siciliano
AU - Abizaid, Alexandre
AU - Marino, Marcos Antonio
AU - Esteves, Vinicius
AU - Andrea, Julio
AU - Godinho, Roger R.
AU - Alfonso, Fernando
AU - Eltchaninoff, Helene
AU - Søndergaard, Lars
AU - Himbert, Dominique
AU - Husser, Oliver
AU - Latib, Azeem
AU - Le Breton, Hervé
AU - Servoz, Clement
AU - Pascual, Isaac
AU - Siddiqui, Saif
AU - Olivares, Paolo
AU - Hernandez-Antolin, Rosana
AU - Webb, John G.
AU - Sponga, Sandro
AU - Makkar, Raj
AU - Kini, Annapoorna S.
AU - Boukhris, Marouane
AU - Gervais, Philippe
AU - Linke, Axel
AU - Crusius, Lisa
AU - Holzhey, David
AU - Rodés-Cabau, Josep
N1 - Funding Information:
Dr del Val was supported by a research grant from the Fundación Alfonso Martin Escudero (Madrid, Spain). Dr Rodés-Cabau holds the Research Chair “Fondation Famille Jacques Larivière” for the Development of Structural Heart Disease Interventions. The authors have no funding sources to declare. Dr Rodés-Cabau has received institutional research grants from Edwards Lifesciences, Medtronic, and Boston Scientific. Dr Tchetche has reported consulting fees from Abbott Vascular, Boston Scientific, Edwards Lifesciences, and Medtronic. Dr Herrmann has received institutional research grants from Abbott, Boston Scientific, Edwards Lifesciences, and Medtronic and consulting fees from Edwards Lifesciences and Medtronic. Dr Webb has has received consulting fees from Edwards Lifesciences and St Jude Medical. Dr Makkar has received research grants from Edwards Lifesciences, Medtronic, Abbott, Capricor, and St Jude Medical, has served as a proctor for Edwards Lifesciences, and has received consulting fees from Medtronic. Dr de Brito has received honoraria from Medtronic and Edwards Lifesciences for symposium speeches and proctoring cases. Dr Lerakis has received consulting fees from Edwards Lifesciences. Dr Le Breton has received lecture fees from Edwards Lifesciences, outside the submitted work. Dr Sinning has received speaker honoraria from Abbott, Boston Scientific, Edwards Lifesciences, and Medtronic and research grants from Boston Scientific, Edwards Lifesciences, and Medtronic, outside the submitted work. Dr Won-Keun has received personal fees from Boston Scientific, Edwards Lifesciences, Abbott, Medtronic, and Meril, outside the submitted work. Dr Stortecky reports grants to his institution from Edwards Lifesciences, Medtronic, Boston Scientific, and Abbott and has received personal fees from Boston Scientific, BTG, and Teleflex, outside the submitted work. Dr Husser has received personal fees from Boston Scientific and payments from Abbott. Dr Mangner has received personal fees from Edwards Lifesciences, Medtronic, Biotronik, Novartis, Sanofi Genzyme, AstraZeneca, Pfizer, and Bayer, outside the submitted work. Dr Linke has received personal fees from Medtronic, Abbott, Edwards Lifesciences, Boston Scientific, Astra Zeneca, Novartis, Pfizer, Abiomed, Bayer, and Boehringer, outside the submitted work. The other authors have no conflicts of interest to disclose.
Funding Information:
Dr del Val was supported by a research grant from the Fundación Alfonso Martin Escudero (Madrid, Spain). Dr Rodés-Cabau holds the Research Chair “Fondation Famille Jacques Larivière” for the Development of Structural Heart Disease Interventions.
Publisher Copyright:
© 2021 Canadian Cardiovascular Society
PY - 2022/1
Y1 - 2022/1
N2 - Background: Staphylococcus aureus (SA) has been extensively studied as causative microorganism of surgical prosthetic-valve infective endocarditis (IE). However, scarce evidence exists on SA IE after transcatheter aortic valve replacement (TAVR). Methods: Data were obtained from the Infectious Endocarditis After TAVR International Registry, including patients with definite IE after TAVR from 59 centres in 11 countries. Patients were divided into 2 groups according to microbiologic etiology: non-SA IE vs SA IE. Results: SA IE was identified in 141 patients out of 573 (24.6%), methicillin-sensitive SA in most cases (115/141, 81.6%). Self-expanding valves were more common than balloon-expandable valves in patients presenting with early SA IE. Major bleeding and sepsis complicating TAVR, neurologic symptoms or systemic embolism at admission, and IE with cardiac device involvement (other than the TAVR prosthesis) were associated with SA IE (P < 0.05 for all). Among patients with IE after TAVR, the likelihood of SA IE increased from 19% in the absence of those risk factors to 84.6% if ≥ 3 risk factors were present. In-hospital (47.8% vs 26.9%; P < 0.001) and 2-year (71.5% vs 49.6%; P < 0.001) mortality rates were higher among patients with SA IE vs non-SA IE. Surgery at the time of index SA IE episode was associated with lower mortality at follow-up compared with medical therapy alone (adjusted hazard ratio 0.46, 95% CI 0.22-0.96; P = 0.038). Conclusions: SA IE represented approximately 25% of IE cases after TAVR and was associated with very high in-hospital and late mortality. The presence of some features determined a higher likelihood of SA IE and could help to orientate early antibiotic regimen selection. Surgery at index SA IE was associated with improved outcomes, and its role should be evaluated in future studies.
AB - Background: Staphylococcus aureus (SA) has been extensively studied as causative microorganism of surgical prosthetic-valve infective endocarditis (IE). However, scarce evidence exists on SA IE after transcatheter aortic valve replacement (TAVR). Methods: Data were obtained from the Infectious Endocarditis After TAVR International Registry, including patients with definite IE after TAVR from 59 centres in 11 countries. Patients were divided into 2 groups according to microbiologic etiology: non-SA IE vs SA IE. Results: SA IE was identified in 141 patients out of 573 (24.6%), methicillin-sensitive SA in most cases (115/141, 81.6%). Self-expanding valves were more common than balloon-expandable valves in patients presenting with early SA IE. Major bleeding and sepsis complicating TAVR, neurologic symptoms or systemic embolism at admission, and IE with cardiac device involvement (other than the TAVR prosthesis) were associated with SA IE (P < 0.05 for all). Among patients with IE after TAVR, the likelihood of SA IE increased from 19% in the absence of those risk factors to 84.6% if ≥ 3 risk factors were present. In-hospital (47.8% vs 26.9%; P < 0.001) and 2-year (71.5% vs 49.6%; P < 0.001) mortality rates were higher among patients with SA IE vs non-SA IE. Surgery at the time of index SA IE episode was associated with lower mortality at follow-up compared with medical therapy alone (adjusted hazard ratio 0.46, 95% CI 0.22-0.96; P = 0.038). Conclusions: SA IE represented approximately 25% of IE cases after TAVR and was associated with very high in-hospital and late mortality. The presence of some features determined a higher likelihood of SA IE and could help to orientate early antibiotic regimen selection. Surgery at index SA IE was associated with improved outcomes, and its role should be evaluated in future studies.
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UR - http://www.scopus.com/inward/citedby.url?scp=85122685546&partnerID=8YFLogxK
U2 - 10.1016/j.cjca.2021.10.004
DO - 10.1016/j.cjca.2021.10.004
M3 - Article
C2 - 34688853
AN - SCOPUS:85122685546
SN - 0828-282X
VL - 38
SP - 102
EP - 112
JO - Canadian Journal of Cardiology
JF - Canadian Journal of Cardiology
IS - 1
ER -