TY - JOUR
T1 - Implantation of cardiac electronic devices in active COVID-19 patients
T2 - Results from an international survey
AU - Tovia-Brodie, Oholi
AU - Rav Acha, Moshe
AU - Belhassen, Bernard
AU - Gasperetti, Alessio
AU - Schiavone, Marco
AU - Forleo, Giovanni Battista
AU - Guevara-Valdivia, Milton E.
AU - Ruiz, David Valdeolivar
AU - Lellouche, Nicolas
AU - Hamon, David
AU - Castagno, Davide
AU - Bellettini, Matteo
AU - De Ferrari, Gaetano M.
AU - Laredo, Mikael
AU - Carvès, Jean Baptiste
AU - Ignatiuk, Barbara
AU - Pasquetto, Giampaolo
AU - De Filippo, Paolo
AU - Malanchini, Giovanni
AU - Pavri, Behzad B.
AU - Raphael, Craig
AU - Rivetti, Luigi
AU - Mantovan, Roberto
AU - Chinitz, Jason
AU - Harding, Melissa
AU - Boriani, Giuseppe
AU - Casali, Edoardo
AU - Wan, Elaine Y.
AU - Biviano, Angelo
AU - Macias, Carlos
AU - Havranek, Stepan
AU - Lazzerini, Pietro Enea
AU - Canu, Antonio M.
AU - Zardini, Marco
AU - Conte, Giulio
AU - Cano, Óscar
AU - Casella, Michela
AU - Rudic, Boris
AU - Omelchenko, Alexander
AU - Mathuria, Nilesh
AU - Upadhyay, Gaurav A.
AU - Danon, Asaf
AU - Schwartz, Arie Lorin
AU - Maury, Philippe
AU - Nakahara, Shiro
AU - Goldenberg, Gustavo
AU - Schaerli, Nicolas
AU - Bereza, Sergiy
AU - Auricchio, Angelo
AU - Glikson, Michael
AU - Michowitz, Yoav
N1 - Funding Information:
Disclosures: Dr Lellouche has received consultant fees from Abbott, Medtronic, and Boston Scientific. Dr Chinitz has received consultant fees from Medtronic, Biosense Webster, and Boston Scientific. Dr Cano has received consultant fees from Medtronic and Boston Scientific. Dr Auricchio has received consultant fees from Boston Scientific, Backbeat, Biosense Webster, CAIRDAC, Corvia Medical, EBR Systems, MicroPort CRM, Philips, and Radcliffe Publisher; speakers’ fee from Boston Scientific, Medtronic, and MicroPort CRM; participated in clinical trials for Boston Scientific, EBR System, Medtronic, and Philips; and discloses intellectual properties in Boston Scientific, Biosense Webster, and MicroPort CRM. Dr Upadhyay has received consultant fees from Abbott, Biotronik, Medtronic, and Zoll Medical. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose. The data underlying this article will be shared on reasonable request to the corresponding author. Funding Sources: The authors report no specific funding related to this article.
Publisher Copyright:
© 2021 Heart Rhythm Society
PY - 2022/2
Y1 - 2022/2
N2 - Background: Cardiac implantable electronic device (CIED) implantation rates as well as the clinical and procedural characteristics and outcomes in patients with known active coronavirus disease 2019 (COVID-19) are unknown. Objective: The purpose of this study was to gather information regarding CIED procedures during active COVID-19, performed with personal protective equipment, based on an international survey. Methods: Fifty-three centers from 13 countries across 4 continents provided information on 166 patients with known active COVID-19 who underwent a CIED procedure. Results: The CIED procedure rate in 133,655 hospitalized COVID-19 patients ranged from 0 to 16.2 per 1000 patients (P <.001). Most devices were implanted due to high-degree/complete atrioventricular block (112 [67.5%]) or sick sinus syndrome (31 [18.7%]). Of the 166 patients in the study survey, the 30-day complication rate was 13.9% and the 180-day mortality rate was 9.6%. One patient had a fatal outcome as a direct result of the procedure. Differences in patient and procedural characteristics and outcomes were found between Europe and North America. An older population (76.6 vs 66 years; P <.001) with a nonsignificant higher complication rate (16.5% vs 7.7%; P = .2) was observed in Europe vs North America, whereas higher rates of critically ill patients (33.3% vs 3.3%; P <.001) and mortality (26.9% vs 5%; P = .002) were observed in North America vs Europe. Conclusion: CIED procedure rates during known active COVID-19 disease varied greatly, from 0 to 16.2 per 1000 hospitalized COVID-19 patients worldwide. Patients with active COVID-19 infection who underwent CIED implantation had high complication and mortality rates. Operators should take these risks into consideration before proceeding with CIED implantation in active COVID-19 patients.
AB - Background: Cardiac implantable electronic device (CIED) implantation rates as well as the clinical and procedural characteristics and outcomes in patients with known active coronavirus disease 2019 (COVID-19) are unknown. Objective: The purpose of this study was to gather information regarding CIED procedures during active COVID-19, performed with personal protective equipment, based on an international survey. Methods: Fifty-three centers from 13 countries across 4 continents provided information on 166 patients with known active COVID-19 who underwent a CIED procedure. Results: The CIED procedure rate in 133,655 hospitalized COVID-19 patients ranged from 0 to 16.2 per 1000 patients (P <.001). Most devices were implanted due to high-degree/complete atrioventricular block (112 [67.5%]) or sick sinus syndrome (31 [18.7%]). Of the 166 patients in the study survey, the 30-day complication rate was 13.9% and the 180-day mortality rate was 9.6%. One patient had a fatal outcome as a direct result of the procedure. Differences in patient and procedural characteristics and outcomes were found between Europe and North America. An older population (76.6 vs 66 years; P <.001) with a nonsignificant higher complication rate (16.5% vs 7.7%; P = .2) was observed in Europe vs North America, whereas higher rates of critically ill patients (33.3% vs 3.3%; P <.001) and mortality (26.9% vs 5%; P = .002) were observed in North America vs Europe. Conclusion: CIED procedure rates during known active COVID-19 disease varied greatly, from 0 to 16.2 per 1000 hospitalized COVID-19 patients worldwide. Patients with active COVID-19 infection who underwent CIED implantation had high complication and mortality rates. Operators should take these risks into consideration before proceeding with CIED implantation in active COVID-19 patients.
KW - Active COVID-19
KW - Cardiac implantable electronic device procedure
KW - Complications
KW - Mortality
KW - Personal protective equipment
UR - http://www.scopus.com/inward/record.url?scp=85120168356&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85120168356&partnerID=8YFLogxK
U2 - 10.1016/j.hrthm.2021.10.020
DO - 10.1016/j.hrthm.2021.10.020
M3 - Article
C2 - 34710561
AN - SCOPUS:85120168356
VL - 19
SP - 206
EP - 216
JO - Heart Rhythm
JF - Heart Rhythm
SN - 1547-5271
IS - 2
ER -