Incidence and outcomes of systemic infections in patients with leadless pacemakers: Data from the Micra IDE study.


Journal

Pacing and clinical electrophysiology : PACE
ISSN: 1540-8159
Titre abrégé: Pacing Clin Electrophysiol
Pays: United States
ID NLM: 7803944

Informations de publication

Date de publication:
08 2019
Historique:
received: 30 04 2019
revised: 04 06 2019
accepted: 19 06 2019
pubmed: 25 6 2019
medline: 21 7 2020
entrez: 25 6 2019
Statut: ppublish

Résumé

The Micra clinical trials have enrolled more than 2500 patients without any reported device-related infections that required removal during follow-up. Leadless pacemakers might be more resistant to bacterial seeding due to smaller surface area and a greater tendency for encapsulation. To analyze the incidence and outcomes of serious infectious events (SIEs: bacteremia or endocarditis) that developed during follow-up in patients with history of Micra leadless pacemaker implantation. SIE and outcomes were characterized based upon adverse event reports. Among 720 patients implanted with Micra in the investigational device exemption trial, we identified 16 patients who had documented 21 SIEs during follow-up. Among patients with SIEs, mean age was 71.9 ± 11.7 years. SIEs occurred at a mean 4.8 ± 4.5 months after implant and patients were followed for 13.1 ± 9.1 months after documentation of SIE. All events were adjudicated as unrelated to the Micra device or procedure. Bacteremia was documented to be related to a gram-positive organism in 13 events (seven Staphylococcus, three Streptococcus, two Enterococcus, and one uncharacterized gram-positive bacteria), and gram-negative organisms in three events. In five events, the type of organism was not characterized (two patients with endocarditis). No persistent cases of bacteremia after antibiotic cessation were seen over the duration of follow-up CONCLUSION: In this small series of Micra patients who developed SIEs postimplant, the occurrence of bacteremia and/or endocarditis did not appear to lead to persistent bacteremia off antibiotics; most events resolved with antibiotic treatment.

Sections du résumé

BACKGROUND
The Micra clinical trials have enrolled more than 2500 patients without any reported device-related infections that required removal during follow-up. Leadless pacemakers might be more resistant to bacterial seeding due to smaller surface area and a greater tendency for encapsulation.
OBJECTIVE
To analyze the incidence and outcomes of serious infectious events (SIEs: bacteremia or endocarditis) that developed during follow-up in patients with history of Micra leadless pacemaker implantation.
METHODS
SIE and outcomes were characterized based upon adverse event reports. Among 720 patients implanted with Micra in the investigational device exemption trial, we identified 16 patients who had documented 21 SIEs during follow-up.
RESULTS
Among patients with SIEs, mean age was 71.9 ± 11.7 years. SIEs occurred at a mean 4.8 ± 4.5 months after implant and patients were followed for 13.1 ± 9.1 months after documentation of SIE. All events were adjudicated as unrelated to the Micra device or procedure. Bacteremia was documented to be related to a gram-positive organism in 13 events (seven Staphylococcus, three Streptococcus, two Enterococcus, and one uncharacterized gram-positive bacteria), and gram-negative organisms in three events. In five events, the type of organism was not characterized (two patients with endocarditis). No persistent cases of bacteremia after antibiotic cessation were seen over the duration of follow-up CONCLUSION: In this small series of Micra patients who developed SIEs postimplant, the occurrence of bacteremia and/or endocarditis did not appear to lead to persistent bacteremia off antibiotics; most events resolved with antibiotic treatment.

Identifiants

pubmed: 31232461
doi: 10.1111/pace.13752
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1105-1110

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Mikhael F El-Chami (MF)

Division of Cardiology, Section of Electrophysiology, Emory University, Atlanta, Georgia.

Kyoko Soejima (K)

Kyorin University Hospital, Tokyo, Japan.

Jonathan P Piccini (JP)

Duke University Medical Center and Duke Clinical Research Institute, Durham, North Carolina.

Dwight Reynolds (D)

Cardiovascular Section, University of Oklahoma Health Sciences Center, OU Medical Center, Oklahoma City, Oklahoma.

Philippe Ritter (P)

Department of Cardiac Pacing and Electrophysiology, CHU/Université de Bordeaux, Pessac, France.

Toshimasa Okabe (T)

The Ohio State University Wexner Medical Center, Columbus, Ohio.

Paul A Friedman (PA)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota.

Yong-Mei Cha (YM)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota.

Kurt Stromberg (K)

Medtronic, plc, Mounds View, Minnesota.

Reece Holbrook (R)

Medtronic, plc, Mounds View, Minnesota.

Dedra H Fagan (DH)

Medtronic, plc, Mounds View, Minnesota.

Paul R Roberts (PR)

University Hospital Southampton, NHS Foundation Trust, Southampton, UK.

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