Assessment of Diagnostic and Therapeutic Practices for Cardiac Implantable Electronic Devices Suspected Infections in Nancy University Hospital

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Completed
CT.gov ID
NCT04501835
Collaborator
(none)
184
1
14
13.1

Study Details

Study Description

Brief Summary

The frequency of cardiac implantable electronic devices (CIED) is constantly increasing.

Devices infections are one of the most serious complications in terms of morbidity and mortality. Although the frequency of cardiac implantable devices infections is difficult to derminate due to divergent definitions, cohort studies report a trend of increasing.

The infection can be localized at the pocket of the implantation, at intravascular or intra-cardiac portion of leads. Infectious endocarditis defined by involvement of the intra-cardiac portion of leads is the most serious form. The diagnosis is based on clinical, biological and multimodal imagery data. Early diagnosis and specific management are necessary to reduce mortality and morbidity.

Since the last European recommendations on infectious endocarditis in 2015, the HeartRythm Society of patient described an algorithm to treat CIED infections and extraction indications.

However, in practice, management of CEID infections remains center-dependent and data from robust international studies are missing.

The main objective of our study is to evaluate the management of CEID suspected infections and the prognosis at 1 year in terms of survival according to the methods of treatment at the Nancy University Hospital and to compare the treatment with the latest recommendations in force

Condition or Disease Intervention/Treatment Phase
  • Other: Diagnostic and treatment evaluation

Study Design

Study Type:
Observational
Actual Enrollment :
184 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Assessment of Diagnostic and Therapeutic Practices for Cardiac Implantable Electronic Devices Suspected Infections in Nancy University Hospital
Actual Study Start Date :
Jul 31, 2019
Actual Primary Completion Date :
Jul 30, 2020
Actual Study Completion Date :
Sep 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Cardiac implantable electronic device infections

Patients hospitalised in Nancy University Hospital for suspected cardiac implantable electronic device infections

Other: Diagnostic and treatment evaluation
No intervention, description of the diagnostic evaluation and the treatment

Outcome Measures

Primary Outcome Measures

  1. Description of the practice [From January 2014 to July 2020]

    Describe the diagnostic and therapeutic practices of patients hospitalized for CIED suspected infection

Secondary Outcome Measures

  1. Evaluation of local practices against current recommendations [From January 2014 to July 2020]

    Classify patients in 3 groups (1 = Cardiac implantable electronic device infection ; 2 Pocket infection without proof of lead involvements ; 3 = systemic infection related to infective valvular endocarditis or not without proof of lead involvements according to our local practices and criteria, to EHRA criteria and modified Duke Li criteria). Compare diagnostic management in our center with EHRA recommendations in each groups Compare therapeutic management including removal/extraction of cardiac implantable electronic device, antibiotic therapy Assessment of adhering to EHRA recommendations Pronostic evaluation according to removal/extraction or not based on survival curve

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All patients who have been hospitalized in Nancy University Hospital between January 2014 et July 2019 for suspected infection of cardiac implantable electronic device
Exclusion Criteria:
  • Minor patients

  • Epicardial CIED

Contacts and Locations

Locations

Site City State Country Postal Code
1 De Ciancio Vandœuvre-lès-Nancy France 54500

Sponsors and Collaborators

  • Central Hospital, Nancy, France

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT04501835
Other Study ID Numbers:
  • 2020PI077
First Posted:
Aug 6, 2020
Last Update Posted:
Jan 27, 2021
Last Verified:
May 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 27, 2021