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Clinical Trials/NCT04501835
NCT04501835
Completed
Not Applicable

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

Central Hospital, Nancy, France1 site in 1 country184 target enrollmentJuly 31, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Implantable Electronic Device Infections
Sponsor
Central Hospital, Nancy, France
Enrollment
184
Locations
1
Primary Endpoint
Description of the practice
Status
Completed
Last Updated
5 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
July 31, 2019
End Date
September 30, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Central Hospital, Nancy, France
Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Description of the practice

Time Frame: From January 2014 to July 2020

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

Secondary Outcomes

  • Evaluation of local practices against current recommendations(From January 2014 to July 2020)

Study Sites (1)

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