Publication:
Clinical Outcomes of Cardiac Implantable Electronic Device-Related Endocarditis: An International ID-IRI Study

dc.contributor.authorAYDIN S.
dc.contributor.authorMERT A.
dc.contributor.authorEMECEN A. N.
dc.contributor.authorSzabo B. G.
dc.contributor.authorAKSOY F.
dc.contributor.authorAkyildiz O.
dc.contributor.authorALKAN S.
dc.contributor.authorCascio A.
dc.contributor.authorSipahi O. R.
dc.contributor.authorLakatos B.
dc.contributor.authoret al.
dc.date.accessioned2025-11-12T21:36:27Z
dc.date.issued2025-10-01
dc.description.abstractBackground/Objectives: Cardiac implantable electronic device-related infective endocarditis (CIED-RIE) is a serious condition with significant morbidity and mortality. Although recent advances in imaging and therapeutic approaches have improved management, diagnosing and treating CIED-RIE continues to be challenging. This study aimed to identify factors associated with mortality in CIED-RIE patients. Methods: We conducted a retrospective, multicenter international study of adult patients diagnosed with CIED-RIE between January 2014 and June 2024. Data on demographics, clinical presentation, microbiological findings, imaging results, treatment modalities, and outcomes were collected and analyzed to determine predictors of short-term mortality. Results: A total of 197 patients (mean age: 65.3 ± 14.4 years; 75.1% male) were included. The most common device type was permanent pacemaker (48.2%). Staphylococcus species were the predominant pathogens (62.4%). Surgical intervention was performed in 67.5% of patients, and 90-day mortality occurred in 19.3%. Multivariable analysis identified higher Charlson comorbidity index (HR: 1.31), tricuspid valve involvement (HR: 2.35), vegetation size ≥ 10 mm (HR: 2.53), pulmonary embolism (HR: 3.92), and absence of surgical intervention (HR: 2.90) as independent predictors of increased 90-day mortality. Conclusions: Early identification of high-risk patients and prompt multidisciplinary management, including surgical intervention when indicated, are critical to improving outcomes in patients with CIED-RIE.
dc.identifier.citationAYDIN S., MERT A., EMECEN A. N., Szabo B. G., AKSOY F., Akyildiz O., ALKAN S., Cascio A., Sipahi O. R., Lakatos B., et al., "Clinical Outcomes of Cardiac Implantable Electronic Device-Related Endocarditis: An International ID-IRI Study", Journal of Clinical Medicine, cilt.14, sa.19, 2025
dc.identifier.doi10.3390/jcm14196816
dc.identifier.issn2077-0383
dc.identifier.issue19
dc.identifier.pubmed41095899
dc.identifier.scopus105018814007
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105018814007&origin=inward
dc.identifier.urihttps://hdl.handle.net/20.500.12645/41342
dc.identifier.volume14
dc.identifier.wosWOS:001593681300001
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectMedicine
dc.subjectHealth Sciences
dc.subjectFundamental Medical Sciences
dc.subjectKlinik Tıp (Med)
dc.subjectKlinik Tıp
dc.subjectTıp Genel & Dahili
dc.subjectClinical Medicine (Med)
dc.subjectClinical Medicine
dc.subjectMedicine General & Internal
dc.subjectGenel Tıp
dc.subjectGeneral Medicine
dc.subjectcardiac implantable electronic device
dc.subjectclinical outcome
dc.subjectendocarditis
dc.subjectmortality
dc.subjecttransvenous lead extraction
dc.titleClinical Outcomes of Cardiac Implantable Electronic Device-Related Endocarditis: An International ID-IRI Study
dc.typearticle
dspace.entity.typePublication
local.avesis.id5c048e71-a162-4f87-a8c9-2be05b962e6c

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