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C8. Endocarditis
Poster Session: Endocarditis
Transcatheter aortic valve replacement (TAVR) is increasingly used for lower risk patients. Incidence of TAVR endocarditis ranges from 0.2% to 3.3%. The purpose of this study was to determine local incidence and risk factors of prosthetic valve infective endocarditis (PVIE) in a contemporary cohort.
Methods:
IRB approved retrospective, nested case-control study evaluated the 1-year incidence and risk factors for PVIE among TAVR recipients from 2015 to 2019. Inclusion: ≥ 18 years, TAVR procedure at Henry Ford Health System. Exclusion: repeat TAVR. PVIE cases were matched with controls who did not experience PVIE. PVIE defined as diagnosis documentation in the electronic medical record.Figure 1. Study Design
Results:
23/1266 patients were identified as cases corresponding to a 1-year incidence of 1.82%. The median time to PVIE was 127 days and 35% occurred within 60 days. The most frequently isolated organisms were streptococci (26%), MRSA (13%), and MSSA (13%). Baseline demographics and comorbidities for 23 PVIE cases and 161 controls are displayed in Table 1. Significant risk factors for PVIE in bivariate analysis included STS-PROM (Society of Thoracic Surgeons Predicted Risk of Mortality), median: 4.1 controls and 6.4 cases (p = 0.012). Age, BMI, and comorbidities were not significantly different. Diabetes was notably more frequent among cases (36% vs 48%, p = 0.274). Patients with PVIE had more post-op RBC transfusions (5% vs 21.7% p = 0.003), ECG changes (23% vs 43.5%, p = 0.035), heart block (15.5% vs 34.8%, p = 0.038), longer length of stay (2 days, range 1 to 4 vs 4 to 11, p = 0.004), and thirty-day readmission (10.6% vs 52.2%, p < 0.001). Results displayed in Table 2.Table 1. Patient Characteristics and Risk Factor AnalysisTable 2. Additional Outcomes
Conclusion: The results from this study give insight to the local incidence, microbiology, and risk of PVIE following TAVR. Future directions include a larger evaluation of modifiable risks such as diabetes management and examining the heart block patients who received permanent pacemaker implants.
Jamison Montes de Oca, PharmD
PGY-2 Infectious Diseases Pharmacy Resident
Henry Ford Health System
Detroit, Michigan, United States
Disclosure: I do not have any relevant financial / non-financial relationships with any proprietary interests.
Rachel Kenney, PharmD
Pharmacy Specialist, Antimicrobial Stewardship
Henry Ford Hospital
Detroit, Michigan, United States
Disclosure: Medtronic, Inc. (Other Financial or Material Support, spouse is an employee and shareholder)
Janet F. Wyman, DNP, CNS-BC, FACC
Administrative Director, Structural Heart Disease Clinical Services
Henry Ford Health
Grosse Pointe Park, Michigan, United States
Disclosure: Edwards Lifesciences (Consultant)
Dee Dee Wang, MD
Henry Ford Hospital
Detroit, Michigan, United States
Disclosure: Edwards LifeSciences (Consultant)
Brian O'Neill, MD
Henry Ford Hospital
Detroit, Michigan, United States
Disclosure: Edwards Lifesciences (Consultant)
Marvin Eng, MD
Henry Ford
Detroit, Michigan, United States
Disclosure: I do not have any relevant financial / non-financial relationships with any proprietary interests.
James Lee, MD
Henry Ford Heart and Vascular Institute
Detroit, Michigan, United States
Disclosure: I do not have any relevant financial / non-financial relationships with any proprietary interests.
Pedro F. Villablanca, MD
Henry Ford Hospital
Detroit, Michigan, United States
Disclosure: I do not have any relevant financial / non-financial relationships with any proprietary interests.
Long To, PharmD, BCPS
Henry Ford Health System
Detroit, Michigan, United States
Disclosure: I do not have any relevant financial / non-financial relationships with any proprietary interests.