Three Decades of Experience with Aortic Prosthetic Valve Endocarditis.
Antonella GaleoneJacopo GardelliniDiletta TrojanVenanzio Di NicolaRenato Di GaetanoGiuseppe FaggianGiovanni Battista LucianiPublished in: Journal of cardiovascular development and disease (2023)
The objective of this study was to evaluate early and long-term outcomes of patients with aortic prosthetic valve endocarditis (a-PVE) treated with a prosthetic aortic valve (PAV), prosthetic valved conduit (PVC), or cryopreserved aortic homograft (CAH). A total of 144 patients, 115 male and 29 female, aged 67 ± 12 years, underwent surgery for a-PVE at our institution between 1994 and 2021. Median time from the original cardiac surgery was 1.9 [0.6-5.6] years, and 47 (33%) patients developed an early a-PVE. Of these patients, 73 (51%) underwent aortic valve replacement (AVR) with a biological or mechanical PAV, 12 (8%) underwent aortic root replacement (ARR) with a biological or mechanical PVC, and 59 (42%) underwent AVR or ARR with a CAH. Patients treated with a CAH had significantly more circumferential annular abscess multiple valve involvement, longer CPB and aortic cross-clamping times, and needed more postoperative pacemaker implantation than patients treated with a PAV. No difference was observed in survival, reoperation rates, or recurrence of IE between patients treated with a PAV, a PVC, or a CAH. CAHs are technically more demanding and more often used in patients who have extensive annular abscess and multiple valve involvement. However, the use of CAH is safe in patients with complex a-PVE, and it shows excellent early and long-term outcomes.
Keyphrases
- aortic valve
- aortic valve replacement
- aortic stenosis
- end stage renal disease
- ejection fraction
- transcatheter aortic valve implantation
- newly diagnosed
- transcatheter aortic valve replacement
- chronic kidney disease
- cardiac surgery
- left ventricular
- peritoneal dialysis
- heart failure
- pulmonary embolism
- percutaneous coronary intervention
- acute kidney injury
- coronary artery disease
- bone marrow
- pulmonary hypertension
- rare case