Authors

• Ana Veljača — University Hospital Centre Zagreb, Zagreb, Croatia — ORCID: 0009-0004-4843-3179
• Irena Ivanac Vranešić — University Hospital Centre Zagreb, Zagreb, Croatia — ORCID: 0000-0002-6910-9720
• Dražen Belina — University Hospital Centre Zagreb, Zagreb, Croatia — ORCID: 0000-0002-9830-1981
• Željko Đurić — University Hospital Centre Zagreb, Zagreb, Croatia — ORCID: 0000-0001-9448-8286
• Kristina Marić Bešić — University Hospital Centre Zagreb, Zagreb, Croatia — ORCID: 0000-0002-4004-7271
• Darko Anić — University Hospital Centre Zagreb, Zagreb, Croatia — ORCID: 0000-0002-7378-944X
• Hrvoje Gašparović — University Hospital Centre Zagreb, Zagreb, Croatia — ORCID: 0000-0001-6871-8746

Keywords

infective endocarditis, absent pulmonary valve syndrome, cardiac surgical procedures

DOI

Full Text

**Introduction:** Absent Pulmonary Valve Syndrome (APVS) is a rare congenital anomaly characterized by features of tetralogy of Fallot with complete absence of pulmonary valve tissue. (1) After complete surgical correction, many patients require reoperation/reintervention later in life due to significant right ventricular outflow tract (RVOT) dysfunction. The Melody transcatheter pulmonary valve (TPV) is an effective option for addressing RVOT dysfunction in patients with previously implanted conduit between the right ventricle (RV) and the pulmonary artery (PA). (2, 3) **Case report:** 24-year-old male underwent complete surgical repair of the APVS at 18 months of age, which was performed in our institution. His initial surgery included the closure of the ventricular septal defect with the implantation of the RV-PA conduit. At the age of 11, he required reoperation due to stenosis of the conduit, and a larger (22 mm) Contegra conduit was implanted. A decade later, he underwent the implantation of a Melody TPV to address restenosis in the RV-PA conduit. Four years after implantation, the patient presented with cough and febrile illness at the local hospital. An echocardiogram showed signs of pulmonary valve (PV) stenosis, which raised suspicion of infective endocarditis (IE). MSCT pulmonary angiography revealed the presence of septic emboli in the lungs, accompanied by lung infarctions. Initial laboratory tests showed leukocytosis, elevated C-reactive protein levels, and blood cultures confirmed the presence of Staphylococcus epidermidis. Subsequently, antibiotic therapy was initiated, and the patient was transferred to our institution where an echocardiography exam confirmed severe PV/conduit stenosis with suspicion of distal conduit thrombosis. Urgent surgery was indicated with the removal of the Melody valve and conduit, followed by the implantation of an aortic homograft in the pulmonary position. The patient completed antibiotic treatment and was doing well at the 3-month follow-up. **Conclusion:** Although a TPV implantation is nowadays a standard treatment procedure for residual RVOT dysfunction in patients with previously implanted PV conduits, it carries a significantly increased risk for IE. Clinicians should be aware that these patients need prompt evaluation for IE if a new febrile illness with PV stenosis occurs.

Literature

1. Jonas RA. Comprehensive Surgical Management of Congenital Heart Disease, 2nd Edition. London: CRC Press, 2014. https://doi.org/10.1201/b13497
2. Bonhoeffer P, Boudjemline Y, Saliba Z, Merckx J, Aggoun Y, Bonnet D, et al. Percutaneous replacement of pulmonary valve in a right-ventricle to pulmonary-artery prosthetic conduit with valve dysfunction. Lancet. 2000 October 21;356(9239):1403–5. https://doi.org/10.1016/S0140-6736(00)02844-0
3. Hascoët S, Acar P, Boudjemline Y. Transcatheter pulmonary valvulation: current indications and available devices. Arch Cardiovasc Dis. 2014 November;107(11):625–34. https://doi.org/10.1016/j.acvd.2014.07.048