Response to the Editor,We want to thank Farkowski et al for the insightful comments on our paper in which we assessed the long-term efficacy and safety of radiofrequency catheter ablation (CA) of atrial fibrillation in patients with cardiac implantable devices (CIEDs) and transvenous leads (TVLs). 1 The authors bring up the potential risk of CIED-related infections in patients undergoing CA. As rightfully mentioned, a little is known on this important subject, and CA in patients with CIED and TVL is not considered a risk factor for CIED-related infections. [2][3][4][5] CA in our center is performed in an electrophysiology laboratory reserved for CA procedures for which antiseptic rules are invariably applied. However, our standard operating procedure for CA does not involve periprocedural antibiotic prophylaxis, including patients with a previously implanted CIED and TVL. Five of in total of 190 patients (2.6%) experienced CIED-related infections during a follow-up of 55.4 ± 38.1 months. Four of those patients experienced pocket infection (two shortly after elective device replacement and development of hematoma; two after cutaneous device perforation). Only in one of those patients, systemic infection with positive blood cultures of Staphylococcus epidermidis was present. The other patient had lead endocarditis with the diagnosis of Staphylococcus aureus in repetitive blood culture samples. In this patient, already five device replacements and an upgrade to cardiac resynchronization therapy with cardioverter-defibrillator function using a dual-coil right ventricular lead were performed. All patients underwent laser lead extraction, as previously described. 6 Empiric antibiotic therapy included vancomycin, gentamycin, and rifampicin, which was adapted to a directed therapy with flucloxacillin after the identification of the infectious agent in one case. Despite the serious adverse events, all patients had a favorable clinical outcome after successful treatment and reimplantation of a new CIED. In all cases, at least 18 months passed after CA until the diagnosis of CIED-related infection, and evidence relating them to CA was not found. Moreover, the overall rate of infections (2.6%) is in line with large studies have addressed this issue in patients without a history of CA. 5 We congratulate Farkowski et al 1,7 on contributing to another piece of the puzzle by going into depth of the current data collected supporting that the risk of CIED-related infection after CA from present observational data appears low. ORCID Leon Dinshaw