On the coattails of the incredible growth in pacemaker and implantable cardioverter-defibrillator implantation over the past decades have come a myriad of device and lead complications. Transvenous lead extraction (TLE) has become the gold standard for the management of many of these complications. Although advances in TLE tools and techniques have improved the safety of the procedure, serious complications including death can occur. Our ability to assess intraprocedural risk has improved, but much work needs to be done. Furthermore, patients with cardiovascular implantable electronic devices (CIEDs) often have other comorbidities but our understanding of how these interact to affect risk of mortality even after a successful TLE is limited. The decision to undertake the risk of TLE must take into account not just the risk of the procedure itself, but also the expected mortality following a successful procedure. Multiple risk factors for TLE complications have been wellestablished including female sex, low body mass index (BMI), history of CVA, severe left ventricular dysfunction, low platelet count, and coagulopathy. 1 Some can have a profound impact on risk of complications. Byrd et al 2 reported a 4.5-fold increased risk of major complications associated with female sex, while Brunner et al 3 reported a 2.7-fold increased risk of major complications in patients with international normalized ratio greater than 1.2. The results of the European Lead Extraction Controlled Study reported by Bongiorini et al 4 illustrated the role of experience, which can mitigate the risk of complications. In that study, a 1.7-fold increase in major, in hospital complications was seen in low vs high volume centers. Even lead type and tools used in TLE may impact the risk of complications. 5,6 Finally, some patients have poor clinical outcomes despite a successful procedure without complications. Extraction for infection is one of the most powerful predictors conferring a 5-to 9.7-fold increased risk of 1-year mortality. 3,7 Similarly, end-stage renal disease has been reported to increase risk of 30-day mortality by 4.8 folds. 3 In an effort to quantify risk, several prediction models have been developed. The IKAR score, developed by Oszczygiel et al 8 , assigns 1 point each for infective indications, age ≥56 years, and removal of a high-voltage lead and 2 points for kidney dysfunction with a glomerular filtration rate ≤ 60 mL/min/m 2 . None of the patients with an IKAR score of 0 died in follow up, while 1-year mortality for those with an IKAR score ≥4 was 94%. Brunner et al 9 used baseline clinical variables and multivariable logistic regression modeling to develop a nomogram to predict 30-day all-cause mortality after TLE. Points are assigned in the nomogram for age, BMI, hemoglobin, end-stage renal disease, ejection fraction, NYHA functional class, extraction for infection, operator experience, and extraction of a dual coil lead. Resultant scores predict 30-day mortality with a high corrected concordance index value (0.867). 2 | ...