TY - JOUR PY - 2024// TI - Risk assessment in patients with symptomatic and asymptomatic pre-excitation JO - Europace A1 - Jemtrén, Anette A1 - Saygi, Serkan A1 - Åkerström, Finn A1 - Asaad, Fahd A1 - Bourke, Tara A1 - Braunschweig, Frieder A1 - Carnlöf, Carina A1 - Drca, Nikola A1 - Insulander, Per A1 - Kennebäck, Göran A1 - Nordin, Astrid Paul A1 - Sadigh, Bita A1 - Rickenlund, Anette A1 - Saluveer, Ott A1 - Schwieler, Jonas A1 - Svennberg, Emma A1 - Tapanainen, Jari A1 - Turkmen, Yusuf A1 - Bastani, Hamid A1 - Jensen-Urstad, Mats SP - euae036 EP - euae036 VL - 26 IS - 2 N2 - AIMS: Controversy remains as to whether the exercise stress test (EST) is sufficient for risk evaluation in patients with pre-excitation. This study aims to clarify the usefulness of EST in risk stratification in both asymptomatic and symptomatic patients presenting with pre-excitation.

METHODS AND RESULTS: This prospective study includes consecutive asymptomatic and symptomatic patients with pre-excitation referred for risk assessment. All participants performed an incremental EST (bicycle) prior to an electrophysiology study (EPS). Primary data from the EST included loss of pre-excitation during exercise, and primary data from the EPS included the measurement of accessory pathway effective refractory period (APERP), shortest pre-excited RR interval (SPERRI), and inducible arrhythmia with the use of a beta-adrenergic receptor agonist if deemed necessary. One hundred and sixty-four patients (59 asymptomatic, 105 symptomatic) completed an EST and EPS. Forty-five patients (27%) demonstrated low-risk findings on EST, of which 19 were asymptomatic and 26 were symptomatic. Six patients with low-risk EST findings had SPERRI/APERP ≤ 250 ms at EPS, and two of them were asymptomatic. The sensitivity, specificity, positive predictive value, negative predictive value (NPV), and accuracy of low-risk EST for excluding patients with SPERRI/APERP ≤ 250 ms were 40, 91, 87, 51, and 60%, respectively. The number of patients with inducible arrhythmia at EPS was similar in the asymptomatic (36, 69%) and symptomatic (73, 61%) groups.

CONCLUSION: Sudden loss of pre-excitation during EST has a low NPV in excluding high-risk APs. The EPS with the use of isoproterenol should be considered to accurately assess the risk of patients with pre-excitation regardless of symptoms (ClinicalTrials.gov Identifier: NCT03301935).

Language: en

LA - en SN - 1099-5129 UR - http://dx.doi.org/10.1093/europace/euae036 ID - ref1 ER -