Prognostic relevance of ventricular arrhythmias in surgical patients with gastrointestinal tumors

• Published in: World journal of gastrointestinal oncology Vol. 16; no. 5; pp. 1787 - 1795
• Main Authors: Xue, Jiao-Jie, Hu, Su-Tian, Wang, Chong-Chong, Chen, Zhi-Chong, Cheng, Shi-Yao, Yu, Shu-Qi, Peng, Hua-Jing, Zhang, Yi-Tao, Zeng, Wei-Jie
• Format: Journal Article
• Language: English
• Published: China Baishideng Publishing Group Inc 15.05.2024
• Subjects: Retrospective Cohort Study; Ventricular arrhythmia; Gastrointestinal tumor; Major adverse cardiovascular events; Surgery; Prognostic
• ISSN: 1948-5204; 1948-5204
• DOI: 10.4251/wjgo.v16.i5.1787

Individuals diagnosed with gastrointestinal tumors are at an increased risk of developing cardiovascular diseases. Among which, ventricular arrhythmia is a prevalent clinical concern. This suggests that ventricular arrhythmias may have predictive value in the prognosis of patients with gastrointestinal tumors. To explore the prognostic value of ventricular arrhythmias in patients with gastrointestinal tumors receiving surgery. We retrospectively analyzed data from 130 patients undergoing gastrointestinal tumor resection. These patients were evaluated by a 24-h ambulatory electrocardiogram (ECG) at the Sixth Affiliated Hospital of Sun Yat-sen University from January 2018 to June 2020. Additionally, 41 general healthy age-matched and sex-matched controls were included. Patients were categorized into survival and non-survival groups. The primary endpoint was all-cause mortality, and secondary endpoints included major adverse cardiovascular events (MACEs). Colorectal tumors comprised 90% of cases. Preoperative ambulatory ECG monitoring revealed that among the 130 patients with gastrointestinal tumors, 100 (76.92%) exhibited varying degrees of premature ventricular contractions (PVCs). Ten patients (7.69%) manifested non-sustained ventricular tachycardia (NSVT). The patients with gastrointestinal tumors exhibited higher PVCs compared to the healthy controls on both conventional ECG [27 (21.3) 1 (2.5), = 0.012] and 24-h ambulatory ECG [14 (1.0, 405) 1 (0, 6.5), < 0.001]. Non-survivors had a higher PVC count than survivors [150.50 (7.25, 1690.50) 9 (0, 229.25), = 0.020]. During the follow-up period, 24 patients died and 11 patients experienced MACEs. Univariate analysis linked PVC > 35/24 h to all-cause mortality, and NSVT was associated with MACE. However, neither PVC burden nor NSVT independently predicted outcomes according to multivariate analysis. Patients with gastrointestinal tumors exhibited elevated PVCs. PVCs > 35/24 h and NSVT detected by 24-h ambulatory ECG were prognostically significant but were not found to be independent predictors.