Key result
High intraoperative complex PVC burden linked to ~2.8-fold higher odds of 30-day MACE.
Why the study?
The prognostic significance of intraoperative premature ventricular contraction burden, particularly complex ventricular ectopy, for 30-day cardiovascular outcomes after liver transplantation was unclear.
Does increased intraoperative complex PVC burden predict an increased risk of 30-day major adverse cardiovascular events in liver transplantation recipients?
Cohort (n=2,290)
No
Does increased intraoperative complex PVC burden predict an increased risk of 30-day major adverse cardiovascular events in liver transplantation recipients?
Odds Ratio: 2.79 (95% CI 1.83–4.27)
Absolute Event Rate: 28.9% vs 11.5%
p-value: p=<0.001
Complex intraoperative ventricular ectopy, but not isolated PVCs, is independently associated with a significantly increased risk of 30-day major adverse cardiovascular events following liver transplantation.
Complex intraoperative PVC burden was associated with higher 30-day MACE risk after liver transplant; extends ambulatory PVC data to the perioperative setting but remains hypothesis-generating.
To examine the association between intraoperative premature ventricular contraction (PVC) burden and 30-day major adverse cardiovascular events (MACE) in liver transplantation (LT) recipients, and to determine whether complex ventricular ectopy carries prognostic significance distinct from isolated PVCs. In this retrospective cohort study, continuous intraoperative ECG recordings from 2,290 consecutive LT recipients were analyzed using a validated AI-based detection pipeline. PVCs were classified as isolated or complex (couplet, NSVT, bigeminy, trigeminy), with total complex PVC burden as the primary exposure. Associations with 30-day MACE were estimated by multivariable logistic regression across burden tertiles. Sensitivity analyses used a hard MACE endpoint excluding arrhythmic components and with additional adjustment for isolated PVC burden. MACE occurred in 515 patients (22.5%). PVCs were detected in 98.2% of patients; isolated PVC prevalence did not differ between those with and without MACE (98.4% vs. 98.0%, P = 0.666), whereas complex PVC prevalence was significantly higher in the MACE group (93.2% vs. 85.8%, P < 0.001). Total complex PVC burden showed a graded association with MACE across tertiles (T1 aOR 1.71, 95% CI 1.11–2.65; T2 aOR 2.26, 95% CI 1.47–3.47; T3 aOR 2.79, 95% CI 1.83–4.27), whereas isolated PVC burden was not associated with MACE in any tertile. The association persisted in both sensitivity analyses. Complex intraoperative ventricular ectopy, but not isolated PVCs, was independently associated with 30-day MACE in LT recipients. AI-enabled PVC quantification may identify an intraoperative signal associated with postoperative cardiovascular risk, although prospective and external validation is required before clinical application.
No takes yet. Share an insight, caveat, or question.
Jang et al. (2026) conducted a cohort in Liver transplantation (LT) recipients (n=2,290). Intraoperative complex premature ventricular contraction (PVC) burden vs. No detected burden of complex PVCs was evaluated on 30-day major adverse cardiovascular events (MACE) (aOR 2.79, 95% CI 1.83-4.27, p=<0.001). Total complex intraoperative premature ventricular contraction burden was independently associated with an increased risk of 30-day MACE (aOR 2.79 for the highest tertile vs no burden).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: