Key result
HeartMate 3 bridge linked to ~2.2-fold higher post-transplant pneumonia risk vs no-LVAD controls.
Why the study?
The HeartMate 3 LVAD's proximity to the lung may expose patients to pulmonary complications during explantation, prompting evaluation of pneumonia risk following heart transplantation among HM3-bridged patients.
Does bridging to heart transplantation with a HeartMate 3 LVAD increase the risk of post-transplant pneumonia compared to bridging without an LVAD in adults undergoing heart transplantation?
Cohort (n=281)
No
Does bridging to heart transplantation with a HeartMate 3 LVAD increase the risk of post-transplant pneumonia compared to bridging without an LVAD in adults undergoing heart transplantation?
Patients bridged to heart transplantation with a HeartMate 3 LVAD face a significantly higher risk of post-transplant pneumonia during index hospitalization and up to one year, highlighting a need for targeted antimicrobial prophylaxis and refined surgical explantation techniques.
Answers are grounded in this paper and cite their sources.
HeartMate 3 bridging was associated with higher post-transplant pneumonia risk; leaves open whether targeted prophylaxis or explant techniques mitigate this in prospective studies.
Background Left ventricular assist devices (LVADs) are commonly used as a bridge to heart transplantation (HT). The HeartMate 3 (HM3) LVAD's proximity to the lung may expose patients to pulmonary complications during explantation. This study aimed to assess the risk of pneumonia following HT among HM3 patients bridged to HT. Methods We retrospectively analyzed all adults who underwent HT at NYP‐Columbia between 2016‐2022. Patients bridged with HM3 LVAD were compared to controls bridged to HT without LVAD. The primary outcome was pneumonia incidence during index hospitalization. Categorical data were compared using Fisher and Wilcoxon tests. Multivariable logistic regression identified predictors of pneumonia. Results 281 patients were included, 82 with HM3 and 199 controls. Average age at HT and race were similar between groups. HM3 patients had more males and COPD/asthma, though less pulmonary hypertension. HM3 patients had a 79% increase in pneumonia incidence during index hospitalization (43% vs. 24%, p = 0.004) and an 83% increase in pneumonia incidence up to one year post‐HT (55% vs. 30%, p = 0.001). HM3 patients had longer intensive care unit stays and mechanical ventilation duration. After adjustment, HM3 remained an independent predictor of post‐HT pneumonia (OR 2.19; 95% CI 1.21‐3.99; p = 0.010). Among HM3 patients, prior coronary artery bypass graft was an additional risk factor for post‐HT pneumonia. Conclusion HM3 as bridge to HT is associated with an increased risk of post‐HT pneumonia. Given these findings, enhanced antimicrobial prophylaxis and surgical techniques warrant further investigation.
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Skoll et al. (2026) conducted a cohort in Heart transplantation (n=281). HeartMate 3 LVAD as bridge to heart transplantation vs. Bridged to heart transplantation without LVAD was evaluated on Pneumonia incidence during index hospitalization (OR 2.19, 95% CI 1.21-3.99, p=0.010). Bridging with a HeartMate 3 LVAD increased post-transplant pneumonia risk during index hospitalization vs controls without LVAD.
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