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Updated: Aug 23, 2025

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Published on: June 12, 2021
Post-Implant Phosphodiesterase-5 Inhibitors in Patients with Left Ventricular Assist Device: A Systematic Review and
Andrew Xanthopoulos1, Dimitrios E Magouliotis2, Konstantinos Tryposkiadis3
1Department of Cardiology, University Hospital of Larissa, 411 10 Larissa, Greece.
Insights
Post-implant phosphodiesterase-5 inhibitors (PDE-5i) in left ventricular assist device (LVAD) patients reduced mortality and thrombotic events like stroke and pump thrombosis. However, PDE-5i use was linked to an increased risk of gastrointestinal bleeding.
Area of Science:
- Cardiology
- Pharmacology
- Medical Technology
Background:
- Hemocompatibility issues persist despite advancements in left ventricular assist device (LVAD) technology.
- Optimizing patient management requires novel pharmacological interventions to mitigate hemocompatibility-related events.
- Third-generation LVADs still face challenges with blood-material interactions.
Purpose of the Study:
- To systematically review and meta-analyze the safety and efficacy of post-implant phosphodiesterase-5 inhibitors (PDE-5i) in reducing hemocompatibility-related events in LVAD patients.
- To evaluate the impact of PDE-5i on mortality, ischemic stroke, pump thrombosis, and gastrointestinal bleeding.
- To synthesize current evidence on PDE-5i as a potential adjunctive therapy for LVAD recipients.
Main Methods:
- Systematic review and meta-analysis of studies retrieved from Pubmed, Scopus, and CENTRAL (1990-2022).
- Inclusion of 15 studies for qualitative synthesis and 9 studies for quantitative synthesis.
- Utilized a fixed-effects model for meta-analysis due to a small number of studies; primary endpoint was all-cause mortality, secondary endpoints included ischemic stroke, pump thrombosis, and gastrointestinal bleeding.
Main Results:
- Phosphodiesterase-5 inhibitors (PDE-5i) were associated with significantly lower all-cause mortality (OR: 0.92 [95% CI: 0.85, 0.98]; p = 0.02).
- Reduced incidence of ischemic stroke (OR: 0.87 [95% CI: 0.78, 0.98]; p = 0.02) and pump thrombosis (OR: 0.90 [95% CI: 0.82, 0.99]; p = 0.04) observed in the PDE-5i group.
- A significantly higher incidence of gastrointestinal bleeding was noted in patients receiving PDE-5i (OR: 1.26 [95% CI: 1.11, 1.44]; p < 0.01).
Conclusions:
- Post-implant use of PDE-5i in LVAD patients demonstrates a benefit in reducing mortality and thrombotic complications.
- The use of PDE-5i is associated with an increased risk of gastrointestinal bleeding, necessitating careful patient monitoring.
- Further research may be warranted to balance the benefits and risks of PDE-5i in LVAD management.
Abstract:
Background: Despite the improvement in left ventricular assist device (LVAD) technology and the advent of third-generation LVADs, hemocompatibility-related events remain a significant issue. Therefore, new pharmacological treatments are necessary to optimize patient management and to further reduce hemocompatibility-related events. The purpose of the present systematic review and meta-analysis was to summarize the existing data regarding the safety and efficacy of post-implant phosphodiesterase-5 inhibitors (PDE-5i) on hemocompatibility-related events. Methods: Among the 258 articles in Pubmed, Scopus, and CENTRAL that were retrieved (1990−2022), 15 studies were included in the qualitative synthesis, and 9 studies were included in the quantitative synthesis. The fixed-effects model was used because it is statistically sound for combining a very small number of studies. The primary endpoint of the study was all-cause mortality, whereas the secondary endpoints were ischemic stroke, pump thrombosis, and gastrointestinal bleeding. Results: Mortality was significantly lower in the PDE-5i group vs. the control group (OR: 0.92 [95% CI: 0.85, 0.98]; p = 0.02). The secondary endpoints ischemic stroke (OR: 0.87 [95% CI: 0.78, 0.98]; p = 0.02) and pump thrombosis (OR: 0.90 [95% CI: 0.82, 0.99]; p = 0.04) were also lower in the PDE-5i group. The incidence of gastrointestinal bleeding was significantly higher in patients with LVAD receiving PDE-5i (OR: 1.26 [95% CI: 1.11, 1.44]; p < 0.01). In the overall analysis, the heterogeneity of outcomes was low, except for pump thrombosis. Conclusions: The use of PDE-5i post-implant was associated with lower mortality and thrombotic events but with a higher risk of gastrointestinal bleeding.
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