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Updated: Feb 14, 2026

Use of a Percutaneous Ventricular Assist Device/Left Atrium to Femoral Artery Bypass System for Cardiogenic Shock
Published on: August 16, 2021
Gastrointestinal Bleeding in Left Ventricular Assist Device: Octreotide and Other Treatment Modalities
Tara L Molina1, Jill C Krisl, Kevin R Donahue
1From the Department of Pharmacy, Houston Methodist Hospital (HMH), Houston, Texas.
Insights
Left ventricular assist devices (LVADs) can cause gastrointestinal bleeding (GIB). Octreotide shows promise in managing this complication by targeting factors like altered blood flow and platelet function.
Area of Science:
- Cardiology
- Gastroenterology
- Pharmacology
Background:
- Left ventricular assist devices (LVADs) are crucial for end-stage heart failure but increase gastrointestinal bleeding (GIB) risk.
- High shear and nonpulsatile flow from continuous-flow LVADs contribute to GIB via arteriovenous malformations and acquired von Willebrand syndrome.
Purpose of the Study:
- To review the pathophysiology of LVAD-associated GIB.
- To discuss current and novel treatment modalities for LVAD-associated GIB.
- To evaluate the role of octreotide in managing LVAD-associated GIB.
Main Methods:
- Literature review of LVADs, GIB pathophysiology, and treatment strategies.
- Analysis of studies investigating octreotide for LVAD-GIB.
- Synthesis of data on octreotide's pharmacologic effects relevant to GIB.
Main Results:
- LVADs induce physiological changes predisposing to GIB.
- Octreotide's mechanisms (e.g., improved platelet aggregation, reduced splanchnic flow) may counteract these changes.
- Existing literature suggests clinical benefit of octreotide in managing LVAD-associated GIB.
Conclusions:
- LVAD-associated GIB is a significant complication requiring effective management strategies.
- Octreotide presents a promising therapeutic option, targeting key pathophysiological mechanisms.
- Further research and clinical trials are warranted to solidify octreotide's role.
Abstract:
Left ventricular assist devices (LVADs) offer a therapeutic strategy for patients with end-stage heart failure. Increased device utilization has also increased the incidence of device-related complications including gastrointestinal bleeding (GIB). Multiple mechanisms have been proposed in the pathophysiology of continuous-flow LVAD-associated GIB including physiologic changes associated with high shear and nonpulsatile flow such as gastrointestinal arteriovenous malformations and acquired von Willebrand syndrome. Strategies to minimize the morbidity and mortality of LVAD-associated GIB are needed. Octreotide, a somatostatin analogue, has been described as an adjunct to current therapies and interventions. Factors that contribute to LVAD-associated GIB may be targeted by the pharmacologic effects of octreotide, including improved platelet aggregation, increased vascular resistance, and decreased splanchnic circulation. Octreotide has demonstrated clinical benefit in several case series and clinical trials for the treatment of LVAD-associated GIB. The focus of this article will be to review the pathophysiology of LVAD-associated GIB, discuss pharmacologic and nonpharmacologic treatment modalities, and review available literature on the role of octreotide in the management of LVAD-associated GIB.
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