# Selection of Flow Modulation Protocols for Patients on Continuous Flow Ventricular Assist Devices (CF-VADs)

> **NIH NIH R01** · UNIVERSITY OF ALABAMA AT BIRMINGHAM · 2023 · $582,195

## Abstract

PROJECT SUMMARY
A major concern with continuous flow ventricular assist devices (CF-VADs) is the resulting non-physiological
flow with diminished pulsatility which has been shown to be a major risk factor for development of arteriovenous
malformations (AVMs) and gastrointestinal (GI) bleeding. To address this issue, flow modulation via rapid
changes in pump impeller speed has been proposed as a technique to introduce ‘artificial pulsatility’. However,
given the inadequacy of large animal models with recreating CF-VAD associated non-surgical bleeding events,
it is still unclear if artificial pulsatility can prevent these adverse events or what level of artificial pulsatility is even
necessary. To evaluate the effects of pulsatility and identify promising flow modulation approaches we developed
a vascular pulse perfusion model (VPPM) to culture Human Aortic Endothelial Cells (HAECs) under conditions
of normal pulsatile flow or flow with diminished pulsatility (CF-VAD support). Our rationale for modeling arterial
vessels is because pulsatility primarily affects the arterial side of the circulatory system and its effects are
transduced by endothelial cells that line the large arterial vessels. The VPPM was validated as relevant model
via direct comparison with aortic samples of patients with and without CF-VADs. Our published data also shows
that loss of pulsatility is associated with an increase in production of pro-angiogenic/inflammatory cytokines. The
relevance of these results is further strengthened by supporting data from patients that experience AVMs and
GI bleeding events (both CF-VAD related and due to other conditions) showing similar elevated levels of pro-
angiogenic/inflammatory cytokines. The VPPM therefore provides a powerful model to evaluate artificial
pulsatility in the context of CF-VAD flow modulation and determine if restoring pulse pressure and/or pulse
frequency can mitigate non-surgical bleeding events. Based on recent studies that suggest that pulse pressure
< 35 mmHg is a major risk factor for development of GI bleeds, we hypothesize that “Diminished pulsatility
associated with ‘CF-VAD support’ results in endothelial dysfunction and pro-inflammatory/pro-angiogenic soluble
factor production. These changes can be mitigated via introduction of artificial pulsatility using flow modulation
strategies where pulse pressure is preserved at > 35 mmHg”. Aim1 will evaluate response of patient derived
endothelial cells within the VPPM to CF-VAD flow and quantify angiogenic/inflammatory soluble factor
production, Aim2 will follow patients for up to 36 months to evaluate serum levels of pro-angiogenic/pro-
inflammatory cytokines and non-surgical bleeding events which will then be compared to results from in-vitro
studies within the VPPM and Aim3 will evaluate different flow modulation strategies using patient-derived
endothelial cells to determine most promising patient-specific approaches via comparison of hemodynamic
profiles and cytok...

## Key facts

- **NIH application ID:** 10576830
- **Project number:** 5R01HL151663-03
- **Recipient organization:** UNIVERSITY OF ALABAMA AT BIRMINGHAM
- **Principal Investigator:** Palaniappan Sethu
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2023
- **Award amount:** $582,195
- **Award type:** 5
- **Project period:** 2021-03-02 → 2025-02-28

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10576830

## Citation

> US National Institutes of Health, RePORTER application 10576830, Selection of Flow Modulation Protocols for Patients on Continuous Flow Ventricular Assist Devices (CF-VADs) (5R01HL151663-03). Retrieved via AI Analytics 2026-05-22 from https://api.ai-analytics.org/grant/nih/10576830. Licensed CC0.

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