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A novel device for air removal from vascular access line: a bench study
Zeping Xu1,2, Lingyan Jin2, Byron Smith3
1Department of Anesthesiology, Jiangsu Cancer Hospital, Nanjing, China.
Journal of Clinical Monitoring and Computing
|February 19, 2018
Summary
A new vascular access line air removal device (VALARD) effectively removes air bubbles without interrupting fluid flow, unlike the Belmont pump. This innovation enhances safety by preventing air embolism during infusions.
Area of Science:
- Medical Devices
- Vascular Access
- Air Embolism Prevention
Background:
- Efficient air removal from vascular access lines is critical for preventing air embolism.
- Current devices, particularly for rapid infusion, have suboptimal performance.
- There is a need for improved air removal technology in medical infusions.
Purpose of the Study:
- To develop and evaluate a novel vascular access line air removal device (VALARD).
- To compare the air removal efficiency and flow interruption of VALARD against the Belmont pump.
- To assess the performance of VALARD under various infusion and air injection rates.
Main Methods:
- Part I: Infusion of saline at 250-750 mL/min with air introduced at 5-15 mL/min, measuring air bubbles >10 µL and flow pause time.
- Part II: Rapid injection of 120 mL air into VALARD at ~500 mL/min, recording air bubbles, flow pause time, and air transit time.
- Comparison between VALARD and Belmont pump performance in air bubble detection and flow interruption.
Main Results:
- VALARD detected no air bubbles >10 µL at any tested flow or air injection rate, without pausing forward flow.
- The Belmont pump allowed air bubbles >10 µL in 60% of tests, often requiring a pause in forward flow.
- VALARD demonstrated efficient air elimination without compromising continuous fluid delivery.
Conclusions:
- The novel VALARD device efficiently removes air from vascular access lines.
- VALARD operates without interrupting forward bulk flow, a significant advantage over existing devices like the Belmont pump.
- Further clinical trials are recommended to validate VALARD's efficiency, safety, and usability in clinical settings.
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