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Performance characteristics of Ultratherm fluid warmer
1Department of Pathology, University of Virginia Health Sciences Center, Charlottesville.
Anesthesia and Analgesia
|December 1, 1993
Summary
The Ultratherm Infusion Fluid Warmer can cause significant hemolysis in blood due to high internal temperatures. Its use is restricted to clear fluids and specific flow rates and times to avoid heat damage.
Area of Science:
- Biomedical Engineering
- Medical Devices
- Fluid Dynamics
Background:
- The Ultratherm Infusion Fluid Warmer (Model 3703-1) is a disposable device for warming intravenous fluids.
- It lacks temperature monitoring and audible alarms, relying on air-activated chemical heating elements.
- Direct contact between heating elements and i.v. tubing raises concerns about temperature control.
Purpose of the Study:
- To evaluate the warming performance and safety of the Ultratherm Infusion Fluid Warmer.
- To assess the impact of the warmer on blood integrity (hemolysis) and fluid temperatures at various flow rates.
- To determine the limitations and appropriate clinical applications for the Ultratherm device.
Main Methods:
- Intratubing thermocouple wire probes were used to measure internal warmer chamber temperatures.
- Blood and saline warming were studied at different flow rates (30, 100, 500 mL/h).
- Free hemoglobin measurements quantified hemolysis in blood samples exiting the warmer.
Main Results:
- Internal warmer chamber temperatures reached a plateau of approximately 65°C and were sustained for hours.
- Blood samples exiting at 47°C and 53°C showed 0.6% and 7% hemolysis, respectively.
- Warming of refrigerated blood at 500 mL/h was insufficient (below 19°C), while room temperature saline reached up to 52°C.
Conclusions:
- High, unmonitored internal temperatures pose a risk of heat damage to blood and sensitive fluids.
- The Ultratherm warmer's use should be limited to clear fluids, room temperature fluids, and specific flow rates (100-500 mL/h) and times (1-6 hours post-activation).
- Clinical application requires careful consideration of these limitations to ensure patient safety.