Bench Validation of a Compact Low-Flow CO Removal Device.

BACKGROUND

There is increasing evidence demonstrating the value of partial extracorporeal CO removal (ECCOR) for the treatment of hypercapnia in patients with acute exacerbations of chronic obstructive pulmonary disease and acute respiratory distress syndrome. Mechanical ventilation has traditionally been used to treat hypercapnia in these patients, however, it has been well-established that aggressive ventilator settings can lead to ventilator-induced lung injury. ECCOR removes CO independently of the lungs and has been used to permit lung protective ventilation to prevent ventilator-induced lung injury, prevent intubation, and aid in ventilator weaning. The Low-Flow Pittsburgh Ambulatory Lung (LF-PAL) is a low-flow ECCOR device that integrates the fiber bundle (0.65 m) and centrifugal pump into a compact unit to permit patient ambulation.

METHODS

A blood analog was used to evaluate the performance of the pump at various impeller rotation rates. In vitro CO removal tested under normocapnic conditions and 6-h hemolysis testing were completed using bovine blood. Computational fluid dynamics and a mass-transfer model were also used to evaluate the performance of the LF-PAL.

RESULTS

The integrated pump was able to generate flows up to 700 mL/min against the Hemolung 15.5 Fr dual lumen catheter. The maximum vCO of 105 mL/min was achieved at a blood flow rate of 700 mL/min. The therapeutic index of hemolysis was 0.080 g/(100 min). The normalized index of hemolysis was 0.158 g/(100 L).

CONCLUSIONS

The LF-PAL met pumping, CO removal, and hemolysis design targets and has the potential to enable ambulation while on ECCOR.