Volume 4 Supplement 1

20th International Symposium on Intensive Care and Emergency Medicine

Open Access

In vitro study of a new vaporization humidifying device: DAR HC 2000®

  • N Bottino1,
  • L Chiaravalli1,
  • M Panigada1,
  • F Carrieri1,
  • E Allegritti1,
  • P Pelosi2 and
  • L Gattinoni1
Critical Care20004(Suppl 1):P107

DOI: 10.1186/cc827

Published: 21 March 2000

Full text

In long-term mechanical ventilation, inspired gas should reach the endotracheal tube with a temperature of 30–32°C, and an absolute humidity (HA) of approximately 28–30 mg H2O/l.

We tested a humidifier (DAR HC 2000® composed of: 1) a vaporising cartridge, containing a hydrophobic membrane that separates the gas flow from the heated water; 2) a heating wire that runs all along the inspiratory line, maintaining the heat and moisture conditions of the inspired gas from the cartridge to the patient; 3) a double temperature control that permits the setting of the desired heating level both at the cartridge (T°c) and at the patient's mouth (T°p).

At first, we studied the system's ability to condition inspired gas at different min ventilation (VE=6, 10, 14 l/min), tidal volume (VT=250, 500, 750 ml), and inspiratory flow (Vi=0.5, 1 l/sec) with different settings of T°c and T°p (32–32, 34–34, 36–36, 34–32, 36–32, 36–34, 38–34, 39–34 °C, respectively). We found that increasing VE from 6 to 10 to 14 l/min led to a progressive decrease of HA from 33.0 ± 4.4 to 27.5 ± 4.4 to 23.4 ± 3.6 mg/l (P<0.01),while VT and Vi had no effects on humidification.

Secondly, we tested the humidifier at different VE (from 4 to 16 l/min, 2 l/min per step) with different T°p (32, 34, 36 °C; T°c initially set at the same level as T°p, and then increased at 1°C at a time until condensate appeared in the thermoregulated tube). Adequate humidification levels (HA= 30 mg/l) can be obtained for each VE and T°p by increasing the temperature set at the cartridge enough.

The third part of the study was to verify the decrease of microbiological contamination by simulating a contaminated patient (using a reservoir containing Micrococcus luteus) and analysing the inspiratory line with the heating wire switched first OFF, then ON: keeping the thermoregulated tube OFF, as supposed, a bacterial growth was seen in the inspiratory line, while switching it ON, no M. luteus colonies were observable.

In conclusion, DAR HC 2000® humidifier allows us to obtain adequate levels of humidity of inspired gas for each ventilatory set, just by increasing the cartridge temperature. Besides, the hydrophobic membrane and the heating wire avoid, respectively, the gas-water contact and the condensate formation in the inspiratory line resulting in a reduction of microbiological contamination of the circuit.

Authors’ Affiliations

1st. Anestesia e Rianimazione, Osp. Maggiore Policlinico-IRCCS
Dip. di Scienze Cliniche e Biologiche, Univ. dell'Insubria


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