Background: Adequate humidification in long-term jet ventilation is a criti
cal aspect in terms of clinical safety.
Aim: To assess a prototype of an electronic jet-ventilator and its humidifi
cation system.
Methods: Forty patients with respiratory insufficiency were randomly alloca
ted to one of four groups. The criterion for inclusion in this study was re
spiratory insufficiency exhibiting a Murray score above 2. The four groups
of patients were ventilated with three different respirators and four diffe
rent humidification systems. Patients in groups A and B received superimpos
ed high-frequency jet ventilation (SHFJV) by an electronic jet-ventilator e
ither with (group A) or without (group B) an additional humidification syst
em. Patients in group C received high-frequency percussive ventilation (HFP
V) by a pneumatic high-frequency respirator, using a hot water humidifier f
or warming and moistening the inspiration gas. Patients in group D received
conventional mechanical ventilation using a standard intensive care unit r
espirator with a standard humidification system. SHFJV and HFPV were used f
or a period of 100 h (4 days).
Results: A significantly low inspiration gas temperature was noted in patie
nts in group B, initially (27.2 +/- 2.5 degrees C) and after 2 days (28.0 /- 1.6 degrees C) (P< 0.05). The percentage of relative humidity of the ins
piration gas in patients in group B was also initially significantly low (6
9.8 +/- 4.1%; P< 0.05) but rose to an average of 98 +/- 2.8% after 2 h. The
average percentage across all four groups amounted to 98 +/- 0.4% after 2
h. Inflammation of the tracheal mucosa was found in patients in group B and
the mucosal injury score (MIS) was significantly higher than in all the ot
her groups. Patients in groups A, C and D showed no severe evidence of airw
ay damage, exhibiting adequate values of relative humidity and temperature
of the inspired gas.
Conclusion: The problems of humidification associated with jet ventilation
can be fully prevented by using this new jet-ventilator. These data were su
stained by nondeteriorating MIS values at the end of the 4-day study period
in groups A, C and D.