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INTRODUCTION
This activity module focuses on aerosol delivery devices used for continuous aerosol therapy. Also,
emphasizes medication delivery devices and techniques.
2. Given a specific clinical situation, select and apply the appropriate aerosol delivery device.
5. Practice communication skills needed to explain the application of an aerosol device to a patient
and confirm patient understanding.
6. Practice medical charting for the therapeutic application of an aerosol delivery device.
7. Apply infection control guidelines and standards associated with aerosol delivery equipment and
procedures, according to OSHA regulations and CDC guidelines.
COMPONENTS OF AN LVN
Examine a large-volume nebulizer and use the following list to identify the labeled
components in Figure 1. Record the components in your laboratory report.
DISS connection
Air entrainment ports
Fio2 adjustment (entrainment selector)
Jet
Baffle
Capillary tube Pressure pop-off (not shown)
Filter
Outlet
ASSEMBLY OF AN LVN
1. Assemble the nebulizer according to the manufacturer’s instructions.
2. Aseptically fill the nebulizer with sterile water. If a prefilled nebulizer is used, be sure not
to contaminate the internal surfaces.
3. Attach the heating element and adjust the settings, if available, to achieve 37°C.
4. Attach the nebulizer to the DISS outlet of a flowmeter.
5. Adjust the Fio2 by turning the entrainment selector to the 100% setting. 6. Turn the flow
to 10 Lpm and observe the mist density and output, the total flow, and the size of the
entrainment port. Record your observations on your laboratory report.
7. Turn the flowmeter to 15 Lpm or as high as it will go. Record the highest flow achievable
on your laboratory report.
8. Return the flow to 10 Lpm.
9. Set the entrainment selector to 35% oxygen. Note any changes in the mist density and
output, the total flow, and the size of the entrainment port. Record your observations on
your laboratory report.
10. Set the entrainment selector in between any two oxygen settings. Record the settings on
your laboratory report.
11. Attach six lengths of corrugated tubing.
12. Place the temperature probe adaptor one tubing length from the patient interface.
Insert the temperature probe. 13. Place another temperature probe adaptor about halfway
between the nebulizer and the patient interface. Insert the temperature probe.
14. Note the time. Record the beginning temperature on both probes on your laboratory
report. 15. Measure the time it takes for the temperature to reach 37°C on each probe.
Record the times and final temperatures on your laboratory report.
16. Analyze the Fio2 and record it on your laboratory report.
17. Adjust the Fio2 by turning the entrainment selector to 0.40. Analyze the Fio2 and
readjust the entrainment selector if necessary to ensure that the nebulizer is delivering 40%
oxygen.
18. Put water in the corrugated tubing so that the lumen of the tube is occluded in the loop,
or “belly,” of the tubing, as shown in Figure 1.
19. Analyze the Fio2 and record it on your laboratory report.
20. Drain the water from the tubing by “milking” the tubing away from the device and into a
waste receptacle.
21. Attach a water trap by cutting the corrugated tubing in the belly of the tubing and
attaching the trap to the ends of the tubing, as shown in Figure 2.
22. Turn the liter flow to 5 Lpm. Observe the mist output and record your observations on
your laboratory report.
A B C D
Figure 1. Aerosol delivery devices.
Figure 2. Aerosol setup with a face mask. Figure 3. Aerosol setup with a face tent.
F
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Laboratory Report
AEROSOL GENERATORS
DATA COLLECTION
EXERCISE 1: Large-Volume Nebulizer
A. JET
B._ Fio2 adjustment (entrainment selector) baffle
C. DISS CONNECTION
D. AIR ENTERTAINMENT PORTS
E. OUTLET
F. FILTER
G. CAPILLARY TUBE
ASSEMBLY OF AN LVN
Type and brand of nebulizer used: _________________________________________
Entrainment Selector at 100%
Mist density at 100%: __________________________________________
Total flow at 100%: ____________
Entrainment port size: ______________________________
Flowmeter at 15 Lpm: ________________
Entrainment Selector at 35%
Mist density at 35%: __________________________________________
Total flow at 35%: ____________
Entrainment port size: ______________________________
Temperature Probes
FIO2 set between _______________________________ Time: _________
Heating element setting: _____________
Initial temperature of probe nearest humidifier: ___________________
Time to achieve 37°C of probe nearest humidifier: _________________
Final temperature of probe nearest humidifier: ____________________
Analysis of FIO2_____________________________________________
Water in Tubing
Analysis of FIO2:_____________________________
5 Lpm flow:________________________________
LARGE-VOLUME USN
Continuous feed inlet
Couplant chamber
On/off switch
Amplitude adjustor
Blower
Diaphragm
Medication chamber
Piezoelectric element
Observations:
___________________________________________________________________________
___________________________________________________________________
Back pressure will be generated by the water in the tubing, preventing the air from being entrained.
As a result, the total flow would be reduced while the FiO2 generated by the unit would increase. If
the total flow does not meet the inspiratory flow demand, the patient can receive FiO2 as room air is
entrained around the delivery system.
2. What effect did increasing the amplitude of the USN have on the aerosol’s density?
What determines the particle size of the USN?
The density of the mist increased as the amplitude was increased.
During the procedure, either titrate the oxygen into the device through a titration
port, titrate in-line, or cover the cannula with the aerosol mask.
4. Under what circumstances would it be necessary to use tandem nebulizers?
When a single unit's flow isn't enough to satisfy the patient's inspiratory flow
demand; otherwise, the required FiO2 can not be provided.
5. What are five factors that should be considered when choosing the proper aerosol
delivery device for a patient?
The medication being administered, the desired deposition location, the patient's
characteristics (age, disease, willingness to obey instructions), the patient's ability to
correctly use the device, and the patient's choice.