Use of Limited EEG Source Devices Survey

Name *

First

Last

Email *

1. Who is primarily responsible for the initial placement of the device [select all that apply]?

Nurse
Medical or nurse assistant
Fellow or physician
Neurodiagnostic technologist
Depends on type of study and-or availability of technologist
Other

If Other, enter here:

2. Is the device used as a substitute for standard or disposable electrodes for the full study or is it replaced with a standard 10-20 setup when a technologist is available [select all that apply]?

Is a substitute used for a full routine EEG test
Is a substitute used for LTM in ICU
Is a substitute used for LTM in EMU
Is a substitute used for pediatric patients
Is replaced with standard 10-20 setup when a technologist is available
Both as a substitute for some studies and for other studies, is replaced with standard 10-20 protocol

3. If the device is replaced with a standard EEG setup, does your facility document the integrity of the device before replacement (i.e., recording inter-electrode impedances, any deviation of the device from the standard 10-20 placement, etc.)?

No. We do not document parameters before or once a device is replaced.
Yes. We document the following parameters when replacing a device with standard 10-20 setup:

If Yes, enter parameters here:

4. In which type of environment(s) is the device used [select all that apply]?

For routine EEG
For long-term monitoring in ICU setting
For LTM in EMU setting
With pediatric
Other

If Other, enter here:

5. Which type of device do you have experience using [select all that apply]?

Cap
Band
Helmet
Other

If Other, enter here:

6. Manufacturer(s):

7. We request your personal feedback on the use of limited EEG-devices (pros and cons):

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