Unit of competency Outline
Date retreived
23/07/2026 7:54 AM AWST
23/07/2026 7:54 AM AWST
Whilst all efforts are made to provide accurate and timely information from the relevant source/documentation, please be aware that the information supplied may not be the most current version. The accuracy of the detail has not been confirmed by the Department and therefore should not be relied upon without first confirming the contents.
Perform polysomnographic recording
Perform polysomnographic recording
Unit of competency
National Code
HLTNE608D
HLTNE608D
State Code
WD223
WD223
TGA Status
Deleted
Deleted
DTWD Status
Deleted
Deleted
State Implementation and Classification
Approved Date
08/08/2014
Field of Education
060301 - General Nursing
Original Release Date
08/08/2014
Nominal Hours
100
Description
DescriptorThis unit of competency describes the skills and knowledge required to prepare a client for and to perform a polysomnographic recording.
Notes
Elements and Performance Criteria
1. Prepare equipment, material and environment
- 1.1 Review client booking list for client details
- 1.2 Identify special needs of clients
- 1.3 Select equipment, materials and location for test
- 1.4 Ensure equipment and materials selected are clean and dry, in working order, and, where applicable, calibrated
- 1.5 Review relevant, current literature and protocols
- 1.6 Arrange client bookings according to organisation procedures, clients' needs, and reason for study
2. Prepare client for procedure
- 2.1 Confirm receipt of information by client
- 2.2 Receive and process request for polysomnographic recording
- 2.3 Correctly identify client, reassure and inform client regarding the procedure
- 2.4 Give opportunities for client/carer to ask questions and discuss areas of concern
- 2.5 Check client consent has been obtained
- 2.6 Review client's medical history, seek clarification on specific details and take actioned, as required
3. Attach monitoring equipment
- 3.1 Utilise personal protective equipment in accordance with standard and additional precautions
- 3.2 Select type and number of electrodes according to client needs, including multiple polygraphic recording electrodes
- 3.3 Conduct head measurement to verify sites for cerebral electrode placement according to current standards and organisation policies and procedures
- 3.4 Identify positioning of monitoring equipment for other physiological measurements
- 3.5 Complete skin preparation according to infection control guidelines and client's needs
- 3.6 Attach other monitoring equipment as required
- 3.7 Correctly connect required leads between interface/head box and machine
- 3.8 Perform pre-test electrode impedance and establish integrity of electrodes and other recording devices, and application
- 3.9 Adjust equipment, electrodes, and other recording devices as required
- 3.10 Enter client details on testing equipment or on paper traces, as required
- 3.11 Perform pre test on machine and biological calibration, including calibration of all polygraphic variables and AC/DC amplifiers
4. Conduct polysomnographic recording
- 4.1 Perform additional validation techniques performed
- 4.2 Apply techniques according to client details and annotate concurrent results on record
- 4.3 Validate electrode impedance throughout test as required
- 4.4 Use troubleshooting methods to isolate problems with any recording device used in the study.
- 4.5 Recognise artefacts are recognised, annotate on the record, and eliminate or reduce on all polygraphic channels
- 4.6 Identify expected waveforms related to clinical conditions and age groups
- 4.7 Identify sleep states and staging
- 4.8 Identify changes in physiological parameters are identified, correlate to client's record and action as required
- 4.9 Identify and action abnormal EEG patterns and waveforms which require immediate attention
- 4.10 Use derivations and machine settings according to test requirements, polygraphic variables, concurrent results and client needs
- 4.11 Add/attach further monitoring equipment and/or electrodes in response to concurrent findings
- 4.12 Annotate on recording any changes throughout the procedure
- 4.13 Determine appropriate length of recording according to standards, medical referral and concurrent polysomnographic results.
- 4.14 Identify and meet client needs during the polysomnographic recording
- 4.15 Identify and respond to severe reactions and complications to in accordance with organisation emergency procedures
5. Complete procedure
- 5.1 Perform post test electrode impedance and verify integrity of electrode and contact
- 5.2 Perform post test machine and biological calibration
- 5.3 Validate existence of the computerised file on hard drive, if required
- 5.4 Identify and action abnormal test patterns which require immediate medical attention
- 5.5 Remove EEG leads and electrodes and other recording devices from client and wash paste/gel off client
- 5.6 Provide client with assistance as required, on completion of the procedure
- 5.7 Confirm timely follow up with referring doctor for results
- 5.8 Record test details for retrieval and statistical purposes according to department procedures
- 5.9 Provide information to client and carer according to duty of care
- 5.10 Clean, dry and store equipment in accordance with manufacturer's guidelines and infection control guidelines
- 5.11 Dispose of disposable EEG electrodes and other materials in accordance with waste management procedures and infection control guidelines
6. Generate report
- 6.1 Review and correct client details reviewed and corrected
- 6.2 Review annotations reviewed and correct to provide accurate and concise information including sleep staging
- 6.3 Forward technical report/results with accompanying documentation to neurologist or respiratory specialist for review or assessment and reporting
RANGE STATEMENT
The Range Statement relates to the unit of competency as a whole. It allows for different work environments and situations that may affect performance. Add any essential operating conditions that may be present with training and assessment depending on the work situation, needs of the candidate, accessibility of the item, and local industry and regional contexts.
Equipment and material may include:
EEG machine; digital, analogue, portable, standard, video and audio
Polygraphic equipment; ECG, EMG, EOG machines, respiration, movement and tremor monitors
Electrodes eg caps, disc, mushroom
Head box
Chair
Bed
Additional - accessories, toys, other stimuli
Gels and Electrode pastes
Tape measure
Video cassette recorder and camera with audio
Resuscitation equipment
CPAP machine
Monitoring equipment including monitors for TCO2, SaO2, sound, body position
Environment may include:
Neurophysiology department
Wards
Sleep Laboratories
Private Neurologist's rooms
Intensive care units
Client details may include:
Referral letter/request
Reason for study/referral
Medical history
Address and telephone number
Date of birth and age
Medications
Client's presenting condition
Sleep patterns
Date of test
Date of previous test
In care client/out of care client
Clients' expectations
Test requested
Referring doctor address and telephone number
Clients may include:
Adults
Children
Neonates
Adolescents
Elderly
Client medical history may include:
Event/s leading to referral
Sleep disorder
Current sleep patterns
Cardiac disorder
Respiratory disorder
Vascular disorder
Neurological disorder
Infectious diseases
Epilepsy type and frequency, and date of last seizure
Psychiatric and behavioural disorders
Developmental disorder
Metabolic disorder
Medications
Action in response to client's medical history may include:
Use of various additional recording devices including: CPAP machine, TCO2 monitors, etc.
Varied activation procedure or disturbances
Alteration of Test procedure time
Waking the client
Personal protective equipment may include:
Gloves
Mask
Goggles
Gown
Positioning of monitoring equipment for other physiological measurement may include:
Respiratory i.e. diaphragm, nasal, oral
EMG
Other monitoring equipment may include:
ECG monitor
Respiration
Actogram
EMG
Oximetry
Movement sensors
CPAP machine
TCO2 monitor
Integrity of electrodes must include:
Ground
Reference
Active
Respiration thermistors or equivalent
Respiration straps
Oximetry
Movement Sensors
CPAP machine
TCO2 monitor
Additional validation techniques must include:
Touch test (of electrodes)
Exchange electrodes
Replace electrodes
Low, and of similar value, impedances
Amplifier calibration for DC and AC
Continuous monitoring of CPAP
Continuous viewing of the sleep study in progress
Techniques applied must include:
Montages
Derivations
Sensitivity
Filter
Display speed
Activations
Sleep states and staging must include:
Wake
REM and REM onset
Non-REM, including stages I, II, III, IV
Sleep onset
Physiological parameters may include:
Respiration
ECG
Oxygen saturation
Actogram
EMG
Causes of changes throughout procedure must include:
EEG findings
ECG findings
Respiration findings
SaO2 findings
TCO2 findings
EMG findings
Clinical events
Equipment
Environmental
Client's physiological and psychological state
Abnormal patterns which require immediate medical attention must include:
Continuous spiking or spike and wave
Hypsarrhythmic EEG
Frequent sub clinical seizure pattern
Status epilepticus
EEG finding consistent with infectious or reportable diseases/conditions eg Herpes Encephalitis, Creutzfeldt Jakob Disease (CJD) or CJD variant
Burst suppression and /or isoelectric EEG
Unilateral abnormality
Any other conditions which may endanger the health and well being of the client, particularly if not expected prior to recording or indicated on the referral letter
Other abnormalities that may be identified on the ECG, respiration or SaO2 channels or other recording devices
Complications and severe reactions may include:
Seizure
Cardio-respiratory arrest
Information provided to client's and carer's may include:
Appropriate follow up period with referring doctor to obtain results
Risks of injury to client following procedure ie. if overtired, or if have ceased medication for test etc.
How to clean the hair etc. appropriately to remove all glues/pastes.
The Range Statement relates to the unit of competency as a whole. It allows for different work environments and situations that may affect performance. Add any essential operating conditions that may be present with training and assessment depending on the work situation, needs of the candidate, accessibility of the item, and local industry and regional contexts.
Equipment and material may include:
EEG machine; digital, analogue, portable, standard, video and audio
Polygraphic equipment; ECG, EMG, EOG machines, respiration, movement and tremor monitors
Electrodes eg caps, disc, mushroom
Head box
Chair
Bed
Additional - accessories, toys, other stimuli
Gels and Electrode pastes
Tape measure
Video cassette recorder and camera with audio
Resuscitation equipment
CPAP machine
Monitoring equipment including monitors for TCO2, SaO2, sound, body position
Environment may include:
Neurophysiology department
Wards
Sleep Laboratories
Private Neurologist's rooms
Intensive care units
Client details may include:
Referral letter/request
Reason for study/referral
Medical history
Address and telephone number
Date of birth and age
Medications
Client's presenting condition
Sleep patterns
Date of test
Date of previous test
In care client/out of care client
Clients' expectations
Test requested
Referring doctor address and telephone number
Clients may include:
Adults
Children
Neonates
Adolescents
Elderly
Client medical history may include:
Event/s leading to referral
Sleep disorder
Current sleep patterns
Cardiac disorder
Respiratory disorder
Vascular disorder
Neurological disorder
Infectious diseases
Epilepsy type and frequency, and date of last seizure
Psychiatric and behavioural disorders
Developmental disorder
Metabolic disorder
Medications
Action in response to client's medical history may include:
Use of various additional recording devices including: CPAP machine, TCO2 monitors, etc.
Varied activation procedure or disturbances
Alteration of Test procedure time
Waking the client
Personal protective equipment may include:
Gloves
Mask
Goggles
Gown
Positioning of monitoring equipment for other physiological measurement may include:
Respiratory i.e. diaphragm, nasal, oral
EMG
Other monitoring equipment may include:
ECG monitor
Respiration
Actogram
EMG
Oximetry
Movement sensors
CPAP machine
TCO2 monitor
Integrity of electrodes must include:
Ground
Reference
Active
Respiration thermistors or equivalent
Respiration straps
Oximetry
Movement Sensors
CPAP machine
TCO2 monitor
Additional validation techniques must include:
Touch test (of electrodes)
Exchange electrodes
Replace electrodes
Low, and of similar value, impedances
Amplifier calibration for DC and AC
Continuous monitoring of CPAP
Continuous viewing of the sleep study in progress
Techniques applied must include:
Montages
Derivations
Sensitivity
Filter
Display speed
Activations
Sleep states and staging must include:
Wake
REM and REM onset
Non-REM, including stages I, II, III, IV
Sleep onset
Physiological parameters may include:
Respiration
ECG
Oxygen saturation
Actogram
EMG
Causes of changes throughout procedure must include:
EEG findings
ECG findings
Respiration findings
SaO2 findings
TCO2 findings
EMG findings
Clinical events
Equipment
Environmental
Client's physiological and psychological state
Abnormal patterns which require immediate medical attention must include:
Continuous spiking or spike and wave
Hypsarrhythmic EEG
Frequent sub clinical seizure pattern
Status epilepticus
EEG finding consistent with infectious or reportable diseases/conditions eg Herpes Encephalitis, Creutzfeldt Jakob Disease (CJD) or CJD variant
Burst suppression and /or isoelectric EEG
Unilateral abnormality
Any other conditions which may endanger the health and well being of the client, particularly if not expected prior to recording or indicated on the referral letter
Other abnormalities that may be identified on the ECG, respiration or SaO2 channels or other recording devices
Complications and severe reactions may include:
Seizure
Cardio-respiratory arrest
Information provided to client's and carer's may include:
Appropriate follow up period with referring doctor to obtain results
Risks of injury to client following procedure ie. if overtired, or if have ceased medication for test etc.
How to clean the hair etc. appropriately to remove all glues/pastes.
EVIDENCE GUIDE
The evidence guide provides advice on assessment and must be read in conjunction with the Performance Criteria, Required Skills and Knowledge, the Range Statement and the Assessment Guidelines for this Training Package.
Critical aspects for assessment and evidence required to demonstrate this competency unit:
The individual being assessed must provide evidence of specified essential knowledge as well as skills
Where, for reasons of safety, space, or access to equipment and resources, assessment takes place away from the workplace, the assessment environment should represent workplace conditions as closely as possible
Consistency of performance should be demonstrated over the required range of situations relevant to the workplace
Context of and specific resources for assessment:
Relevant organisation policy, guidelines, procedures and protocols
Method of assessment:
Clinical skills involving direct client care are to be assessed initially in a simulated clinical setting (laboratory). If successful, a second assessment is to be conducted during workplace application under direct supervision.
Observation of work activities when performing polysomnographic recordings
Observation of simulation and/or role play when performing polysomnographic recordings
Discussion of physical and/or behavioural contingency scenarios involving duty of care
Authenticated transcripts of relevant education/training courses
Recognition of relevant life/work experience
Questioning, written assessments/projects, e-learning can be used to assess knowledge
Authenticated reports of experience in performing polysomnographic recordings (Documentation associated with performance reviews, supervisor/co-ordinator evaluations of work performance)
Training records associated with First Aid, OH Safety training, Orientation/Induction Training, Safe Manual Handing, Universal infection control procedures
Case study and scenario as a basis for discussion of issues and strategies to contribute to best practice
Access and equity considerations:
All workers in the health industry should be aware of access and equity issues in relation to their own area of work
All workers should develop their ability to work in a culturally diverse environment
In recognition of particular health issues facing Aboriginal and Torres Strait Islander communities, workers should be aware of cultural, historical and current issues impacting on health of Aboriginal and Torres Strait Islander people
Assessors and trainers must take into account relevant access and equity issues, in particular relating to factors impacting on health of Aboriginal and/or Torres Strait Islander clients and communities
The evidence guide provides advice on assessment and must be read in conjunction with the Performance Criteria, Required Skills and Knowledge, the Range Statement and the Assessment Guidelines for this Training Package.
Critical aspects for assessment and evidence required to demonstrate this competency unit:
The individual being assessed must provide evidence of specified essential knowledge as well as skills
Where, for reasons of safety, space, or access to equipment and resources, assessment takes place away from the workplace, the assessment environment should represent workplace conditions as closely as possible
Consistency of performance should be demonstrated over the required range of situations relevant to the workplace
Context of and specific resources for assessment:
Relevant organisation policy, guidelines, procedures and protocols
Method of assessment:
Clinical skills involving direct client care are to be assessed initially in a simulated clinical setting (laboratory). If successful, a second assessment is to be conducted during workplace application under direct supervision.
Observation of work activities when performing polysomnographic recordings
Observation of simulation and/or role play when performing polysomnographic recordings
Discussion of physical and/or behavioural contingency scenarios involving duty of care
Authenticated transcripts of relevant education/training courses
Recognition of relevant life/work experience
Questioning, written assessments/projects, e-learning can be used to assess knowledge
Authenticated reports of experience in performing polysomnographic recordings (Documentation associated with performance reviews, supervisor/co-ordinator evaluations of work performance)
Training records associated with First Aid, OH Safety training, Orientation/Induction Training, Safe Manual Handing, Universal infection control procedures
Case study and scenario as a basis for discussion of issues and strategies to contribute to best practice
Access and equity considerations:
All workers in the health industry should be aware of access and equity issues in relation to their own area of work
All workers should develop their ability to work in a culturally diverse environment
In recognition of particular health issues facing Aboriginal and Torres Strait Islander communities, workers should be aware of cultural, historical and current issues impacting on health of Aboriginal and Torres Strait Islander people
Assessors and trainers must take into account relevant access and equity issues, in particular relating to factors impacting on health of Aboriginal and/or Torres Strait Islander clients and communities
Replaces
| State Code | National Code | Title | Type |
|---|---|---|---|
| D8368 | HLTNE608C | Perform polysomnographic recording | Unit of competency |
| State Code | National Code | Title | Type |
|---|---|---|---|
| J117 | HLT60812 | Advanced Diploma of Neurophysiology Technology | Qualification |