Perform rejuvenation, regeneration and/or enhancement of the skin using dermal filler procedures
Overview
This standard coexists alongside, SKANSC1: Implement and maintain safe, hygienic and effective working practices during elective non-surgical cosmetic procedures and SKANSC2: Consult, assess, plan and prepare for elective non-surgical cosmetic procedures within the working environment. This standard is for aesthetic practitioners performing procedures using dermal fillers to temporary disguise signs of ageing, modify facial symmetries and structures. You will also be required to do a post procedure evaluation and reflection for continuous improvement. The aesthetic practitioner must have a First Aid at Work qualification or equivalent and be able to carry out the functions within SFHCHS36: Basic life support and have access to life support equipment as identified in the emergency plan. Users of this standard will need to ensure that their practices reflect up-to-date information, policies, procedures and best practice guidance.
Performance criteria
You must be able to:
carry out a concise and comprehensive consultation face to face with the individual and maintain your responsibilities for health and safety pre, during and post the dermal filler procedure
discuss to establish the individual's objectives, concerns, expectations and desired outcomes to inform the dermal filler procedure plan to include:
2.1 alternative treatment options
develop an emergency plan with the identified healthcare professional/regulated independent prescriber trained to deal with adverse reactions to dermal fillers
establish the dermal filler procedure plan **in accordance with legislative requirements and organisational policies and procedures to include:
4.1 the individual procedure plan
4.2 advice, support and guidance
4.3 emergency plan
4.4 pain management strategy
- reiterate, confirm and agree with the individual, they have understood the proposed dermal filler procedure and pain management to include:
5.1 contra-actions
5.2 adverse reactions
obtain the individual's written informed consent for the dermal filler procedure and pain management, allowing an adequate time scale for the individual to make an informed choice
review the written informed consent for the dermal filler procedure and pain management
select an effective hygiene preparation product to meet the individual's needs in accordance with the manufacturer's instructions
prepare the individual's treatment area in accordance with the dermal filler procedure protocol and associated risk avoidance strategies to include:
9.1 mark out pre-procedure markings if applicable
source and select the hyaluronic acid dermal filler, detailing the G prime, viscosity and longevity of the product to meet the individuals needs and area to be treated, including associated risks
inject the dermal filler with the sterile single use needle and/or cannula in accordance with the dermal filler procedure protocol to include:
11.1 adaptation of injection techniques, depth and placement
11.2 in accordance with the pre-procedure markings if applicable
monitor the individual's health, wellbeing and skin reaction throughout the dermal filler procedure in accordance with legislative requirements and organisational policies and procedures
in the event of an adverse reaction or incident, the aesthetic practitioner must take prompt corrective action as set out within the emergency plan to include:
13.1 seek and implement immediate medical intervention from the identified healthcare professional trained to deal with complications as set out in the emergency plan when a prescription only medication is required
- conclude the procedure in accordance with the dermal filler procedure protocol, legislative requirements and organisational policies and procedures to include:
14.1 removing any pre-procedure markings if applicable
take and store consensual visual media of the individual's treatment area in accordance with insurance requirements, organisational policies and procedures
complete the individual's non-surgical cosmetic procedure records and store in accordance with data legislation
use reflective practice to evaluate the dermal filler procedure and take appropriate action
provide and obtain confirmation of receipt of the verbal and written instructions and advice given to the individual pre and post procedure to include:
18.1 the aesthetic practitioners contact details
18.2 emergency plan
18.3 contingency plan in the event of absence
record the outcome and evaluation of the dermal filler procedure to agree and inform future procedures
discuss and agree future procedures with the individual
Knowledge and Understanding
You need to know and understand:
the importance of collaboration with competent professionals to support effective and safe working practices
your role and responsibilities in performing non-surgical cosmetic procedures and the importance of working within your competence
3. why you must comply with ethical practice and work within the legislative requirements
- the importance to engage in, and document continuous professional development to include, up-to-date information policies, procedures and best practice guidance
5. the anatomy and physiology relevant to this standard
- the types, composition and pharmacological effects of chemical compounds in dermal filler solutions to include:
6.1. the physiological effect of hyaluronic acid solution has on facial anatomy, skin tissue and blood supply
how to adapt injection techniques to place hyaluronic acid solution safely beneath the skin tissue into underlying structures to meet the individual's needs
the adverse reactions associated with a dermal filler procedure to include:
8.1 knowledge and avoidance of danger zones
8.2 non-Hyaluronic Acid dermal fillers (semi-permanent)
- how to implement the correct course of action in the event of an adverse reaction or incident to include:
9.1 why and when immediate medical invention is necessary
the risk avoidance strategies
the importance of obtaining and following instructions from the identified healthcare professional/regulated independent prescriber in the event of an adverse reaction
the purpose, use and limitations of dermal filler procedures in relation to:
12.1* *past and current medical history
12.2 previous non-surgical cosmetic and/or dental procedure history
12.3 relevant lifestyle factors
12.4 contraindicated medication and medical conditions
12.5* *the individual's physical and psychological suitability for the non-surgical cosmetic procedure
12.6 individual's expectations
12.7 hyper-immune response management
12.8 anaphylaxis management
the regulatory and legislative requirements for 'medical devices'
the regulatory and legislative requirements for sourcing, recording and administering dermal filler to include:
14.1 product name
14.2 batch number
14.3 expiry date
14.4 material data sheets
14.5 storage
14.6 disposal
14.7 audit and accountability
the types of pain management and associated risks
the legislative requirements and restrictions for sourcing, storing and using licensed topical anesthetics
the health and safety responsibilities in line with legislation before, during and after the dermal filler procedure
why it is important to discuss and establish the individual's objectives, concerns, expectations, desired outcomes and agree the non-surgical cosmetic procedure plan
the importance of using visual aids to inform the individual of the physical effects
the fee structures and treatment options
the legislative and indemnity requirements of gaining signed, informed consent for the dermal filler procedure
why it is important to allow time for the individual to reflect before confirming and agreeing to receive the elective non-surgical cosmetic procedure
the importance of obtaining written consent for the dermal filler procedure and pain management strategy
the types of hygiene products for the skin and the importance of following manufacturer's instructions
the importance of adhering to the dermal filler procedure protocol
the importance of monitoring the health and wellbeing of the individual during and post procedure
the importance of adhering to the emergency plan in the event of an adverse reaction **
the legislative, insurance and organisational requirements for taking and storing visual media of the individual's treatment area
the legislative and regulatory requirements of completing and storing the individual's non-surgical cosmetic procedure records
the expected outcomes from a dermal filler procedure
the purpose of reflective practice and evaluation and how it informs future procedures
how to collate, analyse, summarise and record evaluation feedback in a clear and concise way
the importance to record the outcome and evaluation of the dermal filler procedure
the instructions and advice pre and post the dermal filler procedure
Scope/range
Additional information
It is expected that the aesthetic practitioner undertaking this standard already has the skills, knowledge and behaviours identified within the aesthetic practitioner's procedure guidance and non-surgical cosmetic National Occupational Standards.
The aesthetic practitioner is expected to already be able to demonstrate competency in determining the relative (restrictive) and absolute (preventative) contraindications for the non-surgical cosmetic procedures. In addition, the aesthetic practitioner should be able to identify adverse reactions or incidents and take prompt corrective action as agreed within the emergency plan.
It is expected that this Standard is used in conjunction with SKANSC1: Implement and maintain safe, hygienic and effective working practices during elective non-surgical cosmetic procedures and SKANSC2: Consult, assess, plan and prepare for elective non-surgical cosmetic procedures.
Items listed within the scope/range should be evidenced in line with the specific type of non-surgical cosmetic procedure being performed.
Scope Performance
Individual's objectives
- safety
- anti-ageing
- skin tissue augmentation
- remedial
Contra-actions
- hyperemia
- wounds
- bruising
- oedema
Injection techniques
- bolus
- intradermal
- micro-papular
- linear threading
- cross hatching
- fanning
- tenting
Scope Knowledge
Anatomy and physiology
- the structure and function of the body systems and their interdependence on each other
- skin and systemic pathologies
- severe adverse event pathologies
- basic knowledge of pharmacology and sciences
- effects of medications have on the skin and muscles
- study of the ageing process of the skin and underlying tissues/ effects of bone reabsorption and understanding of complex facial anatomy and venous and arterial blood supply
* *
Adverse reactions
- infection
- pigment irregularities
- nausea
- allergic reaction
- anaphylaxis
- medicine toxicity/incompatibility/ contraindications
- vasovagal syncope
- asymmetry
- palpability of the filler
- blindness
- necrosis
- nodules
- vascular occlusion
- tindal effect
- arterial occlusion
- compression occlusion
- migration of the dermal filler
- body dysmorphia
- reduced lymphatic drainage
- granulomas
- needlestick injuries
- stroke
- death
- pulmonary embolism
* *
Risk avoidance strategies
- emergency plan
- risk assessment(s)
- acquired medical history
- procedure plan(s)
- restrictive treatment areas
- pre and post instructions and advice
- avoidance of off license use
- inoculations
- first aid at work qualification and basic life support or equivalent
- general health and safety working practices
- infection prevention and control
- working environment
- collaboration with healthcare professional/regulated independent prescriber/appropriate professionals
- legislative prescription protocol
- medicine management
- informed consent
- data management
- audit and accountability
- understanding of the pharmacology
- working knowledge of facial and neck anatomy
- waste management
- assessment of the individual's physical and emotional suitability
* *
Visual aids
- Illustrative images
- Illustrative diagrams
- pre-procedure markings
* *
Dermal filler procedure protocol
- working environment
- health and safety
- risk management plan
- infection prevention and control
- identified healthcare professional/regulated independent prescriber
- emergency plan
- procedure plan
- informed consent
- appropriate professionals
- data management
- audit and accountability
- instructions and advice
- waste management
- evidence based and reflective practice
Instructions
- the individual, regulated independent prescriber and aesthetic practitioner's legal rights and responsibilities
- emergency plan
- post procedure expectations and associated time frames
- pre and post procedure instructions and care
- restrictions and associated risks
- future procedures
- complaints procedure or concerns protocol
Values
Behaviours
Skills
Glossary
Adverse reactions
Adverse reactions are also known as adverse incidents or associated risks. An Adverse reaction is an unexpected physical or physiological reaction from a procedure carried out.
Contra-action
Contra action is an expected temporary reaction from a procedure.
Emergency plan
The emergency plan is the responsibility of the aesthetic practitioner that includes use and access to the emergency kit. An identified healthcare professional will act as the regulated independent prescriber if a prescription only medication is required in the event of an adverse reaction. The regulated independent prescriber has a duty of care to their patients to follow regulatory guidelines set by their Professional, Statutory and Regulated Body.
Pre-procedure markings
Pre-procedure markings should be carried out using a sterile single use surgical pen. Pre-procedure markings are used to create guidelines to identify injection sites as set out in the non-surgical cosmetic procedure plan.
Treatment area
The indicative area to be treated, can also be referred to as treatment site or the anatomical name.
Universal precautions and standard precautions
Universal precautions are relevant if the practitioner is exposed to blood and/or some bodily fluid. It is the responsibility of the practitioner to implement infection prevention and control measures to prevent exposure to blood borne pathogens or Other Potentially Infectious Materials (OPIM).
Standard precautions are the basic level of infection control that should be used at all times within the working environment, such as hand hygiene, personal protective equipment, prevention of needlestick and injuries from sharps, risk assessment, respiratory hygiene and cough etiquette, environmental cleaning and waste disposal.
Visual media
Visual media is evidence generated through photography or video.
Working environment
The working environment requirements should comply with Health and Safety legislation and be in accordance within guidelines set out either by your local authority or governing body.
Risk assessments should be undertaken and control methods implemented and documented, updated regularly and/or if changes occur. The working environment should be hygienic and fit for purpose for the non-surgical cosmetic procedures to be conducted safely and effectively using aseptic techniques. Infection prevention and control procedures are required to minimise risk of infection and transmission of microbes. Personal protective equipment must be fit for purpose and available. Equipment and products must be maintained in line with the manufacturer's instructions and legislative requirements.
It is advisable to create a complication management and/or emergency plan for all non-surgical cosmetic procedures in the event of an adverse reaction or incident.
Links To Other NOS
SKANSC1, SKANSC2, SKANSC3, SKANSC5, SKANSC6, SKANSC7, SKANSC8 and SKANSC9