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The document outlines the requirements for completing a Level 7 Qualification in Aesthetic Medicine. Candidates can choose between a Certificate route requiring portfolio evidence and short answer questions, or a Competency route requiring an Objective Structured Clinical Examination (OSCE). The portfolio must include case histories, a statement of ethics, and a procedure log. The short answer questions cover 8 units of knowledge and understanding. The OSCE involves externally set, internally marked exams in 4 units, with candidate performances filmed for their portfolio.
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- Advise management on quality improvements
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thank you, all the respected peoples, for giving the information to complete this presentation.
this information is free to use by anyone.
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Cleaning physically removes contamination and microorganisms from surfaces but does not necessarily destroy them. It is important to maintain clean and dirty zones to prevent cross-contamination, and work from clean to dirty areas. All surfaces that may become contaminated, such as piercing chairs, should be protected with paper that is changed after each client and waste disposed of properly. There are three levels of decontamination - cleaning, disinfection, and sterilization - with increasing microbial reduction at each level. Sterilization using autoclaves at 134°C for 3 minutes is required for reusable items that contact broken skin.
Section 10 Management of Body Fluids.pdf
Blood and other body fluids can transmit diseases and must be handled safely and immediately. Practitioners should assume all body fluids are infected to prevent transmission. Examples of potential body fluid exposure during procedures include vomit from fainting, urine or feces from seizures, and needlestick injuries or accidents involving blood. Proper personal protective equipment and cleaning procedures, including correct dilution rates and contact times for disinfectants, are necessary to safely manage body fluid spills. Contaminated items that cannot be adequately disinfected must be disposed of.
Section 9 Occupational Exposure Management and PPE.pdf
Individuals working in special procedures may be exposed to occupational hazards like blood and body fluids, physical injuries from needles, and chemicals. Personal protective equipment like disposable aprons, gloves, and eye protection can provide a barrier against hazards and reduce infection risks. Gloves must be single-use, properly disposed of, and changed between different tasks or if torn. Needlestick or sharps injuries require first aid like encouraging bleeding and seeking prompt medical attention to reduce infection risks. Management policies address preventing and controlling exposures, safe sharps use and disposal, cleaning, and first aid responses.
Section 8 Hand Hygiene.pdf
This document discusses proper hand hygiene and its importance in infection control. It outlines the two types of microorganisms on skin - resident and transient - and that transient microbes cause most infections from procedures. Good hand hygiene, including washing with soap and water or using alcohol-based hand rubs, is the most effective way to prevent disease spread. The document provides guidance on when hand washing and disinfection should occur, such as before and after contact with patients or bodily fluids. It also details the proper hand washing technique of lathering and rubbing for 40-60 seconds.
Section 7: Client Consultation and Aftercare.pdf
The document outlines guidelines for client consultations prior to procedures, record keeping, and aftercare advice. It states that consultations should include explaining risks and contraindications, confirming client understanding, and collecting medical information. Records must be easily accessible, contain identifying and procedure details, and be kept confidential. Aftercare advice should promote healing and infection prevention, be provided verbally and in writing, and ensure client understanding.
Section 6: Legal Requirements.pdf
The Public Health (Wales) Act 2017 requires individuals performing special procedures such as acupuncture, electrolysis, body piercing, and tattooing in Wales to be licensed. Licenses are valid for 3 years or 7 days and require practitioners to demonstrate knowledge of infection control, first aid, and legal requirements. Premises where licensed practitioners operate must also be approved, with criteria depending on the risk level of the procedures performed. Non-compliance with licensing conditions that pose significant health risks can result in license revocation or prosecution.
Section 5 The Chain of Infection.pdf
The document discusses the chain of infection, which describes the six steps required for transmission of an infectious disease: 1) an infectious agent, 2) a reservoir, 3) a means of exiting the reservoir, 4) a mode of transmission, 5) a means of entry into a new host, and 6) a susceptible host. To prevent the spread of infection, it is important to break the chain of infection by using standard infection control precautions at all steps, such as proper hand hygiene, use of personal protective equipment, safe disposal of contaminated waste, and cleaning and disinfection of equipment.
Section 4 Common non-infectious hazards and their sources.pdf
Allergic reactions, keloid and hypertrophic scars, and physical injuries are common non-infectious hazards. Allergic reactions can be triggered by metals, latex, and tattoo inks, and cause symptoms like sneezing, coughing, rashes, and headaches. Keloid scars occur when a wound overgrows and becomes lumpy, while hypertrophic scars involve extra tension around a healing wound. Non-infectious hazards are not spread between people and can be caused by genetics, lifestyle, and environment.
Section 3 - The skin - Its reaction to injury and its role in defence against...
The skin protects the body through several layers that act as a barrier against pathogens, chemicals, physical injury, and UV radiation. It regulates temperature and acts as a sensory organ. The circulatory system delivers essential products and removes waste through blood circulation. The lymphatic system runs alongside and defends the body against microorganisms by carrying away bacteria and damaged tissues via lymph. When injured, the skin undergoes an inflammation response and healing process involving clotting, new cell growth, and maturation over time. Factors like nutrition, health, infection, and blood supply can affect wound healing.
Foundation course in dermal fillers hf
The document discusses aging changes that occur in the perioral area, including loss of lip volume, thinning of tissues, and development of wrinkles and lines. Key signs of aging in this region are perioral wrinkles, jowls, marionette lines, and a dimpled chin. These changes occur due to loss of collagen and fat, thinning of the skin and muscles, and repeated muscle activity over time. Careful assessment of the underlying anatomy and causes of aging is important when considering dermal filler treatment for volume restoration in the lips and perioral area.
Fab pres20aug
This document discusses complications of dermal fillers, how to avoid them, and their management. It begins by defining filler complications and categorizing them as immediate, early, or late onset. It then discusses various types of complications including technical errors, inflammatory reactions, infections, and immune reactions. The document provides tips for minimizing risks such as obtaining informed consent, using proper technique, understanding anatomy, and following up with clients. It also reviews how to manage specific complications like nodules, granulomas, necrosis, and unhappy clients. The overall goal is to help practitioners understand, avoid, and address any adverse events from dermal fillers.
Biostimulant dermal fillers
Radiesse and Ellanse are considered biostimulant dermal fillers as they stimulate collagen production in addition to providing immediate volume restoration. Radiesse contains calcium hydroxylapatite microspheres suspended in a gel carrier that provide both immediate correction and induce new collagen formation over time. Ellanse contains polycaprolactone microspheres that degrade slowly and stimulate collagen production. Both fillers have been shown to effectively treat areas such as the cheeks and folds with natural results and high patient satisfaction.
Ace17 lips
This document provides information on lip augmentation using the Teosyal pen. It begins with an introduction to the speaker's qualifications and objectives of the presentation. It then covers anatomy of the lips, how lips age, factors to consider for lip augmentation, and techniques for injection. The main technique discussed is using the Teosyal pen, which offers precise, homogeneous delivery of hyaluronic acid filler for lip augmentation in a minimally invasive manner. Key advantages include less pain on injection and quicker recovery time compared to manual injection techniques.
Anatomy toxin injections
This document provides an overview of the anatomy related to botulinum toxin injections. It discusses the muscles of the forehead, brow, eyes, lips and neck in detail. For each muscle, it describes the origin, insertion, innervation, blood supply, function and related anatomy. It also discusses injection patterns and dosages for treatments like brow lifts, lip treatments, masseter reduction and neck tightening. Potential complications of neck injections are also outlined. The goal is to understand the anatomy to maximize efficacy and safety of botulinum toxin procedures.
MHRA Yellow Card Scheme
The document discusses the Yellow Card Scheme in the UK for reporting adverse drug reactions (ADRs). It defines an ADR and describes how common ADRs are, causing 6.5% of adult hospital admissions. It outlines how ADRs can be classified and factors that influence them. The Yellow Card Scheme acts as an early warning system to identify new ADRs and risks. Healthcare professionals, patients and the public can report suspected ADRs to the scheme to help continual drug safety monitoring.
Regulatory approval process for medical Devices
This document provides an overview of the regulatory approval process for medical devices in the European Union. It discusses key definitions such as the classification of medical devices and relevant EU directives. The approval process involves implementing quality systems, preparing a technical file or design dossier, appointing a notified body for audits and certification, registering the device, and affixing the CE mark. Vigilance reporting and post-market surveillance are also required ongoing responsibilities for device manufacturers.
Guidance for aesthetic medicine qualifications
This guide will help you prepare your responses to the 34 Short Answer Question Essays and your OSCE Assessment
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Section 13 Special Procedures Equipment and Products.pdf
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Section 9 Occupational Exposure Management and PPE.pdf
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Section 3 - The skin - Its reaction to injury and its role in defence against...
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- 1. Save Face Level 7 Recognition of Prior Learning Programme
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