Risk Assessment for Procedure of Botulinum Toxin Injections Paper
Complete a risk assessment of either a procedure or the environment (please state which). Minimum 300 word count, tabular form accepted;
Appraise key regulations, standards codes of practice and guidance relevant to cosmetical/aesthetic injectable practice and explain the impact and consequences of non-compliance for each (see notes for international students)regulation/standards/guidance cited. Minimum 750 wordcount.
NB Marks will be deducted if your answer falls below the recommended minimum word count for each part.
Task Guidance:
Your answer should include the hazards, risks to each hazard, the control to risk that should be implemented with timescales, your evaluation and monitoring timescales. This can be completed in tabular form.
Your answer should include any Acts, regulations, code of practice guidance and quality assurance you are required to adhere to relating to aesthetic injectable therapies. For each cited reference you must explain the impact to your organisation and the consequences of non-compliance. A comprehensive list below is given for guidance. It is not expected that you cite all those listed below but that you pick out those most relevant to your practice.
Guidance notes:
human resources policies and procedures, e.g. diversity & equality, appointment of staff, Disclosure & Barring Service (DBS) checks, bullying and harassment, ‘Whistle Blowing’. Operational procedures, practicing privileges, patient consultation, records management, order and storage of medicines, Medicines Act, GDPR, Freedom of Information Act, patient-centred care, risk assessment and risk management, National Patient Safety Agency (NPSA), Patient Group Directions (PGD), Summary of Product Characteristics (SPC), NICE Guidelines, professional body guidance, MHRA, advertising and promotion of medicines, audit methodologies for the safe selection, procurement, supply, storage, documentation, disposal and review Commercial aspects of cosmetic practice: marketing, advertising, PR, social media Risk assessment, prevention and control of infection, provision and use of work equipment, clinical facility design, fire safety, COSHH Regulations, moving and handling, recording of accidents, needle stick injuries, clinical waste, single use devices, adverse incidents. CME, CPD. External accreditation/registration with appropriate national inspection body, e.g. CQC, voluntary registers, insurance, etc. Seven pillars of clinical governance; Service user, carer and public involvement, Risk management, Clinical audit, Staffing and staff management, Education and training, Clinical effectiveness, Clinical information Equipment management, resuscitation trolleys, automated external defibrillators (AEDs), team working, policies and procedures. Clinical audit.
Risk Assessment of a Procedure and Cosmetical/Aesthetic Injectable Practice
Student’s Name
Institutional Affiliation
Risk Assessment of a Procedure and Cosmetical/Aesthetic Injectable Practice
Risk Assessment for Procedure of Botulinum Toxin Injections
Hazards
Risks to Each Hazard
Control to Risk
Evaluation and Monitoring Timescales
Damage
Damage mainly occurs during the transportation of the medicinal product to be used for Botulinum Toxin injection
Medicines for Botulinum Toxin injections should safely be packaged for transportation
Conducted prior to storing and administering the Botulinum Toxin injection medicine
Mislabeling
Wrongful administration of Botulinum Toxin injection medicine to the unintended patients
Ensure that all medicine include the full directions for use and the targeted patients to be administered with the medicine
Carried out every time when administering the medicine to ensure the correct dosage of injection
Expiration
Expired medicine going to waste for not being used for its intended purposes
Take records on when the medicine should be best used before to ensure that they are administered for intended patients and purpose
Monitor the expiration dates to ensure that all medicines are fit for use for Botulinum Toxin injection before their administration
Theft
The stored medicines for Botulinum Toxin injections can be stolen either by the hospital staff or burglars who might break into the hospital’s pharmacy unit
Improve the security of the hospital facility in general and ensure that specific pharmaceutical personnel are assigned the responsibility of storing the medicine to promote accountability
Install a 24-hour security surveillance activity and the assigned personnel being present at the medicine storage unit around the clock
Disregard of patient information
Failure to adhere to patients need prior to administering the Botulinum Toxin injections
Practitioners should consider the unique needs of the patients before administering Botulinum Toxin injection and inform the patients the products to refrain from using after the injection, as well as informing common side-effects to be aware of
Performed at the time of administering Botulinum Toxin injection
Non-compliance
Patients being subjected to the risk of relapse and readmission to hospital
Assigning patients compliance aids to encourage them on continuing with the Botulinum Toxin injection while either admitted in or discharged from the hospital
During the period required for taking the medicine dosage for Botulinum Toxin injection (Van-Hoeij et al., 2017).
Cosmetical/Aesthetic Injectable Practice
Cosmetical/aesthetic injectable practice is increasingly becoming inclined towards medical specialty as an area of immense interest in medical practice. Therefore, in pursuit of satisfying patients' aesthetic desires and protecting their safety, there are acts, regulations, code of practice guidance, and quality assurance requirements that guide practitioners in this field, some of which are discussed below.
Medicines Act
Medicines Act was enacted in 1968 by the Parliament of United Kingdom and is chiefly intended to make new provisions with regard to medicinal products and the related matters in addition to the associated purposes that are connected therein. The act applies to the aesthetic injectable practice by requiring the specification relating to its use. The usage of injectable aesthetics is dependent on the determination of the strength of the product so that to specify the maximum single dose and maximum daily dose. The determination of the dosage to be used in an aesthetic injectable practice must uniquely correspond to the information of every patient to ensure that their needs are adequately met (Gray, 2018). Non-compliance to the provision of medicines act intended to guide the aesthetic inj...
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