Training activity information
Details
Plan, design and manufacture a custom-made device to support a patient post laryngectomy to improve speech and communication and evaluate against treatment goals
Type
Developmental training activity (DTA)
Evidence requirements
Evidence the activity has been undertaken by the trainee.
Reflection on the activity at one or more time points after the event including learning from the activity and/or areas of the trainees practice for development.
An action plan to implement learning and/or to address skills or knowledge gaps identified.
Considerations
- Patient centred care and support
- Indications for treatment
- Information requirements to complete the device
- Adaption of a stock medical device (tubing/valve) and regulation
- Communication with the multidisciplinary team
- Design requirements and options available, including relationship to anatomical structures
- Retention options
- Selection and use of materials
- Manufacture protocols and device risk assessment
- Patient expectations and experience
- Incidental findings, raising concerns and onward referral for specialist care
- Clinical fitting procedure
- Care and use instructions
- Adaption of the device directly on the clinic
- Impact of plan/design on patient quality of life
- Considerations for ongoing management
- Patient safety, dignity and confidentiality
- Complications and onward referral
Relevant learning outcomes
# | Outcome |
---|---|
# 1 |
Outcome
Deliver quality patient centred care with the best interests of patients in all elements of practice. |
# 2 |
Outcome
Practice in accordance with local and national health and safety policies, regulatory requirements and overall service governance. |
# 3 |
Outcome
Communicate effectively with patients, relatives, healthcare professionals and other stakeholders. |
# 4 |
Outcome
Identify patients who need further specialist support and refer to the appropriate healthcare specialist. |
# 6 |
Outcome
Perform clinical investigations, formulate treatment plans and manufacture medical devices to a safe clinical standard. |
# 8 |
Outcome
Select appropriate biomedical materials and components/instrumentation used in the treatment of patients and the manufacture of custom-made medical devices. |
# 9 |
Outcome
Practice in partnership with other clinical specialisms as part of a multidisciplinary team and understand their roles and their impact on patient care and pathway. |
# 10 |
Outcome
Apply the principals of a quality management system to their professional practice. |
# 12 |
Outcome
Assess and interpret patients’ needs to provide customised treatment dependent on medical, physical, social and psychological requirements. |