E- portfolio assignment .make sure you follow all the instructions mentioned in brief that I attached with it. No plagiarism should be there.

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E- portfolio assignment .make sure you follow all the instructions mentioned in brief that I attached with it. No plagiarism should be there.



CW (40% of the module) - Assessment Brief Read this assessment brief carefully, it tells you how you are going to be assessed, how to submit your assessment on time, and how (and when) you’ll receive your marks and feedback. Module Code ASC_5_WBS_2223 Module Title Work Experience in Biomedical Science Lecturer Shpresa Haliti (ML), Radhika Bhandari (L) Claire Atkinson (L), Mehwish Khalid (HPL) Janki Kavi (HPL) Stefano Tambalo (HPL) Yvonne Obiajulu (HPL) Nikos Trasanidis (HPL) Joaquin Caro (HPL) % Of Module Mark 100% Distributed 23rd January 2023 Submission Method Submit online via this Module’s Moodle site – E-portfolio Face to Face assessment – skills Submission Deadline E-portfolio - Friday 12th May 2023 – 11:59 pm Skills assessment – viva (oral examination) . Feedback on the same day – via Moodle. Release of Feedback E- portfolio - feedback will be available online from 30th May 2023 Release of Marks Provisional marks will be available in the Gradebook on Moodle from (both CW components) - 30th May 2023 Assessment: E-portfolio – each student will complete a portfolio and upload on Moodle for marking. Viva – oral examination Assessment Details: Assessment of your work will consider 1. Content, quality, and organisation of your scientific writing – e-portfolio. You have an opportunity to apply the subject knowledge that you have acquired and reinforced during the semester in this module. This will be assessed according to the following standards (see the marking criteria at the end of this document): 0. Research Use of academic and relevant resources to write the reflective included in the e-portfolio. 0. Subject Knowledge Understanding and application of subject knowledge. Contribution to subject debate by updated research 0. Critical Analysis Analysis and interpretation of real case studies (viva) 1. Practical Competence. Skills to apply theory to practice – skills assessment (viva) 1. The quality of your scientific writing – e-portfolio Structure, quality, and clarity of argument, coherence, use of evidential support and referencing, spelling, grammar, and punctuation. This will be assessed according to the following strands: 1. Communication and Presentation The clear intention in communication -work is well structured in the portfolio. 1. Academic Integrity Acknowledges and gives credit to the work of others follows the conventions and practices of the discipline including appropriate use of referencing standards for discipline. Type Assessment Skills assessment (50%) Coursework 1 (50%) : Demonstrate practical skills including quality assurance for pathology services in the UK – skills assessment– oral assessment. Pass mark = 40% Oral assessment 4 stations – sections assessed by different lecturers: 1. Specimen reception and patient confidentiality – 25% 2. Analytical (including authorisation) – 25% 3. Quality control – 25% 4. Health and safety – 25% Feedback given on the day – final marks to be uploaded on Moodle . *Provisional marks will be available in the Gradebook on Moodle from (both CW components) - 30th May 2023 E-portfolio (50%) Students will compile a portfolio evidence, which will include evidence of work undertaken, nature of tasks, witness statements from employers, a reflective evaluation of the ways in which the work experience (module) has enhanced the students employability, and a careers action plan including an updated CV and cover letter, to further their employability skills following graduation. Pass mark = 40% E-portfolio The following information will be included in the e-portfolio for assessment: 1. E-portfolio content page (student name; ID; course title; module title; school name ) = 5% 2. Answers only 20 training questions from the list (appendix 8). = 30%*Note: answers to Qs should be not more than half a page . Using visulas i.e tables, flow charts when answering Qs will be useful. 3. A personal statement on any of the practicals (template - appendix 1) – not more than 1 page = 5% 4. One witness statement signed by the module lead and one of the NHS staff assessors (template – appendix 2) = 5% 5. Chose a quality control case scenario from the list (appendix 3) and interpret/annotate the results (it can be an IQC/EQA/vertical or horizontal non-compliance etc.) = 10% 6. Chose a set of patient results from the list (appendix 4) and interpret/ annotate findings i.e reporting of critical values, test reference range, patient confidentiality etc. = 5% 7. Risk assessment – choose one of the following activities from appendix 5 and complete a risk assessment - include it in your e-portfolio = 5% 8. Specimen Reception - select one case from the list (appendix 6) and describe actions taken e.g sample mismatch; incorrect sample tubes etc. = 5% 9. Learning reflective report (max = 2500 words) – in your own words reflect on what you learned in this module and how it will help you for the future employment (use template in appendix 7 to write the report) = 20% 10. Include an up to date CV and Cover letter in the portfolio =10% *Note: You can get help from [email protected] on how to write your CV and Cover Letter. E-portfolio will be assessed by the ML and other lecturers – Provisional marks will be available in the Gradebook on Moodle from (both CW components) - 30th May 2023 Extra notes: · Visuals i.e. figures, pictures, graphs and tables used to help explain concepts and summarize information in e-portfolio should be numbered and fully labelled · Written work i.e. reflective report and answers to questions - must be referenced (in the text and a list) using the Harvard system. · All work included in the e-portfolio should be written in Arial font size 12 (or larger if you need to), with a minimum of 1.5 line spacing. Referencing Harvard Referencing should be used when writing short assays; reflective reports etc see your Library Subject Guide for guides and tips on referencing. Regulations Make sure you understand the University Regulations on expected academic practice and academic misconduct. Note in particular: · Your work must be your own. Markers will be attentive to both the plausibility of the sources provided as well as the consistency and approach to the writing of the work. Simply, if you do the research and reading, and then write it up on your own, giving the reference to sources, you will approach the work in the appropriate way and will cause not give markers reason to question the authenticity of the work. · All quotations must be credited and properly referenced. Paraphrasing is still regarded as plagiarism if you fail to acknowledge the source for the ideas being expressed. TURNITIN: When you upload your work to the Moodle site it will be checked by anti-plagiarism software. 15% Turnitin score is the maximum allowed. Resources · Lectures · Tutorials · NHSi platform · Virtual training · Laboratory Health and Safety SOP · Laboratory Risk Assessment document · Laboratory study guide document prepared by lecturers · Health and Care Professions Council. Guidance on Conduct and Ethics for students. Current Edition: Health and Care Professional Council · Ahmed, N., Glencross, H and Wang, Q. Biomedical Science Practice: Experimental and Professional Skills. Current Edition: Oxford University Press. · Institute of Biomedical Science. Get started in your biomedical science career eStudent - Institute of Biomedical Science (ibms.org) · Medical Laboratory Accreditation in UK- www.ukas.com/accreditation/standards/medical-laboratory-accreditation · Harrison, M.A (2018): How to Get Hired: An Insider’s Guide to Applications, Interviews and Getting the Job of Your Dreams · Innes, B. (2016): The interview question & answer book, 2nd Ed. Pearson · Rook, S (2016): Work experience, placements & internships, McMillan Education Learning Outcomes Knowledge and understanding: · Apply scientific skills to a real work situation and appreciate their own role within the organisation as a whole. · Produce reliable and scientific sound results which contribute to the goals of the employer. Intellectual skills · This unit will provide the student with an opportunity to put into practice the intellectual skills acquired in levels · It will test the students’ ability to process the information that has been taught in other units and apply it to “real-life” situations. Practical skills · Develop essential professional skills in biomedical science. Transferable skills · Learn to organise their schedules to complete a given task within a given time scale and meet deadlines. · Co-operate with team members to plan and complete assigned tasks How to get help We will discuss this Assessment Brief in class. However, if you have related questions, please contact the Module Leader via MS TEAMS site or email as soon as possible. Appendix 1. Personal statement template Personal statement - Record Title: Students name: Date of evidence: Details of testimony: 1. Give a short description of any activity that you performed in the professional skills session. 2. What did you learn from this activity ? 3. How will you use this learning in the future? I can confirm the candidate’s evidence is authentic and accurate. Assessor signature: Name: Date: E- PORTFOLIO WITNESS STATEMENT Student : ASSESSOR: ACTIVITY: DATE OF ACTIVITY: Details: Assessor : Signature: Date: Appendix 2. Witness statement template Appendix 3. Quality control – cases EQA Scenarios. Choose any of the EQA results below and annotate the results explaining what each element of the EQA report means. 1. 2. 3. 4. 5. 6. 7. IQC Scenarios. Choose any of the IQC charts below and annotate the results below explaining the errors at different times. A. B. C. D. E. F. Appendix 4. Interpretation and annotation of patient results – cases From the 7 example Biochemistry patient sample results below, annotate at least one and include it in your e-portfolio Appendix 5. Risk assessment – choose one of the following activities (1-5) and complete a risk assessment - include it in your e-portfolio Activity Who might be harmed? What is the hazard and potential consequence What control measures are required or are in place Likelihood (Score 1-5) Severity (score 1-5) 1. Wrong patient sample type was received in the specimen reception 2. Lifting and carrying bulky or heavy loads, boxes of paper, moving heavy equipment, and storage of objects at height 3. Lone working in a clinical laboratory 4. Wrong disposal of glass or sharps 5. Making a cup of coffee at work The average score for likelihood and severity Risk score (Likelihood x severity) = For reference Appendix 6. Patient sample handling – cases (we will upload more ) · Scenario 1: Audit – Waste (Example with model answer & marks) You are completing a waste audit and find Sharps in the clinical waste, clinical waste in the domestic waste, and confidential waste in the domestic waste. Explain what actions you would take on finding the errors and what actions may need to be done to complete the audit process. Purpose: To identify the apprentice who understands waste streams, and the audit process and can communicate with colleagues. Model answer = marks Note: if you wish you can answer all the scenarios but only one is to be included in the E-portfolio Scenario 1- You are working in the specimen reception, and you have received 2 sample tubes from A&E. Tests requested – check table below. Describe what actions you would take. (5 marks) Sample tube Test requested Comment - actions taken Tube 1 – SST (yellow) Glucose, Creatinine, Urea, and Liver Function Tests Tube 2 - Purple Electrolytes, FBC Scenario 2. The order of blood sample drawn . A clinician has requested the following tests: FBC; Blood Culture; U&E, LFT and Creatinine. Put the sample tubes that you have received in order to correspond with the tests requested above. Explain why this order and which department runs these tests. ( 5 marks) Scenario 3. Patient sample identification (5 marks) 1. List three essential and three desirable patient sample identifications prior to running the tests 2. List at least 5 essential identifications and 5 desirables to be included in a patient request form Scenario 4. Incorrectly labelled samples. You are working in specimen reception for a while, and you have noticed that multiple samples are coming from a specific ward labelled incorrectly. How would you investigate this and what corrective action could you take to resolve this issue? (5marks) Scenario 5. Patient confidentiality You receive a phone call in the department that is from a patient asking for their test results. They explain that they have been given the number from their GP and are entitled to receive their results over the phone. How do you proceed? ( 5 marks) Scenario 6. Specimen receipt error (5 marks) You are working in the specimen reception and receive two patient samples and request forms. You noticed
Answered 4 days AfterAug 02, 2023

Answer To: E- portfolio assignment .make sure you follow all the instructions mentioned in brief that I...

Dr Insiyah R. answered on Aug 07 2023
39 Votes
Part 1: Detection of Dengue using Polymerase Chain Reaction (PCR)
Part 2: Estimation of Platelet Count
Part 3: Estimation of CBC
Part 1. Estimation of Dengue Virus using Polymerase Chain Reaction (PCR)
Introduction
Dengue fever is a mosquito-borne viral disease caused by the dengue virus, which belongs to the Flaviviridae family. It is prevalent in tropical and subtropical regions, and its symptoms can range from
mild fever to severe dengue hemorrhagic fever or dengue shock syndrome. The early and accurate detection of dengue virus is crucial for appropriate patient management and control of disease transmission.
Polymerase Chain Reaction (PCR) is a widely used molecular diagnostic technique that allows for the amplification and detection of specific nucleic acid sequences. In the case of the dengue virus, PCR can detect and quantify viral RNA in patient samples, providing a sensitive and specific method for diagnosis.
Materials
· Patient blood sample
· PCR reagents (primers, Taq polymerase, dNTPs, buffer)
· PCR machine
· PPE (Personal Protective Equipment)
· Nucleic acid extraction kit
· Centrifuge
· Micropipettes and sterile tips
· PCR tubes
Procedure
Step 1. Nucleic acid extraction:
· Start by preparing a working area and wearing appropriate PPE.
· Extract viral RNA from the patient's blood sample using a commercial nucleic acid extraction kit according to the manufacturer's instructions.
· Ensure proper handling of the sample to prevent cross-contamination.
Step 2. PCR setup:
· Prepare a master mix containing PCR reagents (primers, Taq polymerase, dNTPs, buffer) according to the PCR protocol.
· Aliquot the master mix into PCR tubes, leaving one tube for negative control (without template DNA).
· Add the extracted nucleic acid template to the appropriate PCR tubes.
Step 3. PCR amplification:
· Place the PCR tubes into the PCR machine and set the appropriate cycling conditions for dengue virus detection.
· Run the PCR program, which typically includes an initial denaturation step, followed by a specific number of cycles for amplification, and a final extension step.
· Monitor the PCR process for any unexpected events or errors.
Step 4. PCR product analysis:
· After PCR amplification, analyze the PCR products using gel electrophoresis or other appropriate methods.
· Visualize the PCR products using a gel imaging system and compare the results with appropriate size markers.
· The presence of a specific band at the expected size indicates a positive result for the dengue virus.
Results and Interpretation
Interpret the PCR results and answer the following questions:
1. Is the PCR result positive or negative for the dengue virus?
2. If positive, what is the size of the PCR product?
3. What does the presence of a specific band at the expected size indicate?
4. Discuss the significance of the PCR result in relation to the diagnosis of dengue fever.
5. How does PCR compare to other diagnostic methods for dengue virus detection?
Discussion
Discuss the importance and limitations of PCR in dengue virus detection, including
1. Sensitivity and specificity of PCR compared to other diagnostic methods.
2. The advantage of PCR in early detection of dengue virus.
3. Factors that can affect the accuracy of PCR results.
4. The clinical implications of PCR results for patient management and disease control.
Conclusion
Summarize the key findings and conclude the report, emphasizing the significance of PCR in the detection of dengue virus and its role in improving patient care and disease surveillance.
Part 2. Estimation of Platelet Count for Dengue Diagnosis
Introduction
Dengue fever is a mosquito-borne viral disease caused by the dengue virus. One of the hallmarks of dengue infection is a significant decrease in platelet count, which can lead to a condition called thrombocytopenia. Platelets play a crucial role in blood clotting, and a low platelet count can result in bleeding complications. Therefore, monitoring platelet count is essential for the diagnosis and management of dengue fever.
Materials
· Patient blood sample
· haematology analyzer
· Microscope
· Reagents for blood smear preparation
· PPE...
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