Course Coordinator:Yoke Lin Fung (ylfung@usc.edu.au) School:School of Health - Biomedicine
UniSC Sunshine Coast |
Blended learning | Most of your course is on campus but you may be able to do some components of this course online. |
Please go to usc.edu.au for up to date information on the
teaching sessions and campuses where this course is usually offered.
Haematology is the area of general pathology that is concerned with diseases that affect the blood, such as blood clotting disorders, anaemia, haemophilia, lymphoma, leukaemia and haemoglobinopathies. This advanced course builds on the fundamentals of haematology developed in the first-year course. After completing this course, you should be able to recognise critical limits and conditions associated with the major haematological tests conducted in pathology services.
| Activity | Hours | Beginning Week | Frequency |
| Blended learning | |||
| Learning materials – Fully independent asynchronous learning | 1.5hrs | Week 1 | 12 times |
| Tutorial/Workshop 1 – On campus discussion and review of haematology theory and concepts to haematology case studies. | 2hrs | Week 2 | 5 times |
| Laboratory 1 – On campus laboratories to gain competency in haematology laboratory investigation including but not limited to blood film morphology and coagulation assays. | 3hrs | Week 1 | 12 times |
Erythrocyte Disorders
Leukocyte Disorders
Coagulation Disorders & Laboratory Assessment
Platelets and vasculature disorders
Malaria
Paediatric, Obstetrics and Geriatric Haematology
Molecular Diagnostics
Flow Cytometric Analysis
Cytogenetics ;Cytochemistry
Bone Marrow and Stem Cell Transplantations
200 Level (Developing)
12 units
| Course Learning Outcomes On successful completion of this course, you should be able to... | Graduate Qualities Mapping Completing these tasks successfully will contribute to you becoming... | Professional Standard Mapping * Australian Institute of Medical and Clinical Scientists | |
| 1 | Demonstrate competency in haematological techniques including preparing blood films, performing full blood counts, microscopic examination and reporting of blood films, and performing coagulation assays. |
Knowledgeable Creative and critical thinker Empowered Engaged Communication Collaboration Problem solving Organisation Applying technologies Information literacy |
1.1.1, 1.1.2, 1.1.3, 1.1.4, 1.2.1, 1.2.3, 1.3.1, 1.3.2, 1.3.3, 1.3.4, 1.3.5, 1.6.1, 1.6.2, 1.6.3, 1.6.4, 1.6.7, 1.5, 2.1.1, 2.1.2, 2.2.1, 2.3.1, 2.3.2, 3.2.1, 3.3.1, 3.3.2, 5.2.1, 5.3.3, 5.3.4, 5.3.9, 7.1.2, 10.4.1, 10.4.2, 10.4.3 |
| 2 | Synthesize haematology results, knowledge of the pathophysiology and clinical features of haematological disorders to support the diagnosis and monitoring of haematological diseases. |
Knowledgeable Creative and critical thinker Empowered Engaged Communication Collaboration Problem solving Organisation Applying technologies Information literacy |
2.1, 2.3, 3.2.1, 3.2.7, 3.3.1, 3.3.2, 3.3.3, 6.5.4 |
| 3 | Appraise current concepts in haematopoiesis, stem cell biology and advanced diagnostic techniques in haematology, including flow cytometry, cytogenetics and molecular diagnostics. |
Knowledgeable Empowered Engaged Problem solving Applying technologies Information literacy |
6.2.4, 6.4.1, 6.5.3, 6.5.7, 7.3.2, 7.4.1, 9.1.1, 10.1.5, 10.3.2, 10.4.2, 10.4.3 |
| CODE | COMPETENCY |
| Australian Institute of Medical and Clinical Scientists | |
| 1.1.1 | Ensure the appropriateness of sample collection procedures: Correct request form is received as set out in established protocol. |
| 1.1.2 | Ensure the appropriateness of sample collection procedures: Identification of patient and demographic information is established. |
| 1.1.3 | Ensure the appropriateness of sample collection procedures: Appropriate action is taken when request appears inconsistent with patient information data. |
| 1.1.4 | Ensure the appropriateness of sample collection procedures: Patient preparation and specimen collection is consistent with test(s) requested. |
| 1.2.1 | Ensure the appropriateness of specimen reception procedures: Documentation is checked to ensure it matches specimen and complies with current regulations. |
| 1.2.3 | Ensure the appropriateness of specimen reception procedures: Specimen suitability for further processing is established. |
| 1.3.1 | Evaluate specimen suitability prior to analysis: Correct and satisfactory labelling and matching of subject details is established. |
| 1.3.2 | Evaluate specimen suitability prior to analysis: Confirmation is made that the nature of the specimen is consistent with requested analysis. |
| 1.3.3 | Evaluate specimen suitability prior to analysis: Specimen is received in correct container (i.e., containing correct anticoagulant or fixative if appropriate) and in accordance with collection and delivery protocols. |
| 1.3.4 | Evaluate specimen suitability prior to analysis: Quality of specimen meets defined acceptability criteria. |
| 1.3.5 | Evaluate specimen suitability prior to analysis: Appropriate action, as per defined criteria, is taken upon receipt of an unsuitable specimen. |
| 1.6.1 | Read and validate results - Equipment based testing: Laboratory instrumentation is operated within established procedures (including quality control, troubleshooting instrument problems and performing preventative and corrective maintenance). |
| 1.6.2 | Read and validate results - Equipment based testing: Validity of test results is confirmed in terms of protocols (including standards, quality control data and performance of analytical systems) and problems are identified and remedied or notified to the appropriate staff member. |
| 1.6.3 | Read and validate results - Equipment based testing: Results are calculated from data outputs according to documented procedures. |
| 1.6.4 | Read and validate results - Equipment based testing: Test data, calculations, results and acceptance/rejection of analytical procedure outcome are documented. |
| 1.6.7 | Read and validate results - Observation based testing: Critical observations are made and recorded. |
| 1.5 | Collection, preparation and analysis of clinical material: Process specimen utilising appropriate techniques |
| 2.1.1 | Assess validity of data/results against possible range of outcomes: Initial observation and limited interpretation for significance of the raw data/results is undertaken. |
| 2.1.2 | Assess validity of data/results against possible range of outcomes: Implausible results, results inconsistent with clinical information or expected outcomes based on other test results or those outside defined criteria are investigated further using defined troubleshooting strategies. |
| 2.2.1 | Validation of results: Possible causes for implausible or inconsistent results or outcomes are determined. |
| 2.3.1 | Make decisions about reporting results, repeating procedures, consulting senior staff and carrying out further tests within established guidelines: Appropriate decisions about repeating procedures, carrying out further tests within established guidelines, rejection or reporting of results are made. Senior staff are appropriately consulted. |
| 2.3.2 | Make decisions about reporting results, repeating procedures, consulting senior staff and carrying out further tests within established guidelines: Rejected results are dealt with appropriately. |
| 2.1 | Correlation and validation of results of investigations using knowledge of method(s) including analytical principles and clinical information: Assess validity of data/results against possible range of outcomes |
| 2.3 | Correlation and validation of results of investigations using knowledge of method(s) including analytical principles and clinical information: Make decisions about reporting results, repeating procedures, consulting senior staff and carrying out further tests within established guidelines |
| 3.2.1 | Use the administrative systems in place to communicate the results: Results are communicated in a timely manner and according to laboratory protocols. |
| 3.3.1 | Ensure that results with important diagnostic or treatment implications are communicated as per established protocols: Significant results, as defined by the laboratory, are identified |
| 3.3.2 | Ensure that results with important diagnostic or treatment implications are communicated as per established protocols: Results are interpreted in the light of clinical information provided and knowledge of the test(s) and limitations. |
| 3.2.7 | Use the administrative systems in place to communicate the results: Relevant reference intervals and, if appropriate, clinical decision limits are included in reports as per established protocols. |
| 3.3.3 | Ensure that results with important diagnostic or treatment implications are communicated as per established protocols: Urgent or significant results are communicated to appropriate personnel so they understand the significance, purpose of the communication and action required. This action is documented. |
| 5.2.1 | Identify and respond to unsafe work practices and breaches of regulations: All safe work practices (as laid down by legislative guidelines) are understood and promoted. |
| 5.3.3 | Ensure correct procedures are followed for acquisition, collection, storage, transportation and disposal of biological, chemical, toxic and radioactive wastes: The disposal of biological, chemical, toxic and radioactive material is performed as per current legislation and guidelines. |
| 5.3.4 | Ensure correct procedures are followed for acquisition, collection, storage, transportation and disposal of biological, chemical, toxic and radioactive wastes: Protocols for incidents such as spills of biological, chemical, toxic and radioactive substances are followed in accordance with current regulations and guidelines. |
| 5.3.9 | Ensure correct procedures are followed for acquisition, collection, storage, transportation and disposal of biological, chemical, toxic and radioactive wastes: Laboratory workplace safety requirements are met when handling biological, chemical, toxic or radioactive substances. |
| 6.5.4 | Complies with profession’s code of ethics: Confidential information gained in a professional capacity is not disclosed to unauthorised persons. |
| 6.2.4 | Maintain and update scientific/technical knowledge and skills: Opportunities to enhance learning from investigation of unusual clinical cases and/or results are pursued. |
| 6.4.1 | Recognises own abilities and level of professional competence: Work is only undertaken within the limits of one's abilities, qualifications and training. |
| 6.5.3 | Complies with profession’s code of ethics: Practices detrimental to patients and others are avoided. |
| 6.5.7 | Complies with profession’s code of ethics: A responsible approach to the community and the environment with respect to the handling and disposal of hazardous materials is maintained. |
| 7.1.2 | Accepts responsibility for own actions/omissions: Tasks are checked to ensure they are completed. |
| 7.3.2 | Demonstrates knowledge of contemporary ethical issues impinging on Medical Science: Rights of individuals/groups are recognised and protected. |
| 7.4.1 | Knowledge of new tests and their potential in the laboratory: Ongoing review of current literature for information on new or improved tests or procedures is performed. |
| 9.1.1 | Research, prepare and deliver appropriate presentations: Educational topics are researched, prepared and presented to health workers and others. |
| 10.4.1 | Prepare and deliver report: Contributions are made regarding the format and presentation of outcomes. |
| 10.4.2 | Prepare and deliver report: Preparation of verbal and/or written reports or article (including for publication) is undertaken. |
| 10.4.3 | Prepare and deliver report: Report is presented for peer review. |
| 10.1.5 | Contribute to planning and design of research and development projects: Relevant information is accessed online, from libraries and other sources. |
| 10.3.2 | Evaluate results and the need for further experimental work: Contributions are made to the interpretation of results and conclusions. |
Refer to the UniSC Glossary of terms for definitions of “pre-requisites, co-requisites and anti-requisites”.
(MLS100 or MLS110) and enrolled in Program UB001 or SC211 or SC355 or SC357
Not applicable
Not applicable
Not applicable
Standard Grading (GRD)
| High Distinction (HD), Distinction (DN), Credit (CR), Pass (PS), Fail (FL). |
You will be reviewing patient case studies, haematology terminology and morphology identification through in-class activities that will provide you with feedback and help you prepare for the assessment tasks in the course.
| Delivery mode | Task No. | Assessment Product | Individual or Group | Weighting % | What is the duration / length? | When should I submit? | Where should I submit it? |
| All | 1 | Activity Participation | Individual | 15% | Student will complete case studies during lab classes. |
Refer to Format | In Class |
| All | 2 | Activity Participation | Group | 15% | Group presentation up to 20 minute |
Refer to Format | In Class |
| All | 3a | Practical / Laboratory Skills, and Written Piece | Individual | 50% | 150 min + 10 min perusal each time |
Refer to Format | In Class |
| All | 3b | Examination - Centrally Scheduled | Individual | 20% | 120min + 10min perusal |
Exam Period | Exam Venue |
| All - Assessment Task 1:Haematology lab learning portfolio | ||||||||||
| Goal: | The goal is for students to relate haematology theory from lectures/learning materials with laboratory practice in the case studies and exercises provided in the lab classes. |
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| Product: | Activity Participation | |||||||||
| Format: | Assessments will be conducted for case studies in labs 3, 5, 9 and 10. |
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| Criteria: |
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| Generic Skills: | Communication, Collaboration, Problem solving, Organisation, Applying technologies, Information literacy |
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| All - Assessment Task 2:Group Case study (15%) | |||||||||||||||||||
| Goal: | Scientific research and communication are key competencies developed in this oral case study activity. You will work collaboratively in a group to prepare and present a case study of a haematological malignancy or disorder. Presentations will take place in either the week 10 or 11 laboratory class. |
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| Product: | Activity Participation | ||||||||||||||||||
| Format: | You will work in a group. All members of the group will have to work together to provide a description of the patient history, full blood count and morphology of the images from the patient slide(s); a description of the diagnostic tests they would request and why; an overview of the treatment and prognosis of the patient. The presentation must be supported by a PowerPoint file. You will participate in a question and answer forum with the class and tutors. The references used for the presentation will follow the Harvard style. The group will also conduct a peer assessment of another group's presentation. Note: This is a group assignment, individual submissions will receive a zero mark. |
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| Criteria: |
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| Generic Skills: | Collaboration, Problem solving, Organisation, Information literacy |
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| All - Assessment Task 3a:Theory & practical assessment | |||||||||||||
| Goal: | To develop advanced laboratory skills and competencies in Haematology that would meet the requirements of AIMS for training of medical laboratory scientists. |
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| Product: | Practical / Laboratory Skills, and Written Piece | ||||||||||||
| Format: | There are 2 practical and theory exams, that will take place during the scheduled week 7 and week 12 lab class. In week 7 it will examine contents from week 1 to 6 inclusive. In week 12 it will examine contents from week 1 to 11 inclusive. Students will review case studies, report on blood films and respond to short answer questions. The exam will assess your competency in haematological techniques, your ability to interpret results, apply haematology knowledge and write a report using appropriate haematology terminology on your findings |
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| Criteria: |
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| Generic Skills: | Communication, Problem solving, Organisation, Applying technologies, Information literacy |
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| All - Assessment Task 3b:Final theory exam | ||||||||||||||||
| Goal: | For the student to - demonstrate their knowledge and understanding of theoratical, diagnostic, practical and clinical concepts of haematology covered in week 1 to 12. - synthesise the elements of the course, analyse information and explain elements of the theories which underpin the concepts in advanced haematology covered as the course progresses. - solve problems based on theoretical material and information covered in lectures and tutorials for paediatric, geriatric and obstetric haematology. |
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| Product: | Examination - Centrally Scheduled | |||||||||||||||
| Format: | The final theory examination will be centrally scheduled, invigilated and take place on campus. It will consist of multiple choice questions, short answer questions & case studies. |
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| Criteria: |
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| Generic Skills: | Communication, Problem solving, Organisation, Applying technologies, Information literacy |
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| Programme Delivery Mode | Assessment Type | Title | Competency | Teaching Methods |
|---|---|---|---|---|
| AIMS - Competency-based Standards for Medical Scientists | ||||
| All delivery modes | Activity Participation | Haematology lab learning portfolio | 1.1.2 | Taught, Practiced, Assessed |
| 1.1.3 | Taught, Practiced, Assessed | |||
| 1.2.3 | Taught, Practiced, Assessed | |||
| 1.5.1 | Taught, Practiced, Assessed | |||
| 1.6.1 | Taught, Practiced, Assessed | |||
| 2.3.1 | Taught, Practiced, Assessed | |||
| Group Case study (15%) | 2.1.1 | Taught, Practiced, Assessed | ||
| 6.2.4 | Taught, Practiced, Assessed | |||
| 9.1.1 | Taught, Practiced, Assessed | |||
| Examination - Centrally Scheduled | Final theory exam | 2.1.1 | Taught, Practiced, Assessed | |
| Practical / Laboratory Skills, and Written Piece | Theory & practical assessment | 1.1.1 | Taught, Practiced, Assessed | |
| 2.1.1 | Taught, Practiced, Assessed | |||
A 12-unit course will have total of 150 learning hours which will include directed study hours (including online if required), self-directed learning and completion of assessable tasks. Student workload is calculated at 12.5 learning hours per one unit.
| Period and Topic | Activities |
n/a |
n/a |
Please note: Course information, including specific information of recommended readings, learning activities, resources, weekly readings, etc. are available on the course Canvas site– Please log in as soon as possible.
Please note that you need to have regular access to the resource(s) listed below. Resources may be required or recommended.
| Required? | Author | Year | Title | Edition | Publisher |
| Recommended | A. Victor Hoffbrand,David P. Steensma | 2019 | Hoffbrand's Essential Haematology | 8th | John Wiley & Sons |
| Recommended | Elaine Keohane,Larry Smith,Jeanine Walenga | 2019 | Rodak's Hematology | n/a | Saunders |
To successfully complete the UB001 Bachelor of Medical Laboratory Science (Pathology) and meet accreditation requirements of AIMS, UB001 students enrolled in MLS201 must attend and participate in all on-campus practical classes. All theory assessments will be invigilated. UB001 students must attain ≥50% for theory and ≥50% laboratory practical assessment.
Academic integrity is the ethical standard of university participation. It ensures that students graduate as a result of proving they are competent in their discipline. This is integral in maintaining the value of academic qualifications. Each industry has expectations and standards of the skills and knowledge within that discipline and these are reflected in assessment.
Academic integrity means that you do not engage in any activity that is considered to be academic fraud; including plagiarism, collusion or outsourcing any part of any assessment item to any other person. You are expected to be honest and ethical by completing all work yourself and indicating in your work which ideas and information were developed by you and which were taken from others. You cannot provide your assessment work to others. You are also expected to provide evidence of wide and critical reading, usually by using appropriate academic references.
In order to minimise incidents of academic fraud, this course may require that some of its assessment tasks, when submitted to Canvas, are electronically checked through Turnitin. This software allows for text comparisons to be made between your submitted assessment item and all other work to which Turnitin has access.
Eligibility for Supplementary Assessment
Your eligibility for supplementary assessment in a course is dependent of the following conditions applying:
(a) The final mark is in the percentage range 47% to 49.4%; and
(b) The course is graded using the Standard Grading scale
Late submissions may be penalised up to and including the following maximum percentage of the assessment task’s identified value, with weekdays and weekends included in the calculation of days late:
(a) One day: deduct 5%;
(b) Two days: deduct 10%;
(c) Three days: deduct 20%;
(d) Four days: deduct 40%;
(e) Five days: deduct 60%;
(f) Six days: deduct 80%;
(g) Seven days: A result of zero is awarded for the assessment task.The following penalties will apply for a late submission for an online examination:
Less than 15 minutes: No penalty
From 15 minutes to 30 minutes: 20% penalty
More than 30 minutes: 100% penalty
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