MLT 276 - Clinical Hematology Practicum

2 credit hours - 120 hours clinical; one term.
Apply practical theory and skills learned in previous MLT courses in the clinical hematology laboratory setting under the supervision of a clinical preceptor. Students will rotate through the areas of a clinical hematology laboratory either through simulation or at an assigned clinical rotation laboratory or a combination of both. Clinical fee $60.

Prerequisite(s): MLT 205  with a grade of C or better, or permission of the MLT Program Coordinator.

Note: Typically offered OF; spring term.

Course Outcomes:
 

1. Explain the impact that the hematopoetic system has on a person’s overall wellness.

2. Discuss the relationship of hematopoetic system and systemic process related to blood

3. Compare and contrast the expected complete blood count (CBC) hematological values in healthy patients vs those with hematological diseases or conditions.

4. Explain the impact of hematological disease states and condition on a patient’s overall health

5. Perform cell counting using automated laboratory equipment, such as Coulter counter

6. Perform manual WBC differentials using microscopy and specialized slides

7. Perform staining techniques to identify shape and size for red blood cells and white blood cells

8. Identify morphological changes in red blood cells, white blood cells and platelets using microscopy and staining procedures

9. Correlate abnormal results (high or low), with disease processes

10. Perform hematology techniques such as sedimentation rates, reticulocyte counts, body fluid assessment, and counts that are performed in the clinical hematology laboratory

11. Perform coagulation testing such as: prothombin time, partial prothombin time, platelet production and factors assays if performed by the laboratory

12. Identify disease conditions related to hemostasis, such as factor deficiencies and coagulopathies

13. Perform quality checks to calibrate automated coagulation instrumentation

14. Apply proper procurement and storage of specimen, such as: additive to specimen ratios, time specified requirements

15. Practice accepted procedures for reporting normal and abnormal results, such as immediate physician notification for abnormal results and high risk situations

16. Document results using site specified methods, such as laboratory information systems