| Literature DB >> 32536919 |
Abstract
Case-based, interactive sessions for small groups (in a large medical school class of 150 students) reinforces basic immunology concepts by including clinical scenarios that stimulate student learning and consolidate critical concepts. Careful design of cases (designing backwards from the key concepts) leads students through successively more complicated and linked group-work questions. This paper details why cases are effective learning tools, how to design an effective case, how to ask appropriate questions and how to help students apply basic immunology concepts to a case. Each group work session is facilitated and followed by a question and answer presentation by faculty, where student groups are directly asked to answer the questions and also challenged with "bonus questions" not presented with the original case. This allows students to "put together" immunology information into a "story" that they can tell and prevents student frustration by summarizing the results at the end of each case. Case design is carefully discussed including clinical relevancy and accuracy, how to write questions that do not give away the answers, how to emphasize mechanistic questions that allow students to "clinically explain as a physician" the immunological basis for the answers. Additionally, students better understand the role of immunity in both normal and disease states. A case-based approach promotes student learning by re-emphasizing basic concepts in the context of the case and promotes better students understanding of critical immunological concepts.Entities:
Keywords: active learning; case-based learning; immunology education; integrated curriculum; key concepts; medical school education; team-based learning
Mesh:
Year: 2020 PMID: 32536919 PMCID: PMC7267000 DOI: 10.3389/fimmu.2020.00995
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561
Immunology Concept Mapping Chart.
| PAMP and DAMP activation of innate immunity | Describe the TLRs that recognize specific PAMPs and DAMPs. | What Toll-like receptors (TLRs) are likely to be activated by this infection? |
| TLR activation and signaling | Explain how TLR activation/signaling primes the innate immune response | What cytokines would you expect to be elevated in the blood in this patient after this infection? |
| Actions of mediators of acute inflammation | Describe the actions of mediators acute inflammation (IL-1/TNF-alpha | Why is the white count elevated? What cell type is most likely to be elevated? Why are the band cells increased? What is the molecular mechanism for the increase on neutrophils and band cells |
| Physiological and effects of acute inflammation. | Describe the physiological effects of elevated IL-1, TNF-alpha and IL-6. | What is the significance of the increasing fever and the presence of bacteria in the blood? What is the molecular mechanism for the fever increase and why does this concern you? |
| Pathological effects of acute inflammation. | Describe the pathological effects of elevated IL-1, TNF-alpha and IL-6. | Why is the blood pressure dropping in this patient? Why is does he have systemic edema? What are the molecular mechanisms for the drop in blood pressure? |