| Literature DB >> 34905444 |
Daniel T Schoenherr1,2, Mary O Dereski1, Kurt D Bernacki3,4, Said Khayyata3,4, Stefanie M Attardi1.
Abstract
Integration of core concepts is an important aspect of medical curriculum enhancement. Challenges to improving integration include the risk of curtailing the basic sciences in the process and the push to decrease contact hours in medical curricula. Self-paced learning tools can be developed that deliberately relate basic and clinical sciences to aid students in making interdisciplinary connections. The purpose of this project was to develop, implement, and evaluate a self-paced learning module that would be applicable to integration of different disciplines in medical education. The module was intended to improve integration between histology and anatomic pathology before a respiratory pathology laboratory session. Qualtrics XM, a survey software commonly available at educational institutions, was used in a novel manner to create the module. Module activities included pre- and post-module quizzes; four short videos emphasizing normal histological features and recalling associated pathologies; three categorization activities designed for students to recognize normal versus abnormal characteristics of lung specimens; and post-activity feedback. Preliminary data from first-year medical students showed that post-module quiz scores were significantly higher than pre-module quiz scores (p < 0.001) and that module users' pre-laboratory pathology self-efficacy was significantly higher than non-users (p < 0.05). These data suggest that module use facilitated short-term knowledge gain and improved pathology self-efficacy before the laboratory session. Online modules can be developed affordably using Qualtrics XM to integrate anatomical sciences with other disciplines, while providing students interactive learning resources without increasing contact hours. The module presented in this report focused on normal versus abnormal morphology, guiding students through recognizing the continuum from healthy to disease states before learning about the pathologies more in depth. A similar module design would likely be effective in integrating other disciplines in medicine, especially in disciplines that require recognition of changes in morphology.Entities:
Keywords: Medical education; histology; integration; online module; pathology
Mesh:
Year: 2022 PMID: 34905444 PMCID: PMC8676635 DOI: 10.1080/10872981.2021.2011692
Source DB: PubMed Journal: Med Educ Online ISSN: 1087-2981
Figure 1.Module Screenshots. (A) Sample screenshot from the bronchus review video. In this frame, the normal thickness for the submucosal glands was reviewed and the names of two conditions were provided that involve changes to the thickness. (B) Sample screen shot from a drag and drop review activity. The user was instructed to move eight specimen images into the corresponding boxes. (C) Answers to drag and drop review activity shown in (B). Histology images were obtained from the Virtual Microscopy Database under an Attribution-NonCommercial-ShareAlike 4.0 Creative Commons License (CC). Image (A) was edited to add arrows and percent
Figure 2.Study Timeline
Figure 3.Pathology Self-Efficacy versus General Self-Efficacy
Pre-laboratory self-efficacy scores
| | Pathology Self-Efficacy | General Self-Efficacy | ||||
| Module Use ( | Median | IQR§ | MW† | Median | IQR§ | MW† |
| Users ( | 24 | 21–24 | 8 | 7–9 | ||
| Non-users ( | 22 | 19–24 | 8 | 7–8 | ||
| Pathology Self-Efficacy | General Self-Efficacy | |||||
| Preparedness Group ( | Median | IQR§ | KW‡ | Median | IQR§ | KW‡ |
| Least Prepared ( | 24 | 22–24.25 | 8 | 7.75–9.25 | ||
| Moderately Prepared ( | 23 | 21–24 | 8 | 8–9 | ||
| Most Prepared ( | 22 | 20–24.75 | 8 | 7–9 | ||
| Pathology Self-Efficacy | General Self-Efficacy | |||||
| Lectures Watched ( | Median | IQR§ | KW‡ | Median | IQR§ | KW‡ |
| 0–1 Lectures ( | 24 | 23–25 | 8 | 8–10 | ||
| 2–3 Lectures ( | 23 | 21–24 | 8 | 7–8 | ||
| 4–5 Lectures ( | 23 | 20.25–24 | 8 | 8–9 | ||
| 6–7 Lectures ( | 22.5 | 20.25–24 | 8 | 7–9 | ||
| Pathology Self-Efficacy | General Self-Efficacy | |||||
| Self-Study Hours ( | Median | IQR§ | KW‡ | Median | IQR§ | KW‡ |
| 0 Hours ( | 23 | 21–24 | 8 | 8–9 | ||
| 1–5 Hours ( | 24 | 21–24 | 8 | 7–9 | ||
| 6–10 Hours ( | 22.5 | 20.75–25.25 | 8 | 7–9 | ||
| 11–15 Hours ( | 20.5 | 20.25–20.75 | 5 | 5–5 | ||
| >15 Hours ( | – | – | – | – | ||
§Interquartile range; †Mann-Whitney U test; ‡Kruskal-Wallis rank sum test; *Significant difference for alpha value set to .05
| Video | Normal Histology Featured | Pathology Correlation |
|---|---|---|
| 1. Respiratory Epithelium | Respiratory epithelium is classified as pseudostratified ciliated columnar from the nasal cavity to distal bronchi (exceptions: nasal vestibules, olfactory region, lingual side of epiglottis, true vocal fold) | Squamous metaplasia is a feature of chronic bronchitis |
| Tall ciliated cells & function | Smoking interferes with ciliary action, preventing mucus clearance | |
| Scattered goblet cells & function | Goblet cell hyperplasia is a feature of chronic bronchitis and asthma | |
| Short neuroendocrine/Kulchitsky cells & function | Origin of neuroendocrine tumors e.g., small cell carcinoma, carcinoid | |
| 2. Bronchus | Lumen clear of neutrophils | Neutrophils in lumen seen in bronchopneumonia |
| Visible basement membrane | Thickened basement membrane seen in asthma | |
| Mucosa can have sparse lymphoid tissue (BALT1) composed of lymphocytes and histiocytes. | Mucosal inflammation seen in bronchitis:
Neutrophils = acute inflammation Plasma cells & lymphocytes = chronic inflammation | |
| Thin layer of crisscrossing smooth muscle bundles in mucosa | Smooth muscle layer thickening seen in asthma | |
| Submucosal glands occupy ~40% of the distance between epithelium and cartilage | >40% in chronic bronchitis, sometimes asthma | |
| 3. Bronchiole | Largest bronchioles: Ciliated simple columnar epithelium with scattered goblet cells | |
| No inflammatory cells in mucosa | Mucosal inflammation seen in bronchiolitis | |
| Thin layer of mucus on epithelial cells but mucus should not clog lumen | Mucus can clog lumen in asthma patients | |
| Thin layer of crisscrossing smooth muscle bundles | Smooth muscle layer thickening is feature of asthma | |
| 4. Alveolus | Approximate diameter is 200um | Alveolar space enlargement seen in emphysema |
| The only normal structure within the lumen is the alveolar macrophage. | Inflammatory exudate within the lumen seen in bacterial pneumonia and ARDS2 | |
| Type I and II pneumocytes & function. | Neoplastic cells in alveolar wall can lead to adenocarcinoma | |
| Thin alveolar septum comprised of type I pneumocytes and their basement membrane sandwiching:
Continuous capillaries and their basement membrane Interstitium (rich in elastic, and reticular fibers) | Thickened interalveolar septum seen in viral pneumonia (interstitial pneumonia). Increased mononuclear cells (lymphocytes, plasma cells) present in thickened alveolar walls in viral infection. |
aBALT: Bronchus-associated lymphoid tissue; 2ARDS: Acute respiratory distress syndrome
| Statement | Strongly disagree | Somewhat disagree | Neither agree nor disagree | Somewhat agree | Strongly agree |
|---|---|---|---|---|---|
| I will be able to achieve most of the goals in respiratory histopathology that have been set for me. | □ | □ | □ | □ | □ |
| When facing difficult tasks in respiratory histopathology, I am certain that I will accomplish them. | □ | □ | □ | □ | □ |
| In general, I think that I can obtain outcomes that are important for histopathology. | □ | □ | □ | □ | □ |
| I believe I can succeed at most any endeavor to which I set my mind. | □ | □ | □ | □ | □ |
| I will be able to successfully overcome many challenges in respiratory histopathology. | □ | □ | □ | □ | □ |
| I am confident that I can perform effectively on many different tasks in respiratory histopathology. | □ | □ | □ | □ | □ |
| Compared to other people, I can do most tasks in histopathology very well. | □ | □ | □ | □ | □ |
| Even when things are tough, I can perform quite well. | □ | □ | □ | □ | □ |
1This self-efficacy survey has been modified for tasks related to histopathology from an original validated self-efficacy survey by Gilad Chen, Stanley M. Gully, and Dov Eden published in Organizational Research Methods (Vol. 4, No. 1) pp. 62–83, copyright © 2001 SAGE Publications, Inc. Reprinted by Permission of SAGE Publications, Inc.