1
Physicians have difficulty recognizing and diagnosing disorders of primary hemostasis. The root of this may lie in their education, where students are oſten taught hemostasis using static graphics. We aimed to create a didactic animation on primary hemostasis for medical students to be used in North American medical schools. To promote widespread use of the animation, we surveyed hemostasis educators from Canada and the US on the animation’s learning objectives. The animation’s script and storyboard were developed using the Animation Processing Model (APM), a psychological processing model that addresses the perceptual limitations of learners. This animation is the first biomedical animation to use the APM in its design. Furthermore, this is the first didactic hemostasis animation which sought peer consensus for its learning objectives. Learning objectives were abstracted from Robbins and Cotran Pathologic Basis of Disease.6 A Likert scale survey was sent via SurveyMonkey (www.surveymonkey.com) to the Association of Hemophilia Clinic Directors of Canada (AHCDC; www.ahcdc.ca) and the Foundation for Women and Girls with Blood Disorders (FWGBD; www.fwgbd.org). For each proposed learning objective, the survey participant was asked: 1. The degree which the educator supported using each learning objective for the animation. 2. The difficulty faced by a typical medical student in learning the concept posed by the objective. Objectives underwent an event unit analysis according to the APM, pairing the entities of primary hemostasis with each of their discrete actions (movement, appearance, or state change). Following this analysis, a script and storyboard was developed. The final animation was created using two techniques: 1. Frame-by-frame animation (Rough Animator and Adobe Photoshop) 2. 2D plus animation (Maxon Cinema 4D[Sketch and Toon module], Adobe Aſter Effects, Adobe Audition, Adobe Premiere Pro) 1. Kirtava A, Crudder S, Dilley A, Lally C, Evatt B. Trends in clinical management of women with von Willebrand disease: A survey of 75 women enrolled in Haemophilia Treatment Centres in the United States. Haemophilia. 2004;10(2):158-161. 2. Lowe RK, Schnotz W. Animation Principles in Multimedia Learning. In: Mayer RE, ed. The Cambridge Handbook of Multimedia Learning, Second Edition. Cambridge: Cambridge University Press; 2014:513-546. 3.Berney S, Bétrancourt M. Does animation enhance learning? A meta-analysis. Comput Educ. 2016;101:150-167. 4. Bajpai S, Semwal M, Bajpai R, Car J, Ho AHY. Health Professions’ Digital Education: Review of Learning Theories in Randomized Controlled Trials by the Digital Health Education Collaboration. J Med Internet Res. 2019;21(3):e12912. 5. Lowe R, Boucheix JM. A Composition Approach to Design of Educational Animations. In: Lowe R, Ploetzner R, eds. Learning from Dynamic Visualization: Innovations in Research and Application. New York City: Springer International Publishing; 2017:5-30. 6. Kumar V, Abbas AK, Aster JC. Robbins and Cotran Pathologic Basis of Disease. In: Kumar V, Abbas AK, Aster JC, eds. 9th ed. Philadelphia: Elsevier Saunders; 2015 First biomedical animation to use the Animation Processing Model to inform its design. First educational animation on primary hemostasis that sought consensus for its learning objectives. Manuscript of results to be submitted for publication. Future plans include: 1. Producing a control animation using a script and storyboard developed prior to the event unit analysis. 2. Performing a randomized study with medical students on learning outcomes between control and APM animations. Physicians have difficulty recognizing and diagnosing primary hemostatic disorders like von Willebrand disease.1 In medical school, hemostasis is often taught using static graphics which may fail to capture the temporal and structural complexity of the subject, leading to incorrect mental models.2 As compared to static graphics, animation has been shown to improve learning outcomes.3 Learning outcomes are statistically higher with medical education digital tools which are developed using a specific learning theory. Furthermore, it is recommended that development of these tools follows establishment of learning objectives for the tool.4 The purpose of this project is to develop an animation for medical students which presents an introduction to primary hemostasis. To inform the animation’s content, we aimed to survey educators with experience in teaching hemostasis in North American medical schools regarding learning objectives for the animation. We elected to use the Animation Processing Model (APM ) as the learning theory which would guide the animation’s pre-production and production. The APM is a psychological processing model that addresses the perceptual limitations of learners viewing educational animations for which the learner has little or no experience with the animation’s content.5 Results Abstract Introduction Materials & Methods Conclusions References We gratefully recognize Nicholas Woolridge (Biomedical Communications, Dept. of Biology, University of Toronto) for his technical support with Cinema 4D, the generous support of the Vesalius Trust, and the AHCDC and FWGBD for their participation in our survey and feedback on the survey instrument. Acknowledgements Animating Primary Hemostasis for Medical Student Education Evelyn Lockhart1,2, Michael Corrin1,3, Paula James4, Ric Lowe5, Jodie Jenkinson1,3 1Biomedical Communications, University of Toronto; 2Dept. of Pathology, University of New Mexico; 3Dept. of Biology, University of Toronto; 4Dept. of Medicine, Queen’s University; 5School of Education, Curtin University Plt 1 flowing/inacve (T1) Plt 1 adhesion (T1) Plt 1 degranulaon (T1, T2) Plt 1 acvaon (T3) Plt 1 flaening (T3) Plt 1 aggregaon (T1, T3) GP 2b3a acvated (T3) GP 2b3a binds Fgn (T1) Fgn binds GP2b3a (T1) Granules release (T1) Blood flow/shear force (T1) VWF synthesized (T3) VWF released (T2) VWF unfurls in shear force (T2) VWF binds GP1b (T1) GP 1b binds VWF (T1) E.C. synthesizes VWF (T3) E.C. injury (T3) E.C. release VWF (T2) Plt 2 adhesion (T1) Plt 2 degranulaon (T1, T2) Plt 2 acvaon (T3) Plt 2 flaening (T3) Plt 2 aggregaon (T1, T3) Blood flow Endothelial cell Von Willebrand factor Platelet 1 Platelet 2 GP 1a GP 2b3a Fibrinogen Granules Very easy Easy Neither difficult nor easy Difficult Very difficult 0 20 40 60 80 100 Percentages n = 25 Strongly agree Agree Neither agree nor disagree Disagree Strongly disagree 0 20 40 60 80 100 Percentages Objecve 1 Objecve 2 Objecve 3 Objecve 4 Objecve 5 Objecve 6 Objecve 7 Objecve 8 Objecve 9 Objecve 10 Objecve 11 Objecve 12 Objecve 13 Agreement in using objecve Difficulty of objecve Figure 3: Frame-by-frame animation Figure 4: 2D plus animation See the proposed learning objectives, animatic, and final animation at www.evelynlockhart.com/thesis Figure 1: Event Unit Analysis of primary hemostasis learning objectives. Entity actions are indicated as follows: T1=movement, T2=appearance, T3=shape change. GP1a: glycoprotein 1a, GP 2b3a: glycoprotein 2b3a. Figure 2: Summary of hemostasis educators survey on animation learning objectives.

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Page 1: Animating Primary Hemostasis for Medical Student Education

Physicians have di�iculty recognizing and diagnosing disorders of primary hemostasis. The root of this may lie in their education, where students are o�en taught hemostasis using static graphics. We aimed to create a didactic animation on primary hemostasis for medical students to be used in North American medical schools. To promote widespread use of the animation, we surveyed hemostasis educators from Canada and the US on the animation’s learning objectives. The animation’s script and storyboard were developed using the Animation Processing Model (APM), a psychological processing model that addresses the perceptual limitations of learners. This animation is the first biomedical animation to use the APM in its design. Furthermore, this is the first didactic hemostasis animation which sought peer consensus for its learning objectives.

Learning objectives were abstracted from Robbins and Cotran Pathologic Basis of Disease.6

A Likert scale survey was sent via SurveyMonkey (www.surveymonkey.com) to the Association of Hemophilia Clinic Directors of Canada (AHCDC; www.ahcdc.ca) and the Foundation for Women and Girls with Blood Disorders (FWGBD; www.fwgbd.org).

For each proposed learning objective, the survey participant was asked:1. The degree which the educator supported using each learning objective for

the animation.2. The di�iculty faced by a typical medical student in learning the concept

posed by the objective.

Objectives underwent an event unit analysis according to the APM, pairing the entities of primary hemostasis with each of their discrete actions (movement, appearance, or state change). Following this analysis, a script and storyboard was developed.

The final animation was created using two techniques:1. Frame-by-frame animation (Rough Animator and Adobe Photoshop)2. 2D plus animation (Maxon Cinema 4D[Sketch and Toon module], Adobe

A�er E�ects, Adobe Audition, Adobe Premiere Pro)

1. Kirtava A, Crudder S, Dilley A, Lally C, Evatt B. Trends in clinical management of women with von Willebrand disease: A survey of 75 women enrolled in Haemophilia Treatment Centres in the United States. Haemophilia. 2004;10(2):158-161.2. Lowe RK, Schnotz W. Animation Principles in Multimedia Learning. In: Mayer RE, ed. The Cambridge Handbook of Multimedia Learning, Second Edition. Cambridge: Cambridge University Press; 2014:513-546.3.Berney S, Bétrancourt M. Does animation enhance learning? A meta-analysis. Comput Educ. 2016;101:150-167.4. Bajpai S, Semwal M, Bajpai R, Car J, Ho AHY. Health Professions’ Digital Education: Review of Learning Theories in Randomized Controlled Trials by the Digital Health Education Collaboration. J Med Internet Res. 2019;21(3):e12912.5. Lowe R, Boucheix JM. A Composition Approach to Design of Educational Animations. In: Lowe R, Ploetzner R, eds. Learning from Dynamic Visualization: Innovations in Research and Application. New York City: Springer International Publishing; 2017:5-30.6. Kumar V, Abbas AK, Aster JC. Robbins and Cotran Pathologic Basis of Disease. In: Kumar V, Abbas AK, Aster JC, eds. 9th ed. Philadelphia: Elsevier Saunders; 2015

First biomedical animation to use the Animation Processing Model to inform its design.

First educational animation on primary hemostasis that sought consensus for its learning objectives.

Manuscript of results to be submitted for publication.

Future plans include:1. Producing a control animation using a script and storyboard

developed prior to the event unit analysis. 2. Performing a randomized study with medical students on

learning outcomes between control and APM animations.

Physicians have di�iculty recognizing and diagnosing primary hemostatic disorders like von Willebrand disease.1

In medical school, hemostasis is often taught using static graphics which may fail to capture the temporal and structural complexity of the subject, leading to incorrect mental models.2

As compared to static graphics, animation has been shown to improve learning outcomes.3

Learning outcomes are statistically higher with medical education digital tools which are developed using a specific learning theory. Furthermore, it is recommended that development of these tools follows establishment of learning objectives for the tool.4

The purpose of this project is to develop an animation for medical students which presents an introduction to primary hemostasis.

To inform the animation’s content, we aimed to survey educators with experience in teaching hemostasis in North American medical schools regarding learning objectives for the animation.

We elected to use the Animation Processing Model (APM) as the learning theory which would guide the animation’s pre-production and production.

The APM is a psychological processing model that addresses the perceptual limitations of learners viewing educational animations for which the learner has little or no experience with the animation’s content.5

ResultsAbstract

Introduction

Materials & Methods

Conclusions

References

We gratefully recognize Nicholas Woolridge (Biomedical Communications, Dept. of Biology, University of Toronto) for his technical support with Cinema 4D, the generous support of the Vesalius Trust, and the AHCDC and FWGBD for their participation in our survey and feedback on the survey instrument.

Acknowledgements

Animating Primary Hemostasis for Medical Student EducationEvelyn Lockhart1,2, Michael Corrin1,3, Paula James4, Ric Lowe5, Jodie Jenkinson1,3

1Biomedical Communications, University of Toronto; 2Dept. of Pathology, University of New Mexico; 3Dept. of Biology, University of Toronto; 4Dept. of Medicine, Queen’s University; 5School of Education, Curtin University

Plt 1 flowing/inactive (T1)

Plt 1 adhesion (T1)

Plt 1 degranulation (T1, T2)

Plt 1 activation (T3)

Plt 1 flattening (T3)

Plt 1 aggregation (T1, T3)

GP 2b3a activated (T3)

GP 2b3a binds Fgn (T1)

Fgn binds GP2b3a (T1)

Granules release (T1)

Blood flow/shear force (T1)

VWF synthesized (T3)

VWF released(T2)

VWF unfurls in shear force (T2)

VWF binds GP1b (T1)

GP 1b binds VWF (T1)

E.C. synthesizes VWF (T3)

E.C. injury(T3)

E.C. release VWF(T2)

Plt 2 adhesion (T1)

Plt 2 degranulation (T1, T2)

Plt 2 activation(T3)

Plt 2 flattening (T3)

Plt 2 aggregation (T1, T3)

Blood flow

Endothelial cell

Von Willebrandfactor

Platelet 1

Platelet 2

GP 1a

GP 2b3a

Fibrinogen

Granules

Very easy

Easy

Neither difficult nor easy

Difficult

Very difficult

0 20 40 60 80 100

Percentages

n = 25

Strongly agree

Agree

Neither agree nor disagree

Disagree

Strongly disagree

0 20 40 60 80 100

Percentages

Objective 1

Objective 2

Objective 3

Objective 4

Objective 5

Objective 6

Objective 7

Objective 8

Objective 9

Objective 10

Objective 11

Objective 12

Objective 13

Agreement in using objective

Difficultyof objective

Figure 3: Frame-by-frame animation Figure 4: 2D plus animation

See the proposed learning objectives, animatic, and �nal animation at www.evelynlockhart.com/thesis

Figure 1: Event Unit Analysis of primary hemostasis learning objectives. Entity actions are indicated as follows: T1=movement, T2=appearance, T3=shape change. GP1a: glycoprotein 1a, GP 2b3a: glycoprotein 2b3a.

Figure 2: Summary of hemostasis educators survey on animation learning objectives.