CURRICULUM - Fakultas Kedokteran Udayana | Just ... · Web viewMoore.K.L, Agar A.M.R :...

Study Guide The Visual System and Disorders

TABLE OF CONTENTS

Page

Content 1

Learning outcomes 2

Block team 4

Fasilitators 5

Core curiculum 6

Time table 9

Time table clinical skill 12

Meeting of student representatives 14

Article review 15

Learning program 17

Practicum and basic clinical skill guides 46

Assessment Form 65

Curriculum map 66

Udayana University Faculty of Medicine, MEU 1


LEARNING OUTCOMES

THE AIMS

1. Comprehend the underlying normal structure and function of the visual system and

its practical or clinical implications.

2. Understanding the pharmacology and pharmacokinetic of the ocular medicines.

3. Able to manage common eye and visual disorders and refer of high risks patient with

visual disorders for further investigation and management.

4. Awareness and responsiveness to the community aspects of health care, needs,

education and promotion.

LEARNING OUTCOMES

1. Able to know and understand anatomy of the eye structures

2. Able to know and understand Histology of the eye structures

3. Able to know and understand Physiology of the eye, and Physiology of vision

4. Able to know and understand the pharmacology and pharmacokinetic of the ocular

medicines

5. Able to establish diagnosis and management patient with Refraction disorders such as Mild Hipermetropia, mild myopia, mild astigmatism and presbyopia.

6. Able to initially diagnose, manage and later refer patient with Refraction disorders such as anisometropia and contact lens problems.

7. Able to establish diagnosis and management patient with external eye diseases such us conjunctivitis, Dry eye Syndrome, Hordeolum, and Episcleritis

8. Able to initially diagnose, manage and later refer patient with external eye diseases such as chalazion, scleritis, keratitis, and uveitis

9. Able to initially diagnose and later refer patient with external eye diseases such as

keratokonjungtivitis sicca and endophthalmitis.

10.Able to initially diagnose, manage and later refer patient with glaucoma disorders.

11.Able to establish diagnosis and management patient with ocular injuries such as

foreign bodies in the conjunctiva and subconjunctival bleeding

12.Able to manage and initially diagnose and later refer patient with ocular injuries such as hyphema and eyelids lacerations.

13.Able to initially diagnose and later refer patient with ocular injuries such as corneal

erosion, foreign bodies on the cornea, thermal corneal burn and lacrimal duct

lacerations.



14.Able to establish diagnosis and management patient with eyelids and lacrimal system disorders such us trichiasis.

15.Able to initially diagnose, manage and later refer patient with eyelids and lacrimal systems disorders such as dacrioadenitis and dacriocystitis

16.Able to initially diagnose and later refer patient with eyelids and lacrimal sytems disorders such as entropion, lagophthalmus, epichantus, ptosis, eyelids retraction

and xanthelasma

17.Able to initially diagnose and later refer patient with cataract, lens dislocation and corneal disorders such as pterygium and keratoconus.

18.Able to initially diagnose and later refer patient with retinal disorders.

19.Able to initially diagnose and later refer patient with neuro ophthalmology & strabismus disorders including amblyopia and binocular diplopia.

20.Able to establish diagnosis and management patient with community ophthalmology disorders such as night blindness

21.Able to initially diagnose, manage and later refer patient with community ophthalmology disorders such as Xerophthalmia

22.Able to initially diagnose and later refer patient with community ophthalmology disorders such as blindness due to 5 most common eye disorders (Cataract,

Glaucoma, refractive errors, infection and immunology eye diseases and retina

disorders)

CURRICULUM CONTENT

1. Anatomy, histology and physiology of the eye.2. Pharmacology of the eye medicines.3. Refractive Errors.4. Infection & Immunologic Eye Diseases.5. Glaucoma disorders 6. Eyelids and Lacrimal systems disorders 7. Ocular Injuries8. Cataract, corneal and lens disorders.9. Vitreous and Retinal disorders 10.Neuro Ophthalmology & strabismus disorders.



BLOCK TEAM

COORDINATOR : dr. I Wyn Eka Sutyawan Sp.M TIME : 11 July 2017 – 31 July 2017

PlannersNo Name

1 dr. Putu Budhiastra, Sp.M (K)2 Prof.dr.NK Niti Susila, SpM (K)3 dr. Ni Made Ayu Surasmiati, M. Biomed, Sp.M4 dr. AAA Sukartini Djelantik, Sp.M (K)5 dr. Made Agus Kusumadjaja, Sp.M (K)6 dr. W.G Jayanegara, Sp.M (K)7 Dr. dr. A.A Mas Putrawati T, Sp.M(K)8 dr. Ariesanti Tri Handayani, Sp.M(K)9 dr. Yuliana,M Biomed

10 Prof.dr.I Dewa Putu Sutjana,PFK,M.Erg11 dr. I.G.A.Dewi Ratnayanti, M. Biomed12 Dr. dr. Made Jawi, M. Kes13 dr. Ni Made Ari Suryathi, M. Biomed, Sp.M14 dr. Ni Made Laksmi Utari, M.Biomed, Sp.M15 dr. IGAM Juliari,Sp.M(K)16 dr. Wayan Eka Sutyawan,SpM17 dr. Ari Andayani,Sp.M(K)18 dr. I Made Krisna Dinata. M. Erg19 dr. Ni Putu Ekawati, M.Repro, SpPA20 dr. Ni Putu Wardani, M. Biomed, SpAn

LecturesNo Name Dept No Telp

1 dr. Putu Budhiastra, Sp.M (K) Ophtalmology 085238238999

2 Prof.dr.NK Niti Susila,SpM (K) Ophtalmology 08123643816

3 dr. Ni Made Ayu Surasmiati, M. Biomed, Sp.M Ophtalmology 0813383418604 dr. AAA Sukartini Djelantik, Sp.M (K) Ophtalmology 081337314911

5 dr. Made Agus Kusumadjaja, Sp.M (K) Ophtalmology 081239813496 dr. W.G Jayanegara, Sp.M (K) Ophtalmology 0818909147

7 Dr. dr. A.A Mas Putrawati T, Sp.M(K) Ophtalmology 08123846995

8 dr. Yuliana,M.Biomed Anatomy 0857926523639 Prof.dr.I Dewa Putu Sutjana,PFK,M.Erg Physiology 08123924477

10 dr. I.G.A.Dewi Ratnayanti, M.Biomed Histology 0361855034411 Dr. dr. Made Jawi, M.Kes Pharmacology 08179787972

12 dr. Ni Made Ari Suryathi, M. Biomed, Sp.M Ophthalmology 085253651928

13 dr. Ni Made Laksmi Utari, M.Biomed, Sp.M Ophthalmology 082340393727

14 dr. IGAM Juliari,Sp.M(K) Ophthalmology 08123615625

15 dr. Wayan Eka Sutyawan,Sp.M Ophthalmology 081338538499

16 dr. Ari Andayani,Sp.M(K) Ophthalmology 08113803666

17 dr. I Made Krisna Dinata, M.Erg Physiology 08174742566

18 dr. I Gusti Ngurah Mayun, SpHK Histology 081237395050

FACILITATORS



Regular Class (Class A)

No Name Group Department Phone Room

1 Prof.dr.GM Aman, Sp.FK A1 Pharmacology 081338770650 2nd floor: R.2.01

2 Prof.Dr.dr.I Putu Adiatmika, M.Kes A2 Physiology 08123811019 2nd floor: R.2.02

3 dr.IG N Wien Aryana, Sp.OT (K) A3 Orthopaedic 0811385263 2nd floor: R.2.03

4 Prof.dr.IDP Sutjana, M.Erg A4 Physiology 08123924477 2nd floor: R.2.04

5 dr.Yuliana, M.Biomed A5 Anatomy 085792652363 2nd floor: R.2.05

6 dr.I Wayan Surudarma, M.Si A6 Biochemistry 081338486589 2nd floor: R.2.06

7 dr.Made Agus Hendrayana, M.Ked A7 Microbiology 08123921590 2nd floor:

R.2.07

8 dr.I Putu Bayu Mayura, S.Ked A8 Microbiology 082236165801 2nd floor: R.2.08

9 Dr.dr. I Made Muliarta, M.Kes A9 Physiology 081338505350 2nd floor: R.2.21

10 dr.IGN Sri Wiryawan, M.Repro A10 Histology 082341768888 2nd floor: R.2.22

English Class (Class B)

No Name Group Department Phone Room

1 dr.Yukhi Kurniawan, Sp.And B1 Andrology 08123473593 2nd floor: R.2.01

2 Dr.dr.BK Satriyasa, M.Repro B2 Pharmacology 087777790064 2nd floor: R.2.02

3 Prof.Dr.dr. Ketut Tirtayasa, MS, AIF AIFO, Sp.Erg B3 Physiology 08123623422 2nd floor:

R.2.03

4 Dr.dr.Tjok Senapati, Sp.An, KAR B4 Anestesiology 081337711220 2nd floor: R.2.04

5 dr.I Wayan Sugiritama, M.Kes B5 Histology 08164732743 2nd floor: R.2.05

6 Dr.dr.Ni Nyoman Sri Budayanti, SP.MK(K) B6 Microbiology 08553711398 2nd floor:

R.2.06

7 dr.IG Kamasan Nyoman Arijana, M.Si, Med B7 Histology 085339644145 2nd floor:

R.2.07

8 dr. I GustiAyu Harry Sundariyati, S.Ked B8 DME 081805380277 2nd floor:

R.2.08

9 dr.IGA Artini,M.Sc B9 Pharmacology 08123650481 2nd floor: R.2.21

10 dr.I Ketut Mariadi, Sp.PD B10 Interna 08123853700 2nd floor: R.2.22

CORE CURRICULUM



BLOCK : VISUAL SYSTEM AND DISORDERSEMESTER : IVSKS : 2

NO DAY LEARNING OUTCOME

EDUCATIONAL STRATEGIES

LEARNING SITUATION

METHOD OF ASSESMENT

1 1 Able to know and understand the Anatomy of the eye

Independent learningIntegrated learningProblem based learning

Introductory lectureStudent ProjectSGDPracticum

MCQ

2 2 Able to know and understand the Histology of the eye



MCQ

3 3 Able to know and understand the Physiology of the eye



MCQ

4 4 Able to know and understand the Pharmacology and Pharmacokinetic of the eye medicines



MCQ

5 5 Able to establish diagnosis and manage patient with REFRACTION DISORDERSsuch as : Myopia, Hyperopia, Astigmatism, Presbyopia, Anisometropia, Buta Senja

Independent learningIntegrated learningProblem/case based learning

Introductory lectureStudent ProjectSGDBCS

MCQOSCE

6 6 Able to establish diagnosis and manage patient with INFECTION & IMMUNOLOGIC EYE DISEASES such as:Conjunctivitis- Hordeoulum, Chalazion and dry eye syndrome- Scleritis, episcleritis- Keratitis,



MCQOSCE



Xeropthalmia,Anterior Uveitis (Iritis & Iridosiklitis), Hipopion.

7 7 Able to establish diagnosis and manage patient with GLAUCOMA DISORDERS such as : - Acute glaucoma- Chronic glaucoma- Secondary glaucoma- Congenital glaucoma



MCQOSCE

8 8 Able to establish diagnosis and manage patient with RECONSTRUCTION, OCULOPLASTY & ONCOLOGY such as :Eyelid and lacrimal laceration, Entropion, Trichiasis, Epicanthus, Ptosis, Dacryoadenitis, Dacryocystitis


Introductory lectureSGDBCS

MCQ

9 9 Able to establish diagnosis and manage patient with CORNEA & LENS DISORDERS such as : - Pterygium, Keratoconus- Senile Cataract, Lens Dislocasion



MCQOSCE

10 10 Able to establish diagnosis and manage patient with VITREO RETINAL DISORDERS such as : - Retinal detachment- Retinal vessel occlusion- Degeneration macula- Diabetic retinopathy- Hypertensive


Introductory lectureSGD

MCQ



retinopathy11 11 Able to establish

diagnosis and manage patient with NEURO OPHTHALMOLOGY such as :Diplopia BinocularHemianopia:

bitemporal dan Homonymous

Visual Filed Disturbance

Edema PapilNeuropathy Optic

(Atrophy + Neuritis)


Introductory lectureSGDBCS

MCQOSCE

12 12 Able to establish diagnosis and manage patient with STRABISMUS DISORDERS such as : - Eye movement- Esotropia - Eksotropia


Introductory lectureSGD

MCQ



TIME TABLE

DAY PROGRAMME LEARNING ACTIVITIES CLASS A CLASS B PIC

I11/7/2017

LEARNING OUTCOME 1

INTRODUCTIONLECTURE :- Anatomy of the EyeIndependent LearningSGDBreakStudent ProjectPlenary session

08.00-08.1508.15-09.00

09.00-10.3010.30-12.0012.00-12.3012.30-14.0014.00-15.00

09.00-09.15 09.15-10.00

12.00-13.3013.30-15.0011.30-12.0010.00-11.3015.00-16.00

BudiYuliana

YulianaII

12/7/2017

LEARNING OUTCOME 2,3

LECTURE:- Histology of the eye

Independent LearningSGDBreakStudent ProjectPlenary session

08.00-09.00

09.00-10.3010.30-12.0012.00-12.3012.30-14.0014.00-15.00

09.00-10.00

12.00-13.3013.30-15.0011.30-12.0010.00-11.3015.00-16.00

Ratna/Mayun

Ratna/MayunIII

13/7/2017

LEARNING OUTCOME 3

LECTURE :- Physiology of the eye


08.00-09.00

09.00-10.3010.30-12.0012.00-12.3012.30-14.0014.00-15.00

09.00-10.00

12.00-13.3013.30-15.0011.30-12.0010.00-11.3015.00-16.00

Sutjana/Krisna

Sutjana/Krisna

IV14/7/2017

LEARNING OUTCOME

3,4

LECTURE:- Chronic Glaucoma and Congenital glaucoma- Acute Glaucoma and Secondary glaucoma


08.00-08.30

08.30-09.00

09.00-10.3010.30-12.0012.00-12.3012.30-14.0014.00-15.00

09.00-09.30

09.30-10.00

12.00-13.3013.30-15.0011.30-12.0010.00-11.3015.00-16.00

Agus

Ari Surya

Agus, Ari Surya

V17/7/2017

LEARNING OUTCOME

5,6,22

LECTURE:-Ocular Injuries-Eyelids and Lacrimal Disorders


08.00-08.30

08.30-09.00

09.00-10.3010.30-12.0012.00-12.3012.30-14.0014.00-15.00

09.00-09.30

09.30-10.00

12.00-13.3013.30-15.0011.30-12.0010.00-11.3015.00-16.00

Sukartini

Laksmi U

Sukartini, Laksmi U

VI18/7/2017

LEARNING OUTCOME 7,8,9,21,22

LECTURE:- Infection eye disorders- Imunologic eye

disorders

08.00-08.3008.30-09.00

09.00-09.3009.30-10.00

Niti Juliari




09.00-10.3010.30-12.0012.00-12.3012.30-14.0014.00-15.00

12.00-13.3013.30-15.0011.30-12.0010.00-11.3015.00-16.00 Niti, Juliari

VII19/7/2017

LEARNING OUTCOME

10,22

LECTURE :- Physiology of the eye

- Pharmacology of the ocular medicine


08.00-08.30

08.30-09.00

09.00-10.3010.30-12.0012.00-12.3012.30-14.0014.00-15.00

09.00-09.30

09.30-10.00

12.00-13.3013.30-15.0011.30-12.0010.00-11.3015.00-16.00

Krisna

Jawi

Krisna, JawiVIII

20/7/2017

LEARNING OUTCOME

11,12,13,14,15,16

LECTURE:- Visus and Refraction- Refraction disorders


08.00-08.3008.30-09.00

09.00-10.3010.30-12.0012.00-12.3012.30-14.0014.00-15.00

09.00-09.3009.30-10.00

12.00-13.3013.30-15.0011.30-12.0010.00-11.3015.00-16.00

Eka

Eka

IX21/7/2017

BCS

X24/7/2017

LEARNING OUTCOME

17,18,22

LECTURE 1Cornea and Lens disorderLECTURE 2Retina


08.00-08.30

08.30-09.00

09.00-10.3010.30-12.0012.00-12.3012.30-14.0014.00-15.00

09.00-09.30

09.30-10.00

12.00-13.3013.30-15.0011.30-12.0010.00-11.3015.00-16.00

Jaya

Ari

Jaya, Ari

XI25/7/2017

BCS

XII26/7/2017

BCS

XIII27/7/2017

BCS

XIV28/7/2017

BCS



XV31/7/2017

LEARNING OUTCOME

19,20

LECTURE 1Neuro OphthalmologyLECTURE 2Strabismus


08.00-08.30

08.30-09.00

09.00-10.3010.30-12.0012.00-12.3012.30-14.0014.00-15.00

09.00-09.30

08.30-09.00

12.00-13.3013.30-15.0011.30-12.0010.00-11.3015.00-16.00

Mas

Surasmiati

Juliari Mas,

Surasmiati

XVI24-

28/7/2017

ARTICLE REVIEW PRESENTATION TEAM

XVII1/8/

2017

PRE-EVALUATION BREAK TEAM

XVIII2/8/

2017

FINAL ASSESSMENT TEAM

Note. Lecture: at class room (4.02), 4rd floor start on time Class will be locked while the lecture begin, please do not late for the class Student Presentation: at class room (4.02)

TIME TABLE BASIC CLINICAL SKILL

DAY LEARNING ACTIVITY CLASS A CLASS B PIC



I21/7/17

LECTURE :- Histology

Examination- Physiology Practice

Lecture : Ishihara Plucido Kampimetri

Practicum Histology

BreakPracticum Physiology

08.00-08.30

08.30-09.00

09.30-11.30

11.30-12.0012.00-14.00

09.00-09.30

09.30 -10.00

13.00-15.00

12.30-13.0010.30-12.30

Ratna

Krisna

Histology team

PHYSIOLOGY TEAM

II25/7/17

LECTURE:VISUAL ACUITY EXAMINATIONBCS Visual Acuity Exam+ Anterior segmen

BreakStudent Project Presentation

08.00 – 09.00

09.30-11.30

11.30-12.0012.00-14.00

09.00 – 10.00

13.00-15.00

12.30-13.0010.30-12.30

Laksmi Utari

TEAM

Eka

III26/7/17

LECTURE :- TONOMETRY- VISUAL

FIELD/KONFRONTASI

- AMSLER GRID

BCS Tonometry + Konfrontasi + Amsler GridBreakStudent Project Presentation

08.00-09.00

09.30-11.30

11.30-12.0012.00-14.00

09.00-10.00

13.00-15.00

12.30-13.0010.30-12.30

Mas Putrawati

TEAM

Surasmiati

IV27/7/17

LECTURE :- Anterior Segment

Examination- Therapeutic

Instillation & Drug Prescription

BCS Ant Segment Exam+ TerupeutisBreakStudent Project

08.00-08.30

08.30-09.00

09.30-11.30

11.30-12.0012.00-14.00

09.00-09.30

09.30-10.00

13.00-15.00

12.30-13.0010.30-12.30

Ari Suryathi

TEAM

Laksmi Utari

V28/7/17

LECTURE :- POST SEGMENT

EXAMINATION

BCS Post Segment ExamBreak

08.00-09.00

09.30-11.3011.30-12.0012.00-14.00

09.00-10.00

13.00-15.0012.30-13.0010.30-12.30

Surasmiati

TEAM

Budi/Ari



Student Project presentation

Note:

Lecture for BCS Ophthalmology, Histology and Physiology will be held at Class Room (R.4.02)

BCS Ophthalmology will be held at Skill Lab. Histology Practicum will be demonstrated in classroom. Physiology Practicum will be held in Physiology Dept.

Each BCS will be divided into 4 small groups:- ENGLISH CLASS (CLASS B):

Group AGroup BGroup CGroup D

- REGULAR CLASS (CLASS A):Group AGroup BGroup CGroup D

MID BLOCK MEETING

The meeting between block planner team, facilitators and the student group representatives will be held on 18 Juli 2017 at classroom (4.02) if necessary. In this meeting all the facilitator and student group representative are expected to give suggestion and input as an evaluation to improve the study guide and educational process of visual system and



disorder. Because of the important of this meeting, all the facilitators and student group representative are strongly expected to attend the meeting. All of student group representatives (approximately 10 students) are expected to give suggestion and input or complain to the team planner for improvement. For this purpose, every student group must choice one student as their representative to attend the meeting.

PLENARY SESSION

For each learning task, the student is requested to prepare a group report. The report will be presented in plenary session. Lecturer in charge will choose the group randomly. The aim of this presentation is to make similar perception about the topic that has been given.

ASSESSMENT METHOD

Assessment will be held on Wednesday, 2 August 2017. The Final examination will be held with the format of Computer Based Test. There are 100 questions for the examination that consist out Multiple Choice Questions (MCQ). The time provision is 100 minutes. The number of MCQ is 100. The minimal passing score for the assessment is 70. The proportions of examination score are: Small Group Discussion : 5%Article Review (Student Project) : 15%Final assessment (MCQ) : 80%

The Prerequisites of Final Examination:Attend 75% of total student activitiesUniform for Examination: white shirt, black trouser/ skirt, shoes. NO SANDALS ALLOWED to be wear at the classBring Student ID card with photoBe present 15 minute before the examination starting time

Other than the examination score, the student performance and attitude during group discussion and all block activities will be considered for the average final score.

ARTICLE REVIEW

Students have to write an Article Review with topics that has not been given by lecturer. The topic will be chosen randomly on day one. Each small group discussion is going to write one Article Review with different tittle. One topic shall be wroten by 10-12 students with the direction from facilitator. Students make one review as student project and will be presented



in front of the class and scored by respective facilitators and evaluators.

Format of Article Review

1. Cover: Title Article Review writed at top left cornerUdayana SymbolNameStudent Registration NumberUdayana University, School of Medicine, 2015

2. Introduction3. Content: From Definition to Treatment 4. Summary5. Reference (minimal 10 references) VancouverExample: Journal.John L, Kaplan El. Nonparametric estimation from incomplete observations. J Am Stat Assoc 2008;45:456-481.

Tex bookRootman J, Lapointe JS: Masenchymal Tumor. In Rootman J (ed): Diseases of the orbit. Philadelphia: JB Lippincott CO, 2000,pp 455-469.

Note:8-10 pages, 1.5 space, Time New Roman 12, page at right bottom.

Supervisor (Facilitator) Score with 60% qualification, while Evaluator Score the Presentation with 40% qualification.

TOPIC OF ARTICLE REVIEWEnglish Class

Date SGD Presentation Time

Title Evaluator



24/7/17

25/7/17

26/7/17

27/7/17

28/7/17

B1 10.00-10.30 Corneal Ulcer Niti/JuliariB2 10.30-11.00 Endophthalmitis Niti/Juiari

B3 10.00-10.30 Amblyopia Eka SB4 10.30-11.00 Ainsometria in children Eka S

B5 10.00-10.30 Congenital Esotropia SurasmiatiB6 10.30-11.00 Eksotropia Intermitten Surasmiati

B7 10.00-10.30 Age Macular Degeneration Budiastra/Ari AB8 10.30-11.00 Diabetic Retinopathy Budiastra/Ari A

B9 10.00-10.30 Dacriosistitis Laksmi UtariB10 10.30 -11.00 Ptosis Laksmi Utari

Note. Student presentation: at class room (4.02)

Regular ClassDate SGD Presentation

TimeTitle Evaluator

24/7/17

25/7/17

26/7/17

27/7/17

28/7/17

A10 12.30-13.00 Endofthalmitis Niti/JuliariA9 13.00-13.30 Corneal Ulcer Niti/Juliari

A8 13.00-13.30 Ainsometria in children Eka SA7 13.00-13.30 Amblyopia Eka S

A6 12.30-13.00 Eksotropia Intermitten SurasmiatiA5 13.00-13.30 Congentital Esotropia Surasmiati

A4 12.30-13.00 Diabetic Retinopathy Budiastra/ Ari AA3 13.00-13.30 Age Macular Degeneration Budiastra/Ari A

A2 12.30-13.00 Ptosis Laksmi UtariA1 13.00-13.30 Dacriosistitis Laksmi Utari

Note. Student presentation: at class room (4.02)

LEARNING PROGRAM

Day 1ANATOMY OF THE EYE

dr. Yuliana



SUMMARY

The eyes lie within two bony orbits, located on either side of the root of the nose. The medial walls of the orbits are almost parallel. They border the nasal cavity anteriorly and the ethmoidal air cell and the sphenoid sinus posteriorly. The lateral walls border the middle cranial, temporal, and pterygopalatine fossae. Superior to the orbit is the anterior cranial fossa and the frontal and supraorbital sinus. The maxillary sinus and the palatine air cell are located inferiorly. Seven bones make up the bony orbit such as frontal, zygomatic, maxillary, ethmoidal, sphenoid, lacrimal, and palatine. The four rectus muscles insert anteriorly on the globe along the Spiral of Tillaux. Two oblique muscles are superior and inferior oblique muscle.Six of the twelve cranial nerves (CV II-VII) directly innervates the eye and periocular tissue. The principal arterial supply of the orbit and its structures derives from the ophthalmic artery, the first major branch of the intracranial portion of the internal carotid artery.

LEARNING TASK:1. Describe four walls of orbit and the bones that construct the walls.

2. Describe blood supply of the eye

3. Describe about lacrimal apparatus components4. Describe about orbit muscles 5. Describe about layers of eyeball6. Describe about nerve supply of the eyes

SELF ASSESSMENT:1. Describe about the position of bones that construct the walls 2. Describe about the position of lacrimal apparatus

LEARNING RESOURSES:1. Moore.K.L, Agar A.M.R : Essensial Clinical Anatomy, Second Edition, Lippincott Williams & Wilkins. 1995, USA

Day 2HISTOLOGY OF THE EYE

dr. Ratnayanti

Abstract

Like any other senses, eye is our window to the external world. Eye captures image continuously and transmits it to the brain for next processing and understanding. The structure of the eye is perfectly designed to perform its course. The light reflected by object enters the eye through cornea and pupil. The amount of light permitted is regulated by iris by dilating or constricting the pupil. Then, the refractive structures, lens and vitreous body, directing the light to the retina where it translated to a signal the brain can understand and perceived as an image. The shape and structure of the other eye walls support the photoreceptor function of the eye. The rigid and opaque sclera protects the eye and maintains the spherical shape needed for precise image in the back of the eye. The uvea provides nutrition and its melanin blocks lights from other angles, thus, only light comes from cornea is received. The accessory structures of the eye also support and protect the



eye. It is consist of lacrimal gland, which produce tears; conjunctiva, covered the anterior part of the eye; and eye lids, the “on and off button” of the eye.

VignetteA 25 year old woman came to your private practice with a symptom of pink eye. She already had it since 2 days ago and it getting worse by now. It also followed by a yellowish secret which usually noticed when she got up from sleeping in the morning. She also felt pain and her eyes felt watery. From the examination you found redness in the white area of both eyes and also on the inside of the eyelids. Learning Task:

1. What histologic structure mainly affected in the case?2. Describe that histologic structure involve in the case above!

A 89 year old man came to a private practice due to dryness in the eye. He often felt itchy, gritty, and sometime burning. After the feeling he was tearing then when the tearing stopped he felt the symptoms again. It became worst if he read, watched television or went out especially in a windy day. He was in regular use of beta blocker because of heart problem. The doctor took Schimer’s test and found the result was minimal wetting of the paper.

Learning Task:1. What is the main structure disturbed in the case above?2. Describe about the structure, which layer is mainly affected in the case above?3. Describe all of the accessory structures that contributing in the formation of the

structure mentioned!

Self Assessment:1. Describe in detail about the accessory structure involve in the case above 2. Describe the accessory structures that contributing in the formation of tear film!3. Describe about the circulation and function of aqueous humor and tears!3. Describe about the refractive media of the eye:

1. Cornea2. Aqueous humor3. Lens4. Vitreous humor

4. Describe in detail about the histologic structure of the eye’s wall:1. Sclera2. Choroid3. Retina

5. Describe about the structure that holds the lens, including the choroid body!6. What fluid drains from the eye to the canal of Schlemm?7. What structures absorb the light that enters the eye?8. The area in the retina that contains no photoreceptor cells is called….9. What is the sclera made of?10. What cells in the conjunctiva which produce substance that constitute the tear film?

References: 1. Gartner, L. P. & Hiatt, J. L. 2011. Color Textbook of Histology. 3rd Ed. Philadelphia:

Saunders Elsevier. Pp. 514-526.2. Fawcett, D. W. & Jensh, R. P. 2002. Concise Histology. 2nd Ed. London: Arnold.

Pp.301-313.DAY 3

PHYSIOLOGY OF THE EYEBy Prof.dr.I Dewa Putu Sutjana, PFK,M.Erg



INTRODUCTIONThe human know the environment because they had special senses, such as visual

system, auditory, smell, taste, tactile which are call five senses. The visual system was control around 90% of the daily activity. The visual system detects and interprets light stimulations. The light stimulations are in form of electromagnetic waves of lengths between 400 to 700 nm, which make up visible light. The human can be known the environment because they had:

1. The optic system, for reflected the light enters the eye and focuses it on the retina

2. The retina as photoreceptors transducer light energy into an nerves impulses3. The optical neural, Neural pathways from the retina to the visual cortex at

occipital lob of brain.4. The visual cortex of the brain process nerve impulses into visual images.

I.OPTIC SYSTEM OF THE EYEThe optics system of the eye is equivalent to the usually photographic camera. It has

a lens system, aperture system (call pupil) and retina that correspond to the film. The lens system of the eye is composed of four refractive interfaces. If all the refractive surfaces of the eye are added together and considered to be one single lens known as reduced eye. In reduced eye total refractive power 59 diopters when the eye accommodated for distant vision.

FORMATION OF AN IMAGE ON THE RETINAThe light from the objects refracted and focused by the optics system of the eye on

the retina. The image is inverted and reversed with respect to the object. However, the mind perceives objects in the upright position.

PUPILLARY DIAMETERLike in the camera the eye had the pupil which is formed by the iris. The major function of the iris is to control the diameter of the pupil. The diameter of the pupil is control the amount of light enters the eye. The stimulation of the parasympathetic nerve increases the diameter of pupil. The change of pupil diameter followed the accommodation ACCOMODATION

The eye can be adjusted automatically the vision changes from the near to par objects, by changes the refractive power of the eye which is known as accommodation. In human eye the accommodation is due to change the refractive power of the lens (from 20 diopters to about 34 diopters), especially in children or the young person. The ability of eye accommodation (lens refractive power) is reduced with increased of age, and than followed by presbyopia. NORMAL VISION AND ERROR OF REFACTIONNormal vision known as an emmetropic eye, if parallel light rays from distant objects are in sharp focus on the retina, when ciliary muscle completely relaxed. If the parallel light rays are focus behind the retina is known as hyperopia, if parallel light rays focus in the front of retina known as myopia, but if the different of the curvature of the cornea is known as astigmatism. The correction of refractive error is use of lens, concave spherical lens for myopia, convex lens for hyperopia and cylindrical lens for astigmatism.

VISUAL ACUITYVisual acuity is the ability of the person to distinguished two bright pin point spots of

light 10 meters away can barely distinguished the spots as separate entities when they are 1.5 to 2 millimeters apart. Clinical method to tested the visual acuity use the Snellen’s chart,



consist of letter of different sizes placed 20 feet away from the person being tested, with the formula:

V = d/D V= visual acuity, d = distant of the person can read the letter, and D=distant of normal vision can read that letter.

FLUID SYSTEM OF THE EYEFor normal vision, the eye filled with intraocular fluid, which maintains sufficient

pressure in the eyeball to keep it distended. The fluid can be divided into two portions: aqueous humor, which lies in front of the lens and vitreous humor, which is between the posterior surface of the lens and the retina. The aqueous humor is a freely flowing fluid, whereas the vitreous humor sometimes called the vitreous body, is gelatinous mass. Both water and dissolved substances can diffuse slowly in the vitreous humor but there is little flow of fluid. Aqueous humor is continually being formed and reabsorbed. The balance between formation and reabsorption of aqueous humor regulates the total volume and pressure of intra ocular fluid.

RECEPTOR AND NEURAL FUNCTION OF THE RETINARetina is the light sensitive portion of the eye, contain 9 layers from outside to inside

as follows (1) pigmented layer, (2) layer of rods and cones, (3) outer nuclear layer, (4) outer plexiform layer, (5) inner nuclear layer, (6) inner plexiform layer, (7) ganglionic layer, (8) layer of optic nerve fiber, (9) inner limiting membrane. After the light passes through the lens system of the eye and then through the vitreous humor, it enters the retina from the inside layer and then finally reaches the layer of rods and cones. Cones located at the central fovea, a minute area in the center of retina occupying a total area around 1 square millimeter. The central fovea only 0.3 millimeters in diameter is composed almost entirely of cones. Outer of the center fovea located by rods.

PHOTORECEPTOR RHODOPSIN-RETINAL VISUAL CYCLEAND EXCITATION OF THE RODS

When light energy is absorbed by rhodopsin the rhodopsin begins to decompose within a very small fraction, cause photoactivation of electron, and then re-formation of rhodopsin again, which is call rhodopsin-retinal cycle. In that cycle vitamin A more important for normal vision, but if vitamin A is not enough, the night blindness occurs.

PHOTOCHEMISTRY OF COLOR VISION BY CONESPhoto chemicals in the cones have almost same to the rhodopsin at the rods. The

difference is the protein portions, call the opsins (photopsins). According to the Young-Helmholtz theory, there are three type of color pigment in the cones cells (blue, green, red): blue sensitive pigment, green sensitive pigment, and red sensitive pigment. So different cones (three type of cone) are sensitive to different colors of light.Color blindness. When a single group of color-receptive cones is missing from the eye, the person is unable to distinguish some colors from others, call color blindness. If the person loss of red cones it is called a protanope, if lacks of green called deuteranope. Red green color blindness is a genetic disorders, that at the female X chromosome. So that the color blindness almost in males.

NEURAL FUNCTION OF THE RETINANeural organization at the retina is more complex. The function of the neural

pathways is to transmit the neural impulse from the retina (rods and cone) through the optic nerve to the brain. It is different at the peripheral retina and in the center foveal retina. That is way the center foveal retina for detail and color vision LEARNING TASK

1. Describe the equivalent and the different optic system of the human eye to the photographic camera.



2. Describe the optic system of the eye3. Describe the different of emmetropia, hyperopia and myopia.4. What is accommodation, and in the human eyes which part of the optic system most

important.5. Describe the circulation of the eye fluid6. Describe the different of rods and cones in the vision perception7. Describe the rhodopsin-retinal cycle, during light exposure to the rod8. Describe the role of vitamin A in rhodopsin retinal cycle9. Describe the Young-Helmholtz theory of the color vision10. Describe many kind of color blindness

SELF ASSESSMENT1. Can you mention the part of optic system2. What is mean by presbyopia and why it is occur in the human?3. Can you explain the role of cilliary muscle during accommodation?4. Can you explain why color blindness almost occur in males.5. Can you explain the neural function of the retina6. Can you explain why the niktalopia person difficult to see in the afternoon but not

problem at the morning?

RESOURCES:1. Guyton, A. The Textbook of Medical Physiology2. Silverthorn, D.U. 2010. Human physiology. An Integrated Approach.Fifth Ed.

Pearson. San Fransisco.

DAY 4 GLAUCOMA

By Md Agus Kusumadjaja,MD, Ari Suryathi,MD

AIMS:Describe the signs, symptoms, patophysiology and inital management of glaucoma disorders

LEARNING OUTCOMES:Can describe the signs, symptoms, pathophysiology and inital management of:

1. Acute angle closure2. Primary Acute angle closure glaucoma3. Secondary glaucoma 4. Primary open angle glaucoma5. Congenital glaucoma

CURRICULUM CONTENT:1. Acute angle closure 2. Primary Acute angle closure glaucoma3. Secondary glaucoma due to lens opacity and trauma (hyphema)4. Primary open angle glaucoma5. Congenital glaucoma

ABSTRACT / SUMMARY



Glaucoma is a group of eye disorders characterized by progressive optic nerve damage causing typical visual field defects, and increase of intraocular pressure (IOP) as one of risk factors. Glaucoma can be classified into primary, secondary, congenital and absolute glaucoma. Glaucoma also can de differentiated into acute and chronic glaucoma based on their onset. Visual acuity examination, IOP measurement, Gonioscopy, Ophthalmoscopy and Visual field examination are required to establish glaucoma diagnosis. Primary acute angle closure glaucoma (PACG) occurs when sufficient iris bombe develops to cause occlusion of the anterior chamber angle by the peripheral iris. This blocks aqueous outflow and the intraocular pressure rises rapidly, causing severe pain, redness, and blurring of vision. Angle closure is likely to develop only in eyes with preexisting anatomic narrowing of the anterior chamber angle usually when it is exacerbated by enlargement of the crystalline lens associated with aging. The acute attack is often precipitated by papillary dilatation. This occurs spontaneously in the evenings when the level of illumination is reduced.

Primary open angle glaucoma (POAG) / chronic glaucoma is the most common form in blacks and whites. The chief pathologic feature of POAG is a degenerative process in the trabecular meshwork, including deposition of extra cellular material within the meshwork and beneath the endothelial lining of Schlemm’s canal. The consequence is a reduction in adequate drainage leading to a rise in intraocular pressure. The major problem in detection of (POAG) is the absent of symptoms until relatively late in the disease.

SELF DIRECTING LEARNING (In depth learning of above lecture)1. Basic knowledge of aquous humor production and outflow2. Mechanism of primary and secondary acute angle closure3. Signs, symptoms and diagnosis of acute angle closure and acute angle closure

glaucoma4. Initial management of acute angle closure angle and acute angle closure

glaucoma5. Mechanism of primary and secondary open angle glaucoma6. Signs, symptoms and diagnosis of open angle glaucoma7. Initial management of open angle glaucoma8. Mechanism of congenital glaucoma9. Signs, symptoms and diagnosis of congenital glaucoma

SCENARIOCase 1.

A woman, 45 yo complained her eye suddenly painful, nausea and vomiting when she worked in her office. On the examination doctors found there is visual acuity decreasing and hyperemia of conjunctiva and pericorneal, corneal edema, and high intra ocular pressure.

1. Mention things you should elaborate from the patient during anamnesis2. Mention physical examination you should do to this patient3. Explain about the result from the examination4. Mention differential diagnosis of the case5. Which diagnosis is the most appropriate?6. Explain about the initial management of this case

Case 2.A man, 65 yo complained about blur vision and narrowing visual field since three months ago. There was no redness and pain on his eye, but the blur vision getting worse every time.

1. Mention thing you should elaborate from the patient during anamnesis2. Mention physical examination you should do to this patient3. Explain about the result from the examination 4. Mention differential diagnosis of the case



5. Which diagnosis is the most appropriate?6. Explain about the management of this case.

Case 3.A man 65 years old complained about blur vision since six months ago and the blur vision getting worse every time. Ophthalmology examination found increasing intra ocular pressure on right eye, decreasing visual acuity both eye caused by lens opacity. There was no redness and pain on his eye.

1. Mention thing you should elaborate from the patient during anamnesis2. Mention physical examination you should do to this patient3. Explain about the result from the examination 4. Mention differential diagnosis of the case5. Which diagnosis is the most appropriate? 6. Explain about the management of this case.7. What is the suggestion for the patient?

SELF ASSESSMENT:

1. Describe definition of acute glaucoma & chronic glaucoma.2. Explain about pathogenesis of acute glaucoma & chronic glaucoma.3. Mention classification of glaucoma based on onset and pathogenesis.4. Mention symptoms could be found in acute glaucoma & chronic glaucoma.5. Mention the examination needed to make diagnosis of acute glaucoma & chronic

glaucoma.6. Explain how you can establish diagnosis of acute glaucoma & chronic glaucoma.7. What should you do if you have a patient with acute glaucoma & chronic glaucoma?8. Mention what you should tell to the patient who has history of acute glaucoma &

chronic glaucoma.9. Mention about the pathogenesis, signs and symptoms of congenital glaucoma

LEARNING RESOURCES:

1. Vaughan: General Ophthalmology2. Ilyas S: Ilmu Penyakit Mata. FK UI3. Deborah PL: Manual Diagnostic &Ocular Treatment.4. PERDAMI: Panduan Ketrampiilan dan Klinis Penyakit Mata, Jakarta, 2006

DAY 5 RECONSTRUCTION, OCULOPLASTY & ONCOLOGY

By Sukartini AAA D, Laksmi Utari, MD

AIMS:Describe the sign, symptoms, pathophysiology and management of reconstruction, oculoplasty & oncology cases

LEARNING OUTCOMES:Can Describe the signs, symptoms, pathophysiology and management of:

1. Eyelid and lacrimal laceration2. Entropion3. Trichiasis4. Epicanthus5. Ptosis



6. Dacryoadenitis7. Dacryocystitis

CURRICULUM CONTENTS:1. Ocular injury

a. Sharp injury (Laceration of the eyelid & Lacrimal system)b. Blunt injury (Sub Conjunctiva Bleeding & Hypema)

2. Eyelid disorders3. Lacrimal system disorders

ABSTRACT / SUMMARY OF LECTURE:Ocular injury is most often found in cases of reconstruction and oculoplastic division.

There are two mechanisms that cause injury to the eye, which is due to sharp and blunt object. Both of them can cause damage to all orbital tissue. Eyelid and lacrimal apparatus most frequently injured. Laceration of the eyelid and lacrimal system need special management. The wound should be cleaned thoroughly and given antibiotics. Laceration must be repaired carefully to maintain its contour and prevent any complication such as epiphora, trichiasis, entropion or ectropion, lagophthalmos and ptosis.

Entropion is turning inward of the eyelid, and may be involutional (spastic, senile), cicatrical, or congenital. The most common entropion is involutional which occurs as a result of aging.

Ectropion (sagging and eversion of the lower eyelid) is usually bilateral and is frequent findings in older persons. It may be caused by relaxation of orbicularis oculi muscle, either as part of the aging process or following seventh nerve palsy. The symptoms are tearing and irritation, and exposure keratitis may occur.

Trichiasis is impingement of eyelashes on the cornea and may be due to entropion, epibhlepharon, or simply misdirected growth. It causes corneal irritation and encourages ulceration.

Epichantus characterized by vertical folds of skin over the medial canthi. It is typical of Asian and is present to some degree in most children of all races. The skinfolds is often too large to cover the part of nasal sclera and cause “pseudoesotropia”.

Normally, the upper eyelid rests approximately midway between the superior limbus and the pupillary margin. Ptosis or bhlepharoptosis is the condition in which one or both upper eyelids assume an abnormally low position. Ptosis may be congenital or acquired and can be hereditary in either case.

Excessive tearing (epiphora) is occasionally due to canalicular stenosis or obstruction of the common canaliculus and lacrimal sac. Most cases of the stenosis are acquired, due to the result of viral infections.

Dacryoadenitis is the inflammation of lacrimal gland, which can be acute or chronic inflammation. It is a rare condition, which is most often seen in children as a complication of mumps, measles, or influenza and in adults in association with gonorrhea.

Dacryocystitis is the infection of the lacrimal sac. It is moft often unilateral and always secondary to obstruction of nasolacrimal duct. Usually occurs in infants or postmenopausal women.

SELF DIRECTING LEARNING (In depth learning of above lecture) 1. Anatomy of eyelid and lacrimal system (punctum, canaliculi, lacrimal sac and duct)2. Physiology of lacrimal system3. Patophysiology of sharp and blunt injury4. Sign & symptom of eyelid disorders5. Sign & symptom of lachrymal apparatus disorders

SCENARIO:



1. A woman 30 years old came to the eye clinic with chief complained left eye bleeding after felt down in the bathroom since 5 hours ago. Ophthalmology examination on left eye found there are eyelid ruptures. The visual acuity both eyes were good. According case above:a. Describe things you should elaborate from the patient to make diagnosis?b. Explain about diagnosis of the patient!c. What is the first aid for this case?d. What we should do after the first aid?

2. A woman 16 years old came to the eye clinic with chief complained redness and watery on her right eye since 2 weeks ago. Ophthalmology examination on right eye found on her inferior eyelid there are eyelashes touching her cornea, with conjunctival hyperemia The visual acuity both eyes still good. According case above:a. Describe things you should elaborate from the patient to make diagnosis?b. Explain about diagnosis of the patient!c. What we should do for this patient?

3. A man 45 years old came to the eye clinic with chief complained swollen and pain on his left eye since 2 weeks ago. He also mention that his left eye always watery since 2 months ago after he had an accident and trauma on his face. Ophthalmology examination on left eye found there are redness and swollen on his inferior left eyelid. The visual acuity both eyes were good. According case above:a. Describe things you should elaborate from the patient to make diagnosis?b. Explain about diagnosis of the patient!c. What is the management for this patient?

SELF ASSESMENT:1. Explain about lacrimal system (tear outflow)2. Explain about sign & symptoms of dacryoadenitis3. Explain about sign & symptoms of dacryocystitis

LEARNING RESOURCES:1. Vaughan: General Ophthalmology2. Ilyas S: Ilmu Penyakit Mata. FK UI3. Deborah PL: Manual Diagnostic &Ocular Treatment.4. PERDAMI: Panduan Ketrampiilan dan Klinis Penyakit

DAY 6 INFECTION AND IMMUNOLOGIC EYE DISEASE

By N.K. Niti S,MD/IGAM Juliari, MD

AIMS:Describe the Signs, Symptom, Patophysiology and management of CONJUNCTIVITIS INFECTION AND IMMUNOLOGIC IN CORNEA, CILLIARY BODY, AND ANTERIOR CHAMBER , HORDEOLUM AND CALAZION, SCLERITIS AND EPISCLERITIS, DRY EYE DISORDERS.

LEARNING OUTCOMES:Can describe the Signs, Symptoms, Patophysiology and Management of:1. Keratitis



2. Xeropthalmia3. Anterior Uveitis (Iritis & Iridosiklitis)4. Hipopion 5. Conjunctivitis 6. Hordeolum and Chalazion7. Scleritis and Episcleritis8. Dry eye disorders

SELF DIRECTING LEARNING ( in depth learning of above lecture)

1. Keratitis a. Pathogenesis of keratitisb. Definition of keratitisc. Aetiology of keratitisd. Signs and symptoms of keratitise. Diagnosis of keratitisf. Prognosis of keratitis g. Management of keratitish. Different diagnosis of keratitisi. Prognosis of kearatitisj. Complication of keratitis

2. Xeropthalmia a. Pathogenesis of xeropthalmiab. Definition of xeropthalmiac. Aetiology of xeropthalmiad. Signs and symptoms of xeropthalmiae. Diagnosis of xeropthalmiaf. Prognosis of xeropthalmiag. Management of xeropthalmiah. Different diagnosis of xeropthalmia

3. Uveitis anteriora. Pathogenesis of uveitis anteriorb. Definition of iritis and iridocyclitisc. Aetiology of iritis and iridocyclitisd. Signs and symptoms of iritis and iridocyclitise. Diagnosis of iritis and iridocyclitis f. Prognosis of iritis and iridocyclitis g. Management of iritis and iridocyclitish. Different diagnosis of iritis and iridocyclitisi. Prognosis of iritis and iridocyclitis j. Complication of iritis and iridocyclitis

4. Hypopiona. Physiology of hypopionb. Pathogenesis of hypopionc. Definition of hypopiond. Aetiology of hypopione. Signs and symptoms of hypopionf. Diagnosis of hypopion



g. Prognosis of dry eye h. Management of dry eye i. Different diagnosis of dry eye j. Prognosis of dry eye k. Complication of dry eye

1. Conjunctivitis a. Pathogenesis of conjunctivitis (Allergy, viral, bacterial)b. Definition of conjunctivitisc. Aetiology of conjunctivitisd. Signs and symptoms of conjunctivtse. Diagnosis of conjunctivitisf. Management of conjunctivitisg. Prognosis of conjunctivitish. Differential diagnosis conjunctivitis due to aetiologyi. Complication of conjunctivitis

2. Hordeolum

a. Pathogenesis of hordeolumb. Definition of external and internal hordeolumc. Aetiology of external and internal hordeolumd. Signs and symptoms of external and internal hordeolume. Diagnosis of external and internal hordeolumf. Management of external and internal hordeolumg. Complication of external and internal hordeolum

3. Chalaziona. Pathogenesis of chalazionb. Definition of chalazionc. Aetiology of chalaziond. Signs and symptoms of chalazione. Diagnosis of chalazionf. Management of chalaziong. Complication of chalazion

4. Scleritis a. Pathogenesis of infection scleritis non infection scleritisb. Definition of infection or non infection scleritisc. Aetiology of infection or non infection scleritisd. Signs and symptoms of infection or non infection scleritise. Diagnosis of infection or non infection scleritisf. Prognosis of infection or non infection scleritis g. Management of infection or non infection scleritish. Different diagnosis of infection or non infection scleritisi. Complication of scleritis

5. Episcleritis Pathogenesis of episcleritisDefinition of episcleritisAetiology of episcleritisSigns and symptoms of episcleritis



Diagnosis of episcleritisPrognosis of episcleritis Management of episcleritisDifferent diagnosis of episcleritis

6. Dry eye disordersPhysiology of tear filmPathogenesis of dry eye syndromeDefinition of dry eye Aetiology of dry eye Signs and symptoms of dry eye Diagnosis of dry eye Prognosis of dry eye Management of dry eye Different diagnosis of dry eye Prognosis of dry eye Complication of dry eye

ABSTRACT / SUMMARY

The external eye is the most crucial part of the body exposed to outside word. The normal structure and function of the healthy eye rely on homeostasis of the entire body for protection against an adverse environment. Genetic and nutrition determine the embryogenesis and growth of the eye. Intact vascular and nervous systems stable metabolism, and immune system maintains surveillance.

The cushioning effect of the periocular tissues and local barriers such as the orbital rim are needed to safeguard the globe. The eyebrows and eyelashes catch small particles, and cilia also work as sensors to stimulate reflex eyelid closure. Blinking augments the lacrimal pump to rinse tears over the eye and flush off foreign material. The tear film also dilute toxins and allergens and contains proteins that control the normal flora. Mucin stabilizes that tear film and demarcates the living cells of the ocular surface from surrounding environment.

The epidermis and epithelium of healthy eyelids, conjunctiva, and cornea adhere tightly to their basement membranes. Regulation of cellular growth and metabolism are critical to maintenance of an intact ocular surface and transparent cornea. The underlying extracellular matrix of the eye's mucous membrane is rich in blood vessels and conjunctiva-associated lymphoid tissue (CALT). The anterior segment of the eye provides a clear, protected entrance for light that is to be processed by the visual pathways through the central nervous system.

Understanding the eye's innate defenses requires study of ocular histology and biochemistry and observation of many people, both healthy and ill. The practice of corneal and external eye disease builds on this understanding and extends from clinical examination to clinic-pathologic problem solving, molecular medicine, and microsurgery. The student should become familiar with ocular embryology, anatomy, physiology and biochemistry, ocular immunology, and ophthalmic pathology.

Although the protections of the eye are very strong but the eye still can also be infected by bacteria, virus, fungi, and parasites.

A detailed history and physical examination are essential to proper diagnosis of external eye infections or inflammatory etiology. The patient's chief complaint and a complete systemic and ocular history, including the presence of risk factors for infections of the external eye, should be noted. A complete eye examination should included special attention to skin of the face and eyelids, the preauricular lymph node, the globe-orbit relationship, ocular discharge, and conjunctiva and corneal morphology. Diagnostic tests are chose to differentiate between likely diagnostic entities and to assist in therapy. (eg. Antimicrobial sensitivity testing in microbial keratitis.)



1. KeratitisKeratitis is an inflammation of cornea. The specific symptoms are pain and photophobia. Examination is often fascilitated by instillation of a local anesthetic. Fluorescein staining can outline a superficial epithelial lesion that might otherwise be impossible to see. A patient's history is important in corneal disease. A history of trauma, corneal disease, and local medications should be investigated.

2. XeropthalmiaXeropthalmia is a medical condition in which the aye fail to produce tears. It may caused by vitamin A deficiency, which is sometime used to describe that condition, although there may be other causes. Xeropthalmia caused by a severe vitamin A deficiency is described by pathologic dryness of the conjunctiva and cornea. The conjunctiva becomes dry, thick and wrinkled. If untreated, it can lead to corneal ulceration and ultimately to blindness as a result of corneal damage.

3. Anterior Uveitis (Iritis & Iridocyclitis)Anterior uveitis is most common and is usually unilateral and acute in onset. Typical symptoms include pain, photophobia, and blurred vision. Examination usually revealed circumcorneal redness with minimal palpebral conjunctival injection or discharge. The pupil may be miosis or irregular due to the formation of posterior synechiae. Inflammation limited to the anterior chamber is called "iritis"; inflammation involving both anterior chamber and the anterior vitreous is called "iridocyclitis". 4. HypopionHypopion is a medical condition invoving inflammatory cells in the anterior chamber of the eye. It is a leukocytic exudate, seen in the anterior chamber, usually accompanied by redness of the conjunctiva and the underlying episclera. It is a sign of inflammation of the anterior uvea and iris, i.e. iritis, which is a form of anterior uveitis. The exudate settles at the dependent aspect of the eye due to gravity. It can be sterile (in bacterial corneal ulcer) or not sterile (fungal corneal ulcer).

5. ConjunctivitisConjunctivitis is inflammation of the conjunctiva. It is the most common eye disease worldwide. There were several causes of conjunctivitis, such as bacterial, chlamydial, viral, rickettsial, fungal, parasitic, immunologic (allergic), chemical (irritative), systemic disease, secondary to dacryocystitis or canaliculitis, or unknown etiology. The important symptoms of conjunctivitis are foreign body sensation, a scratching or burning sensation, a sensation of fullness around the eye, itching, and photofobia. The signs of conjunctivitis are hyperemia conjunctiva, tearing, exudation, pseudoptosis, papillary hypertrophy, chemosis, follicles, pseudomembranes and membranes. Specific therapy for conjunctivitis depends on the causes.

The specific symptoms are pain and photophobia. Examination is often fascilitated by instillation of a local anesthetic. Fluorescein staining can outline a superficial epithelial lesion that might otherwise be impossible to see. A patient's history is important in corneal disease. A history of trauma, corneal disease, and local medications should be investigated.

6. Hordeolum and ChalaziaHordeolum is infection of the glands of the eyelid. It could involve meibomian gland (internal hordeolum) or Zeis's or Moll's glands (external hordeolum or stye). Pain, redness, and swelling are the principal symptoms. Most hordeola are caused by staphylococcal infections, usually Staphylococcal aureus. Treatment consists of warm compresses three or four times a day for 10-15 minutes, antibiotic ointment applied to the conjunctival sac every



3 hours. If the process does not begin to resolve within 48 hours, incision and drainage is indicated. A chalazion is an idiopathic sterile chronic granulomatous inflammation of a meibomian gland, usually characterized by painless localized swelling. Surgical excision is performed via a vertical incision into the tarsal gland from the conjunctival surface followed by curettement. Intralesional steroid injection maybe usefull for small lesions.

7. Scleritis & EpiscleritisEpiscleritis is a relatively common localized inflammation of the vascularized connective tissue overlying the sclera. It tends to affect young people, third or fourth decade, affects woman three times as frequently as men. Symptoms of episcleritis include redness and mild irritation or discomfort. The condition is benign, and the course is generally self-limited in 1-2 weeks. Others therapy was needed in special causes. Scleritis is an uncommon disorder characterized by cellular infiltration, destruction of collagen, and vascular remodeling. These changes may be immunologically mediated or less commonly, the result of infection. Laboratory studies are often helpful in identifying associated systemic disease. There were 2 types of scleritis, anterior and posterior. Initial treatment of scleritis is with systemic nonsteroidal anti-inflammatory agents. If there is no response in 1-2 weeks, or if vascular closure becomes apparent, oral prednisone, 0.5-1.5 mg/kg/d, should be started.8. Dry Eye Syndrome Dryness of the eye may result from any disease associated with deficiency of the tear film components (aqueous, mucin, or lipid), lid surface abnormalities, or epithelial abnormalities. Patients with dry eyes complain most frequently of a scratchy or sandy (foreign body) sensation. Other common symptoms are itching, excessive mucus secretion, inability to produce tears, a burning sensation, photosensitivity, redness, pain, and difficulty in moving the eyelid. The most characteristic feature on slitlamp examination is the interrupted or absent tear meniscus at the lower lid margin. Tenacious yellowish mucus strands are sometimes seen in the lower conjunctival fornix. The bulbar conjunctival loses its normal luster and may be thickened, edematous, and hyperemic. Diagnosis and grading of the dry eye conditions can be achieved with good accuracy using the following diagnostic methods, such as schirmer test, tear film break-up time, ocular ferning test, impression cytology, fluorescein staining, rose Bengal staining, tear lysozyme assay, tear osmolality, and lactoferrin. The treatment is according to the gradation of the dry eye.

SCENARIO

1. A 35-year-old complained of pain in his left eye for several days, watery discharge, and blurred vision. He thinks he has the same symptoms before. He admits to stress on the job as well as a recent cold sore.a. What is the diagnosis?b. What are you looking for on fluorescein staining?c. What are the signs of the herpes simplex keratitis?d. What is the complication of herpes simplex keratitis?e. How should the patient be treated?

2. A 30-year-old man presents with severe phtophobia, pain, tearing, and decreased vision in his right eye for two days. This condition has occurred several times before. He says that it was better by using drops. On exam, his vision 20/50 in the right eye and 20/20 in the left eye. His pupil is poorly reactive on the right and miotic. The right eye is diffuse injected, especially the limbus. The anterior chamber is deep, but cell and flare are present with few fine keratic-precipitates.

a. What is the diagnosis?b. What is the etiology of anterior uveitis?



c. What are differences between nongranulomatous anterior uveitis and granulomatous anterior uveitis?

d. What is the complication of anterior uveitis?e. How should the patient be treated?

3. A 27-year-old man present with foreign-body sensation and photophobia in both eyes after sleeping with soft contact lenses during his call night.

a. What is the diagnosis?b. What is the etiology?c. What is the complication that could be happened?d. How should the patient be treated?

4. A 67 -year-old man has red eye on both eye since 1 week. No pain, no blur vision. There is a yellow secrets on both eyes, provious. His palpebral were swelling and difficult to open. History of medication on the eye was positive, but he didn’t remember the brand. History of traditional medicine was positive, he used urine for wash his eye

a. What is the diagnosis of this case?b. Mention about the type of conjunctivitisc. What is the etiology of this case?d. What are differences between bacterial and viral conjunctivitis?e. How to manage the bacterial conjunctivitis?

5. A 79-year-old woman complains of red eyes that constantly tear and burn. She also feels foreign-body sensation and reports that her vision is not clear as before. The vision varies with tear blink. She has noticed this condition over past several years. On exam find a poor tear film filled with debris.

What is the diagnosis?What is the definition of dry eye?What are the components of the tear film?What are the most common signs of dry eye?What are the treatments for dry eye patients?

SELF ASSESMENTS1. Mention and explain about types of keratitis2. Mention and explain about types of xeropthalmia3. Mention about symptom and sign of anterior uveitis4. Mention about hypopion 5. Mention and explain about types of conjunctivitis6. Mention about tear film components and dry eye examination

LEARNING RESOURCES:1. Vaughan: General Ophthalmology2. Ilyas S: Ilmu Penyakit Mata. FK UI3. Deborah PL: Manual Diagnostic &Ocular Treatment.4. PERDAMI: Panduan Ketrampiilan dan Klinis Penyakit Mata, Jakarta, 2006

DAY 7PHYSIOLOGY OF THE EYE – Visual Pathways



dr. I Made Krisna Dinata, M.Erg

AbstractThe Visual Pathways

The visualnerve signals leave the retinas through the opticnerves. At the optic chiasm, the optic nerve fibersfrom the nasal halves of the retinas cross to theopposite sides, where they join the fibers from theopposite temporal retinas to form the optic tracts. The fibers of each optic tractthen synapse in the dorsal lateral geniculate nucleus of the thalamus, and fromthere, geniculocalcarine fibers pass by way of the optic radiation (also called thegeniculocalcarine tract) to the primary visual cortex in the calcarine fissure areaof the medial occipital lobe. Visual fibers also pass to several older areas of the brain:

1. From the optic tracts to the suprachiasmatic nucleus of the hypothalamus, presumably tocontrol circadian rhythms that synchronize various physiologic changes of the body with night and day

2. Into the pretectal nuclei in the midbrain, to elicit reflex movements of the eyes to focus on objects of importance and to activate the pupillary light reflex

3. Into the superior colliculus, to control rapid directional movements of the two eyes 4. Into the ventral lateral geniculate nucleus of the thalamus and surrounding basal

regions of the brain, presumably to help control some of the body’s behavioral functions.

The visual pathways can be divided roughly into an old systemto the midbrain and base of the forebrain and a new system for direct transmissionof visual signals into the visual cortex located in the occipital lobes. Inhuman beings, the new system is responsible for perception of virtually allaspects of visual form, colors, and other conscious vision.

Function of the Dorsal Lateral Geniculate Nucleusof the ThalamusThe optic nerve fibers of the new visual system terminate in the dorsal

lateralgeniculate nucleus, located at the dorsal end of the thalamus and also calledsimply the lateral geniculate body, as shown in Figure 51–1. The dorsal lateralgeniculate nucleus serves two principal functions: First, it relays visual informationfrom the optic tract to the visual cortex by way of the optic radiation(also called the geniculocalcarine tract). This relay function is so accurate thatthere is exact point-to-point transmission with a high degree of spatial fidelityall the way from the retina to the visual cortex.

Visual FieldThe field of vision is the visual area seen by an eye at agiven instant. The area seen

to the nasal side is calledthe nasal field of vision, and the area seen to the lateralside is called the temporal field of vision.Each called monocular visual field . The area which are seen by two eyes is called binocular visual field

Fusion of the Visual Images From the Two EyeTo make the visual perceptions more meaningful, thevisual images in the two eyes

normally fuse with eachother on “corresponding points” of the two retinas.The visual cortex plays an important role in fusion. Itwas pointed out earlier in the chapter that correspondingpoints of the two retinas transmit visual signals todifferent neuronal layers of the lateral geniculatebody, and these signals in turn are relayed to parallelneurons in the visual cortex. Interactions occurbetween these cortical neurons to cause interferenceexcitation in specific neurons when the two visualimages are not “in register”—that is, are not precisely“fused.”

Case



A woman, 65 yo, came to physician with complainthat hervisual doesn’t work properly. The examination found that she had bipolar hemianopia.

Learning Task1. Which area in visual pathways had been damage in that patient?2. Describe the transmit of visual impulse from retina to the brain3. What is called the monocular and binocular visual field4. Differentiate the nasal and temporal visual field, and what tool for evaluation of the

visual field5. Describe how the visual image can be fusion

Self Assessment1. Explain the different of visual field from left and right visual field2. What is called the monocular and binocular visual field3. Discribe the neural pathways to control pupillary light reflex4. Describe the neural pathways to the optic nerve to form the consensual reflex

Refferences1. Medical Physiology eleventh edition, Guyton & Hall.2. Physiology fifth edition, Linda S. Costanzo.3. Silvertharn, D.U. 2010. Human Physiology. An Integrated Approach. Fifth Ed.

Pearson. San Fransisco

DAY 7OCULAR PHARMACOLOGY

By Dr. dr. I Made Jawi, M.Kes

Abstract

Various pharmacologic agents are used for the treatment of eye disorders. The major challenge faced by today’s pharmacologist and formulation scientist is ocular drug delivery. Topical eye drop is the most convenient and patient compliant route of drug administration, especially for the treatment of anterior segment diseases. Delivery of drugs to the targeted ocular tissues is restricted by various precorneal, dynamic and static ocular barriers. Also, therapeutic drug levels are not maintained for longer duration in target tissues. In the past two decades, ocular drug delivery research acceleratedly advanced towards developing a novel, safe and patient compliant formulation and drug delivery devices/techniques, which may surpass these barriers and maintain drug levels in tissues. Anterior segment drug delivery advances are witnessed by modulation of conventional topical solutions with permeation and viscosity enhancers. Also, it includes development of conventional topical formulations such as suspensions, emulsions and ointments. Various nanoformulations have also been introduced for anterior segment ocular drug delivery. On the other hand, for posterior ocular delivery, research has been immensely focused towards development of drug releasing devices and nanoformulations for treating chronic vitreoretinal diseases. These novel devices and/or formulations may help to surpass ocular barriers and associated side effects with conventional topical drops. Also, these novel devices and/or formulations are easy to formulate, no/negligibly irritating, possess high precorneal residence time, sustain the drug release, and enhance ocular bioavailability of therapeutics. An update of current research advancement in ocular drug delivery necessitates and helps drug delivery scientists to modulate their think process and develop novel and safe drug delivery strategies. Systemic administration of a drug to treat eye disease would require a high concentration of circulating drug in the plasma to achieve therapeutic quantities in the aqueous humours, with the increased risk of side effect. Three



important factors have to be considered when attempting drug delivery to the eye: (1) how the blood-eye barrier (systemic to ocular) or cornea (external to ocular) is crossed to reach the site of action; (2) how to localize the pharmacodynamic action at the eye and minimize drug action on other tissues; (3) how to prolong the duration of drug action so that the frequency of drug administration can be reduced. Many of the pharmacological agents commonly used for the treatment of eye disorders have been discussed in other blocks, such as anti bacterial, anti viral, anti allergy and anti inflammation agents. A number of antibacterial antibiotics have been formulated for topical ocular use. Natamycin is the only ophthalmic antifungal in use. Autonomic agents have several uses in ophthalmology, including diagnostic evaluation of anisocoria, as adjunctive therapy in laser and incisional surgeries, and in the treatment of glaucoma. Glaucoma is a condition of the eye in which there is an increase in the intraocular pressure (IOP), causing progressive atrophy of the optic nerve with deterioration of vision. Drugs reduce IOP either by increasing outflow of aqueous humour, by decreasing aqueous production (beta-adrenergic blocking drugs, alpha-adrenergic agonists, and carbonic anhydrase inhibitors), or transiently reducing the volume of intraocular fluids (osmotic agents).

SELF-DIRECTED LEARNING1. Basic principles of drug that affect outonomic nervus system 2. Pharmacokinetic and pharmacodynamic of some drugs that use in visual system3. Important side effects of drugs that use in visual system4. Important drug for glaucoma treatment, cycloplegic and antibiotic.

SCENARIO

VignetteNyoman Dewi,70 y.o, is diagnosed by an ophthalmologist as having glaucoma. Your initial assessment reveals that she has high blood pressure and appears to have difficulty in following instructions. Please discuss the following issues.

Learning Tasks1. Which anti-glaucoma will you give to the patient according to the patient condition?

Explain your answer.2. What is the mechanism of action on the muscle of the iris and cilia?3. What receptor mediates the action?4. List parts of the eyes that are innervated by the autonomic nervous system and

explain the effects of sympathetic and parasympathetic drugs to those parts. 5. List the drugs that can be used to treat glaucoma and explain their mechanism of

action to reduce the intraocular pressure6. Please explain, why topical application sometimes has systemic effect?7. List the important side effects of anti-glaucoma agents.8. Which drug can produce cycloplegia? Explain the mechanism of action of this drug.9. Please compare the advantages and disadvantages between eye drops and eye

ointments.

Self Assessments1. Please explain the factors that determine the rate and the extent of absorption of the

drug after topical application to the eye.2. Please explain the possible absorption pathways of an ophthalmic drug following

topical application to the eye. Which routes are desired to localize ocular drug effects?

3. Please explain, why topical eye medication can cause systemic side effects?4. Please explain how to apply eye drop to the eye to get optimal effect.5. Please explain the characteristics of cholinoceptors in the peripheral nervous

system.



6. Please explain the characteristic of adrenoceptors in the ANS.7. Please explain the effects of sympathetic and parasympathetic drugs on the eye.8. Please list some drugs used in glaucoma and explain their mechanisms of action.9. Please list important side effects of drugs used in glaucoma.10. Please list some drugs used in ophthalmology diagnostic.

RESOURCESStandard textbook

1. Trevor AJ, Katzung BG, and Masters SB. Katzung & Trevor’s Pharmacology Examination & Board Review. Seventh Ed. Singapore: McGraw Hill 2005.

Additional Readings1. Moroi SE, Lichter PR. Ocular Pharmacology in Goodman & Gillman’s: The

Pharmacology Basis of Therapeutics. 10th Ed. New York: McGraw Hill. 2001.

DAY 8REFRACTION DISORDERS

By Eka Sutyawan,MD

AIMS:Describe the Signs, Symptoms, Patophysiology and Management of refractive errors

LEARNING OUTCOMES:Can describe the Signs, Symptoms, Patophysiology and Management of:

1. Myopia2. Hyperopia3. Astigmatism4. Presbyopia5. Anisometropia6. Buta Senja

CURRICULUM CONTENTS1. Optics and Refraction2. Refraction examination3. Emetropia and Ametropia / Refractive Errors

ABSTRACT / SUMMARY OF LECTUREThe eye change refractive power to focus on near object by a process call it

accommodation. Emetropia is absence of refractive errors and ammetropia is the present of refractive errors.

Light rays are focused on the retina to create sharp image. The light has to pass trough refractive media of the eye such as cornea, lens and vitreous body to reach retina. Some equipment are needed to examine refraction as follows Snellen chart, Trial lenses, trial frame, pupil distance ruler, lensometer, astigmatism chart, streak retinoscopy and autorefractor. The technique used in subjective refraction is trial and errors technique, while Astigmatic Clock Dial technique and Jackson Cross Cylinder technique were used to find astigmatism of the patient. Emmetropia is term used for eye with parallel light from distant object focused on retisna without accommodation of the eye. Ametropia is condition where parallel light is not focused on retina without eye accommodation. Classification of ammetropia is myopia, hypermetropia and astigmatism.

Miopia is a refractive error in which focus for light rays from a distant object is anterior to the retina. Hypermetropia is a refractive error in which the focus of light rays from a distant object is behind the retina. Astigmatism is a refractive error that prevents the



light rays from coming to a point focus on the retina because of different degrees of refraction in the various meridians of the cornea or crystalline lens. Presbyopia (“old sight”) is a physiologically blurred near vision, commonly evident soon after age 40, due to reduction in the power of accommodation.

The management of refractive errors could be glasses, contact lens and refractive surgery. Contact lens could be used to treat refractive errors, theraphy for some ocular pathologies as well as cosmetic or prosthetic use. Some complication could be developed regarding the inappropriate handle and use of contact lens, such as allergic, Keratitis and corneal ulcer.

SELF DIRECTING LEARNING (in depth learning of above lecture)1. Physiology of Optics and refraction2. Definition of Emetropia and Ametropia 3. Refraction examination4. Refractive error: Myopia5. Refractive Error: Hyperopia6. Refractive Error: Astigmatism7. Refractive Error: Presbyopia8. Anisometropia9. Managements of refractive errors10. Benefits and complications of Contact lens use

SCENARIO

1. A 8 years old boy complain about intermittent blurred vision and headache at the frontal region. Everyday, the patient spent his time in front of his gadget all day. From physical examination found that he able to read all the letters from the Snellen chart. After given mydriatic drops and done the refraction, he can read all the letters with correction of S+2.00 D in both eyes. a. What is the diagnosis of this case?b. Mention about the types of hypermetropia based on the accomodationc. What kind of glasses should be prescripse for hypermetropia patientd. What are the complications of hypermetropia and how it can happened?e. What is the differences between hypermetropia and presbyopia

2. A 25 years old woman complained of blurred vision and headache especially in frontal region. From the examination there are C-1.50 A 180° found in the right eyes and S-2.00 C-0.50 A0° in the left eye.

a. What is the diagnosis of the both eye?b. Mention about the types of regular astigmatismc. Mention about the symptoms of astigmatism

3. A 30 years old man come to the ophthalmologist and has checked his visual acuity. From the right eye there is S-6.00 and his BCVA is 6/10 and from his left eye there is 6/6 with S-0.50

a. What is the diagnosis of this patient?b. What is the complication of myopia?c. What happen if the patient is given maximum correction of glasses?d. So what is the best treatment in this case to make better visual acuity and

avoid the complication?

SELF ASSESSMENTS



1. Mentions and explain about types of myopia2. Methods of objective refraction:

a. Trial and errors techniquesb. Streak retinoscopyc. Astigmatic clock diald. Fogging techniquee. Jackson cross cylinder

LEARNING RESOURSES:1. Vaughan: General Ophthalmology2. Ilyas S: Ilmu Penyakit Mata. FK UI3. Deborah PL: Manual Diagnostic &Ocular Treatmentt.4. PERDAMI: Panduan Ketrampiilan dan Klinis Penyakit Mata, Jakarta, 2007

DAY 10CORNEA LENS PROBLEM

By IWG Jayanegara, MD

AIMS:Describe the signs, symptoms, patophysiology and management of pterygium, keratoconus, senile cataract, lens dislocation

LEARNING OUTCOMES:Can describe the signs, symptoms, patophysiology and management of pterygium, keratoconus, senile cataract, lens dislocation

CURRICULUM CONTENTS1. Pterygium2. Keratoconus3. Senile Cataract4. Lens Dislocasion

ABSTRACT / SUMMARY OF LECTURE

A pterygium is an elevated, wedged-shaped growth of the scleral conjunctiva that invades the cornea. Pterygium are benign (non-cancerous) growths, but contain blood vessels and form scar tissue on the eye. Because a pterygium resembles tissue or film growing over the eye, a person who has one may become concerned about personal appearance. Prolonged exposure to ultraviolet light from the sun may play a role in the formation of pterygium.

Keratoconus is a degenerative disorder of the eye in which structural changes within the cornea cause it to thin and change to a more conical shape than its normal gradual curve. Keratoconus can cause substantial distortion of vision, with multiple images, streaking and sensitivity to light.

A cataract is a clouding of the lens inside the eye that leads to a decrease in vision. It is the most common cause of blindness and is conventionally treated with surgery. Visual loss occurs because opacification of the lens obstructs light from passing and being focused on to the retina at the back of the eye. It is most commonly due to biological aging. Over time, yellow-brown pigment is deposited within the lens and this, together with disruption of the normal architecture of the lens fibers, leads to reduced transmission of light, which in turn leads to visual problems. Those with cataract commonly experience difficulty



appreciating colors and changes in contrast, driving, reading, recognizing faces, and experience problems coping with glare from bright lights.

Lens dislocation is a displacement or malposition of the eye's crystalline lens from its normal location. A partial dislocation of a lens is termed subluxated lens; a complete dislocation of a lens is termed lens luxation or luxated lens. Lens dislocation can cause by blunt injury to the eye, zonullar weakness. The lens may be dislocation in any direction, including posteriorly into the vitreous cavity or anteriorly into the anterior chamber. Symptoms and signs of lens dislocation include fluctuation of vision, impaired accommodation, monocular diplopia, iridodenesis or phacodenesis is present.

SELF DIRECTING LEARNING (in depth learning of above lecture)1. Physiology and pathophysiology of pterygium, keratoconus, senile cataract, lens

dislocation2. Definition of pterygium, keratoconus, senile cataract, lens dislocation3. Management of pterygium, keratoconus, senile cataract, lens dislocation

SCENARIO1. A 70 years old man complains of difficulty driving because of reduced vision. His

best corrected visual acuity is 20/80 OD and 20/40 OS. Progressive nearsightedness. Problems with glare during the day.

a. What need to be asking to the patient to make the diagnosis?b. Make the physical examination of this patient with imagination in correlation

with the story above.c. What is the diagnosis of this case?d. How to diagnose this kind of cases?e. How to treated this case?

2. A 35 years old man came to the ophthalmologist and has checked his eyes. He complained of on both eye usually be seen as a fleshy, pink growth on the white of the eye. They occur between the eyelids ,on the right eye, in the corner of the eye, close to the nose, extend onto the cornea.


with the story above.c. What is the diagnosis of this case?d. How to diagnosed this case?e. What is the best treatment in this case?

3. A 50 years old woman came to eye emergency with complain blurred vision on left eye after got hit by wood 5 hours ago. There’s no bleeding dan wound on her eyes. The eye examination was visual acuity 1m counting finger, IOP was 25mmHg, lens’s position was more toward to anterior chamber.


with the story above.c. What is the diagnosis of this case?d. How to diagnosed this case?e. What is the best treatment in this case?



SELF ASSESSMENTS1. Mention and explain about Pterygium2. Mention and explain about Keratoconus3. Mention and explain about Senile Cataract4. Mention and explain about Lens Dislocation5. Referal procedure

LEARNING RESOURSES:1. Vaughan: General Ophthalmology2. Ilyas S: Ilmu Penyakit Mata. FK UI3. Deborah PL: Manual Diagnostic &Ocular Treatment.4. PERDAMI: Panduan Ketrampilan dan Klinis Penyakit Mata, Jakarta, 20065. Buku Panduan Belajar Koas. Ilmu Kesehatan Mata. UNUD. 2017

DAY 10VITREORETINAL DISORDERS

By : Budhiastra MD and Ari Andayani MD

AIMS : Describe the Signs, Symptoms, Patophysiology and Management of Vitreo Retina disorders.

LEARNING OUTCOMESCan describe the Signs, Symptoms, Patophysiology and Management of:

1. Diabetic Retinopathy2. Hypertensiv Retinopathy3. Retinal Occlusion Retinal Disease4. Retinal Detachment5. Age Related Macular Degeneration

CURRICULUM CONTENT1. Fundus Examination by Funduscopy Direct, Slit lamp with lens , Fundus Camera

and OCT2. Laser Photocoagulation3. Anti VEGF Injection Intra Vitreal4. Sceral Buckling dan Vitrectomy

ABSTRACT / SUMMARY OF LECTUREDiabetic Retinopathy is progressive microangiopathy characteristized by small

vessel damage and occlusion. The earliest pathologic changes are thickening of the capillary endothelial basement membrane and reduction of the number of pericytes. In term both prognosis and treatment, it is useful to divide DR into Nonproliferative (NPDR) and Proliferative Diabetic Retinopathy (PDR). Diabetic Macular Edema (DME) can occur in both conditions.

Hypertensive retinopathy is the retinal change in hypertension is secondary to focal ischemia. Hypertension causes increases arterioral light reflex called copper and silver wiring. Classification of hypertensive retinopathy according to Keith-Wagener-Baker (KW): 1.KW 1: sclerosis, mild stenosis of arterial vessel, 2.KW 2: a-v crossing, hard exudates, 3 KW 3:hemorrhagic,soft exudates,4.KW 4:KW 3+papillaedema (optic disc edema).

Retinal detachment is separation of the sensory retina (photoreceptor and inner tissue layers) from underlying retinal pigment epithelium (RPE) layer. RD can be divided into:



1. Rhegmatogenous retinal detachment (RRD) with retinal tear (due to myopia, aphakia, trauma, degeneration or can be spontaneous).

2. Exudative (serous) retinal detachment with serous fluid under retina without tear, found in hypertensive retinopathy, eclampsia.

3. Tractional retinal detachment, due to traction on vitreous body by fibrotic tissue, found vitreous bleeding at diabetic retinopathy or trauma. The main treatment of Rhegmatogenous detachment are Drainage, Air (gas) injection, Cryo and Explants (DACE), but Tractional RD commonly need vitrectomy surgery.

Vascular disorders retinal occusion includes central retinal vein occlusion (CRVO), branch retinal vein occlusion (BRVO), and central retinal arterial occlussion (CRAO), branch (BRAO). Usually present with sudden loss of visual field and with painless visual loss. CRVO is a common and easily diagnose retinal vascular disorders with potentially blind complication. Retinal artery occlusion can be caused by embolism, arteriosclerosis, infection, and phlebitis. We distinguish between ischemic and non - ischemic vein occlusion. The causes of retinal vein occlusion include compression of the veins, arteriosclerosis, infection, phlebitis cardiovascular diseases, hypertension and diabetes mellitus. The main treatment CRVO is anti-VEGF intra vitreal and laser photocoagulation.

Age-Related Macular degeneration is a atrophy and degeneration of outer retina, retinal pigment epithelium, Bruch’s membrane and choriocapillaris. The disease includes a broad spectrum of clinical and pathologic finding that can classify into two groups: non exudative (“dry”) and exudative (“wet”). The exat cause is unknown, but the incidence increased with each decade over age 50, race usually Caucasian, sex slight female predominan, family history and a history of cigarette smoking. The main treatment of wet is injection anti-VEGF intravitral.

SELF DIRECTING LEARNING (in depth learning of above lecture)1. History of Vitreo Retinal Diseases2. Vitreo Retina Examination3. Sign and Symptoms Vitreo Retinal Diseases.4. Complications of Vitreo Retinal Diseases5. Medication of Retinal Deseases6. Treatment Vitreo Retinal Diseases by Laser Photocoagulation7. Surgery of Vitreo Retinal Diseases by Surgery such as Screla Buckling, Cryo and

Vitrctomy.8. Prognosis of Vitreo- Retinal Diseases.

SCENARIO1. A 50 years old male patient complained blurry vision on both of his eyes since 2

months prior. He has a history of hypertension, and diabetes mellitus. Redness and history of accident was denied. From the examination, the visual acuity was 6/30, hard to be corrected, anterior segment was normal, intraocular pressure was normal. From funduscopy examination there were flame shaped hemorrhages on all quadrants, exudates, microaneurysma, NVD on posterior pole.

a. What kind of anamnesis that would be needed on this patient?b. Laboratory examination that would be needed on this patient?c. Opthalmology examination that would be needed on this patient?d. Explain retinal hemorrhages patophisiology on this patiente. What would be the Predisposision factors that influence retinal hemorhages

on this casef. What would be the differential diagnosis for this case?



g. What would be the therapy for this case?h. How would be the follow up for this patient?

2. A 55 years old man complained blurry vision on his left eye since 3 days before. He was diagnosed with hypertension and diabetes mellitus 3 years ago. From examination, visual acuity was 3/60, IOP was normal, anterior segment was normal. From funduscopy examination there were flame shaped hemorrhages on all quadrants, exudates, cotton woll spots, the optic nerve head was not well demarcated, the vessel were bending, and hemorrhaging.

a. What kind of anamnesis that would be needed on this patient?b. Laboratory examination that would be needed on this patient?c. Opthalmology examination that would be needed on this patient?d. Explain retinal hemorrhages patophisiology on this patiente. What would be the Predisposision factors that influence retinal hemorhages

on this casef. What would be the differential diagnosis for this case?g. What would be the therapy for this case?h. How would be the follow up for this patient?

3. A 41 years old woman complained a sudden blurry vision on her left eye since 5 days before. She has been wearing glasses since high school. From the examination, the visual acuity was 1/60 and was hard to be corrected, IOP was 10 mmhg, The anterior segment was normal, from funduscopy examination vitreous was clear and the retina was elevated on the inferior.

a. What kind of anamnesis that would be needed on this patient?b. Laboratory examination that would be needed on this patient?c. Opthalmology examination that would be needed on this patient?d. Explain the patophisiology of this casee. What would be the Predisposision factors on this casef. What would be the differential diagnosis for this case?g. What would be the therapy for this case?h. How would be the follow up for this patient?

SELF ASSESSMENTS

1. Describe definition of retinal detachment, central artery & vein occlusion vitreous hemorrhagic, hypertensive retinophaty, and diabetic retinophaty.

2. Explain about pathogenesis of retinal detachment, central artery & vein occlusion vitreous hemorrhagic, hypertensive retinophaty, and diabetic retinophaty.

3. Mention classification of retinal detachment, central artery & vein occlusion vitreous hemorrhagic, hypertensive retinophaty, and diabetic retinophaty.

4. Mention symptoms could be found in retinal detachment, central artery & vein occlusion vitreous hemorrhagic, hypertensive retinophaty, and diabetic retinophaty.

5. Mention the examination needed to make diagnosis of retinal detachment, central artery & vein occlusion vitreous hemorrhagic, hypertensive retinophaty, and diabetic retinophaty.

6. Explain how you can establish diagnosis of retinal detachment, central artery & vein occlusion vitreous hemorrhagic, hypertensive retinophaty, and diabetic retinophaty.

7. What should you do if you have a patient with retinal detachment, central artery & vein occlusion vitreous hemorrhagic, hypertensive retinophaty, and diabetic retinophaty?



8. Mention what you should tell to the patient who has history of retinal detachment, central artery & vein occlusion vitreous hemorrhagic, hypertensive retinophaty, and diabetic retinophaty.

LEARNING RESOURSES :1. Vaughan, Asburhy : General Ophthalmology2. Deborah P Langstone : Manual Diagnosis and Ocular Tretment.3. Perdami : Panduan Ketrampilan dan Klinis Penyakit Mata, Jakarta, 2006.4. American Academy of Ophthalmology : 2012

DAY 15NEURO-OPHTHLMOLOGY DISORDERS

By AA Mas Putrawati Triningrat, MD

AimsDescribe: the sign, symptoms, patophysiology and management of neuro ophthalmology disorder

LEARNING OUTCOMES:

Can describe about Diplopia Binocular, Hemianopia: bitemporal dan Homonymous, Visual Filed Disturbance, Edema Papil, Neuropathy Optic (Atrophy + Neuritis)

Curriculum contents.Can describe the:

1. Diplopia Binocular2. Hemianopia: bitemporal dan Homonymous3. Visual Filed Disturbance 4. Edema Papil5. Neuropathy Optic (Atrophy + Neuritis)

Abstract / summary of lectureIt is important to recognize that any disturbance in afferent function may result in the

same complaints of visual loss seen with pathology affecting the retina, optic nerve and visual pathways. The optic nerve begins anatomically at optic disc but physiology and functionally within the ganglion cell layer that covers the entire retina.

Diplopia commonly known as double vision and the most common symptoms for which patients seek ophthalmic care. Double vision in one eye is known as monocular double vision. Double vision continues when the unaffected eye is covered, but it should be able to see normally when the affected eye is covered. It can be caused by an irregularly shaped cornea (astigmatism) which is refractive error, a rare type of cataract, abnormalities of the iris, lens, or fluid within the eye and even dry eye. Binocular diplopia is where the brain is unable to combine the images from the right and left eyes into one picture and the double vision resolve when either eye is covered. The double vision can be the same in all fields of gaze (comitant), or vary with gaze direction (incomitant). Diplopia can be horizontal, vertical, oblique or torsional. It can be caused by a number of condition. Damage which affecting the eye mucles that move the eyes or the nerves that control movement, the diplopia can be created.

The visual field is the portion of the subject’s surrounding that can be seen at any one time. The normal extent of field vision is 50 superiorly, 60 nasally, 70 inferiorly and 90 temporally. A Visual field defect is a loss of part of the usual field of vision, can be one or



both eyes. The lesion may be anywhere along the optic pathway, retina to occipital cortex. Hemianopia bitemporal and homonymous is visual field disturbance that affecting visual pathway (Chiasma opticum and tractus opticum).

Optic neuropathies typically are associated with visual field loss, most demonstrate an afferent pupillary defect, although in case with very mild optic nerve dysfunction or with bilateral symmetric dysfunction, the defect may not detectable. The optic disc may be abnormal or normal in appearance; abnormal disc maybe oedematous or may show other abnormalities, such as excavation, or atrophy. Certain causes of optic neuropathy may present in more than one way; for example, orbital compressive or infiltrate lesions may initially demonstrate either normal, oedematous or atrophic. Optic atrophy is a nonspecific response to optic nerve damage from any causes since optic nerve consist of retinal ganglion cell axons, optic atrophy may be the consequences of primary retinal disorder, such as retinitis pigmentosa, CRAO. Optic neuritis is a disk swelling caused by inflammation at the nerve head (intraocular optic nerve). Loss of vision is the cardinal symptom of optic neuritis and is particularly useful in differentiating papilitis from papiledema which it may resemble on ophthalmoscopic examination. Optic neuritis may be due to a variety of causes, but the most common is demyelinating dss, including multiple sclerosis.

Edema papil is an optic disk swelling due to raised intracranial pressure of which the most common causes are cerebral tumour, abscess, subdural haematom, arteriovenous malformations, subarachnoid hemorrhage acquired hydrocephalus, meningitis and encephalitis.

Self directing learning1. Anatomy of optic nerve2. Visual pathways3. Extraocular muscle and Ocular movement4. Pupillary reactivity5. Relative afferent pupillary defect6. Optic disc evaluation7. Edema papil8. Atrophy optic9. Neuritis optic10. Abnormal Visual Filed

Scenario

Case 1Woman, 20 years old, complained about double vision and feel headache since 3 days before admission to hospital. There are history of traffic accident particularly in eye area.

1. Mention things you should elaborate from the patien during anamnesis2. Mention physical examination you should do for this patient3. Explain about the result from the examination4. Mention differential diagnosis of the case5. Which diagnosis is the most appropriate?6. Explain about the management of this case

Case 2Woman 30 years old, complained about sudden blur vision, and visual filed disturbance on her left eye since two days before. He also complained about pain when moving her eye. On ophthalmology examination, doctor found decreasing visual acuity (VOS 3/60).Mention things you should elaborate from the patien during anamnesisMention physical examination you should do for this patient



Explain about the result from the examinationMention differential diagnosis of the caseWhich diagnosis is the most appropriate?Explain about the management of this case

Case 3Man 45 years old, complained about headache, nausea, vomit and disturbance visual field on both eyes since 3 days before. On the ophthalmology examination, doctor found no disturbance of vision, but there was edema optic nerve both eyes.

1. Mention things you should elaborate from the patien during anamnesis2. Mention physical examination you should do for this patient3. Explain about the result from the examination4. Mention differential diagnosis of the case5. Which diagnosis is the most appropriate?6. Explain about the management of this case

Self assessment NO1. Describe definition of edema papil, atrophy optic, neuropathy optic, neuritis optic2. Explain about pathogenesis of edema papil, atrophy optic, neuropathy optic, neuritis

optic3. Mention symptom could be found in edema papil, atrophy optic, neuropathy optic,

neuritis optic4. Mention the examination needed to make diagnosis of edema papil, atrophy optic,

neuropathy optic, neuritis optic5. Explain how you can establish diagnosis of edema papil, atrophy optic, neuropathy

optic, neuritis optic

LEARNING RESOURSES:1. Vaughan: General Ophthalmology2. American Academy of Ophthalmology, Basic and clinical science course, section 5,

neuro-ophthalmology3. PERDAMI: Panduan Ketrampiilan dan Klinis Penyakit Mata, Jakarta, 20

DAY 15STRABISMUS

By Surasmiati MD

AIMS:Describe about eye movement, esotropia and eksotropia

LEARNING OUTCOMES:Can describe about eye movement, esotropia and eksotropia

CURRICULUM CONTENTS:1. Eye movement2. Esotropia 3. Eksotropia

ABSTRACT / SUMMARY OF LECTURE:

EYE MOVEMENT



Eye movement are controlled by six extraocular muscles innervated by cranial nerves III, IV and VI. Ductions are monocular eye movements. Movement of the eye nasally is adduction; temporal movement is abduction. Elevation and depression of the eye are termed sursumduction (supraduction) and deorsumduction (infraduction), respectively. Incycloduction (intorsion) is nasal rotation of the vertical meridian; excycloduction (extorsion) is temporal rotation of the vertical meridian. Binocular eye movements are either conjugate (versions) or disconjugate (vergences). Versions are movements of both eyes in the same direction. Dextroversion is movement of both eyes to the right, and levoversion is movement of both eyes to the left. Sursumversion (supraversion) and deorsumversion (infraversion) are elevation and depression of both eyes, respectively. Convergence is movement of both eyes nasally, and divergence is movement of both eyes temporally.

STRABISMUSOcular position when the eye is looking straight ahead with the visual axis parallel to the sagittal plane of the head, is called primary position. Orthotropia, when the eyes properly aligned. Strabismus is a misalignment of the eyes. There are many different types of strabismus. Strabismus is most commonly described by the direction of the eye misalignment; common types of strabismus are esotropia, exotropia, hypotropia, and hypertropia.

EsotropiaEsotropia is inward turning of the eyes (aka "crossed eyes"). Types of esotropia include infantile esotropia, accommodative esotropia, and sixth nerve palsy. Infantile esotropia usually appears before 6 month old. Accommodative esotropia (also called refractive esotropia) is an inward turning of the eyes due to efforts of accommodation. It is often seen in patients with moderate amounts of hyperopia.

ExotropiaExotropia refers to outward deviation of the eyes. Exotropia may occur from time to time (intermittent exotropia) or may be constant.

Strabismus ExaminationA. Hirschberg Method – the patient fixates a light at a distance about 33 cm.

decentering of the light reflection is noted in the deviating eye. B. Krimsky method -- uses reflections produced on both corneas by a penlight and

placing prisms in front of the fixation eyeC. Cover tes consist of four parts: (1) the cover/ uncover test (2) alternate cover test

(3) the prism alternate cover test and (4) Simultaneous prism cover test

SELF DIRECTING LEARNING (In depth learning of above lecture) 1. Definition of binocular single vision.2. Definition of Orthophoria, Heterotropia, Heterophoria3. Describe muscle action and field of action of Extra ocular muscle

SCENARIOA 6 years old girl complain blurred vision and eye discomport. From the visual acuity examination of the right eye is 6/30 with correction ∫ -2.25 visual acuity improve 6/12 and the left eye the visual acuity 6/6. Hirschberg test result that the corneal light reflex on the right eye fall in the lateral side at limbus

a. What is the diagnosis of this case?b. What is the choice of medical treatment of this case?c. How about Hirschberg test?d. What is the complication of uncorrected refractive error?e. What is the treatment of amblyopia?



SELF ASSESSMENT:1. Mention and explain about type of strabismus 2. Management of strabismus,

LEARNING RESOURSES:1. Vaughan: General Ophthalmology2. Ilyas S: Ilmu Penyakit Mata. FK UI3. Deborah PL: Manual Diagnostic & Ocular Treatmentt.4. PERDAMI: Panduan Ketrampiilan dan Klinis Penyakit Mata, Jakarta, 20065. Wright, KW. Handbook of Pediatric Strabismus and Amblyopia, 2006



PRACTICUM DAN BASIC CLINICAL SKILL STUDY GUIDE

I. BASIC CLINICAL SKILL VISUAL PHYSIOLOGY STUDY GUIDE

A. GOALThe goals of the study are to enchand the knowledge and the student skill for examination of:1. Visual acuity (visus)2. Visual field3. Pupil reflex, consensual reflex and pupil reflex during accomodation.4. Organic and functional color blindness5. Cornea arch

B. EQUIPMENT USE:1. Optotype snellen2. Perimeter3. flashlight4. Ishihara chart and wall thread5. Keratoskope placido

C. WORK METHOD:

1. VISUAL ACUITY, (Snellen chart)a. Hang the Snellen chart at the wall at eye height during sitting b. Ask the subject sit on the chair which 6 meter distance from the Snellen chartc. For examination of the right eye, close the left eye with the left hand.d. Ask the subject to read the letter on the chart, begin with the upper to the

lower raw, without any mistakee. Repeat this test to the other eye, with same method.f. Visual acuity (visus) is calculatefrom the formula: V = d/D, where V= visual

acuity, d= the distance of subject from Snellen chart, and D= the distance that normal person can be read correctly (this is write at the Snellen chart).

g. Must be remember that the value from d/D, can’t be to simplified.

Learning task: Comprehend the influence of aging process to the visual acuity, what is the cause that problem? 2. VISUAL FIELD (use perimeter)

a. The equipment for visual field test is perimeter. Place the perimeter on the laboratory table

b. Ask the subject sitting face to the perimeter, and close one eye which is note test. If the right eye would be tested, close the feft eye and visepersa.

c. Palace the subject chic on the chic support and ajust the height so the lower margin of their eye and the eye level equal to the center of perimeter.

d. Fit he perimeter fist so the perimeter arc on the plane surfacee. Ask the subject to focus their sight to the centre of perimeter during the

examination.f. Take the sign tool (white) and move it along the perimeter arc from side to

the center , and stop when the subject begin sea it, and read the number at the perimeter arc, and than write on the form.

g. Repeated again that method after move the perimeter arc 30 degree clock wise direction

h. Do it to the other eye with the same method.



Learning task: comprehend the difference of visual field of right and left eye. What is the mono and binocular vision?. 3. PUPIL REFLEX, CONSENSUIL REFLEX and PUPIL REFLEX DURING ACCOMMODATION (use flashlight)

a. Ask the subject sitting on the chair and relaxb. Beam of light to the right eye of the subject with flashlight, and look at the

change of pupil diameter of the right eye (if the pupil diameter is smaller, it mean pupil reflex positive).

c. Repeat it again but now look the change of pupil diameter of the left eye (consensual reflex, If the diameter of left eye is smaller, it mean consensual reflex positive)

d. Ask the subject to watch the examiner’s fingers from distance around 50 cm and than moving it approach the subject (focusing the eyes or accommodation), and the examiner watching the changes of pupil diameter .During accommodation the pupil diameter should be smaller.

Learning task: describe the mechanism of pupil reflex and consensual reflex. Why the pupil diameter change to smaller during accommodation? 4. ORGANIC AND FUNCTIONAL COLOR BLINDNESS (use Ishihara chart and wall thread).4.1. Organic visual blindness:

a. Ask the subject to select many color of wall thread and collect it with same color. The examiner write the incorrect color.

b. Ask the subject to read the Ishihara chart, and write their mistake, use the guide of the Ishihara chart.

4.2. Functional color blindness.a. Ask the subject to watch the white sky through the green or red glass for view

minute, and than ask them to watch the wall thread or read the Ishihara chart.

b. The subject difficult to choose the wall thread or read the Ishihara chart. It is functional color blindness.

Learning task: Describe the mechanism of organic or functional color blindness. 5. CORNEA ARCH (use keratoskope placido)

a. Ask the subject to sit down back to the light, and place the keratoskope placido 20 cm front of the subject.

b. Ask the subject always watch the keratoskope placido during examination, and the examiner watch the cornea of the subject through the hole at the center of keratoskope palcido. The image of the keratoskope placido can be watch at front surface of the cornea in form of black circle.

c. If the image form is full and concentric circle, it mean the surface of cornea is normal

d. If the image form is crooked on one side and difference to the other side, it mean the front surface of the cornea is abnormal.

Learning task: what is call astigmatism? what is to correct it? STUDY GUIDE BASIC CLINICAL SKILL OPHTHALMOLOGY

CONTENTS:



1. Subjective visual examination2. External inspection:

Eyelid Conjunctiva Sclera Lachrymal apparatus Pupil Light reflex and convergence Cornea Camera Oculi Anterior Iris Lens

3. Intra Ocular Pressure Palpation Tonometry Schiotz

4. Therapeutic Skill Eyelid eversion Eye drops installation Eye ointment installation Applying eye dressing Removal conjunctiva foreign body Removal corneal foreign body (with cotton bud)

I. SUBJECTIVE VISUAL EXAMINATION

Eye Examination:• Visual Acuity• Visual field examination with confrontation test, perimetry (kinetic and static)• Dark adaptation – measurement of least luminance required to produce a visual

sensation • Contrast sensitivity – is measurement of the smallest distinguishable contrast, it is

assessment of quality of vision• Colour vision –with lantern test (Edridge green lantern) and Isochromatic charts

Subjective examination of the function of eye Definition-It is defined as the measurement of the smallest retinal image which can be appreciated with reference to its shape and size. it is actually measure of form sense.

• Central or direct vision

• Distance vision with Snellen test type

• Near vision with Snellen test type or Jaeger’s test type

• The principal of assessment is measurement of spatial resolution of the eye i.e. an estimation of ability of eye to discriminate between two points.

DISTANCE VISION

Two distant points can be visible as separate only when they subtend an angle of 1 minute at the nodal point of eye.

Principle



• Each individual letter subtends an angle of 5 minutes and each component of letter subtends an angle of 1 minute at the nodal point of eye from the distance in meters written as numerical.

• Snellen chart is having different number of letters in different rows and the letter at top line should be read clearly at distance of 60 m. similarly the letters at subsequent lines as are read at 36, 24,18,12,9,6,5mts respectively

• Numerical convention is used for recording visual acuity. In fraction, the numerator is the distance at which the patient is sitting from chart and the denominator is the distance at which person (with normal vision) should be able to read the last line that person is able to read.

Procedure of testing• Patient is seated at the distance of 6 meters from Snellen’s chart (distance of 6 mts

is taken as at this distance it is assumed that the rays are almost parallel and patient exert minimum accommodation)

• The chart should be properly illuminated at minimum of 20 feet candles. Patient is asked to wear trial frame. It is adjusted according to patient inter pupillary distance.



• Ask the patient to read with one eye from the top letter while the contra lateral eye is closed gently with the patient palm or with occulder in the trial frame.

• Now patient is asked to reads the Snellen’s chart from top letter to smaller letter, and depending upon the smallest line that the patient can read from distance of 6mt. His vision is recorded as 6/6, 6/9, 6/12,6/18, 6/24, 6/36, 6/60.

• But if patient is not able to see the top line from 6mts he is asked to count the examiner finger at 5,4, 3, 2, 1 mts (or reverse, from 1 to 5 mts) and noted as 5/60,4/60,3/60,2/60,1/60 respectively (or CF=counting finger 1m, CF 2m, CF 3m,CF 4m, CF 5m)

• If patient not able to count examiner finger close to face then examiner waves or moves his hand in about 25 cm from the patient eye and asks patient whether he is able to see hand movement or not. Visual acuity then recorded as HM+ or 1/300

• When patient cannot distinguish hand movements, the examiner use penlight in front of the patient eye (± 20 – 25cm) and notes whether the patient can perceive light or not. If he perceive light it is noted as LP (light perception) +ve otherwise as LP-ve. The examiner then reflect the penlight from four directions (nasal, superior, temporal, inferior) and asked the patient to mention the direction of the light.

• Record accordingly if present patient perceive light from all directions it is marked as PR (Projection of rays ) present or else mark as absent or defective. The test is repeated for the other eye in similar fashion

Pin hole test Method

• Place the pin hole occluder in front of the eye with reduced vision

• Ask the patient to move their eye and head until some letters can be read on the letter chart

• Ask the patient to read the lowest line of letters he can see looking through the pinhol

Interpretation • If patient vision is improved with pin hole it means the poor acuity is due to refractive

errors. (eg. 6/12 PH 6/6 means visual acuity 6/12 can be improved with pinhole until 6/6)

• If static acuity means may be due to structural or organic cause.(eg.6/12 NI PH = non improved PH means the visual acuity still 6/12 with non improvement with pin hole)

• If reduced the poor visual acuity may be due to corneal opacity or lenticular opacity occupying papillary area or macular pathology.

Charts for testing near vision are :1) Snellen near vision chart 2) Jaeger chart3) Roman test type

Method of recording near vision• Ask the patient to sit with his back to the light



• If the patient is using glasses for distance the same number will be put on the trial frame. Occlude one eye with an occulder

• Ask the patient to hold the near vision by his right hand at a distance of 25 to 33 cms.

• Note the near vision as per the letter read

• Repeat the test for the other eye.

II. EXTERNAL INSPECTION

1. EyelidsEyelids conditions

Diffuse swollen or edema, usually found in nephritic syndrome, heart disease, anemia, dacryoadenitis and hyperthyroid..

Eyelid swollen with sharp edge in chalazion, tumor. Blepharospasm, happened on corneal erosin, anterior uveitis, acute

glaucoma. Essential Blepharospasm did not result from organic disorders and usually happened billateraly. Blepharospasm could also be found at psychiatric patient with hysteria.

Echymosis, the color of the eyelid changes as a result of blood extravatation after trauma.

Ectropion, is turning outward of the eyelids, could be found in elderly, paralise of the muscles, cikatriks and other.

Entropion, turning inward of the eyelids.In Trachomas patient the entropion usually happen in upper eyelids. Entropion could also happen due to parese of the muscles, cikatriks and senile condition.

Lagoftalmos: inabillity to close the eyelids completely. Redness, inflamation, squama, tumour Merah, radang, keropeng (skuama),

tumor. Pseudoptosis, difficulties to open the eyelids as if it is drooping. Happen on

enophthalmos, phtisis bulbi, chalazion or the other eyelids tumour, eyelids edema and blepharochalazis.

Ptosis, drooping eyelids. Usually happen in elderly with history of intraocular surgery, Myasthenia gravis, Horner Syndrome, N III palsy, botulinum toxin injection

Cikatriks, scar on the eyelids Trikiasis, silia atau bulu mata tumbuh salah arah sehingga dapat merusak

kornea. Trikiasis dapat disebabkan blefaritis dan entropion. Xantelasma, penimbunan deposit berwarna kekuning-kuningan pada

kelopak, terutama nasal atas dan bawah. Xantelasma biasanya dihubungkan dengan hiperlipidemia dan dapat tanpa hiperlipidemia seperti pada histiosis dan retikulohistositoma.

Abnormality of lower eyelids: Similar with upper eyelids Swollen of lacrimal sac, redness and sometimes pus came out when it be

pushed. Madarosis.

Inerpalpebral Fissure Normal



Narrow or small, if there is eyelids edema, blepharitis, ptosis, pseudoptosis, blepharophymosis

Wide or bigger, happened in hyperthyroid or intraocular tumour.

Eyelids margin Complete cilia Trichiasis Meibomian gland punctum secretion Redness, pain and ulceration

2. Conjunctiva

Upper Tarsal Conjunctiva Can be checked by eversion the upper eyelids using finger or cotton tip applicator. Abnormality of the conjunctiva:

Cobble stone follicles, deposite of macrophages and lymphoid cells under the conjunctiva. Dome shaped appearance, about 1 mm. Most follicles can be seen in forniks area because in this area consist of a lot of lymphoid tissues.

Membrane, inflammatory cells beyond the conjunctiva that will be bleed iwhen excised. This membrane usually appears like mass surrounding tarsal or bulbar conjunctiva. It is consists of necrotic tissues, penetrated to the deeper layer and greyish, usually can be found in patient with bacteria conjunctivitis or rarely happened on viral conjunctivitis.

Pseudomembrane, membranes that not get bleed if excised. Happened in ocular pemphygoid and Steven Johnson Syndrome.

Papillae, tiny dome shaped nodule that consist of hyperemic central core blood vessels of the conjunctiva that protrude up and perpendicular to the tarsal plate surrounded by edema and inflammatory cells

Giant Papillae, polygonal shaped, flat and coukd be found in vernal conjunctivitis, superior limbic keratitis, and iatrogenic conjunctivitis.

Cicatriks, in trachoma usually the direction of the cicatriks is parallel with eyelids margin.

Simblepharon, stickyness of tarsal and bulbar conjunctiva and kornea. Can be found in chemical trauma or Steven Johnson Syndromes

Hordeolum or Stye Chalazion.

Inferior tarsal conjunctiva Konjungtiva tarsal inferiorThe abnormalities could be:

Cobble stone follicles. Papil. cicatriks Hordeolum or Stye. Chalazion.

Bulbar conjunctiva The abnormalities could be:

Discharge Conjunctival Injection, vasodilatation of superior conjunctival arteries



Cilliary Injection, vasodilatation of pericorneal arteries or anterior cilliaris arteries.

Episcleral injection, vasodilatation of episcleral vessels Subconjunctival bleeding. Flickten, inflammatory surrounded with neovascularization on conjunctiva Simblepharon. Degeneration plaque Pinguecula, conjunctival degeneration plaque in palpebral fissure area,

triangular shape in nasal and temporal cornea Pterygium, proliferation of fibrous tissues process with neovascularization on

conjunctiva, triangular shape with the apeks toward the cornea Pseudopterygium. Flickten, inflammatory cells and neovascularization on the cornea.

3. ScleraAbnormalities that coulb be found in sclera:

Local or diffuse episcleral injection. Nodulle.

4. Lacrimal Apparatus The abnormalities includes:

Epifora. Stenosis or obstruction of lacrimal punctum Lacrmal sac inflammation Peradangan di sakus lakrimal. Yellowish discharge or pus in lacrimal punctum

5. Pupil Pupil abnormalities:

Isokoria, similarities of shape and size of pupil in both eyes Anisokoria, the size of both pupil is different, found in monocular granuloma

uveitis and Afferent pupillary defect Midriasis, happened as a results of parasympatolitik drugs (atropine,

skopolamine) atau sympatomimetik (adrenaline and cocaine). Miosis, happened in miotic spastics (meningitis, ensephalitis dan ventrikel

haemorraghe), morfine and antikolinesterase intoxication. In miotic paralitic or simpatic parese as Horner syndrome, miosis, ptosis dan anhidrosis were the Trias.

Hippus, also known as pupillary athetosis, is spasmodic, rhythmic, but irregular dilating and contracting pupillary movements between the sphincter and dilator muscles

Pupil occlusion, pupil covered by inflammatory tissues in front of the lens Seklusi pupil, the whole pupil is attached to anterior lens Leukokoria, white pupil or whitish reflex of the pupil. Can be found in

cataract, retrolental fibroplasia, endophthalmitis, vitreous hyperplasia, high myopia, retinal detachment andretinal tumour as retinoblastoma

No pupil reaction, can be found in intoxication of mydriatics and miotic drug, sphincter pupil rupture, posterior sinekia, blind

Light reflex and convergence Positive light reflex, miotic effect when pupil get exposed to the light


http://en.wikipedia.org/wiki/Pupillary_response

http://en.wikipedia.org/wiki/Eye_muscles


Negative light reflex, happened on sphincter pupillae rupture, no Light perception patient, parasympatic abnormalities, drug induced angd posterior synekia

Convergence reflex consist of accommodation, miosis and convergence if there is a changes focus from far point to near point.

KorneaAbnormalities of the cornea:

Normal corneal diameter is 12 mm Macrocornea: diameter of the corena is larger than normal Microcornea: diameter of the cornea is smaller than normal Arkus senilis, whitish or grey ring in outer segement of cornea Corneal edema, the cornea is unclear and thickened, happened in congenital

glaucoma as well as acute glaucoma, after intra ocular surgeries, endothelial decompensation, trauma and corneal infection

Erosion, corneal epithelial detachment, give rise to positive fluourescein test Infiltrat, deposit of inflammatory cells on the cornea that makes cornea

unclear and positive placido test Pannus, inflammatory cells with neovascularization, usually at the superior

limbal area of the cornea, happened in trachoma, contact lens warpage, flicten, superior limbic keratoconjunctivitis and corneal burn

Corneal Ulcer, loss half of corneal layer due to necrosis in infection or allergic condition

Corneal Xerosis, the dryness of the corneal surface and unclear cornea. Keratomalasia, softened and protruded cornea Cicatriks, scar on the cornea, consist of nebula, macula and lecoma Leukoma adheren, cornea is attached to the iris Corneal Staphyloma, protrusion of the cornea due to corneal ulcer or cornea

become thin with exposed uvea in the back of the cornea Keratik presipitat, inflammatory cell in the corneal endothel

6. Anterior ChamberAbnormalities:

Shallow anterior chamber in lens dislocation, iris tumour, anterior synekia, iris bombe due to pupillary block and acute glaucoma

Deep anterior chamber, in aphakia, myopia, congenital glaucoma and angle resession

Flare, deposit of inflammatory cells and fibrin in anterior chamber Hipopion, the deposit of inflammatory cells in lower part of anterior chamber.

7. IrisAbnormalities:

Coloboma Aniridia Iris atrophy Rubeosis iridis, neovascularization in the iris Anterior Synekia, attachment of the iris with cornea Posterior Synekia, attachment of the iris to the lens

8. Lens



Abnormalities: Cataract, clouding of the lens Lens dislocation, changes in lens position from its normal position, can be

subluxated or luxated to anterior or posterior

II. TONOMETRI

1.PALPATION TONOMETRI

Basic: intra ocular pressure measurement by examiner finger

Instrument: examiner finger tekanan bola mata dengan jari pemeriksa.

Technique

The patient close his eyes Penderita memejamkan mata with down gaze

One of the pointing finger pushed the eyeball while the other finger constantly hold

the eyeball, and the other finger hold the forehead and patient chin.

Interpretation

The eyeball soft enough when it is pushed by finger (N = normal palpation)

N+1, N+2, N+3 atau N-1, N-2, N-3 is the notation that show the higher or lower

intraocular pressure

If the intraocular pressure is higher than normal the glaucoma is suspicious

Notes

This methods can be used if tonometry is not available or the tonometry could not be used

in some eye condition such as cicatriks on the cornea, irregular cornea and corneal

infection. This methods need more practical skill because of subjective interpretation.

Beware of oculo cardiac reflex if the eyeball being pushed innapropiatelly.



2. SCHIOTZ TONOMETRI

The Schiotz tonometer was once the most widely used tonometer. It is used much less often in today’s office setting, but still serves as an accurate, inexpensive, portable, autoclavable instrument for use in the operating room or in nonophthalmologic or nonoptometric settings. The instrument is a simple mechanical device that employs a weight to press a freely moving plunger against the cornea, indenting it. The amount of indentation produced by this weight is read from a scale with a needle indicator moved by the plunger. The plunger must move freely within the cylinder of the tonometer, so the instrument must be kept scrupulously clean. Any debris or oils from the hands can accumulate in the cylinder and affect the movement of the plunger.

The Schiotz tonometer. (Courtesy of Sklar Instruments.)

Cleaning the TonometerThe entire instrument must be carefully cleaned between each patient to avoid the possible spread of infection. The instrument is made entirely of metal, so it can withstand steam sterilization and noncorrosive chemical disinfection. However, it is more common to clean the tonometer with isopropyl alcohol.

Calibrating the SchiotzA metal test block is provided with every instrument. It is in the corner of the storage box and should be wiped clean before use. The calibration is checked by resting the tonometer perpendicularly on the test block. The needle should indicate zero on the left end of the scale. If it does not, a small screw at the base of the needle can be loosened to rezero the needle. The needle itself should be perfectly straight because bending it will give a false reading.



The instrument is placed on the test block to test calibration. (Photo by Mark Arrigoni.) (Reprinted from HerrinMP. Ophthalmic Examination and Basic Skills. Thorofare, NJ: SLACK Incorporated; 1990.)

Performing Schiotz TonometryThe patient must be reclining so that the eyes are looking straight up at the ceiling. A drop of anesthetic is instilled in each eye. The patient is instructed to relax and keep both eyes open and positioned straight ahead; a target placed on the ceiling is helpful. The tonometer should already have been cleaned and tested.A right-handed assistant should hold the tonometer in the right hand using the 2 curved arms attached to the side of the cylinder. The scale mount rotates easily and should be turned so that the scale is facing the assistant. The left hand is used to gently hold the lids of the patient’s right eye apart, anchoring them against the orbital rim so that no pressure is applied to the globe. An alternative hand position is to hold the upper lid with the left hand and the lowerLids with the small finger of the right hand. In either case, the hand holding the tonometer can rest on the patient’s cheek or forehead for stability. The tonometer is gently lowered onto the eye so that the footplate rests on the central cornea and the instrument is perpendicular. The cylinder is then lowered slightly, so that the tonometer is resting on the eye and the assistant is providing only lateral support. The cylinder should neither lift up nor press down on the footplate at this point. Looking straight at the scale, the needle position is noted. If the scale is not directly facing the assistant, an erroneous reading will be made. The tonometer is quickly lifted straight up off. Because the plunger indents the cornea, any movement of the tonometer while it is on the eye may cause an abrasion. The scale readings do not indicate IOP in mm Hg but must be converted according to a table provided with the instrument. The scale readings are inversely proportional to the IOP; lower numbers indicate higher pressures. The standard weight on the plunger is 5.5 gm, and 2 additional weights (2.0 and 4.5 gm) may be added to this for a total of 7.5 and 10.0 gm, respectively. If the scale reading is less than 3 (ie, the IOP is more than 25), the next weight is added, and the measurement is taken again. If the 7.5 weight still gives a reading of less than 3, then the third weight is added, and the measurement is retaken. Along with the IOP, the assistant should also document the weight used.



Manual technique for Schiotz tonometry. (Courtesy of Sklar Instruments.)

IV. THERAPEUTIC SKILL

1. EYELID EVERSION2. EYE DROP INSTILATION3. EYE OINTMENT INSTILLATION4. APPLY EYE DRESSING5. REMOVAL CONJUNCTIVAL FOREIGN BODY6. REMOVAL CORNEAL FOREIGN BODY (WITH COTTON BUD)

1. EYELID EVERSION

INFERIOR CONJUNCTIVA AND FORNIKS EXAMINATION 1. Patient look down, pushed the skin in the inferior part of inferior eyelids with

thumb or point finger then pulled toward the maxilar bone. 2. Patient asked to see upgaze so the inferior forniks can be exposed and inferior

SUPERIOR PALPEBRAL CONJUNCTIVA EXAMINATION (2 HANDS TECHNIQUE) 1. Using thumb or point finger, pull several eyelashes, and pull away the edge of

superior eyelids against the eyeball 2. Put cotton tip applicator (cotton bud) in the sulcus of superior eyelids, along

theegde of tarsus and pushed the applicator to the temporal part of the eye. 3. Pull the edge of superior eyelids outward and upward to see the superior bulbar

conjunctiva, through the applicator. Pulled the applicator and hold the edge of the eyelids to the skin of superior orbital rim with thumb to see the superior palpebral conjunctiva.



SUPERIOR PALPEBRAL CONJUNCTIVA EXAMINATION (1 HAND TECHNIQUE) 1. Ask the patient to look up, Pasien diminta untuk melihat ke atas, use the hand

that temporal to the checked eye, and placed the thumb in inferior eyelids, then pull up.

2. Placed the edge of point finger to press superior eyelids up. Patient then asked to look down, hold for a couple of second. Pinch the superior eyelids using thumb and point finger

3. Rotate with the finger and wrist so the superior eyelids could be seen. The point finger holds the resistance in the lid crease. Thumb holds the edge of superior eyelids to the superior orbits.

2.EYE DROP INSTALLATION1. Patient look up gaze 2. Hold the inferior eyelids under the eyelashes and pull the eyelids out from the

eyeball. 3. Give 1 drop into cul –de –sac, do not touch the eyelashes or eyelids to avoid

contamination. 4. Gently pull the inferior eyelids upward until touching the superior eyelid while the eye

looking downgaze. 5. Close the eyelids for about 3 minutes and try not to blink, so the drug can be pump

into the nose and increase systemic absorption. 6. The excessive drug in medial canthal should be wipe out before open the eyelids.

Another drug that should be instilled may be given in 10 minutes after the first drug instilled..

3.EYE OINTMENT INSTALLATION1. Ointment used if the eye need longer duration of drug. Diperlukan bila

menginginkan kontak dengan mata yang lebih lama.2. Similar with application of eyedrops, but the amount that given to the patient

usually as much as needed. 3. Patient asked to extend his head or lay in bed in supine position 4. Give the ointment into the cul – de – sac and keep away the tube from the

eyelashes or eyelids. 5. Gently pull the inferior eyelids upward until touching the superior eyelid while the

eye looking downgaze 6. For about 2 minutes press with thumb and point finger with closed eyelids.



4.APPLICATION OF A PRESSURE PATCH 1. The patient closes both eyes; the examiner must ensure good closure of the eyelids. 2. The examiner applies an eye pad to the closed eyelids, either lengthwise or folded in

half 3. The examiner places a second patch lengthwise over the first patch.4. Finally, the examiner secures the patches with tape placed from the center of the

forehead to the angle of the jaw across the patched eye. Usually, an antibiotic ointment is applied before patching, and the patient’s progress should be monitored daily

A B

C D

(Taken from Pallay DA, Krachmer JH, M.D. Primary Care Ophthalmology, Mosby,2005)

5. REMOVAL CONJUNCTIVAL FOREIGN BODY1. Patient could be seat or lay in supine position. Extend the head while the patient sit. 2. Separate the eyelids with thumb and point finger in 1 hand or use the eye spreader /

speculum.3. Wet the cotton bud with topical anesthesia, or normal saline or artifisial tears. Do not

use the dry cotton bud because the cotton could leave its part in the eye.4. Swab and rotate the mucous so it can be bond to the cotton bud. Usually swaping is

done to inner canthal or inferior forniks.5. Swab cotton bud through the superior and inferior forniks to clean the debris..6. Conjunctival sac can be filled with sterile isotonic liquid.

6. REMOVAL CORNEAL FOREIGN BODY (WITH COTTON BUD)1. Instill 1 drop of topical anesthesia 2. Open the eyelids with thumb and point finger, remove the foreign body with wet

cotton bud. 3. Rmove the foreign body that embedded in the cornea using 1 cc spuit with slitlamp.4. If there is rust still stay in cornea, do the kuretase with needle or ring rust removal.

Ring rust should not be remove all if unnecessary to avoid cicatriks of the cornea.5. Do the eye patching. Evealuate within 24 hours. (as the corneal erosion protocol))



V. DIRECT FUNDUSCOPY

Purpose:Test to know the posterior segment condition, including optic nerve, retina, blood vessel, vitreous and macula

The funduscopy or direct ophthalmoscopy (taken from Funduscopy made easy, Wong Yee Ming, 2009)

Basic :The light that come into the posterior segment will give fundal reflex. Orange reflex is seen in clear media and called positive fundal reflex. Negative fundal reflex if there is no orange reflex or dark reflex (black)

Instruments:

1. Ophtalmoscopy2. Midriatic drug

1. tropicamide 0.5%-1% (mydriacyl)2. fenilefrin hidroklorida 2.5% (kerja lebih cepat)

Notes:To dilated the pupil, at first we should measure the intraocular pressure. Beware of these condition and avoid the dilatation of the pupil:- Shallow anterior chamber- Head trauma - Iris fixated IOL- The patient drive the vehicles alone - Narrow angle glaucoma

Technique Funduscopy should be done on the same side for patient andthe examiner. This

being said, while examining the right eye, hold the funduscope with your right hand, and examining with your right eye on the right side of the patient

Setting the illuminated lens disc at positive (Green) usually from 4-10, stand from



approximately 1 arm’s length from the patient while illuminating the patient’s both eyes using the large aperture. This enable you to examine the red reflex of the patient

Select “0” on the illuminated lens disc and start with the small aperture as you approach the patient while fixing the “red reflex” pupil as your target. Remember to ask the patient to look straight at the distance to maintain pupil dilation

Tilting slightly at 15-25° lateral to the patient, move forward as you direct the light beam into the pupil. The optic disc should be within view as you are about 1-2 inches from the patient’seye. Remember that the optic disc is slightly towards the nasal aspect of the fundus.

Do not panic if you do not see the optic disc initially. Look for anearby retinal blood vessels. You’ll most likely find the optic disc by tracing at either one “end” or the other of the vessel. This is due to the developmental fact that retinal vessels branch from optic disc to the peripheral retina

The optic disc may not be focused as you see it, as hypermetropic patients require more “plus” (green numbers) lenses for clear focus of the fundus while myopia patients require more “minus” (red numbers).

Examine the optic disc for (the 4C’s):

Color (pink, pale, hyperemia, etc) Contour (margin, shape, elevation, etc) Cup-disc ratio (compare the vertical diameter)Caliber of vessels (normal AV ratio around 2:3)

the AV ratio mentioned is measured from the width of the vessels before 3rd bifurcation from the origin of optic disc

Follow each vessel as far to the periphery as you can look for any abnormalities such as venous dilatation, AV nipping,etc

To examine the periphery, ask the patient to:o Look up for examination of the superior retinao Look down for inferior retinao Look temporally for temporal retinao Look nasally for nasal retina

Lastly, locate the macula which is approximately 2 disc diameters temporally from the optic disc, between the superotemporal and inferotemporal vessels. Or you can ask the patient to look at the light of the ophthalmoscope, which would put the macula in good view. Look for abnormalities. Red filter facilitates the view of the macula

For the examination of the left eye, the same procedure can be repeated, but with left hand and left eye on the left side



LEARNING TASK BASIC CLINICAL SKILL OPHTHALMOLOGY

A. Please demonstrate the subjective visual acuity examinationB. Please demonstrate how to external inspection of anterior segment C. Please demonstrate how to measure intraocular pressure using Palpation and

Schiotz tonometry D. Please demonstrate how to apply eye drops E. Please demonstrate how to apply eye ointment F. Please demonstrate how to remove foreign body from the conjunctiva and corneaG. Please demonstrate how to examine the posterior segment using direk

ophthalmoscope



Article Review Assessments Form

Block of Visual system and Disorders

Name :…………………………………………..Student Reg. Number :…………………………………………..Facilitator :…………………………………………..Title :…………………………………………..

Time Table of Consultation

No Point of Discussion Date Supervisor Sign1 Outline of Paper2 Final Discussion

No Item Assessment Range Score (%) Score1 Ability to find the literature 0-202 Communication/attitude/presentation 0-303 Quality of material (SOAP) 0-404 Student interest and motivation 0-10

TOTAL 100Facilitator,

(………………………………………)NIP

No Item Assessment Range Score (%) Score1 Quality of material 0-602 Capability of Information Searching 0-103 Critical Thinking 0-30

TOTAL 100Evaluator/Supervisor,

(………………………………………)NIP



CURRICULUM MAPSmstr Program or curriculum blocks

10 Senior Clerkship9 Senior Clerkship8 Senior Clerkship

7Health System-based Practice(3 weeks)BCS (1 weeks)

Community-based practice(4 weeks)

Evidence-based Medical Practice(2 weeks)Special topics :Health Ergonomy & Health Environment(2 weeks)

Elective StudyIV (evaluation)

(3 weeks)

Comprehensive Clinic Orientation (Clerkship)+ medical ethic(4 weeks)

19 weeks

6The Cardiovascular System and Disorders(3 weeks)BCS (1 weeks)

Medical Emergency(2 weeks)

BCS (1 weeks)

The Urinary System and Disorders(3 weeks)BCS (1 weeks)

The Reproductive System and Disorders (4 weeks)BCS (1 weeks)

Elective StudyIII

(3 weeks)

19 weeks

5Neuroscience andneurologicaldisorders(3 weeks)BCS (1 weeks)

The Respiratory System and Disorders(4 weeks)

BCS (1 weeks)

The skin & hearing system& disorders(3 weeks)

BCS (1 weeks)

Special Topic : - Palliative med- Complemnt & Alternative Med.- Forensic(3 weeks)

Elective Study II(2 weeks)

18 weeks

4Musculoskeletal system &connective tissue disorders(3 weeks)BCS (1 weeks)

Alimentary & hepatobiliary systems & disorders(3 Weeks)

BCS (1 weeks)

The Endocrine System, Metabolism and Disorders(4 weeks)BCS (1 weeks)

Clinical Nutrition and Disorders(2 weeks)

BCS (1 weeks)

The Visualsystem &disorders(2 weeks)

BCS (1weeks)

19 weeks

3Basic microbiology & parasitology(3 weeks)Basic Infection & infectiousdiseases(3 weeks)BCS (1 weeks)

Immune system &disorders(2 weeks)

BCS (1 weeks)

Hematologicsystem & disorder & clinical oncology(3 weeks)BCS (1 weeks)

Special Topic- Andro & aging- Geriatri-Travel medicine (4 weeks)

Basic Pharmaceutical medicine & drug etics

(1 weeks)

19 weeks

2Medicalcommunication(3 weeks)Basic pharmacology(2 weeks)BCS (1 weeks)

Medical Professionalism(2 weeks) + medical ethic (1 weeks)Basic Anatomy Pathology & Clinical pathology (3 weeks)BCS (1 weeks)

Behavior Changeand disorders(3 weeks)

BCS (1 weeks)

Elective Study I(2 weeks)

19 weeks

1Studium Generale and Humaniora(2 weeks)

Basic Anatomy ( 4 weeks) Pratikum Anatomy(1 Weeks)

The cellas bioche-mical machinery(2 weeks)

Basic Histology (2 weeks) & Basic Physiology(2 weeks)BCS (1 weeks)

Growth &development(2 weeks)

Basic Biochemistry (2 weeks)BCS (1 weeks)

19 weeks

Pendidikan Pancasila & Kewarganegaraan ( 3 weeks )


CURRICULUM - Fakultas Kedokteran Udayana | Just ... · Web viewMoore.K.L, Agar A.M.R :...

Documents

Transcript of CURRICULUM - Fakultas Kedokteran Udayana | Just ... · Web viewMoore.K.L, Agar A.M.R :...