Topcon DRI OCT-1 Triton, DRI OCT-1 Triton plus User Manual

USER MANUAL 3D OPTICAL COHERENCE TOMOGRAPHY

DRI OCT-1

Model Triton

DRI OCT-1

Model Triton (plus)

INTRODUCTION

0123

CAUTION : Federal law restricts this device to the sale by or on the order of a physician.

Thank you for purchasing the TOPCON DRI OCT-1 Model Triton 3D Optical Coherence Tomography.

INTENDED USE / INDICATIONS FOR USE

The TOPCON DRI OCT-1 Model Triton is a non-contact, high-resolution tomographic and bio-microscopic imaging device. It is indicated for in-vivo viewing, axial cross-sectional and three dimensional imaging, and measurement of posterior ocular structures, including the retina, retinal nerve fiber layer, ganglion cell plus inner plexiform layer, ganglion cell complex, macula, optic nerve head, and choroid. The DRI OCT-1 Model Triton is intended for use as a diagnostic device to aid in the detection and management of ocular diseases including, but not limited to, macular holes, cystoid macular edema, diabetic retinopathy, age-related macular degeneration, and glaucoma.

FEATURES

This instrument is a special photography device to observe, photograph and record the image and tomogram of fundus and the image of anterior segment and to present its electronic image for diagnosis. By mounting the anterior segment attachment kit, which is an optional accessory, you can observe, photograph and record the tomogram of anterior segment. After photographing, the images and tomograms of fundus and anterior segment can be recorded in a personal computer where the analysis software is installed. This instrument is classified into two types depending on the combination of the installed functions:

DRI OCT-1 Model Triton:Not equipped with the FA photography function and with the FAF

photography function.

DRI OCT-1 Model Triton plus*:Equipped with the FA photography function and with the FAF

photography function.

(* "plus" is a catalog symbol.)

PURPOSE OF THIS MANUAL

This manual outlines the DRI OCT-1 Model Triton 3D Optical Coherence Tomography, including operating procedures, troubleshooting, maintenance and cleaning. Before using the instrument, carefully read the "DISPLAYS AND SYMBOLS FOR SAFE USE" and the "GENERAL SAFETY INFORMATION" to familiarize yourself with the features of the TOPCON DRI OCT-1 Model Triton 3D Optical Coherence Tomography and to ensure that you operate it safely. Always keep this User Manual at hand.

Trademarks

• Microsoft®, Windows®, Windows® 8.1, SQL Server® and Internet Explorer® are either registered trademarks or trademarks of Microsoft Corporation in the United States and/or other countries.

• Core™ i7 is trademark of Intel Corporation.

• IBM® is a registered trademark of International Business Machines Corporation.

* In general, other company names and product names in this manual are trademarks or the regis-

tered trademarks of those companies.

IPA Font License

IPA font is used in some parts for DRI OCT-1 Model Triton. Any and all terms and conditions of "IPA Font License Agreement v1.0" shall be deemed to be accepted and agreed by you if you use DRI OCT-1 Model Triton. For IPA Font License v1.0, refer to the following URL.

http://ipafont.ipa.go.jp/ipa_font_license_v1.html

1. No part of this manual may be copied or reprinted, in whole or in part, without prior written permission.

2. The contents of this manual are subject to change without prior notice and without legal obligation.

3. The contents of this manual are correct to the best of our knowledge. Please inform us of any ambiguous or erroneous descriptions, missing information, etc.

4. Original Instructions This manual was originally written in English.

CONTENTS

INTRODUCTION ......................................................................................................................... 1

DISPLAYS AND SYMBOLS FOR SAFE USE .................................................................... 5

GENERAL SAFETY INFORMATION .................................................................................... 6

HOW TO USE THIS MANUAL ................................................................................................ 8

GENERAL MAINTENANCE INFORMATION ...................................................................... 8

DISCLAIMERS ............................................................................................................................ 8

POSITIONS OF WARNING AND CAUTION INDICATIONS .......................................... 9

STANDARD ACCESSORIES ................................................................................................ 10

COMPONENTS .................................................................................................................................. 11

COMPONENT NAMES .................................................................................................................. 11

COMPOSITION OF PARTS WHICH CONTACT THE HUMAN BODY .......................................... 11

CONTROL PANEL COMPONENTS .............................................................................................. 12

OPERATION METHOD OF TOUCH DISPLAY .............................................................................. 13

NAMES ON THE TOUCH DISPLAY .............................................................................................. 14

PREPARATIONS ............................................................................................................................... 29

INSTALLING THE INSTRUMENT .................................................................................................. 29

CONNECTING THE POWER CORD ............................................................................................. 30

CONNECTING THE EXTERNAL DEVICE ..................................................................................... 31

RESET FROM POWER SAVE STATE .......................................................................................... 32

BASIC OPERATIONS ....................................................................................................................... 33

FLOW OF OPERATION ................................................................................................................. 33

PREPARATION FOR PHOTOGRAPHY ........................................................................................ 34

FUNDUS TOMOGRAPHY ............................................................................................................. 35

DELETING DATA ........................................................................................................................... 48

SAVING DATA ............................................................................................................................... 48

PRINTING DATA ............................................................................................................................ 48

HOW TO FINISH ............................................................................................................................ 49

OBJECTIVE OPERATIONS ............................................................................................................ 50

COLOR FUNDUS PHOTOGRAPHY .............................................................................................. 50

FUNDUS PERIPHERAL PHOTOGRAPHY .................................................................................... 54

STEREOSCOPIC PHOTOGRAPHY .............................................................................................. 56

FA PHOTOGRAPHY (DRI OCT-1 Model Triton plus) .................................................................... 60

FAF PHOTOGRAPHY (DRI OCT-1 Model Triton plus) .................................................................. 63

ANTERIOR SEGMENT TOMOGRAPHY ....................................................................................... 65

DETAILS OF THE SETTING MENU ............................................................................................. 73

MAINTENANCE ................................................................................................................................. 89

DAILY CHECKUPS ........................................................................................................................ 89

ORDERING CONSUMABLES ....................................................................................................... 89

REPLACING THE XENON LAMP ................................................................................................. 90

REFILLING THE Chinrest tissue .................................................................................................... 91

MAINTENANCE BY THE DEALER ................................................................................................ 91

CLEANING ........................................................................................................................................... 92

CLEANING THE EXTERNAL COVER, TOUCH DISPLAY AND OTHERS ................................... 92

CLEANING OF THE PARTS WHICH COME INTO CONTACT WITH THE PATIENT .................. 92

CLEANING THE TOUCH DISPLAY ............................................................................................... 92

CLEANING THE OBJECTIVE LENS ............................................................................................. 93

BEFORE REQUESTING SERVICE .............................................................................................. 94

TROUBLESHOOTING ................................................................................................................... 94

SPECIFICATIONS AND PERFORMANCE ............................................................................... 101

SYSTEM DIAGRAM ..................................................................................................................... 101

SPECIFICATIONS ....................................................................................................................... 102

OTHER SPECIFICATIONS .......................................................................................................... 103

SPECIFICATIONS OF THE PERSONAL COMPUTER (COMMERCIAL

PRODUCT) TO BE CONNECTED ............................................................................................... 104

SAFETY OF LED PRODUCT ....................................................................................................... 105

GENERAL INFORMATION ON USAGE AND MAINTENANCE ......................................... 108

INTENDED PATIENT POPULATION ........................................................................................... 108

INTENDED USER PROFILE ........................................................................................................ 108

ENVIRONMENTAL CONDITIONS FOR USE .............................................................................. 108

STORAGE, USAGE PERIOD ...................................................................................................... 108

ENVIRONMENTAL CONDITIONS FOR PACKAGING IN STORAGE ......................................... 108

ENVIRONMENTAL CONDITIONS FOR PACKAGING IN TRANSPORTATION ......................... 108

ELECTRIC RATING ..................................................................................................................... 109

DIMENSIONS AND WEIGHT ....................................................................................................... 109

SYSTEM CLASSIFICATION ........................................................................................................ 109

OPERATION PRINCIPLE ............................................................................................................ 110

CHECKPOINTS FOR MAINTENANCE ........................................................................................ 110

DISPOSAL ................................................................................................................................... 111

PATIENT’S ENVIRONMENT ....................................................................................................... 112

Requirements for the EXTERNAL DEVICE ................................................................................. 113

ELECTROMAGNETIC COMPATIBILITY ..................................................................................... 114

RELATION BETWEEN THE SETTING OF THE ILLUMINATION/FLASH LEVEL AND MAXIMUM RADIANCE

................................................................................................................... 118

OPTIONAL ACCESSORIES ......................................................................................................... 120

ANTERIOR SEGMENT ATTACHMENT KIT AA-1 ...................................................................... 120

REFERENCE MATERIAL .............................................................................................................. 121

TYPE OF PLUG ........................................................................................................................... 123

DRI OCT-1 Model Triton SOFTWARE LICENSE TERMS .................................................... 124

DISPLAYS AND SYMBOLS FOR SAFE USE

To encourage safe and proper use and to prevent injury to the operator and others or potential damage to property, important messages are put on the instrument body and inserted in the manual. We suggest that everyone understand the meaning of the following displays, icons and text before reading the "GENERAL SAFETY INFORMATION" and observe all listed instructions.

DISPLAY

Display Meaning

Situations in which the device should not be used because the

CONTRAINDICATION

WARNING

CAUTION

NOTE

risk of use clearly outweighs any possible benefit.

Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.

Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury.

Useful functions to know. Paying attention to these will prevent the noted problems.

SYMBOL

Symbol IEC/ISO Publication Description Description (French)

IEC 60417-5032 Alternating Current Courant alternatif

IEC 60417-5008

IEC 60417-5007

IEC 60878-02-02 Type B applied part Partie appliquée du Type B

ISO 7010-W001 General warning sign

ISO 7010-M002

ISO 7000-2497 Date of manufacture Date de fabrication

ISO 7000-2498 Serial number Numéro de série

Off (power: disconnection from the mains)

On (power: connection to the mains)

Refer to instruction manual/ booklet

Éteint (courant: coupure avec le secteur)

Allumé (courant: raccordement sur le secteur)

Symbole d'avertissement général

Voir le manuel/la brochure

ISO 7000-3082 Manufacturer Fabricant

ISO 15223-1

Authorised Representative in the European Community

Représentant autorité pour l’Union européenne

GENERAL SAFETY INFORMATION

CONTRAINDICATION

When used for red-free photography only, this instrument must not be used for the following patients.

• Patients who are hypersensitive to light

• Patients who recently underwent photodynamic therapy (PDT)

• Patients taking medication that causes photosensitivity.

WARNING

Ensuring the Safety of Patients and Operators

Be careful not to hit the patient's eyes or nose with the instrument during operation. The patient may be injured.

Handling the cord on this product or cords associated with accessories sold with this product, will expose you to lead, a chemical known to the State of California to cause birth detects or other reproductive harm.

Wash hands after handling.

Preventing Electric Shocks and Fires

To avoid fire and electric shock, install the instrument in a place free of water and other liquids.

To avoid fire and electric shock, do not put cups or vessels containing liquids near the instrument.

To avoid fire in the event of an instrument malfunction, immediately turn OFF ( ) the Power switch and unplug the cable if you see smoke coming from the instrument or if you detect other problems. Don't install the instrument where it is difficult to unplug the cable from the instrument body. Ask your dealer for repairs.

CAUTION

Ensuring the Safety of Patients and Operators

Use this instrument carefully on the following patients.

• Patients who have epidemic corneitis, conjunctivitis or any other infectious disease

• Patients who are taking medications that cause light hypersensitivity.

When operating the chin-rest up/down button, be careful not to pinch the patient's hand to avoid possible injury

To avoid injury of the patient, be careful not to bump the patient's eye or nose with the instrument when operating the touch panel.

Preventing Electric Shock

To avoid electric shock, do not insert metal objects into any vents and/or slots.

To avoid electric shock, do not open the instrument. Request service from an authorized Topcon distributor.

Do not put any substance over the vent on the top surface of the power supply unit. If the vent is covered, the temperature of the power supply unit may rise abnormally to cause a malfunction. To prevent the instrument from malfunction, do not drop any liquid into the vent.

Electromagnetic Compatibility (EMC)

This instrument has been tested (with 100V/120V/230V) and found to comply with IEC60601-1-2:

2007. This instrument radiates radio frequency energy within standard and may affect other devices in the vicinity. If you have discovered that turning on/off the instrument affects other devices, we recommend you change its position, keep a proper distance from other devices, or plug it into a different outlet. Please consult the dealer from whom you purchased the instrument if you have any additional questions.

HOW TO USE THIS MANUAL

• Read the instructions on pages 1 to 9 before using the machine.

• Regarding connection to various devices, see "CONNECTING THE EXTERNAL DEVICE"on page

31.

• If you would like an overview of the system, begin by reading "BASIC OPERATIONS" (page 33).

GENERAL MAINTENANCE INFORMATION

USER MAINTENANCE

To ensure the safety and performance of the instrument, all maintenance work, unless specified in this manual, shall be conducted by trained service engineers. The following maintenance tasks may be done by the user. For details, see the relevant part of this manual.

Cleaning the objective lens:

The objective lens may be cleaned by the user. For details, see "CLEANING THE OBJECTIVE LENS" on page 93.

DISCLAIMERS

• TOPCON shall not take any responsibility for damage due to fire, earthquakes, actions by third persons and other accidents, or damage due to negligence and misuse by the user and any use under unusual conditions.

• TOPCON shall not take any responsibility for damage derived from inability to properly use this instrument, such as loss of business profit and suspension of business.

• TOPCON shall not take any responsibility for damage caused from using this instrument in a manner other than that described in this Instruction Manual.

• Diagnoses made shall be the responsibility of pertaining doctors and TOPCON shall not take any responsibility for the results of such diagnoses.

• The customer shall take the responsibility to save data and perform backup in case data should be lost. When the customer has obtained data through this software and has saved or backed up the data in a server or personal computer, TOPCON shall not take any responsibility for the loss of the data, loss of profit or other damages on the customer.

POSITIONS OF WARNING AND CAUTION INDICATIONS

Optional accessory: Attachment kit for Anterior segment (Anterior segment lens unit)

To ensure safety, this machine provides warning displays. Use the instrument correctly by observing the display instructions. If any of the following display labels are missing, contact your TOPCON dealer at the address listed on the back cover.

No. Label Meaning Signification

WARNING

To avoid electric shock, do not open the instrument. Request service from an authorized Topcon distributor.

Pour éviter un choc électrique, ne pas ouvrir l'appareil. Demander le service d'un concessionaire autorisé de Topcon.

WARNING

When operating the chinrest up/down button, be careful not to pinch the patient's hand to avoid possible injury.

Quand vous fonctionnez le bouton pour élever/baisser le mentonniére, faire attention de ne pas pincer la main du patient, ce qui causerait une blessure.

CAUTION

To avoid potential injury during operation, do not touch the patient’s eyes or nose with the instrument.

Pour éviter une blessure pendant le fonctionnement, ne pas faire toucher l'appareil aux yeux ou au nez du patient.

CAUTION

To avoid injury of the patient, be careful not to bump the patient's eye or nose with the instrument when operating the touch panel.

CAUTIONCLASS 3B INVISIBLE LED RADIATION WHEN OPEN AVOID EXPOSURE TO THE BEAM.

Pour éviter une blessure du patient, faire attention de ne pas heurter les yeux ou le nez du patient contre l'appareil pendant le fonctionnement du touche-panneau.

ATTENTION RAYONNEMENT LED INVISIBLE DE CLASSE 3B - EN CAS D’OUVERTURE EXPOSITION AU FAISCEAU DANGEREUSE

CAUTION

To avoid injury, be careful not to pinch your fingers when operating the main unit up and down.

CLASS 1 LASER PRODUCT (IEC60825-1:2001)

Degree of protection against electric shock : TYPE B APPLIED PART

To avoid injury of the patient, be careful not to bump the patient's eye or nose with the lens unit when operating the instrument.

CAUTION

Pour éviter une blessure, faire attention de ne pas se pincer les doigts pendant le fonctionnement vers le haut et vers le bas de l’unité principale.

PRODUIT LASER DE CLASSE 1 (CEI60825-1:2001)

Degré de protection contre les chocs électriques : TYPE B PARTIE D'APPLICATION

Pour éviter une blessure, faire attention que l’unité de lentille ne heurte pas les yeux ou le nez du sujet pendant le fonctionnement de l’unité principale.

MISE EN GARDE

PRÉCAUTION

STANDARD ACCESSORIES

Upon unpacking, make sure that all the following standard accessories are included. Figures in ( ) are the quantities.

Power cord (1) Chinrest tissue (1) External fixation target (1)

Monitor cleaner (1) User manual, Unpacking and

Dust cover (1) assembly manual and Analysis software DVD (1 each)

UNPACKING AND ASSEMBLY MANUAL

3D OPTICAL COHERENCE TOMOGRAPHY

USER MANUAL

3D OPTICAL COHERENCE TOMOGRAPHY

DRI OCT-1

Model Triton

DRI OCT-1

Model Triton (plus)

DRI OCT-1

Model Triton

Accessory case (1) Chinrest tissue pins (2) LAN cable (1)

COMPONENTS

Main unit

Power supply unit

Chinrest unit

External fixation target

Diopter compensation lens selector

Focusing knob

Base clamping knob

Touch display

External connection terminal

External cover

Photography button Control lever

Vertical position mark

Sliding board

Power lamp

Forehead rest *1

Eye height mark

Forehead rest base

Chinrest tissue pin

Chinrest *1

Objective lens (Laser aperture)

Lamp house cover screw

Lamp house cover

*1: Contacting part (class B)

Power switch

Control panel

COMPONENT NAMES

COMPOSITION OF PARTS WHICH CONTACT THE HUMAN BODY

Forehead rest : Silicone rubber Chinrest : Acrylonitrile butadiene styrene resin Chinrest tissue : Paper Chinrest tissue pin : Polyamide resin

COMPONENTS

CONTROL PANEL COMPONENTS

Base clamping knob

Chinrest up/down button

Power lamp

Photography button

Internal fixation target position move button (Up/Down/Left/Right/Reset)

Small pupil diaphragm selector button

Split button

External fixation target selector button

Chinrest up/down button : Adjusts the chinrest up/down movement.

Internal fixation target

: Adjusts the internal fixation target position finely.

position move button

Power lamp : Displays "power ON" (this lamp is ON), "power OFF" (this lamp is

OFF) and "power save" (this lamp blinks).

Photography button : Starts photography.

Base clamping knob : Locks and unlocks the base.

Small pupil diaphragm

: Sets the small pupil diaphragm to ON/OFF.

selector button

Split button : Sets the split lines to ON/OFF.

External fixation target selector button

: Sets the external fixation target to ON/OFF.

COMPONENTS

OPERATION METHOD OF TOUCH DISPLAY

Tap → To select any relevant item.

Touch the screen softly with a finger.

Operate the touch display by your fingers. Don't use any sharp tool such as a

NOTE

ball point pen. The touch display may be damaged to cause an incorrect operation.

COMPONENTS

NAMES ON THE TOUCH DISPLAY

Capture icon display area

Patient ID display area

[SET UP] button

Message display area

Capture icon tab

[Follow-up] button

 Display areas and functions on the touch display

Information is displayed on the touch display and you can perform a variety of operations by touching the screen.

Capture icon selection screen



You can select the optimal mode for various types of photography.

Patient ID display area : Displays the patient ID. Capture icon tab : By selecting a tab, the capture icons registered in each tab are dis-

[SET UP] button : Shifts to the setting menu screen. Message display area : Displays the message. Capture icon display area : Displays the capture icons. [Follow-up] button : • Each time you press this button, "Follow-up ON" (button is orange)

played.

and "Follow-up OFF" (button is black) is changed each other. In case of "ON", Follow-up photography is done. In case of "OFF", it is not done.

• Follow-up photography is applied to the following cases.

• When selecting the photography icon to which Follow-up photography is unapplied, Follow-up photography is not done even if this button is set to "ON".

• When the [Follow-up] button is set to "ON", "Follow up" is displayed in yellow on the capture icon which is applicable to Follow-up photography.]

• Line ("12mm" is not the object of Follow-up photography.)

• 5 Line Cross

• Radial

COMPONENTS

Follow-up photography function in DRI OCT-1 Model Triton is as follows: the

処理中です。

しばらくお待ちください。

system searches the same scan position as the last photographed data* by using the live IR image of the present photography to decide the scan position.

NOTE

* "The last photographed data" means the data photographed at the date in the

past. The data captured at the same date as the present photography is not used for searching in Follow-up photography.

Reading the base line data for Follow-up photography

• Tap the photography icon (to which the Follow-up mode is applied) on condition that the [Follow-up mode] button is ON (orange). The system reads the last photography data (base line data) that is relevant to the entered patient ID and the selected photography icon.

• The following message is displayed when the relevant data does not exist.

• One eye data of the relevant data does not exist.

• Both eyes data of the relevant data does not exist.

COMPONENTS

Photography screen (OCT photography)

Tomogram live image area

Area 1

Area 2

Patient ID display area Timer button

Fundus/anterior segment live image area

Patients ID display area : Displays the patients ID. Timer button

(Only in DRI OCT-1 Model Triton plus)

Area 1 : Displays the operation mode buttons and changes the modes. Area 2 : Changes the internal fixation target and performs other operations. Tomogram live image area : Displays the tomogram live image. You can perform a variety of oper-

Fundus/anterior segment live image area

: Used in FA photography. (Refer to page 61.)

ations on the live image. (Refer to page 22.)

: This area displays the live image of fundus or anterior segment and

the graphic image of the scan pattern, which is set on the selected capture icon, with an interrupted line. The right/left eye, flash level and illumination level are displayed around the image. You can adjust the flash level and illumination level with the touch display. (Refer to page 20.) In the scan position adjustment mode, the scan position adjustment range and fine adjustment buttons are displayed. So you can adjust the scan position with the touch display. (Refer to page 39.)

COMPONENTS

Area 1

Menu button Capture mode button Preview mode button

Internal fixation target position selector button

Scan position button

Tracking button

Internal fixation target shape selector button

Color fundus photography button

FAF photography button

OCT-LFV image button

TRACKING

Area1 displays the operation mode buttons.You can change to each mode. The current operation mode is highlighted in orange. The mode that cannot be selected according to the current status is displayed in gray unclearly. The mode cannot be selected even if you touch the button in this status.

Menu button : Returns to the photography icon selection screen.

Capture mode button : Shifts to the photography screen to take a picture.

Preview mode button : It is displayed by highlight during a preview.

Area 2

In Area 2, set or change the internal fixation target and adjust the scan position. Set or change data with the buttons.

• Tracking button <"Line" scan/"Radial" scan/"5 Line Cross" scan>

Set the button to "ON". The system searches the position specified by the scan position adjustment mode according to IR image. In Follow-up photography, the tracking button is always ON and this status cannot be changed. The system searches the same position as the base line according to IR image.

• Color fundus photography button:

Displays the color fundus photography status (ON/OFF). You can change ON/OFF of color fundus photography.

• FAF photography button: (Only in DRI OCT-1 Model Triton plus)

Displays the FAF photography status (ON/OFF). You can change ON/OFF of FAF photography.

• OCT-LFV image button:

You can set whether the OCT-LFV image should be displayed on the live image. When "ON" is selected for "ON/OFF" after selecting "Setting menu" → "Page 2" → "OCT·FLV" → "ON/OFF", the tomogram is optimized and then "OFF" is changed to "ON" automatically. So the OCT-LFV image is displayed.

COMPONENTS

• Scan position button

* Displayed only in Radial/5 Line

Cross scan.

Scan possible range (red)

Fine adjustment button (right)

Fine adjustment button (down)

Fine adjustment button (left)

Scan pattern display (green and yellow)

Button to reset the change of position

Fine adjustment button (up)

Rotation button

* Displayed only in Line/5 Line Cross

scan.

Line 5 Line CrossRadial

The scan position adjustment mode is accessed. The selected scan pattern, the scan position adjustment range, the scan possible range (only in "Radial" and "5 Line Cross" scan) and other fine adjustment buttons are displayed on the fundus live image area.

Radial scan

5 Line Cross scan

Scan pattern display (green and yellow) Displays the graphic image of the scan pattern kinds. The green line shows the scan position, and the arrow shows the scan advance direction. (In case of "Radial" and "5 Line Cross", the arrow direction for the right eye is reversed for the left eye.) The yellow line is displayed for the scan pattern except "Line" . For "3D", the yellow line shows the scan range and, for other scan patterns, the scan position in addition to the position indicated by the green line. When scan is performed once, it is done at the positions indicated by the green and yellow lines.

COMPONENTS

Scan position adjustment range (blue) Displays the "Scan width × Scan width" range at the focal point on fundus. In the "Scan width × Scan width" range, it is easy to obtain the sufficient output sensitivity for tomograms.

Scan possible range (red) Displayed only for "5 Line Cross" and "Radial" scan patterns. This range shows the "12.0mm×

12.0mm" range at the focal point on fundus. This is the limit range where you can get a tomogram by using this instrument. If a tomogram exceeds the range indicated by the blue line, you cannot always get the sufficient output sensitivity because the pupil and others obstruct the photography.

Fine adjustment buttons (up/down/right/left) Each time you touch these buttons, the scan position is moved by about 0.03mm (on fundus) in the arrow direction.

Rotation buttons (clockwise/counterclockwise) Displayed only for "Line" and "5 Line Cross" scans. Each time you touch these buttons, the scan line is rotated by 1° in the arrow direction.

RESET button Press this button. The changes for the position, which were performed by the fine adjustment buttons and rotation buttons, are reset. The initial position is set again.

• Internal fixation target position selector button

When selecting the fundus capture icon, the internal fixation target position (one of "D", "C" and "M") is displayed according to the setting. The fixation target position is changed to "D", "C" and "M" in turn by touching this button. In "Wide" scan, "Wide" is fixed.

D (Disc): Optic disc is the center of the screen.

C (Center): The middle position between macula and optic disc is the center of the screen.

M (Macula): Macula is the center of the screen.

• Internal fixation target shape selector button

Displays the selected internal fixation target shape. You can select the internal fixation target shape among the following five shapes by pressing this button.

• 1 dot/4-dot rectangle/4-dot rhomb/×/cross

COMPONENTS

Fundus/anterior segment live image area

Right/left eye display

Live image

Flash level display

Scan pattern display (green and yellow) * Dotted line

Illumination level display

3D (H) Line

5 Line CrossRadial

This area displays the fundus live image, the right/left eye, illumination level and besides, the graphic image of the scan pattern, which is set on the selected capture icon, with an interrupted line. You can set ON/OFF of the illumination level by the touch display. In the scan position adjustment mode, the interrupted line of the scan pattern display is changed to the solid line display. The scan position adjustment range and fine adjustment buttons are displayed. You can adjust the scan position by the touch display.

• Live image:

Displays the fundus live image.

• Scan pattern display (green and yellow):

Displays the graphic image of the scan pattern, which is set on the selected capture icon. The green line shows the scan position, and the arrow shows the scan advance direction. (The arrow direction for the right eye is reversed for the left eye.) The yellow line is displayed for the scan pattern except "Line". For "3D", the yellow line shows the scan range and, for other scan patterns, the scan position in addition to the position indicated by the green line. When scan is performed once, it is done at the positions indicated by the green and yellow lines. The length and size of the lines are changed according to the set value of scan size.

• Right/left eye display:

COMPONENTS

In the case of left eye, "OS(L)" is displayed at the upper right position of the live image. In the case of right eye, "OD(R)" is displayed at the upper left position.

• Illumination level display:

Displays the illumination level (level) by five steps (value: 1 to 5). You can adjust the illumination level by touching the screen. (Refer to P.40.)

• Flash level display:

Displays the flash level (level) by nine steps (value: 1 to 9). You can adjust the flash level by touching the screen. (Refer to P. 40.)

• Tracking photography

The display color of the scan pattern on the IR fundus image shows whether tracking is successful or not in "Radial", "Line" and "5 Line Cross" scan.

• When tracking is OFF, the green dotted line is displayed.

• When the scan position is not specified on condition that tracking is ON or when the base is pulled forward, the yellow dotted line is displayed.

• After tracking is ON and the scan position is specified or when tracking is OK in Follow-up photography, the light blue solid line is displayed.

• After tracking is ON and the scan position is specified or when tracking is NG in Follow-up photography, the red solid line blinks.

COMPONENTS

Tomogram live image area

Stereoscopic image

[Image Quality] level meter

Image Quality value (IQV)

Z lock position display bar

Z lock position

[Optimize] button

[Manual] button

Live image

Z lock position is moved.

This area displays the tomogram live image. Perform the operation on the live image.

• Z lock position : Displays the center position of the displayed tomogram.

• Z lock position display bar : Indicates the Z lock position changeable range. By touching an

optional position on the bar, you can move the center position of the displayed tomogram to the touched position.

COMPONENTS

• Image Quality value (IQV) : Displays the "Image Quality" level with a value.

Optimize

Manual

• Image Quality value (IQV) is the image quality evaluation standard peculiar to TOPCON. IQV shows the image quality of the tomograms obtained by the DRI OCT-1 Model Triton with a value quantitatively. When you need a tomogram applicable to image analysis or other processing, the IQV must be 40 or

NOTE

higher. If the IQV is 40 or higher, the tomogram has a proper image quality. If the IQV is less than 40, image analysis can be performed for the tomogram but the reliability on the analysis result is reduced. So the tomogram is not applicable for analysis.

• If only the images of poor image quality are obtained, contact your dealer or TOPCON listed on the back cover.

• [Image Quality] level meter

• Live image : Displays the live tomogram image.

• Stereoscopic image : Displays the image of the anterior segment stereoscopic camera.

• [Optimize] button : After detecting the retina position automatically, this button optimizes

• [Manual] button : If the tomogram is not found automatically by the button, tap

When pressing the button, the Z lock position indicates the position

NOTE

against the reference mirror operating range. The Z lock position when pressing the button does not have the function to move the displayed tomo-

gram center position.

: Displays the "Image Quality" level with meter.

the image output sensitivity to display a clear tomogram. Moreover, this button performs the OCT auto focus operation according to the setting (default).

the button and operate the Z lock position. You can search the retina position.

COMPONENTS

Preview screen (OCT photography)

Tomogram preview area

Fundus photographed image

Scanned range

Delete button

Scan position (icon)

After OCT photography, the preview screen shown below appears.

Tomogram preview area : Previews the photographed tomograms.

When there are two or more images in "3D" or "Radial" scan, the typical image is displayed in this area. In "3D" scan, the two images at both ends are regarded as the typical images and, in "Radial" scan, the two images (vertical and horizontal) are regarded so. For each image, an icon that indicates the scan position is displayed.

Fundus photographed image : Displays the fundus image taken by each photographing action. Delete button : Deletes the photography result.

COMPONENTS

 Setting menu screen

Page forward/backward button

Capture icon tab

Icon layout setting area

Function button

Page number

Capture icon list

Menu selector button

[Add icon] button

[Delete icon] button

[Edit Tab name] button

[Edit Capture] button

[Reset to default] button

You can set many kinds of data for this instrument on this screen. On the capture icon selection screen, which is the initial screen, press the [SET UP] button. This screen appears.

• Capture select screen Set the icon display on the capture icon select screen and the parameters for each capture icon.

Function button : Saves and cancels the setting. Menu selector button : You can change the setting screens for the photography mode and for

Capture icon list : Displays all the capture icons. You can view the hidden capture icons

Page number : Displays the current setting menu page's number in page order. Icon layout setting area : Sets the icons that will be displayed on the Capture icon selection

Page forward/backward button

[Edit Capture] button : Shifts to the parameter setting screen to check and change the param-

Capture icon tab : Select a tab, and the photography icons, which are registered in each

the information to each other.

using the scroll bar at the right.

screen, which is the initial screen.

: Shifts to the other pages in the setting menu.

eters for the capture icon selected in the icon layout setting area.

tab, are displayed.

COMPONENTS

[Add icon] button : Adds the icon, which is selected on the capture icon list, to the icon

layout setting area. When you select a capture icon in the icon layout setting area, the icon is added to the left side or upper right corner of the capture icon.

[Delete icon] button : Deletes the capture icon, which is selected in the icon layout setting

area. After deleting, the remaining capture icons are placed in order

on the left. [Edit Tab name] button : Changes the name of the capture icon tab. [Reset to default] button : Returns the changed capture icon to the default.

COMPONENTS

•

Item name

Capture icon name

Item value selector button

OK button

Cancel button

Parameter setting screen Set the parameters for the capture icon selected in the icon layout setting area.

Display of the capture icon

: Displays the selected capture icon name.

name Item name : Displays the objective items of the parameters for the selected cap-

ture icon. Item value selector button : Displays the set value of each item. Select the desired item. OK button : Validates the changed contents and returns to the menu screen. Cancel button : Returns to the menu screen. The changed contents are not validated.

COMPONENTS

• Photography setting screen • Auto operation setting screen • System setting screen

Utility button

Function button

Page number

Item button

Item value display area

Page forward/backward button

You can set data about photography and system.

Function button : Saves and cancels the setting. Page number : Displays the current setting menu page's number in page order. Utility button : Displays the objective items on the current setting menu page.

Page forward/backward button

Item button : Changes the set status of the selected item. Item value display area : Displays the current set status of each item.

Select the desired item.

: Shifts to other pages in the setting menu.

COMPONENTS

+ 102 hidden pages

Topcon DRI OCT-1 Triton, DRI OCT-1 Triton plus User Manual

Specifications and Main Features

Frequently Asked Questions

User Manual

COMPONENTS

COMPONENT NAMES

COMPOSITION OF PARTS WHICH CONTACT THE HUMAN BODY

CONTROL PANEL COMPONENTS

OPERATION METHOD OF TOUCH DISPLAY

NAMES ON THE TOUCH DISPLAY