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Printed: April 2017
The Henson 9000 is manufactured in the United Kingdom by
Elektron Technology UK Ltd.
Broers Building
J.J. Thompson Avenue
Cambridge
Cambridgeshire
CB3 0FA
Tel : 01803 407 700
Fax : 01803 407 724
Email: info@elektron-healthcare.com
at our manufacturing site in Torquay.
Elektron Technology
Woodland road
Torquay
Devon
TQ2 7AY
Table of Contents
3Cont ent s
Part I
............................................................................................................... 81 Ele ktro n co mp a ny no tice s
............................................................................................................... 92 Impo rta nt w arnin gs
............................................................................................................... 103 Re visio n hist ory
............................................................................................................... 124 He lp /Man ua l info rma tion
............................................................................................................... 135 Ackn ow led ge me nt s
Part II
............................................................................................................... 151 Sin gle s timu lu s te st
............................................................................................................... 162 Multip le s timulus te s t
............................................................................................................... 173 ZATA th e s hold t es t
............................................................................................................... 184 Drive rs te st
Part III
............................................................................................................... 201 Sup ra -th re sh old te st s
............................................................................................................... 392 Za ta t hres ho ld te st
Welcome
Quick start
Visual field tests
Presenting and selecting different multiple stimulus
patterns
7
14
19
21Multiple stimulus
23Patient instructions
24
25Missed stimuli in multiple stimulus suprathreshold test
26Single stimulus
28Patient instructions
29Setting the test intensity
31Single stimulus algorithm
32Multiple Stimulus algorithm
33Test status indicator
34Extending the test
35Adding and correcting presentations
36Changing the supra-threshold increment
37Analysing the results
38Toolbar
41Blind spot
42Fovea measurement
43Global Indices
44Mean Defect
45Standard Deviation
46Hemifield Test
............................................................................................................... 643 Drive rs te sts
56GSS2
58Printing
59Patient instructions
60Stimulus locations
61Using existing patient details
63ZATA toolbar
65Patient Instructions
66Options
67Stimulus locations
Part IV
............................................................................................................... 711 P re pa ring t h e p atie nt
............................................................................................................... 752 Aut o t imin g
............................................................................................................... 763 C atch Tria ls
............................................................................................................... 774 C han ging e yes
............................................................................................................... 785 De mon stra tin g the t es t
............................................................................................................... 796 En te rin g t he p atie nt's da te o f b irth
............................................................................................................... 807 Fixa tio n t arg e ts
............................................................................................................... 818 He lp fa cilit y
............................................................................................................... 829 P rint ing th e re sults o f a fie ld te s t
............................................................................................................... 8410 Re spo ns e bu tto n
............................................................................................................... 8511 Sa ving visu al fie ld d ata
............................................................................................................... 8712 Vid eo ca me ra
Part V
............................................................................................................... 891 Add re ss
............................................................................................................... 902 Te s ts
............................................................................................................... 913 C omp ute r
............................................................................................................... 924 Da ta ba se
............................................................................................................... 945 Ba ckup
............................................................................................................... 966 Vid eo Se tup
............................................................................................................... 977 Int eg ra tio n
............................................................................................................... 988 P DF
............................................................................................................... 999 Sa ve /C ance l
General information
Options program
68
72Aligning the patient
73Patient Instructions
74Refractive correction
88
Part VI
............................................................................................................... 10 31 Ba cku p co py of th e da ta ba s e
............................................................................................................... 10 42 Cha nging th e a ctive d ata ba se
............................................................................................................... 10 53 De le ting a re co rd from t he d ata ba se
............................................................................................................... 10 64 Ed itin g d ata in th e da ta ba se
............................................................................................................... 10 75 Find ing a re co rd in th e d a ta ba se
............................................................................................................... 10 86 Mo vin g t hro ug h t he d ata ba se
............................................................................................................... 10 97 Ima ge file s
............................................................................................................... 11 08 Prin tin g a da tab as e re co rd
............................................................................................................... 11 19 Sa vin g re co rd s in d a ta ba se
............................................................................................................... 11 210 P ro gre ss io n An alysis
............................................................................................................... 11 811 Imp ort from s pre ad sh ee t
5Cont ent s
113Progression Screen
115Glaucoma Staging System: GSS II
117Printing
Part VII
............................................................................................................... 12 01 Op en ing a n e xis t ing vis ual fie ld d ata ba se
............................................................................................................... 12 12 Cre a tin g a n ew vis ua l fie ld d ata ba se
............................................................................................................... 12 23 Cop ying a vis ual fie ld d ata ba se
............................................................................................................... 12 34 De le ting a re co rd
............................................................................................................... 12 45 Me rg ing d ata ba se s
............................................................................................................... 12 56 Tra ns fe rring re co rd s b e tw e en da ta ba se s
............................................................................................................... 12 67 Imp orting d ata fro m a He ns on 5/60 00 Da ta ba se
Part VIII
Utilities program
Appendix 1 - 9000 Technical
specifi cation
Part IX
Appendix 2 - 9000
Connection details
Part X
Part XI
Appendix 3 - Instal lation
Appendix 4 - Maintenance
and warranty
............................................................................................................... 13 51 Reg ular ins pe ctio n an d ma int ena nce
............................................................................................................... 13 92 Up grad in g t he s oftw a re
............................................................................................................... 14 03 Cle an in g
............................................................................................................... 14 14 Preve nta tive main t en ance
............................................................................................................... 14 25 Rep la ce me nt pa rts
............................................................................................................... 14 36 Rep airs a nd re ca libra tio n
............................................................................................................... 14 47 Wa rra nty
119
127
130
131
134
Part XII
............................................................................................................... 14 61 Ba ckg ro und o ut of to le ra nce
............................................................................................................... 14 72 Bow l e rro r
............................................................................................................... 14 83 LE D e rro r
............................................................................................................... 14 94 Chinre st
............................................................................................................... 15 05 Key vio la tio n
............................................................................................................... 15 16 Dat ab as e e rro rs
The Henson 9000 is manufactured in the United Kingdom by
Elektron Technology Uk Ltd.,
Broers Building,
J.J. Thompson Avenue,
Cambridge.
CB3 0FA
The Henson unit must be used in accordance with the operating instructions.
Please read the instructions before attempting operation.
The instructions in this guide are to be view ed as an accompaniment to correct
training on this equipment.
Contact your sales agent for details of on-site training or contact the
manufacturer for details of training videos and webinar training sessions.
The results of a test are only to be analysed by a suitable qualified person, and
it is the responsibility of the practice manager/owner to ensure that only
suitably trained personnel are operating this equipment.
The only warranties for Elektron Technology UK Ltd. products and services are
set forth in the express warranty statements accompanying such products and
services. Nothing herein should be construed as constituting an additional
warranty.
This symbol on the product or on its packaging indicates that to
preserve the environment, this product must be recycled after its useful life as
required by law and must not be disposed of with your household or
commercial waste. It is your responsibility to dispose of your waste electrical
and electronic equipment by handing it over to a designated collection point for
the proper recycling of such equipment. The separate collection and recycling of
your waste equipment at the time of disposal will help to conserve natural
resources and ensure that it is recycled in a manner that protects human
health and the environment. For more information about the authorized
collection location nearest to you, please contact your local city office, your
household waste disposal service or the agent from whom you purchased the
product.
This unit must be
connected to an earthed
mains supply
Hazardous voltages are
present inside this unit.
No user-serviceable parts
inside
No modification of this
equipment is allow ed
This equipment is not
suitable for use in an
oxygen rich environment
The instrument is not
suitable for operation in
environments where
handling of fluids is
normal use.
This equipment should be
kept dry at all times
1. 2
Important warnings
Backing up your data
It is strongly recommended that you regularly back up the database of patient
records on a USB memory stick, or other suitable removable media, to avoid
any possibility of data loss.
This simple procedure is described later in this manual in Database Backup.
103
Allergy advice
The chin and head rest pads are made from a low allergy Silicone, but you
should check with the patient that the do not have an allergy to silicone before
allowing them to touch the Henson.
Changes to patient instructions in
the first person. Additional
formatting changes and
corrections.
Version 1.5
Novembe
r 2015
Added Progression information to
coincide with Version 3.4
Software release
Version 1.6
April
2017
Changes for Version 3.5 Softw are
release - addition of integration,
changes to Database images,
additional language support.
Henson Perimeter User Manual
1. 3
Revision history
To determine the version of installed software, click ABOUT on the main menu.
Info rma t io n fo r th e Ve rs io n 3 .5 re le as e
The release version of softw are called 3.5 contains some important changes to
the way the softw are operates. These may not affect your operation of the
instrument if you do not use the database or have any practice management
integration, but it is important that you understand them if you do.
The previous versions of the software stored a PDF copy of the printout
alongside the database in an images folder and this has now changed to a
jpeg picture file. The database will operate in the same way as before except
that the 2 eyes plots (threshold tests) are shown on different tabs.
The quality of the jpeg picture file can be set in the options program.
If you currently use the PDF file for another reason, and the Jpeg file cannot be
substituted then an additional PDF file can still be created when saving. The
location for this can be set in the options program (PDF tab)
Many of the images in this manual have 'hot spots'. If you place the cursor over
one of these and click then you will jump to a new page giving further
information on a topic.
Some of the screen shots in this manual may differ slightly from the software
installed on your machine.
The information contained in this manual is subject to change without notice.
All rights reserved. Reproduction, translation, or adaptation of this manual
without prior written permission of Elektron Technology UK Ltd. is prohibited,
except as allowed under copyright laws.
Elektron Technology UK Ltd. shall not be liable for technical or editorial errors or
omissions contained herein.
The following symbols are used in the manual and on the instrument.
The following visual field tests are available with the Henson 9000:
Multiple Stimulus Supra-Threshold: Choose this if speed is
21
important. It is approximately twice as fast as the Single Stimulus suprathreshold strategy in patients with little or no defect. This is a SemiAutomated test.
Single Stimulus Supra-Thresho ld: Choose this test to
26
screen large numbers of patients. This is a fully automated test where
the patient presses a response button every time they see a
84
stimulus.
ZATA(Zippy Adaptive Threshold Algorithm): This strategy replaces
39
the classic Full threshold algorithm. It is much faster than the Full and
Fast Threshold programs and will normally be the program of choice for
monitoring visual field loss. The ZATA program uses a Bayesian algorithm
and adaptive terminating criteria to make the best use of prior data. This
is a fully automated test where the patient presses a response button
84
every time they see a stimulus.
Drivers: The Drivers Test program is designed to see whether or
64
not a patient meets the UK DVLA visual field requirements for Group 1
and Group 2 driving. Again, this is a fully automated test where the
patient presses a response button every time they see a stimulus.
Multiple stimulus supra-threshold tests are used to rapidly screen the visual
field. Multiple stimulus tests are approximately twice as fast as a single stimulus
test. The multiple stimulus tests are semi-automated and require more
perimetrist involvement than the single stimulus tests. With a skilled perimetrist
this can result in more reliable results with less variability.
Each presentation is composed of a pattern of 2, 3 or 4 stimuli.
1. The patient tells the perimetrist how many stimuli they saw .
2. If they give the wrong number then the perimetrist should repeat the
presentation.
3. If on the second presentation the patient still reports the wrong
number, the perimetrist asks the patient where the stimuli they saw
were. Any missed stimuli are then marked as misses. It is often
35
useful when trying to establish which stimuli were missed to ask the
patient to report the clock hour positions of the seen stimuli.
4. If on the second presentation the patient reported the correct number
then the perimetrist should proceed to the next pattern. In this case it is
assumed that the error in the first presentation was a false one.
5. If there is some doubt, the perimetrist can re-present the pattern. There
is no limit to the number of times it can be presented.
Missed locations can be tested at higher intensity levels to quantify the
36
depth of any defect.
At the beginning of the test the threshold is determined. Stimuli are then
32
initially presented at 5dB above this threshold estimate.
The test has 3 levels, it starts testing just 26 points. It can be extended
3434
to 68 and 136 locations.
The test can be customised with the addition of extra stimulus locations.
35
To g et mo re h e lp o n a te s t s cre e n ite m click o ve r th e it em in th e ima g e b elo w .
3.1.1.2Pre se nt in g a nd s ele cting d iffere nt mu ltip le s timulus p att erns
The currently selected multiple stimulus pattern is displayed on the screen by
the red circles.
To present this pattern to the patient click Present or press the
space bar.
To go onto the next pattern click Fwd or press right arrow key on
keyboard.
To go back click Bwd or press left arrow key on keyboard.
All the patterns within the current test level are represented by a line of buttons
along the bottom of the screen:
To go to a specific pattern click the pattern button.
Each of the pattern buttons gives the number of stimuli in the pattern. This
number starts off in green and goes to black once the pattern has been
presented. If there is a missed stimulus in the selected pattern then the
number is shown in red.
When extending the test to a higher level, additional pattern buttons will
3.1.1.3Mis se d s timuli in mu ltip le s timulus s upra thre sh old te st
It is not unusual for a patient with no visual field loss to miss the occasional
stimulus. To differentiate between these and misses due to genuine field loss,
the pattern should be presented a second time.
If the incorrect number is given twice then establish which stimuli were missed
by:
1. Asking the patient where they saw stimuli. It is often helpful at this
stage to tell the patient to consider the bow l as a clock face and to give
the hour positions of the stimuli.
2. With the Miss button selected (down) click over the location of the
missed stimulus, or click the right mouse button when the cursor is over
the missed location.
To correct mistakes (i.e. remove stimuli marked as missed) make sure the Rmv
25Visual field tests
button is selected (down) and touch or click over the mistake.
Stimuli missed at a 5dB increment should be tested at a higher intensity
level.
The Supra-threshold tests present stimuli at intensities that are above the
patients estimated threshold. It uses one of 2 techniques to establish a
patients threshold:
Age related. The level is simply set by the age of the patient. This is
the fastest method but can lead to errors when a patient's threshold
departs from the average value for their age, e.g. when there are media
opacities.
Threshold related. The level is set by a series of measurements
taken at the onset of the test. The algorithm is different for Single
and Multiple stimulus tests.
32
When your machine was installed one of these techniques would have been
set as the default method, i.e. the method first selected when a suprathreshold test is undertaken. You can change the default method within the
Options program.
88
You can also opt to change the method at the onset of a test. For example, you
might want to regularly use the age setting method but then for a particular
patient, maybe one who has a cataract, want to set it according to their
threshold.
31
To select a different method at the onset of a test:
1. Click on the tool bar.
2. Select a method from the popup screen, see below, and then click OK.