LETTERS TO THE JOURNAL

osity about the progress of my own macular degeneration, but now, in my seventies, I

should be happy to leave further development

and clinical trials to others who may think it worthwhile.

763

(Omega 5500) onto a screen to give an x 10

magnification, and the area of the optic disc

and disc pallor measured using a compensat­

ing planimeter and expressed as relative units. The reproducibility of duplicate measure­

Last year the local youth training work­

ments (expressed as coefficient of variation,

were sold in aid of the Macular Disease

2.5% for the colour measurements and 3.9 +

shop3 kindly made three dozen PPs which Society's Research Fund.

mean/standard deviation x 100%) was 4.2 +

2.9% for the red free measurements.

The area of optic disc pallor (expressed as a

E. R. Ellis, AE, CEng, MIMechE

Riverside Cottage,

percentage of optic disc area) was 36.6 +

21A City Walls,

16.5% for the colour photographs, and 38.1 +

Chester CH1 1SB.

16.2% for the red-free photographs. There

References

mean values (p

1

was no significant difference between the

A. Chopdar, FRCS, Department of Ophthalmology, East Surrey Hospital.

2

E.

Gowler,

Chairman

of

the

Macular

Disease

Society. 3

Cheshire County Council, County Youth Workshop, Ellesmere Port.

=

0.95). The Spearman rank

correlation co-efficient between the colour

and

red-free

pallor

areas

was

r

=

0.89

(p 0.0001). Subjectively there was little differ­

ence in the ease or difficulty with which the

pallor boundary was outlined with either the colour or red-free images.

Sir, Optic disc pallor measurement

The major ophthalmoscopic features of optic

Comment

nerve damage in glaucoma are pathological

Optic disc pallor area has previously been

studies indicate that the appearance of optic

roretinal rim areall and visual field 10ss!2 in

cupping and pallor of the disc.! Histological

disc pallor reflects loss of neural tissue and

changes in light transmission of the atrophic optic nerve.2.3 Thus disc pallor is a valuable

shown to be significantly correlated with neu­

glaucoma. Measurement of pallor area can be

made from monoscopic disc photographs and

this represents an advantage over neuroreti­

clinical sign in the assessment and manage­

nal rim area measurement, which requires

subjects. A number of different techniques

to get a true representation of depth at the

ing colorimetry,4 densitometry,S planimetry,6

nuclear sclerosis, can affect the colour of the

sis.s-IO A review of the methods used shows

and red-free fundus photographs. Circular

ment of ocular hypertensive and glaucoma

have been used to measure disc pallor includ­

photometr/ and computerised image analy­

that several of the studies used colour photo­

graphs,4,8,9 while others used black and white or monochromatic images.5.6,7,10

It is not

known how well the colour and monochro­

stereoscopic views (preferably simultaneous)

optic nerve head. Lens opacities, in particular

optic disc affecting the quality of both colour

light polarisers have been suggested as a means of improving the quality of fundus imaging in cataractous eyes.13 Similarly, lens

opacities affect the quality of stereoscopic disc

matic pallor measurements correspond. To

photographs making it difficult to get topo­

measured and correlated using colour and

field testing unreliable. The variety of tech­

address this, the area of optic disc pallor was red-free fundus photographs.

Optic disc colour photographs (Zeiss fun­

dus camera) of 25 ocular hypertensive and

glaucoma patients were used to give a wide

range of pallor values. The monochromatic

images were obtained by taking red-free photographs (Wratten 58 filter) of the colour

images. The 35 mm slides were projected

graphic measurements, and also make visual niques to measure pallor have used colour and monochromatic/black and white images inter­

changeably without knowing how well the colour and monochromatic pallor measure­

ments correlated. The results of this study

show that optic disc pallor area may be reliably and accurately measured from red­ free fundus photographs.

LETTERS TO THE JOURNAL

764

Colm O'Brien FRCS, FCOphth

factors which predispose to the development

Old Hall Street

been associated with maternal diabetes melli­

St Paul's Eye Hospital Liverpool L3 9PF

References 1

2

Schwartz B: Cupping and pallor of the optic disc. Arch Ophthalmol1973, 89: 272-7. Quigley HA and Anderson DR: The histological basis of optic disc pallor in experimental optic

3

atrophy. Am J Ophthalmol1977, 83: 709-17. Quigley HA, Hohman RM, Addicks EM: Quantita­ tive study of optic nerve head capillaries in experi­ mental optic disc pallor. Am J Ophthalmol1982, 93: 689-99.

4

Gloster]: Colorimetry of the optic disc. Trans Oph­ thalmol Soc UK 1973, 93: 243-9.

5

Schwartz B and Kern]: Scanning microdensitometry of optic disc pallor in glaucoma. Arch ophthalmol 1977,95: 2159-65.

6

Schwartz B, Reinstein NM, Lieberman DM: Pallor of the optic disc. Quantitative photographic eval­ uation. Arch Ophthalmol1973, 89: 278-86.

7

Robert Y and Hendrikson P: Color appearance of the papilla in normal and glaucomatous eyes. Arch Ophthalmol1984, 102: 1772-5.

8

Nagin P, Schwartz B, Nanba K: The reproducibility of computerised analysis for measuring optic disc pallor in the normal optic disc. Ophthalmology 1985,92: 243-51.

9 Miller ]M and Caprioli ]: Videographic quantifica­ tion of optic disc pallor. Invest Ophthalmol Vis Sci 10

1988,29: 320-3. Cox M] and Wood IC]: Computer-assisted optic nerve head assessment. Ophthalmol Physiol Opt

11

1991, 11: 27-35. Tuulonen A, Airaksinen P], Schwartz B et al: Corre­ lation of optic disc pallor and neuroretinal rim area in glaucoma and ocular hypertension. Invest

12

Ophthalmol Vis Sci1990,31: 566. Schwartz B: Correlation of pallor of optic disc with asymmetrical visual field loss in glaucoma. XXII

13

Concilium Ophthalmologicum 1974,2: 632-8. Fariza E, ]alkh AE, Thomas ]V, O'Day T, Peli E, Acosta ]: Use of circularly polarised light in fun­ dus and optic disc photography. Arch Ophthalmol 1988, 106: 1001-4.

of ONH are unknown. The condition has

tus/post-mature birth7, young maternal age,8 first born children9 and maternal ingestion of drugs during pregnancy, especially alcohol.

We have carried out a questionnaire survey

study involving the mothers of 27 patients

with bilateral ONH. Patients were identified

from the records of the Royal Hospital for

Sick Children in Glasgow which is a referral centre for a population of 2.5 million. The aim

of the study was to gather information regard­

ing the maternal history during pregnancy.

The study also included 65 mothers of age matched normal children. The main factors

reviewed

included

the

timing

birth,

smoking during pregnancy.

The results obtained regarding the timing

of birth demonstrated a slightly higher preva­

lence of both premature and post-mature

birth in the patient group, the latter result agreeing with a previous report of slightly

raised prevalence of post-maturity in children

with ONH.9 Our results were also, as in that

report, not statistically significant. Our results

which

demonstrated lower

maternal age in mothers of patients with

ONH (25.5 years compared to 27.4 years in the normal group) were in accordance with

previous reports.8,9 However, this difference

was not statistically significant (0.2

Optic disc pallor measurement.

LETTERS TO THE JOURNAL osity about the progress of my own macular degeneration, but now, in my seventies, I should be happy to leave further develop...
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