Biomedical subjects

F Fitzke

Publications and source records attributed to F Fitzke.

17 recordsLinked to original sources

PubMed2005

Pars plana vitrectomy for diabetic macular oedema: OCT and functional correlations.

PURPOSE: A prospective study to evaluate the macular structural and functional effects of pars plana vitrectomy (PPV) for persistent diffuse clinically significant macular oedema (CSMO). METHOD: A total of 12 patients with persistent diffuse CSMO were recruited and underwent assessment including best-corrected visual acuity, fundus fluorescein angiography, optical coherence tomography (OCT) and fine matrix mapping (FMM) at baseline and over a period of a year poststandard three-port PPV. RESULTS: The median baseline ETDRS letters score for all 12 patients was 52 (range 41-63) while at 12 months it had increased to 65 (range of 27-68), an improvement of two complete ETDRS lines (P=0.037). Similarly, there was an improvement in the perifoveal cone thresholds (P=0.02). The foveal thickening for all 12 patients ranged from a median of 183 to 751 microm (normal range 126-180 microm) and the macular volume ranged from a median of 2.13 to 6.42 mm(3) (normal <1.66 mm(3)). After surgery, both the median foveal thickness (from 334 to 280 microm) and median macular volume (from 3.24 to 2.61 mm(3)) demonstrated decreases over 12 months (P=0.01). On baseline OCT, the patients fell into two anatomically distinct groups: Group 1 (n=4) had a dome-shaped thickened macula with a partial posterior hyaloid separation and a significantly higher foveal thickness and macular volume than Group 2 (n=8) which had a diffuse low-elevation profile of the thickened macula (P=0.007). CONCLUSIONS: In this prospective study of PPV for persistent fovea-involving CSMO there was structural and functional improvement.

Aged↗

PubMed2005

Diabetic macular oedema: pilot randomised trial of pars plana vitrectomy vs macular argon photocoagulation.

INTRODUCTION: Focal macular photocoagulation for clinically significant macular oedema (CSME) is the proven method for treatment of this condition, but with little chance of visual improvement. Pars plana vitrectomy (PPV) may produce resolution of macular oedema and improvement in visual acuity. However, there have been no randomised trials to ascertain role of vitrectomy in the management of persistent CSME. METHODS: Patients with persistent CSME despite previous macular photocoagulation and Snellen visual acuity 6/15 to 6/60 were recruited. Dilated fundoscopy, best-corrected visual acuity including Early Treatment Diabetic Retinopathy Study (ETDRS) vision, ocular coherence tomography and fundus fluorescein angiography (FFA) at baseline and up to 12 months post-treatment was performed. Exclusion criteria were signs of posterior vitreous detachment, macular traction or the taut posterior hyaloid face syndrome, or macular ischaemia on FFA. In all, 20 patients were randomised (10 in each arm) to either standard macular photocoagulation or PPV and removal of the posterior hyaloid face. RESULTS: Of the 20 patients recruited, seven patients completed the protocol in the vitrectomy and eight in the laser arms, respectively. There was little evidence of any difference in the foveal thickness at 12 months between the two treatment arms despite a gradual improvement. Only one patient, from the vitrectomy arm, suffered moderate visual loss (defined as loss of 15 ETDRS letters) (our primary outcome). DISCUSSION: In this pilot RCT, standard PPV provides little visual benefit compared to macular photocoagulation, but a larger definitive study is required to confirm this early appraisal.

Aged↗

PubMed2003

Macular pigment: quantitative analysis on autofluorescence images.

BACKGROUND: Macular pigment (MP) reduces oxidative damage in the central retina and can be quantified by flicker-photometric analysis (HFP) of MP optical density. These analyses demonstrate a very good correlation with central absorption by MP on autofluorescence (AF) images. With these techniques different types of MP-distribution have been described. In the present study a quantification analysis of MP in AF images was developed to verify these MP types and to compare MP distribution patterns between healthy individuals and those with age-related macular degeneration (AMD). METHODS: AF images (HRA) were analysed with respect to the area of central and paracentral absorption in 400 eyes with a computerised analysis program of MP optical density. The patients were between 41 and 90 years old (mean 67.2 years); 168 were male and 232 female, and 253 had early AMD and 147 showed no AMD characteristics. The central MP concentrations (peak) were measured, the amount of MP values within the first 8-pixel radius ("C"), the total amount of MP within a 120-pixel radius ("T") were calculated as the volume of the MP values over the regarded radius and the C/T ratio was registered. RESULTS: Four types of MP distribution (type 1, intense central and paracentral MP; type 2, less intense central and paracentral MP; type 3, only central MP; type 4, only paracentral MP) were identified. The differences in MP distribution were confirmed and clearly characterised by quantitative analyses of peak, total MP ("T"), central MP ("C") and C/T ratio: mean peak in type 1, 0.65; type 2, 0.42; type 3, 0.42; type 4, 0.29; mean total amount of MP in 120-pixel radius ("T") in type 1, 5829.0; type 2, 4412.5; type 3, 2709; type 4, 4302.8. MP types with lower levels of MP were significantly more often observed in the AMD group (AMD: type 1, 120=47.4%; types 2-4, 133=52.6%; healthy eyes: type 1, 112=76.2%; types 2-4, 35=23.8%) ( P<0.0001) CONCLUSIONS: Analysis of MP on AF images is a quantitative method for investigation of MP. With this method a wide variation in concentration and distribution of MP could be seen in the population. Four different types of MP distribution could be characterised and quantitatively distinguished. Reduced levels of MP seem to be associated with a higher risk of development of AMD as they were significantly more often observed in the AMD group. This strategy of quantitative MP analysis on AF images is easily practicable and may be used in further studies to investigate the role of MP as a potential risk factor for AMD.

Adult↗

PubMed2003

Genotype-phenotype correlation in British families with X linked congenital stationary night blindness.

AIM: To correlate the phenotype of X linked congenital stationary night blindness (CSNBX) with genotype. METHODS: 11 CSNB families were diagnosed with the X linked form of the disease by clinical evaluation and mutation detection in either the NYX or CACNA1F gene. Phenotype of the CSNBX patients was defined by clinical examination, psychophysical, and standardised electrophysiological testing. RESULTS: Comprehensive mutation screening identified NYX gene mutations in eight families and CACNA1F gene mutations in three families. Electrophysiological and psychophysical evidence of a functioning but impaired rod system was present in subjects from each genotype group, although the responses tended to be more severely affected in subjects with NYX gene mutations. Scotopic oscillatory potentials were absent in all subjects with NYX gene mutations while subnormal OFF responses were specific to subjects with CACNA1F gene mutations. CONCLUSIONS: NYX gene mutations were a more frequent cause of CSNBX than CACNA1F gene mutations in the 11 British families studied. As evidence of a functioning rod system was identified in the majority of subjects tested, the clinical phenotypes "complete" and "incomplete" do not correlate with genotype. Instead, electrophysiological indicators of inner retinal function, specifically the characteristics of scotopic oscillatory potentials, 30 Hz flicker and the OFF response, may prove more discriminatory.

Base Sequence↗

PubMed1995

Choroidal hypoperfusion in acute posterior multifocal placoid pigment epitheliopathy. An indocyanine green angiography study.

BACKGROUND: The pathogenesis of acute posterior multifocal placoid pigment epitheliopathy remains obscure. The placoid lesions and characteristic findings on fluorescein angiography have been interpreted as representing either primary disease of the retinal pigment epithelium or disease of the choroidal vasculature. This study used indocyanine green (ICG) choroidal videoangiography to investigate this controversy. METHODS: Sequential choroidal videoangiography was performed with ICG and a scanning laser ophthalmoscope on patients with acute posterior multifocal placoid pigment epitheliopathy. Image analysis was used to differentiate between masking and ischemia as to the cause of hypofluorescence on the angiograms. RESULTS: Indocyanine green angiograms of acute posterior multifocal placoid pigment epitheliopathy showed areas of hypofluorescence in both the early and late pictures that correlated with the placoid lesions. Image analysis identified these as areas of choroidal hypoperfusion. Successive films showed partial or complete resolution of these hypofluorescent areas. CONCLUSIONS: Indocyanine green choroidal videoangiography has shown choroidal hypoperfusion to underlie the pathogenesis of acute posterior multifocal placoid pigment epitheliopathy.

Acute Disease↗

PubMed1994

Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow gene.

BACKGROUND: Recently, mutations in the retinal degeneration slow (rds) gene which codes for peripherin-rds have been implicated as a cause of autosomal dominant retinitis pigmentosa. Because this gene is expressed in both rods and cones, mutations in the rds gene might be expected to cause degeneration affecting either the scotopic or photopic systems. Mutations at codon 172 of the rds gene have been identified in three families with autosomal dominantly inherited, progressive macular dystrophy. METHODS: Affected individuals underwent ophthalmic examination, scotopic perimetry, dark adaptometry, measurement of color-contrast sensitivity, and electroretinography to characterize the photoreceptor dysfunction. RESULTS: In all but one affected member, symptoms of progressive central visual loss developed in the third or fourth decade of life accompanied by central scotoma and well-demarcated atrophy of the retinal pigment epithelium and choriocapillaris of the macula. In general, cone and rod thresholds were elevated, and color-contrast sensitivity was absent in the central visual field. Peripherally, the scotopic sensitivities were normal, as was the recovery from bleach. Cone electroretinograms were diminished in amplitude, and delayed in all affected adults except one. Rod electroretinograms were normal or near normal in amplitude, and had normal implicit times. Affected asymptomatic children had macular changes, abnormal color-contrast sensitivity, and reduced pattern and cone electroretinograms. CONCLUSION: These results indicate that mutations in the rds gene can be expressed as a macular dystrophy, with evidence of primary cone dysfunction and preservation of peripheral rod function.

Adolescent↗

PubMed1994

Electrophysiology and psychophysics in ocular hypertension and glaucoma: evidence for different pathomechanisms in early glaucoma.

It is not clear whether glaucomatous optic nerve damage is the end result of one pathological process or whether there are several mechanisms by which the final disease is manifest. The use of electrophysiological and psychophysical tests which measure the function of specific subdivisions of the visual pathways have been shown to be of use in the early diagnosis of glaucoma. In addition these results may help to elucidate the mechanisms of loss of visual function in patients with early glaucoma. One hundred and ninety-three patients with ocular hypertension (intraocular pressure > 24 mmHg, with normal visual fields and optic discs), 30 with glaucoma and 35 controls underwent pattern electroretinogram (PERG), peripheral colour contrast thresholds, motion detection thresholds (MDT) and Humphrey automated visual fields at the same visit. For each test there was a significant proportion of patients with abnormal results as has been found in previous studies of these techniques. However, there was a significant lack of correlation between the groups with only a small number of patients having abnormalities on more than one test. Of the patients demonstrating abnormal PERGs, 36% had abnormal colour contrast and 32% abnormal MDT, but only 15% were abnormal on both tests. Early glaucomatous damage may be focal or diffuse in nature. Similarly there may be preferential damage to ganglion cells subserving different visual functions or damage at different retinal layers. The results lend support to these hypotheses and give further evidence that more than one pathomechanism may be involved early in the glaucomatous process.

Color Perception↗

PubMed1994

The role of light scatter in the degradation of visual performance before and after Nd:YAG capsulotomy.

The aim of this study was to determine whether capsulotomy size influences visual performance. Snellen visual acuity and forward light scatter (light scattered towards the patient's retina, but out of the focussed retinal image) measurements using simple computer graphics based on van den Berg's technique were used to measure visual performance. Twelve patients were studied: 4 had small central capsulotomies through undilated pupils and 8 had wide capsulotomies through dilated pupils. The two groups were matched for age and pre-laser Snellen acuity. Following treatment, both groups had equal improvements in Snellen acuity. There was only a significant (p < 0.001) improvement in forward light scatter readings in the group who received wide capsulotomies. Measurements of forward light scatter are more sensitive than Snellen acuity testing in demonstrating loss of visual performance in patients with media opacities. It is recommended that pupils are dilated prior to Nd:YAG capsulotomy if forward light scatter from capsule remnants and the consequent glare disability are to be minimised.

Aged↗

PubMed1994

The primary treatment trial: changes in the visual field analysis by computer-assisted perimetry.

Computer-assisted perimetry was performed 6-monthly on patients entered into the Primary Treatment Trial using the 30-2 program. Those patients with a minimum of five visual fields had pointwise linear regression analysis (Progressor) carried out. Two consecutive slopes significant at the 0.05 level were taken as evidence for change, either improvement or worsening. Forty-eight patients in the surgery group, 40 in the medical group and 20 in the laser group were suitable for analysis. A comparison of the eyes showing 'improvement' or 'worsening' in the surgery and medicine groups showed no difference between them. This lack occurred despite a significant difference in intraocular pressure between the two groups. The reasons for this lack of difference are discussed.

Diagnosis, Computer-Assisted↗

PubMed1994

[Sensitivity to glare before and after Nd:YAG capsulotomy. Comparison between small and large capsulotomy].

AIM OF THE STUDY: The aim of this study was to determine whether capsulotomy size influences visual performance. PATIENTS AND METHODS: Twenty eyes were included in this study and were divided into two groups: 10 eyes had small central capsulotomies without dilating the pupil, and 10 eyes had large capsulotomies through dilated pupils. We measured both, visual acuity and glare due to forward light scatter using a computer system. RESULTS: Following treatment both groups had equally significant (< 0.001) improvements in visual acuity. However, a significant (p < 0.001) improvement of glare due to forward light scatter was only observed in the eyes with a large size capsulotomy. CONCLUSIONS: Our study showed that measurements of forward light scatter are more sensitive than visual acuity testing in demonstrating loss of visual performance in patients with media opacities. It is recommended that pupils are dilated prior to Nd:YAG capsulotomy if forward light scatter from capsule remnants and the subsequent glare disability are to be minimised.

Aged↗

PubMed1994

Correlation of peripheral displacement thresholds and optic disc parameters in ocular hypertension.

Both peripheral displacement thresholds and measurement of optic disc parameters have been advocated in the early diagnosis of glaucoma at the stage before scotomata are detected on conventional visual field assessment. The peripheral movement displacement thresholds were measured in 50 eyes of 50 patients with ocular hypertension and a significant correlation was found with neuroretinal rim areas measured using a computerised image system. There was also a significant correlation with optic disc diameter but no correlation with cup-disc ratio. The results support the proposition that measurement of peripheral movement displacement thresholds may be a useful tool in the detection of early glaucomatous optic nerve damage.

Cohort Studies↗

PubMed1993

Corneal light scattering and visual performance in myopic individuals with spectacles, contact lenses, or excimer laser photorefractive keratectomy.

Corneal transparency and visual performance are currently receiving much attention after excimer laser surgery. To date, emphasis has been on comparison of eyes on which laser surgery has been performed to eyes with emmetropia. A more appropriate comparison should be between eyes on which laser surgery has been performed and eyes with other forms of correction for myopia. Forward-scattered light, back-scattered light, and visual acuity were investigated and data were collected from 35 myopic individuals with various types of correction for myopia (spectacles, hard and soft contact lenses, and excimer laser surgery). Forward-scattered light was measured by using a new computerized technique, back-scattered light was measured with a charge coupled device-camera system, and visual acuity was measured with a computerized system at various levels of contrast. Spectacles, hard contact lenses, and excimer laser surgery are all superior to soft contact lenses in terms of light scatter and low-contrast visual acuity and excimer laser photorefractive keratectomy produces comparable results to spectacles one year postoperatively. At low-contrast visual acuity, mean visual acuity was 2.45 minutes of arc for the spectacle wearers, 3.21 minutes of arc for the hard contact-lens wearers, and 5.04 minutes of arc for the soft contact-lens wearers. Excimer laser patients had a mean visual acuity of 9.04 minutes of arc three months postoperatively, and 2.53 minutes of arc after one year. A mean value of 2.4% contrast for forward light scatter was obtained for spectacle wearers compared with a level of 3.84% contrast for hard contact-lens wearers and 16.1% contrast for soft contact-lens wearers. The mean value for excimer laser patients was 20% contrast three months postoperatively and 2.1% contrast one year postoperatively.

Contact Lenses↗

PubMed1993

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy.

Mutations in the RDS gene, which encodes the photoreceptor glycoprotein peripherin, have been sought in families with autosomal dominant retinal dystrophies. A cysteine deletion at codon 118/119 is associated with retinitis pigmentosa in one. Three families with similar macular dystrophy have mutations at codon 172, arginine being substituted by tryptophan in two and by glutamine in one. A stop sequence at codon 258 exists in a family with adult vitelliform macular dystrophy. These findings demonstrate that both retinitis pigmentosa and macular dystrophies are caused by mutations in RDS and that the functional significance of certain amino-acids in peripherin-RDS may be different in cones and rods.

Adult↗

PubMed1993

Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study.

Twenty five symptomatic individuals and six asymptomatic obligate gene carriers from four families with autosomal dominant retinitis pigmentosa (adRP) showing apparent incomplete penetrance have been studied. Symptomatic individuals from three families showed early onset of night blindness, non-recordable rod electroretinograms, and marked elevation of both rod and cone thresholds in all subjects tested. In the fourth family, there was more variation in the age of onset of night blindness and some symptomatic individuals showed well preserved rod and cone function in some retinal areas. All asymptomatic individuals tested had evidence of mild abnormalities of rod and cone function, indicating that these families show marked variation in expressivity rather than true non-penetrance of the adRP gene. No mutations of the rhodopsin or RDS genes were found in these families and the precise genetic mutation(s) remain to be identified.

Adolescent↗

PubMed1992

A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa.

Recently it has been demonstrated that some families with autosomal dominant retinitis pigmentosa (adRP) have mutations in the rhodopsin gene while others do not. Previously we have identified six such mutations in seven adRP families in this laboratory, one of which was previously described in US patients. We now present a completed screen of the rhodopsin gene in a panel of 39 adRP families, by a rapid screening technique which will be of use for routine diagnosis. Nine different mutations were ultimately found, in a total of twelve of the 39 families. These include the six previously identified mutations, in codons 68-71, 190, 211, 255, 296 and 347, two new ones in codons 53 and 106, and another mutation first identified in a single US patient, in codon 58. Thus approximately 30% of adRP families have 'Rhodopsin RP' while the remainder probably have a defect elsewhere in the genome. Of those families in which rhodopsin mutations have been found, four have been classified D type, three as sectorial RP and the remainder are of uncertain classification. All families excluded from chromosome 3q by linkage have been classified R type. These data suggest a correlation between clinical sub-classification and the underlying rhodopsin/non-rhodopsin heterogeneity.

Amino Acid Sequence↗

PubMed1992

[Corneal opacity after photorefractive keratectomy with an excimer laser. Cause, objective measurement and functional consequences].

A marginal loss of corneal transparency or 'haze' is a phenomenon commonly experienced after photorefractive keratectomy using excimer lasers (193 nm). The putative causes of this phenomenon are the presence in the surgical site of (1) activated keratocytes, (2) vacuoles and (3) newly synthesized collagen. A CCD camera device was employed in order to measure the corneal transparency. Both scattered and reflected light in the slit image of patients' corneas was measured using polarizing filters and image analysis software. We observed an increase in reflected and scattered light until the second postoperative month, followed by a subsequent decline. However, the combined signal generated by reflected and scattered light showed a second increase at 4 months postoperatively, whereas the signal generated by scattered light alone stayed at lower levels. These objective measures of changes in corneal transparency were correlated with changes in visual performance using psychophysical tests measuring visual acuity at different contrast levels (100%, 20% and 5%). In all patients we observed a good correlation between the signal generated by scattered light alone and the reduction in the 5% contrast visual acuity performance. These disturbances in low contrast visual performance were only significant during the first 3-4 months postoperatively, and thereafter most patients returned to their preoperative value. Eighteen percent of our patients discontinued topical steroids postoperatively. No difference in corneal transparency was observed.

Adult↗

PubMed1982

Cyclic macular edema.

Three patients with macular edema noted that their vision improved during the course of the day. In one patient, a 25-year-old man, visual acuity improved from 20/40 to 20/30; in the second, a 53-year-old woman, it improved from 20/60 to 20/40; in the third, a 30-year-old man, it improved from 20/25 to 20/20. The Rayleigh match showed a wider divergence in color matches to test wavelengths during the morning hours in one patient. The Stiles-Crawford effect was abnormal in all three patients but showed no cyclic pattern. All three patients had difficulty with Arden plates, but no cyclic pattern was apparent. The cyclic change in visual acuity could not be corrected by a change in refraction and may have been the result of a change in the macular edema.

Adult↗