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Clinical and experimental evidence that the pattern electroretinogram (PERG) is generated in more proximal retinal layers than the focal electroretinogram (FERG).

A TV monitor was used to evoke either a pattern ERG to a contrast-reversing checkerboard (PERG), or a focal ERG to alternate increases and decreases of luminance of the blank screen within a bright surround (FERG). Both responses are small (approx 2 microV) and fast (approx 50 msec to peak) and are similar in several other properties. However, they differ in timing and respond differently to changes in contrast. Each frame of a TV picture evokes a "raster ERG," even though the screen is blank. The response is focal and specific to a small central strip of the screen. It is simpler to record than the FERG, where the whole screen is flashing. Because the FERG summation area is about 4 deg, small squares (checks) reversing in contrast produce little luminance response. In 5 of 7 cases where the PERG is unilaterally reduced, the FERGs or raster responses were not affected. Thus clinical evidence also suggests that the PERG may be a separate phenomenon to the FERG and produced at a different site. Toxic, traumatic, congenital, and degenerative diseases of the optic nerve reduce the PERG. The comparison is most easily made in unilateral disease. Ten weeks after an optic nerve insult, the PERG becomes reduced in the affected eye as if retrograde degeneration was occurring. In 27 amblyopes of various types, the PERG was reduced in 23 where orthoptic treatment had failed. In 4 patients responding to treatment, PERGs of the amblyopic eye were as large as, or larger than, those of the fellow eye. The loss is greater with smaller checks. Retinal changes do occur after age 4 but so slowly that responses in heavily occluded eyes are not reduced. An additional level in the visual pathway is thus accessible to evoked potential investigation.

Amblyopia↗

Binocular vision after lens implantation.

Orthoptic tests for binocular vision were performed on 107 patients with intraocular lenses 3 to 10 months after surgery. The tests carried out were: cover test, Worth-test, Lang's two-pencil-test, the TNO-test and Lang's stereo-test. The implanted lenses were of the four-loop Binkhorst type. They were all implanted after planned extracapsular surgery. Visual acuity 3 to 10 months after operation was 0.5 or more in 95% of the patients (0.8 or more in 53% of the patients). Refraction in spheric equivalents was -0.7 +/- 1.26 diopters. The calculated optical aniseikonia was 2.2% +/- 1.8%. Orthotropia as disclosed by the unilateral cover-test prevailed in 81% of the patients. Most of the patients were exotrop (14 patients for the near, 6 patients for the near and the far). The results of Lang's two-pencil-test were positive in 89%. The Worth-test (polarized, for distance) showed suppression in 23% of the patients. The random-dot-test (TNO-test) showed positive results in 68% (retinal disparities 1980 arc seconds or less), in 57% (480 arc seconds or less), and the new Lang stereotest in 58% (1200 arc seconds or less) of the patients.

Diplopia↗

Dyslexia; ophthalmological aspects 1991.

Dyslexia or specific reading disability is an important and frequent handicap afflicting 5-10% of the population. It is basically a disorder of acquisition of written language, probably due to a poorly developed phonological awareness, which in turn may be neurologically related. As anatomical correlates symmetry of the planum temporale and ectopies in the cerebral cortex have been suggested. Functional correlates are discovered with brain electrical mapping and stimulation of brain structures during neuro surgery. From an ophthalmological point of view there are no relations between dyslexia and ocular problems including refractive errors and accommodation, problems of binocular control and stereopsis, eye dominance instability etc. However, contrast sensitivity seems to be reduced in dyslexics for the middle range of spatial frequencies, which may be related to impaired function of the 'transient' visual system. With regard to eye movements, there is no firm experimental proof for any disturbances in dyslexia, be it with the different movement systems or in the best movement direction. 'Backward saccades' or regressions are typical not only for dyslexic reading but in all types of reading when comprehension is poor. Although there is no treatment for dyslexia itself that can be based on ophthalmological findings, the ophthalmologist must after careful examination discover and treat any ocular, orthoptic or neuroophthalmological problem that may make reading difficult for the dyslexic child. The ophthalmologist must explain to the child and the parents that dyslexia usually has no ophthalmological or visual cause but is a disability with a neurobiological background, still unknown, in which the only efficient treatment is within the area of pedagogy.

Dyslexia↗

A controlled trial of parent initiated and conventional preschool health surveillance using personal child health records.

OBJECTIVES: A comparison of parent initiated preschool surveillance, using personal child health records, with the then current system of child health surveillance using child health records. DESIGN: Prospective, controlled trial with randomisation of five general practices into two groups. SETTING: Five general practices, a well baby clinic, and an orthoptic clinic at Yeovil District Hospital. SUBJECTS: 538 babies born between 1 April 1992 and 1 November 1994, from within the five general practices. MAIN OUTCOME MEASURES: The number of screenable abnormalities in the two groups that were missed in the first 3 years of a baby's life. RESULTS: 163 babies from the parent initiated preschool surveillance group and 107 from the conventional group completed the study. Although all the mothers from the parent initiated preschool surveillance group understood the concept of parent initiated surveillance, 117 stated their health visitor had made their appointments. Only 45 mothers made their own appointments. The abnormality rates were: 12 of 163 and eight of 107 at 1 year and nine of 163 and six of 107 at 3 years. No medically important conditions were missed. Most mothers did not want to make their own appointments because it was inconvenient. The system was unpopular with health visitors. CONCLUSION: Parent initiated preschool surveillance is as safe as the current system. Implementing the idea involved a small change in work practice and a large change conceptually for some of the primary health care team. It was not adopted in east Somerset.

Appointments and Schedules↗

Reduction of ocular muscle torque by splitting of the rectus muscle II: technique and results.

AIM: To present the results of a new technique that the authors have developed to weaken the extraocular muscles. The biomechanics of this technique, which is termed "Y-split recession," are given in the companion paper. METHODS: A retrospective study, testing the effects of a new surgical technique on strabismus, nystagmus, and visual acuity. 228 patients (aged 6.8 (SD 6.0) years) with variable angle strabismus and nystagmus were treated by splitting and detaching two rectus muscles, and re-attaching the two halves at an angle of about 65 degrees to each other. Subjects were examined with the usual orthoptic tests immediately after the operation, and up to 96 months later. RESULTS: The operation reduced the strabismus, eliminated or weakened the nystagmus in primary position, and improved binocular vision and the development of visual acuity. Only minor side effects were observed. CONCLUSIONS: The Y-split recession can be used to reduce the torque for extraocular rectus muscles, and provides an alternative to "Cuppers Fadenoperation," recession, and similar procedures.

Adolescent↗

In the absence of strabismus what constitutes a visual deficit in children?

AIM: To examine the range of monocular crowded logMAR acuity and cycloplegic refraction of children aged 3 years and 4 years without strabismus. METHODS: Data were collected prospectively. All children had full orthoptic and ophthalmic examination. Inclusion principally required the absence of strabismus, symptoms, and ocular pathology. Criteria were used to categorise the refraction findings as normal, borderline, or abnormal. RESULTS: 118 children aged 3 years (mean 3 years 6 months (SD 2 months) and 67 children aged 4 years (mean 4 years 4 months (SD 3 months) fulfilled the inclusion criteria. For the children with normal refraction, the mean monocular logMAR acuity was 0.200 (SD 0.09) for 3 year olds (n = 84) and 0.140 (SD 0.08) for 4 year olds (n = 45); the mean interocular acuity difference (IAD) was 0.03 (SD 0.06) for 3 year olds and 0.03 (SD 0.04) for 4 year olds. The 95% confidence limits were calculated for monocular acuity and IAD and compared to the acuity scores of the children with borderline (n = 17) and abnormal refractive error (n = 38). 15 borderline and 16 abnormal cases had a visual acuity within these limits. CONCLUSION: A wide range of refraction may be associated with a good level of visual acuity in children aged 3 years and 4 years.

Child, Preschool↗

Do infants of birth weight less than 1500 g require additional long term ophthalmic follow up?

AIM: To survey existing ophthalmic follow up protocols in the United Kingdom for very low birthweight (VLBW) children. In addition, relative risk analysis was performed using data from a cohort study to assess which factors (birth weight, gestational age, retinopathy of prematurity (ROP) status) led to a high risk of developing amblyogenic factors. METHODS: Questionnaires were sent to every orthoptic department in the United Kingdom (n = 288) for information on their policy on the follow up of VLBW children. RESULTS: Responses were received from 125 departments (43%). There was a large variation in criteria used for follow up; 21% of respondents using birth weight (BW) and gestational age (GA), 22% using stage 3 or treated ROP, the remainder using a combination of these factors. There was no consensus regarding when follow up should commence (from 3 months to 3 years) or cease (1-8 years). Relative risk analysis revealed that birth weight under 1500 g, GA under 33 weeks, and the presence of severe ROP were significant risk factors for developing one or more amblyogenic factors. CONCLUSION: There is no consensus on whether VLBW children need to be reviewed. There is a greatly increased risk of ophthalmic deficits in those with severe ROP or severe neurological disorders, and also in those with mild or no ROP. Children in the latter group who are not routinely followed up, have a high risk of developing treatable refractive errors and strabismus. This raises the question of whether an additional screening examination is merited.

Age Factors↗

Effect of refractive surgery on binocular vision and ocular alignment in patients with manifest or intermittent strabismus.

OBJECTIVE: To evaluate the effect of refractive surgery on binocular vision and ocular alignment in patients with manifest or intermittent strabismus, with or without vertical component. SETTING: University Hospital Antwerp, Edegem, Belgium. PATIENTS AND METHODS: 13 patients (22 eyes) with strabismus underwent refractive surgery. Five of these patients presented with an esotropia and four of them with a small vertical deviation. Five patients had a manifest exotropia, of whom two presented with a small vertical deviation. Two patients had an intermittent exotropia with binocular vision, of whom one patient had a vertical deviation. One patient had a hypertropia with a dissociated vertical deviation. RESULTS: Ocular alignment and binocular function remained unchanged postoperatively in all except two patients with high anisometropia who experienced an improvement in binocular function. In these patients, the preoperative manifest deviation became intermittent or latent after surgery, allowing fusion and stereopsis. Vertical deviation was found preoperatively in 8 of the 13 patients. This vertical deviation remained unchanged postoperatively, but improved in one patient with anisometropia. CONCLUSION: Preoperative intermittent or manifest strabismus is not a contraindication for refractive surgery provided some specific recommendations are taken into account, such as an adequate preoperative orthoptic examination and aiming at emmetropia for both eyes.

Adult↗

On the relationship between strabismic amblyopia and eccentric fixation.

Landolt C and grating acuity are compared with that normally expected of the eccentric fixation region for 10 strabismic amblyopes. The findings suggest that 2 populations of amblyopes exist. For some amblyopes visual function is that predicted of the eccentric region used for fixation, whereas for other amblyopes there is a further pathological reduction in visual function. These findings may have an important bearing on the type of orthoptic treatment used for amblyopia.

Adolescent↗

Acquired Brown's syndrome associated with Hurler-Scheie's syndrome.

A 5-year-old Caucasian girl with known Hurler-Scheie's syndrome (mucopolysaccharidosis) developed a right Brown's syndrome while under orthoptic review. There was no evidence of trauma or inflammation of the superior oblique tendon, trochlea, or surrounding tissues. The Brown's syndrome in this case may be due to shortening of the superior oblique tendon, associated with the shortening of long tendons of the arms and feet, which is common in Hurler-Scheie's syndrome.

Child, Preschool↗

Prospective multicentre study of the accuracy of surgery for horizontal strabismus.

Eight centres throughout the United Kingdom cooperated with a prospective evaluation of the accuracy of surgery for horizontal strabismus. The eight centres were divided into four with a specialist interest in strabismus and four offering a general ophthalmic service. Each participating surgeon was asked to indicate the anticipated outcome of surgery and, thereafter, orthoptic examinations were made post-operatively to determine the actual outcome. Two hundred and five cases were included in the study and it is hoped the results will serve as useful guidelines for those departments wishing to undertake audit of their own strabismus surgery. There was no statistically significant difference in the accuracy of surgical alignment achieved by strabismus specialists and general ophthalmologists.

Clinical Competence↗

Emmetropisation, axial length, and corneal topography in teenagers with Down's syndrome.

AIM: To study the refractive status and corneal topography in Down's syndrome. METHOD: A matched cohort subgroup of 50 individuals with Down's syndrome in the Manchester area aged 15-22 years was studied by refraction, corneal topography, A-scan biometry, slit lamp examination, and orthoptic examination. RESULTS: (1) A linear relation was found between axial length and spherical equivalent refraction. There was no statistical relation between keratometry and the axial length. (2) 80% of the group had a hyperopic refraction (mean +2.46 D, range +0.5 to +7.5 D); 18% were myopic (mean -2.75 D, range -0.5 to -8.0 D); and 2% were emmetropic (within plus or minus 0.5 D of zero). The overall mean spherical equivalent refraction was +1.43 (SD 2.86) D. 63% of eyes could see 6/12 or better and 66% of the individuals had a binocular vision of 6/12 or better. (3) Corneal topography was generally of a regular "bow tie" pattern, but there was a high incidence of oblique cylinders. Mean cylinder strength was 1.14 (1.15) D. (4) The prevalence of overt keratoconus was 2%. 6% had corneal topography with inferior steepening which may be a preclinical keratoconic process. CONCLUSIONS: In this cohort of late teenagers with Down's syndrome, emmetropisation has failed to occur in most individuals. In a similar aged group of non-disabled individuals one would expect about 83% emmetropic (plus or minus 0.25 D), 13% myopic, and 4% hyperopic. The wide spread of oblique cylinders and the small proportion of with the rule astigmatism is probably related to this failure of emmetropisation. The prevalence of 2% keratoconus in Down's syndrome compares with that found by other authors of between 5.5 and 15%. The 6% with inferior steepening on topography will be followed up over the next few years to see if there is any development of clinical keratoconus. Hence we will see if corneal topography is useful as a screening tool for preclinical keratoconus in this high risk group.

Adolescent↗

Movement hyperacuity in childhood amblyopia.

BACKGROUND: Amblyopia results in deficits in a number of visual functions in both the amblyopic and dominant eye. The present work describes oscillatory movement displacement thresholds (OMDT) in childhood amblyopia. METHODS: The OMDT from the dominant and amblyopic eyes of 50 orthoptic patients (aged 74 (SD 16) months) were compared with those from a group of 24 controls (79 (21) months). OMDT were measured using a forced choice staircase procedure. Subjects were asked to identify which of the computer controlled monitors displayed the oscillating stimulus. Visual acuity and stereoscopic responses were noted from clinical records. RESULTS: Amblyopic children demonstrating stereopsis showed no significant OMDT deficit in the amblyopic eye. Those children having no stereopsis had elevated OMDT in the amblyopic eye (p < 0.05). Results suggest that the dominant eye of children with amblyopia may also have a pattern of visual development which is anomalous (difference in correlation coefficient with age; p < 0.05). CONCLUSION: OMDT deficits demonstrated in some amblyopic eyes indicate that amblyopia is incompletely described by its "clinical" definition. Results suggest that the dominant eye in those with unilateral amblyopia may not be "normal".

Aging↗

Non-cycloplegic screening for amblyopia via refractive findings with the Nikon Retinomax hand held autorefractor in 3 year old kindergarten children.

AIMS: To assess non-cycloplegic screening for amblyopia with the hand held Nikon Retinomax autorefractor in 3 year old kindergarten children. METHODS: 427 three year old children were examined in kindergarten with the Retinomax without cycloplegia. A gold standard was established in all children by two orthoptic examinations in kindergarten. If there were missing, abnormal, or inconsistent findings, children were referred for ophthalmological examination. If, by the ophthalmological examination, a new case of amblyopia requiring treatment was diagnosed, the gold standard was set "positive." RESULTS: In 404 children the gold standard was obtained. 10 children (2.5%) had a "positive" gold standard of unknown and untreated amblyopia. Screening sensitivity was 0.80, specificity 0.58, accuracy 0.58, and the likelihood ratio 1.89. CONCLUSION: Non-cycloplegic refractive screening with the Retinomax led to many false positive referrals due to instrument myopia and "inconclusive" results. Hence specificity, accuracy, and the likelihood ratio were too low to conduct screening effectively.

Amblyopia↗

Differences in the management of amblyopia between European countries.

BACKGROUND: Amblyopia treatment is not standardised and differences between centres and countries have not been systematically investigated. This survey compares the different patterns of orthoptic treatment of amblyopia in the United Kingdom (UK) and three German speaking countries (GSC). METHODS: Questionnaires were sent to orthoptists in the UK and the GSC asking for their preferred choices of treatment of amblyopia between the ages of 6 months to 10 years. RESULTS: The following significant differences in management of amblyopia were found: (1) the number of hours of occlusion per week was higher in the GSC, p<0.0001, (2) orthoptists in the GSC treat amblyopia up to an older age. Orthoptists in the GSC and in the UK predicted similar treatment outcomes. CONCLUSION: Orthoptists in the GSC usually treat patients more intensively and for longer, while the prediction of visual outcome does not differ significantly between countries. These results highlight the lack of standardisation in the treatment of the various types of amblyopia.

Age Factors↗

The clinical features of albinism and their correlation with visual evoked potentials.

AIM: To investigate the relation between the clinical and electrophysiological abnormalities of patients undergoing visual evoked potential investigation for albinism. METHODS: 40 subjects with a probable or possible clinical diagnosis of albinism underwent pattern appearance and/or flash visual evoked potential (VEP) examination. The VEP findings are correlated with the clinical features of albinism determined by clinical examination and orthoptic assessment. RESULTS: The majority of patients with clinical evidence of albinism showed a contralateral predominance in the VEPs. There was close correlation between the clinical signs of albinism and the degree of contralateral VEP predominance. This manifested as an interhemispheric latency asymmetry to monocular pattern appearance stimulation but amplitude asymmetry to flash stimulation. The strongest correlation for pattern appearance interhemispheric latency difference was with foveal hypoplasia (rho = 0.58; p = 0.0003) followed by nystagmus (rho = 0.48; p = 0.0027) and iris transillumination (rho = 0.33; p = 0.039). The VEP abnormalities were of greater magnitude in those patients with most features of albinism. Several patients with apparently mild disorders of ocular pigmentation had small but significantly abnormal VEP latency asymmetries. CONCLUSION: There is a strong association between the magnitude of the interhemispheric latency asymmetry of the pattern appearance VEP, and of amplitude asymmetry of the flash VEP, with the clinical signs of albinism. The data are consistent with a spectrum of abnormalities in albinism involving both clinical expression and electrophysiological misrouting, which is wider than previously recognised.

Adolescent↗

Interaction of somatoform and vestibular disorders.

BACKGROUND: The high coincidence of organic vestibular and somatoform vertigo syndromes has appeared to support pathogenic models showing a strong linkage between them. It was hypothesised that a persisting vestibular dysfunction causes the development of anxiety disorders. OBJECTIVE: To determine the relation between vestibular deficits and somatoform vertigo disorders in an interdisciplinary prospective study. METHODS: Participants were divided into eight diagnostic groups: healthy volunteers (n=26) and patients with benign paroxysmal positioning vertigo (BPPV, n=11), vestibular neuritis (n=11), Menière's disease (n=7), vestibular migraine (n=15), anxiety (n=23), depression (n=12), or somatoform disorders (n=22). Neuro-otological diagnostic procedures included electro-oculography with rotatory and caloric testing, orthoptic examination with measurements of subjective visual vertical (SVV) and ocular torsion, and a neurological examination. Psychosomatic diagnostic procedures comprised interviews and psychometric instruments. RESULTS: Patients with BPPV (35.3%) and with vestibular neuritis (52.2%) had pathological test values on caloric irrigation (p<0.001). Otolith dysfunction with pathological tilts of SVV and ocular torsion was found only in patients with vestibular neuritis (p<0.001). Patients with Menière's disease, vestibular migraine, and psychiatric disorders showed normal parameters for vestibular testing but pathological values for psychometric measures. There was no correlation between pathological neurological and pathological psychometric parameters. CONCLUSIONS: High anxiety scores are not a result of vestibular deficits or dysfunction. Patients with Menière's disease and vestibular migraine but not vestibular deficits showed the highest psychiatric comorbidity. Thus the course of vertigo syndromes and the possibility of a pre-existing psychopathological personality should be considered pathogenic factors in any linkage between organic and psychometric vertigo syndromes.

Adult↗

Role of visual dysfunction in postural control in children with cerebral palsy.

INTRODUCTION: Deficient postural control is one of the key problems in cerebral palsy (CP). Little, however, is known about the specific nature of postural problems of children with CP, nor of the relation between abnormal posture and dysfunction of the visual system. AIM OF THE STUDY: To provide additional information on the association of abnormalities in postural control and visual dysfunction of the anterior or posterior part of the visual system. METHODS: Data resulting from ophthalmologic, orthoptic, neurological, neuro-radiological, and ethological investigations of more than 313 neurologically impaired children were retrospectively analyzed. RESULTS: Abnormal postural control related to ocular and ocular motor disorders consisted of anomalous head control and subsequent abnormal head posture and torticollis. The abnormal postural control related to retrochiasmatical damage of the visual system consisted of a torticollis combined with adjustment of the upper part of the body, as if at the same time adapting to a combination of defects and optimizing residual visual functions. CONCLUSION: Visual dysfunctions play a distinct role in the postural control of children with CP.

Adolescent↗