- •Foreword
- •Preface
- •Contributors
- •Contents
- •1. Epidemiology of Pediatric Strabismus
- •1.1 Introduction
- •1.2 Forms of Pediatric Strabismus
- •1.2.1 Esodeviations
- •1.2.1.1 Congenital Esotropia
- •1.2.1.2 Accommodative Esotropia
- •1.2.1.3 Acquired Nonaccommodative Esotropia
- •1.2.1.4 Abnormal Central Nervous System Esotropia
- •1.2.1.5 Sensory Esotropia
- •1.2.2 Exodeviations
- •1.2.2.1 Intermittent Exotropia
- •1.2.2.2 Congenital Exotropia
- •1.2.2.4 Abnormal Central Nervous System Exotropia
- •1.2.2.5 Sensory Exotropia
- •1.2.3 Hyperdeviations
- •1.3 Strabismus and Associated Conditions
- •1.4.1 Changes in Strabismus Prevalence
- •1.4.2 Changes in Strabismus Surgery Rates
- •1.5 Worldwide Incidence and Prevalence of Childhood Strabismus
- •1.6 Incidence of Adult Strabismus
- •References
- •2.1 Binocular Alignment System
- •2.1.2 Vergence Adaptation
- •2.1.3 Muscle Length Adaptation
- •2.2 Modeling the Binocular Alignment Control System
- •2.2.1 Breakdown of the Binocular Alignment Control System
- •2.2.4 Changes in Basic Muscle Length
- •2.2.6 Evidence Against the “Final Common Pathway”
- •2.3 Changes in Strabismus
- •2.3.1 Diagnostic Occlusion: And the Hazard of Prolonged Occlusion
- •2.3.2.1 Supporting Evidence for Bilateral Feedback Control of Muscle Lengths
- •2.4 Applications of Bilateral Feedback Control to Clinical Practice and to Future Research
- •References
- •3.1 Dissociated Eye Movements
- •3.2 Tonus and its relationship to infantile esotropia
- •3.5 Pathogenetic Role of Dissociated Eye Movements in Infantile Esotropia
- •References
- •4.1 Introduction
- •4.2.1 Binocular Correspondence: Anomalous, Normal, or Both?
- •4.3 MFS with Manifest Strabismus
- •4.3.1 Esotropia is the Most Common Form of MFS
- •4.3.2 Esotropia Allows for Better Binocular Vision
- •4.3.3 Esotropia is the Most Stable Form
- •4.4 Repairing and Producing MFS
- •4.4.1 Animal Models for the Study of MFS
- •References
- •5.1 Esotropia as the Major Type of Developmental Strabismus
- •5.1.2 Early Cerebral Damage as the Major Risk Factor
- •5.1.3 Cytotoxic Insults to Cerebral Fibers
- •5.1.5 Development of Binocular Visuomotor Behavior in Normal Infants
- •5.1.6 Development of Sensorial Fusion and Stereopsis
- •5.1.7 Development of Fusional Vergence and an Innate Convergence Bias
- •5.1.8 Development of Motion Sensitivity and Conjugate Eye Tracking (Pursuit/OKN)
- •5.1.9 Development and Maldevelopment of Cortical Binocular Connections
- •5.1.10 Binocular Connections Join Monocular Compartments Within Area V1 (Striate Cortex)
- •5.1.11 Too Few Cortical Binocular Connections in Strabismic Primate
- •5.1.12 Projections from Striate Cortex (Area V1) to Extrastriate Cortex (Areas MT/MST)
- •5.1.15 Persistent Nasalward Visuomotor Biases in Strabismic Primate
- •5.1.16 Repair of Strabismic Human Infants: The Historical Controversy
- •5.1.18 Timely Restoraion of Correlated Binocular Input: The Key to Repair
- •References
- •6. Neuroanatomical Strabismus
- •6.1 General Etiologies of Strabismus
- •6.2 Extraocular Myopathy
- •6.2.1 Primary EOM Myopathy
- •6.2.2 Immune Myopathy
- •6.2.4 Neoplastic Myositis
- •6.2.5 Traumatic Myopathy
- •6.3 Congenital Pulley Heterotopy
- •6.4 Acquired Pulley Heterotopy
- •6.5 “Divergence Paralysis” Esotropia
- •6.5.1 Vertical Strabismus Due to Sagging Eye Syndrome
- •6.5.2 Postsurgical and Traumatic Pulley Heterotopy
- •6.5.3 Axial High Myopia
- •6.6 Congenital Peripheral Neuropathy: The Congenital Cranial Dysinnervation Disorders (CCDDs)
- •6.6.1 Congenital Oculomotor (CN3) Palsy
- •6.6.3 Congenital Trochlear (CN4) Palsy
- •6.6.4 Duane’s Retraction Syndrome (DRS)
- •6.6.5 Moebius Syndrome
- •6.7 Acquired Motor Neuropathy
- •6.7.1 Oculomotor Palsy
- •6.7.2 Trochlear Palsy
- •6.7.3 Abducens Palsy
- •6.7.4 Inferior Oblique (IO) Palsy
- •6.8 Central Abnormalities of Vergence and Gaze
- •6.8.1 Developmental Esotropia and Exotropia
- •6.8.2 Cerebellar Disease
- •6.8.3 Horizontal Gaze Palsy and Progressive Scoliosis
- •References
- •7.1 Congenital Cranial Dysinnervation Disorders: Facts About Ocular Motility Disorders
- •7.1.1 The Concept of CCDDs: Ocular Motility Disorders as Neurodevelopmental Defects
- •7.1.1.1 Brainstem and Cranial Nerve Development
- •7.1.1.2 Single Disorders Representing CCDDs
- •7.1.1.3 Disorders Understood as CCDDs
- •7.2 Congenital Cranial Dysinnervation Disorders: Perspectives to Understand Ocular Motility Disorders
- •7.2.1.1 Brown Syndrome
- •Motility Findings
- •Saccadic Eye Movements
- •Comorbidity
- •Epidemiologic Features
- •Laterality
- •Sex Distribution
- •Incidence
- •Heredity
- •Potential Induction of the Syndrome
- •Radiologic Findings
- •Natural Course in Brown Syndrome
- •Intra-and Postoperative Findings
- •References
- •8.1 Amblyopia
- •8.2 What Is Screening?
- •8.2.1 Screening for Amblyopia, Strabismus, and/or Refractive Errors
- •8.2.1.1 Screening for Amblyopia
- •8.2.1.2 Screening for Strabismus
- •8.2.1.3 Screening for Refractive Error
- •8.2.1.4 Screening for Other Ocular Conditions
- •8.3 Screening Tests for Amblyopia, Strabismus, and/or Refractive Error
- •8.3.1 Vision Tests
- •8.3.3 Stereoacuity
- •8.3.4 Photoscreening and/or Autorefraction
- •8.3.6 Who Should Administer the Screening Program?
- •8.4 Treatment of Amblyopia
- •8.4.1 Type of Treatment
- •8.4.2 Refractive Adaptation
- •8.4.3 Conventional Occlusion
- •8.4.4 Pharmacological Occlusion
- •8.4.5 Optical Penalization
- •8.4.7 Treatment Compliance
- •8.4.8 Other Treatment Options for Amblyopia
- •8.4.9 Recurrence of Amblyopia Following Therapy
- •8.5 Quality of Life
- •8.5.1 The Impact of Amblyopia Upon HRQoL
- •8.5.3 Reading Speed and Reading Ability in Children with Amblyopia
- •8.5.4 Impact of Amblyopia Upon Education
- •8.5.6 The Impact of Strabismus Upon HRQoL
- •8.5.7 Critique of HRQoL Issues in Amblyopia
- •8.5.8 The Impact of the Condition or the Impact of Treatment?
- •References
- •9. The Brückner Test Revisited
- •9.1 Amblyopia and Amblyogenic Disorders
- •9.1.1 Early Detection of Amblyopia
- •9.1.2 Brückner’s Original Description
- •9.2.1 Physiology
- •9.2.2 Performance
- •9.2.3 Shortcomings and Pitfalls
- •9.3.1 Physiology
- •9.3.2 Performance
- •9.3.3 Possibilities and Limitations
- •9.4.1 Physiology
- •9.4.2 Performance
- •9.4.3 Possibilities and Limitations
- •9.5 Eye Movements with Alternating Illumination of the Pupils
- •References
- •10. Amblyopia Treatment 2009
- •10.1 Amblyopia Treatment 2009
- •10.1.1 Introduction
- •10.1.2 Epidemiology
- •10.1.3 Clinical Features of Amblyopia
- •10.1.4 Diagnosis of Amblyopia
- •10.1.5 Natural History
- •10.2 Amblyopia Management
- •10.2.1 Refractive Correction
- •10.2.2 Occlusion by Patching
- •10.2.3 Pharmacological Treatment with Atropine
- •10.2.4 Pharmacological Therapy Combined with a Plano Lens
- •10.3 Other Treatment Issues
- •10.3.1 Bilateral Refractive Amblyopia
- •10.3.3 Maintenance Therapy
- •10.4 Other Treatments
- •10.4.1 Filters
- •10.4.2 Levodopa/Carbidopa Adjunctive Therapy
- •10.5 Controversy
- •10.5.1 Optic Neuropathy Rather than Amblyopia
- •References
- •11.1 Introduction
- •11.1.2 Sensory or Motor Etiology
- •11.1.4 History
- •11.1.5 Outcome Parameters
- •11.2 Outcome of Surgery in the ELISSS
- •11.2.1 Reasons for the ELISSS
- •11.2.2 Summarized Methods of the ELISSS
- •11.2.3 Summarized Results of the ELISSS
- •11.2.4 Binocular Vision at Age Six
- •11.2.5 Horizontal Angle of Strabismus at Age Six
- •11.2.6 Alignment is Associated with Binocular Vision
- •11.3 Number of Operations and Spontaneous Reduction into Microstrabismus Without Surgery
- •11.3.1 The Number of Operations Per Child and the Reoperation Rate in the ELISSS
- •11.3.2 Reported Reoperation Rates
- •11.3.3 Test-Retest Reliability Studies
- •11.3.6 Spontaneous Reduction of the Angle
- •11.3.7 Predictors of Spontaneous Reduction into Microstrabismus
- •Appendix
- •References
- •12.1 Overview
- •12.1.2 Manifest Latent Nystagmus (MLN)
- •12.1.2.1 Clinical Characteristics of Manifest Latent Nystagmus (MLN)
- •12.1.3 Congenital Periodic Alternating Nystagmus (PAN)
- •12.1.3.1 Clinical characteristics of congenital periodic alternating nystagmus
- •12.2 Compensatory Mechanisms
- •12.2.1 Dampening by Versions
- •12.2.2 Dampening by Vergence
- •12.2.3 Anomalous Head Posture (AHP)
- •12.2.3.4 Measurement of AHP
- •12.2.3.6 Testing AHP at Near
- •12.3 Treatment
- •12.3.1 Optical Treatment
- •12.3.1.1 Refractive Correction
- •12.3.1.2 Spectacles and Contact Lenses (CL)
- •12.3.1.3 Prisms
- •12.3.1.4 Low Visual Aids
- •12.3.2 Medication
- •12.3.3 Acupuncture
- •12.3.4 Biofeedback
- •12.3.6 Surgical Treatment of Congenital Nystagmus
- •12.3.6.1 Management of Horizontal AHP
- •12.3.6.2 Management of Vertical AHP
- •12.3.6.3 Management of Head Tilt
- •Retro-Equatorial Recession of Horizontal Rectus Muscles
- •The Tenotomy Procedure
- •References
- •13.1 Dissociated Deviations
- •13.2 Surgical Alternatives to Treat Patients with DVD
- •13.2.1 Symmetric DVD with Good Bilateral Visual Acuity, with No Oblique Muscles Dysfunction
- •13.2.2 Bilateral DVD with Deep Unilateral Amblyopia
- •13.2.3 DVD with Inferior Oblique Overaction (IOOA) and V Pattern
- •13.2.4 DVD with Superior Oblique Overaction (SOOA) and A Pattern
- •13.2.5 Symmetric vs. Asymmetric Surgeries for DVD
- •13.3 Dissociated Horizontal Deviation
- •13.4 Dissociated Torsional Deviation. Head tilts in patients with Dissociated Strabismus
- •13.5 Conclusions
- •References
- •14.1 Introduction
- •14.2 Clinical and Theoretical Investigations
- •References
- •15.1 General Principles of Surgical Treatment in Paralytic Strabismus
- •15.1.1 Aims of Treatment
- •15.1.2 Timing of Surgery
- •15.1.3 Preoperative Assessment
- •15.1.4 Methods of Surgical Treatment
- •15.2 Third Nerve Palsy
- •15.2.1 Complete Third Nerve Palsy
- •15.2.2 Incomplete Third Nerve Palsy
- •15.3 Fourth Nerve Palsy
- •15.4 Sixth Nerve Palsy
- •References
- •16.1 Graves Orbitopathy (GO): Pathogenesis and Clinical Signs
- •16.1.1 Graves Orbitopathy is Part of a Systemic Disease: Graves Disease (GD)
- •16.1.2 Graves Orbitopathy−Clinical Signs
- •16.1.2.1 Clinical Changes Result in Typical Symptoms
- •16.1.3 Clinical Examination of GO
- •16.1.3.1 Signs of Activity
- •16.1.3.2 Assessing Severity of GO
- •16.1.3.3 Imaging
- •16.2 Natural History
- •16.3 Treatment of GO
- •16.3.1.1 Glucocorticoid Treatment
- •16.3.1.2 Orbital Radiotherapy
- •16.3.1.3 Combined Therapy: Glucocorticoids and Orbital Radiotherapy
- •16.3.1.4 Other Immunosuppressive Treatments and New Developments
- •16.3.2 Inactive Disease Stages
- •16.3.2.1 Orbital Decompression
- •16.3.2.2 Extraocular Muscle Surgery
- •16.3.2.3 Lid Surgery
- •16.4 Thyroid Dysfunction and GO
- •16.5.1 Relationship Between Cigarette Smoking and Graves Orbitopathy
- •16.5.2 Genetic Susceptibility
- •16.6 Special Situations
- •16.6.1 Euthyroid GO
- •16.6.2 Childhood GO
- •16.6.3 GO and Diabetes
- •References
who should conduct screening based upon personnel costs alone may not be appropriate.
Summary for the Clinician
■Content of vision screening programs vary widely. Most involve assessment of VA for which a large number of tests are available. The gold standard is a crowded logMAR-based test. Referral criteria should be specific for the test used.
■The use of photoscreeners and/or autorefractors in vision screening programs is not universal. The use of photoscreeners and/or autorefractors will have an impact upon the cost e ectiveness of screening.
■The inclusion of stereotests in pre-school vision screening programs could be questioned.
■Recommendations state that pre-school vision screening programs be conducted by orthoptists or by professionals trained and supported by orthoptists.
8.4 Treatment of Amblyopia
8.4 Treatment of Amblyopia |
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8.4.1 Type of Treatment
Amblyopia is treated by obscuring the image from the good eye to promote the use of the amblyopic eye. This can be achieved through occlusion treatment (patching or pharmacological occlusion, in the form of atropine), or through optical penalization. There are notable advantages and disadvantages to di erent treatment modalities in terms of compliance, ease of administration, and VA outcome. Comparison of studies investigating the e ectiveness of treatment of amblyopia is hindered, due to differing definitions of both “amblyopia” and “treatment success”. In addition, clinicians have long recognized that the amount of treatment prescribed and the amount of treatment actually undertaken may di er. Objective measurement of the amount of occlusion worn has been made possible with the introduction of occlusion dose monitors (ODM). ODMs were developed and validated by the Monitored Occlusion Treatment for Amblyopia Study (MOTAS) Cooperative (UK), and since then, have been used to examine whether there is a dose response to occlusion therapy.
8.4.2Refractive Adaptation
The clinical management of amblyopia is determined following careful consideration on a case-per-case basis, taking into account a number of factors including the type of amblyopia present, the patient’s age, and the level of VA in the amblyopic eye. Nonetheless, advances in evidence-based medicine have led to a number of recognized studies that have reinforced or altered clinical practice in the management of this condition. The Pediatric Eye Disease Investigator Group (PEDIG), based in the USA, is a multi-centre group dedicated to clinical research in strabismus, amblyopia and other eye disorders a ecting children. Funded by the National Eye Institute (NEI), this group has investigated many aspects of the clinical course of amblyopia and its treatment.The Monitored Occlusion Treatment of Amblyopia Study Cooperative (MOTAS Cooperative) is a multidisciplinary group of ophthalmologists, orthoptists, basic scientists, and statisticians dedicated to investigating amblyopia treatment. Based in London (UK), it is funded by the charities Guide Dogs for the Blind Association, and Fight for Sight. They have conducted two clinical trials to identify the response of amblyopia to occlusion therapy. Data from both the studies conducted by PEDIG and the MOTAS Cooperative have contributed to our understanding of the management of amblyopia.
One of the main concepts that have arisen over the recent years in amblyopia treatment is that of refractive adaptation (or “optical treatment of amblyopia” as it is sometimes known [26]. There has been increasing evidence to suggest that the treatment of amblyopia in the presence of refractive error should incorporate observation of VA following the prescription of glasses alone [26–29]. These studies report increases in VA in subjects such that some did not require any additional treatment for their amblyopia. Prior to such studies, it was uncertain whether observed improvements in VA achieved were the result of amblyopia therapy (i.e. occlusion) or due to glasses-wear alone.
It is becoming increasingly clear that refractive adaptation is a recognized period in amblyopia therapy. The time taken to reach this period, however, remains under debate. The MOTAS studies utilized a period of 18-week observation [27–29]; however, the PEDIG reported that 83% of their study group demonstrated stability of improvement in VA before 15 weeks, but one patient improved in 30 weeks [26]. Improvements in VA have been described to occur after 20 weeks, but not considerably, with the majority of improvement having occurred in weeks 4–12 [30].
One of the arguments supporting the notion of vision screening is the detection of bilateral refractive error.
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8 The Value of Screening for Amblyopia Revisited |
Wallace et al. [31], as part of the PEDIG study, examined the improvements in VA in children with bilateral refractive amblyopia aged between 3 and 10 years.They reported that correction of refractive error improved VA, with only
812% of the cohort requiring additional amblyopia therapy in the form of occlusion or atropine.
8.4.3Conventional Occlusion
Patching treatment is often initiated as the first-line approach in amblyopia therapy. One advantage of patching treatment is that the e ects are reversible; that is, once the patch is removed, the non-amblyopic eye is favored, which is not the case with pharmacological occlusion. Since the acknowledgement of refractive adaptation, it has been necessary to confirm that occlusion therapy is also e ective in the management of amblyopia.PEDIG compared the e ect of daily patching vs. a control group of amblyopes in children aged 3–7 years, following a period of refractive adaptation. An improvement in VA was observed in both the groups after 5 weeks, and as expected, a greater improvement was reported in the patched group [32].
The MOTAS Cooperative investigated the amount of occlusion required to improve VA and explored the doseresponse relationship in amblyopia therapy [28]. They found that most children required between 150 and 250h of occlusion, irrespective of the type of amblyopia present. Specific characteristics were observed to a ect the response, such as the age of the patient; where older children required a greater amount of occlusion to achieve similar gains in VA compared with their younger counterparts. Younger children have been observed to respond more quickly and with less occlusion than older children; however, the final level of VA achieved has been similar for all ages [29].
Traditionally, clinicians have recommended near-visual activities whilst occlusion therapy is undertaken; however, there has been little research to justify such advice. The PEDIG investigated whether performing such activities influenced the improvement in VA outcome when treating amblyopia in conjunction with occlusion therapy [33]. No statistical evidence to support the notion that near visual activities improved VA outcome in their study group was found. It should be noted that the study group were prescribed only 2h of patching per day, and that the authors made no inference as to whether the results would be similar in subjects patched for a greater or lesser time.
One disadvantage of pharmacological occlusion is that the e ects are not readily reversible; it can take several weeks for the e ects of atropine to wear o . Concerns also exist regarding its e cacy as a treatment modality, with some clinicians believing it to be a less e ective treatment when compared with conventional occlusion. Studies conducted by PEDIG examined the e ectiveness of conventional occlusion vs. pharmacological occlusion in the treatment of moderate amblyopia (20/40–20/80) [34] and severe amblyopia (20/100–20/400) [35]. Either treatment modality was found to be appropriate with similar improvements in VA in either group. The decision towards which therapy should be adopted may now be based on other factors. One such factor may be the instillation of the atropine itself. The e ect of di erent atropine regimens in the treatment of moderate amblyopia (20/40– 20/80) was investigated.Comparisons were made between the observed e ects of daily atropine instillation and those of weekend-only atropine instillation [36]. Both groups were observed to show improvements in VA of similar magnitudes. It could be argued that the need for daily atropine instillation is redundant, thereby improving the therapeutic experience for the child. This in itself may encourage parents and/or clinicians to adopt this treatment modality.
8.4.5Optical Penalization
Another treatment option in the management of amblyopia is that of optical penalization. This is where lenses are used to induce a defocused image of the non-amblyopic eye. Tejedor and Ogallar [37] directly compared the e ects of atropine vs. optical penalization in the treatment of mild to moderate amblyopia (VA of at least 20/60). This small study found greater improvements in VA in the atropine group after 6 months of therapy, which may be attributed to the child peeking over or around the glasses and thereby not achieving the desired e ect of optical penalization. Although optical penalization remains a useful treatment option in specific clinical situations, it is often not considered as an appropriate firstline choice of therapy in the management of amblyopia.
8.4.6E ective Treatment of Amblyopia
in Older Children (Over the Age of 7 Years)
8.4.4Pharmacological Occlusion
Pharmacological occlusion (i.e. atropine) has notable benefits; it could be argued that it carries with it less of a social stigma compared with the wearing of an eye patch.
There has been strong evidence that treatment for amblyopia is more e ective prior to the age of 7 years. Despite this, amblyopia therapy has been reported to be successful in older children with either anisometropic [38–42] and/or strabismic amblyopia [40–42].Treatment
of strabismic amblyopia in the older child should be pursued with caution, as there is a notable risk of reducing the density of suppression, and thereby inducing intractable diplopia in these patients. A number of studies that reported on improvements in VA in older children with strabismic or mixed etiology amblyopia following treatment have not reported on whether the density of suppression had been measured, or if any other side-e ects had been observed [40–42]. Despite some evidence to suggest that successful treatment of amblyopia in the older child is possible, earlier intervention is more advantageous, and to that end supports the notion of pre-school vision screening.
8.4.7 Treatment Compliance
The successful management of amblyopia is intrinsically linked to treatment compliance and adherence to therapy. This in itself is multi-factorial in nature. The development and application of ODMs has meant that reasons for non-compliance can be more thoroughly investigated. In particular, ODMs have highlighted the discrepancy between the amount of occlusion prescribed and the amount administered. Clinicians have long recognized that the amount of occlusion carried out often falls short of their recommended treatment plan. Stewart et al. [29] reported on the e ect of 6 h a day occlusion compared with 12 h a day occlusion in the treatment of strabismic and/or anisometropia amblyopia. They found that the amount of occlusion received was 66 and 50% of their prescribed 6 and 12 h a day, respectively. Such information ought to be taken into account when prescribing occlusion therapy.
Loudon et al. [43] examined some of the limiting factors of occlusion therapy for amblyopia and reported that parental fluency in the national language and level of education were both predictors of low compliance. Parental understanding of the condition and treatment has also been reported as being an important factor in the successful management of amblyopia.
Adherence to treatment must be considered not only in terms of the child complying with therapy, but in the parent/guardian administering the treatment as advocated by the ophthalmologist and/or orthoptist. Searle et al. [44] found two variables that were significant predictors of compliance with occlusion therapy. They reported that self-e cacy (the belief in the ability to patch their child) was positively associated with treatment compliance. The parental belief that occlusion therapy inhibits the child’s activities was negatively associated with treatment compliance.
8.4 Treatment of Amblyopia |
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8.4.8Other Treatment Options for Amblyopia
The use of photorefractive keratectomy (PRK) for the treatment of anisometropia in children has not been fully investigated and concerns exist surrounding the longterm response to refractive surgery in terms of VA and corneal status. However, it could be postulated that if the amblyopic risk factor of high anisometropia is removed early, then the possibility of development of dense amblyopia would be reduced. Paysse et al. [45] reported the results of a small study of children with high anisometropia, and found improvements in both VA and stereopsis following treatment. However, compliance with amblyopia therapy remained una ected in this study group following treatment. The use of refractive surgery in children is not commonplace and there remains a need for a large randomized clinical trial to fully investigate the possible benefits of this form of treatment.
8.4.9Recurrence of Amblyopia Following Therapy
Recurrence of amblyopia has been observed in patients following the cessation of treatment, with rates varying widely. Some recent studies have sought to identify factors that may influence whether recurrence is likely to occur [46–49]. These include age of termination of treatment, VA at the time of cessation of treatment, and the type of amblyopia present. Recurrence in amblyopia was noted in 7–27%, with a low reported recurrence in children who underwent treatment after the age of 7 years [49]. Age of the child at the cessation of treatment does appear to be a factor, with recurrence inversely correlated with patient age [46].
Summary for the Clinician
■Treatment of amblyopia associated with refractive error should incorporate a period of observation with glasses-wear alone to allow for “refractive adaptation” or “optical treatment of amblyopia”. Improvements in VA can occur up to and beyond 20 weeks after glasses are prescribed, but most improvement occurs in weeks 4–12. In some cases, further amblyopia therapy may not be required.
■There is evidence to suggest that children who undergo amblyopia therapy at an early age respond more quickly to occlusion than older children, and require less occlusion in total.
