This document presents a case study of a 7-month-old male child brought to the pediatric ophthalmology clinic with watering and mucopurulent discharge from the left eye for 7 months. Examination found enlarged discs and asymmetric cupping between the eyes. The child was diagnosed with nasolacrimal duct obstruction and congenital glaucoma in the left eye. Over several follow up visits, treatment with eye drops and surgery was performed to manage intraocular pressure and treat the glaucoma. The case highlights the evaluation, management, and long term follow up of congenital glaucoma in infants.
This document discusses scleritis, an inflammation of the sclera. It defines scleritis and notes it is less common than episcleritis. Scleritis can be classified as anterior or posterior, with anterior scleritis subdivided into non-necrotizing diffuse/nodular or necrotizing forms with or without inflammation. Associated systemic diseases are common in 45% of patients. Signs, symptoms, investigations, and treatment are described depending on the classification of scleritis. Surgical treatment may be needed for extreme scleral thinning or corneal complications.
Benign epithelial tumors of the ocular surface include papillomas, which are caused by HPV infection and can be either pedunculated or sessile. Sessile papillomas have a risk of malignant transformation. Malignant epithelial tumors include ocular surface squamous neoplasia (OSSN), which presents as dysplasia or carcinoma in situ and can invade the cornea or globe if not treated with surgical excision or topical chemotherapy. Neuroectodermal tumors of the ocular surface include freckles, benign acquired melanosis (BAM), and primary acquired melanosis (PAM), which has a risk of progressing to conjunctival melanoma. Close monitoring is important to detect malignant transformation
This document discusses branch retinal vein occlusion (BRVO), including its pathogenesis, clinical features, complications, investigations, and management. BRVO is caused by obstruction of one of the retinal veins, usually at the arteriovenous crossing point. It can lead to macular edema, neovascularization, vitreous hemorrhage, and retinal detachment. Treatment involves anti-VEGF injections, steroids, laser photocoagulation, and occasionally surgery. Several clinical trials have evaluated therapies for BRVO, finding that anti-VEGF drugs and steroids reduce macular edema but laser provides little additional benefit when combined with anti-VEGF treatment.
Chalazion is a chronic inflammatory nodule of the meibomian gland in the eyelid. It is the most common benign eyelid lesion, occurring more often in adults. Chalazions start as small, tender swellings and are caused by obstruction and retention of secretions in the meibomian gland. On pathology, they show chronic inflammation with lipid-filled giant cells. Clinically, they appear as painless, hard swellings of the eyelid that can cause blurry vision. Treatment involves warm compresses, antibiotics, steroids, or incision and curettage for larger lesions. Complications include infection, cyst formation, or recurrence.
This document defines and classifies different types of amblyopia, including strabismic amblyopia, stimulus deprivation amblyopia, anisometropic amblyopia, meridional amblyopia, and bilateral ametropic amblyopia. It discusses the pathogenesis and pathophysiology of amblyopia, noting that visual deprivation during early development can cause changes in visual system neurons. The evaluation, diagnosis, and management of amblyopia are also outlined, including prevention through early vision screening, treatment by eliminating causes of visual deprivation and correcting refractive errors, and occlusion therapy to correct ocular dominance.
Global estimates indicate that the prevalence of glaucoma is 3.54% worldwide, and the number of people affected is projected to increase from 64.3 million in 2013 to 111.8 million in 2040. Glaucoma is the leading cause of irreversible blindness, with open-angle glaucoma affecting an estimated 4.5 million people and angle-closure glaucoma affecting 3.9 million people globally. Pseudoexfoliation syndrome is the most common cause of secondary open-angle glaucoma worldwide and is characterized by the deposition of pseudoexfoliative material in various structures of the anterior eye segment.
Congenital Glaucoma is one of the most common causes of irreversible childhood blindness. This presentation covers this topic in detail that can aid physicians in effective patient care.
PS: The slides in the preview look skewed, download the presentation to view the font used in Office 2012 and upwards.
This document discusses scleritis, an inflammation of the sclera. It defines scleritis and notes it is less common than episcleritis. Scleritis can be classified as anterior or posterior, with anterior scleritis subdivided into non-necrotizing diffuse/nodular or necrotizing forms with or without inflammation. Associated systemic diseases are common in 45% of patients. Signs, symptoms, investigations, and treatment are described depending on the classification of scleritis. Surgical treatment may be needed for extreme scleral thinning or corneal complications.
Benign epithelial tumors of the ocular surface include papillomas, which are caused by HPV infection and can be either pedunculated or sessile. Sessile papillomas have a risk of malignant transformation. Malignant epithelial tumors include ocular surface squamous neoplasia (OSSN), which presents as dysplasia or carcinoma in situ and can invade the cornea or globe if not treated with surgical excision or topical chemotherapy. Neuroectodermal tumors of the ocular surface include freckles, benign acquired melanosis (BAM), and primary acquired melanosis (PAM), which has a risk of progressing to conjunctival melanoma. Close monitoring is important to detect malignant transformation
This document discusses branch retinal vein occlusion (BRVO), including its pathogenesis, clinical features, complications, investigations, and management. BRVO is caused by obstruction of one of the retinal veins, usually at the arteriovenous crossing point. It can lead to macular edema, neovascularization, vitreous hemorrhage, and retinal detachment. Treatment involves anti-VEGF injections, steroids, laser photocoagulation, and occasionally surgery. Several clinical trials have evaluated therapies for BRVO, finding that anti-VEGF drugs and steroids reduce macular edema but laser provides little additional benefit when combined with anti-VEGF treatment.
Chalazion is a chronic inflammatory nodule of the meibomian gland in the eyelid. It is the most common benign eyelid lesion, occurring more often in adults. Chalazions start as small, tender swellings and are caused by obstruction and retention of secretions in the meibomian gland. On pathology, they show chronic inflammation with lipid-filled giant cells. Clinically, they appear as painless, hard swellings of the eyelid that can cause blurry vision. Treatment involves warm compresses, antibiotics, steroids, or incision and curettage for larger lesions. Complications include infection, cyst formation, or recurrence.
This document defines and classifies different types of amblyopia, including strabismic amblyopia, stimulus deprivation amblyopia, anisometropic amblyopia, meridional amblyopia, and bilateral ametropic amblyopia. It discusses the pathogenesis and pathophysiology of amblyopia, noting that visual deprivation during early development can cause changes in visual system neurons. The evaluation, diagnosis, and management of amblyopia are also outlined, including prevention through early vision screening, treatment by eliminating causes of visual deprivation and correcting refractive errors, and occlusion therapy to correct ocular dominance.
Global estimates indicate that the prevalence of glaucoma is 3.54% worldwide, and the number of people affected is projected to increase from 64.3 million in 2013 to 111.8 million in 2040. Glaucoma is the leading cause of irreversible blindness, with open-angle glaucoma affecting an estimated 4.5 million people and angle-closure glaucoma affecting 3.9 million people globally. Pseudoexfoliation syndrome is the most common cause of secondary open-angle glaucoma worldwide and is characterized by the deposition of pseudoexfoliative material in various structures of the anterior eye segment.
Congenital Glaucoma is one of the most common causes of irreversible childhood blindness. This presentation covers this topic in detail that can aid physicians in effective patient care.
PS: The slides in the preview look skewed, download the presentation to view the font used in Office 2012 and upwards.
Hypertensive retinopathy refers to changes in the retina and choroid that occur due to high blood pressure. There are three main factors that contribute to its pathogenesis: vasoconstriction, arteriosclerotic changes, and increased vascular permeability. Clinically, it presents as arteriolar narrowing, AV nicking, cotton wool spots, hemorrhages, and hard exudates. It can be chronic or malignant, with malignant seeing a more rapid progression. Treatment involves strict blood pressure control.
This document defines and describes phthisis bulbi, a condition where the eye shrinks and its contents become disorganized due to severe injury or disease damage. It outlines the causes of phthisis bulbi, including trauma, infection, inflammation, surgery, retinal detachment, and malignancy. A grading system is proposed based on clinical features, from atrophy without shrinkage to phthisis bulbi with intraocular ossification or calcium deposition. Signs, symptoms, pathophysiology, diagnosis, and management are discussed, with management focusing on alleviating pain and cosmetic rehabilitation rather than restoring vision.
Myopia, or nearsightedness, is a refractive condition where parallel rays of light focus in front of the retina. There are several types of myopia based on etiology. Simple myopia is the most common type and results from axial elongation of the eyeball. Pathological myopia can lead to degenerative changes in the retina and choroid over time like myopic crescents if left untreated. Treatment options include optical correction with glasses or contacts, refractive surgeries like LASIK, and low vision aids for advanced cases. Proper diet and genetic counseling can help manage risk of progression.
This document summarizes key concepts related to strabismus and eye movement examination. It defines terms like strabismus, visual axis, anatomical axis, orthophoria and describes tests to evaluate eye alignment and movement including:
- Hirschberg test to measure strabismus angle
- Cover-uncover test and alternate cover test to detect heterotropia and heterophoria
- Prism bar cover test for measuring strabismus angle
- Synoptophore for grading binocular vision
- Maddox rod test for detecting horizontal and vertical phorias
- Extraocular muscle actions and innervations are also summarized.
The document discusses the anatomy, embryology, and function tests of the macula lutea. It describes the macula lutea as a 5.5mm circular area at the posterior pole of the retina that subserves central vision. It notes the macula's delayed development until 8 months gestation and specialization of the fovea which contains the highest concentration of cones. The document outlines various macular function tests used to evaluate macular diseases, including visual acuity, Amsler grid, microperimetry, and electroretinography. It provides details on the anatomy and cell layers of the fovea centralis and techniques for assessing macular integrity with tests like the Maddox rod.
Ocular injuries can be classified as open globe, closed globe, or periocular injuries. Open globe injuries involve a full thickness break in the eye wall, while closed globe injuries do not penetrate the full thickness. Periocular injuries involve the tissues surrounding the eye. Common closed globe injuries include conjunctival and corneal abrasions, hyphema, and retinal detachment. Lid lacerations may require repair depending on their location. Blunt eye trauma requires examination of visual acuity and eye anatomy to check for injuries like ruptured globe or optic nerve damage. Suspected open globe injuries or those with vision loss require emergent ophthalmology referral.
The cornea is the transparent front part of the eye that transmits and focuses light. It has 3 main layers - an outer epithelial layer, a thick middle stromal layer made of collagen, and an inner single-cell endothelial layer. The cornea derives its strength and curvature from the orderly arrangement of collagen in the stroma. It remains transparent due to its regular structure without blood vessels and the deturgescent properties maintained by the endothelial pump. The cornea has a high metabolic rate powered by glucose and oxygen and is innervated by nerves for vision and protection.
This document summarizes various clinical features of lid disorders including nodules, cysts, tumors, infections, malpositions, and traumatic injuries. It describes conditions such as chalazion, hordeolum, molluscum, xanthelasma, blepharitis, herpes, entropion, ectropion, and ptosis. It also lists systemic causes of lid edema and malignant conditions that can affect the lids.
Chronic conjunctivitis can be caused by infection or allergy. Infectious causes include trachoma caused by Chlamydia trachomatis, which is the leading cause of preventable blindness worldwide. If left untreated, repeated trachoma infections can lead to scarring of the conjunctiva and complications like trichiasis and corneal opacity. Granulomatous conjunctivitis presents with localized conjunctival granulomas and lymphadenopathy in conditions like cat scratch disease or tuberculosis. Non-specific chronic conjunctivitis can be caused by chronic irritation or hypersensitivity reactions.
This document discusses primary angle closure glaucoma (PACG), a type of glaucoma where the iris occludes the drainage angle of the eye, obstructing aqueous outflow. PACG is a leading cause of glaucoma worldwide and is particularly common in East Asian populations. It is classified based on the degree of iris occlusion and presence of optic nerve damage and vision loss. Risk factors include older age, female sex, Asian ethnicity, family history, hypermetropia, and shorter axial length. Symptoms include blurred vision, halos around lights, eye pain, and headache. Signs include elevated eye pressure, shallow anterior chamber, iris changes, and optic nerve damage. The document outlines methods for diagnosing
Lacrimation refers to watering of the eye due to excessive tear production from the lacrimal gland, while epiphora is watering caused by obstruction of the tear drainage system. Differentiating the two is important to provide proper treatment. The document discusses the anatomy and physiology of tear production, drainage, and evaluates causes of watering eye including lacrimation, dry eye, blepharitis, and epiphora due to punctal stenosis or nasolacrimal duct obstruction. Treatment depends on the underlying cause and may include punctal dilation, dacryocystorhinostomy, Jones tube insertion, or endoscopic lacrimal surgery.
Primary open angle glaucoma (POAG) is characterized by adult onset, elevated intraocular pressure (IOP) above 21 mmHg with an open iridocorneal angle, optic disc cupping, and visual field loss. Risk factors include older age, family history, higher IOP, and certain medical conditions. POAG is caused by reduced outflow of aqueous humor from the eye due to thickening of the trabecular meshwork. Diagnosis requires evidence of optic nerve damage and visual field loss in addition to elevated IOP. Treatment aims to lower IOP and prevent further vision loss through medications, laser trabeculoplasty, or surgery.
This document discusses the treatment of non-healing corneal ulcers. It begins by describing the signs and symptoms of a non-healing corneal ulcer. Risk factors include compromised ocular surfaces, dry eye, previous trauma or surgery, and systemic conditions like diabetes or malnutrition. Treatment involves topical antibiotics, debridement of necrotic tissue, bandage contact lenses, and in severe cases, therapeutic keratoplasty.
Maddox Rod
Use of Maddox Rod
Method of Assessment MR
Double MR Test procedure
Recording procedure of MR Test
Heterophoria, Cyclophoria, Esophoria,Exophoria,Hyperphoria,Hypophoria
This document discusses intermediate uveitis (IU), which involves inflammation in the anterior vitreous, pars plana, and peripheral retina. IU accounts for 8-22% of uveitis cases. Clinically, it is characterized by "snowballs" or yellow-white exudates in the peripheral vitreous. Treatment involves topical/periocular steroids initially, with cryotherapy, vitrectomy or immunosuppressants for non-responsive cases. Complications include cystoid macular edema, cataracts, glaucoma, and retinal detachment. Proper diagnosis requires excluding other causes like syphilis, Lyme disease, multiple sclerosis and sarcoidosis.
This document provides information on entropion, including anatomy of the eyelid, causes of entropion, classification, symptoms, assessment, differential diagnosis, and surgical and non-surgical management. Entropion is defined as inward rotation of the eyelid margin. It discusses various procedures for correcting entropion such as Quickert-Rathbun eversion sutures, lower lid retractor advancement combined with lateral tarsal strip or wedge resection, tarsal fracture/transverse tarsotomy, and use of posterior lamellar grafts for severe cicatricial entropion. Non-surgical management includes artificial tears, bandage contact lenses, lower lid taping, and botulinum
Keratoconus is a non-inflammatory condition where the cornea progressively thins and changes from a dome shape to a cone shape. It typically develops between ages 8-45. The cornea thins and breaks occur in the Bowman's layer and Descemet's membrane. Diagnosis involves examining for Fleischer's ring, Vogt's striae, and irregular topography. Mild cases are treated with glasses or soft contacts while more severe cases require rigid gas permeable contacts or surgical interventions like intracorneal ring segments, lamellar keratoplasty, or penetrating keratoplasty.
Keratoconus is a non-inflammatory thinning of the cornea that causes it to take on a conical shape. It typically develops in adolescence and causes vision impairment due to irregular astigmatism. It is classified into four stages based on refractive error, corneal thickness and shape. While the exact cause is unknown, theories include genetic and enzymatic factors. It is often associated with eye rubbing and connective tissue disorders. Clinical features include corneal thinning, Fleischer's ring, Munson's sign, and scarring in advanced cases. Diagnosis involves topography, pachymetry and biomicroscopy to detect corneal shape changes.
This document provides information on the anatomy and diseases of the vitreous humor. It discusses that the vitreous humor is a jelly-like structure that fills the back of the eye and provides support. Common diseases include vitreous liquefaction, detachment, hemorrhage, and opacities. Vitreous liquefaction is the most common degenerative change and causes floaters. Posterior vitreous detachment often occurs in older individuals and may lead to retinal tears or breaks. Vitreous opacities can result from inflammatory cells, aggregates, tumors or hemorrhages. Vitreous hemorrhage usually stems from retinal vessels and can cause vision loss.
Approach to cases of congenital glaucoma, developmentalBipin Bista
This document discusses approaches to congenital glaucoma and developmental glaucoma associated with ocular and systemic disorders. It covers signs and symptoms, diagnostic examinations including vision testing, tonometry, and imaging. Primary congenital glaucoma is described along with theories of abnormal development. Specific conditions like Axenfeld-Rieger syndrome are also outlined. Management options are mentioned including medical therapy, various surgical procedures, and postoperative care.
Approach to cases of congenital glaucoma, developmentalShahrukh Kc
This document discusses approaches to congenital glaucoma and developmental glaucoma associated with ocular and systemic disorders. It covers signs and symptoms, diagnostic examinations including vision testing, external examination, and specific tests like tonometry and gonioscopy. Etiology and theories of abnormal development are explained. Primary congenital glaucomas, Axenfeld-Rieger Syndrome, Peters Anomaly, and Aniridia are discussed in detail including clinical features, management, genetics, and histopathology where relevant. Surgical and medical management strategies are also outlined.
Hypertensive retinopathy refers to changes in the retina and choroid that occur due to high blood pressure. There are three main factors that contribute to its pathogenesis: vasoconstriction, arteriosclerotic changes, and increased vascular permeability. Clinically, it presents as arteriolar narrowing, AV nicking, cotton wool spots, hemorrhages, and hard exudates. It can be chronic or malignant, with malignant seeing a more rapid progression. Treatment involves strict blood pressure control.
This document defines and describes phthisis bulbi, a condition where the eye shrinks and its contents become disorganized due to severe injury or disease damage. It outlines the causes of phthisis bulbi, including trauma, infection, inflammation, surgery, retinal detachment, and malignancy. A grading system is proposed based on clinical features, from atrophy without shrinkage to phthisis bulbi with intraocular ossification or calcium deposition. Signs, symptoms, pathophysiology, diagnosis, and management are discussed, with management focusing on alleviating pain and cosmetic rehabilitation rather than restoring vision.
Myopia, or nearsightedness, is a refractive condition where parallel rays of light focus in front of the retina. There are several types of myopia based on etiology. Simple myopia is the most common type and results from axial elongation of the eyeball. Pathological myopia can lead to degenerative changes in the retina and choroid over time like myopic crescents if left untreated. Treatment options include optical correction with glasses or contacts, refractive surgeries like LASIK, and low vision aids for advanced cases. Proper diet and genetic counseling can help manage risk of progression.
This document summarizes key concepts related to strabismus and eye movement examination. It defines terms like strabismus, visual axis, anatomical axis, orthophoria and describes tests to evaluate eye alignment and movement including:
- Hirschberg test to measure strabismus angle
- Cover-uncover test and alternate cover test to detect heterotropia and heterophoria
- Prism bar cover test for measuring strabismus angle
- Synoptophore for grading binocular vision
- Maddox rod test for detecting horizontal and vertical phorias
- Extraocular muscle actions and innervations are also summarized.
The document discusses the anatomy, embryology, and function tests of the macula lutea. It describes the macula lutea as a 5.5mm circular area at the posterior pole of the retina that subserves central vision. It notes the macula's delayed development until 8 months gestation and specialization of the fovea which contains the highest concentration of cones. The document outlines various macular function tests used to evaluate macular diseases, including visual acuity, Amsler grid, microperimetry, and electroretinography. It provides details on the anatomy and cell layers of the fovea centralis and techniques for assessing macular integrity with tests like the Maddox rod.
Ocular injuries can be classified as open globe, closed globe, or periocular injuries. Open globe injuries involve a full thickness break in the eye wall, while closed globe injuries do not penetrate the full thickness. Periocular injuries involve the tissues surrounding the eye. Common closed globe injuries include conjunctival and corneal abrasions, hyphema, and retinal detachment. Lid lacerations may require repair depending on their location. Blunt eye trauma requires examination of visual acuity and eye anatomy to check for injuries like ruptured globe or optic nerve damage. Suspected open globe injuries or those with vision loss require emergent ophthalmology referral.
The cornea is the transparent front part of the eye that transmits and focuses light. It has 3 main layers - an outer epithelial layer, a thick middle stromal layer made of collagen, and an inner single-cell endothelial layer. The cornea derives its strength and curvature from the orderly arrangement of collagen in the stroma. It remains transparent due to its regular structure without blood vessels and the deturgescent properties maintained by the endothelial pump. The cornea has a high metabolic rate powered by glucose and oxygen and is innervated by nerves for vision and protection.
This document summarizes various clinical features of lid disorders including nodules, cysts, tumors, infections, malpositions, and traumatic injuries. It describes conditions such as chalazion, hordeolum, molluscum, xanthelasma, blepharitis, herpes, entropion, ectropion, and ptosis. It also lists systemic causes of lid edema and malignant conditions that can affect the lids.
Chronic conjunctivitis can be caused by infection or allergy. Infectious causes include trachoma caused by Chlamydia trachomatis, which is the leading cause of preventable blindness worldwide. If left untreated, repeated trachoma infections can lead to scarring of the conjunctiva and complications like trichiasis and corneal opacity. Granulomatous conjunctivitis presents with localized conjunctival granulomas and lymphadenopathy in conditions like cat scratch disease or tuberculosis. Non-specific chronic conjunctivitis can be caused by chronic irritation or hypersensitivity reactions.
This document discusses primary angle closure glaucoma (PACG), a type of glaucoma where the iris occludes the drainage angle of the eye, obstructing aqueous outflow. PACG is a leading cause of glaucoma worldwide and is particularly common in East Asian populations. It is classified based on the degree of iris occlusion and presence of optic nerve damage and vision loss. Risk factors include older age, female sex, Asian ethnicity, family history, hypermetropia, and shorter axial length. Symptoms include blurred vision, halos around lights, eye pain, and headache. Signs include elevated eye pressure, shallow anterior chamber, iris changes, and optic nerve damage. The document outlines methods for diagnosing
Lacrimation refers to watering of the eye due to excessive tear production from the lacrimal gland, while epiphora is watering caused by obstruction of the tear drainage system. Differentiating the two is important to provide proper treatment. The document discusses the anatomy and physiology of tear production, drainage, and evaluates causes of watering eye including lacrimation, dry eye, blepharitis, and epiphora due to punctal stenosis or nasolacrimal duct obstruction. Treatment depends on the underlying cause and may include punctal dilation, dacryocystorhinostomy, Jones tube insertion, or endoscopic lacrimal surgery.
Primary open angle glaucoma (POAG) is characterized by adult onset, elevated intraocular pressure (IOP) above 21 mmHg with an open iridocorneal angle, optic disc cupping, and visual field loss. Risk factors include older age, family history, higher IOP, and certain medical conditions. POAG is caused by reduced outflow of aqueous humor from the eye due to thickening of the trabecular meshwork. Diagnosis requires evidence of optic nerve damage and visual field loss in addition to elevated IOP. Treatment aims to lower IOP and prevent further vision loss through medications, laser trabeculoplasty, or surgery.
This document discusses the treatment of non-healing corneal ulcers. It begins by describing the signs and symptoms of a non-healing corneal ulcer. Risk factors include compromised ocular surfaces, dry eye, previous trauma or surgery, and systemic conditions like diabetes or malnutrition. Treatment involves topical antibiotics, debridement of necrotic tissue, bandage contact lenses, and in severe cases, therapeutic keratoplasty.
Maddox Rod
Use of Maddox Rod
Method of Assessment MR
Double MR Test procedure
Recording procedure of MR Test
Heterophoria, Cyclophoria, Esophoria,Exophoria,Hyperphoria,Hypophoria
This document discusses intermediate uveitis (IU), which involves inflammation in the anterior vitreous, pars plana, and peripheral retina. IU accounts for 8-22% of uveitis cases. Clinically, it is characterized by "snowballs" or yellow-white exudates in the peripheral vitreous. Treatment involves topical/periocular steroids initially, with cryotherapy, vitrectomy or immunosuppressants for non-responsive cases. Complications include cystoid macular edema, cataracts, glaucoma, and retinal detachment. Proper diagnosis requires excluding other causes like syphilis, Lyme disease, multiple sclerosis and sarcoidosis.
This document provides information on entropion, including anatomy of the eyelid, causes of entropion, classification, symptoms, assessment, differential diagnosis, and surgical and non-surgical management. Entropion is defined as inward rotation of the eyelid margin. It discusses various procedures for correcting entropion such as Quickert-Rathbun eversion sutures, lower lid retractor advancement combined with lateral tarsal strip or wedge resection, tarsal fracture/transverse tarsotomy, and use of posterior lamellar grafts for severe cicatricial entropion. Non-surgical management includes artificial tears, bandage contact lenses, lower lid taping, and botulinum
Keratoconus is a non-inflammatory condition where the cornea progressively thins and changes from a dome shape to a cone shape. It typically develops between ages 8-45. The cornea thins and breaks occur in the Bowman's layer and Descemet's membrane. Diagnosis involves examining for Fleischer's ring, Vogt's striae, and irregular topography. Mild cases are treated with glasses or soft contacts while more severe cases require rigid gas permeable contacts or surgical interventions like intracorneal ring segments, lamellar keratoplasty, or penetrating keratoplasty.
Keratoconus is a non-inflammatory thinning of the cornea that causes it to take on a conical shape. It typically develops in adolescence and causes vision impairment due to irregular astigmatism. It is classified into four stages based on refractive error, corneal thickness and shape. While the exact cause is unknown, theories include genetic and enzymatic factors. It is often associated with eye rubbing and connective tissue disorders. Clinical features include corneal thinning, Fleischer's ring, Munson's sign, and scarring in advanced cases. Diagnosis involves topography, pachymetry and biomicroscopy to detect corneal shape changes.
This document provides information on the anatomy and diseases of the vitreous humor. It discusses that the vitreous humor is a jelly-like structure that fills the back of the eye and provides support. Common diseases include vitreous liquefaction, detachment, hemorrhage, and opacities. Vitreous liquefaction is the most common degenerative change and causes floaters. Posterior vitreous detachment often occurs in older individuals and may lead to retinal tears or breaks. Vitreous opacities can result from inflammatory cells, aggregates, tumors or hemorrhages. Vitreous hemorrhage usually stems from retinal vessels and can cause vision loss.
Approach to cases of congenital glaucoma, developmentalBipin Bista
This document discusses approaches to congenital glaucoma and developmental glaucoma associated with ocular and systemic disorders. It covers signs and symptoms, diagnostic examinations including vision testing, tonometry, and imaging. Primary congenital glaucoma is described along with theories of abnormal development. Specific conditions like Axenfeld-Rieger syndrome are also outlined. Management options are mentioned including medical therapy, various surgical procedures, and postoperative care.
Approach to cases of congenital glaucoma, developmentalShahrukh Kc
This document discusses approaches to congenital glaucoma and developmental glaucoma associated with ocular and systemic disorders. It covers signs and symptoms, diagnostic examinations including vision testing, external examination, and specific tests like tonometry and gonioscopy. Etiology and theories of abnormal development are explained. Primary congenital glaucomas, Axenfeld-Rieger Syndrome, Peters Anomaly, and Aniridia are discussed in detail including clinical features, management, genetics, and histopathology where relevant. Surgical and medical management strategies are also outlined.
Dr. Atul Kumar Anand discusses primary congenital glaucoma, which occurs due to a developmental defect in the trabecular meshwork and anterior chamber angle. It affects about 1 in 10,000 births and is usually diagnosed within the first year of life. The main symptoms are photophobia, epiphora, and blepharospasm. Examination reveals corneal edema, enlargement, and increased intraocular pressure. The primary treatment is surgical, through procedures like goniotomy or trabeculotomy to relieve pressure and allow drainage of fluid from the eye. Follow-up is required over an indefinite period to monitor intraocular pressure and optic nerve changes.
An 8-year-old Russian boy presented with haziness in vision for two years. Examination found high intraocular pressures and severe optic disc cupping, indicating primary congenital glaucoma. He was diagnosed with primary congenital open angle glaucoma and successfully managed with medications, with intraocular pressures and vision stabilized over one year follow up.
The document discusses congenital glaucoma, defining it as glaucoma present at birth associated with developmental anomalies of the eye. It covers the epidemiology, genetics, classification, pathogenesis, clinical features, evaluation, and management of congenital glaucoma. The main treatment involves surgical options like goniotomy, trabeculotomy, and trabeculectomy to lower intraocular pressure and clear the cornea.
This document presents a case of congenital glaucoma in an 8-year-old female. Examination under anesthesia revealed increased intraocular pressure and a hazy cornea in the left eye, while the right eye was normal. A provisional diagnosis of congenital glaucoma in the left eye was made. Medical treatment was initiated but surgery was declined. The patient was followed up regularly with good intraocular pressure control on medication. The document then reviews definitions, epidemiology, genetics, classifications, theories of development and clinical features of congenital glaucoma.
Primary congenital glaucoma is caused by abnormal development of the trabecular meshwork, resulting in impaired aqueous outflow and elevated intraocular pressure. It occurs in children under 2 years old and clinical features include photophobia, corneal edema, corneal enlargement, and optic disc cupping. Diagnosis involves assessing intraocular pressure, eye examination for signs of glaucoma, and refractive error. Treatment involves medications and surgeries to lower intraocular pressure and prevent vision loss.
A 39-year-old male presented with a three-year history of decreased and fluctuating vision in his left eye. Examination revealed essential iris atrophy in the left eye, which was causing fluctuating intraocular pressure and visual acuity due to corneal changes. The patient has been managed with hypertonic saline drops and has not experienced further pressure spikes, though his vision remains fluctuating.
congenital glaucoma and congenital cataractRegina Lr
The document summarizes congenital glaucoma and congenital cataract. It discusses the epidemiology, genetics, pathogenesis, clinical features, diagnosis and management of congenital glaucoma. Congenital glaucoma is caused by developmental defects of the trabecular meshwork and anterior chamber angle that obstruct aqueous outflow. Signs include corneal enlargement, Haab's striae, elevated intraocular pressure, and optic nerve cupping. Treatment involves medical therapy with topical medications or surgical procedures like goniotomy to remove obstructing tissue from the anterior chamber angle.
- Three cases of bilateral corneal opacities are presented
- All cases show central corneal opacity without signs of inflammation or vascularization
- This suggests a diagnosis of corneal dystrophy, which is a hereditary condition causing bilateral corneal opacity that is non-inflammatory in nature
- Corneal dystrophy can be classified anatomically based on the layer of the cornea involved, or by the new IC3D classification system which integrates phenotype, pathology, and genetics
This document discusses primary congenital glaucoma, including its history, terminology, classification, management, and associated anomalies. It notes that primary congenital glaucoma is a leading cause of childhood blindness and can be inherited in an autosomal recessive pattern. The classical signs are epiphora, blepharospasm, and photophobia. Examination involves measuring intraocular pressure and corneal diameter. Surgical options for treatment include goniotomy and trabeculotomy to lower IOP and clear the cornea. Developmental glaucomas can be associated with conditions like Axenfeld-Rieger syndrome, aniridia, Peters anomaly, and Sturge Weber syndrome.
Congenital or infantile glaucoma occurs in babies and young children, usually within the first year of life. It is a rare condition caused by incorrect development of the eye's drainage system before birth. The mainstay treatment is surgical, through procedures like goniotomy or trabeculotomy to create an opening in the trabecular meshwork and improve aqueous outflow. These surgeries may need to be repeated if the first procedure fails to sufficiently lower intraocular pressure.
Case Report and Clinical Findings of Central Serous RetinopathyDan Mulder
Central Serous Retinopathy (CSR) is a retinal disease caused by a serous detachment of the retina. The case report details examination findings and diagnostic testing for a patient diagnosed with CSR. Imaging including fundus photos, OCT, and angiography can help diagnose CSR by identifying fluid detachments and leakages. While the cause is unknown, CSR is often self-limiting and treatments may include observation, anti-inflammatory drugs, or laser photocoagulation depending on severity and chronicity. This patient was initially observed but later prescribed NSAIDs due to the chronic nature of the detachment.
Strabismus, also known as squint, refers to misalignment of the eyes. The document provides an overview of strabismus, including types, causes, signs and symptoms, diagnosis, and treatment approaches. Specifically, it discusses pseudo-strabismus versus real strabismus, classifications based on age of onset, fusional status, direction of deviation, and variation with gaze. Diagnosis involves assessing visual acuity, ocular movements, binocular vision, refractive error, and ruling out underlying conditions. Management may include glasses, eye exercises, prism therapy, or surgical correction depending on the type and severity of strabismus. The goal is to restore or maintain binocular vision and eye
Pediatric eye disorders can affect vision development in children. A childhood eye exam evaluates visual acuity, ocular alignment and structure, and eye health. The exam includes tests of the red reflex, pupil response, and visual focus and tracking. Common childhood eye conditions include strabismus, amblyopia, and infections like conjunctivitis. Early detection through regular eye exams is important to address any vision problems and prevent long-term amblyopia.
glaucoma and cataract.pdf, After the class the students will be able :
Explain the structures and function of eye.
Explain the age affect on vision.
Describe the definition , etiology, risk factors, pathophysiology, medical management, surgical management and Nursing management of Glaucoma.
Describe the definition , etiology, risk factors, pathophysiology, medical management, surgical management and Nursing management of cataract.
List down the health education for Glaucoma and cataract.
This document provides classifications and definitions for different types of pediatric glaucoma, including primary congenital glaucoma, secondary infantile glaucoma, primary juvenile glaucoma, and developmental glaucomas. It discusses the epidemiology, pathophysiology, clinical features, examination findings, differential diagnosis, management, and long-term prognosis of these conditions. It also describes various ocular and systemic anomalies that can be associated with developmental glaucomas, such as Axenfeld-Rieger syndrome, Peters anomaly, aniridia, Sturge-Weber syndrome, and neurofibromatosis.
The document provides an overview of various pathologies that can affect the eye and orbit, including calcifications, retinoblastoma, melanoma, persistent hyperplastic primary vitreous, globe rupture, retinal detachment, choroidal detachment, coloboma, optic nerve glioma, thyroid eye disease, pseudotumor, periocular abscess, orbital cellulitis, venous vascular malformation, and orbital varix. Each condition is briefly described and accompanied by example images to illustrate associated imaging findings.
This document provides an overview of childhood glaucoma, including terminology, classification systems, epidemiology, pathogenesis, clinical presentation, diagnosis, and management. It discusses primary and secondary childhood glaucomas. Primary childhood glaucomas are further classified based on the presence of ocular anomalies, systemic diseases/syndromes, or acquired conditions. The document outlines evaluation procedures such as examination under anesthesia and diagnostic testing. It also reviews medical and surgical treatment options for childhood glaucoma.
A hordeolum is a common infection of the eyelid margin. Lesions appear as a red, swollen nodule that resembles a pimple in appearance. The infection may be on the external or internal surface of the eyelid and could lead to redness and edema of the lid. Recognition of these lesions requires an understanding of eyelid anatomy. The objective of this case is to review etiology of these lesions and appropriate treatment.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Clinic ^%[+27633867063*Abortion Pills For Sale In Tembisa Central19various
Clinic ^%[+27633867063*Abortion Pills For Sale In Tembisa Central Clinic ^%[+27633867063*Abortion Pills For Sale In Tembisa CentralClinic ^%[+27633867063*Abortion Pills For Sale In Tembisa CentralClinic ^%[+27633867063*Abortion Pills For Sale In Tembisa CentralClinic ^%[+27633867063*Abortion Pills For Sale In Tembisa Central
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kol...rightmanforbloodline
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Versio
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Version
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Version
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
Osteoporosis - Definition , Evaluation and Management .pdfJim Jacob Roy
Osteoporosis is an increasing cause of morbidity among the elderly.
In this document , a brief outline of osteoporosis is given , including the risk factors of osteoporosis fractures , the indications for testing bone mineral density and the management of osteoporosis
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
There is increasing confidence that cell therapies will soon play a role in the treatment of autoimmune disorders, but the extent of this impact remains to be seen. Early readouts on autologous CAR-Ts in lupus are encouraging, but manufacturing and cost limitations are likely to restrict access to highly refractory patients. Allogeneic CAR-Ts have the potential to broaden access to earlier lines of treatment due to their inherent cost benefits, however they will need to demonstrate comparable or improved efficacy to established modalities.
In addition to infrastructure and capacity constraints, CAR-Ts face a very different risk-benefit dynamic in autoimmune compared to oncology, highlighting the need for tolerable therapies with low adverse event risk. CAR-NK and Treg-based therapies are also being developed in certain autoimmune disorders and may demonstrate favorable safety profiles. Several novel non-cell therapies such as bispecific antibodies, nanobodies, and RNAi drugs, may also offer future alternative competitive solutions with variable value propositions.
Widespread adoption of cell therapies will not only require strong efficacy and safety data, but also adapted pricing and access strategies. At oncology-based price points, CAR-Ts are unlikely to achieve broad market access in autoimmune disorders, with eligible patient populations that are potentially orders of magnitude greater than the number of currently addressable cancer patients. Developers have made strides towards reducing cell therapy COGS while improving manufacturing efficiency, but payors will inevitably restrict access until more sustainable pricing is achieved.
Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
2. CASE 1
21-06-2019
A 7 month old MALE child ,brought to Paediatric Ophthalmology OPD at
SSN with –
Complain of – watering from left eye (OS) associated with mucopurulent
discharge since last 7 months.
HISTORY OF UNKNOWN EYE DROP INSTILLATION IN LEFT EYE (OS) FOR 3
MONTHS.
3. OD OS
VISION CSM CSM
LIDS N N
CONJUNCTIVA N N
CORNEA NORMAL NORMAL
COVER TEST ORTHO ORTHO
ANTERIOR CHAMBER NORMAL NORMAL
IRIS NORMAL NORMAL
PUPIL NORMAL NORMAL
LENS CLEAR CLEAR
IOP(FINGER TENSION) NORMAL NORMAL
DISC CDR 0.2 CDR 0.5
DIAGNOSIS : LEFT EYE (OS)- NASOLACRIMAL DUCT OBSTRUCTION
- LARGE DISC
ACTION PLAN : CONJUCTIVAL SWAB FOR SENSITIVITY AND GLAUCOMA CLINIC OPINION
4. 21-06-2019
Case seen by Glaucoma clinic Doctor.
O/E –
Cornea – Clear
Pupil – Dilated
IOP (TONOPEN) OD- 36 OS- 43
ACTION PLAN : OBSERVE FOR SIX WEEKS AND REVIEW AFTER THAT
DIAGNOSIS : OU- NASOLACRIMAL DUCT OBSTRUCTION
- ASYMMETRIC CUP
5. 28-06-2019
Case seen by Pediatric ophthalmologist and based on culture sensitivity
report , the child was started on –
TOBRAMYCIN E/D - 3 TIMES / DAY X 2 weeks
TOBRAMYCIN E/O - 2 TIMES / DAY X 2 weeks
CRIGGLER MASSAGE
ADVICED TO REVIEW AFTER 1 MONTH
6. 30-07-2019
Case seen by Paediatric Ophthalmologist first, and noticed improvement in
symptoms, so was advised to continue CRIGGLER MASSAGE and to Review in
Glaucoma clinic.
GLAUCOMA CLINIC –
O/E –
Cornea – Clear, Appears larger
Pupil – Dilated
No haab’s striae
IOP (TONOPEN) OD- 21 OS- 41/43
DIAGNOSIS : OU- NASOLACRIMAL DUCT OBSTRUCTION
- ASSYMETRIC CUP
OS - CONGENITAL GLAUCOMA
- MEGALOCORNEA
ADVICE: EUA (SEVOFLURANE) +/-
REFRACTION,CCT,BIOMETRY,FUNDUS PHOTO +/- SYRINGING
7. 16-09-2019 OD OS
HEAD CIRCUMFERENCE --- ---
FACE NAD NAD
ORBIT NORMAL NORMAL
LID NORMAL NORMAL
CONJUCTIVA NORMAL NORMAL
CORNEA CLEAR
12 MM
CLEAR
13MM
ANTERIOR CHAMBER DEEP DEEP
IRIS NORMAL NORMAL
PUPIL NORMAL NORMAL
LENS CLEAR CLEAR
IOP (TONOPEN) 17mm of Hg 33mm of Hg
GONIOSCOPY Anterior insertion of iris
with prominent iris process
Anterior insertion of iris
with prominent iris process
FUNDUS 0.5 VCDR ,PINK, HEALTHY 0.2 VCDR,PINK,HEALTHY
KERATOMETRY K1- 38.25
K2- 40.75 *66°
K1- 36.25
K2- 38.25 *27°
8. ADVICE: GONIOTOMY ON TABLE
Patient was started on –
Tobramycin E/D - 6 TIMES / DAY x 7 DAYS
- 4 TIMES / DAY x 7 DAYS
- 2 TIMES / DAY x 7 DAYS
9. 17-09-2019 ( FIRST POST –OP)
O/E - Clear cornea with white and quite eye
- No abnormal lid swelling noted
ADVICE: EUA , REFRACTION AND IDO AFTER 1 MONTH
19-09-2019 ( SECOND POST OP)
O/E - Clear cornea with white and quite eye
- Minimal conjunctival congestion
- No abnormal lid swelling noted
IOP (Tonopen ) – left eye (OS) - 10 mm Hg
ADVICE: EUA , REFRACTION AND IDO AFTER 1 MONTH
10. 18-10-2019
OD OS
FACE NAD NAD
ORBIT NORMAL NORMAL
LID LACERATION – UPPER EYE LID NORMAL
CONJUCTIVA NORMAL NORMAL
CORNEA ABRASSION ON RIGHT SIDE CLEAR
ANTERIOR CHAMBER DEEP DEEP
IRIS NORMAL NORMAL
PUPIL NORMAL NORMAL
LENS CLEAR CLEAR
IOP (TONOPEN) 9mm of Hg 13/14mm of Hg
GONIOSCOPY Anterior insertion of iris with
prominent iris process
Anterior insertion of iris with
prominent iris process
FUNDUS 0.4:1 0.9:1
REFRACTION -1.50 D sph -1.50 D sph
OS- SUTURE REMOVED
ADVICE: REPEAT EUA AFTER 6 MONTHS, VISUAL REHABILITATION IN PEDIATRIC OPHTHALMOLOGY CLINIC
ADV: TOBRAMYCINE E/D-
TDS x 7 DAYS
11. DEFINITION
Buphthalmos is a term used to describe the abnormal enlargement of
an infant’s eye secondary to elevated IOP.
In extreme cases,these eyes are vulnerable to lens-subluxationand
rupture even with even minor trauma.
12. Isolated congenital glaucoma
1. Isolated maldevelopment of the trabecular meshwork
2. No other developmental ocular anomalies or ocular diseases that can raise IOP.
3. Recognized with in first month
Infantile glaucoma
1. Synonymous with congenital glaucoma.
2. 1 month to 3 years
Juvenile glaucoma
1. Primary glaucoma occurring later in child hood or early adulthood
2. 3 years to 35 years
13. Three years of age is generally taken as the division between infantile and
juvenile glaucoma.
After this age the eye no longer expands in response to raised intraocular
pressure.
Juvenile glaucoma doesn’t havecorneal enlargement or Haabstriae
14. EPIDEMIOLOGY
1. 1 in 10000births
2. 50%isolated congenital
3. 60%diagnosed by 6 months and 80%by 1 year
4. 65%affected are males
5. 70%bilateral involvement
15. CLINICALFEATURES
Classic Triad ……symptoms
1. Epiphora
2. Photophobia
3. Blepharospasm
Other symptoms are
cloudy cornea , red eye, enlarged cornea or eye , irritability , poor vision and pain
In older children, astigmatism, progressive axial myopia cause symptomatic decreased VA and
refractive amblyopia.
17. 1. Breaks in Descmet’s membrane –as
cornea stretches- acute localized edema
& deposition of new basement
membrane into hyalineridges.
2. Horizontal, curvilinear and parallel to
the limbus in the peripheralcornea.
Haab’s striae
20. 1. Anterior chamber becomesdeep
2. Optic nerve cupping
◦ Develop early and rapidly
◦ Reversalof cupping with IOPreduction
21. EVALUATION
Examination in clinic
Observe
1. Cornea Size and Clarity
2. degree of tearing/photophobia
3. Any discharge /swelling –sac area
4. Iris/pupil Hypoplasia/corectopia andAniridia
22. EVALUATION UNDERGA
OTHER USEFUL DIAGNOSTIC TESTS:
CCT
Ultrasound (Axial Length Measurement / B
Scan)
Optic Nerve Photography
Refraction
1. Vision Testing (Acuity and Visual field)
2. Tonometry ( After Induction And Before Intubation )
3. External Examination
4. Anterior Segment Examination
5. Corneal Diameter Measurement
6. Gonioscopy
7. Optic Nerve &Fundus Examination
23. VISION TESTING :
Varies with patient’s age and Cognitive function
Central , maintained fixation behaviour and absent Nystagmus – Infants
Optotype Testing with Proper Refraction – Older Children
VISUAL FIELD TESTING:-
Difficult in children with Nystgmus and in Young Children.
Children with associated Neurological condition ( sturgeweber
syndrome) may have underlying homonymous hemifield vision loss
independent of Glaucoma.
24. EXTERNAL EXAMINATION:
Important to identify evidence of other associated abnormalities –
o Neurofibromatosis
o Facial haemangioma
o Photophobia
o Nasolacrimal duct obstruction
o Facial features s/o Metabolic disorder , Connective tissue disorder, Chromosomal
abnormalities.
-Exclude other causes of epiphora, photophobia and blepharospasm.
-Most common cause of epiphora in new-born and infant – congenital NLDO
-Others :- Conjunctivitis (infectious, chemical)
Corneal epithelial defect/ abrasion
Keratitis
Inflamed ant segment (uveitis, trauma)
26. Horizontal diameter from white to white……..
The vertical diameter is fallaciously lowered by
encroachment of sclera at the superior limbus
27. Also Document
Corneal edema/ clouding, breaks in Descemet’s membrane (Haab’s striae)
Other causes of corneal clouding
Sclerocornea
Tears in D membrane
Ulcers
Metabolic disease
Peters anomaly
Endothelial dystrophies
Dystrophy e.g congenital hereditary stromal dystrophy
28. TONOMETRY:
1. IOPshould be measured using Perkin’shand-held applanation tonometer or
tonopen
2. Most anesthetic agents reduceIOP
3. Should be measured early during earliest possible moments afteranesthesia
induction, before intubation.
4. AsymmetricIOPmore suggestiveof abnormality than B/Lborderline IOP
31. ANTERIOR SEGMENT EXAMINATION
(BIO-MICROSCOPY) :
Assess corneal size, symmetry, clarity.
Bio microscopy ( handheld slit lamp) adds improved examination and detail of
corneal architecture specially Haab’s striae.
IOP normalised Descemet's tear repair corneal edema clears , but
linear corneal opacities persists associated with reduced endothelial count
Permanent scaring Refractive errors.
Limbus may be dramatically stretched and thinned by ocular stretching in
infant eye with Glaucoma and Anterior chamber deepens.
32. GONIOSCOPY:
Koeppe (14-16mm) lens provides surgeon with appropriate view of the
angle.- Infants
Indirect Goniocopy – Zeiss or Sussman lens – Older Children.
In normal newborn
1. Iris inserts posterior to scleral spur.
2. TM appears more translucent than that of adult.
In primary congenital glaucoma
1. Anterior insertion of iris (flat or concave) directly into TM.
2. Surface of TM has stippled appearance and meshwork may appear thicker
3. Occasionally loops of blood vessels from major arterial circle may be seen
(LOCH NESS monster phenomenon)
33. OPTICNERVE & FUNDUS:
1. C:D ratio >0.3 and asymmetry are suggestive evidence of glaucoma.
2. The infant glaucomatous cup is more often round , steep walled central &
surrounded by uniform pink NRR. Tends to enlarge circumferentially with
progression of glaucoma.
3. Cupping is reversible
34. REFRACTION :-
Enlargement of globe due to elevated IOP , creates myopic shift in refractive
error Amblyopia , if significant anisometropia is present.
Haab’s striae significant Astigmatism Amblyopia ,especially in unilateral /
asymmetric cases.
35. ULTRASONOGRAPHY:-
Important ,because stabilisation and even reduction in axial length can occur
in enlarged eye with stable IOP.
In aphakic eyes of infants after filtration surgery OR implantation of Glaucoma
drainage device – axial length changes within days after a significant IOP
reduction.
Glaucoma filtration surgery – size of implant
B- scan helps in confirming Retinal status in eyes with opaque media -- aids in
assessing patency of glaucoma drainage devices when bleb is not seen.
36. CENTRAL CORNEAL THICKNESS:-
CHILDREN ( 6- 23 MONTHS ) – 540 µm
OLDER CHILDREN – 550- 560 µm
White people thinner CCT than Black people.
CCT is thinner in children with congenital glaucoma than other children.
Eyes with Aniridia, Aphakia -- thicker CCT
Importance of CCT in evaluation & management in children with Glaucoma
is still uncertain…...
37. IMAGING TECHNIQUES:-
FUNDUS PHOTOGRAPHY -
OPTICAL COHERENCE TOPOGRAPHY (OCT) –
Documentation
OCT – measure thickness of peripapillary nerve fibre layer ,
Macular area ,
Volume
Newly developed Handheld Spectral- domain OCT may be used, in uncoop
or children who can not assessed by standard technology.