- •Contents
- •General Introduction
- •Objectives
- •1 The Pediatric Eye Examination
- •Preparation
- •Examination: General Considerations and Strategies
- •Examination: Specific Elements
- •Visual Acuity Assessment
- •Alternative Methods of Visual Acuity Assessment in Preverbal Children
- •Red Reflex Examination (Brückner Test)
- •Dynamic Retinoscopy
- •Visual Field Testing
- •Pupil Testing
- •Anterior Segment Examination
- •Intraocular Pressure Measurement
- •Cycloplegic Refraction
- •Fundus Examination
- •Examination of the Uncooperative Child
- •2 Strabismus Terminology
- •Prefixes and Suffixes
- •Prefixes
- •Suffixes
- •Strabismus Classification Terms
- •Age of Onset
- •Fixation
- •Variation of the Deviation Size With Gaze Position or Fixating Eye
- •Miscellaneous Terms
- •Abbreviations for Types of Strabismus
- •3 Anatomy of the Extraocular Muscles
- •Horizontal Rectus Muscles
- •Vertical Rectus Muscles
- •Oblique Muscles
- •Levator Palpebrae Superioris Muscle
- •Relationship of the Rectus Muscle Insertions
- •Blood Supply of the Extraocular Muscles
- •Arterial System
- •Venous System
- •Structure of the Extraocular Muscles
- •Orbital and Fascial Relationships
- •Adipose Tissue
- •Muscle Cone
- •Muscle Capsule
- •The Tenon Capsule
- •Pulley System
- •Anatomical Considerations During Surgery
- •4 Amblyopia
- •Epidemiology
- •Detection and Screening
- •Pathophysiology
- •Classification
- •Strabismic Amblyopia
- •Refractive Amblyopia
- •Visual Deprivation Amblyopia
- •Evaluation
- •Treatment
- •Cataract Removal
- •Refractive Correction
- •Occlusion and Penalization
- •Complications of Therapy
- •5 Motor Physiology
- •Basic Principles and Terms
- •Axes of Fick and Ocular Rotations
- •Positions of Gaze
- •Extraocular Muscle Action
- •Eye Movements
- •Motor Units
- •Monocular Eye Movements
- •Binocular Eye Movements
- •Supranuclear Control Systems for Eye Movement
- •6 Sensory Physiology and Pathology
- •Physiology of Normal Binocular Vision
- •Retinal Correspondence
- •Fusion
- •Selected Aspects of the Neurophysiology of Vision
- •Visual Development
- •Effects of Abnormal Visual Experience on the Retinogeniculocortical Pathway
- •Abnormalities of Binocular Vision
- •Visual Confusion
- •Diplopia
- •Sensory Adaptations in Strabismus
- •Suppression
- •Anomalous Retinal Correspondence
- •Monofixation Syndrome
- •History and Presenting Features of Strabismus
- •Assessment of Ocular Alignment
- •Positions of Gaze
- •Cover Tests
- •Corneal Light Reflex Tests
- •Subjective Tests
- •Assessment of Eye Movements
- •Ocular Rotations
- •Convergence
- •Fusional Vergence
- •Special Tests
- •Motor Tests
- •Assessment of the Field of Single Binocular Vision
- •3-Step Test
- •Prism Adaptation Test
- •Torticollis: Differential Diagnosis and Evaluation
- •Ocular Torticollis
- •Tests of Sensory Adaptation and Binocular Cooperation
- •Red-Glass Test
- •Bagolini Lenses
- •4Δ Base-Out Prism Test
- •Afterimage Test
- •Amblyoscope Testing
- •Worth 4-Dot Test
- •Stereoacuity Testing
- •Related Videos
- •8 Esodeviations
- •Epidemiology
- •Pseudoesotropia
- •Infantile (Congenital) Esotropia
- •Pathogenesis
- •Evaluation
- •Management
- •Accommodative Esotropia
- •Pathogenesis and Types of Accommodative Esotropia
- •Evaluation
- •Management
- •Acquired Nonaccommodative Esotropias
- •Basic Acquired Nonaccommodative Esotropia
- •Cyclic Esotropia
- •Sensory Esotropia
- •Divergence Insufficiency
- •Spasm of the Near Reflex
- •Consecutive Esotropia
- •Nystagmus and Esotropia
- •Incomitant Esotropia
- •Sixth Nerve Palsy
- •Other Forms of Incomitant Esotropia
- •9 Exodeviations
- •Pseudoexotropia
- •Exophoria
- •Intermittent Exotropia
- •Clinical Characteristics
- •Evaluation
- •Classification
- •Treatment
- •Convergence Weakness Exotropia
- •Constant Exotropia
- •Infantile Exotropia
- •Sensory Exotropia
- •Consecutive Exotropia
- •Other Forms of Exotropia
- •Exotropic Duane Retraction Syndrome
- •Neuromuscular Abnormalities
- •Dissociated Horizontal Deviation
- •Convergence Paralysis
- •10 Pattern Strabismus
- •Etiology
- •Clinical Features and Identification
- •V Pattern
- •A Pattern
- •Y Pattern
- •X Pattern
- •λ Pattern
- •Management
- •General Principles
- •Treatment of Specific Patterns
- •11 Vertical Deviations
- •A Clinical Approach to Vertical Deviations
- •Incomitant Vertical Tropias
- •Overelevation and Overdepression in Adduction
- •Superior Oblique Muscle Palsy
- •Inferior Oblique Muscle Palsy
- •Other Incomitant Vertical Tropias
- •Comitant Vertical Tropias
- •Monocular Elevation Deficiency
- •Orbital Floor Fractures
- •Other Comitant Vertical Tropias
- •Dissociated Vertical Deviation
- •Clinical Features
- •Management
- •Related Videos
- •12 Special Forms of Strabismus
- •Congenital Cranial Dysinnervation Disorders
- •Duane Retraction Syndrome
- •Congenital Fibrosis of the Extraocular Muscles
- •Möbius Syndrome
- •Miscellaneous Special Forms of Strabismus
- •Brown Syndrome
- •Third Nerve Palsy
- •Sixth Nerve Palsy
- •Thyroid Eye Disease
- •Chronic Progressive External Ophthalmoplegia
- •Myasthenia Gravis
- •Esotropia and Hypotropia Associated With High Myopia
- •Internuclear Ophthalmoplegia
- •Ocular Motor Apraxia
- •Superior Oblique Myokymia
- •Strabismus Associated With Other Ocular Surgery
- •13 Childhood Nystagmus
- •General Features
- •Nomenclature
- •Evaluation
- •History
- •Ocular Examination
- •Types of Childhood Nystagmus
- •Congenital Nystagmus
- •Acquired Nystagmus
- •Nystagmus-Like Disorders
- •Convergence-Retraction Nystagmus
- •Opsoclonus
- •Treatment
- •Prisms
- •Surgery for Nystagmus
- •14 Surgery of the Extraocular Muscles
- •Evaluation
- •Indications for Surgery
- •Planning Considerations
- •Visual Acuity
- •General Considerations
- •Incomitance
- •Cyclovertical Strabismus
- •Prior Surgery
- •Surgical Techniques for the Extraocular Muscles and Tendons
- •Approaches to the Extraocular Muscles
- •Rectus Muscle Weakening Procedures
- •Rectus Muscle Strengthening Procedures
- •Rectus Muscle Surgery for Hypotropia and Hypertropia
- •Adjustable Sutures
- •Oblique Muscle Weakening Procedures
- •Oblique Muscle Tightening (Strengthening) Procedures
- •Stay Sutures
- •Transposition Procedures
- •Posterior Fixation
- •Complications of Strabismus Surgery
- •Diplopia
- •Unsatisfactory Alignment
- •Iatrogenic Brown Syndrome
- •Anti-Elevation Syndrome
- •Lost and Slipped Muscles
- •Pulled-in-Two Syndrome
- •Perforation of the Sclera
- •Postoperative Infections
- •Foreign-Body Granuloma and Allergic Reaction
- •Epithelial Cyst
- •Conjunctival Scarring
- •Adherence Syndrome
- •Dellen
- •Anterior Segment Ischemia
- •Change in Eyelid Position
- •Refractive Changes
- •Anesthesia for Extraocular Muscle Surgery
- •Methods
- •Postoperative Nausea and Vomiting
- •Oculocardiac Reflex
- •Malignant Hyperthermia
- •Chemodenervation Using Botulinum Toxin
- •Pharmacology and Mechanism of Action
- •Indications, Techniques, and Results
- •Complications
- •Related Videos
- •15 Growth and Development of the Eye
- •Normal Growth and Development
- •Dimensions of the Eye
- •Refractive State
- •Orbit and Ocular Adnexa
- •Cornea, Iris, Pupil, and Anterior Chamber
- •Intraocular Pressure
- •Extraocular Muscles
- •Retina
- •Visual Acuity and Stereoacuity
- •Abnormal Growth and Development
- •16 Decreased Vision in Infants and Children
- •Normal Visual Development
- •Evaluation of the Infant With Decreased Vision
- •Classification of Visual Impairment in Infants and Children
- •Delayed Visual Maturation
- •Pregeniculate Visual Impairment
- •Retrogeniculate Visual Impairment, or Cerebral Visual Impairment
- •Pediatric Low Vision Rehabilitation
- •17 Eyelid Disorders
- •Congenital Eyelid Disorders
- •Telecanthus
- •Dystopia Canthorum
- •Cryptophthalmos
- •Ablepharon
- •Congenital Coloboma of the Eyelid
- •Ankyloblepharon
- •Congenital Ectropion
- •Congenital Entropion
- •Epiblepharon
- •Congenital Tarsal Kink
- •Distichiasis
- •Euryblepharon
- •Epicanthus
- •Palpebral Fissure Slants
- •Blepharophimosis–Ptosis–Epicanthus Inversus Syndrome
- •Congenital Ptosis
- •Marcus Gunn Jaw-Winking Syndrome
- •Infectious and Inflammatory Eyelid Disorders
- •Neoplasms and Other Noninfectious Eyelid Lesions
- •Capillary Malformations
- •Congenital Nevocellular Nevi of the Skin
- •Other Acquired Eyelid Conditions
- •Trichotillomania
- •Excessive Blinking
- •18 Orbital Disorders
- •Craniosynostosis
- •Nonsynostotic Craniofacial Conditions
- •Infectious and Inflammatory Conditions
- •Preseptal Cellulitis
- •Orbital Cellulitis
- •Childhood Orbital Inflammation
- •Neoplasms
- •Differential Diagnosis
- •Primary Malignant Neoplasms
- •Metastatic Tumors
- •Hematopoietic, Lymphoproliferative, and Histiocytic Neoplasms
- •Benign Tumors
- •Ectopic Tissue Masses
- •Cystic Lesions
- •Teratoma
- •Ectopic Lacrimal Gland
- •19 Lacrimal Drainage System Abnormalities
- •Congenital and Developmental Anomalies
- •Atresia of the Lacrimal Puncta or Canaliculi
- •Congenital Lacrimal Fistula
- •Dacryocystocele
- •Nasolacrimal Duct Obstruction
- •Clinical Features
- •Nonsurgical Management
- •Surgical Management
- •20 Diseases of the Cornea, Anterior Segment, and Iris
- •Congenital and Developmental Anomalies of the Cornea
- •Abnormalities of Corneal Size and Shape
- •Abnormalities of Peripheral Corneal Transparency
- •Abnormalities of Central and Diffuse Corneal Transparency
- •Treatment of Corneal Opacities
- •Congenital and Developmental Anomalies of the Globe
- •Microphthalmos
- •Anophthalmos
- •Nanophthalmos
- •Abnormalities of the Iris
- •Abnormalities in the Size, Shape, or Location of the Pupil
- •Acquired Corneal Conditions
- •Keratitis
- •Systemic Diseases Affecting the Cornea or Iris
- •Metabolic Disorders Affecting the Cornea or Iris
- •Other Systemic Diseases Affecting the Cornea or Iris
- •Tumors of the Cornea, Iris, and Anterior Segment
- •Cornea
- •Iris
- •Ciliary Body
- •Miscellaneous Clinical Signs
- •Pediatric Iris Heterochromia
- •Anisocoria
- •21 External Diseases of the Eye
- •Infectious Conjunctivitis
- •Ophthalmia Neonatorum
- •Bacterial Conjunctivitis
- •Viral Conjunctivitis
- •Inflammatory Disease
- •Blepharitis
- •Ocular Allergy
- •Ligneous Conjunctivitis
- •Miscellaneous Conjunctival Disorders
- •Papillomas
- •Conjunctival Epithelial Inclusion Cysts
- •Conjunctival Nevi
- •Ocular Melanocytosis
- •Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis
- •22 Pediatric Glaucomas
- •Genetics
- •Classification
- •Primary Childhood Glaucoma
- •Primary Congenital Glaucoma
- •Juvenile Open-Angle Glaucoma
- •Secondary Childhood Glaucoma
- •Glaucoma Associated With Nonacquired Ocular Anomalies
- •Glaucoma Associated With Nonacquired Systemic Disease or Syndrome
- •Secondary Glaucoma Associated With an Acquired Condition
- •Glaucoma Following Cataract Surgery
- •Treatment
- •Surgical Therapy
- •Medical Therapy
- •Prognosis and Follow-Up
- •Pediatric Cataracts
- •General Features
- •Morphology
- •Evaluation
- •Examination
- •Cataract Surgery in Pediatric Patients
- •Timing of the Procedure
- •Intraocular Lens Use in Children
- •Management of the Anterior Capsule
- •Lensectomy Without Intraocular Lens Implantation
- •Lensectomy With Intraocular Lens Implantation
- •Postoperative Care
- •Complications
- •Visual Outcome After Cataract Extraction
- •Structural or Positional Lens Abnormalities
- •Congenital Aphakia
- •Spherophakia
- •Coloboma
- •Dislocated Lenses in Children
- •Isolated Ectopia Lentis
- •Ectopia Lentis et Pupillae
- •Marfan Syndrome
- •Homocystinuria
- •Weill-Marchesani Syndrome
- •Sulfite Oxidase Deficiency
- •Treatment
- •24 Uveitis in the Pediatric Age Group
- •Epidemiology and Genetics
- •Classification
- •Anterior Uveitis
- •Juvenile Idiopathic Arthritis
- •Tubulointerstitial Nephritis and Uveitis Syndrome
- •Kawasaki Disease
- •Other Causes of Anterior Uveitis
- •Intermediate Uveitis
- •Posterior Uveitis
- •Toxoplasmosis
- •Toxocariasis
- •Panuveitis
- •Sarcoidosis
- •Familial Juvenile Systemic Granulomatosis
- •Vogt-Koyanagi-Harada Syndrome
- •Other Causes of Posterior Uveitis and Panuveitis
- •Masquerade Syndromes
- •Evaluation of Pediatric Uveitis
- •Treatment of Pediatric Uveitis
- •Management of Inflammation
- •Surgical Treatment of Uveitis Complications
- •25 Disorders of the Retina and Vitreous
- •Congenital and Developmental Abnormalities
- •Persistent Fetal Vasculature
- •Retinopathy of Prematurity
- •Hereditary Retinal Disease
- •Hereditary Macular Dystrophies
- •Hereditary Vitreoretinopathies
- •Infections
- •Herpes Simplex Virus and Cytomegalovirus
- •Human Immunodeficiency Virus
- •Tumors
- •Choroidal and Retinal Pigment Epithelial Lesions
- •Retinoblastoma
- •Acquired Disorders
- •Coats Disease
- •Diabetes Mellitus
- •Albinism
- •26 Optic Disc Abnormalities
- •Developmental Anomalies
- •Optic Nerve Hypoplasia
- •Morning Glory Disc Anomaly
- •Coloboma of the Optic Nerve
- •Myelinated Retinal Nerve Fibers
- •Tilted Disc Syndrome
- •Bergmeister Papilla
- •Megalopapilla
- •Peripapillary Staphyloma
- •Optic Nerve Aplasia
- •Melanocytoma
- •Optic Atrophy
- •Dominant Optic Atrophy, Kjer Type
- •Recessive Optic Atrophy
- •Behr Optic Atrophy
- •Leber Hereditary Optic Neuropathy
- •Optic Neuritis
- •Papilledema
- •Idiopathic Intracranial Hypertension
- •Pseudopapilledema
- •Drusen
- •27 Ocular Trauma in Childhood
- •Accidental Trauma
- •Superficial Injury
- •Penetrating Injury
- •Blunt Injury
- •Orbital Fractures
- •Traumatic Optic Neuropathy
- •Nonaccidental Trauma
- •Abusive Head Trauma
- •Ocular Injury Secondary to Nonaccidental Trauma
- •28 Ocular Manifestations of Systemic Disease
- •Diseases due to Chromosomal Abnormalities
- •Inborn Errors of Metabolism
- •Familial Oculorenal Syndromes
- •Phakomatoses
- •Neurofibromatosis
- •Tuberous Sclerosis
- •Von Hippel–Lindau Disease
- •Sturge-Weber Syndrome
- •Ataxia-Telangiectasia
- •Incontinentia Pigmenti
- •Wyburn-Mason Syndrome
- •Klippel-Trénaunay-Weber Syndrome
- •Intrauterine or Perinatal Infection
- •Toxoplasmosis
- •Rubella
- •Cytomegalovirus
- •Herpes Simplex Virus
- •Syphilis
- •Lymphocytic Choriomeningitis
- •Malignant Disease
- •Leukemia
- •Neuroblastoma
- •Basic Texts
- •Related Academy Materials
- •Requesting Continuing Medical Education Credit
CHAPTER 21
External Diseases of the Eye
This chapter focuses on external diseases of the eye that are seen in the pediatric population. Many of the topics covered in this chapter are also discussed in BCSC Section 8, External Disease and Cornea.
Infectious Conjunctivitis
Bacterial and viral infections are the most common causes of infectious conjunctivitis in children in developed countries. Patients with infectious conjunctivitis commonly present with burning, stinging, foreign-body sensation, ocular discharge, and matting of the eyelids. Symptoms and signs may present unilaterally or bilaterally. The character of the discharge, which can provide some diagnostic help, may be serous, mucopurulent, or purulent. Purulent discharge suggests a polymorphonuclear response to a bacterial infection; mucopurulent discharge suggests a viral or chlamydial infection; and a serous or watery discharge suggests a viral or allergic reaction. Membrane or pseudomembrane formation may be seen in severe viral or bacterial conjunctivitis, Stevens-Johnson syndrome, ligneous conjunctivitis, and chemical burns. Table 21-1 lists common causes of conjunctival injection, or red eye, in infants and children.
Table 21-1
Ophthalmia Neonatorum
Ophthalmia neonatorum refers to conjunctivitis occurring in the first month of life. This condition can be caused by bacterial, viral, and chemical agents. Widespread effective prophylaxis has diminished its occurrence to very low levels in industrialized countries, but ophthalmia neonatorum remains a significant cause of ocular infection, blindness, and even death in medically underserved areas around the world.
Epidemiology and etiology
Worldwide, the incidence of ophthalmia neonatorum is greater in areas with high rates of sexually transmitted disease and poor health care. The prevalence ranges from 0.1% in highly developed countries with effective prenatal and perinatal care to 10% in areas such as East Africa. Because a mother may have multiple sexually transmitted diseases, infants with one type of ophthalmia neonatorum should be screened for other such diseases. Public health authorities should be contacted to initiate evaluation and treatment of other maternal contacts in cases of sexually transmitted
diseases.
The causative organism usually infects the infant through direct contact during passage through the birth canal. Infection can ascend to the uterus, especially if there is prolonged rupture of membranes, so even infants delivered by cesarean section can be infected.
Neisseria gonorrhoeae
Ophthalmia neonatorum caused by Neisseria gonorrhoeae typically presents in the first 3–4 days of life. Patients may present with mild conjunctival hyperemia and discharge. In severe cases, there is marked chemosis, copious discharge, and potentially rapid corneal ulceration and perforation of the eye (Fig 21-1). Systemic infection can cause sepsis, meningitis, and arthritis.
Figure 21-1 Neisseria gonorrhoeae conjunctivitis.
Gram stain of the conjunctival exudate showing gram-negative intracellular diplococci allows for a presumptive diagnosis of N gonorrhoeae infection; treatment should be started immediately. Ophthalmia neonatorum from Neisseria meningitidis has also been reported. Definitive diagnosis is based on culture of the conjunctival discharge. Treatment of gonococcal ophthalmia neonatorum includes systemic ceftriaxone and topical irrigation with saline. Topical antibiotics may be indicated if there is corneal involvement.
Chlamydia trachomatis
Chlamydia trachomatis is an obligate intracellular bacterium that causes neonatal inclusion
conjunctivitis. Onset of conjunctivitis usually occurs around 1 week of age, although onset may be earlier, especially in cases with premature rupture of membranes. Eye infection is characterized by minimal to moderate discharge, mild swelling of the eyelids, and hyperemia with a papillary reaction of the conjunctiva. Severe cases may be accompanied by more copious discharge and pseudomembrane formation. Chlamydial infection in infants differs from that in adults in several ways: in infants, there is no follicular response, membrane formation may occur, and there is greater mucopurulent discharge.
Chlamydial infections can be diagnosed by culture of conjunctival scrapings, polymerase chain reaction, direct fluorescent antibody tests, and enzyme immunoassays. Systemic treatment of neonatal chlamydial disease is indicated because of the risk of pneumonia and otitis media. The treatment of choice is oral erythromycin, 50 mg/kg per day in 4 divided doses for 14 days.
Herpes simplex virus
Infection with herpes simplex virus (HSV) is usually secondary to HSV type 2 and typically presents later than infection with N gonorrhoeae or C trachomatis, frequently in the second week of life. See the discussion of congenital HSV infection in Chapter 28.
Chemical conjunctivitis
Chemical conjunctivitis refers to a mild, self-limited irritation and redness of the conjunctiva occurring in the first 24 hours after instillation of silver nitrate, a preparation used for prophylaxis against ophthalmia neonatorum. This condition improves spontaneously by the second day of life.
Prophylaxis for ophthalmia neonatorum
In 1880, Credé introduced the concept of widespread prophylaxis for gonorrheal ophthalmia neonatorum with 2% silver nitrate. Silver nitrate prophylaxis significantly reduced the incidence of gonorrheal conjunctivitis and is still used in some parts of the world. Silver nitrate is not effective against C trachomatis and thus has been supplanted by agents that act against both N gonorrhoeae and C trachomatis, such as erythromycin and tetracycline ointments.
A clinical trial for ophthalmia neonatorum conducted in Kenya showed that povidone-iodine drops are more effective and less toxic than erythromycin or silver nitrate ointment. Povidone-iodine is particularly useful in developing countries because of its low cost and ease of application.
Bacterial Conjunctivitis
The most common causes of bacterial conjunctivitis in school-aged children are Streptococcus pneumoniae, Haemophilus species, Staphylococcus aureus, and Moraxella. The incidence of infection from Haemophilus has decreased because of widespread immunization. More severe forms of bacterial conjunctivitis accompanied by copious discharge suggest infection with more virulent organisms, including N gonorrhoeae and N meningitidis.
Diagnosis is by clinical presentation. Culture to identify the offending agent is usually not necessary in mild cases but should be done in severe cases. If untreated, symptoms are self-limited but may last up to 2 weeks. A broad-spectrum topical ophthalmic drop or ointment should shorten the course to a few days. Topical medications that are usually effective include polymyxin combinations, aminoglycosides, erythromycin, bacitracin, fluoroquinolones, and azithromycin. The fluoroquinolones are considerably more expensive than other medications and may give rise to drugresistant organisms. Patients with N meningitidis conjunctivitis, and others exposed to these patients, require systemic treatment because of the high risk of meningitis.
Parinaud oculoglandular syndrome
Parinaud oculoglandular syndrome (POS) manifests as unilateral granulomatous conjunctivitis associated with preauricular and submandibular adenopathy that can be very marked (Fig 21-2). Bartonella henselae, a pleomorphic gram-negative bacillus that is endemic in cats and causes catscratch disease, is the most common cause of POS. Other causative organisms include
Mycobacterium tuberculosis, Mycobacterium leprae, Francisella tularensis, Yersinia pseudotuberculosis, Treponema pallidum, and C trachomatis. Cat-scratch disease is usually associated with a scratch from a kitten, but a cat bite or even touching the eye with a hand that has been licked by an infected kitten can cause the disease.
Figure 21-2 Parinaud oculoglandular syndrome. A, Marked follicular reaction in lower fornix. B, Massive enlargement of submandibular lymph node on affected right side. (Courtesy of David A. Plager, MD.)
Serologic testing is an effective means of diagnosing POS. Presence of antibodies to B henselae, detected by indirect fluorescent antibody testing or enzyme immunoassay, can confirm a diagnosis of cat-scratch disease. Treatment can be supportive in mild cases of cat-scratch disease because the disease is self-limited. In more severe cases systemic treatment, usually with azithromycin, may be indicated. Appropriate systemic antibiotics are used to treat the other organisms that cause POS.
Chlamydial infections
Two different diseases can be caused by C trachomatis in children and adolescents: trachoma and adult inclusion conjunctivitis.
Trachoma Trachoma is the most common cause of preventable blindness in the world. This disease is uncommon in Europe and the United States, except in areas of the southern United States and on Native American reservations. It is caused by poor hygiene and inadequate sanitation and is spread from eye to eye or by flies or fomites. Clinical manifestations include acute purulent conjunctivitis, a follicular reaction, papillary hypertrophy, vascularization of the cornea, and progressive cicatricial changes of the cornea and conjunctiva. Diagnosis is made by Giemsa stain, cell culture, or polymerase chain reaction. Treatment includes both topical and systemic erythromycin. Tetracycline can be used in children 8 years of age and older.
Adult inclusion conjunctivitis Adult inclusion conjunctivitis is a sexually transmitted disease that can be
