Inflammation of conjunctiva due to allergic or hypersensitivity reactions which may be immediate (humoral) or delayed (cellular) to specific antigens
Types :
Simple allergic conjunctivitis
Hay fever conjunctivitis
Seasonal Conjunctivitis (SAC)
Perennial allergic conjunctivitis (PAC)
Vernal keratocon...
Inflammation of conjunctiva due to allergic or hypersensitivity reactions which may be immediate (humoral) or delayed (cellular) to specific antigens
Types :
Simple allergic conjunctivitis
Hay fever conjunctivitis
Seasonal Conjunctivitis (SAC)
Perennial allergic conjunctivitis (PAC)
Vernal keratoconjunctivitis (VKS)
Atopic keratoconjunctivitis (AKC)
Giant papillary conjunctivitis (GPC)
Phlyctenular keratoconjunctivitis (PKC)
H1 antihistamine – vasoconstrictor : Antazoline phosphate 0.5% + Naphazoline hydrochloride 0.5%
Antihistamine with mast cell stabilization property: Olopatadine 0.1%, Epinastine, Azelastine, Ketotifin
H1 antihistamine : Levocabastine, emedastine
Mast cell stabilizer : Cromolyn sodium 4%, pemirolast potassium, Nedocromil, iodoxamide
Topical NSAIDS: Ketrorolac, Flurbiprofen
Topical Steroids : rarely necessary
Immunosuppressant’s (cyclosporin) for steroid resistant cases
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Conjunctivitis – Allergic and Trachoma Dr Sambandha Dhoj Khati 2 nd year resident LEIRC 1
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Allergic conjunctivitis Inflammation of conjunctiva due to allergic or hypersensitivity reactions which may be immediate ( humoral ) or delayed (cellular) to specific antigens Types : Simple allergic conjunctivitis Hay fever conjunctivitis Seasonal Conjunctivitis (SAC) Perennial allergic conjunctivitis (PAC) Vernal keratoconjunctivitis (VKS) Atopic keratoconjunctivitis (AKC) Giant papillary conjunctivitis (GPC) Phlyctenular keratoconjunctivitis (PKC) 3
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Simple allergic conjunctivitis Mild form of disease Type I Hypersensitivity reaction Two forms : Seasonal allergic conjunctivitis (SAC) Perennial allergic conjunctivitis (PAC) 5
Etiology : Hay fever conjunctivitis : associated with allergic rhinitis Allergens : pollen , grass, animal dandruffs SAC : common and recurrent condition Caused by airborne allergen Worse during spring and summer PAC : from the allergens that exist year round : dust mites, animal dander or mold Less common and milder than SAC 6
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Symptoms : Itching (hallmark) Redness Tearing Burning sensation in eyes Sneezing and nasal discharge may be associated 8
Investigation Generally not done Conjuctival scrapping : eosinophils Specific IgE level : increased in serum and tear Tear cytology : eosinophils , neutrophils Positive skin test : for specific allergens 10
Treatment Elimination of allergen if possible Preventive : limit time spent outdoor using air conditioner with filter avoiding animal dander Cold compression 11
Vernal Keratoconjunctivitis Derived from Greek word “vernal” meaning occurring in spring Rare but serious form of ocular allergy Recurrent bilateral disorders IgE and cell mediated immune mechanism plays role 13
Predisposing factors : 4-20 years, remission by late teen Common in males More in late spring and summer Prevalent in warm dry climates, middle east, north America , non-existent in cold climate Atopic condition – asthma, eczema present in 90% 2/3 rd have family history of atopy 14
VKC pathology Conjunctival epithelium: hyperplasia and downward projection into the sub-epithelial tissue Adenoid layer : cellular infiltration by eosinophil’s, plasma cells, lymphocytes and histiocytes Fibrous layer: proliferation which later undergoes hyaline changes Conjunctival vessls : proliferation, increased permeability and vasodilation ALL THESE CHANGES LEADS TO MULTIPLE PAPILLAE FORMATION IN UPPER TARSAL CONJUNCTIVA 16
S ymptoms Intense itching Photophobia Lacrimation FB sensation Burning sensation Mucoid discharge – copious, tenacious, cord like 17
Signs Palpebral Disease : Early mild disease: conjunctival hyperemia, diffuse velvety papillary hypertrophy in upper tarsal plate Macro papillae (<1mm) : focal or diffuse, may progress to giant papillae (>1mm) over upper tarsal plate, Mucus deposition between giant papillae 18
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Limbal / bulbar form May start as a thickening and opacification of limbus Limbal nodules- mucoid nodules, which are gelatinous, elevated Horner – trantas dot – composed mainly of eosinophil's and epithelial debris ( limbal apices) 20
Limbal Vernal 21
Vernal keratopathy / corneal involvement Punctate epithelial erosion to macro erosions Sub epithelial scarring Pseudogerantoxon , Shield Ulcers – oval ulceration with thickened, opaque edges in upper part of cornea Superficial corneal vascularization keratoconus 22
Shield Ulceration pathophysiology 23
Hypothesis Mechanical hypothesis : Abrasion of cornea occurs by giant papillae on upper tarsal conjunctiva Hence there is superior location of shield ulcer Toxin hypothesis: Eosinophil granule contain major basic protein which are cytotoxic and inhibits epithelial healing Hence removal of inflammatory debris promotes epithelization 24
Grade I Transparent clear base Responds to medical management Minimal scarring, no vascularization Good outcome Grade II Inflammatory debris in ulcer base Responds poorly to medical management Surgical debridment of ulcer base required Re- epithelization in a week CAMERON’S GRADING OF SHIELD ULCER 25
Grade III Elevated plaque above surrounding epithelium Responds best to surgical treatment Promotes epithelization Antiscarring Antivascularization Anti inflammatory Acts as BCL 26
Progression of vernal keratopathy 27
Treatment Topical antihistamins Mast cell stablizers : Sodium chromoglycate 2% drops 4-5 times/day Topical steroid : every 4 hour for 2 days followed by 3-4 times a day for 2 weeks MONITOR IOP TO PREVENT STEROID INDUCED GLAUCOMA Acetylcysteine (10%) Topical cyclosporine (0.05%) : severe unresponsive case 28
Oral antihistamine : for itching Oral steroid : short course for very severe non responsive case Treatment of large papillae by supratarsal injection of long acting steroid or surgical removal General measures: dark goggles, cold compress, change of place from hot to cold 29
Supratarsal steriod injection TRICOT BEFORE AFTER 30
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The greater the papillary size, the more probable is the persistence or worsening of symptoms in the long term follow up period. Also indicated in poor prognosis for the persistence of the disease and its evolution into a chronic, perennial condition DOI: 10.1016/s0161-6420(00)00092-0 32
Other treatment modalities for giant papillae Surgical resection and autologous conjunctival graft in refractory cases Surgical resection and cryotherapy Superficial tarsectomy (compromises accessory lacrimal and meibomian gland function) Surgical resection and buccal mucous membrane graft 33
Differential diagnosis Bacterial/ viral conjunctivitis Rhinitis, dry eye Meibomian gland disease (resulting in tear film abnormality or insufficiency) Blepharitis Contact lens wear Topical and systemic medication use 34
Atopic keratoconjunctivitis Ocular manifestation of atopy Rare, billateral disease Peak incidence : 30-50 years of age No gender predilection Tends to be chronic and unremitting Both IgE and cell mediated immune response play role 35
Symptoms: Itching Soreness and dry sensation Mucoid discharge Photophobia Blurred of vision tearing 36
Signs Eyelids : Lid margin are chronically inflammed Maceration of inner and outer canthus Chornic blepharitis and madarosis may present Keratinization of lid margin may be present 37
Hertoghe sign Absense of the lateral portion of the eyebrow Dennie - morgan folds Lid skin folds caused by persistent rubbing 38
Conjunctiva Normally involves inferior palpebral conjunctiva Hyperemia, chemosis and watery discharge present Papillae are usually small Diffuse conjunctival infiltration, and scarring present 39
Cicatricial changes causes symblepharon formation and forniceal shortening Keratinization of caruncle Horner- trantas dots sometime present 40
Corneal Involvement : Punctate epithelial erosion over inferior third of cornea Peripheral vascularization and stromal scarring present Persistent epithelial defect may progress to cornea perforation and descematocele formation 41
Other: Anterior and posterior shield like cataract are common Retinal detachment and degenerative changes is common Risk of endophthalmitis are common after cataract surgery 42
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Investigation Serum and tear IgE : increased Conjunctival scrapping : eosinophil and mononuclear cells Tear assay : increased histamine, allergen specific IgE , tryptase 45
Treatment General measures: Allergen avoidance Cold compression Maintainance of eyelid hygiene Bandage contact lens 46
NSAIDS Topical steroids along with topical antibiotics Mucolytic agents: N- acetylcysteine Immunomodulators : cyclosporin 0.05%, tacrolimus 0.03% ointment Supratarsal steroid injection : in severe palpebral disease and noncompliant 48
Systemic medication: Oral histamines, Oral antibiotics: to reduce blepharitis aggravated inflammtion . doxycyclin , azithromycin Immunosuppresive agent: steroids, cyclosporin , tacrolimus , azathioprine, mainly in AKC unresponsive to other treatment Other treatment: allergen desensitization, plasmapheresis in patient with high serum level of IgE 49
Surgery Superificial keratectomy: to remove plaque Surface maintenance/ restoration surgery : Amniotic membrane overlay graft or Lamellar keratoplasty Eyelid procedure – botulinum induced ptosis or lateral tarsorrhaphy – persistent ED or ulceration 50
Giant papillary conjunctivits Not a true allergic reaction Inflammatory reaction of upper tarsal conjunctiva associated with Contact lens use Surgical suture barbs Ocular prosthesis 51
Clinical features Symptoms Thick mucous discharge , I nflammed superior papillae B lurry vision FB sensation R edness Signs: Mild conjunctival hyperemia Papillary hypertrophy on upper tarsal conjunctiva Milky white discharge between the papillae 52
Treatment Offending cause should be removed Ensure effective cleaning of contact lens, prosthesis Topical medication : mast cell stabilizers, antihistaminics , NSAIDS can be used Steroids have limited role 53
Phlyctenular conjunctivitis Usually self limiting condition Delayed type hypersensitivity (type 4 ) reaction to tuberculous , staphylococcus antigens, moraxella axenfeld baccilus , parasites Common in developing countries Predisposing factors: Age: peak age group 3-15 years Gender : girls than boys Living condition : overcrowded and unhygenic 54
Pathology Stage of nodule formation : exudation and infiltration of lymphocytes Stage of ulceration : necrosis of apex of nodule leading to ulcer formation Stage of granulation Stage of healing 55
Signs: Simple : most common Typically pinkish-white nodule at limbus or conjunctiva surrounded by hyperemia, often solitary Necrotizing : very large phlycten with necrosis and ulceration Miliary : mulitple phlyctens , may be arranged like a ring around 57
Phlyctenular keratitis Ulcerative : Sacrofulous ulcer: shallow marginal ulcer Fascicular ulcer : has prominent parallel leash of vessels Miliary ulcer: multiple ulcers scattered all over Diffuse infiltrative: Central infiltration of cornea Characteristic rich vascularization all around limbus 58
Treatment Local therapy: Topical steroid eye drop and ointment Topical antibiotic eyedrop and ointment Atropine eye ointment when cornea involved Systemic therapy : Diagnosis and management of TB Septic foci like caries, folliculitis, tonsilitis , adenoiditis to be adequately treated Parasitic infestation to be ruled out and treated if present GENERAL MEASURES: improve hygiene and supplement high-protein diet 59
Contact dermoconjunctivitis Allergic reaction in the conjunctiva and eyelid skin to medications (or other toxic products like cosmetics) Etiology: delayed type hypersensitivity response to prolong contact with chemicals and ophthalmic medicines (atropine, neomycin, soframycin ) 60
Clinical feature Cutaneous involvement : Weeping eczema around the area involved with medication Conjunctival response : Lower fornix and lower palpebral conjunctiva 61
Treatment Discontinuing of causative chemical or medication Antihistamine NSAIDS Topical steroid eye drop Steroid ointment in involved surrounding area 62
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Comparison of VKC and AKC 64
TRACHOMA 65
Trachoma Formely called as egyptian ophthalmia Chronic keratoconjunctivitis Affecting superficial epithelium of cornea and conjunctiva Leading cause of preventable irreversible blindness Caused by Chlamydia trachomatis serovars A,B,Ba,C 66
Chlamydia trachomatis Three species: A, B, Ba and C trachoma (C is commenest ) D- K inclusion conjunctivitis L1, L2 and L3 lymphogranuloma venerum 67
Predisposing factors Age : infancy and childhood Gender : more in female Climate : dry and dusty weather Socio-economic status : poor, overcrowding, poor hygiene Environmental exposure to dust, irritant, smoke, sunlight 68
Source of infection : Conjunctival discharge of affected person Superimposed bacterial infection speed up process Mode of infection : Direct spread by airborne/water borne modes Vector transmission by flies ( Musca domestica ) Through contaminated fingers, clothing,bedding Incubation period : 5-21 days 69
Risk factors 6D’s Dry Dusty Dirty Dung Discharge Density (crowding) Transmission of Trachoma 5 F’s Fingers Flies Face Faeces Fomites 70
Development life cycle 71
Pathology C.trachomatis – prokaryotic, obligatory intracellular parasite Papillary hyperplasia Lymphoid infiltration Localized aggregation of lymphocytes form follicles Follicle is invaded by multinucleated macrophages Fibroblast grow from periphery and form scar Cicatricial conjunctiva undergo hyaline or amyloid degeneration 72
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Clinical features Symptoms Foreign body sensation Occasional lacrimation Stickiness of lids Scanty mucoid discharge Diminution of vision Photophobia 75
Signs: Divided into active trachoma and cicatricial trachoma Active trachoma Common in preschool children Mixed follicular and papillary reactions Mucopurulent discharge Superior epithelial keratitis Pannus formation 76
Pannus Progressive pannus : infiltration of cornea ahead of vessels Regressive pannus : vessels extend beyond the area of infiltration 77
Cicatricial trachoma : Prevalent in middle age Eyelid signs : trichiasis , distichiasis , cicatricial entropion Conjunctival signs : Linear or stellate conjunctival scars – mild cases Arlt’s line (broad confluent scar) – severe disease 78
The WHO simplified system for the assessment of trachoma (1987) 80
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Mc callans classification Stage 1 – incipient trachoma / stage of infiltration Hypermia of palpebral conjunctiva and immature follicles Stage 2 – stage of florid infiltration Mature follicles, papillae, progressive pannus Stage 3- cicatrizaing trachoma/ stage of scarring Stage 4- healed trachoma / stage of sequale 82
Diagnosis Requires at least 2 of the following clinical features : Follicles on the upper tarsal conjunctiva Limbal follicles and their sequale ( herbert pits) Typical tarsal conjunctival scarring Vascular pannus most marked on the superior limbus 83
Laboratory Diagnosis Detection of Halberstaedter - Prowazek bodies on smear done by conjunctival scrapping Lugol’s iodine Giemsa stain Immunofluorescent stain Cytology Isolation of chlamydia Yolk culture McCoy type II cells tritated with cyclohexamide Hela cell line 87
Serology Complement fixation test Immunodiffusion assay Radioisotope assay Micro- immunofluorescent antibody test ELSIA DNA probes and PCR 88
Management Treat the affected and the family members Topical therapy Oint . Tetracyclin 1% / Oint . Erythromycin 2-4times/day X 6 weeks Gtt. Azithromycn 1% BD X 2-3 days 89
Systemic antibiotics Tab . Azithromycin 20mg/kg single dose Tab. Tetracycline 250mg PO QID X 3-4 weeks Tab. Erythromycin 250mg PO QID X 3-4 weeks Tab Doxycyclin 100mg PO OD X 3-4 weeks 90
WHO recommendation for antibiotic treatment for trachoma Determine the district level prevalence of TF in 1-9 years old children: If prevalence is 10% or more, mass treatment with antibiotic throughout the district If prevalence is less than 10%, assessment at the community level in area of known disease 91
In assessment at the community level: In communities in which the prevalence of TF in 1-9 year-old children is 10% or more – mass treatment with antibiotic In communities in which the prevalence of TF in 1-9 years old children is 5% or more, but <10% - targeted treatment should be considered In communities in which the prevalence of TF in 1-9 year old children is <5% - antibiotic distribution is not recommended 92
Surgical management Concretion Removed with hypodermic needle Trichiasis Lash treatment Corrective lid surgery 93
Posterior Lamellar Tarsal Rotation Posterior lamellar incision Dividing posterior and anterior lamella Horizontal mattress sutures Postoperative lid eversion 97
Tarsal Advance and Rotation Posterior lamellar incision and division between posterior and anterior lamella Rotation and suturing of terminal tarsus, inferior advancement and suturing of posterior lamella 98
Prophylaxis Hygiene measure Health education Environment sanitation Good water supply Early treatment of conjunctivitis Blanket antibiotic therapy Intermittent treatment WHO recommendation – endemic areas Minimize intensity and severity of disease Regimen – 1% tetracyclin eye ointment BD X 5 days in a month for 6 months 99
Prevention of trachoma blindness Effective intervention (SAFE strategy) S urgery Correct lid deformity Prevent blindenss A ntibiotics Acute infection Community control F acial hygiene E nvironment changes Health education Sanitation Water supply 100
Achievement Nepal : first country in south- east Asia validated for eliminating trachoma (21 st MAY , 2018, 71 st General Assembly of WHO) https://www.who.int/news/item/21-05-2018-nepal-first-country-in-south-east-asia-validated-for-eliminating-trachoma 101