Glaucoma classification: Difference between revisions
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{{CMG}} {{AE}}{{RBS}} | {{CMG}} {{AE}}{{RBS}} | ||
== Overview == | |||
The glaucoma is typically classified is as open angle or closed angle and as primary or secondary. There have been multiple schemes proposed for the classification for glaucoma. However the classification of the | The glaucoma is typically classified is as open angle or closed angle and as primary or secondary. There have been multiple schemes proposed for the classification for glaucoma. However the classification of the | ||
glaucomas based on initial events and classification based on mechanisms of outflow obstruction are commonly used. | glaucomas based on initial events and classification based on mechanisms of outflow obstruction are commonly used. | ||
==Classification | ==Classification Based Upon Angle== | ||
== | {| class="wikitable" | ||
! colspan="2" |Open-angle Glaucoma | |||
|- | |||
|Primary open-angle glaucoma (POAG) (H40.11) | |||
| | |||
:* Not associated with known ocular or systemic disorders that cause increased resistance to aqueous outflow or damage to optic nerve | |||
:* Elevated IOP | |||
|- | |||
|Normal-tension glaucoma (H40.12) | |||
| | |||
:* Continuum of POAG | |||
:* IOP is not elevated | |||
|- | |||
|Juvenile open-angle glaucoma | |||
== | | | ||
:* Open-angle glaucoma diagnosed at young age (typically 10-30 years of age) | |||
|- | |||
|Glaucoma suspect (H40.0) | |||
| | |||
:* Normal optic disc and visual field associated with elevated IOP | |||
:* Suspicious optic disc and/or visual field with normal IOP | |||
|- | |||
|Secondary open-angle glaucoma | |||
: | |||
| | |||
:* Increased resistance to trabecular meshwork outflow associated with other conditions (e.g. pigmentary-, phacolytic-, steroid-induced-) | |||
:* Increased post-trabecular resistance to outflow secondary to elevated episcleral venous pressure (e.g. carotid cavernous sinus fistula) | |||
|} | |||
{| class="wikitable" | |||
! colspan="2" |Angle-Closure Glaucoma | |||
|- | |||
|Primary ACG with relative | |||
pupillary block | |||
| | |||
:*Movement of aqueous humor from posterior chamber to anterior chamber restricted | |||
:*Peripheral iris in contact with trabecular meshwork | |||
|- | |||
|Acute angle closure | |||
: | |||
| | |||
:*Occurs when IOP rises rapidly as a result of relatively sudden blockage of the trabecular meshwork | |||
|- | |||
|Subacute angle closure (intermittent angle closure) | |||
: | |||
| | |||
:*Repeated, brief episodes of angle closure with mild symptoms and elevated IOP, often a prelude to acute angle closure | |||
|- | |||
|Chronic angle closure | |||
| | |||
:*IOP elevation caused by variable portions of anterior chamber angle being permanently closed by PAS | |||
|- | |||
|Secondary ACG with pupillary block | |||
| | |||
:*Swollen lens, secluded pupil | |||
|- | |||
|Secondary ACG without pupillary block | |||
: | |||
| | |||
:* Posterior pushing mechanism: lens-iris diaphragm pushed forward (e.g. posterior segment tumor, scleral buckling procedure, uveal effusion) | |||
:* Anterior pulling mechanism: anterior segment process pulling iris forward to form PAS (e.g. iridocorneal endothelial syndrome, neovascular glaucoma, inflammation) | |||
|- | |||
|Plateau iris syndrome | |||
| | |||
:*Primary angle closure with or without component of pupillary block, but pupillary block is not predominant mechanism of angle closure | |||
|} | |||
==Classification | {| class="wikitable" | ||
|+ | |||
!Childhood Glaucoma | |||
! | |||
|- | |||
|Primary congenital/infantile glaucoma | |||
: | |||
| | |||
:*Primary glaucoma present from birth to first few years of life | |||
|- | |||
|Glaucoma associated with congenital anomalies | |||
: | |||
| | |||
:*Associated with ocular disorders (e.g. anterior segment dysgenesis, aniridia) | |||
:* Associated with systemic disorders (e.g. rubella, Lowe syndrome) | |||
|- | |||
|Secondary glaucoma in infants and children | |||
: | |||
| | |||
:*Glaucoma secondary to retinoblastoma or trauma | |||
|} | |||
==Classification based upon initial event== | |||
=== Congenital and Developmental Glaucoma (Q15.0)=== | === Congenital and Developmental Glaucoma (Q15.0)=== | ||
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===Absolute Glaucoma (H44.5)=== | ===Absolute Glaucoma (H44.5)=== | ||
*Absolute glaucoma | *Absolute glaucoma | ||
==Classification based upon mechanism of outflow obstruction== | |||
===Open Angle Glaucoma Mechanisms=== | |||
#Pre-trabecular (membrane overgrowth) | |||
#:*Fibrovascular membrane (neovascular glaucoma) | |||
#:*Endothelial layer, often with Descemet-like membrane (iridocorneal endothelial syndrome, posterior polymorphous dystrophy, penetrating and non-penetrating trauma) | |||
#:*Epithelial downgrowth | |||
#:*Fibrous ingrowth | |||
#:*Inflammatory membrane (Fuchs heterochromic iridocyclitis,luetic interstitial keratitis) | |||
#Trabecular | |||
#:*Idiopathic (chronic open-angle glaucoma, juvenile open-angle glaucoma) | |||
#:*"Clogging” of trabecular meshwork | |||
#::*Red blood cells (hemorrhagic-, ghost cell-, sickled red blood cells) | |||
#::*Macrophages (hemolytic-, phacolytic-, melanomalytic-) | |||
#::*Neoplastic cells (primary ocular tumors, neoplastic tumors, juvenile xanthogranuloma) | |||
#::*Pigment particles (pigmentary-, exfoliation syndrome / glaucoma capsulare, malignant melanoma) | |||
#::*Protein (uveitis, lens-induced glaucoma) | |||
#::*Viscoelastic agents | |||
#::*α-chymotrypsin-induced glaucoma | |||
#::*Vitreous | |||
#:*Alterations of the trabecular meshwork | |||
#::*Steroid-induced glaucoma | |||
#::*Edema (uveitis, scleritis, episcleritis, alkali burns) | |||
#::*Trauma (angle recession) | |||
#::*Intraocular foreign bodies (hemosiderin, chalcosis) | |||
#Post-trabecular | |||
#:*Obstruction of Schlemm’s canal (e.g. collapse at canal) | |||
#:*Elevated episcleral venous pressure | |||
#:*Carotid cavernous fistula | |||
#:*Cavernous sinus thrombosis | |||
#:*Retrobulbar tumors | |||
#:*Thyroid ophthalmopathy | |||
#:*Superior vena cava obstruction | |||
#:*Mediastinal tumors | |||
#:*Sturge-Weber syndrome | |||
#:*Familial episcleral venous pressure elevation | |||
===Angle Closure Glaucoma Mechanisms=== | |||
#Anterior (“pulling”) | |||
#:*Contracture of membranes | |||
#::*Neovascular glaucoma | |||
#::*Iridocorneal endothelial syndrome | |||
#::*Posterior polymorphous dystrophy | |||
#::*Penetrating and non-penetrating trauma | |||
#:*Consolidation of inflammatory products | |||
#Posterior (“pushing”) | |||
#:*With pupillary block | |||
#::*Pupillary block glaucoma | |||
#::*Lens-induced mechanisms (phacomorphic lens, ectopia lentis) | |||
#::*Posterior synechiae (iris-vitreous block, pseudophakia, uveitis) | |||
#:*Without pupillary block | |||
#::*Ciliary block (malignant) glaucoma | |||
#::*Lens-induced mechanisms (phacomorphic lens, ectopia lentis) | |||
#::*Following lens extraction (forward vitreous shift) | |||
#::*Anterior rotation of ciliary body (following scleral buckling or panretinal photocoagulation, central retinal vein occlusion) | |||
#::*Intraocular tumors (retinoblastoma, malignant melanoma) | |||
#::*Cysts of the iris and ciliary body | |||
#::*Retrolenticular tissue contracture (retinopathy of prematurity, persistent hyperplastic primary vitreous) | |||
===Developmental Anomalies of Angle=== | |||
#Incomplete development of trabecular meshwork / Schlemm’s canal | |||
#:*Congenital (infantile) glaucoma | |||
#:*Axenfeld-Rieger syndrome | |||
#:*Peter’s anomaly | |||
#:*Glaucomas associated with other developmental anomalies | |||
#Iridocorneal adhesions | |||
#:*Broad strands (Axenfeld-Rieger syndrome) | |||
#:*Fine strands that contract to close angle (aniridia) | |||
===Combined Mechanism Glaucoma=== | |||
#Combination of two or more forms of glaucoma present either sequentially or simultaneously | |||
#IOP elevation can occur as a result of either or both of the following: | |||
#:*The intrinsic resistance of the trabecular meshwork to aqueous outflow in open-angle glaucoma | |||
#:*The direct anatomic obstruction of the filtering meshwork by synechiae in ACG | |||
==References== | ==References== | ||
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[[Category:Emergency medicine]] | [[Category:Emergency medicine]] | ||
[[Category:Mature chapter]] | [[Category:Mature chapter]] | ||
[[Category:Needs overview]] | [[Category:Needs overview]] |
Latest revision as of 21:52, 29 July 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Rohan Bir Singh, M.B.B.S.[2]
Overview
The glaucoma is typically classified is as open angle or closed angle and as primary or secondary. There have been multiple schemes proposed for the classification for glaucoma. However the classification of the glaucomas based on initial events and classification based on mechanisms of outflow obstruction are commonly used.
Classification Based Upon Angle
Open-angle Glaucoma | |
---|---|
Primary open-angle glaucoma (POAG) (H40.11) |
|
Normal-tension glaucoma (H40.12) |
|
Juvenile open-angle glaucoma |
|
Glaucoma suspect (H40.0) |
|
Secondary open-angle glaucoma
|
|
Angle-Closure Glaucoma | |
---|---|
Primary ACG with relative
pupillary block |
|
Acute angle closure
|
|
Subacute angle closure (intermittent angle closure)
|
|
Chronic angle closure |
|
Secondary ACG with pupillary block |
|
Secondary ACG without pupillary block
|
|
Plateau iris syndrome |
|
Childhood Glaucoma | |
---|---|
Primary congenital/infantile glaucoma
|
|
Glaucoma associated with congenital anomalies
|
|
Secondary glaucoma in infants and children
|
|
Classification based upon initial event
Congenital and Developmental Glaucoma (Q15.0)
- Developmental glaucoma
- Primary congenital glaucoma
- Infantile glaucoma
- Glaucoma associated with hereditary of familial diseases
Primary Glaucoma and its Variants (H40.1-H40.2)
- Primary glaucoma
- Variants of primary glaucoma
- Pigmentary glaucoma
- Exfoliation glaucoma, also known as pseudoexfoliative glaucoma or glaucoma capsulare
Secondary Glaucoma (H40.3-H40.6)
- Secondary glaucoma
- Inflammatory glaucoma
- Uveitis of all types
- Fuchs heterochromic iridocyclitis
- Phacogenic glaucoma
- Angle-closure glaucoma with mature cataract
- Phacoanaphylactic glaucoma secondary to rupture of lens capsule
- Phacolytic glaucoma due to phacotoxic meshwork blockage
- Subluxation of lens
- Glaucoma secondary to intraocular hemorrhage
- Traumatic glaucoma
- Angle recession glaucoma: Traumatic recession on anterior chamber angle
- Postsurgical glaucoma
- Neovascular glaucoma
- Drug-induced glaucoma
- Corticosteroid induced glaucoma
- Alpha- chymotrypsin glaucoma. Postoperative ocular hypertension from use of alpha chymotrypsin.
- Glaucoma of miscellaneous origin
- Associated with intraocular tumors
- Associated with retinal detachments
- Secondary to severe chemical burns of the eye
- Associated with essential iris atrophy
Absolute Glaucoma (H44.5)
- Absolute glaucoma
Classification based upon mechanism of outflow obstruction
Open Angle Glaucoma Mechanisms
- Pre-trabecular (membrane overgrowth)
- Fibrovascular membrane (neovascular glaucoma)
- Endothelial layer, often with Descemet-like membrane (iridocorneal endothelial syndrome, posterior polymorphous dystrophy, penetrating and non-penetrating trauma)
- Epithelial downgrowth
- Fibrous ingrowth
- Inflammatory membrane (Fuchs heterochromic iridocyclitis,luetic interstitial keratitis)
- Trabecular
- Idiopathic (chronic open-angle glaucoma, juvenile open-angle glaucoma)
- "Clogging” of trabecular meshwork
- Red blood cells (hemorrhagic-, ghost cell-, sickled red blood cells)
- Macrophages (hemolytic-, phacolytic-, melanomalytic-)
- Neoplastic cells (primary ocular tumors, neoplastic tumors, juvenile xanthogranuloma)
- Pigment particles (pigmentary-, exfoliation syndrome / glaucoma capsulare, malignant melanoma)
- Protein (uveitis, lens-induced glaucoma)
- Viscoelastic agents
- α-chymotrypsin-induced glaucoma
- Vitreous
- Alterations of the trabecular meshwork
- Steroid-induced glaucoma
- Edema (uveitis, scleritis, episcleritis, alkali burns)
- Trauma (angle recession)
- Intraocular foreign bodies (hemosiderin, chalcosis)
- Post-trabecular
- Obstruction of Schlemm’s canal (e.g. collapse at canal)
- Elevated episcleral venous pressure
- Carotid cavernous fistula
- Cavernous sinus thrombosis
- Retrobulbar tumors
- Thyroid ophthalmopathy
- Superior vena cava obstruction
- Mediastinal tumors
- Sturge-Weber syndrome
- Familial episcleral venous pressure elevation
Angle Closure Glaucoma Mechanisms
- Anterior (“pulling”)
- Contracture of membranes
- Neovascular glaucoma
- Iridocorneal endothelial syndrome
- Posterior polymorphous dystrophy
- Penetrating and non-penetrating trauma
- Consolidation of inflammatory products
- Posterior (“pushing”)
- With pupillary block
- Pupillary block glaucoma
- Lens-induced mechanisms (phacomorphic lens, ectopia lentis)
- Posterior synechiae (iris-vitreous block, pseudophakia, uveitis)
- Without pupillary block
- Ciliary block (malignant) glaucoma
- Lens-induced mechanisms (phacomorphic lens, ectopia lentis)
- Following lens extraction (forward vitreous shift)
- Anterior rotation of ciliary body (following scleral buckling or panretinal photocoagulation, central retinal vein occlusion)
- Intraocular tumors (retinoblastoma, malignant melanoma)
- Cysts of the iris and ciliary body
- Retrolenticular tissue contracture (retinopathy of prematurity, persistent hyperplastic primary vitreous)
Developmental Anomalies of Angle
- Incomplete development of trabecular meshwork / Schlemm’s canal
- Congenital (infantile) glaucoma
- Axenfeld-Rieger syndrome
- Peter’s anomaly
- Glaucomas associated with other developmental anomalies
- Iridocorneal adhesions
- Broad strands (Axenfeld-Rieger syndrome)
- Fine strands that contract to close angle (aniridia)
Combined Mechanism Glaucoma
- Combination of two or more forms of glaucoma present either sequentially or simultaneously
- IOP elevation can occur as a result of either or both of the following:
- The intrinsic resistance of the trabecular meshwork to aqueous outflow in open-angle glaucoma
- The direct anatomic obstruction of the filtering meshwork by synechiae in ACG