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Foster Classification and GPAC Clinical Picture

The document outlines a classification system for glaucoma based on the evolution of the disease, emphasizing the relationship between angle closure and glaucomatous optic neuropathy. It describes different stages, including suspicion of primary angle closure, primary angle closure, and primary closed-angle glaucoma, along with their symptoms and clinical manifestations. The classification also includes acute, intermittent, and chronic forms of angular closure, highlighting the importance of clinical assessment in identifying at-risk patients.
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0% found this document useful (0 votes)
32 views3 pages

Foster Classification and GPAC Clinical Picture

The document outlines a classification system for glaucoma based on the evolution of the disease, emphasizing the relationship between angle closure and glaucomatous optic neuropathy. It describes different stages, including suspicion of primary angle closure, primary angle closure, and primary closed-angle glaucoma, along with their symptoms and clinical manifestations. The classification also includes acute, intermittent, and chronic forms of angular closure, highlighting the importance of clinical assessment in identifying at-risk patients.
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd

Classification based on the evolution of the disease

This classification suggests a continuum of the disease, in which the angle closure process
and that of glaucomatous optic neuropathy represent associated alterations. Thus, the term
"glaucoma" is restricted to individuals who present with optic nerve damage.

• Suspicion of primary angular closure

Term used for the individual at risk of suffering from primary angle closure.
The identification of this condition is based on the inability to observe, at gonioscopy, the
pigmented portion of the trabecular meshwork at 180 or more, without complementary maneuvers, in
primary position of the gaze, in a dark environment, with a narrow light slot and without
to illuminate the pupil to prevent the opening of the angle. There are no pigmentary remnants of
previous iridotrabecular placement (imprint), goniosynechiae, or glaucomatous optic neuropathy,
and the levels of IOP are within the limits of normality.

• Primary angular closure

It is the term used when the individual already shows signs of the angular closure process.
primary.

In this condition, in addition to the gonioscopic alterations observed in individuals with


suspects of angle closure, show imprint or goniosynchia and/or increase in IOP.
However, there is no glaucomatous optic neuropathy.

The evolution of the "suspected angle closure" to the "primary angle closure" can occur.
in the presence or absence of symptoms.

Comment: the term "acute glaucoma" was replaced by the term "angle closure"
acute primary". This clinical presentation represents the most symptomatic form of the process of
angular closure, in which the filtering trabeculation is abruptly obstructed by the periphery
of the iris, which leads to a sharp increase in IOP and the characteristic symptoms. In the current
classification, the term 'glaucoma' is restricted to eyes that already show signs of neuropathy
glaucomatous optic nerve. The eyes that show sequelae of this acute clinical picture but without
Signs of glaucomatous neuropathy are characterized as eyes with 'acute angle closure'
primary." On the other hand, eyes with sequelae of primary acute angle closure and signs of
glaucomatous neuropathy is classified as "primary angle-closure glaucoma with
previous episodes of primary acute angle closure.

Note: The term "acute glaucoma" may remain in consensus during this period of
transition.

• Primary Closed-Angle Glaucoma

This condition is characterized by the alterations found in individuals with closure


primary angle, associated with the presence of glaucomatous optic neuropathy and/or defect
campimetric compatible with glaucoma.
Classification of the angular closure process by symptoms

The process of angular closure can manifest through three clinical forms: acute,
intermittent and chronic

Acute shape

More aggressive/symptomatic clinical manifestation of the angle closure process, generally


unilateral.

Symptoms:

• Intense eye pain


• Headache, in general, hemicrania and ipsilateral
• Blurred vision
• Vision of color halos
• Nausea and vomiting

Signs:

• High PIO, often above 40 mmHg


• Reduction of visual acuity
• Corneal edema, predominantly epithelial
• Midriasis media paralytica or hyporeactive pupil
• Previous flat camera
• Peripheral bulging of the iris (iris bombé)
• Angular closure generally at 360 or
• Conjunctival hyperemia with ciliary injection
• Tyndall inflammatory and/or pigmentary

NOTE: The optical disc may show edema, with venous congestion and/or hemorrhage in
candle flame associated.

Intermittent form

Clinical picture similar to that of the acute form, but with milder manifestations.
recurrent, which resolve spontaneously.

Symptoms

• Vision of halos, eye pain and/or mild ipsilateral headache at the time of the crisis

Signs:

• PIO elevated during crises, but normal between crises


• Imprint
• Presence or absence of goniosynchia
• Previous flat camera

• Chronic form

They represent the cases in which the angular closure process occurs asymptomatically.

Note: this classification refers to symptomatology and not to the duration of


disease.
Symptoms:

• Absent

Signs:

• high or normal PIO


• Presence or absence of goniosynchia
• Possible concomitance of intermittent or acute angle closure
• Flat front camera

Comments: In the different clinical presentations based on the symptoms, one can
observe or not glaucomatous optic neuropathy. The presence of the lesion in the optic nerve
It depends on individual susceptibility and the duration and intensity of elevated IOP.
the patient may migrate from one category to another over time, depending on the evolution of
the anatomical alterations and/or interventions performed. Ex: Patient with the chronic form
that eventually develops an acute angle closure, or a patient with the acute form that,
Even after the iridectomy, it becomes chronic.

Clinical assessment

The detection of patients at risk of primary angle closure should be carried out through the
biomicroscopic evaluation of the central and peripheral anterior chamber.

In patients with suspected primary angle closure, the ophthalmological examination should
include refraction, applanation tonometry, and anterior segment biomicroscopy
posterior.

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