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10.3 Primary Glaucoma 253

Perimetry. Noise field perimetry is suitable as a screening test as it makes the patient aware of scotomas and makes it possible to detect and describe them. The patient is shown a flickering monitor displaying what resembles image noise on a television set. The patient will not see the flickering points in the region of the scotoma. After this test, the defect should be quantified by more specific methods. Automatic grid perimetry is suitable for the early stages of glaucoma. Special programs (such as the G1 program on the Octopus perimeter and the 30–2 program on the Humphrey perimeter devices) reveal the earliest glaucomatous changes. In advanced glaucoma, kinetic hand perimetry with the Goldmann perimeter device is a useful preliminary examination to evaluate the remaining field of vision.

Differential diagnosis: Two disorders are important in this context:

Ocular hypertension. Patients with ocular hypertension have significantly increased intraocular pressure over a period of years without signs of glaucomatous optic nerve damage or visual field defects. Some patients in this group will continue to have elevated intraocular pressure but will not develop glaucomatous lesions; the others will develop primary open angle glaucoma. The probability that a patient will develop definitive glaucoma increases the higher the intraocular pressure, the younger the patient, and the more compelling the evidence of a history of glaucoma in the family.

Low-tension glaucoma. Patients with low-tension glaucoma exhibit typical progressive glaucomatous changes in the optic disk and visual field without elevated intraocular pressure. These patients are very difficult to treat because management cannot focus on the control of intraocular pressure. Often these patients will have a history of hemodynamic crises such as gastrointestinal or uterine bleeding with significant loss of blood, low blood pressure, and peripheral vascular spasms (cold hands and feet). Patients with glaucoma may also experience further worsening of the visual field due to a drop in blood pressure.

Caution should be exercised when using cardiovascular and anti-hyper- tension medications in patients with glaucoma.

Treatment: Indications for initiating treatment.

Glaucomatous changes in the optic cup: Medical treatment should be initiated where there are signs of glaucomatous changes in the optic cup or where there is a difference of more than 20% between the optic cups of the two eyes.

Any intraocular pressure exceeding 30 mm Hg should be treated.

Increasing glaucomatous changes in the optic cup or increasing visual field defects: Regardless of the pressure measured, these changes show that the current pressure level is too high for the optic nerve and that additional medical therapy is indicated. This also applies to patients with advanced

254 10 Glaucoma

glaucomatous damage and threshold pressure levels (around 22 mm Hg). The strongest possible medications are indicated in these cases to lower pressure as much as possible (10–12 mm Hg).

Early stages: It is often difficult to determine whether therapy is indicated in the early stages, especially where intraocular pressure is elevated slightly above threshold values. Patients with low-tension glaucoma exhibit increasing cupping of the optical disk even at normal pressures (less than 22 mm Hg), whereas patients with elevated intraocular pressure (25–33 mm Hg) may exhibit an unchanged optic nerve for years.

Patients with suspected glaucoma and risk factors such as a family history of the disorder, middle myopia, glaucoma in the other eye, or differences between the optic cup in the two eyes should be monitored closely. Follow-up examinations should be performed three to four times a year, especially for patients not undergoing treatment.

Medical therapy. Available options in medical treatment of glaucoma (see also Fig. 10.1):

Inhibit aqueous humor production.

Increase trabecular outflow.

Increase uveoscleral outflow.

Fig. 10.14 and Table 10.3 list the various active ingredients and substance groups available for medical treatment of glaucoma. For the sake of completeness, Fig. 10.14 also lists traditional substances that are no longer used today; these include substances that have too many side effects or have been replaced by more efficient medications. Table 10.3 lists only those medications that are actually used today.

Principles of medical treatment of primary open angle glaucoma:

Medical therapy is the treatment of choice for primary open angle glaucoma. Surgery is indicated only where medical therapy fails.

There is no one generally applicable therapy plan. However, several principles may be formulated:

Where miosis is undesirable, therapy should begin with beta blockers (Table 10.3).

Where miosis is not a problem (as is the case with aphakia), therapy begins with miotic agents.

Miotic agents may be supplemented with beta blockers, epinephrine derivatives, guanethidine, dorzolamide and/or latanoprost maximum topical therapy).

Osmotic agents or carbonic anhydrase inhibitors (administered orally or intravenously) inhibit the production of aqueous humor. They can be administered temporarily in addition to topical medications. Their side effects usually make them unsuitable for prolonged treatment. The general rule is to try to use the weakest possible medications required to

10.3 Primary Glaucoma 255

Options in medical treatment of glaucoma.

 

 

 

 

 

 

 

Direct

 

Pilocarpine

 

 

 

 

 

 

 

 

(cholinergic agents)

Carbachol

 

 

 

 

 

 

 

 

Parasympatho-

Aceclidine

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

mimetic agents

Physostigmine (Eserine)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Reversible

 

 

 

 

 

 

 

 

 

Neostigmine

 

 

 

 

 

 

 

 

Indirect

 

 

 

 

 

 

 

 

Demecarium bromide

 

 

 

 

 

 

 

 

(cholinesterase

 

 

 

 

 

 

 

 

 

inhibitors)

Echothiophate iodide

 

ointments

 

 

 

 

Irreversible

 

 

 

 

 

Diisopropyl fluorophosphate

 

 

 

 

Prostaglandin

 

Latanoprost

 

 

 

 

analogues

 

 

and

 

 

 

 

 

 

 

 

 

 

 

 

 

eyedrops

 

 

 

Sympatho-

Direct

Epinephrine (α- und β-agonist)

 

 

 

 

sympatho-

Dipivefrin (clonidine central

 

 

 

 

mimetic

 

 

 

 

mimetic

α2-agonist)

 

 

 

 

agents

 

Topical

 

 

 

 

agents

Apraclonidine, Brimonidine

 

 

 

 

 

Direct

Beta blockers

 

 

 

 

 

 

 

 

 

sympatho-

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Sympatho-

lytic agents

 

 

 

 

 

 

 

 

 

lytic agents

Indirect

Guanethidine

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

sympatho-

 

 

 

 

 

 

 

 

 

6-hydroxy dopamine

 

 

 

 

 

 

 

 

 

lytic agents

 

 

 

 

 

 

 

 

Carbonic anhydrase

 

 

medication

 

 

 

Dorzolamide (eyedrops)

 

 

 

 

 

 

inhibitors

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Acetazolamide (systemic)

 

 

 

 

 

 

Dichlorphenamide

 

Systemic

 

 

 

Osmotic

 

Mannitol

 

 

 

 

 

Glycerine

 

 

 

 

agents

 

 

 

 

 

 

Ethyl alcohol

 

 

 

 

 

 

 

 

 

 

 

 

Fig. 10.14

Improve drainage of aqueous humor

Inhibit production of aqueous humor

Reduce ocular volume via osmotic gradient

achieve normal pressure over a 24-hour period: as much as necessary, and as little as possible.

The effectiveness of any pressure-reducing therapy should be verified by pressure analysis on the ward or on an outpatient basis.

The effect of the eyedrops should not interfere with the patient’s ability to work. Tolerance, effects, and side effects of the eyedrops should be

repeatedly verified on an individual basis during the course of treatment.

256 10 Glaucoma

Surgical treatment of primary open angle glaucoma. Indications:

Medical therapy is insufficient.

The patient does not tolerate medical therapy. Reactions include allergy, reduced vision due to narrowing of the pupil, pain, and ciliary spasms, and ptosis.

The patient is not a suitable candidate for medical therapy due to lack of compliance or dexterity in applying eyedrops.

Table 10.3 Medical treatment of glaucoma

Active ingredients and preparations (examples)

Parasympathomimetic

agents

Direct parasympathomimetic agents: Cholinergic agents

Pilocarpine

Carbachol

Aceclidine

Mode of action

Indications

Side effects

Improve

Primary

Younger pa-

drainage of

open angle

tients frequent-

aqueous humor

glaucoma

ly do not

in primary

Acute angle

tolerate the

open angle

closure

temporary

glaucoma. The

glaucoma

myopia due to

effect is prob-

 

contraction of

ably purely

 

the ciliary

mechanical via

 

muscle.

contraction of

 

Miosis with

the ciliary

 

worsening of

muscle and ten-

 

the night vision

sion on the

 

and narrowing

trabecular

 

of the peri-

meshwork and

 

pheral field of

scleral spur.

 

vision.

In acute angle

 

 

closure glau-

 

 

coma, the

 

 

forced narrow-

 

 

ing of the pupil

 

 

and the extrac-

 

 

tion of the iris

 

 

from the angle

 

 

of the anterior

 

 

chamber are

 

 

most impor-

 

 

tant.

 

 

 

 

 

 

 

Continued !

 

10.3 Primary Glaucoma

257

 

 

Table 10.3 (Continued)

 

 

 

 

 

 

 

 

 

 

 

Active ingredients and

Mode of action

Indications

Side effects

 

preparations (examples)

 

 

 

 

 

 

 

 

 

 

 

 

Improve

Primary

Cholinesterase

Indirect parasym-

pathomimetic

drainage. Con-

open angle

inhibitors are

agents: cholin-

traction of the

glaucoma

no longer rou-

esterase inhibitors

ciliary muscle

if other

tinely used

Neostigmine

and sphincter

miotic

today because

 

pupillae muscle

agents are

of their signifi-

 

is more pro-

no longer

cant ocular and

 

nounced than

effective.

systemic side

 

with other

 

effects. They

 

miotic agents.

 

are only used in

 

 

 

isolated cases

 

 

 

such as when

 

 

 

other medica-

 

 

 

tions fail to

 

 

 

control intra-

 

 

 

ocular pressure.

 

 

 

 

 

Direct sympathomi-

Improve

Primary

10 – 15% of pa-

metic agents

drainage of

open angle

tients develop

Dipivefrin

aqueous humor

glaucoma

an allergy.

(epinephrine deriva-

and reduce pro-

 

Paradoxical in-

tive)

duction of

 

crease in intra-

 

aqueous hu-

 

ocular pressure

 

mor.

 

occasionally

 

Used in combi-

 

occurs.

 

nation with

 

Epinephrine de-

 

pilocarpine and

 

rivatives have

 

carbonic anhy-

 

been shown to

 

drase inhibitors,

 

cause cystoid

 

these agents

 

maculopathy in

 

also reduce

 

patients with

 

intraocular

 

aphakia.

 

pressure.

 

Oxidation prod-

 

 

 

ucts of epine-

phrine derivatives form deposits in the conjunctiva (adrenochrome deposits) and can lead to obstruction of the canaliculus (see Fig. 4.24 h).

258

10 Glaucoma

 

 

Table 10.3 (Continued)

 

 

 

Active ingredients and

Mode of action

Indications

Side effects

preparations (examples)

 

 

 

Clonidine:

 

Reduces

Particularly

Lowers blood

 

 

intraocular

suitable for

pressure.

 

 

pressure by

young

Should be used

 

 

about 20%, pri-

patients

only in low con-

 

 

marily by vaso-

with pri-

centrations

 

 

constriction

mary open

(1/16% and

 

 

without in-

angle glau-

1/8%) because

 

 

fluencing the

coma.

the effect on

 

 

size of the pupil

 

intraocular

 

 

and accommo-

 

pressure is the

 

 

dation.

 

same as with

 

 

 

 

higher concen-

 

 

 

 

trations but the

 

 

 

 

side effects are

 

 

 

 

significantly

 

 

 

 

less.

Apraclonidine:

 

Also reduces

Very good

Beware of car-

 

 

aqueous humor

reduction

diovascular dis-

 

 

production.

of intraocu-

ease.

 

 

In contrast to

lar pressure

 

 

 

clonidine, this

in decom-

 

 

 

agent does not

pensated

 

 

 

reduce sys-

glaucoma.

 

 

 

temic blood

 

 

 

 

pressure.

 

 

Brimonidine:

 

Improves

As with apra-

As with apra-

 

 

drainage of

clonidine.

clonidine.

 

 

aqueous humor

 

 

 

 

by reducing

 

 

episcleral venous pressure and reducing aqueous humor production by decreasing ciliary body perfusion.

Continued !

10.3 Primary Glaucoma 259

Table 10.3 (Continued)

Active ingredients and

Mode of action

Indications

Side effects

preparations (examples)

 

 

 

Sympatholytic agents

Direct sympatholytic agents: beta blockers

Timolol:

Betaxolol:

Carteolol:

Levobunolol:

Metipranolol:

Indirect sympatholytic agents:

Guanethidine:

Reduce pres-

Primary

sure by de-

open angle

creasing pro-

glaucoma

duction of

Secondary

aqueous humor

open angle

without in-

glaucoma

fluencing pupil

Secondary

size and accom-

angle clo-

modation.

sure glau-

 

coma

Reduce heart rate and increase bronchiospasms in asthma patients.

Contraindications: Beta blockers should used with caution in patients with obstructive lung disease, cardiac insufficiency, or cardiac arrhythmia and only after consulting an internist. Absorption from topical application can produce systemic side effects.

Decrease

Reduce

Red eyes.

aqueous humor

pressure

 

production.

only

 

 

slightly.

 

 

 

 

 

 

Continued !

 

260

10 Glaucoma

 

 

Table 10.3 (Continued)

 

 

 

Active ingredients and

Mode of action

Indications

Side effects

preparations (examples)

 

 

 

Prostaglandin ana-

Increase

Suitable for

No known sys-

logues:

 

uveoscleral

all patients

temic side

Latanoprost:

aqueous humor

with pri-

effects.

 

 

 

drainage.

mary open

Local changes

 

 

 

 

angle glau-

in the color of

 

 

 

 

coma.

the iris in 16%

 

 

 

 

Adjunctive

of all patients.

 

 

 

 

therapy

 

 

 

 

 

with beta

 

 

 

 

 

blockers,

 

 

 

 

 

epine-

 

 

 

 

 

phrine deri-

 

 

 

 

 

vatives,

 

 

 

 

 

pilocarpine,

 

 

 

 

 

and car-

 

 

 

 

 

bonic anhy-

 

 

 

 

 

drase inhib-

 

 

 

 

 

itors.

 

Carbonic anhydrase

Reduces

Acute glau-

Prolonged ther-

inhibitors:

 

aqueous humor

coma.

apy causes

Dorzolamide:

production. The

Surgical

malaise, nau-

 

 

 

enzyme car-

procedures

sea, depres-

Acetazolamide:

bonic anhy-

that can

sion, anorexia,

Dichlorphenamide:

drase con-

increase

weight loss,

tributes to the

intraocular

and decreased

 

 

 

 

 

 

production of

pressure.

libido in

 

 

 

aqueous humor

 

40 – 50% of

 

 

 

via active secre-

 

glaucoma

 

 

 

tion of bicar-

 

patients.

 

 

 

bonate.

 

 

Continued !

 

 

10.3 Primary Glaucoma

261

Table 10.3 (Continued)

 

 

 

 

Active ingredients and

Mode of action

Indications

Side effects

preparations (examples)

 

 

 

 

Osmotic agents:

Decrease

Exclusively

 

 

Mannitol:

intraocular

indicated in

 

 

Glycerine:

pressure pre-

acute in-

 

 

sumably by

creases of

 

 

 

 

 

 

 

 

producing an

intraocular

 

 

 

 

osmotic pres-

pressure

 

 

 

 

sure gradient

such as

 

 

 

 

by means of

angle clo-

 

 

 

 

the hyper-

sure glau-

 

 

 

 

osmotic sub-

coma due

 

 

 

 

stances re-

to its short

 

 

 

 

leased into the

duration of

 

 

 

 

bloodstream.

action (only

 

 

 

 

This draws

a few

 

 

 

 

water from the

hours).

 

 

 

 

fluid-filled

 

 

 

 

 

spaces,

 

 

 

 

 

especially from

 

 

 

 

 

the vitreous

 

 

 

 

 

body and

 

 

 

 

 

aqueous

 

 

 

 

 

humor.

 

 

 

Argon laser trabeculoplasty:

Principle: Laser burns in the trabecular meshwork cause tissue contraction that widens the intervening spaces and improves outflow through the trabecular meshwork.

Technique: Fifty to 100 focal laser burns are placed in the anterior trabecular meshwork (Fig. 10.15).

Comment: Laser surgery in the angle of anterior chamber is possible only if the angle is open. The surgery itself is largely painless, may be performed as an outpatient procedure, and involves few possible complications. These may include bleeding from vascular structures near the angle and synechiae between the iris and individual laser burns. Argon laser trabeculoplasty can bring improvement with intraocular pressures up to 30 mm Hg. It decreases intraocular pressure by about 6–8 m Hg for about two years. Argon laser trabeculoplasty is only effective in about every second patient. The full effect occurs about four to six weeks postoperatively.

262 10 Glaucoma

Argon laser trabeculoplasty.

Canal of Schlemm

Cornea

 

 

 

 

 

 

 

 

 

 

 

Trabecular

 

 

 

eshwork

 

 

meshwork

 

 

 

 

 

 

 

ularm

 

 

 

 

ec

 

 

 

 

ab

 

 

 

 

 

Tr

 

 

 

 

 

 

 

 

 

Argon

laser

beam

 

 

 

 

 

 

 

 

 

 

 

 

Iris

 

 

 

 

 

Ciliary body

 

 

 

Lens

 

 

Fig. 10.15 An argon laser beam is focused on the trabecular meshwork through a gonioscope and slit lamp. Approximately 100 laser burns are placed in a circle in the trabecular meshwork to improve aqueous humor drainage.

Filtration surgery:

Principle: The aqueous humor is drained through the anterior chamber through a subconjunctival scleral opening, circumventing the trabecular meshwork. Formation of a thin-walled filtration bleb is a sign of sufficient drainage of aqueous humor.

Technique (Fig. 10.16a – c): First a conjunctival flap is raised, which may be either fornix-based or limbal-based. Then a partial-thickness scleral flap is raised. Access to the anterior chamber is gained via a goniotomy performed with a 1.5 mm trephine at the sclerocorneal junction or via a rectangular trabeculectomy performed with a scalpel and dissecting scissors. A peripheral iridectomy is then performed through this opening. The scleral flap is then loosely closed and covered with conjunctiva.

Comment: A permanent reduction in intraocular pressure is achieved in 80–85% of these operations.

Cyclodialysis:

Principle: The aqueous humor is drained through an opening into the suprachoroidal space.

Technique: A full-thickness scleral incision is made down to the ciliary body 4 mm posterior to the limbus. The sclera is then separated from the