Ординатура / Офтальмология / Английские материалы / Ophthalmology A Short Textbook_Lang_2000
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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.
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Direct |
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Pilocarpine |
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(cholinergic agents) |
Carbachol |
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Parasympatho- |
Aceclidine |
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mimetic agents |
Physostigmine (Eserine) |
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Reversible |
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Neostigmine |
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Indirect |
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Demecarium bromide |
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(cholinesterase |
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inhibitors) |
Echothiophate iodide |
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ointments |
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Irreversible |
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Diisopropyl fluorophosphate |
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Prostaglandin |
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Latanoprost |
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analogues |
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and |
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eyedrops |
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Sympatho- |
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Epinephrine (α- und β-agonist) |
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sympatho- |
Dipivefrin (clonidine central |
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mimetic |
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mimetic |
α2-agonist) |
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agents |
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Topical |
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agents |
Apraclonidine, Brimonidine |
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Direct |
Beta blockers |
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sympatho- |
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Sympatho- |
lytic agents |
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lytic agents |
Indirect |
Guanethidine |
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sympatho- |
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6-hydroxy dopamine |
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lytic agents |
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Carbonic anhydrase |
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medication |
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Dorzolamide (eyedrops) |
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inhibitors |
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Acetazolamide (systemic) |
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Dichlorphenamide |
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Systemic |
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Osmotic |
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Mannitol |
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Glycerine |
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Ethyl alcohol |
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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- |
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contraction of |
ably purely |
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the ciliary |
mechanical via |
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muscle. |
contraction of |
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Miosis with |
the ciliary |
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worsening of |
muscle and ten- |
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the night vision |
sion on the |
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and narrowing |
trabecular |
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of the peri- |
meshwork and |
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pheral field of |
scleral spur. |
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vision. |
In acute angle |
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closure glau- |
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coma, the |
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forced narrow- |
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ing of the pupil |
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and the extrac- |
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tion of the iris |
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from the angle |
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of the anterior |
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chamber are |
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most impor- |
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tant. |
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Continued ! |
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10.3 Primary Glaucoma |
257 |
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Table 10.3 (Continued) |
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Active ingredients and |
Mode of action |
Indications |
Side effects |
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preparations (examples) |
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Improve |
Primary |
Cholinesterase |
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Indirect parasym- |
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pathomimetic |
drainage. Con- |
open angle |
inhibitors are |
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agents: cholin- |
traction of the |
glaucoma |
no longer rou- |
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esterase inhibitors |
ciliary muscle |
if other |
tinely used |
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– Neostigmine |
and sphincter |
miotic |
today because |
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pupillae muscle |
agents are |
of their signifi- |
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is more pro- |
no longer |
cant ocular and |
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nounced than |
effective. |
systemic side |
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with other |
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effects. They |
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miotic agents. |
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are only used in |
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isolated cases |
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such as when |
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other medica- |
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tions fail to |
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control intra- |
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ocular pressure. |
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Direct sympathomi- |
Improve |
Primary |
10 – 15% of pa- |
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metic agents |
drainage of |
open angle |
tients develop |
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– Dipivefrin |
aqueous humor |
glaucoma |
an allergy. |
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(epinephrine deriva- |
and reduce pro- |
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tive) |
duction of |
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crease in intra- |
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aqueous hu- |
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ocular pressure |
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mor. |
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occasionally |
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Used in combi- |
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nation with |
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Epinephrine de- |
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pilocarpine and |
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rivatives have |
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carbonic anhy- |
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been shown to |
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drase inhibitors, |
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cause cystoid |
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these agents |
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maculopathy in |
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also reduce |
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patients with |
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intraocular |
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aphakia. |
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pressure. |
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Oxidation prod- |
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ucts of epine- |
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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 |
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Table 10.3 (Continued) |
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Active ingredients and |
Mode of action |
Indications |
Side effects |
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preparations (examples) |
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Clonidine: |
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Reduces |
Particularly |
Lowers blood |
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intraocular |
suitable for |
pressure. |
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pressure by |
young |
Should be used |
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about 20%, pri- |
patients |
only in low con- |
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marily by vaso- |
with pri- |
centrations |
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constriction |
mary open |
(1/16% and |
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without in- |
angle glau- |
1/8%) because |
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fluencing the |
coma. |
the effect on |
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size of the pupil |
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intraocular |
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and accommo- |
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pressure is the |
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dation. |
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same as with |
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higher concen- |
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trations but the |
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side effects are |
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significantly |
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less. |
Apraclonidine: |
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Also reduces |
Very good |
Beware of car- |
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aqueous humor |
reduction |
diovascular dis- |
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production. |
of intraocu- |
ease. |
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In contrast to |
lar pressure |
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clonidine, this |
in decom- |
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agent does not |
pensated |
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reduce sys- |
glaucoma. |
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temic blood |
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pressure. |
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Brimonidine: |
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Improves |
As with apra- |
As with apra- |
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drainage of |
clonidine. |
clonidine. |
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aqueous humor |
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by reducing |
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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) |
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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- |
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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 |
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production. |
only |
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slightly. |
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Continued ! |
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260 |
10 Glaucoma |
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Table 10.3 (Continued) |
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Active ingredients and |
Mode of action |
Indications |
Side effects |
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preparations (examples) |
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Prostaglandin ana- |
Increase |
Suitable for |
No known sys- |
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logues: |
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uveoscleral |
all patients |
temic side |
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– |
Latanoprost: |
aqueous humor |
with pri- |
effects. |
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drainage. |
mary open |
Local changes |
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angle glau- |
in the color of |
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coma. |
the iris in 16% |
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Adjunctive |
of all patients. |
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therapy |
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with beta |
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blockers, |
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epine- |
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phrine deri- |
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vatives, |
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pilocarpine, |
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and car- |
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bonic anhy- |
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drase inhib- |
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itors. |
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Carbonic anhydrase |
Reduces |
Acute glau- |
Prolonged ther- |
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inhibitors: |
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aqueous humor |
coma. |
apy causes |
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– |
Dorzolamide: |
production. The |
Surgical |
malaise, nau- |
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enzyme car- |
procedures |
sea, depres- |
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– |
Acetazolamide: |
bonic anhy- |
that can |
sion, anorexia, |
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Dichlorphenamide: |
drase con- |
increase |
weight loss, |
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tributes to the |
intraocular |
and decreased |
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production of |
pressure. |
libido in |
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aqueous humor |
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40 – 50% of |
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via active secre- |
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glaucoma |
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tion of bicar- |
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patients. |
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bonate. |
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Continued !
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10.3 Primary Glaucoma |
261 |
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Table 10.3 (Continued) |
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Active ingredients and |
Mode of action |
Indications |
Side effects |
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preparations (examples) |
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Osmotic agents: |
Decrease |
Exclusively |
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– |
Mannitol: |
intraocular |
indicated in |
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Glycerine: |
pressure pre- |
acute in- |
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sumably by |
creases of |
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producing an |
intraocular |
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osmotic pres- |
pressure |
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sure gradient |
such as |
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by means of |
angle clo- |
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the hyper- |
sure glau- |
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osmotic sub- |
coma due |
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stances re- |
to its short |
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leased into the |
duration of |
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bloodstream. |
action (only |
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This draws |
a few |
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water from the |
hours). |
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fluid-filled |
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spaces, |
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especially from |
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the vitreous |
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body and |
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aqueous |
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humor. |
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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 |
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Trabecular |
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eshwork |
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meshwork |
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ularm |
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ab |
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Tr |
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Argon |
laser |
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Iris |
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Ciliary body |
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Lens |
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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
