eMedicine Specialties > Ophthalmology > Intraocular Pressure

Glaucoma, Unilateral: Treatment & Medication

Author: Ingrid U Scott, MD, MPH, Professor, Department of Ophthalmology and Public Health Sciences, Penn State College of Medicine
Contributor Information and Disclosures

Updated: Mar 8, 2007

Treatment

Medical Care

  • Increased EVP
    • Although topical glaucoma medications and oral carbonic anhydrase inhibitors may be used initially to control IOP, the underlying etiology must be resolved to achieve long-term IOP control.
    • Medications that decrease aqueous production are more effective than drugs that increase aqueous outflow.
  • ICE syndrome
    • Medications that reduce aqueous production can often control the early stages of glaucoma.
    • Epinephrine may be effective in some cases.
    • The benefit of topical prostaglandins remains to be demonstrated.
    • Miotics are generally ineffective due to mechanical obstruction of the trabecular meshwork.

Surgical Care

  • Increased EVP
    • Laser trabeculoplasty is generally ineffective unless there are secondary changes in the outflow channels.
    • Glaucoma filtering surgery may be necessary in cases refractory to medical therapy to completely bypass the resistance due to increased EVP; ciliochoroidal effusions or suprachoroidal hemorrhage may complicate filtering surgery.
    • The optimal treatment of a direct carotid-cavernous sinus fistula is closure of the abnormal arteriovenous communication with preservation of internal carotid artery patency. Techniques to achieve this result include surgical repair of the damaged portion of the intracavernous internal carotid artery, electrothrombosis, embolization, or balloon occlusion of the fistula.
    • Dural carotid-cavernous sinus fistulae may close spontaneously, but, for those lesions causing progressive or unacceptable symptoms and signs, standard embolization or endovascular balloon occlusion is generally performed. If these techniques are unsuccessful, direct surgery on the cavernous sinus may be considered. In cases where anatomy makes a standard intravascular approach impossible, the superior ophthalmic vein can be cannulated and a balloon or coil can be threaded into the area of a direct communication.
  • ICE syndrome
    • Laser trabeculoplasty is usually ineffective.
    • Patients with ICE syndrome generally do well with glaucoma filtering surgery, although late failure may develop due to endothelialization of the fistula, which, in some cases, may be reopened with the Nd:YAG laser.

Consultations

  • Increased EVP
    • Consultation is indicated depending on the coexisting conditions.
    • Oculoplastic consultation for management of orbital tumors
    • Vitreoretinal consultation for management of choroidal hemangiomas
    • Patients with thyroid ophthalmopathy may benefit from neuro-ophthalmic and/or oculoplastic consultation for management of optic neuropathy.
    • Corneal consultation for management of exposure keratitis
  • ICE syndrome - Cornea consultation for management of corneal edema

Medication

Medications used to decrease aqueous production include beta-blockers (topical), carbonic anhydrase inhibitors (topical and/or oral), and alpha 2-agonists.

Beta-adrenergic blockers

Decrease IOP by reducing aqueous production. Reduce elevated and normal IOP, with or without glaucoma.


Timolol 0.25%, 0.5% (Timoptic, Timoptic XE, Blocadren)

May reduce elevated and normal IOP, with or without glaucoma, by reducing production of aqueous humor or by outflow.

Adult

Timoptic: 1 gtt bid
Timoptic XE: 1 gtt qd

Pediatric

Administer as in adults

May cause bradycardia and asystole when used in combination with systemic beta-blockers (may cause additive effects)

Documented hypersensitivity; cardiac disease; low blood pressure; low pulse rate; pulmonary disease (eg, asthma, COPD); history of depression; history of hyperlipidemia

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

May exacerbate or precipitate heart block, asthma, COPD, and mental changes (especially in elderly persons); may alter blood lipid profile


Levobunolol 0.25% or 0.5% (AK Beta, Betagan)

Nonselective beta-adrenergic blocking agent that lowers IOP by reducing aqueous humor production and possibly increases outflow of aqueous humor.

Adult

1 gtt bid

Pediatric

Administer as in adults

May cause bradycardia and asystole when used in combination with systemic beta-blockers (may cause additive effects)

Documented hypersensitivity; bronchial asthma; severe COPD; sinus bradycardia; second- and third-degree AV block; overt cardiac failure; cardiogenic shock

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

May potentiate muscle weakness that is consistent with certain myasthenic symptoms (eg, diplopia, ptosis, generalized weakness); product may have sulfites, which may cause allergic-type reactions in certain susceptible persons


Metipranolol 0.3% (OptiPranolol)

Beta-adrenergic blocker that has little or no intrinsic sympathomimetic effects and membrane-stabilizing activity. Has little local anesthetic activity. Reduces IOP by reducing production of aqueous humor.

Adult

1 gtt bid

Pediatric

Administer as in adults

May cause bradycardia and asystole when used in combination with systemic beta-blockers (may cause additive effects)

Documented hypersensitivity; sinus tachycardia; cardiac failure; cardiogenic shock; second- and third-degree AV block

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

May exacerbate or precipitate heart block, asthma, COPD, and mental changes (especially in elderly persons); may alter blood lipid profile


Carteolol 1.0% (Ocupress)

Blocks beta 1- and beta 2-receptors and has mild intrinsic sympathomimetic effects.

Adult

1 gtt bid

Pediatric

Administer as in adults

May cause bradycardia and asystole when used in combination with systemic beta-blockers (may cause additive effects)

Documented hypersensitivity; congestive heart failure; asthma; cardiac conduction defects; breastfeeding

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Product may have sulfites, which may cause allergic-type reactions in certain susceptible persons


Betaxolol 0.25% or 0.5% (Betoptic)

Selectively blocks beta 1-adrenergic receptors with little or no effect on beta 2-receptors. Reduces IOP by reducing production of aqueous humor.

Adult

1 gtt bid

Pediatric

Administer as in adults

May have additive systemic effects if patient is already on systemic beta-blockers

Documented hypersensitivity; bronchial asthma; severe COPD; sinus bradycardia; second- and third-degree AV block; overt cardiac failure; cardiogenic shock

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Beta-blockade may potentiate muscle weakness consistent with myasthenic symptoms; product may have sulfites, which may cause hypersensitivity reactions in susceptible persons

Alpha 2-adrenergic agonists

Act to decrease aqueous humor formation.


Brimonidine 0.2% (Alphagan)

Selective alpha 2-receptor that reduces aqueous humor formation and increases uveoscleral outflow.

Adult

1 gtt tid

Pediatric

Administer as in adults

Coadministration with topical beta-blockers may further decrease IOP; tricyclic antidepressants may decrease effects of brimonidine; CNS depressants (eg, barbiturates, opiates, sedatives) may potentiate effects of brimonidine

Documented hypersensitivity; patients receiving MAOIs

Pregnancy

B - Usually safe but benefits must outweigh the risks.

Precautions

May exacerbate or precipitate ocular irritation, topical sensitivity, vasovagal attack, and optic nerve ischemia in patients with advanced glaucomatous optic neuropathy


Apraclonidine 0.5% or 1% (Iopidine)

Reduces elevated, as well as normal, IOP whether or not accompanied by glaucoma. A relatively selective alpha-adrenergic agonist that does not have significant local anesthetic activity. Has minimal cardiovascular effects.

Adult

1 gtt tid prelaser and postlaser or surgery, short term

Pediatric

Not established

Monitor pulse and BP frequently when giving cardiovascular drugs; not for use concurrently with MAOIs

Documented hypersensitivity; patients on MAOIs or have taken them in the past 14 d

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

May exacerbate or precipitate ocular irritation, topical sensitivity, vasovagal attack, and optic nerve ischemia in patients with advanced glaucomatous optic neuropathy

Carbonic anhydrase inhibitors

Enzyme found in many tissues of the body, including the eye. Catalyzes a reversible reaction where carbon dioxide becomes hydrated and carbonic acid dehydrated. By slowing the formation of bicarbonate ions with subsequent reduction in sodium and fluid transport, it may inhibit CA in the ciliary processes of the eye. This effect decreases aqueous humor secretion, reducing IOP.


Acetazolamide (Diamox, Diamox Sequels)

Inhibits enzyme CA, reducing the rate of aqueous humor formation, which, in turn, reduces IOP. Used for adjunctive treatment of chronic simple (open angle) glaucoma and secondary glaucoma and preoperatively in acute angle-closure glaucoma when delay of surgery desired to lower IOP.

Adult

125 mg or 250 mg PO bid/qid or 5-10 mg/kg q6-8h or 500 mg SR cap bid

Pediatric

5 mg/kg PO q6h

Can decrease therapeutic levels of lithium and alter excretion of drugs (amphetamines, quinidine, phenobarbital, salicylates) by alkalinizing urine

Documented hypersensitivity; hepatic disease; severe renal disease; adrenocortical insufficiency; severe pulmonary obstruction

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

May exacerbate or precipitate lethargy, depression, weight loss, acidosis, renal stones, and bone marrow suppression; patients with impaired hepatic function may go into coma; may cause substantial increase in blood glucose in some diabetic patients


Dorzolamide 2% (Trusopt)

Used concomitantly with other topical ophthalmic drug products to lower IOP. If more than one ophthalmic drug is being used, administer the drugs at least 10 min apart. Reversibly inhibits CA, reducing hydrogen ion secretion at renal tubule and increasing renal excretion of sodium, potassium bicarbonate, and water to decrease production of aqueous humor.

Adult

1 gtt tid

Pediatric

Not established

Coadministration with high-dose salicylate therapy may increase toxicity; may have additive systemic effects if patient is already on oral CA inhibitors

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Local ocular adverse effects, primarily conjunctivitis and lid reactions, may occur with long-term administration of dorzolamide (discontinue therapy and evaluate patient before restarting therapy)


Methazolamide (Neptazane)

Reduces aqueous humor formation by inhibiting enzyme CA, which results in decreased IOP.

Adult

25-50 mg PO bid/tid

Pediatric

Not established

May increase toxicity of salicylate, digoxin; coadministration with other diuretics may induce hypokalemia; decreases effects of lithium and alters excretion of other drugs by alkalinizing urine

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Caution in respiratory acidosis and diabetes mellitus; impairs mental alertness and/or physical coordination; hematuria, glycosuria, polyuria, hepatic insufficiency, bone marrow suppression, thrombocytopenia/purpura, agranulocytosis, urticaria, pruritus, and rash may occur


Brinzolamide 1% (Azopt)

Catalyzes reversible reaction involving hydration of carbon dioxide and dehydration of carbonic acid. May use concomitantly with other topical ophthalmic drug products to lower IOP. If more than one topical ophthalmic drug is being used, administer drugs at least 10 min apart.

Adult

1 gtt tid

Pediatric

Not established

May have additive systemic effects if patient is already on oral CA inhibitors

Pregnancy

B - Usually safe but benefits must outweigh the risks.

Precautions

Local ocular adverse effects, primarily conjunctivitis and lid reactions, may occur with long-term administration (discontinue therapy and evaluate patient before restarting therapy)

Prostaglandin derivatives

These agents may decrease intraocular pressure by increasing the outflow of aqueous humor.

They are administered once per day (except for unoprostone, which is administered twice daily). Potential adverse effects of these medications are similar to latanoprost (eg, eyelash growth, increased iris pigmentation). These agents are considered by some glaucoma specialists as first-line agents for glaucoma, mainly because of the lack of systemic adverse effects.


Bimatoprost ophthalmic solution (Lumigan)

A prostamide analogue with ocular hypotensive activity. Mimics the IOP-lowering activity of prostamides via the prostamide pathway. Used to reduce IOP in open-angle glaucoma or ocular hypertension.

Adult

1 gtt of 0.03% solution in affected eye(s) hs; not to exceed 1 dose/d

Pediatric

Not established

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

May cause permanent increase in pigment to iris (ie, increases brown pigment) and eyelid; may increase eyelash growth; may cause bacterial keratitis; caution in uveitis or macular edema; do not instill if wearing contact lenses


Travoprost ophthalmic solution (Travatan)

Prostaglandin F2-alpha analog. Selective FP prostanoid receptor agonist believed to reduce IOP by increasing uveoscleral outflow. Used to treat open-angle glaucoma or ocular hypertension.

Adult

1 gtt in affected eye(s) hs; not to exceed 1 dose/d

Pediatric

Not established

Documented hypersensitivity; pregnancy

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Commonly causes ocular hyperemia; may cause permanent increase in pigment to iris (ie, increases brown pigment) and eyelid; may increase eyelash growth; may cause bacterial keratitis; caution in uveitis or macular edema; do not instill if wearing contact lenses


Unoprostone ophthalmic solution (Rescula)

Prostaglandin F2-alpha analog. Selective FP prostanoid receptor agonist believed to reduce IOP by increasing uveoscleral outflow. Used to treat open-angle glaucoma or ocular hypertension.

Adult

1 gtt in affected eye(s) bid

Pediatric

Not established

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Commonly causes ocular hyperemia; may cause permanent increase in pigment to iris (ie, increases brown pigment) and eyelid; may increase eyelash growth; may cause bacterial keratitis; caution in uveitis or macular edema; do not instill if wearing contact lenses

More on Glaucoma, Unilateral

Overview: Glaucoma, Unilateral
Differential Diagnoses & Workup: Glaucoma, Unilateral
Treatment & Medication: Glaucoma, Unilateral
Follow-up: Glaucoma, Unilateral
References

References

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  3. Cibis GW, Tripathi RC, Tripathi BJ. Glaucoma in Sturge-Weber syndrome. Ophthalmology. Sep 1984;91(9):1061-71. [Medline].

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  5. Gandolfi SA, Cimino L, Sangermani C, et al. Improvement of spatial contrast sensitivity threshold after surgical reduction of intraocular pressure in unilateral high-tension glaucoma. Invest Ophthalmol Vis Sci. Jan 2005;46(1):197-201. [Medline].

  6. Jain SS, Rao P, Kothari K, et al. Posterior scleritis presenting as unilateral secondary angle-closure glaucoma. Indian J Ophthalmol. Sep 2004;52(3):241-4. [Medline].

  7. Kirsch M, Henkes H, Liebig T, et al. Endovascular management of dural carotid-cavernous sinus fistulas in 141 patients. Neuroradiology. Jul 2006;48(7):486-90. [Medline].

  8. Manor RS, Kurz O, Lewitus Z. Intraocular pressure in endocrinological patients with exophthalmos. Ophthalmologica. 1974;168(4):241-52. [Medline].

  9. Uram M, Zubillaga C. The cutaneous manifestations of Sturge-Weber syndrome. J Clin Neuroophthalmol. Dec 1982;2(4):245-8. [Medline].

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Further Reading

Keywords

open angle, closed angle, vision loss, visual deficit, open-angle glaucoma, episcleral venous pressure, EVP, glaucoma associated with iridocorneal endothelial syndrome, ICE syndrome

Contributor Information and Disclosures

Author

Ingrid U Scott, MD, MPH, Professor, Department of Ophthalmology and Public Health Sciences, Penn State College of Medicine
Ingrid U Scott, MD, MPH is a member of the following medical societies: American Academy of Ophthalmology, American Medical Association, American Society of Cataract and Refractive Surgery, American Society of Retina Specialists, Association for Research in Vision and Ophthalmology, Macula Society, Phi Beta Kappa, and Retina Society
Disclosure: Nothing to disclose.

Medical Editor

Bradford Shingleton, MD, Assistant Clinical Professor of Ophthalmology, Harvard Medical School; Consulting Staff, Department of Ophthalmology, Massachusetts Eye and Ear Infirmary
Bradford Shingleton, MD is a member of the following medical societies: Alpha Omega Alpha and American Academy of Ophthalmology
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Martin B Wax, MD, Clinical Professor, Department of Ophthalmology, University of Texas Southwestern Medical School; Vice President, Ophthalmology Research and Development, Head, Ophthalmology Discovery Research, Alcon Labs, Inc
Martin B Wax, MD is a member of the following medical societies: American Academy of Ophthalmology, American Glaucoma Society, and Society for Neuroscience
Disclosure: Alcon Labs Salary Employment

CME Editor

Lance L Brown, OD, MD, Ophthalmologist, Affiliated With Freeman Hospital and St John's Hospital, Regional Eye Center, Joplin, Missouri
Disclosure: Nothing to disclose.

Chief Editor

Hampton Roy Sr, MD, Associate Clinical Professor, Department of Ophthalmology, University of Arkansas for Medical Sciences
Hampton Roy Sr, MD is a member of the following medical societies: American Academy of Ophthalmology, American College of Surgeons, and Pan-American Association of Ophthalmology
Disclosure: Nothing to disclose.

 
 
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