You are in: eMedicine Specialties > Ophthalmology > INTRAOCULAR PRESSURE Glaucoma, Lens-ParticleArticle Last Updated: Aug 16, 2006AUTHOR AND EDITOR INFORMATIONAuthor: Brian R Sullivan, MD, Associate Professor, Department of Ophthalmology, University of Texas Southwestern Medical Center Brian R Sullivan is a member of the following medical societies: American Academy of Ophthalmology and American Society of Cataract and Refractive Surgery Editors: Richard W Allinson, MD, Associate Professor, Department of Ophthalmology, Texas A&M University Health Science Center, Scott and White Clinic; Simon K Law, MD, PharmD, Assistant Professor of Ophthalmology, Jules Stein Eye Institute; Chief of Section of Ophthalmology Surgical Services, Department of Veterans Affairs Healthcare Center, West Los Angeles; 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; Lance L Brown, OD, MD, Ophthalmologist, Affiliated With Freeman Hospital and St John's Hospital, Regional Eye Center, Joplin, Missouri; Hampton Roy Sr, MD, Associate Clinical Professor, Department of Ophthalmology, University of Arkansas for Medical Sciences Author and Editor Disclosure Synonyms and related keywords: lens-particle glaucoma, lens particle glaucoma, vision loss, visual deficit, lens-induced glaucoma, open-angle glaucoma, open angle glaucoma INTRODUCTIONBackgroundLens-particle glaucoma, a subclassification of lens-induced glaucoma, is a type of secondary open-angle glaucoma involving intraocular retention of fragmented lens debris. Following surgery or injury, lens material may be sequestered within the capsular bag or dislocated into other areas of either the posterior eye or anterior eye. Characteristically, large lens pieces spontaneously fragment further into small (sometimes invisible) particles that eventually migrate into the anterior chamber and obstruct aqueous outflow. Lens-particle glaucoma is not associated with decentration or dislocation of an intact lens. PathophysiologyThe mechanism involves the following 4 processes: (1) presence of a nonintact lens capsule, usually violated during trauma or intraocular surgery; (2) dislocation of lens fragments into the anterior or posterior segment, with subsequent release of lens particles into the anterior chamber; (3) obstruction of trabecular meshwork by lens debris and inflammatory components; and (4) reduction of the outflow facility of an open anterior chamber angle, resulting in elevation of intraocular pressure (IOP). FrequencyUnited StatesIncidence has not been reported. Mortality/MorbidityMortality is not associated with this condition. Morbidity is rare. RaceNo known racial predilection exists. SexNo known gender predilection exists for the condition. Penetrating eye trauma, a risk factor for lens-particle glaucoma, has been reported to occur more commonly in young adult males. Alcohol abuse is a significant comorbidity in this population. AgeAll ages are affected, ranging from infancy (especially when involving congenital cataract surgery) to late adulthood. Penetrating eye injuries occur most frequently in young adults. However, lens-particle glaucoma probably occurs most commonly in elderly persons as a complication of cataract surgery. CLINICALHistory
Physical
Causes
DIFFERENTIALSEndophthalmitis, Postoperative Foreign Body, Intraocular Glaucoma, Angle Closure, Acute Glaucoma, Angle Recession Glaucoma, Aphakic And Pseudophakic Glaucoma, Hyphema Glaucoma, Malignant Glaucoma, Phacolytic Glaucoma, Primary Open Angle Phacoanaphylaxis
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Drug Name | Levobunolol (Betagan, AKBeta) 0.25%, 0.5% |
|---|---|
| Description | Nonselective beta-adrenergic blocking agent that lowers IOP by reducing aqueous humor production and possibly increases outflow of aqueous humor. |
| Adult Dose | 1 gtt bid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; COPD; CHF; asthma; cardiac conduction defects; breastfeeding |
| Interactions | May cause bradycardia and asystole when used in combination with systemic beta-blockers (may cause additive effects) |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Beta-blockade 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 |
| Drug Name | Betaxolol (Betoptic) 0.25%, 0.5% |
|---|---|
| Description | Selectively blocks beta1-adrenergic receptors with little or no effect on beta2-receptors. Reduces IOP by reducing production of aqueous humor. |
| Adult Dose | 1 gtt bid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; CHF; cardiac conduction defects (possibly less effect on airways due to beta1 selectivity); breastfeeding |
| Interactions | May have additive systemic effects if patient is already on systemic beta-blockers |
| 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 |
| Drug Name | Carteolol HCl (Ocupress) 1% |
|---|---|
| Description | Blocks beta1- and beta2-receptors and has mild intrinsic sympathomimetic effects. |
| Adult Dose | 1 gtt bid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; CHF; asthma; cardiac conduction defects; breastfeeding |
| Interactions | May cause bradycardia and asystole when used in combination with systemic beta-blockers (may cause additive effects) |
| 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 |
| Drug Name | Timolol maleate (Timoptic, Timoptic XE) 0.25%, 0.5% |
|---|---|
| Description | May reduce elevated and normal IOP, with or without glaucoma, by reducing production of aqueous humor or by outflow. |
| Adult Dose | 1 gtt bid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; bronchial asthma; sinus bradycardia; second- and third-degree AV block; severe COPD; overt cardiac failure; cardiogenic shock |
| Interactions | May cause bradycardia and asystole when used in combination with systemic beta-blockers (may cause additive effects) |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Product may have sulfites, which may cause allergic-type reactions in susceptible patients; may exacerbate or precipitate heart block, asthma, COPD, and mental changes (especially in elderly persons) |
Topical adrenergic agonists (sympathomimetics) decrease aqueous production and reduce resistance to aqueous outflow. Adverse effects include dry mouth and allergenicity.
| Drug Name | Brimonidine (Alphagan) |
|---|---|
| Description | Selective alpha2-receptor that reduces aqueous humor formation and increases uveoscleral outflow. |
| Adult Dose | 1 gtt bid (bid dosing may be as effective as tid) |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; patients receiving MAOIs |
| Interactions | Coadministration with topical beta-blockers may further decrease IOP; tricyclic antidepressants may decrease effects of brimonidine; CNS depressants, such as barbiturates, opiates, and sedatives, may potentiate effects of brimonidine |
| 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 |
| Drug Name | Apraclonidine (Iopidine) 0.5%, 1% |
|---|---|
| Description | Reduces elevated, as well as normal, IOP whether or not accompanied by glaucoma. Apraclonidine is a relatively selective alpha-adrenergic agonist that does not have significant local anesthetic activity. Has minimal cardiovascular effects. |
| Adult Dose | 1 gtt tid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; patients on MAOIs or have taken them in the past 14 d |
| Interactions | Monitor pulse and BP frequently when giving cardiovascular drugs; not for use concurrently with MAOIs |
| 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 |
Reduce secretion of aqueous humor by inhibiting carbonic anhydrase (CA) in the ciliary body. These drugs are less effective, and their duration of action is shorter than many other classes of drugs. Adverse effects are relatively rare but include superficial punctate keratitis, acidosis, paresthesias, nausea, depression, and lassitude. Corneal decompensation has been reported when this class of drugs is used in patients with corneal endothelial dysfunction.
| Drug Name | Dorzolamide HCl (Trusopt) 2% |
|---|---|
| Description | 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 increases renal excretion of sodium, potassium bicarbonate, and water to decrease production of aqueous humor. |
| Adult Dose | 1 gtt tid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | 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) |
| Drug Name | Brinzolamide (Azopt) 1% |
|---|---|
| Description | 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 Dose | 1 gtt tid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | 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 (discontinue therapy and evaluate patient before restarting therapy) |
| Drug Name | Dorzolamide HCl/timolol maleate (Cosopt) |
|---|---|
| Description | Combination drug of carbonic anhydrase inhibitor and beta-blocker. |
| Adult Dose | 1 gtt bid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; COPD; CHF; asthma; cardiac conduction defects; breastfeeding |
| Interactions | 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); product may have sulfites, which may cause allergic-type reactions in susceptible patients |
| Drug Name | Acetazolamide (Diamox) |
|---|---|
| Description | Inhibits enzyme carbonic anhydrase, reducing 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 Dose | 125-250 mg tab PO qid or 500 mg cap PO bid; total dose not to exceed 1 g/24 h |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; hepatic disease; severe renal disease; adrenocortical insufficiency; severe pulmonary obstruction |
| Interactions | Can decrease therapeutic levels of lithium and alter excretion of drugs (eg, amphetamines, quinidine, phenobarbital, salicylates) by alkalinizing urine. |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Patients with impaired hepatic function may go into coma; may cause substantial increase in blood glucose in some diabetic patients; severe toxicities include decrease of potassium level and blood dyscrasia such as aplastic anemia |
| Drug Name | Methazolamide (Neptazane) |
|---|---|
| Description | Reduces aqueous humor formation by inhibiting enzyme CA, which results in decreased IOP. |
| Adult Dose | 25-100 mg PO bid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; renal impairment |
| Interactions | 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 |
Cholinergic antagonists commonly are used in the management of anterior intraocular inflammation, and, occasionally, they may be used in eyes with lens-particle glaucoma that have an active phacoantigenic uveitis. These topical drugs exert mydriatic and cycloplegic effects on the iris and ciliary body and reduce the permeability of the blood-aqueous barrier.
| Drug Name | Scopolamine 0.25% (I-Hyoscine) |
|---|---|
| Description | Topical antimuscarinic agent with potent mydriatic and cycloplegic action. Blocks action of acetylcholine at parasympathetic sites in the smooth muscle, producing pupillary dilation (mydriasis) and paralysis of accommodation (cycloplegia). |
| Adult Dose | 1 gtt bid/tid/qid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; narrow-angle glaucoma; bladder outlet obstruction; ileus/GI obstruction |
| Interactions | None reported |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Avoid excessive systemic absorption by compressing lacrimal sac using digital pressure for 1-3 min after instillation; may produce drowsiness, blurred vision, or sensitivity to light (due to dilated pupils); observe caution while driving or performing other tasks requiring alertness, coordination, or physical dexterity |
| Drug Name | Homatropine 5% (AK-Homatropine, Isopto homatropine) |
|---|---|
| Description | Topical antimuscarinic agent with moderate cycloplegic and mydriatic effects. Homatropine is less potent than scopolamine, and the toxicity of homatropine is one fiftieth of that of atropine. |
| Adult Dose | 1 gtt bid/tid/qid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; narrow-angle glaucoma |
| Interactions | None reported |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in elderly persons where increased IOP may be present; toxic anticholinergic systemic adverse effects can occur but are rare when used sparingly; adverse effects are more common in children, especially infants; compressing lacrimal sac by digital pressure for 1-3 min following instillation minimizes systemic absorption |
Corticosteroid agents commonly are used in combination with topical cycloplegics in the management of anterior uveitis. In cases of lens-particle glaucoma, the use of steroids is limited to eyes that have coexisting intraocular inflammation.
| Drug Name | Prednisolone acetate 1% (Pred Forte) |
|---|---|
| Description | Topical ophthalmic corticosteroid with approximately 3-5 times the potency of hydrocortisone. Topical corticosteroid therapy should be withdrawn by tapering the dosage. |
| Adult Dose | 1 gtt 1-8 times/d; dosage may be adjusted according to severity of inflammation, up to 1 gtt q1h |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; infectious diseases of the eye, particularly those associated with herpes simplex virus, zoster, fungi, and mycobacteria |
| Interactions | None reported |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in elderly persons where increased IOP may be present; toxic anticholinergic systemic adverse effects can occur but are rare when used sparingly; adverse effects are more common in children, especially infants; compressing lacrimal sac by digital pressure for 1-3 min following instillation minimizes systemic absorption |
| Drug Name | Loteprednol etabonate 0.5% (Lotemax) |
|---|---|
| Description | Topical ophthalmic corticosteroid. Although less potent, loteprednol may be associated with a lower risk of steroid-induced IOP elevation when compared to prednisolone and may be preferred in patients with glaucoma who have mild-to-moderate intraocular inflammation. Topical corticosteroid therapy should be withdrawn by tapering the dosage. |
| Adult Dose | 1 gtt 1-6 times/d; dosage may be adjusted according to severity of inflammation, up to 1 gtt q1h |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; infectious diseases of the eye, particularly those associated with herpes simplex virus, zoster, fungi, and mycobacteria |
| Interactions | None reported |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Steroid-induced elevation of IOP is a particular risk in patients with glaucoma; topical corticosteroid also associated with secondary ocular infections involving bacterial, viral, and fungal pathogens; caution in cases with erosive ocular surface disease, especially in eyes with exposure or other risk factors for corneal ulceration |
| Media file 1: Lens nucleus dislocated into the inferior vitreous during cataract surgery. Reprinted from Survey of Ophthalmology, Vol 43. Monshizadeh R, Nasrollah S, Haimovici R: Management of retained intravitreal lens fragments after cataract surgery. 397-403. Copyright 1999, with permission from Elsevier Science. | |
![]() | View Full Size Image | Media type: Photo |
| Media file 2: Ruptured lens capsule with elevated intraocular pressure following trauma. Courtesy of KS Kooner, MD. | |
![]() | View Full Size Image | Media type: Photo |
Glaucoma, Lens-Particle excerpt
Article Last Updated: Aug 16, 2006