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Guideline Summary
Guideline Title
Primary angle closure.
Bibliographic Source(s)
American Academy of Ophthalmology Glaucoma Panel. Primary angle closure. San Francisco (CA): American Academy of Ophthalmology; 2010. 29 p. [149 references]
Guideline Status

This is the current release of the guideline.

This guideline updates a previous version: Glaucoma Panel, Preferred Practice Patterns Committee. Primary angle closure. San Francisco (CA): American Academy of Ophthalmology (AAO); 2005. 23 p.

All Preferred Practice Patterns are reviewed by their parent panel annually or earlier if developments warrant and updated accordingly. To ensure that all Preferred Practice Patterns are current, each is valid for 5 years from the "approved by" date unless superseded by a revision.

Jump ToGuideline ClassificationRelated Content

Scope

Disease/Condition(s)

Primary angle closure (PAC)

Note: Primary angle closure is appositional or synechial closure of the anterior chamber angle caused by multiple mechanisms. Pupil block is considered to be a key element in the pathogenesis of most instances of PAC. The pressure in the posterior chamber is higher than the anterior chamber, causing an anterior bowing of the iris, which may crowd the angle in predisposed eyes.

Guideline Category
Diagnosis
Evaluation
Management
Prevention
Treatment
Clinical Specialty
Ophthalmology
Intended Users
Health Plans
Physicians
Guideline Objective(s)

To preserve visual function and maintain quality of life by preventing primary angle-closure glaucoma (PACG) or acute angle-closure crisis (AACC) from developing by addressing the following goals of therapy:

  • Identify those patients who are at risk of developing PACG or AACC or in whom it is present
  • Manage an acute attack of angle closure
  • Reverse or prevent angle closure by using laser iridotomy and/or, iridoplasty or, if necessary, incisional iridectomy to alleviate pupil block
  • Observe patients for chronic intraocular pressure (IOP) elevation, progression of synechial angle closure, identification of unsuspected plateau iris by repeat gonioscopy after iridotomy, or optic nerve damage, and manage as indicated
  • Evaluate the fellow eye for evidence of angle closure or an anatomic narrow angle in AACC and appropriately perform an iridotomy
  • Educate the patient and family members about the characteristics of the disease and involve them in the management of it
Target Population

Individuals of all ages, most of whom are adults over 50 who have risk factors that include abnormally high transpupillary resistance to aqueous humor movement, most often in association with pupil block

Interventions and Practices Considered
  1. Ophthalmic examination, including assessment of refractive status and pupil, determination of intraocular pressure (IOP), slit-lamp biomicroscopy, gonioscopy, evaluation of the fundus and optic nerve head, anterior segment imaging
  2. Medical therapy, including:
    • Topical beta-adrenergic antagonists
    • Topical alpha2-adrenergic agonists
    • Topical or systemic carbonic anhydrase inhibitors
    • Topical miotics
    • Systemic hyperosmotic agents
  3. Surgical treatment
    • Laser iridotomy
    • Incisional iridectomy
    • Prophylactic laser peripheral iridotomy of the fellow eye
  4. Pre- and post-operative care
  5. Vision rehabilitation and social services referral
  6. Follow-up evaluation
Major Outcomes Considered
  • Visual function
  • Quality of life

Methodology

Methods Used to Collect/Select the Evidence
Searches of Electronic Databases
Description of Methods Used to Collect/Select the Evidence

In the process of revising this document, a detailed literature search of PubMed and the Cochrane Library was conducted on December 3, 2008 and April 24, 2009 on the subject of primary angle closure (PAC) for the years from January 1, 2004 to the date of the search. Details of the literature search are available at www.aao.org/ppp External Web Site Policy.

Number of Source Documents

Not stated

Methods Used to Assess the Quality and Strength of the Evidence
Weighting According to a Rating Scheme (Scheme Given)
Rating Scheme for the Strength of the Evidence

Ratings of Strength of Evidence

Level I includes evidence obtained from at least one properly conducted, well-designed, randomized controlled trial. It could include meta-analyses of randomized controlled trials.

Level II includes evidence obtained from the following:

  • Well-designed controlled trials without randomization
  • Well-designed cohort or case-control analytic studies, preferably from more than one center
  • Multiple-time series with or without the intervention

Level III includes evidence obtained from one of the following:

  • Descriptive studies
  • Case reports
  • Reports of expert committees/organizations (e.g., Preferred Practice Pattern [PPP] panel consensus with external peer review)
Methods Used to Analyze the Evidence
Systematic Review
Description of the Methods Used to Analyze the Evidence

Not stated

Methods Used to Formulate the Recommendations
Expert Consensus
Description of Methods Used to Formulate the Recommendations

The results of a literature search on the subject of primary angle closure were reviewed by the Glaucoma Panel and used to prepare the recommendations, which they rated in two ways. The panel first rated each recommendation according to its importance to the care process. This "importance to the care process" rating represents care that the panel thought would improve the quality of the patient's care in a meaningful way. The panel also rated each recommendation on the strength of the evidence in the available literature to support the recommendation made.

Rating Scheme for the Strength of the Recommendations

Ratings of Importance to Care Process

Level A, defined as most important

Level B, defined as moderately important

Level C, defined as relevant, but not critical

Cost Analysis

A formal cost analysis was not performed and published cost analyses were not reviewed.

Method of Guideline Validation
Internal Peer Review
Description of Method of Guideline Validation

These guidelines were reviewed by Council and approved by the Board of Trustees of the American Academy of Ophthalmology (October 2010).

Recommendations

Major Recommendations

Ratings of importance to the care process (A-C) and ratings of strength of evidence (I-III) are defined at the end of the "Major Recommendations" field.

Diagnosis

History

The patient should be asked about symptoms that suggest intermittent angle-closure attacks (e.g., blurred vision, halos around lights, eye pain, headache, eye redness). [A:III] Review of the patient's family history may identify a relative with acute angle-closure glaucoma. Specific questioning includes asking about the use of topical or systemic medication (e.g., sulfonamides, topiramate [e.g., Topamax; Ortho-McNeil Neurologics, Titusville, NJ], phenothiazines, and anticholinergics) that may induce angle narrowing.

Ophthalmic Examination

Refractive Status [A:III]

Hyperopic eyes, especially in older patients, have narrower anterior chamber angles and are at increased risk of primary angle closure (PAC). Assessment of actual refractive status by retinoscopy or manifest refraction in the acute angle closure crisis (AACC) eye may be postponed until a subsequent visit. However, approximating the refractive status is appropriate by measuring the eyeglass power to determine the possibility of hyperopia or refracting the fellow eye.

Pupil [A:III]

  • Size and shape (may be asymmetric or oval in involved eye during or following an acute attack)
  • Reactivity (may be poorly reactive or mid-dilated during an acute attack and tonic after an attack)
  • Relative afferent pupillary defect (may be present in chronic angle closure or asymmetric optic nerve damage)

Slit-Lamp Biomicroscopy [A:III]

  • Conjunctival hyperemia (in acute cases)
  • Central and peripheral anterior chamber depth narrowing
  • Anterior chamber inflammation suggestive of a recent or current attack
  • Corneal swelling with or without microcystic edema (in acute cases)
  • Iris abnormalities, including diffuse or focal atrophy, posterior synechiae, abnormal pupillary function, irregular pupil shape, and a mid-dilated pupil (suggestive of a recent or current attack)
  • Lens changes including cataract and glaukomflecken (patchy, localized, anterior subcapsular lens opacities)
  • Corneal endothelial cell loss

Determination of Intraocular Pressure (IOP) [A:III]

Intraocular pressure is measured in each eye, preferably using a contact applanation method (typically Goldmann tonometry) before gonioscopy. Measuring central corneal thickness should be postponed until resolution of an acute attack (Aghaian et al., 2004). [A:III]

Gonioscopy [A:III]

Gonioscopy of both eyes should be performed on all patients in whom angle closure is suspected to evaluate the angle anatomy, appositional closure, and presence of peripheral anterior synechiae (PAS). Compression (indentation) gonioscopy with a four-mirror or similar lens is particularly helpful to determine if visible appositional closure is actually permanent, synechial closure and, if so, for the extent of such PAS.

Other Components of the Initial Evaluation

Although a dilated examination may not be advisable in patients with iridotrabecular contact (ITC), an attempt should be made to evaluate the fundus and optic nerve head using the direct ophthalmoscope or indirect ophthalmoscopy at the slit-lamp biomicroscope with a 90-diopter lens. [A:III] For patients with PAC or PAC suspect who are not having an acute attack, pupil dilation is not recommended until an iridotomy has been performed, since dilation can precipitate acute attacks (Wolfs et al., 1997). [A:III]

Management

Goals

The goals of managing a patient with PAC are as follows:

  • Reverse or prevent angle-closure process
  • Control intraocular pressure (IOP)
  • Prevent damage to the optic nerve

Primary Angle-Closure Suspect

In patients with ITC, and normal IOP without PAS, iridotomy may be considered to reduce the risk of developing angle closure. [A:III] Alternatively, patients with ITC may be followed for development of IOP elevation, evidence of progressive narrowing, or synechial angle closure, [A:III] since iridotomy can be associated with bothersome postoperative glare/diplopia.

Patients with PAC suspect who have not had an iridotomy should be warned that they are at risk for AACC and that certain medicines (e.g., over-the-counter decongestants, motion-sickness medication, anticholinergic agents) could cause pupil dilation and induce AACC (Wolfs et al., 1997). [A:III] They should also be informed about the symptoms of AACC and instructed to notify their ophthalmologist immediately if symptoms occur (Wilensky et al., 1993). [A:III]

Primary Angle Closure and Primary Angle-Closure Glaucoma

Iridotomy is indicated for eyes with PAC or primary angle-closure glaucoma (PACG) (Weinreb & Friedman, 2006; Saw, Gazzard, & Friedman, 2003). [A:III]

Acute Angle-Closure Crisis

Acute Attack Management

In AACC, medical therapy is usually initiated first to lower the IOP to reduce pain and clear corneal edema. [A:III] Iridotomy should then be performed as soon as possible. [A:III] Laser iridotomy is the preferred surgical treatment, because it has a favorable risk-benefit ratio (Quigley, 1981; American Academy of Ophthalmology Committee on Ophthalmic Procedures Assessment, 1994; Robin & Pollack, 1982). [A:II]

When laser iridotomy is not possible or if the AACC cannot be medically broken, laser peripheral iridoplasty (even with a cloudy cornea) (Lam et al., "Argon laser," 2002), paracentesis (Lam et al., "Efficacy and safety," 2002), and incisional iridectomy remain effective alternatives. [A:III]

Fellow-Eye Management

The fellow eye of a patient with AACC should be evaluated because it is at high risk for a similar event. The fellow eye should receive a prophylactic laser iridotomy promptly if the chamber angle is anatomically narrow, [A:II] since approximately half of fellow eyes of acute angle-closure patients can develop acute attacks within 5 years (Bain, 1957; Lowe, 1962; Wilensky et al., 1993; Saw, Gazzard, & Friedman, 2003; Edwards, 1982; Ang, Aung, & Chew, 2000; Snow, 1977).

Surgery and Postoperative Care

The ophthalmologist who performs the laser iridotomy or incisional iridectomy has the following responsibilities (American Academy of Ophthalmology, "Pretreatment assessment," 2006; American Academy of Ophthalmology, "An ophthalmologist's duties," 2006) [A:III]:

  • Obtain informed consent from the patient or the patient's surrogate decision maker after discussing the risks, benefits, and expected outcomes of surgery [A:III]
  • Ensure that preoperative evaluation confirms the need for surgery [A:III]
  • Perform at least one IOP check within 30 minutes to 2 hours of surgery (Robin, Pollack, & deFaller, 1987; Rosenblatt & Luntz, 1987; Barnes et al., 1999) [A:III]
  • Prescribe topical corticosteroids in the postoperative period [A:III]
  • Ensure that the patient receives adequate postoperative care [A:III]

Preoperative miotics facilitate laser iridotomy or iridectomy. Medications should be used perioperatively to avert sudden IOP elevation, particularly for patients who have severe disease (Robin, Pollack, & deFaller, 1987). [A:III]

Follow-up evaluation after surgery should include the following elements: [A:III]

  • Evaluation of the patency of iridotomy
  • Measurement of IOP
  • Gonioscopy with compression/indentation to assess the extent of PAS, if it was not performed immediately after iridotomy
  • Pupil dilation to decrease the risk of posterior synechiae formation
  • Fundus examination as clinically indicated

Follow-up Evaluation

Following iridotomy, patients with a residual open angle or a combination of open angle and some PAS with or without glaucomatous optic neuropathy should be followed at least annually, with special attention to repeat gonioscopy to determine interval changes such as increased extent of PAS or development of secondary angle closure from cataract progression and increased lens thickness. [A:III] Subsequent follow-up intervals depend on the clinical findings and judgment of the treating ophthalmologist.

Counseling/Referral

If the diagnosis or management of PAC, PAC suspect, AACC, or PACG is in question or is refractory to treatment, consultation with or referral to an ophthalmologist with special training or experience in managing this condition may be desirable. Patients with significant visual impairment or blindness may benefit from appropriate vision rehabilitation and social services. More information on vision rehabilitation, including materials for patients, is available at www.aao.org/smartsight External Web Site Policy.

Definitions:

Ratings of Importance to Care Process

Level A, defined as most important

Level B, defined as moderately important

Level C, defined as relevant, but not critical

Ratings of Strength of Evidence

Level I includes evidence obtained from at least one properly conducted, well-designed, randomized controlled trial. It could include meta-analyses of randomized controlled trials.

Level II includes evidence obtained from the following:

  • Well-designed controlled trials without randomization
  • Well-designed cohort or case-control analytic studies, preferably from more than one center
  • Multiple-time series with or without the intervention

Level III includes evidence obtained from one of the following:

  • Descriptive studies
  • Case reports
  • Reports of expert committees/organizations (e.g., Preferred Practice Pattern [PPP] panel consensus with external peer review)
Clinical Algorithm(s)

An algorithm for the management of patients with acute primary angle-closure crisis is provided in Appendix 3 in the original guideline document.

Evidence Supporting the Recommendations

References Supporting the Recommendations
Type of Evidence Supporting the Recommendations

The type of supporting evidence is identified and graded for most recommendations (see "Major Recommendations" field).

Benefits/Harms of Implementing the Guideline Recommendations

Potential Benefits

Prevention and appropriate treatment of primary angle closure

Potential Harms
  • Complications of laser iridotomy include increased intraocular pressure (IOP); laser burn of cornea, lens, or retina; late onset corneal edema; development of posterior synechiae; hyphema; iritis; and the development of a ghost image in vision.
  • Chronic miotic therapy is not an appropriate alternative, either for prophylaxis of the fellow eye or for treatment of established angle closure, and it is not a substitute for iridotomy. About 40% of fellow eyes treated with miotics can develop an acute attack within 5 years, and many eyes with angle closure can develop progressive formation of synechial angle closure with miotic use.

Qualifying Statements

Qualifying Statements
  • The Preferred Practice Pattern® (PPP) guidelines are based on the best available scientific data as interpreted by panels of knowledgeable health professionals. In some instances, such as when results of carefully conducted clinical trials are available, the data are particularly persuasive and provide clear guidance. In other instances, the panels have to rely on their collective judgment and evaluation of available evidence.
  • Preferred Practice Pattern guidelines provide the pattern of practice, not the care of a particular individual. While they should generally meet the needs of most patients, they cannot possibly best meet the needs of all patients. Adherence to these PPPs will not ensure a successful outcome in every situation. These practice patterns should not be deemed inclusive of all proper methods of care or exclusive of other methods of care reasonably directed at obtaining the best results. It may be necessary to approach different patients' needs in different ways. The physician must make the ultimate judgment about the propriety of the care of a particular patient in light of all of the circumstances presented by that patient. The American Academy of Ophthalmology is available to assist members in resolving ethical dilemmas that arise in the course of ophthalmic practice.
  • Preferred Practice Pattern guidelines are not medical standards to be adhered to in all individual situations. The Academy specifically disclaims any and all liability for injury or other damages of any kind, from negligence or otherwise, for any and all claims that may arise out of the use of any recommendations or other information contained herein.
  • References to certain drugs, instruments, and other products are made for illustrative purposes only and are not intended to constitute an endorsement of such. Such material may include information on applications that are not considered community standard, that reflect indications not included in approved U.S. Food and Drug Administration (FDA) labeling, or that are approved for use only in restricted research settings. The FDA has stated that it is the responsibility of the physician to determine the FDA status of each drug or device he or she wishes to use, and to use them with appropriate patient consent in compliance with applicable law.

Implementation of the Guideline

Description of Implementation Strategy

An implementation strategy was not provided.

Implementation Tools
Clinical Algorithm
Foreign Language Translations
Patient Resources
Quick Reference Guides/Physician Guides
For information about availability, see the Availability of Companion Documents and Patient Resources fields below.

Institute of Medicine (IOM) National Healthcare Quality Report Categories

IOM Care Need
Getting Better
Living with Illness
IOM Domain
Effectiveness
Patient-centeredness

Identifying Information and Availability

Bibliographic Source(s)
American Academy of Ophthalmology Glaucoma Panel. Primary angle closure. San Francisco (CA): American Academy of Ophthalmology; 2010. 29 p. [149 references]
Adaptation

Not applicable: The guideline was not adapted from another source.

Date Released
2000 Sep (revised 2010)
Guideline Developer(s)
American Academy of Ophthalmology - Medical Specialty Society
Source(s) of Funding

American Academy of Ophthalmology (AAO)

Guideline Committee

Glaucoma Panel; Preferred Practice Patterns Committee

Composition of Group That Authored the Guideline

Glaucoma Panel Members: Bruce E. Prum, Jr., MD, (Chair); David S. Friedman, MD, MPH, PhD, American Glaucoma Society Representative; Steven J. Gedde, MD; Leon W. Herndon, MD; Young H. Kwon, MD, PhD; Michele C. Lim, MD; Lisa F. Rosenberg, MD; Rohit Varma, MD, MPH, Methodologist

Preferred Practice Patterns Committee Members: Christopher J. Rapuano, MD, (Chair); David F. Chang, MD; Emily Y. Chew, MD; Robert S. Feder, MD; Stephen D. McLeod, MD; Bruce E. Prum, Jr., MD; R. Michael Siatkowski, MD; David C. Musch, PhD, MPH, Methodologist

Academy Staff: Flora C. Lum, MD; Nancy Collins, RN, MPH; Doris Mizuiri

Financial Disclosures/Conflicts of Interest

The panel and committee members have disclosed the following financial relationships occurring from January 2009 to September 2010:

David F. Chang, MD: Advanced Medical Optics - Consultant/Advisor; Alcon Laboratories, Inc. - Consultant/Advisor; Allergan, Inc. - Lecture fees; Calhoun Vision, Inc. - Consultant/Advisor, Equity owner; Eyemaginations, Inc. - Consultant/Advisor, Patent/Royalty; Ista Pharmaceuticals - Consultant/Advisor, Grant support; LensAR - Consultant/Advisor; Hoya - Consultant/Advisor; Peak Surgical - Consultant/Advisor; Revital Vision - Equity owner; SLACK, Inc. - Patent/Royalty; Transcend Medical - Consultant/Advisor; Visiogen, Inc. - Consultant/Advisor, Equity owner

Emily Y. Chew, MD: No financial relationships to disclose.

Robert S. Feder, MD: No financial relationships to disclose.

David S. Friedman, MD, MPH, PhD: Alcon Laboratories, Inc. - Grant support; NiCox - Consultant/Advisor; Novartis Pharmaceuticals Corp. - Consultant/Advisor; ORBIS International - Consultant/Advisor; Pfizer, Inc. - Consultant/Advisor, Lecture fees, Grant support; Promedior - Consultant/Advisor; Zeiss Meditec - Grant support

Steven J. Gedde, MD: Lumenis, Inc. - Lecture fees

Leon W. Herndon, MD: Alcon Laboratories, Inc. - Consultant/Advisor, Lecture fees; Allergan, Inc. - Lecture fees; iScience - Lecture fees; Ista Pharmaceuticals - Consultant/Advisor, Lecture fees; Merck & Co., Inc. - Lecture fees; Optonol, Ltd. - Lecture fees; Pfizer, Inc. - Lecture fees; Reichert, Inc. - Lecture fees

Young H. Kwon, MD, PhD: Allergan, Inc. - Consultant/Advisor; Free Educational Publications, Inc. - Equity owner; Pfizer, Inc. - Consultant/Advisor

Michele C. Lim, MD: No financial relationships to disclose.

Stephen D. McLeod, MD: Abbott Medical Optics - Consultant/Advisor, Equity owner; Visiogen, Inc. - Consultant/Advisor, Equity owner

David C. Musch, PhD, MPH: Glaukos Corp. - Consultant/Advisor; MacuSight, Inc. - Consultant/Advisor; National Eye Institute - Grant support; NeoVista, Inc. - Consultant/Advisor; Neurotech USA, Inc. - Consultant/Advisor; OPKO Health, Inc. - Consultant/Advisor; Oraya Therapeutics, Inc. - Consultant/Advisor; Pfizer Ophthalmics - Grant support; Washington University - Grant support

Bruce E. Prum, Jr., MD: Alcon Laboratories, Inc. - Grant support; Allergan, Inc. - Consultant/Advisor

Christopher J. Rapuano, MD: Alcon Laboratories, Inc. - Lecture fees; Allergan, Inc. - Consultant/Advisor, Lecture fees; Bausch & Lomb - Lecture fees; Inspire - Lecture fees; EyeGate Pharma - Consultant/Advisor; Inspire - Lecture fees; Rapid Pathogen Screening - Equity owner; Vistakon Johnson & Johnson Visioncare, Inc. - Lecture fees

Lisa F. Rosenberg, MD: No financial relationships to disclose.

R. Michael Siatkowski, MD: National Eye Institute - Grant support

Rohit Varma, MD, MPH: Alcon Laboratories, Inc. - Consultant/Advisor, Lecture fees; Allergan, Inc. - Consultant/Advisor, Grant support; Aquesys - Consultant/Advisor, Equity owner, Grant support; Bausch & Lomb Surgical - Consultant/Advisor; Genentech, Inc. - Consultant/Advisor, Grant support; Merck & Co., Inc. - Consultant/Advisor; National Eye Institute - Grant support; Optovue - Grant support; Pfizer, Inc. - Consultant/Advisor, Lecture fees, Grant support; Replenish, Inc. - Consultant/Advisor, Equity owner, Grant support

Guideline Status

This is the current release of the guideline.

This guideline updates a previous version: Glaucoma Panel, Preferred Practice Patterns Committee. Primary angle closure. San Francisco (CA): American Academy of Ophthalmology (AAO); 2005. 23 p.

All Preferred Practice Patterns are reviewed by their parent panel annually or earlier if developments warrant and updated accordingly. To ensure that all Preferred Practice Patterns are current, each is valid for 5 years from the "approved by" date unless superseded by a revision.

Guideline Availability

Electronic copies: Available from the American Academy of Ophthalmology (AAO) Web site External Web Site Policy.

Print copies: Available from American Academy of Ophthalmology, P.O. Box 7424, San Francisco, CA 94120-7424; telephone, (415) 561-8540.

Availability of Companion Documents

The following is available:

Print copies: Available from American Academy of Ophthalmology, P.O. Box 7424, San Francisco, CA 94120-7424; telephone, (415) 561-8540.

Patient Resources

The following are available:

Also, there are a variety of other patient education products available for purchase in English and Spanish from the American Academy of Ophthalmology (AAO) Web site External Web Site Policy.

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC Status

This summary was completed by ECRI on November 20, 2000. The information was verified by the guideline developer on December 20, 2000. This NGC summary was updated by ECRI on January 6, 2006. The updated information was verified by the guideline developer on February 9, 2006. This NGC summary was updated by ECRI Institute on February 21, 2011.

Copyright Statement

This National Guideline Clearinghouse (NGC) summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions. Information about the content, ordering, and copyright permissions can be obtained by calling the American Academy of Ophthalmology at (415) 561-8500.

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