ICD-10: H40.139

Pigmentary glaucoma, unspecified eye

Additional Information

Description

Pigmentary glaucoma is a specific type of secondary open-angle glaucoma characterized by the deposition of pigment granules in the trabecular meshwork, which can lead to increased intraocular pressure (IOP) and potential vision loss. The ICD-10 code H40.139 specifically refers to pigmentary glaucoma that is unspecified regarding which eye is affected.

Clinical Description of Pigmentary Glaucoma

Pathophysiology

Pigmentary glaucoma occurs when pigment from the iris is released into the aqueous humor, the fluid in the front part of the eye. This pigment can accumulate in the trabecular meshwork, the drainage system of the eye, leading to obstruction and increased IOP. The condition is often associated with a genetic predisposition and is more common in individuals with myopia (nearsightedness) and those of Caucasian descent.

Symptoms

Patients with pigmentary glaucoma may experience:
- Visual disturbances: These can include blurred vision or halos around lights, particularly during activities that involve rapid eye movement.
- Increased IOP: This may be asymptomatic initially but can lead to optic nerve damage if untreated.
- Peripheral vision loss: As the disease progresses, patients may notice a gradual loss of peripheral vision.

Diagnosis

Diagnosis typically involves:
- Comprehensive eye examination: This includes measuring IOP, assessing the optic nerve for damage, and evaluating the visual field.
- Gonioscopy: This procedure allows the eye care professional to examine the angle of the anterior chamber where the trabecular meshwork is located.
- Visual field testing: To detect any loss of peripheral vision.

Treatment

Management of pigmentary glaucoma may include:
- Medications: Topical medications such as prostaglandin analogs, beta-blockers, or carbonic anhydrase inhibitors to lower IOP.
- Laser therapy: Procedures like laser peripheral iridotomy or laser trabeculoplasty may be considered to improve aqueous outflow.
- Surgical options: In cases where medications and laser treatments are insufficient, surgical interventions may be necessary to create a new drainage pathway.

Coding Details for H40.139

ICD-10 Code Structure

  • H40: This is the general category for glaucoma.
  • H40.1: This subcategory refers to open-angle glaucoma.
  • H40.13: This further specifies pigmentary glaucoma.
  • H40.139: This code indicates pigmentary glaucoma that is unspecified regarding the eye affected, meaning it does not specify whether it is in the right eye, left eye, or both.

Clinical Implications

The unspecified nature of H40.139 means that when coding for this condition, the healthcare provider may not have determined which eye is affected, or the condition may be bilateral but not explicitly documented. Accurate coding is essential for proper billing and treatment planning, as it impacts the management strategies and potential reimbursement for services rendered.

Conclusion

Pigmentary glaucoma, classified under ICD-10 code H40.139, is a significant ocular condition that requires careful monitoring and management to prevent vision loss. Understanding its clinical presentation, diagnostic criteria, and treatment options is crucial for healthcare providers in delivering effective care to patients diagnosed with this condition. Regular follow-ups and patient education about the disease's nature and management are essential components of successful treatment outcomes.

Clinical Information

Pigmentary glaucoma, classified under ICD-10 code H40.139, is a specific type of glaucoma characterized by the deposition of pigment in the trabecular meshwork, leading to increased intraocular pressure (IOP) and potential optic nerve damage. Understanding its clinical presentation, signs, symptoms, and patient characteristics is crucial for timely diagnosis and management.

Clinical Presentation

Definition and Pathophysiology

Pigmentary glaucoma is a form of secondary open-angle glaucoma that occurs when pigment granules from the iris are released into the aqueous humor, subsequently obstructing the trabecular meshwork. This obstruction can lead to elevated IOP, which is a significant risk factor for optic nerve damage and vision loss[1].

Patient Characteristics

  • Demographics: Pigmentary glaucoma is more prevalent in younger individuals, typically affecting those between the ages of 20 and 50. It is more common in males than females, with a higher incidence reported in individuals of Caucasian descent[2].
  • Family History: A positive family history of glaucoma can increase the risk of developing pigmentary glaucoma, indicating a genetic predisposition[3].

Signs and Symptoms

Symptoms

Patients with pigmentary glaucoma may experience a range of symptoms, although many may remain asymptomatic in the early stages. Common symptoms include:
- Blurred Vision: Patients may report intermittent blurriness, particularly during physical activities or after exercise due to changes in IOP[4].
- Halos Around Lights: Some individuals may notice halos around lights, especially at night, which can be attributed to corneal edema or changes in the anterior chamber[5].
- Eye Pain or Discomfort: As the condition progresses and IOP increases, patients may experience ocular pain or discomfort[6].

Signs

During a comprehensive eye examination, several signs may indicate the presence of pigmentary glaucoma:
- Increased Intraocular Pressure: Measurement of IOP often reveals elevated levels, which can be confirmed through tonometry[7].
- Pigment Dispersion: The presence of pigment granules in the anterior chamber and on the corneal endothelium is a hallmark sign. This can be observed during slit-lamp examination[8].
- Optic Nerve Changes: Fundoscopic examination may reveal changes in the optic nerve head, such as cupping, which indicates potential damage due to elevated IOP[9].
- Visual Field Defects: As the disease progresses, visual field testing may show characteristic defects, often starting in the peripheral vision[10].

Conclusion

Pigmentary glaucoma, classified under ICD-10 code H40.139, presents with specific clinical features that can significantly impact patient quality of life if not diagnosed and managed promptly. Awareness of the demographic characteristics, symptoms, and clinical signs associated with this condition is essential for healthcare providers. Early detection through regular eye examinations and appropriate management strategies can help mitigate the risk of vision loss associated with this form of glaucoma. Regular monitoring and patient education about the disease's progression and management options are vital for optimal outcomes.

References

  1. Clinical and Economic Burden of Glaucoma by Disease.
  2. Primary Open-Angle Glaucoma Preferred Practice Pattern.
  3. ICD-10-CM Codes for Glaucoma.
  4. Complications and Management of Glaucoma Filtering.
  5. Nationwide Glaucoma Incidence in End Stage Renal Disease.
  6. ICD-10 Emergency Codes 10/1/2023 - DC Medicaid.
  7. ICD-10 International Statistical Classification of Diseases and Related Health Problems.
  8. Primary Open-Angle Glaucoma Preferred Practice Pattern.
  9. Glaucoma H40 - ICD-10-CM Codes.
  10. Primary Open-Angle Glaucoma Preferred Practice Pattern.

Approximate Synonyms

Pigmentary glaucoma, classified under the ICD-10-CM code H40.139, is a specific type of glaucoma characterized by the deposition of pigment in the trabecular meshwork, which can lead to increased intraocular pressure and potential vision loss. Understanding alternative names and related terms for this condition can enhance clarity in medical documentation and communication. Below are some alternative names and related terms associated with H40.139.

Alternative Names for Pigmentary Glaucoma

  1. Pigmentary Dispersion Syndrome: This term refers to the condition where pigment is released from the iris and deposited in various parts of the eye, potentially leading to pigmentary glaucoma.
  2. Pigmentary Glaucoma: Often used interchangeably with H40.139, this term emphasizes the glaucoma aspect of the pigmentary dispersion.
  3. Secondary Glaucoma: Since pigmentary glaucoma can arise as a secondary condition due to pigment dispersion, it may be referred to in this context.
  4. Iris Pigmentary Glaucoma: This term highlights the role of iris pigment in the development of the condition.
  1. Intraocular Pressure (IOP): A critical measurement in diagnosing and managing glaucoma, including pigmentary glaucoma.
  2. Trabecular Meshwork: The structure in the eye where aqueous humor drains; its obstruction by pigment can lead to increased IOP.
  3. Visual Field Loss: A common consequence of untreated glaucoma, including pigmentary glaucoma, where peripheral vision may be affected.
  4. Ocular Hypertension: A condition that can precede the development of glaucoma, including pigmentary types, characterized by elevated IOP without optic nerve damage.
  5. Glaucomatous Optic Neuropathy: Refers to the optic nerve damage that can occur as a result of glaucoma, including pigmentary glaucoma.

Conclusion

Understanding the alternative names and related terms for ICD-10 code H40.139 is essential for healthcare professionals involved in the diagnosis and treatment of glaucoma. These terms not only facilitate better communication among medical practitioners but also enhance patient education regarding their condition. For accurate coding and billing, it is crucial to use the correct terminology in medical records and insurance claims, ensuring that patients receive appropriate care and coverage.

Treatment Guidelines

Pigmentary glaucoma, classified under ICD-10 code H40.139, is a type of secondary open-angle glaucoma characterized by the deposition of pigment in the trabecular meshwork, which can lead to increased intraocular pressure (IOP) and potential vision loss. The management of pigmentary glaucoma typically involves a combination of medical, laser, and surgical interventions aimed at controlling IOP and preserving vision. Below is a detailed overview of standard treatment approaches for this condition.

Medical Management

1. Topical Medications

The first line of treatment for pigmentary glaucoma often involves the use of topical medications to lower IOP. Common classes of medications include:

  • Prostaglandin Analogues: These are often the first choice due to their efficacy in reducing IOP. Examples include latanoprost and bimatoprost, which work by increasing uveoscleral outflow.
  • Beta-Blockers: Such as timolol, these medications reduce aqueous humor production and are frequently used in combination with other agents.
  • Alpha Agonists: Medications like brimonidine can also decrease aqueous humor production and increase outflow.
  • Carbonic Anhydrase Inhibitors: These can be used topically (e.g., dorzolamide) or orally (e.g., acetazolamide) to further reduce aqueous humor production.
  • Rho Kinase Inhibitors: A newer class of medications, such as netarsudil, can enhance outflow through the trabecular meshwork.

2. Monitoring and Follow-Up

Regular monitoring of IOP and visual field testing is essential to assess the effectiveness of treatment and make necessary adjustments. Patients should be educated about the importance of adherence to prescribed medications.

Laser Treatment

1. Laser Peripheral Iridotomy (LPI)

While LPI is more commonly used for angle-closure glaucoma, it may be considered in certain cases of pigmentary glaucoma to improve aqueous outflow, especially if there is any component of angle closure.

2. Selective Laser Trabeculoplasty (SLT)

SLT is a minimally invasive procedure that targets the trabecular meshwork to enhance aqueous outflow. It can be an effective option for patients who are not adequately controlled on medications alone.

Surgical Options

1. Trabeculectomy

In cases where medical and laser treatments are insufficient to control IOP, surgical intervention may be necessary. Trabeculectomy involves creating a new drainage pathway for aqueous humor, thereby lowering IOP.

2. Tube Shunt Surgery

For patients with more advanced disease or those who have failed previous surgeries, tube shunt surgery (e.g., Ahmed or Baerveldt implants) may be indicated. This procedure involves implanting a device to facilitate aqueous drainage.

Conclusion

The management of pigmentary glaucoma (ICD-10 code H40.139) requires a tailored approach that may include a combination of medical therapy, laser treatment, and surgical intervention, depending on the severity of the disease and the patient's response to initial treatments. Regular follow-up and monitoring are crucial to ensure effective management and to prevent progression of the disease. As with any medical condition, collaboration between the patient and healthcare provider is essential for optimal outcomes.

Diagnostic Criteria

Pigmentary glaucoma is a specific type of glaucoma characterized by the dispersion of pigment from the iris, which can lead to increased intraocular pressure and potential damage to the optic nerve. The ICD-10 code H40.139 refers to "Pigmentary glaucoma, unspecified eye." To diagnose this condition, healthcare professionals typically follow a set of criteria that includes clinical evaluation, patient history, and specific diagnostic tests.

Diagnostic Criteria for Pigmentary Glaucoma

1. Patient History

  • Symptoms: Patients may report symptoms such as blurred vision, halos around lights, or eye discomfort. A thorough history of any previous eye conditions or family history of glaucoma is also essential.
  • Age and Gender: Pigmentary glaucoma often occurs in younger individuals, typically between the ages of 20 and 50, and is more common in males.

2. Clinical Examination

  • Visual Acuity Test: Initial assessments include measuring visual acuity to determine if there is any loss of vision.
  • Intraocular Pressure (IOP) Measurement: Elevated IOP is a hallmark of glaucoma. Tonometry is used to measure the pressure inside the eye, with readings above 21 mmHg often indicating potential glaucoma.

3. Slit-Lamp Examination

  • Iris Examination: A slit-lamp examination allows the clinician to observe the iris for pigment dispersion. The presence of pigment granules in the anterior chamber or on the corneal endothelium is indicative of pigmentary glaucoma.
  • Pupil Reaction: The response of the pupil to light and accommodation can also provide insights into the condition.

4. Gonioscopy

  • This procedure involves using a special lens to examine the angle of the anterior chamber where the iris meets the cornea. In pigmentary glaucoma, the angle may appear open, but pigment can be seen deposited in the trabecular meshwork.

5. Visual Field Testing

  • Perimetry: This test assesses the peripheral vision, which can be affected in glaucoma. Defects in the visual field can help confirm the diagnosis.

6. Optic Nerve Assessment

  • Fundoscopy: A thorough examination of the optic nerve head is crucial. Signs of damage, such as cupping of the optic disc, can indicate glaucoma progression.

7. Additional Diagnostic Tests

  • Optical Coherence Tomography (OCT): This imaging test provides detailed images of the optic nerve and retinal nerve fiber layer, helping to assess for any structural changes associated with glaucoma.
  • Pachymetry: Measuring corneal thickness can also be relevant, as thinner corneas are associated with a higher risk of glaucoma.

Conclusion

The diagnosis of pigmentary glaucoma (ICD-10 code H40.139) involves a comprehensive approach that includes patient history, clinical examination, and various diagnostic tests. The combination of elevated intraocular pressure, characteristic findings during slit-lamp examination, and visual field defects are critical in confirming the diagnosis. Early detection and management are essential to prevent vision loss associated with this condition. If you have further questions or need more specific information, feel free to ask!

Related Information

Description

  • Pigment from iris released into aqueous humor
  • Pigment accumulates in trabecular meshwork
  • Obstruction leads to increased intraocular pressure
  • Increased IOP can lead to optic nerve damage
  • Peripheral vision loss is common symptom
  • Condition often associated with genetic predisposition
  • More common in individuals with myopia and Caucasian descent

Clinical Information

  • Pigmentary glaucoma is a form of secondary open-angle glaucoma
  • Caused by pigment granules from iris released into aqueous humor
  • Obstructing trabecular meshwork and leading to elevated IOP
  • Risk factor for optic nerve damage and vision loss
  • More prevalent in younger individuals (20-50 years)
  • Common in males than females, especially Caucasian descent
  • Positive family history increases risk of developing pigmentary glaucoma
  • Early symptoms include blurred vision, halos around lights, eye pain or discomfort
  • Signs include increased IOP, pigment dispersion, optic nerve changes, visual field defects

Approximate Synonyms

  • Pigmentary Dispersion Syndrome
  • Pigmentary Glaucoma
  • Secondary Glaucoma
  • Iris Pigmentary Glaucoma
  • Intraocular Pressure (IOP)
  • Trabecular Meshwork Obstruction
  • Visual Field Loss
  • Ocular Hypertension
  • Glaucomatous Optic Neuropathy

Treatment Guidelines

  • Latanoprost reduces IOP effectively
  • Timolol beta-blockers reduce aqueous production
  • Brimonidine alpha agonists decrease IOP
  • Dorzolamide CA inhibitors reduce IOP
  • Netarsudil rho kinase inhibitors enhance outflow
  • LPI improves aqueous outflow in angle closure
  • SLT targets trabecular meshwork for drainage
  • Trabeculectomy creates new drainage pathway
  • Tube shunt surgery facilitates aqueous drainage

Diagnostic Criteria

  • Symptoms of blurred vision
  • Halos around lights reported
  • Eye discomfort reported
  • Previous eye conditions in history
  • Family history of glaucoma
  • Elevated intraocular pressure measured
  • Visual acuity tested initially
  • Iris examination via slit-lamp
  • Pupil reaction observed
  • Gonioscopy to examine angle
  • Defects in visual field detected
  • Optic nerve head examined by fundoscopy
  • Structural changes by OCT imaging
  • Corneal thickness measured by pachymetry

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