ICD-10: H40.132

Pigmentary glaucoma, left 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 H40.132 specifically refers to pigmentary glaucoma affecting the left eye.

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 young to middle-aged males.

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 sensitivity to light: This is due to the changes in the iris and the dispersion of pigment.
- Eye pain or discomfort: This may occur during episodes of elevated IOP.

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 clinician to examine the angle of the anterior chamber and assess for pigment deposition.
- Visual field testing: To detect any peripheral vision loss, which is common in glaucoma.

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 indicated to improve aqueous outflow.
- Surgical intervention: In cases where medical and laser treatments are insufficient, surgical options may be considered to create a new drainage pathway.

ICD-10 Code H40.132: Specifics

Code Breakdown

  • H40: This is the general category for glaucoma.
  • H40.1: This subcategory refers to primary open-angle glaucoma.
  • H40.13: This further specifies secondary open-angle glaucoma due to pigment dispersion.
  • H40.132: This code indicates that the condition is specifically affecting the left eye.

Clinical Implications

The use of the ICD-10 code H40.132 is crucial for accurate medical billing and coding, ensuring that healthcare providers can document the specific type of glaucoma affecting the patient. This specificity aids in treatment planning and tracking the prevalence of different glaucoma types in clinical practice.

Prognosis

With appropriate management, many patients with pigmentary glaucoma can maintain good vision. Regular monitoring and adherence to treatment are essential to prevent progression and preserve visual function.

Conclusion

Pigmentary glaucoma, particularly as denoted by the ICD-10 code H40.132 for the left eye, is a significant ocular condition that requires careful diagnosis and management. Understanding its clinical features, treatment options, and implications for patient care is vital for healthcare providers involved in ophthalmology and general practice. Regular follow-ups and patient education are key components in managing this condition effectively.

Clinical Information

Pigmentary glaucoma, classified under ICD-10 code H40.132, 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. These granules can obstruct the trabecular meshwork, leading to elevated IOP. The condition often develops in young to middle-aged adults and is more prevalent in males than females[1].

Signs and Symptoms

Patients with pigmentary glaucoma may present with a variety of signs and symptoms, which can include:

  • Elevated Intraocular Pressure (IOP): One of the hallmark signs of pigmentary glaucoma is increased IOP, which can be measured during a comprehensive eye examination. Normal IOP ranges from 10 to 21 mmHg, and values above this range may indicate glaucoma[2].

  • Visual Field Loss: As the disease progresses, patients may experience peripheral vision loss. This is often detected through visual field testing, which can reveal characteristic patterns of vision loss associated with glaucoma[3].

  • Pigment Dispersion: Clinicians may observe pigment deposits on the corneal endothelium (known as Krukenberg's spindle) and on the trabecular meshwork during a slit-lamp examination. These deposits are indicative of the pigmentary process occurring within the eye[4].

  • Symptoms of Glaucoma: Patients may report symptoms such as blurred vision, halos around lights, and difficulty adjusting to changes in lighting conditions. However, many individuals may be asymptomatic in the early stages of the disease[5].

Patient Characteristics

Certain demographic and clinical characteristics are commonly associated with pigmentary glaucoma:

  • Age: The condition typically affects younger individuals, often between the ages of 20 and 50 years[6].

  • Gender: There is a higher prevalence of pigmentary glaucoma in males compared to females, which may be attributed to anatomical differences in the eye[7].

  • Family History: A family history of glaucoma can increase the risk of developing pigmentary glaucoma, suggesting a genetic predisposition[8].

  • Ethnicity: Some studies indicate that pigmentary glaucoma may be more common in individuals of Caucasian descent, although it can occur in any ethnic group[9].

  • Myopia: There is a noted association between myopia (nearsightedness) and pigmentary glaucoma, with myopic individuals being at a higher risk for developing this condition[10].

Conclusion

Pigmentary glaucoma (ICD-10 code H40.132) is a significant ocular condition that requires careful monitoring and management. Early detection through regular eye examinations is essential, especially for individuals at higher risk due to age, gender, family history, or myopia. Understanding the clinical presentation, signs, symptoms, and patient characteristics can aid healthcare providers in diagnosing and treating this potentially sight-threatening condition effectively. Regular follow-ups and appropriate therapeutic interventions can help manage intraocular pressure and preserve vision in affected patients.

References

  1. Glaucoma H40 - ICD-10-CM Codes
  2. ICD-10 Glaucoma Reference Guide
  3. Primary Open-Angle Glaucoma Preferred Practice Pattern
  4. ICD-10-CM TABULAR LIST of DISEASES and INJURIES
  5. Scanning Computerized Ophthalmic Imaging
  6. ICD-10-AM Disease Code List
  7. ICD-10 International statistical classification of diseases and ... - IRIS
  8. ICD-10-CM Code for Pigmentary glaucoma H40.132
  9. ICD-10-CM Code for Pigmentary glaucoma H40.13
  10. ICD-10 International statistical classification of diseases ... - IRIS

Approximate Synonyms

Pigmentary glaucoma, specifically coded as H40.132 in the ICD-10-CM system, is a 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 H40.132.

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: While this is the primary term, it is often used interchangeably with the specific designation of left eye involvement (H40.132).

  3. Secondary Open-Angle Glaucoma: Pigmentary glaucoma is classified as a secondary form of open-angle glaucoma due to its specific etiology related to pigment dispersion.

  4. Iris Pigment Dispersion: This term describes the initial phase of the condition where pigment granules are released from the iris, which can lead to the development of pigmentary glaucoma.

  1. Intraocular Pressure (IOP): A critical measurement in diagnosing and managing glaucoma, including pigmentary glaucoma, as elevated IOP is a hallmark of the disease.

  2. Trabecular Meshwork: The structure in the eye where aqueous humor drains; its obstruction by pigment can lead to increased intraocular pressure.

  3. Visual Field Loss: A common consequence of untreated pigmentary glaucoma, where peripheral vision may be affected.

  4. Glaucomatous Optic Neuropathy: This term refers to the optic nerve damage that can occur as a result of prolonged elevated intraocular pressure, characteristic of pigmentary glaucoma.

  5. Ocular Hypertension: A condition where the intraocular pressure is higher than normal, which can precede the development of glaucoma, including pigmentary types.

  6. Angle-Closure Glaucoma: While not directly related, it is important to differentiate pigmentary glaucoma from other types of glaucoma, such as angle-closure, which has different pathophysiological mechanisms.

Conclusion

Understanding the alternative names and related terms for ICD-10 code H40.132 (Pigmentary glaucoma, left eye) is essential for accurate diagnosis, treatment, and communication among healthcare providers. These terms not only facilitate better understanding of the condition but also aid in the documentation and coding processes necessary for effective patient care and billing practices. If you have further questions or need additional information on this topic, feel free to ask!

Treatment Guidelines

Pigmentary glaucoma, classified under ICD-10 code H40.132, is a type of secondary open-angle glaucoma characterized by the deposition of pigment in the trabecular meshwork, leading 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: Medications like timolol can reduce aqueous humor production, thereby lowering IOP.
  • Alpha Agonists: Brimonidine is another option that decreases aqueous humor production and increases uveoscleral outflow.
  • Carbonic Anhydrase Inhibitors: Topical agents such as dorzolamide can also be used to reduce aqueous humor production.
  • Rho Kinase Inhibitors: Newer medications like netarsudil may be considered for their dual mechanism of action, enhancing outflow and reducing production.

2. Oral Medications

In cases where topical medications are insufficient, oral carbonic anhydrase inhibitors (e.g., acetazolamide) may be prescribed to further decrease IOP.

Laser Treatment

1. Laser Peripheral Iridotomy (LPI)

While LPI is more commonly used for angle-closure glaucoma, it may be considered in pigmentary glaucoma if there is evidence of angle narrowing or if the patient has a history of acute angle-closure episodes.

2. Selective Laser Trabeculoplasty (SLT)

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

Surgical Options

1. Trabeculectomy

For patients with advanced disease or those who do not respond to medical or laser treatments, trabeculectomy may be indicated. This surgical procedure creates a new drainage pathway for aqueous humor, effectively lowering IOP.

2. Aqueous Shunts

In cases where trabeculectomy is not successful or feasible, the implantation of aqueous shunts (e.g., Ahmed or Baerveldt implants) can be considered. These devices help to drain excess fluid from the eye, thereby reducing IOP.

Monitoring and Follow-Up

Regular follow-up appointments are crucial for monitoring IOP and assessing the effectiveness of treatment. Patients should be educated about the importance of adherence to prescribed medications and the need for routine eye examinations to detect any progression of the disease.

Conclusion

The management of pigmentary glaucoma (ICD-10 code H40.132) involves a comprehensive approach tailored to the individual patient's needs. Initial treatment typically focuses on medical management with topical medications, followed by laser treatments or surgical interventions as necessary. Ongoing monitoring is essential to ensure effective control of IOP and to prevent vision loss. As with any medical condition, collaboration between the patient and healthcare provider is key to achieving optimal outcomes.

Diagnostic Criteria

Diagnosing pigmentary glaucoma, specifically under the ICD-10 code H40.132 for the left eye, involves a comprehensive evaluation that includes clinical history, symptom assessment, and specific diagnostic tests. Below is a detailed overview of the criteria used for diagnosis.

Clinical History and Symptoms

  1. Patient History:
    - A thorough medical history is essential, focusing on any previous eye conditions, family history of glaucoma, and any symptoms the patient may be experiencing.
    - Symptoms of pigmentary glaucoma can include blurred vision, halos around lights, and peripheral vision loss, which may progress over time.

  2. Age and Demographics:
    - Pigmentary glaucoma typically affects younger individuals, often between the ages of 20 and 50, and is more common in males. This demographic information can guide the clinician's suspicion of the condition.

Clinical Examination

  1. Visual Acuity Testing:
    - Initial assessments include measuring visual acuity to determine if there is any impact on the patient's vision.

  2. Intraocular Pressure (IOP) Measurement:
    - Elevated intraocular pressure is a hallmark of glaucoma. Tonometry is used to measure IOP, with readings above 21 mmHg often indicating potential glaucoma.

  3. Slit-Lamp Examination:
    - A slit-lamp exam allows the clinician to inspect the anterior segment of the eye, where pigment dispersion can be observed. The presence of pigment granules in the anterior chamber or on the corneal endothelium is indicative of pigmentary glaucoma.

  4. Gonioscopy:
    - This procedure involves using a special lens to examine the angle of the anterior chamber. In pigmentary glaucoma, the angle may appear open, but pigment can be seen deposited in the trabecular meshwork.

  5. Optic Nerve Assessment:
    - The optic nerve head is evaluated for signs of damage, such as cupping, which is indicative of glaucoma. This can be assessed through direct examination or imaging techniques like optical coherence tomography (OCT).

  6. Visual Field Testing:
    - Perimetry tests are conducted to assess the visual field for any defects, which can indicate progression of the disease. Typical findings in pigmentary glaucoma include peripheral vision loss.

Diagnostic Criteria Summary

To diagnose pigmentary glaucoma (ICD-10 code H40.132) for the left eye, the following criteria are typically met:

  • Elevated IOP: Consistently high intraocular pressure readings.
  • Pigment Dispersion: Evidence of pigment in the anterior chamber and on the trabecular meshwork.
  • Optic Nerve Damage: Signs of glaucomatous optic neuropathy, such as increased cup-to-disc ratio.
  • Visual Field Defects: Documented loss of peripheral vision consistent with glaucoma.

Conclusion

The diagnosis of pigmentary glaucoma is multifaceted, requiring a combination of patient history, clinical examination, and specific diagnostic tests. Accurate diagnosis is crucial for effective management and treatment to prevent vision loss. If you suspect pigmentary glaucoma, it is essential to consult an eye care professional for a comprehensive evaluation and appropriate management strategies.

Related Information

Description

  • Pigment deposition in trabecular meshwork
  • Increased intraocular pressure (IOP)
  • Potential vision loss
  • Glaucoma affecting left eye
  • Visual disturbances and blurred vision
  • Increased sensitivity to light
  • Eye pain or discomfort during elevated IOP

Clinical Information

  • Pigment granules cause trabecular meshwork obstruction
  • Increased intraocular pressure (IOP) is a hallmark sign
  • Elevated IOP can lead to optic nerve damage
  • Peripheral vision loss occurs in late stages
  • Pigment dispersion on corneal endothelium and trabecular meshwork
  • Symptoms include blurred vision, halos around lights, and difficulty adjusting to lighting changes
  • Asymptomatic in early stages of disease
  • Typically affects younger individuals (20-50 years)
  • Higher prevalence in males compared to females
  • Family history increases risk of developing pigmentary glaucoma
  • More common in Caucasians, but can occur in any ethnic group
  • Myopia is associated with increased risk of developing pigmentary glaucoma

Approximate Synonyms

  • Pigmentary Dispersion Syndrome
  • Secondary Open-Angle Glaucoma
  • Iris Pigment Dispersion
  • Intraocular Pressure (IOP)
  • Trabecular Meshwork Obstruction
  • Visual Field Loss
  • Glaucomatous Optic Neuropathy

Treatment Guidelines

  • Topical prostaglandin analogues first line
  • Beta-blockers reduce aqueous humor production
  • Alpha agonists decrease IOP
  • Carbonic anhydrase inhibitors oral or topical
  • Rho kinase inhibitors for resistant cases
  • Laser peripheral iridotomy for angle narrowing
  • Selective laser trabeculoplasty enhance outflow
  • Trabeculectomy create new drainage pathway
  • Aqueous shunts implantation as last resort

Diagnostic Criteria

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