ICD-10: H44.13

Sympathetic uveitis

Additional Information

Approximate Synonyms

Sympathetic uveitis, classified under the ICD-10-CM code H44.13, is a specific type of uveitis that occurs as a reaction to an injury or disease in one eye, leading to inflammation in the other eye. Understanding alternative names and related terms for this condition can enhance clarity in medical communication and documentation. Below are some of the alternative names and related terms associated with sympathetic uveitis.

Alternative Names

  1. Sympathetic Ophthalmia: This is the most common alternative name for sympathetic uveitis. It refers to the bilateral inflammation of the uveal tract that occurs after trauma or surgery to one eye, affecting the other eye due to an autoimmune response.

  2. Uveitis, Sympathetic: This term is often used interchangeably with sympathetic uveitis, emphasizing the uveal involvement in the inflammatory process.

  3. Post-traumatic Uveitis: While this term is broader, it can refer to uveitis that develops following trauma, including sympathetic uveitis as a specific subset.

  1. Uveitis: A general term for inflammation of the uvea, which includes the iris, ciliary body, and choroid. Sympathetic uveitis is a specific type of uveitis.

  2. Autoimmune Uveitis: This term encompasses uveitis caused by autoimmune reactions, which is relevant since sympathetic uveitis is believed to be an autoimmune response triggered by an injury to the other eye.

  3. Bilateral Uveitis: This term describes uveitis affecting both eyes, which is characteristic of sympathetic uveitis following an initial unilateral injury.

  4. Choroiditis: While not synonymous, choroiditis (inflammation of the choroid) can be a component of sympathetic uveitis, as the condition involves inflammation of the uveal tract.

  5. Iritis: Inflammation of the iris, which can occur in sympathetic uveitis, although it is a more specific term that refers to inflammation of just one part of the uveal tract.

  6. Ciliary Body Inflammation: This term refers to inflammation of the ciliary body, another component of the uveal tract that may be involved in sympathetic uveitis.

Conclusion

Understanding the alternative names and related terms for ICD-10 code H44.13 (sympathetic uveitis) is essential for accurate diagnosis, treatment, and documentation in medical settings. These terms not only facilitate clearer communication among healthcare professionals but also enhance patient understanding of their condition. If you have further questions or need more specific information, feel free to ask!

Description

Sympathetic uveitis, classified under ICD-10 code H44.13, is a specific type of uveitis that occurs as a secondary response to an injury or inflammation in one eye, leading to inflammation in the fellow eye. This condition is part of a broader category of uveitis, which refers to inflammation of the uveal tract, including the iris, ciliary body, and choroid.

Clinical Description of Sympathetic Uveitis

Pathophysiology

Sympathetic uveitis is primarily an autoimmune response triggered by trauma or surgical intervention in one eye, often referred to as the "injured eye." The immune system mistakenly targets the uveal tissue of the unaffected eye, leading to inflammation. This phenomenon is thought to be mediated by the release of antigens from the injured eye that provoke an immune response in the other eye.

Symptoms

Patients with sympathetic uveitis may experience a range of symptoms, including:
- Blurred vision: Due to inflammation affecting the clarity of the ocular media.
- Photophobia: Increased sensitivity to light, which can be quite uncomfortable.
- Redness: Inflammation can cause conjunctival injection, leading to a red appearance of the eye.
- Pain: Patients may report ocular pain or discomfort, particularly in the affected eye.
- Floaters: The presence of floaters can occur due to inflammatory debris in the vitreous humor.

Diagnosis

Diagnosis of sympathetic uveitis typically involves:
- Clinical Examination: An ophthalmologist will perform a comprehensive eye examination, including visual acuity tests and slit-lamp examination to assess the extent of inflammation.
- History Taking: A detailed medical history is crucial, particularly regarding any recent eye injuries or surgeries.
- Imaging: In some cases, imaging studies such as optical coherence tomography (OCT) may be utilized to evaluate the extent of inflammation and any associated complications.

Treatment

Management of sympathetic uveitis focuses on controlling inflammation and preventing complications. Treatment options may include:
- Corticosteroids: Systemic or topical corticosteroids are commonly prescribed to reduce inflammation.
- Immunosuppressive Therapy: In cases where corticosteroids are insufficient, immunosuppressive agents may be considered.
- Management of Underlying Conditions: Addressing any underlying causes or associated conditions is essential for effective treatment.

Prognosis

The prognosis for sympathetic uveitis varies depending on the severity of the initial injury and the promptness of treatment. Early intervention can lead to better outcomes, while delayed treatment may result in complications such as cataracts, glaucoma, or permanent vision loss.

Conclusion

ICD-10 code H44.13 for sympathetic uveitis encapsulates a complex condition that arises from an autoimmune response following ocular trauma. Understanding its clinical presentation, diagnostic criteria, and treatment options is crucial for effective management and improved patient outcomes. If you suspect sympathetic uveitis, it is essential to seek prompt evaluation by an eye care professional to initiate appropriate treatment.

Clinical Information

Sympathetic uveitis, classified under ICD-10 code H44.13, is a rare but serious inflammatory condition affecting the uveal tract of the eye, typically following trauma or surgery to one eye, which can lead to inflammation in the fellow eye. Understanding its clinical presentation, signs, symptoms, and patient characteristics is crucial for timely diagnosis and management.

Clinical Presentation

Definition and Etiology

Sympathetic uveitis is characterized by bilateral inflammation of the uveal tissue, which includes the iris, ciliary body, and choroid. It often occurs after an inciting event, such as penetrating ocular trauma or surgical procedures, particularly in the affected eye. The condition is thought to be an autoimmune response triggered by antigens released from the injured eye into the systemic circulation, leading to inflammation in the unaffected eye[1].

Patient Characteristics

Patients who develop sympathetic uveitis typically have a history of ocular trauma or surgery. The condition is more common in younger individuals, particularly males, due to the higher incidence of eye injuries in this demographic. However, it can occur in any age group following the appropriate inciting event[1][2].

Signs and Symptoms

Initial Symptoms

The onset of sympathetic uveitis can be insidious, often presenting weeks to months after the initial injury. Common initial symptoms include:
- Blurred vision: Patients may experience a gradual decline in visual acuity.
- Photophobia: Increased sensitivity to light is frequently reported.
- Eye pain: Patients may describe a dull ache or sharp pain in the affected eye.

Ocular Signs

Upon examination, several signs may be observed:
- Redness: Conjunctival injection may be present, indicating inflammation.
- Anterior chamber reaction: There may be an accumulation of inflammatory cells (flare and cells) in the anterior chamber.
- Iritis: Inflammation of the iris can lead to miosis (constricted pupil) and irregular pupil shape.
- Ciliary flush: A ring of redness around the cornea may be noted, indicating deeper ocular inflammation.
- Retinal changes: Fundoscopic examination may reveal changes in the retina, such as edema or exudates, depending on the severity of the inflammation[2][3].

Systemic Symptoms

In some cases, patients may also experience systemic symptoms, including:
- Fever: Low-grade fever may accompany the ocular symptoms.
- Malaise: A general feeling of discomfort or unease can occur.

Conclusion

Sympathetic uveitis is a significant ocular condition that requires prompt recognition and management to prevent complications such as vision loss. Understanding the clinical presentation, including the characteristic signs and symptoms, as well as the typical patient profile, is essential for healthcare providers. Early intervention can help mitigate the inflammatory response and preserve visual function in affected individuals. If you suspect sympathetic uveitis in a patient, a thorough ocular examination and referral to an ophthalmologist are recommended for further evaluation and treatment[1][2][3].

Diagnostic Criteria

Sympathetic uveitis, classified under the ICD-10-CM code H44.13, is a type of uveitis that occurs as a response to trauma or inflammation in one eye, leading to inflammation in the other eye. The diagnosis of sympathetic uveitis involves a combination of clinical evaluation, patient history, and specific diagnostic criteria. Below are the key criteria and considerations used in diagnosing this condition.

Clinical Criteria for Diagnosis

1. Patient History

  • Trauma or Surgery: A history of ocular trauma or surgical intervention in one eye is often a significant factor. This can include penetrating injuries or surgical procedures that may trigger an inflammatory response in the other eye.
  • Symptoms: Patients may report symptoms such as blurred vision, photophobia (sensitivity to light), redness, and pain in the affected eye.

2. Ocular Examination

  • Visual Acuity Testing: Assessing the visual acuity in both eyes is crucial. A decrease in vision in the eye that was not initially injured may indicate sympathetic uveitis.
  • Slit-Lamp Examination: This examination allows for detailed observation of the anterior segment of the eye. Signs of inflammation, such as keratic precipitates, anterior chamber cells, and flare, are indicative of uveitis.
  • Fundoscopic Examination: A thorough examination of the retina and vitreous is performed to check for any signs of inflammation or other abnormalities.

3. Diagnostic Tests

  • Intraocular Pressure Measurement: Elevated intraocular pressure may be observed in cases of uveitis.
  • Imaging Studies: Optical coherence tomography (OCT) or ultrasound may be utilized to assess the extent of inflammation and any associated complications.

4. Exclusion of Other Conditions

  • Differential Diagnosis: It is essential to rule out other causes of uveitis, such as infectious uveitis (e.g., viral, bacterial, or fungal infections) and other non-infectious types of uveitis. This may involve serological tests or cultures to identify infectious agents.

Additional Considerations

1. Systemic Associations

  • Autoimmune Disorders: Sympathetic uveitis may be associated with systemic autoimmune conditions. A thorough medical history and possibly additional testing may be warranted to identify any underlying systemic issues.

2. Follow-Up and Monitoring

  • Regular Monitoring: Patients diagnosed with sympathetic uveitis require ongoing monitoring to assess the response to treatment and to check for potential complications, such as cataract formation or glaucoma.

3. Treatment Response

  • Response to Treatment: The effectiveness of corticosteroids or other immunosuppressive therapies can also provide insight into the diagnosis, as sympathetic uveitis typically responds to anti-inflammatory treatment.

Conclusion

The diagnosis of sympathetic uveitis (ICD-10 code H44.13) is multifaceted, relying on a combination of patient history, clinical examination, and exclusion of other potential causes of uveitis. Accurate diagnosis is crucial for effective management and treatment, as sympathetic uveitis can lead to significant visual impairment if not addressed promptly. Regular follow-up and monitoring are essential to ensure optimal outcomes for affected patients.

Treatment Guidelines

Sympathetic uveitis, classified under ICD-10 code H44.13, is a rare but serious condition characterized by inflammation of the uveal tract in one eye, which can subsequently affect the fellow eye. This condition often arises following trauma or surgery to one eye, leading to an immune response that targets both eyes. Understanding the standard treatment approaches for sympathetic uveitis is crucial for effective management and prevention of complications.

Overview of Sympathetic Uveitis

Sympathetic uveitis is typically a bilateral condition, although it may initially present in only one eye. The inflammation can lead to significant visual impairment if not treated promptly. Symptoms may include redness, pain, photophobia, and vision changes in the affected eye, with potential involvement of the fellow eye manifesting later.

Standard Treatment Approaches

1. Corticosteroids

Corticosteroids are the cornerstone of treatment for sympathetic uveitis. They help reduce inflammation and control the immune response. The administration can be systemic (oral or intravenous) or local (intraocular injections).

  • Systemic Corticosteroids: High-dose oral corticosteroids, such as prednisone, are often initiated to quickly control inflammation. The dosage may be tapered based on the clinical response and side effects.
  • Intraocular Corticosteroids: In cases where systemic therapy is insufficient or not tolerated, intraocular implants (e.g., fluocinolone acetonide) may be used to deliver sustained corticosteroid therapy directly to the eye[3].

2. Immunosuppressive Therapy

For patients who do not respond adequately to corticosteroids or who require long-term treatment, immunosuppressive agents may be considered. These can include:

  • Methotrexate: Often used in cases of chronic uveitis, it helps to modulate the immune response.
  • Azathioprine: Another option for long-term management, particularly in patients with recurrent episodes.
  • Biologics: Newer agents, such as TNF-alpha inhibitors, may be utilized in refractory cases[3].

3. Management of Underlying Conditions

Identifying and managing any underlying conditions that may contribute to sympathetic uveitis is essential. This may involve:

  • Surgical Intervention: If the sympathetic uveitis is secondary to trauma or surgical complications, addressing the primary issue may alleviate the inflammatory response.
  • Regular Monitoring: Patients should be monitored for complications such as cataracts, glaucoma, or retinal detachment, which can arise from prolonged inflammation or treatment side effects[2].

4. Supportive Care

Supportive measures are also important in managing symptoms and improving quality of life:

  • Pain Management: Analgesics may be prescribed to manage discomfort associated with inflammation.
  • Patient Education: Educating patients about the condition, potential complications, and the importance of adherence to treatment regimens is vital for successful outcomes.

Conclusion

The management of sympathetic uveitis (ICD-10 code H44.13) requires a comprehensive approach that includes corticosteroids, immunosuppressive therapy, and addressing any underlying causes. Early intervention is critical to prevent complications and preserve vision. Regular follow-up and monitoring are essential to adjust treatment as needed and to manage any side effects or complications that may arise during the course of therapy. As research continues, new therapeutic options may emerge, enhancing the management of this complex condition.

Related Information

Approximate Synonyms

  • Sympathetic Ophthalmia
  • Uveitis, Sympathetic
  • Post-traumatic Uveitis
  • Autoimmune Uveitis
  • Bilateral Uveitis
  • Choroiditis
  • Iritis
  • Ciliary Body Inflammation

Description

  • Autoimmune response triggered by trauma
  • Inflammation of unaffected eye
  • Blurred vision due to inflammation
  • Photophobia and increased sensitivity
  • Redness and conjunctival injection
  • Pain or discomfort in affected eye
  • Floaters from inflammatory debris

Clinical Information

  • Bilateral inflammation of the uveal tissue
  • Inciting event triggers autoimmune response
  • Common in younger individuals, particularly males
  • History of ocular trauma or surgery is common
  • Blurred vision and photophobia are initial symptoms
  • Redness and anterior chamber reaction are signs
  • Iritis, ciliary flush, and retinal changes can occur
  • Fever and malaise may accompany ocular symptoms

Diagnostic Criteria

  • History of ocular trauma or surgery
  • Decreased visual acuity in other eye
  • Keratic precipitates, anterior chamber cells, flare
  • Elevated intraocular pressure
  • Imaging studies (OCT, ultrasound)
  • Exclusion of infectious uveitis
  • Systemic autoimmune disorder association

Treatment Guidelines

  • Corticosteroids reduce inflammation
  • Systemic corticosteroids high-dose oral treatment
  • Intraocular corticosteroids sustained eye delivery
  • Methotrexate modulates immune response
  • Azathioprine long-term immune suppression
  • Biologics refractory case management
  • Surgical intervention primary cause correction
  • Regular monitoring for complications prevention

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