ICD-10: H18.61
Keratoconus, stable
Additional Information
Treatment Guidelines
Keratoconus is a progressive eye condition characterized by the thinning and bulging of the cornea, leading to visual distortion. The ICD-10 code H18.61 specifically refers to stable keratoconus, which indicates that the condition has not progressed significantly over time. Treatment approaches for stable keratoconus focus on managing symptoms and preserving vision. Below, we explore the standard treatment options available for this condition.
1. Regular Monitoring
For patients with stable keratoconus, regular eye examinations are crucial. These assessments typically include:
- Visual Acuity Tests: To monitor any changes in vision.
- Corneal Topography: This imaging technique maps the surface curvature of the cornea, helping to detect any subtle changes in the corneal shape over time.
- Pachymetry: Measuring corneal thickness to assess the health of the cornea and the risk of progression[1][2].
2. Corrective Lenses
Soft Contact Lenses
- Initial Treatment: Many patients with stable keratoconus can achieve satisfactory vision correction with soft contact lenses, which provide a smoother optical surface than the irregular cornea[3].
Rigid Gas Permeable (RGP) Lenses
- Preferred Option: RGP lenses are often recommended as they provide better vision correction by creating a new refractive surface over the cornea. They are particularly effective for patients whose vision cannot be adequately corrected with soft lenses[4].
Scleral Lenses
- Advanced Cases: For patients with more advanced keratoconus or those who cannot tolerate RGP lenses, scleral lenses may be used. These larger lenses vault over the cornea and rest on the sclera, providing comfort and improved vision[5].
3. Corneal Cross-Linking (CXL)
While primarily used for progressive keratoconus, corneal cross-linking can be considered in stable cases if there is a risk of future progression. This procedure strengthens the corneal tissue by using riboflavin (vitamin B2) and ultraviolet light, which can help stabilize the cornea and prevent further deterioration[6].
4. Intacs (Intrastromal Corneal Ring Segments)
Intacs are small, crescent-shaped devices implanted in the cornea to flatten its shape and improve vision. This option is typically reserved for patients who do not achieve satisfactory vision with contact lenses and is considered when the keratoconus is stable[7].
5. Surgical Options
In cases where vision cannot be adequately corrected with lenses, surgical interventions may be considered:
Corneal Transplantation
- Penetrating Keratoplasty (PK): This is a full-thickness corneal transplant that may be necessary for patients with severe keratoconus who have significant visual impairment and have not responded to other treatments[8].
Lamellar Keratoplasty
- Selective Replacement: This technique replaces only the affected layers of the cornea, preserving more of the patient's original tissue and potentially leading to faster recovery times[9].
Conclusion
The management of stable keratoconus primarily involves regular monitoring and the use of corrective lenses, with options like corneal cross-linking and surgical interventions available for specific cases. Patients should work closely with their eye care professionals to determine the most appropriate treatment plan based on their individual needs and the stability of their condition. Regular follow-ups are essential to ensure that any changes in the cornea are promptly addressed, maintaining optimal visual health.
Description
Keratoconus is a progressive eye disorder characterized by the thinning and conical shape of the cornea, which can lead to visual impairment. The ICD-10-CM code H18.61 specifically refers to Keratoconus, stable, indicating that the condition is not currently progressing.
Clinical Description of Keratoconus
Definition and Pathophysiology
Keratoconus is defined as a non-inflammatory condition where the cornea thins and bulges outward into a cone shape. This abnormal shape distorts light entering the eye, leading to various visual disturbances. The exact cause of keratoconus is not fully understood, but it is believed to involve genetic, environmental, and biochemical factors.
Symptoms
Patients with stable keratoconus may experience:
- Blurred or distorted vision
- Increased sensitivity to light and glare
- Frequent changes in prescription glasses
- Difficulty seeing at night
In stable keratoconus, these symptoms may be present but do not worsen over time, distinguishing it from progressive forms of the disease.
Diagnosis
Diagnosis typically involves:
- Visual Acuity Tests: Assessing the clarity of vision.
- Corneal Topography: Mapping the surface curvature of the cornea to identify irregularities.
- Pachymetry: Measuring corneal thickness to evaluate the extent of thinning.
Treatment Options
While stable keratoconus may not require immediate intervention, treatment options include:
- Corrective Lenses: Glasses or soft contact lenses may be sufficient for mild cases.
- Rigid Gas Permeable (RGP) Lenses: These lenses can help improve vision by providing a smooth surface for light to focus on.
- Corneal Cross-Linking: A procedure that strengthens corneal tissue to prevent progression.
- Surgical Options: In advanced cases, procedures such as corneal transplants may be necessary.
ICD-10-CM Code H18.61
Code Details
- Code: H18.61
- Description: Keratoconus, stable
- Classification: This code falls under the category of diseases of the cornea in the ICD-10-CM coding system, which is used for medical billing and documentation.
Importance of Accurate Coding
Accurate coding is crucial for:
- Insurance Reimbursement: Ensuring that healthcare providers are reimbursed for services rendered.
- Patient Records: Maintaining clear and precise medical records for ongoing patient care.
- Epidemiological Studies: Facilitating research and data collection on the prevalence and treatment outcomes of keratoconus.
Conclusion
Keratoconus, stable (ICD-10-CM code H18.61), represents a non-progressive form of this corneal disorder, allowing for various management strategies to maintain visual acuity. Understanding the clinical aspects and coding details of keratoconus is essential for healthcare providers in delivering effective patient care and ensuring proper documentation and billing practices.
Clinical Information
Keratoconus is a progressive eye disorder characterized by the thinning and conical shape of the cornea, which can lead to visual impairment. The ICD-10 code H18.61 specifically refers to stable keratoconus, indicating that the condition has not progressed significantly over time. Understanding the clinical presentation, signs, symptoms, and patient characteristics associated with this condition is crucial for effective diagnosis and management.
Clinical Presentation
Signs and Symptoms
-
Visual Disturbances: Patients with stable keratoconus often experience blurred or distorted vision. This distortion can manifest as ghosting or multiple images, particularly when looking at lights or reading text. The irregular shape of the cornea disrupts the normal focusing of light onto the retina, leading to these visual anomalies[1].
-
Sensitivity to Light: Many individuals report increased sensitivity to bright lights (photophobia), which can be uncomfortable and may lead to squinting or avoidance of bright environments[1].
-
Changes in Prescription: Patients may notice frequent changes in their eyeglass prescription, as the condition can alter the refractive error of the eye. This variability can be frustrating and may prompt individuals to seek further evaluation[1].
-
Corneal Scarring: In some cases, stable keratoconus can lead to scarring of the cornea, which may be visible during an eye examination. This scarring can further impact visual acuity and may require intervention if it progresses[1].
Patient Characteristics
-
Age of Onset: Keratoconus typically begins in the late teens to early twenties, although it can be diagnosed at any age. The stable form of the condition may be more common in older patients who have had the disorder for a longer duration without significant progression[2].
-
Family History: There is a genetic component associated with keratoconus, and individuals with a family history of the condition are at a higher risk. This familial tendency suggests a hereditary link that may influence the onset and stability of the disease[2].
-
Associated Conditions: Patients with keratoconus may have other ocular conditions, such as allergies or atopic diseases, which can exacerbate the symptoms. Additionally, conditions like Down syndrome and Ehlers-Danlos syndrome have been associated with a higher prevalence of keratoconus[2][3].
-
Gender: Some studies suggest that keratoconus may be more prevalent in males than females, although the reasons for this discrepancy are not fully understood[3].
Diagnosis and Management
Diagnostic Tools
-
Corneal Topography: This imaging technique is essential for diagnosing keratoconus, as it provides detailed maps of the cornea's shape and curvature. It helps in assessing the severity and stability of the condition[4].
-
Slit-Lamp Examination: An eye care professional will perform a slit-lamp examination to evaluate the cornea's structure and look for signs of thinning or scarring[4].
Management Strategies
-
Eyeglasses and Contact Lenses: In the stable phase, many patients can manage their symptoms with corrective lenses. Rigid gas permeable (RGP) contact lenses are often preferred as they can provide better vision correction by creating a smooth surface over the irregular cornea[4].
-
Collagen Cross-Linking: For patients at risk of progression, collagen cross-linking may be recommended to strengthen the corneal tissue and prevent further deterioration. This procedure is particularly beneficial for those with unstable keratoconus but may also be considered for stable cases if there are concerns about future progression[5].
Conclusion
Keratoconus, particularly in its stable form (ICD-10 code H18.61), presents with a range of visual disturbances and patient characteristics that are essential for diagnosis and management. Understanding the clinical signs, symptoms, and associated factors can aid healthcare providers in delivering effective care and improving patient outcomes. Regular monitoring and appropriate interventions are crucial to managing this condition and maintaining visual health.
Approximate Synonyms
Keratoconus is a progressive eye condition characterized by the thinning and bulging of the cornea, leading to visual distortion. The ICD-10-CM code for stable keratoconus is H18.61. Below are alternative names and related terms associated with this condition:
Alternative Names for Keratoconus
- Keratoconus, stable: This is the primary term used in the ICD-10 coding system to describe the condition when it is not progressing.
- Stable keratoconus: Often used interchangeably with the ICD-10 code, emphasizing the non-progressive nature of the condition.
- Corneal ectasia: A broader term that can include keratoconus as well as other conditions where the cornea becomes distorted.
- Keratoconus, right eye: Specifically refers to keratoconus affecting the right eye, coded as H18.611 in ICD-10.
- Keratoconus, left eye: Refers to keratoconus affecting the left eye, coded as H18.612.
- Keratoconus, bilateral: Indicates that keratoconus is present in both eyes, coded as H18.613.
Related Terms and Concepts
- Corneal thinning: A key feature of keratoconus, where the cornea becomes thinner than normal.
- Visual distortion: A common symptom of keratoconus, where vision becomes blurred or distorted due to the irregular shape of the cornea.
- Contact lenses for keratoconus: Specialized lenses, such as gas permeable or scleral lenses, are often used to manage the visual impairment caused by keratoconus.
- Corneal transplant: In severe cases of keratoconus, a corneal transplant may be necessary to restore vision.
- Pachymetry: A diagnostic procedure used to measure the thickness of the cornea, which is crucial in assessing keratoconus.
Conclusion
Understanding the various terms associated with ICD-10 code H18.61 for stable keratoconus is essential for accurate diagnosis, treatment, and billing in medical settings. These alternative names and related concepts help healthcare professionals communicate effectively about the condition and its management. If you need further information on treatment options or diagnostic procedures related to keratoconus, feel free to ask!
Diagnostic Criteria
Keratoconus is a progressive eye disorder characterized by the thinning and bulging of the cornea, leading to visual impairment. The ICD-10-CM code H18.61 specifically refers to "Keratoconus, stable," indicating that the condition has not progressed significantly over time. The diagnosis of keratoconus, particularly in its stable form, involves several criteria and diagnostic methods.
Diagnostic Criteria for Keratoconus
1. Clinical Symptoms
Patients with keratoconus may present with various symptoms, including:
- Blurred or distorted vision
- Increased sensitivity to light and glare
- Frequent changes in eyeglass prescriptions
- Difficulty seeing at night
These symptoms can help clinicians suspect keratoconus, but they are not definitive for diagnosis.
2. Ocular Examination
A comprehensive eye examination is crucial for diagnosing keratoconus. Key components include:
- Visual Acuity Testing: Assessing the clarity of vision, which may reveal irregularities.
- Slit-Lamp Examination: This allows the eye care professional to observe the cornea's shape and thickness, identifying any bulging or thinning characteristic of keratoconus.
3. Corneal Topography
Corneal topography is a critical diagnostic tool for keratoconus. It provides a detailed map of the cornea's surface, highlighting:
- Irregularities in curvature
- Areas of steepening, which are indicative of keratoconus
- The overall shape of the cornea, which can help differentiate keratoconus from other conditions
4. Pachymetry
Pachymetry measures the thickness of the cornea. In keratoconus, the cornea is often thinner than normal, particularly at the apex of the cone. This measurement can help confirm the diagnosis and assess the severity of the condition.
5. Refraction Tests
Refraction tests help determine the degree of refractive error. Patients with keratoconus may exhibit irregular astigmatism, which can be detected through these tests. The presence of significant astigmatism that cannot be corrected with standard lenses may suggest keratoconus.
6. Family History and Risk Factors
A family history of keratoconus can increase the likelihood of diagnosis. Additionally, certain risk factors, such as eye rubbing, allergies, and other connective tissue disorders, may contribute to the development of keratoconus.
Conclusion
The diagnosis of keratoconus, particularly the stable form represented by ICD-10 code H18.61, relies on a combination of clinical symptoms, detailed ocular examinations, and advanced diagnostic techniques such as corneal topography and pachymetry. By utilizing these criteria, eye care professionals can accurately diagnose and monitor the condition, ensuring appropriate management and treatment for affected patients.
Related Information
Treatment Guidelines
- Regular eye examinations
- Visual Acuity Tests
- Corneal Topography
- Pachymetry
- Soft Contact Lenses for initial treatment
- RGP Lenses for better vision correction
- Scleral Lenses for advanced cases
- Corneal Cross-Linking for risk of progression
- Intacs for improved vision when lenses fail
- Corneal Transplantation (PK) as last resort
- Lamellar Keratoplasty for selective replacement
Description
- Progressive eye disorder caused by thinning cornea
- Abnormal corneal shape distorts light entering the eye
- Causes blurred or distorted vision, sensitivity to light
- Corneal thinning can lead to visual impairment
- Stable form of keratoconus is not currently progressing
- Symptoms may include frequent changes in prescription glasses
- Difficulty seeing at night due to conical cornea shape
Clinical Information
- Visual disturbance with blurred vision
- Increased sensitivity to light (photophobia)
- Frequent changes in eyeglass prescription
- Corneal scarring visible during examination
- Typically begins in late teens to early twenties
- Genetic component with family history risk
- Associated with ocular conditions and syndromes
- Males may have higher prevalence than females
- Diagnostic tools include corneal topography and slit-lamp examination
- Management strategies involve eyeglasses, contact lenses, and collagen cross-linking
Approximate Synonyms
- Keratoconus stable
- Stable keratoconus
- Corneal ectasia
- Keratoconus right eye
- Keratoconus left eye
- Keratoconus bilateral
Diagnostic Criteria
Subcategories
Related Diseases
Medical Disclaimer: The information provided on this website is for general informational and educational purposes only.
It is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with questions about your medical condition.