ICD-10: G37.3

Acute transverse myelitis in demyelinating disease of central nervous system

Clinical Information

Inclusion Terms

  • Acute transverse myelopathy
  • Acute transverse myelitis NOS

Additional Information

Diagnostic Criteria

Acute transverse myelitis (ATM) is a neurological condition characterized by inflammation of the spinal cord, leading to varying degrees of motor, sensory, and autonomic dysfunction. The ICD-10 code G37.3 specifically refers to acute transverse myelitis in the context of demyelinating diseases of the central nervous system. Diagnosing ATM involves a combination of clinical evaluation, imaging studies, and laboratory tests. Below, we outline the key criteria used for diagnosis.

Clinical Criteria

  1. Symptoms: The onset of symptoms is typically rapid, occurring over hours to days. Common symptoms include:
    - Weakness or paralysis in the legs and/or arms.
    - Sensory disturbances such as numbness, tingling, or loss of sensation.
    - Bowel and bladder dysfunction.
    - Pain in the back or limbs.

  2. Neurological Examination: A thorough neurological examination is essential. Findings may include:
    - Asymmetrical motor weakness.
    - Hyperreflexia or hyporeflexia.
    - Sensory level indicating loss of sensation below a certain spinal level.

  3. Duration of Symptoms: Symptoms must persist for at least 24 hours to differentiate acute transverse myelitis from other conditions that may cause transient neurological deficits.

Diagnostic Imaging

  1. Magnetic Resonance Imaging (MRI): MRI of the spinal cord is the gold standard for diagnosing ATM. Key findings may include:
    - Hyperintense lesions on T2-weighted images, typically spanning multiple segments of the spinal cord.
    - Evidence of edema or inflammation in the affected areas.

  2. Contrast Enhancement: In some cases, the use of gadolinium contrast may reveal areas of active inflammation, which can help differentiate ATM from other conditions such as tumors or infections.

Laboratory Tests

  1. Cerebrospinal Fluid (CSF) Analysis: A lumbar puncture may be performed to analyze CSF. Typical findings in ATM include:
    - Elevated protein levels.
    - Normal glucose levels.
    - Presence of oligoclonal bands, which may indicate an underlying demyelinating process.

  2. Blood Tests: Tests may be conducted to rule out other causes of myelitis, such as infections (e.g., viral or bacterial), autoimmune disorders, or paraneoplastic syndromes.

Exclusion of Other Conditions

To confirm a diagnosis of acute transverse myelitis, it is crucial to exclude other potential causes of the symptoms, including:
- Multiple sclerosis (MS) or other demyelinating diseases.
- Infectious myelitis (e.g., due to viruses like West Nile or enteroviruses).
- Vascular events such as spinal cord infarction.
- Neoplastic processes or compressive lesions.

Conclusion

The diagnosis of acute transverse myelitis (ICD-10 code G37.3) is a multifaceted process that requires careful clinical assessment, imaging studies, and laboratory evaluations to confirm the presence of inflammation in the spinal cord while ruling out other potential causes. Early diagnosis and intervention are critical for improving outcomes and managing symptoms effectively. If you suspect ATM, it is essential to consult a healthcare professional for a comprehensive evaluation.

Clinical Information

Acute transverse myelitis (ATM) is a neurological condition characterized by inflammation of the spinal cord, leading to a range of clinical presentations, signs, and symptoms. The ICD-10 code G37.3 specifically refers to acute transverse myelitis occurring in the context of demyelinating diseases of the central nervous system (CNS). Below is a detailed overview of the clinical presentation, signs, symptoms, and patient characteristics associated with this condition.

Clinical Presentation

Acute transverse myelitis typically presents with a rapid onset of neurological symptoms, often following a viral infection or other triggering events. The condition can affect individuals of any age but is most commonly seen in young adults and children. The hallmark of ATM is the bilateral nature of symptoms, which can vary significantly in severity and duration.

Signs and Symptoms

  1. Motor Symptoms:
    - Weakness: Patients often experience weakness in the legs (paraparesis) or arms (quadriparesis), depending on the level of spinal cord involvement. This weakness can range from mild to complete paralysis.
    - Spasticity: Increased muscle tone and reflexes may be observed, leading to stiffness and spasms.

  2. Sensory Symptoms:
    - Numbness and Tingling: Patients may report sensory disturbances, including numbness, tingling, or a "pins and needles" sensation, typically below the level of the lesion.
    - Loss of Sensation: There may be a complete or partial loss of sensation, particularly in a "saddle" distribution around the buttocks and inner thighs.

  3. Autonomic Symptoms:
    - Bladder and Bowel Dysfunction: Many patients experience urinary urgency, incontinence, or retention, as well as bowel dysfunction, due to autonomic nervous system involvement.
    - Sexual Dysfunction: Changes in sexual function may also occur.

  4. Pain:
    - Radicular Pain: Patients may experience sharp, shooting pain that radiates along the nerve roots, often exacerbated by movement or certain positions.
    - Central Pain: Some may develop chronic pain syndromes due to central nervous system damage.

Patient Characteristics

  • Demographics: Acute transverse myelitis can affect individuals of any age, but it is most prevalent in young adults (ages 10-19 and 30-39) and children. There is a slight female predominance in many studies.
  • Pre-existing Conditions: Many patients with ATM have a history of demyelinating diseases, such as multiple sclerosis (MS), neuromyelitis optica (NMO), or other autoimmune disorders. A significant proportion of cases may follow viral infections, particularly those caused by the Epstein-Barr virus, cytomegalovirus, or SARS-CoV-2[4][5].
  • Clinical Course: The clinical course of ATM can vary widely. Some patients may experience a complete recovery, while others may have persistent neurological deficits. The prognosis often depends on the underlying cause and the promptness of treatment.

Conclusion

Acute transverse myelitis is a serious neurological condition that requires prompt diagnosis and management. Understanding the clinical presentation, signs, symptoms, and patient characteristics associated with ICD-10 code G37.3 is crucial for healthcare providers to ensure timely intervention and improve patient outcomes. Early recognition and treatment can significantly influence the recovery trajectory, making awareness of this condition essential in clinical practice.

Approximate Synonyms

Acute transverse myelitis (ATM) is a neurological condition characterized by inflammation of the spinal cord, leading to varying degrees of motor and sensory dysfunction. The ICD-10 code G37.3 specifically refers to acute transverse myelitis in the context of demyelinating diseases of the central nervous system. Here, we will explore alternative names and related terms associated with this condition.

Alternative Names for Acute Transverse Myelitis

  1. Transverse Myelitis: This is the most common alternative name, often used interchangeably with acute transverse myelitis, although it can refer to both acute and chronic forms of the condition.

  2. Acute Myelitis: This term emphasizes the acute nature of the inflammation affecting the spinal cord.

  3. Demyelinating Transverse Myelitis: This name highlights the demyelinating aspect of the condition, indicating that it is associated with the loss of myelin, the protective sheath around nerve fibers.

  4. Acute Inflammatory Demyelinating Polyneuropathy: While this term is more general and can refer to broader conditions, it may sometimes be used in discussions about acute transverse myelitis, particularly in the context of autoimmune responses.

  1. Demyelinating Diseases: This broader category includes various conditions that result in the loss of myelin in the central nervous system, such as multiple sclerosis (MS) and neuromyelitis optica (NMO).

  2. Multiple Sclerosis (MS): A common demyelinating disease that can lead to acute transverse myelitis as a presenting symptom or complication.

  3. Neuromyelitis Optica (NMO): Another demyelinating condition that can cause transverse myelitis, often associated with specific antibodies (AQP4).

  4. Spinal Cord Inflammation: A general term that encompasses various inflammatory conditions affecting the spinal cord, including acute transverse myelitis.

  5. Acute Flaccid Myelitis (AFM): Although distinct from ATM, AFM is another condition that affects the spinal cord and can present with similar symptoms, particularly in children.

  6. Post-Infectious Myelitis: This term refers to myelitis that occurs following an infection, which can sometimes lead to acute transverse myelitis.

Conclusion

Understanding the alternative names and related terms for ICD-10 code G37.3 is essential for accurate diagnosis and treatment of acute transverse myelitis. These terms not only facilitate communication among healthcare professionals but also help in the classification and management of demyelinating diseases of the central nervous system. If you have further questions or need more specific information about acute transverse myelitis, feel free to ask!

Treatment Guidelines

Acute transverse myelitis (ATM) is a neurological condition characterized by inflammation of both sides of one segment of the spinal cord, leading to varying degrees of motor, sensory, and autonomic dysfunction. The ICD-10 code G37.3 specifically refers to acute transverse myelitis in the context of demyelinating diseases of the central nervous system. Understanding the standard treatment approaches for this condition is crucial for effective management and recovery.

Overview of Acute Transverse Myelitis

Acute transverse myelitis can occur as a result of various underlying conditions, including multiple sclerosis, infections, autoimmune diseases, and post-infectious syndromes. Symptoms typically include weakness, sensory alterations, and bladder or bowel dysfunction, which can significantly impact a patient's quality of life. The acute phase of the condition often requires prompt medical intervention to mitigate long-term complications.

Standard Treatment Approaches

1. Corticosteroids

Corticosteroids are the cornerstone of treatment for acute transverse myelitis. They are used to reduce inflammation and expedite recovery. High-dose intravenous corticosteroids, such as methylprednisolone, are commonly administered in the acute phase. The typical regimen involves:

  • Methylprednisolone: 1,000 mg IV daily for 3 to 5 days.

This treatment aims to decrease inflammation in the spinal cord and improve neurological function[1][2].

2. Plasmapheresis

For patients who do not respond adequately to corticosteroids, plasmapheresis (also known as therapeutic apheresis) may be considered. This procedure involves the removal of plasma from the blood, which can help eliminate circulating antibodies that may be contributing to the inflammatory process. Plasmapheresis is typically reserved for severe cases or those with significant disability[3][4].

3. Symptomatic Management

In addition to addressing the underlying inflammation, symptomatic treatment is essential for managing the various complications associated with ATM. This may include:

  • Pain Management: Analgesics or neuropathic pain medications (e.g., gabapentin, pregabalin) to alleviate pain.
  • Physical Therapy: Rehabilitation services to improve mobility, strength, and function. Early physical therapy can help prevent complications such as muscle atrophy and contractures.
  • Occupational Therapy: To assist patients in adapting to daily activities and improving their quality of life.
  • Bladder and Bowel Management: Interventions may include medications, catheterization, or bowel regimens to manage dysfunction[5][6].

4. Long-term Rehabilitation

Following the acute treatment phase, many patients require ongoing rehabilitation to address residual deficits. This may involve:

  • Continued Physical and Occupational Therapy: To enhance recovery and adapt to any lasting changes in function.
  • Psychological Support: Counseling or support groups to help patients cope with the emotional impact of their condition.

5. Monitoring and Follow-up

Regular follow-up with a neurologist is crucial for monitoring recovery and managing any long-term effects. This may include periodic MRI scans to assess for any new lesions or changes in the central nervous system, particularly in cases associated with multiple sclerosis or other demyelinating diseases[7][8].

Conclusion

The management of acute transverse myelitis (ICD-10 code G37.3) involves a multifaceted approach that includes corticosteroids, plasmapheresis for refractory cases, and comprehensive symptomatic management. Early intervention and rehabilitation are key to optimizing recovery and minimizing long-term disability. Ongoing monitoring and support are essential to address the evolving needs of patients as they navigate the challenges associated with this condition.


References

  1. Article - Billing and Coding: Botulinum Toxins (A52848).
  2. ICD-10 International statistical classification of diseases.
  3. Plasmapheresis/Plasma Exchange/Therapeutic Apheresis.
  4. Multiple Sclerosis (MS) - Defining in Administrative Data.
  5. Pediatric acquired demyelinating syndromes: a nationwide study.
  6. Marked increase in severe neurological disorders after vaccination.
  7. ICD-10-CM Diagnosis Code G37.3 - Acute transverse myelitis in demyelinating disease of central nervous system.
  8. G37.3: Acute transverse myelitis in demyelinating disease of central nervous system.

Description

Acute transverse myelitis (ATM) is a neurological condition characterized by inflammation of the spinal cord, leading to varying degrees of motor, sensory, and autonomic dysfunction. The ICD-10 code G37.3 specifically refers to acute transverse myelitis occurring in the context of demyelinating diseases of the central nervous system (CNS). Below is a detailed overview of this condition, including its clinical description, symptoms, diagnosis, and management.

Clinical Description

Definition

Acute transverse myelitis is defined as a neurological syndrome that results from inflammation of both sides of a segment of the spinal cord. This inflammation disrupts the transmission of nerve signals, leading to a range of neurological deficits. When classified under ICD-10 code G37.3, it indicates that the myelitis is associated with underlying demyelinating diseases, such as multiple sclerosis (MS) or neuromyelitis optica (NMO) [1][2].

Etiology

The exact cause of acute transverse myelitis can vary. It may be triggered by:
- Infectious agents: Viral infections, including those caused by the herpes virus, cytomegalovirus, and more recently, SARS-CoV-2, have been implicated in the onset of ATM [7][8].
- Autoimmune responses: Conditions like multiple sclerosis or neuromyelitis optica can lead to demyelination and subsequent inflammation of the spinal cord [1][4].
- Post-infectious syndromes: Following infections, some individuals may develop an autoimmune response that targets the spinal cord [6].

Symptoms

The symptoms of acute transverse myelitis can vary widely among individuals but typically include:
- Motor symptoms: Weakness or paralysis in the legs or arms, often presenting as difficulty walking or maintaining balance.
- Sensory symptoms: Numbness, tingling, or altered sensations in the limbs or trunk. Patients may experience a "band-like" sensation around the torso.
- Autonomic dysfunction: Issues such as bladder and bowel dysfunction, sexual dysfunction, and changes in blood pressure may occur due to disrupted autonomic pathways.
- Pain: Some patients report severe back pain or neuropathic pain in the affected areas [3][5].

Diagnosis

Diagnosing acute transverse myelitis involves a combination of clinical evaluation and diagnostic testing:
- Clinical history and examination: A thorough neurological examination is essential to assess motor and sensory function.
- Magnetic Resonance Imaging (MRI): MRI of the spinal cord is crucial for identifying areas of inflammation and demyelination. It can help differentiate ATM from other conditions such as spinal cord tumors or vascular issues [4][5].
- Lumbar puncture: Analyzing cerebrospinal fluid (CSF) can provide insights into inflammatory processes and rule out infections. Elevated levels of oligoclonal bands in the CSF may indicate a demyelinating process [1][2].
- Blood tests: These may be performed to identify underlying infections or autoimmune conditions.

Management

The management of acute transverse myelitis typically involves:
- Corticosteroids: High-dose intravenous corticosteroids are often the first line of treatment to reduce inflammation and improve recovery outcomes [3][4].
- Plasmapheresis: In cases where corticosteroids are ineffective, plasmapheresis may be considered to remove harmful antibodies from the bloodstream.
- Rehabilitation: Physical therapy and occupational therapy are essential for helping patients regain strength and function post-episode.
- Symptomatic treatment: Addressing specific symptoms such as pain, bladder dysfunction, and spasticity is crucial for improving the quality of life [5][6].

Conclusion

Acute transverse myelitis, classified under ICD-10 code G37.3, is a serious neurological condition that requires prompt diagnosis and management. Understanding its clinical features, potential causes, and treatment options is vital for healthcare providers to optimize patient outcomes. Ongoing research into the underlying mechanisms and effective therapies continues to be essential, especially in light of emerging associations with viral infections like SARS-CoV-2. For individuals experiencing symptoms suggestive of ATM, early medical intervention is critical to mitigate long-term complications and enhance recovery.

Related Information

Diagnostic Criteria

  • Rapid onset of weakness or paralysis
  • Sensory disturbances such as numbness or tingling
  • Bowel and bladder dysfunction present
  • Asymmetrical motor weakness found on examination
  • Hyperreflexia or hyporeflexia present
  • Sensory level indicates loss of sensation below certain spinal level
  • Symptoms persist for at least 24 hours
  • MRI shows hyperintense lesions in spinal cord
  • Edema or inflammation evident on MRI
  • Elevated protein levels in CSF analysis
  • Normal glucose levels in CSF analysis
  • Presence of oligoclonal bands in CSF analysis

Clinical Information

  • Rapid onset of neurological symptoms
  • Bilateral nature of symptoms
  • Weakness in legs or arms
  • Spasticity and increased muscle tone
  • Numbness and tingling sensations
  • Loss of sensation in saddle distribution
  • Bladder and bowel dysfunction
  • Sexual dysfunction
  • Radicular pain and central pain syndromes
  • Prevalent in young adults and children
  • Female predominance
  • Follows viral infections and demyelinating diseases

Approximate Synonyms

  • Transverse Myelitis
  • Acute Myelitis
  • Demyelinating Transverse Myelitis
  • Acute Inflammatory Demyelinating Polyneuropathy

Treatment Guidelines

  • High-dose corticosteroids used to reduce inflammation
  • Methylprednisolone administered IV daily for 3-5 days
  • Plasmapheresis considered for non-responsive patients
  • Pain management with analgesics or neuropathic pain medications
  • Physical therapy to improve mobility and strength
  • Occupational therapy to adapt to daily activities
  • Bladder and bowel management interventions
  • Long-term rehabilitation with physical and occupational therapy
  • Regular follow-up with neurologist for monitoring recovery

Description

Coding Guidelines

Excludes 1

  • acute flaccid myelitis (G04.82)
  • multiple sclerosis (G35)
  • neuromyelitis optica [Devic] (G36.0)

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