Find comprehensive information on Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's Disease. This resource offers guidance on ALS diagnosis, clinical documentation, and medical coding for healthcare professionals. Learn about the symptoms, diagnostic criteria, and ICD-10 codes related to ALS for accurate and efficient medical record keeping. Explore resources for managing and documenting ALS patient care.
Also known as
Amyotrophic lateral sclerosis
Progressive degeneration of motor neurons.
Systemic atrophies primarily affecting the central nervous system
Includes conditions like spinal muscular atrophy and progressive bulbar palsy.
Diseases of the nervous system
Encompasses various neurological disorders affecting the brain, spinal cord, and nerves.
Follow this step-by-step guide to choose the correct ICD-10 code.
Is the diagnosis amyotrophic lateral sclerosis (ALS)?
Yes
Is there familial history of ALS?
No
Do not code as ALS. Review the clinical documentation for the correct diagnosis.
When to use each related code
| Description |
|---|
| Progressive neurodegenerative disease affecting nerve cells in brain and spinal cord. |
| Progressive muscle weakness and wasting due to spinal cord anterior horn cell degeneration. |
| Group of rare, progressive neurodegenerative disorders affecting motor neurons. |
Ensure accurate coding for ALS type (e.g., familial vs. sporadic) to avoid underpayment and support quality reporting. Consider G12.21 vs. G12.29.
Properly document and code common ALS comorbidities like respiratory failure (J96.00-J96.99) or dysphagia (R13.1) for accurate reimbursement.
CDI review should confirm diagnostic criteria for ALS per El Escorial criteria to prevent incorrect coding of similar conditions like primary lateral sclerosis.
Q: What are the most effective diagnostic strategies for differentiating Amyotrophic Lateral Sclerosis (ALS) from other neuromuscular disorders mimicking ALS?
A: Differentiating Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig's Disease) from mimicking conditions like multifocal motor neuropathy (MMN), Kennedy's disease, or cervical spondylotic myelopathy requires a multi-pronged approach. Electrodiagnostic studies, specifically electromyography (EMG) and nerve conduction studies (NCS), are crucial for identifying lower and upper motor neuron involvement characteristic of ALS. Serum creatine kinase levels can help rule out muscle disorders, while magnetic resonance imaging (MRI) of the brain and spinal cord can exclude structural abnormalities mimicking ALS symptoms. Consider implementing a thorough review of the patient's clinical presentation, including symptom onset and progression, alongside genetic testing for known ALS-associated mutations. Explore how comprehensive clinical, electrophysiological, and imaging data, combined with appropriate laboratory investigations, can enhance diagnostic accuracy in ALS.
Q: How can clinicians effectively manage respiratory dysfunction in patients with progressive Amyotrophic Lateral Sclerosis?
A: Respiratory dysfunction is a major concern in the progressive stages of Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease). Effective management involves proactive monitoring of respiratory function through regular assessments like spirometry and nocturnal oximetry. Non-invasive ventilation (NIV), particularly bilevel positive airway pressure (BiPAP), is often initiated when forced vital capacity (FVC) falls below 50% predicted or symptoms like dyspnea and orthopnea emerge. Patient education on the benefits of NIV and effective cough augmentation techniques is crucial for improving quality of life. Learn more about strategies for optimizing respiratory care in ALS, including airway clearance techniques and the role of mechanical insufflation-exsufflation. Consider implementing a multidisciplinary approach involving pulmonologists, respiratory therapists, and palliative care specialists for comprehensive respiratory management in ALS patients.
Patient presents with progressive muscle weakness, consistent with the clinical presentation of amyotrophic lateral sclerosis (ALS, also known as Lou Gehrig's disease). Symptoms include both upper and lower motor neuron involvement, manifesting as muscle atrophy, fasciculations, spasticity, dysarthria, and dysphagia. The patient reports increasing difficulty with activities of daily living (ADLs), including ambulation, dressing, and swallowing. Diagnostic workup including electromyography (EMG) and nerve conduction studies (NCS) demonstrates evidence of denervation and reinnervation, supporting the ALS diagnosis. Differential diagnoses considered included progressive muscular atrophy, primary lateral sclerosis, and spinal muscular atrophy. Based on the patient's clinical picture, the El Escorial criteria for ALS were reviewed and met. The prognosis for ALS is discussed with the patient and family, including the progressive nature of the disease and the impact on respiratory function. A multidisciplinary care plan is initiated, focusing on symptom management, supportive care, and optimizing quality of life. This plan includes referral to physical therapy, occupational therapy, speech therapy, respiratory therapy, and nutritional counseling. Patient education regarding assistive devices, such as walkers, canes, and communication aids, is provided. Advanced care planning and discussions regarding palliative care options are initiated. ICD-10 code G12.21 is assigned for ALS. The patient is scheduled for follow-up to monitor disease progression and adjust the treatment plan as needed.