Guillain-Barre syndrome
- G61.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM G61.0 became effective on October 1, 2023.
- This is the American ICD-10-CM version of G61.0 – other international versions of ICD-10 G61.0 may differ.
Applicable To
- Acute (post-)infective polyneuritis
- Miller Fisher Syndrome
The following code(s) above G61.0 contain annotation back-references
that may be applicable to G61.0:
- G00-G99 Diseases of the nervous system
- G60-G65 Polyneuropathies and other disorders of the peripheral nervous system
Approximate Synonyms
- Acute infective polyneuritis
- Acute inflammatory demyelinating polyneuropathy
- Fisher’s syndrome
- Guillain barre syndrome
- Guillain-barrè syndrome
- Miller fischer variant of guillain barre syndrome
- Polyneuritis, acute infectious
- Polyneuropathy (multiple nerve disorder)
Clinical Information
- A variant of the guillain-barre syndrome characterized by the acute onset of oculomotor dysfunction, ataxia, and loss of deep tendon reflexes with relative sparing of strength in the extremities and trunk. The ataxia is produced by peripheral sensory nerve dysfunction and not by cerebellar injury. Facial weakness and sensory loss may also occur. The process is mediated by autoantibodies directed against a component of myelin found in peripheral nerves. (Adams et al., Principles of Neurology, 6th ed, p1313; neurology 1987 sep;37(9):1493-8)
- An acute inflammatory autoimmune neuritis caused by t cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occurs in peripheral nerves and nerve roots. The process is often preceded by a viral or bacterial infection, surgery, immunization, lymphoma, or exposure to toxins. Common clinical manifestations include progressive weakness, loss of sensation, and loss of deep tendon reflexes. Weakness of respiratory muscles and autonomic dysfunction may occur. (from Adams et al., Principles of Neurology, 6th ed, pp1312-1314)
- An acute, autoimmune inflammatory process affecting the peripheral nervous system and nerve roots. It results in demyelination. It is often caused by an acute viral or bacterial infection.
- Guillain-barre syndrome is a rare disorder that causes your immune system to attack your peripheral nervous system (pns). The pns nerves connect your brain and spinal cord with the rest of your body. Damage to these nerves makes it hard for them to transmit signals. As a result, your muscles have trouble responding to your brain. No one knows what causes the syndrome. Sometimes it is triggered by an infection, surgery or a vaccination. The first symptom is usually weakness or a tingling feeling in your legs. The feeling can spread to your upper body. In severe cases, you become almost paralyzed. This is life-threatening. You might need a respirator to breathe. Symptoms usually worsen over a period of weeks, then stabilize. Most people recover. Recovery can take a few weeks to a few years. Treatment options during the symptom period include medicines or a procedure called plasma exchange.
- Progressive ascending motor neuron paralysis of unknown etiology, frequently following an enteric or respiratory infection.
ICD-10-CM G61.0 is grouped within Diagnostic Related Group(s) (MS-DRG v41.0):
- 094 Bacterial and tuberculous infections of nervous system with mcc
- 095 Bacterial and tuberculous infections of nervous system with cc
- 096 Bacterial and tuberculous infections of nervous system without cc/mcc
Convert G61.0 to ICD-9-CMCode History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- 2024 (effective 10/1/2023): No change
Diagnosis Index entries containing back-references to G61.0:
- Barré-Guillain disease or syndrome G61.0
- Disease, diseased – see also Syndrome
- Guillain-Barré G61.0
- Landry’s G61.0
- Encephalomyeloradiculitis G61.0 (acute)
- Encephalomyeloradiculoneuritis G61.0 (acute) (Guillain-Barré)
- Guillain-Barré disease or syndrome G61.0
- Landry-Guillain-Barré, syndrome or paralysis G61.0
- Landry’s disease or paralysis G61.0
- Miller Fisher syndrome G61.0
- Neuritis (rheumatoid) M79.2
- multiple – see also Polyneuropathy
- infective, acute G61.0
- infectious G61.0 (multiple)
- multiple – see also Polyneuropathy
- NeuromyelitisG36.9
- ascending G61.0
- Ophthalmoplegia – see also Strabismus, paralytic
- ataxia-areflexia G61.0
- Paralysis, paralytic (complete) (incomplete) G83.9
- Polyneuritis, polyneuritic – see also Polyneuropathy
- acute G61.0 (post-)
- febrile, acute G61.0
- idiopathic, acute G61.0
- infective G61.0 (acute)
- postinfective G61.0 (acute)
- Polyradiculoneuropathy G61.0 (acute) (postinfective) (segmentally demyelinating)
- Sclerosis, sclerotic
- Syndrome – see also Disease
- Barré-Guillain G61.0
- Fisher’s G61.0
- Guillain-Barré G61.0 (-Strohl)
- Miller-Fisher G61.0