chronic inflammatory demyelinating polyradiculoneuropathy: A slowly progressive autoimmune demyelinating disease of peripheral nerves and nerve roots. Clinical manifestations include weakness and sensory loss in the extremities and enlargement of peripheral nerves. The course may be relapsing-remitting or demonstrate a step-wise progression. Protein is usually elevated in the spinal fluid and cranial nerves are typically spared. GUILLAIN-BARRE SYNDROME features a relatively rapid progression of disease which distinguishes it from this condition. (Adams et al., Principles of Neurology, 6th ed, p1337)
| Name | G6_POLYOTHUNS |
|---|---|
| Long name | Other and unspecified polyneuropathies, also in other diseases |
| Hospital Discharge registry | ICD-10: G619/G629/G63/G628/G611/G618, ICD-8: 3540[8-9] |
| Cause of Death registry | ICD-10: G63/G628/G619/G629/G611/G618, ICD-8: 3540[8-9] |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF2 |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 2629 | 1076 | 1553 |
| Unadjusted prevalence (%) | 1.21 | 0.88 | 1.65 |
| Mean age at first event (years) | 60.42 | 58.72 | 61.60 |
| Case fatality at 5-years (%) | 5.90 | 4.00 | 7.21 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 2.0 | 2.0 | 2.0 |
| Recurrence at 6 months (%) | 46.44 | 46.38 | 46.49 |
before Other and unspecified polyneuropathies, also in other diseases
after Other and unspecified polyneuropathies, also in other diseases
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