2012
DOI: 10.1016/j.ejpn.2011.12.003
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Childhood chronic inflammatory demyelinating polyneuroradiculopathy – Three cases and a review of the literature

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Cited by 26 publications
(29 citation statements)
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References 60 publications
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“…In summary, the evidence shows that a good response to initial treatment with IVIG occurred in 78% ( n =59), corticosteroids in 70% ( n =44), and plasma exchange in 14% ( n =7) …”
Section: Resultsmentioning
confidence: 98%
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“…In summary, the evidence shows that a good response to initial treatment with IVIG occurred in 78% ( n =59), corticosteroids in 70% ( n =44), and plasma exchange in 14% ( n =7) …”
Section: Resultsmentioning
confidence: 98%
“…Three further series ( n =7) found good response with first‐line IVIG in 71%, which specifically improved sensory or motor function. Further treatment was required in 40% of responders . A series ( n =2) of patients with childhood multiple sclerosis on interferon who were subsequently diagnosed with CIDP had a limited response to steroids but a good response to IVIG …”
Section: Resultsmentioning
confidence: 99%
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“…Steroids induced short-term improvement in 71% -100% of children in small series (63). As a first-line therapy, oral prednisone is usually administered at a dose of 1 -2 mg/kg/day in the initial four to six weeks, then reduced over the next four to six weeks (45,64), or even by tapering over 3 -6 months.6 Interval therapy (2 mg/kg/day for 3 -8 days, repeated every four weeks) and also alternating therapy (2 mg/kg/alternate day) have been designated (58,65). In some patients, high-dose 'pulse' methylprednisolone therapy (15 -20 mg/kg/day for three days) was intravenously administered before the origination of oral prednisone therapy (31,33,48).…”
Section: Prednisonementioning
confidence: 99%