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Intravenous Immunoglobulin Treatment in Patients With Chronic Inflammatory Demyelinating PolyneuropathyClinical and Laboratory Characteristics Associated With Improvement
P. A. van Doom, MD;
M. Vermeulen, MD;
A. Brand, MD;
P. G. H. Mulder, PhD;
H. F. M. Busch, MD
Arch Neurol. 1991;48(2):217-220.
Abstract
Of 52 patients fulfilling the criteria of chronic inflammatory demyelinating polyneuropathy, 20 (38%) did not improve after intravenous immunoglobulin treatment, two (4%) had a short-lasting improvement and subsequent infusions had no effect, nine (17%) reached a spontaneously or therapeutically induced complete remission, and 21 patients (40%) needed intermittent infusions to maintain improvement. All patients who improved initially had symptoms that significantly interfered with life-style. After treatment, 90% of these patients were independent in their daily activities. Significantly associated with improvement were disease duration of less than 1 year, progression of weakness until treatment, absence of discrepancy in weakness between arms and legs, areflexia of the arms, and slowed nerve conduction velocity of the motor median nerve. The probability of improvement if all these features are present is 93%.
Author Affiliations
From the Department of Neurology, University Hospital Dijkzigt, Rotterdam (Drs van Doom, Vermeulen, and Busch); the Department of Immunohematology and Bloodbank, University Hospital, Leiden (Dr Brand); and the Department of Biostatistics, Erasmus University, Rotterdam (Dr Mulder), the Netherlands.
Footnotes
Accepted for publication May 11, 1990.
Reprint requests to Department of Neurology, University Hospital Dijkzigt, Dr Molewaterplein 40, 3015 GD Rotterdam, the Netherlands (Dr van Doom).
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