Clinical Neurology and Neurosurgery
Volume 112, Issue 6 , Pages 467-469, July 2010

Identification and comparison of adverse events for preparations of IVIG in patients with neuromuscular diseases

Department of Clinical Neurosciences and the University of Calgary, Calgary, Alberta, Canada

Received 4 May 2009; received in revised form 15 January 2010; accepted 16 February 2010.

Abstract 

Objective

Risk factors for adverse events in intravenous immunoglobulin (IVIG) therapy are uncertain. We sought to determine the associations of IVIG-related adverse events in patients with neuromuscular disorders.

Patients and methods

We determined the prevalence of adverse events with the use of different forms of IVIG in a tertiary care patient population with neuromuscular diseases. A retrospective assessment for over two decades of patient care was performed.

Results

Adverse events occurred in 43% of patients over time and during 10% of infusions. Prevalence of adverse events, especially headache, was higher for lyophilized forms of IVIG, and increased with cumulative IVIG delivery. Fortunately, serious adverse events were rare for all IVIG preparations. Discontinuation of IVIG therapy occurred most commonly due to perceived inefficacy or adverse events with lyophilized forms of IVIG.

Conclusion

IVIG is generally well tolerated and only rarely associated with serious adverse events, but lyophilized forms of IVIG may be associated with greater prevalence of adverse events in patients with neuromuscular diseases.

Keywords: Chronic inflammatory demyelinating polyneuropathy, Guillain-Barre syndrome, Intravenous immunoglobulin, Myasthenia gravis, Neuromuscular disorders

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0303-8467(10)00052-1

doi:10.1016/j.clineuro.2010.02.008

Clinical Neurology and Neurosurgery
Volume 112, Issue 6 , Pages 467-469, July 2010