Display options
Share it on

Autoimmune Dis. 2014;2014:962530. doi: 10.1155/2014/962530. Epub 2014 Dec 18.

Intravenous immunoglobulin treatment in chronic neurological diseases: do we have maintenance dose right?.

Autoimmune diseases

Ondrej Dolezal

Affiliations

  1. NHS Scotland, Dumfries and Galloway Royal Infirmary, Bankend Road, Dumfries DG14AP, UK.

PMID: 25580286 PMCID: PMC4281444 DOI: 10.1155/2014/962530

Abstract

Objectives. We tried to define, on individual basis, minimal effective maintenance dose of intravenous immunoglobulins (IVIG) in 26 patients with chronic neurological conditions requiring long-term IVIG treatment. Methods. Clinical criteria were reviewed in individual cases (Phase 1) followed by titration phase (Phase 2, 12 months) and posttitration/follow-up phase (Phase 3, 3 months). Objective neurological examination and patient self-reports were used for clinical follow-up. Results. 69.2% of patients reported condition as stable, 26.9% as better, and 3.9% as mildly worse. Original mean monthly dose was 1 g/kg; over the period of 12 months we reduced dose of IVIG to mean dose 0.67 g/kg (range 0.3-2.5 g/kg, P < 0.0001) which meant reduction by 36.4%. We identified 4 nonresponders and diagnosis in one case was reclassified to degenerative disease. In follow-up phase we reduced dose further to 0.60 g/kg. Cumulative monthly dose dropped from 2040 g to 1298 g and to 991 g, respectively. Financial expenses were reduced significantly (by -36.4% during titration phase and by -51.4% during follow-up phase) (comparing with baseline) (P < 0.0001). Conclusion. Individual dose titration leads to significant maintenance IVIG dose reduction with preserved clinical efficacy. Maintenance dose below 1 g/kg (in our study around 0.7 g/kg) has acceptable risk/benefit ratio.

References

  1. J Peripher Nerv Syst. 2013 Jun;18(2):130-40 - PubMed
  2. Neurology. 2001 Feb 27;56(4):445-9 - PubMed
  3. Curr Treat Options Neurol. 2014 Feb;16(2):269 - PubMed
  4. J Peripher Nerv Syst. 2009 Jun;14(2):93-100 - PubMed
  5. Blood Coagul Fibrinolysis. 2005 Jul;16(5):313-8 - PubMed
  6. N Engl J Med. 2001 Sep 6;345(10):747-55 - PubMed
  7. Can J Neurol Sci. 2013 May;40(3):384-8 - PubMed
  8. J Neuroimmunol. 2000 Mar 1;103(2):195-201 - PubMed
  9. J Neuroimmunol. 2001 Mar 1;114(1-2):160-7 - PubMed
  10. Drugs. 2009 May 29;69(8):987-1001 - PubMed
  11. J Neurosci Res. 1996 Feb 1;43(3):273-281 - PubMed
  12. J Peripher Nerv Syst. 2010 Sep;15(3):185-95 - PubMed
  13. Brain. 1996 Aug;119 ( Pt 4):1067-77 - PubMed
  14. Lancet Neurol. 2008 Feb;7(2):136-44 - PubMed
  15. J Neuroimmunol. 1996 Mar;65(1):11-9 - PubMed
  16. Ann Neurol. 1994 Dec;36(6):838-45 - PubMed
  17. Immunol Rev. 1994 Jun;139:79-107 - PubMed
  18. J Neurol. 2009 Apr;256(4):608-14 - PubMed
  19. Arch Neurol. 2010 Sep;67(9):1082-8 - PubMed
  20. J Neuroimmunol. 2014 Sep 15;274(1-2):225-9 - PubMed
  21. J Neurol Neurosurg Psychiatry. 1996 Apr;60(4):388-92 - PubMed
  22. Clin Exp Immunol. 1994 Jul;97 Suppl 1:49-51 - PubMed
  23. Scand J Immunol. 1994 Jul;40(1):37-42 - PubMed
  24. J Autoimmun. 1993 Dec;6(6):683-9 - PubMed
  25. J Peripher Nerv Syst. 2010 Mar;15(1):1-9 - PubMed
  26. Eur J Neurol. 2013 May;20(5):836-42 - PubMed
  27. J Immunol Methods. 1998 Jul 1;216(1-2):117-37 - PubMed
  28. Ned Tijdschr Geneeskd. 1993 Sep 25;137(39):1955-8 - PubMed
  29. Eur J Neurol. 2014;21(1):147-52 - PubMed
  30. Postgrad Med. 2013 Mar;125(2):65-72 - PubMed
  31. Am J Hematol. 2000 Sep;65(1):30-4 - PubMed
  32. Cochrane Database Syst Rev. 2009 Jan 21;(1):CD001797 - PubMed
  33. J Peripher Nerv Syst. 2010 Dec;15(4):295-301 - PubMed

Publication Types