[CIS PIDD] [cis-pidd] IGSC for autoimmune disorders

[CIS-PIDD]

Yes we have used in dermatomyositis split dose and give twice weekly
Patients have tolerated well.

In addition to ref below I have seen abstracts at JACI meeting

Misbah S, Baumann A, Fazio R, et al. A smooth transition protocol for patients with multifocal motor neuropathy going from intravenous to subcutaneous immunoglobulin therapy: an openlabel proof-of-concept study. J Peripher Nerv Syst. 2011;16:92-97.

Danieli MG, Pettinari L, Moretti R, Logullo F, Gabrielli A. Subcutaneous immunoglobulin in polymyositis and dermatomyositis: a novel application. Autoimmun Rev. 2011;10:144-149


Best regards
Maite


Maite de la Morena, MD
Professor of Pediatrics  and Internal Medicine
Division of Allergy and Immunology
University of Texas Southwestern Medical Center in Dallas
5323 Harry HInes Blvd
Dallas, Texas 75390-9063
Phone 214 456-5161
Fax: 214 456-8317
Email: maite.delamorena at utsouthwestern.edu



From: CIS-PIDD [mailto:cis-pidd at lists.clinimmsoc.org]
Sent: Wednesday, June 15, 2016 5:50 PM
To: CIS-PIDD
Subject: [cis-pidd] IGSC for autoimmune disorders

Colleagues:

Has anyone used the subcutaneous route to administer 'high dose' immunoglobulin (2g/kg) to patients with autoimmune disease?

Joe Church
Children's Hospital Los Angeles

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