Subcutaneous Immunoglobulins: Product Characteristics and Their Role in Primary Immunodeficiency Disease

被引:15
作者
Melamed, Isaac [1 ]
Testori, Alessandro [1 ]
Spirer, Zvi [2 ]
机构
[1] IMMUNOe Int Res Ctr, Centennial, CO 80112 USA
[2] Edmond & Lily Safra Childrens Hosp, Sheba Med Ctr, Tel Hashomer, Israel
关键词
adverse drug reactions; immunoglobulin G; immunologic deficiency syndrome; intravenous immunoglobulin therapy; primary immunodeficiency disease; QUALITY-OF-LIFE; PRIMARY ANTIBODY DEFICIENCIES; REPLACEMENT THERAPY; GAMMA-GLOBULIN; INTRAVENOUS IMMUNOGLOBULINS; SAFETY; EFFICACY; PHARMACOKINETICS; INFUSIONS; CHILDREN;
D O I
10.3109/08830185.2012.732631
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Research on the role of subcutaneous immunoglobulin in primary immunodeficiency disease (PIDD) is ongoing. We analyzed pivotal studies for four subcutaneous immunoglobulin products: IGSC 10% (Gammagard (R) Liquid), IGIV-C 10% (Gamunex (R)-C), IGSC 16% (Vivaglobin (R)) and IGSC 20% (Hizentra (R)). To identify similarities and differences between products, we examined infusion parameters, adverse event profiles and improvements in tolerability over time. Maximum volume infused was 30mL/site for IGSC 10%, 34mL/site for IGIV-C 10%, 15mL/site for IGSC 16% and 25 mL/site for IGSC 20%. Maximum number of simultaneous infusion sites was 10 for IGSC 10%, 8 for IGIV-C 10%, 6 for IGSC 16% and 4 for IGSC 20%. Local adverse reaction rate per infusion was 0.02 for IGSC 10%, 0.59 for IGIV-C, 0.49 for IGSC 16% and 0.58 for IGSC 20%. IGSC products have similar efficacy profiles; however, their tolerability profiles vary. Reasons for these differences are unknown and warrant further research.
引用
收藏
页码:451 / 461
页数:11
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