Human normal immunoglobulin in the treatment of primary immunodeficiency diseases

被引:9
作者
Wood, Philip [1 ]
机构
[1] St James Univ Hosp, Leeds LS9 7TF, W Yorkshire, England
来源
THERAPEUTICS AND CLINICAL RISK MANAGEMENT | 2012年 / 8卷
关键词
antibody deficiency; immunoglobulin therapy; common variable immunodeficiency; COMMON VARIABLE IMMUNODEFICIENCY; PRIMARY ANTIBODY DEFICIENCY; QUALITY-OF-LIFE; X-LINKED AGAMMAGLOBULINEMIA; SUBCUTANEOUS GAMMA-GLOBULIN; PRIMARY IMMUNE-DEFICIENCY; INTRAVENOUS IMMUNOGLOBULIN; REPLACEMENT THERAPY; PRIMARY HYPOGAMMAGLOBULINEMIA; HUMORAL IMMUNODEFICIENCY;
D O I
10.2147/TCRM.S22599
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
The primary antibody deficiency syndromes are a rare group of disorders that can present at any age, and for which delay in diagnosis remains common. Replacement therapy with immunoglobulin in primary antibody deficiencies increases life expectancy and reduces the frequency and severity of infection. Higher doses of immunoglobulin are associated with reduced frequency of infection. Late diagnosis and delayed institution of immunoglobulin replacement therapy results in increased morbidity with a wide variety of organ-specific complications and increased mortality. Risks of immunoglobulin therapy are minimized by modern manufacturing processes, although patients can experience both immediate and delayed adverse reactions, and concerns remain over the transmission of prions in plasma. Immunoglobulin therapy leads to improvements in overall quality of life, and many of the improvements relate to reduced infection rates and fear of future infections, strongly suggesting that the immunoglobulin therapy itself is the major factor in this improvement. There are limited data on the economic benefits of immunoglobulin therapy, with the fluctuating costs of immunoglobulins making comparison between different studies difficult. However, estimates suggest that early intervention with immunoglobulin replacement compares favorably with prolonged therapy for other more common chronic diseases.
引用
收藏
页码:157 / 167
页数:11
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