Cited by 185Immunodeficiency and Autoimmune DisordersMonoclonal and Polyclonal Antibodies ResearchNeutropenia and Cancer Infections

Home-Based Subcutaneous Immunoglobulin Versus Hospital-Based Intravenous Immunoglobulin in Treatment of Primary Antibody Deficiencies: Systematic Review and Meta Analysis

Abolhassani, Hassan, Sadaghiani, Mohammad Salehi, Aghamohammadi, Asghar, Ochs, Hans D., Rezaei, Nima·2012·Journal of Clinical Immunology

Abstract

Immunoglobulin replacement by the subcutaneous route (SCIg) for the prophylactic treatment of primary or secondary antibody deficient patients has been introduced as an alternative to conventional intravenous administration (IVIg). This is a systematic review of all eligible studies comparing efficacy and safety of IVIg and SCIg. Retrospective and prospective cohort studies and randomized, controlled trials comparing SCIg to IVIg were identified from MEDLINE, EMBASE, CINAHL, AMED, CSR, ISI and Cochrane Database without restriction on publication date and language. If possible, meta-analysis was performed by using the Review Manager software. A total of 47 articles with 1,484 compared cases were reviewed. Subcutaneous immunoglobulin replacement achieved acceptable IgG trough level, low incidence of side effects, efficacy similar to IVIg infusions, better health related quality of life and treatment satisfaction, and faster functional recovery with less time off work. Because of the heterogeneity of the reports, meta-analysis had to be performed by random effect method for IgG trough levels [OR (odds ratio) = 1.00, range = 0.84-1.15; p < 0.01], infection rates (OR = 0.59, range = 0.36-0.97; p = 0.04), and adverse events (OR = 0.09, range = 0.07-0.11; p < 0.001), which showed significant preference of SCIg over IVIg. Based on the analysis of published reports, changing immunoglobulin replacement therapy from IVIg to SCIg may be of benefit to qualified patients with primary immunodeficiency. These advantages, having been demonstrated in numerous studies,make medical, practical and economic sense to consider switching patients with antibody deficiency from IVIg to SCIg.

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Crossref · 10.1007/s10875-012-9720-1

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References 77 · Cited by 185

Authors
Abolhassani, H., Sadaghiani, M. S., Aghamohammadi, A., Ochs, H. D., & Rezaei, N.
Affiliations
  • Children's Medical Center (IR)
  • Seattle Children's Hospital (US)
Corresponding author
  • Ochs, Hans D.
  • Rezaei, Nima
Venue
Journal of Clinical Immunology
Published
2012-06-23
Volume
32
Issue
6
Pages
1180-1192
ISSN
  • 0271-9142 (ISSN-L)
  • 1573-2592
OpenAlex
W2037581442
Cited by
185
References
77
Citations by year
2026: 8 · 2025: 11 · 2024: 14 · 2023: 11 · 2022: 20 · 2021: 15 · 2020: 15 · 2019: 9 · 2018: 11 · 2017: 12 · 2016: 19 · 2015: 14 · 2014: 17 · 2013: 8 · 2012: 1
FWCI
1.18
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Clinical Immunology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
  • Health Sciences › Medicine › Oncology › Neutropenia and Cancer Infections
Keywords
subcutaneous immunoglobulin, intravenous immunoglobulin, primary antibody deficiency, immunoglobulin replacement therapy, IgG trough levels, infection rate, adverse events, health-related quality of life, treatment satisfaction, functional recovery
MeSH terms
Humans, Immunoglobulin G, Immunization, Passive, Immunologic Deficiency Syndromes, Prospective Studies, Quality of Life, Retrospective Studies, Self Administration, Randomized Controlled Trials as Topic, Databases, Bibliographic, Immunoglobulins, Intravenous, Infusions, Subcutaneous

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