Subcutaneous Immunoglobulin for Primary and Secondary Immunodeficiencies: an Evidence-Based Review
Abstract
Background Substitution with immunoglobulin can be administered intravenously (IV) or subcutaneously (SC) to patients with immunodeficiency, but it is not clear which route is to be preferred.Objective The aim of this study was to compare IV and SC administration of immunoglobulin regarding efficacy, safety, health-related quality of life and health economics in patients with primary or secondary immunodeficiency.Method PubMed and other databases were searched. Reference lists of retrieved articles were scanned and major immunoglobulin producers were contacted for additional articles. Randomized and non-randomized clinical studies that compared SC with IV immunoglobulin substitution in patients with immunodeficiency were included. The validity of the findings in the included studies was evaluated and summarized in accordance with the GRADE approach.Results Twenty-five studies were included; two randomized and 17 non-randomized studies of patients with primary immunodeficiency, one non-randomized study of patients with secondary immunodeficiency and five studies of health economics. The quality of evidence as assessed by the GRADE score was found to be moderate or low for all outcomes. Both IV and SC administration of immunoglobulin was found to be highly effective in preventing serious bacterial infections. IgG trough levels were higher with SC immunoglobulin substitution. Both therapy forms were concluded to be safe, as no serious adverse event was reported. Minor adverse events, consisting of local symptoms that were usually mild, were more frequent with SC immunoglobulin substitution. Health-related quality of life improved when patients switched from hospital-based IV immunoglobulin substitution to SC immunoglobulin substitution at home. The studies that evaluated health economics all found that SC administration was considerably more cost effective in comparison with IV immunoglobulin substitution. The main difference was that the number of lost work or school days was lower in patients with SC administration.Conclusion Both SC and IV immunoglobulin substitution offer protection from serious bacterial infections and have good safety. On the basis of available studies it is not possible to rate one of the two substitution modes as superior to the other, at least not regarding efficacy and safety. Improvement of health-related quality of life with SC immunoglobulin substitution largely seems to be related to home therapy. Studies including patients with secondary immunodeficiency were few, as were randomized studies of patients with primary immunodeficiency.
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An evidence-based review of 25 randomized and non-randomized trials and health-economic assessments comparing SCIG versus IVIG substitution therapy in patients with immunodeficiency showed that improvements in quality of life with SCIG were mainly related to home therapy.
“An evidence-based review of 25 randomized and non-randomized trials as well as health-economic assessments comparing SCIG versus IVIG substitution therapy in patients with immunodeficiency showed that improvements in QoL with SCIG were mainly related to home therapy.”
From Subcutaneous Administration of Biotherapeutics: An Overview of Current Challenges and Opportunities (2018) · cites this paper as [59]
The main advantage from an economical point of view lies in fewer days of school or work absence.
“It was found that the main advantage from an economical point of view lies in fewer days of school or work absence [59].”
From Subcutaneous Administration of Biotherapeutics: An Overview of Current Challenges and Opportunities (2018) · cites this paper as [59]
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References 78 · Cited by 71
- Authors
- Lingman-Framme, J., & Fasth, A.
- Affiliations
- Drottning Silvias barn- och ungdomssjukhus (SE)
- Corresponding author
- Fasth, Anders
- ORCID
- Fasth, Anders
- Venue
- Drugs
- Published
- 2013-07-17
- Volume
- 73
- Issue
- 12
- Pages
- 1307-1319
- ISSN
- 0012-6667 (ISSN-L)
- 1179-1950
- OpenAlex
- W2050987772
- Cited by
- 71
- References
- 78
- Citations by year
- 2026: 5 · 2025: 2 · 2024: 6 · 2023: 2 · 2022: 4 · 2021: 3 · 2020: 4 · 2019: 6 · 2018: 8 · 2017: 8 · 2016: 7 · 2015: 7 · 2014: 9
- FWCI
- 0.65
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Drugs (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Baxter International
- National Institute for Health and Care Research
- Sveriges Regering
- National Institutes of Health
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
- Health Sciences › Medicine › Oncology › Neutropenia and Cancer Infections
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Keywords
- subcutaneous immunoglobulin, intravenous immunoglobulin, primary immunodeficiency, secondary immunodeficiency, serious bacterial infection, IgG trough levels, adverse events, health-related quality of life, home-based therapy, cost-effectiveness, work and school absenteeism
- MeSH terms
- Cost-Benefit Analysis, Home Care Services, Humans, Immunoglobulin G, Immunologic Deficiency Syndromes, Quality of Life, Randomized Controlled Trials as Topic, Infusions, Subcutaneous, Administration, Intravenous
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