Current experience with manual push subcutaneous immunoglobulin (SCIg) in patients with immune deficiencies.

Publication date: Jun 24, 2025

Immunoglobulin G replacement therapy prevents infections in patients with antibody deficiencies. Subcutaneous immunoglobulin (SCIg) has typically been administered via infusion pump, but the manual push technique offers a simple, convenient alternative method. The manual push technique is efficacious, well tolerated, quick to administer, offers increased dosing flexibility, and does not rely on a pump. Having various administration options available to patients provides greater treatment satisfaction and feelings of self-empowerment, which may improve compliance. Currently available literature published before 10 February 2022, that reported patient and healthcare professional experience with SCIg administered via manual push, were reviewed. Literature searches were performed using PubMed, Google and ClinicalTrials. gov using key words ‘manual push’, ‘rapid push’, ‘immunoglobulin’, ‘subcutaneous immunoglobulin’, ‘SCIg’, and ‘primary immunodeficiency’. Real-world evidence demonstrates all delivery techniques provide similar efficacy, so treatment administration becomes about patient preference, hospital resources, cost-effectiveness/recovery and clinician attitude. To establish newer administration modalities such as manual push or prefilled syringes, there needs to be patient awareness of these options, then education and finally confidence in recommending these options. Adoption of newer administration modalities will help ensure patients receive the widest range of choice, thus improving compliance and their risk of recurrent and severe infection.

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Concepts Keywords
Clinicaltrials Home-based therapy
February immunoglobulin replacement therapy
Google individualized dosing
Satisfaction manual push
primary immunodeficiency (PID)
rapid push
subcutaneous immunoglobulin (SCIg)

Semantics

Type Source Name
disease MESH infections
pathway KEGG Primary immunodeficiency
disease IDO primary immunodeficiency
disease IDO infection
drug DRUGBANK Coenzyme M
disease MESH Inflammation
disease MESH defects
disease IDO site
disease MESH nosocomial infection
disease MESH COVID 19
drug DRUGBANK Phenindione
disease MESH SID
disease IDO history
pathway REACTOME Reproduction
disease IDO production
drug DRUGBANK Immune Globulin Human
disease MESH chest pain
disease MESH tachycardia
disease MESH renal failure
disease IDO immunodeficiency
drug DRUGBANK Indoleacetic acid
disease MESH bacterial infections
drug DRUGBANK Methionine
drug DRUGBANK Trestolone
disease MESH lifestyle
drug DRUGBANK Tropicamide
disease MESH anaphylactic reactions
disease MESH hypersensitivity

Original Article

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