Shift from intravenous or 16% subcutaneous replacement therapy to 20% subcutaneous immunoglobulin in patients with primary antibody deficiencies
@article{Canessa2017ShiftFI, title={Shift from intravenous or 16\% subcutaneous replacement therapy to 20\% subcutaneous immunoglobulin in patients with primary antibody deficiencies}, author={Clementina Canessa and Jessica Iacopelli and Antonio Pecoraro and Giuseppe Spadaro and Andrea Matucci and Cinzia Milito and Alessandra Vultaggio and Carlo Agostini and Francesco Cinetto and Maria Giovanna Danieli and Simona Gambini and Carolina Marasco and Antonino Trizzino and Angelo Vacca and Domenico De Mattia and Baldassarre Martire and Alessandro Plebani and Mario Di Gioacchino and Alessia Gatta and Andrea Finocchi and Francesco Licciardi and S. Martino and Marco de Carli and Viviana Moschese and Chiara Azzari}, journal={International Journal of Immunopathology and Pharmacology}, year={2017}, volume={30}, pages={73 - 82} }
In patients with primary antibody deficiencies, subcutaneous administration of IgG (SCIG) replacement is effective, safe, well-tolerated, and can be self-administered at home. A new SCIG replacement at 20% concentration (Hizentra®) has been developed and has replaced Vivaglobin® (SCIG 16%). An observational prospective multi-centric open-label study, with retrospective comparison was conducted in 15 Italian centers, in order to investigate whether and to what extent switching to Hizentra® would…
21 Citations
Delivery of subcutaneous immunoglobulin by rapid “push” infusion for primary immunodeficiency patients in Manitoba: a retrospective review
- MedicineAllergy, Asthma & Clinical Immunology
- 2020
In a real-life setting, in the Manitoba adult PIDD population, SCIG push is an effective method of preventing severe infections, with most patients preferring to continue this therapy once initiated.
Replacement and Immunomodulatory Activities of 20% Subcutaneous Immunoglobulin Treatment: A Single-Center Retrospective Study in Autoimmune Myositis and CVID Patients
- Medicine, BiologyFrontiers in Immunology
- 2021
It is suggested that 20% SCIg treatment represents a viable and safe treatment for PM/DM patients and a valid therapeutic alternative to IVIg, with important advantages for patients’ quality of life.
Patient experience with subcutaneous immunoglobulin 20%, Ig20Gly, for primary immunodeficiency diseases: a prespecified post hoc analysis of combined data from 2 pivotal trials
- MedicineBMC Immunology
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Patients with primary immunodeficiency diseases reported high levels of treatment satisfaction, convenience, and preference for Ig20Gly, with consistent results across studies and use of multiple patient-reported outcome measures.
Correlations Among Subcutaneous Immunoglobulin Dosage, Immunoglobulin G Serum Pre-infusional Levels and Body Mass Index in Primary Antibody Deficiency Patients: A Pooled Analysis from the SHIFT/IBIS Studies
- Medicine, BiologyClinical Drug Investigation
- 2020
Findings support the concept that the cumulative monthly dose ofSCIG and the dose of SCIG per kilogram of body weight affect IgG trough levels in PAD patients, irrespective of BMI.
Subcutaneous Immunoglobulin Twenty Percent Every Two Weeks in Pediatric Patients with Primary Immunodeficiencies: Subcohort Analysis of the IBIS Study.
- MedicinePediatric allergy, immunology, and pulmonology
- 2019
Biweekly Hizentra is a noninferior option with respect to previous IVIG/SCIG-based treatment in patients with PID, and there were no differences in the number of infections.
Long-term efficacy, safety, and tolerability of recombinant human hyaluronidase-facilitated subcutaneous infusion of immunoglobulin (Ig) (fSCIG; HyQvia(®)) in immunodeficiency diseases: real-life data from a monocentric experience
- Biology, MedicineClinical and Experimental Medicine
- 2020
Real-life data suggest that long-term repeated self-administration of recombinant human hyaluronidase-facilitated subcutaneous infusion of immunoglobulins results in a reduced rate of infectious events if compared to the pre-treatment rate.
Pediatric subset of primary immunodeficiency patients treated with SCIG: post hoc analysis of SHIFT and IBIS pooled data
- MedicineAllergy, Asthma & Clinical Immunology
- 2020
In pediatric PID patients, weekly and biweekly Hizentra ® administrations appeared equally effective treatment options.
Czech Hizentra Noninterventional Study With Rapid Push: Efficacy, Safety, Tolerability, and Convenience of Therapy With 20% Subcutaneous Immunoglobulin.
- Medicine, BiologyClinical therapeutics
- 2019
Assessment of renal function in patients with myositis and treated with subcutaneous immunoglobulin: a series of 24 cases
- Medicine, BiologyTherapeutic advances in musculoskeletal disease
- 2018
The use of high-dose SCIg is generally feasible and safe in patients with inflammatory myopathies andRenal function was stable over the study period in all patients and the treatment was not withdrawn during the first year in any patient for safety issues.
Immunoglobulin replacement therapy in primary and secondary antibody deficiency: The correct clinical approach
- Medicine, BiologyInternational immunopharmacology
- 2017
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