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Facilitated Subcutaneous Immunoglobulin Treatment Increases the Quality of Life and Decreases the Number of Infections and Hospitalizations in Children with Primary Immunodeficiencies.
Erbas Açici, Nida; Topyildiz, Ezgi; Aygün, Ayse; Geyik, Mehmet; Edeer Karaca, Neslihan; Aksu, Guzide; Kutukculer, Necil.
Afiliación
  • Erbas Açici N; Department of Pediatrics, Ege University Faculty of Medicine, Izmir, Turkey.
  • Topyildiz E; Department of Pediatric Immunology, Ege University Faculty of Medicine, Izmir, Turkey.
  • Aygün A; Department of Pediatric Immunology, Ege University Faculty of Medicine, Izmir, Turkey.
  • Geyik M; Department of Pediatric Immunology, Ege University Faculty of Medicine, Izmir, Turkey.
  • Edeer Karaca N; Department of Pediatric Immunology, Ege University Faculty of Medicine, Izmir, Turkey.
  • Aksu G; Department of Pediatric Immunology, Ege University Faculty of Medicine, Izmir, Turkey.
  • Kutukculer N; Department of Pediatric Immunology, Ege University Faculty of Medicine, Izmir, Turkey.
Int Arch Allergy Immunol ; 185(4): 382-391, 2024.
Article en En | MEDLINE | ID: mdl-38246144
ABSTRACT

INTRODUCTION:

Immunoglobulin replacement therapy is an effective lifelong treatment modality used in patients with primary immunodeficiency to prevent and/or reduce the incidence of serious infections. Facilitated subcutaneous immunoglobulin (fSCIG) was developed to combine the advantages of intravenous immunoglobulin (IVIG) and subcutaneous immunoglobulin (SCIG) and is the latest method of immunoglobulin G (IgG) administration. In this study, switching to fSCIG administration in primary immunodeficiency patients receiving regular IVIG or SCIG therapy was evaluated, and serum IgG trough levels, frequency of infections, frequency and duration of hospitalizations, duration of absence from school/work, and quality of life were determined.

METHODS:

In this study, fifteen patients with primary immunodeficiency who were previously receiving IVIG or SCIG treatment, followed by fSCIG, were evaluated retrospectively. Age, diagnosis, current complications, mean IgG value, frequency of infection, frequency of hospitalization, and duration of absenteeism from school and work were recorded during and before fSCIG treatment. At the beginning of fSCIG treatment, at 6th and 12th months, "The Quality of Life Scale" was also evaluated in patients and parents.

RESULTS:

The most common indications for initiation of fSCIG treatment were the difficulty of access to the hospital and the long transfusion periods. No systemic adverse reactions were reported except for redness, swelling, and mild pain on the injection site. The median IgG values for the last 1 year were 529.6 mg/dL for IVIG (n = 9), 876.2 mg/dL for SCIG (n = 6) and 856.7 mg/dL for fSCIG (n = 15, all patients) treatment. The frequency of infections and the number of hospitalizations decreased significantly in the fSCIG group compared to both previous treatment modalities. There was a significant increase in the quality of life score of the patients and their families when compared with previous treatment modalities.

CONCLUSION:

fSCIG is an effective treatment method and is well tolerated in patients with immunodeficiency. It provides stable immunoglobulin levels and excellent protection against infections and offers the patients the possibility of home-based therapy.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Calidad de Vida / Inmunoglobulinas Intravenosas Límite: Child / Humans Idioma: En Revista: Int Arch Allergy Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Calidad de Vida / Inmunoglobulinas Intravenosas Límite: Child / Humans Idioma: En Revista: Int Arch Allergy Immunol Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Turquía