Adverse Reactions to Intravenous Immunoglobulin in Children with Primary Immunodeficiencies: A Single Center Experience
Abstract
Aim: This study evaluated the clinical outcomes of patients diagnosed with immunodeficiency who regularly received intravenous immunoglobulin therapy.
Material and Methods: This study was performed on 0-18-year-olds. 35 patients diagnosed with primary immunodeficiency were included in our study. Patients’ data regarding gender, age, primary diagnosis, family history of immunodeficiency, consanguineous marriage, growth and developmental delay, lymphoid tissue involvement, systemic findings, infection frequency before and after intravenous immunoglobulin therapy, and the existence of hospitalization history were analyzed retrospectively.
Results: Thirteen (%37,1) female and 22 (%67,9) male patients were evaluated in this study. Twenty-one patients (%60) were diagnosed with common variable immunodeficiency, 6 were (%17,1) severe combined immunodeficiency, 3 were (%8,6) ataxia telangiectasia, 3 were (%8,6) hyper immunoglobulin M syndrome and 2 were (%5,7) Bruton agammaglobulinemia. All the patients (%100) had a history of hospitalization for recurrent infection. Before the immunoglobulin treatment, it was observed that one patient (%2,9) had 4-6 times, 15 patients (%42,9) had 7-10 times, and 19 patients (%54,3) had more than ten times history of infection per a year. However, after the immunoglobulin treatment, it has been observed that the infection frequency of all the patients (%100) was 1-3 times per year. Pretreatment median IgG values were 224 mg/dL (25-1339) and posttreatment 510 mg/dL (218-1568), who were entered into this study.
Conclusion: Early identification of PIDs before the emergence of serious infections is important for prognosis and providing timely genetic counseling to the family. Treatment with intravenous immunoglobulin therapy reduces recurrent infections, hospitalization, and morbidity.
Keywords
Ethical Statement
References
- Thampakkul S, Ballow M. Replacement intravenous immune serum globulin therapy in patients with antibody immune deficiency. Immunol Allergy Clin North Am. 2001;21(1):165-84. doi:10.1016/S0889-8561(05)70198-3.
- Gayretli Aydın ZG, Tanır G. Clinical indications of intravenous immunoglobulin use in pediatric infectious diseases. Clinic. J Pediatr Inf. 2017;11(4):148-53. doi:10.5578/ced.201741.
- Anderson D, Ali K, Blanchette V, Brouwers M, Couban S, Radmoor P, et al. Guidelines on the use of intravenous immune globulin for hematologic conditions. Transfus Med Rev. 2007;21(2 Suppl 1):S9-56. doi:10.1016/j.tmrv.2007.01.001.
- Stiehm ER. Adverse effects of human immunoglobulin therapy. Transfus Med Rev. 2013;27(3):171-8. doi:10.1016/j.tmrv.2013.05.004.
- Geha RS, Notarangelo LD, Casanova JL, Chapel H, Conley ME, Fischer A, et al. Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee. J Allergy Clin Immunol. 2007;120(4):776-94. doi:10.1016/j.jaci.2007.08.053.
- Yorulmaz A, Artaç H, Kara R, Keleş S, Reisli İ. Primer immün yetmezlikli 1054 olgunun retrospektif değerlendirilmesi. Astım Alerji İmmünoloji. 2008;6(3):127-34.
- Wu J, Zhong W, Yin Y, Zhang H. Primary immunodeficiency disease: a retrospective study of 112 Chinese children in a single tertiary care center. BMC Pediatr. 2019;19(1):410. doi:10.1186/s12887-019-1729-7.
- Galal N, Meshaal S, Elhawary R, ElAziz DA, Alkady R, Lotfy S, et al. Patterns of primary immunodeficiency disorders among a highly consanguineous population: Cairo University Pediatric Hospital’s 5-year experience. J Clin Immunol. 2016;36(7):649-55. doi:10.1007/s10875-016-0314-1.
Details
Primary Language
English
Subjects
Health Services and Systems (Other)
Journal Section
Research Article
Authors
Fatih Karagözlü
*
0000-0001-6861-8163
Türkiye
Murat Sütçü
0000-0002-2078-9796
Türkiye
Ayper Somer
0000-0002-7827-1113
Türkiye
Publication Date
June 26, 2026
Submission Date
September 19, 2024
Acceptance Date
February 26, 2025
Published in Issue
Year 2026 Volume: 18 Number: 2


