A pilot study about subcutaneous administration of 10% immunoglobulin in patients with primary immune deficiencies: Single center experience
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Dosyalar
Tarih
2017
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Aim: In this study, we aimed to see the safety, protectivity and adverse events of rapid infusion subcutaneous immunoglobulin (SCIG)
therapy in our patients for one year duration.
Material and methods: 10 patients diagnosed with primary immune deficiency and receiving regular intravenous immunoglobulin
(IVIG) were randomly included to the study, then their IVIG replacement therapy changed as rapidly infused SCIG in same monthly
dose. Patients were evaluated in different times for following aspects; serum IgG levels, frequency of infections, side effects, local
reactions, and improvement of life quality. IgG levels of patients were measured at the beginning, 3, 6, and 12 months of SCIG
replacement treatment.
Results: Local reactions were high at the beginning, then decreased with recurrent infusions. Any severe systemic reactions were not
observed in patients. Less infection rate was seen in four patients who were not receiving IVIG regularly before with good compliance
in all patients. Infection frequency remained same in 4patients. Increased levels of IgG were achieved eight of the patients at end of
the 6months and their levels remained as stable at the end of a year.
Conclusion: Our study showed that rapid SCIG therapy in same monthly dose with IVIG is as effective as IVIG for preventing infections
without any worse systemic reactions
Açıklama
Anahtar Kelimeler
Kaynak
Annals of Medical Research
WoS Q DeÄŸeri
Scopus Q DeÄŸeri
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Künye
Cansever, M., Bektas Kut, F., & Patiroglu, T. (2021). A pilot study about subcutaneous administration of 10% immunoglobulin in patients with primary immune deficiencies: Single center experience . Annals of Medical Research, 24(4), 0457–0461. Retrieved from https://annalsmedres.org/index.php/aomr/article/view/1580
