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Pregled bibliografske jedinice broj: 538127

Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS)


Burton, B.K.; Whiteman, D.A.; HOS investigators; Barišić, Ingeborg; Barić, Ivo
Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS) // Molecular genetics and metabolism, 103 (2011), 2; 113-120 doi:10.1016/j.ymgme.2011.02.018 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 538127 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS)

Autori
Burton, B.K. ; Whiteman, D.A. ; HOS investigators ; Barišić, Ingeborg ; Barić, Ivo

Izvornik
Molecular genetics and metabolism (1096-7192) 103 (2011), 2; 113-120

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Hunter syndrome

Sažetak
Objective was to evaluate the occurrence of infusion-related reactions (IRRs) in patients with mucopolysaccharidosis type II (MPS II) receiving idursulfase enrolled in the observational database HOS - the Hunter Outcome Survey. Information in HOS regarding the frequency, timing and severity of reported IRRs during the first year of treatment with idursulfase was analyzed, and formation of antibodies to idursulfase was characterized. The analysis was restricted to patients who started treatment with idursulfase at or after enrolment in HOS and for whom at least 1 year of follow-up data was available (n=104 ; data collected on or before 16 October 2009). A total of 65 IRRs were reported in 33 (31.7%) patients in the first year of enzyme replacement therapy (ERT). Six of these patients experienced more than three events. Nearly all of the initial IRRs occurred during the first 3months of ERT ; five patients (4.8% of the total patient population) experienced their first IRR after 3months of treatment. Only two patients (1.9% of the total patient population) experienced their first IRR after more than 6 months of ERT. Most of the IRRs were of mild-to-moderate severity. After initially stopping the infusion, IRRs were generally readily managed by slowing the infusion and/or use of antihistamines or antipyretics. No patient in this analysis discontinued ERT because of an IRR event. IgG antibodies to idursulfase were detected in 32/63 patients (50.8%) for whom samples were taken ; no patient developed IgE to idursulfase. Serum antibody levels were measured within 24h of an IRR for 10 IRRs in 7 patients ; 7/9 samples contained IgG to idursulfase, 2 of which had neutralizing activity. IRRs in patients receiving idursulfase can typically be readily managed without interruption of treatment. Initial IRRs usually occur in the first 3 months of treatment, but in rare instances may occur after more than 6 months of therapy. Physicians using ERT to treat patients with MPS II, either in the clinic or at home, should therefore be familiar with the timing, nature and recommended management of IRRs.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA


Projekti:
072-1083107-0365 - Istraživanje epidemiologijskih i genetičkih osnova prirođenih mana (Barišić, Ingeborg, MZOS ) ( CroRIS)
108-1081870-1885 - Nasljedne metaboličke i ostale monogenske bolesti djece (Barić, Ivo, MZOS ) ( CroRIS)

Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta,
Medicinski fakultet, Zagreb

Profili:

Avatar Url Ivo Barić (autor)

Avatar Url Ingeborg Barišić (autor)

Poveznice na cjeloviti tekst rada:

doi ac.els-cdn.com www.sciencedirect.com dx.doi.org

Citiraj ovu publikaciju:

Burton, B.K.; Whiteman, D.A.; HOS investigators; Barišić, Ingeborg; Barić, Ivo
Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS) // Molecular genetics and metabolism, 103 (2011), 2; 113-120 doi:10.1016/j.ymgme.2011.02.018 (međunarodna recenzija, članak, znanstveni)
Burton, B., Whiteman, D., HOS investigators, Barišić, I. & Barić, I. (2011) Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS). Molecular genetics and metabolism, 103 (2), 113-120 doi:10.1016/j.ymgme.2011.02.018.
@article{article, author = {Burton, B.K. and Whiteman, D.A. and Bari\v{s}i\'{c}, Ingeborg and Bari\'{c}, Ivo}, year = {2011}, pages = {113-120}, DOI = {10.1016/j.ymgme.2011.02.018}, keywords = {Hunter syndrome}, journal = {Molecular genetics and metabolism}, doi = {10.1016/j.ymgme.2011.02.018}, volume = {103}, number = {2}, issn = {1096-7192}, title = {Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS)}, keyword = {Hunter syndrome} }
@article{article, author = {Burton, B.K. and Whiteman, D.A. and Bari\v{s}i\'{c}, Ingeborg and Bari\'{c}, Ivo}, year = {2011}, pages = {113-120}, DOI = {10.1016/j.ymgme.2011.02.018}, keywords = {Hunter syndrome}, journal = {Molecular genetics and metabolism}, doi = {10.1016/j.ymgme.2011.02.018}, volume = {103}, number = {2}, issn = {1096-7192}, title = {Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: a perspective from the Hunter Outcome Survey (HOS)}, keyword = {Hunter syndrome} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


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