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Infliximab administered with shortened infusion times in a specialized IBD infusion unit: A prospective cohort study
Authors:Gert Van Assche  Séverine Vermeire  Maja Noman  Christine Amant  Ellen Weyts  Anita Vleminckx  Marie-Josée Vermeyen  Paul Rutgeerts
Affiliation:1. Key Laboratory of Food Processing Technology and Quality Control in Shandong Province, College of Food Science and Engineering, Shandong Agricultural University, Tai''an 271018, China;2. Department of Chemical and Biological Engineering, Iowa State University, Ames, IA 50011, USA;1. Faculty of Environment, University of Tehran, Tehran, Iran
Abstract:Background and aimsBiological therapy with anti TNF agents requires parenteral administration and in the case of infliximab this involves in hospital treatment. We aimed to prospectively assess the safety and tolerance of infliximab infusion in patients with IBD in a specialized unit adhering to strict standard operation procedures including switch to accelerated 1 h infusions.MethodsA prospective audit of a referral center IBD infusion unit was performed. We recorded infusion times and all adverse events including hypersensitivity reactions. Patients were also polled about the impact of the treatment on quality of life (QOL).ResultsOn 20 consecutive days 177 patients were treated with infliximab and all participated. Of those infliximab 117 received 1 h infusions and 4 (2.2%) had an immediate infusion reaction. Median time on unit was optimal for those with 1 h infusions [1:35 h (IQR: 1:25–1:50)] without an increased risk of infusion reactions. Prophylactic therapy significantly increased the time on unit [3:20 h (IQR: 2:50–3:45), p < 0.001]. Patients reported a high global satisfaction and a good tolerability of the infusions with a considerable or strong impact on studies, work or QOL in one third.ConclusionsA dedicated IBD infusion unit can achieve high quality of care and shortened 1 h infliximab infusions are well tolerated in patients with scheduled maintenance therapy.
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