Befrits Ragnar, Wikman Ola, Blomquist Lars, Hjortswang Henrik, Hammarlund Per, Bajor Antal, Klintman Daniel, Blom Håkan
Department of Gastroenterology and Hepatology, Karolinska University Hospital, 17176 Stockholm, Sweden.
Scand J Gastroenterol. 2013 Sep;48(9):1027-32. doi: 10.3109/00365521.2013.819442. Epub 2013 Jul 29.
Iron deficiency and anemia are being increasingly recognized as a complication of inflammatory bowel disease (IBD). The aim of this study was to observe, in a non-interventional way, how Swedish gastroenterologists adhere to guidelines in IBD outpatients treated with intravenous ferric carboxymaltose (FCM), and the result of treatment.
Altogether 394 IBD patients (Crohn's disease (CD) 60%, ulcerative colitis (UC) 40%) from 14 centers were included. Group A (n = 216) was observed from November 2008 and group B (n = 178) from March 2010. Time of observation ranged from 12 to 29 months.
S-Ferritin (µmol/l) and transferrin saturation (T-Sat; %) were recorded at baseline in 62% and 50% in group A. Median values for Hb, ferritin and T-Sat at baseline were 111 g/l, 10 µmol/l and10%, respectively, and 134 g/l, 121 µmol/l and 20% after iron treatment (p < 0.001 for all three parameters). Similar results were found in group B. Approximately three-quarters of all patients had only one iron infusion during the study period. Median time to reinfusion was 6 (1-25) months. Only previously described infusion reactions occurred in 27 (7%) patients.
Adherence to European guidelines was rather poor and needs to be improved. The effect on iron parameters of intravenous FCM was significant, and resulted in a ferritin level that indicates an effect on the iron stores. The effect was mostly sustained for a year since only one-quarter of the patients were given repeated iron infusions. No unforeseen safety concerns emerged during the observation period.
缺铁和贫血日益被视为炎症性肠病(IBD)的一种并发症。本研究的目的是以非干预方式观察瑞典胃肠病学家在接受静脉注射羧麦芽糖铁(FCM)治疗的IBD门诊患者中遵循指南的情况以及治疗结果。
纳入了来自14个中心的共394例IBD患者(克罗恩病(CD)占60%,溃疡性结肠炎(UC)占40%)。A组(n = 216)于2008年11月开始观察,B组(n = 178)于2010年3月开始观察。观察时间为12至29个月。
A组分别有62%和50%的患者在基线时记录了血清铁蛋白(µmol/l)和转铁蛋白饱和度(T-Sat;%)。基线时血红蛋白、铁蛋白和T-Sat的中位数分别为111 g/l、10 µmol/l和10%,铁治疗后分别为134 g/l、121 µmol/l和20%(所有三个参数的p均<0.001)。B组也有类似结果。在研究期间,约四分之三的患者仅接受了一次铁输注。再次输注的中位时间为6(1 - 25)个月。仅27例(7%)患者出现了先前描述的输注反应。
对欧洲指南的遵循情况相当差,需要改进。静脉注射FCM对铁参数的影响显著,并导致铁蛋白水平表明对铁储备有影响。由于只有四分之一的患者接受了重复铁输注,这种效果大多持续了一年。在观察期内未出现意外的安全问题。