Mahey Reeta, Kriplani Alka, Mogili Krishna D, Bhatla Neerja, Kachhawa Garima, Saxena Renu
Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, New Delhi, India.
Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, New Delhi, India.
Int J Gynaecol Obstet. 2016 Apr;133(1):43-8. doi: 10.1016/j.ijgo.2015.09.007. Epub 2015 Dec 23.
To evaluate the efficacy and safety of intravenous ferric carboxymaltose (FCM) in comparison with intravenous iron sucrose (ISC) in the treatment of anemia due to abnormal uterine bleeding (AUB).
A randomized controlled trial was conducted between April 2013 and May 2014 in patients older than 18 years of age presenting at a hospital in New Delhi, India, with anemia due to AUB. Patients were randomized in a 1:1 ratio to receive treatment with intravenous FCM or ISC. The primary outcome, increase in hemoglobin above baseline, was monitored over a 12-week period. Patients completing the full treatment and follow-up protocol were included in the analyses. Participants and investigators were not masked to treatment allocations.
Overall, 30 patients were assigned to each group. Increases in mean hemoglobin levels from baseline were significantly higher in the FCM group at 6 weeks (P=0.005). At 12 weeks, there was no significant difference in hemoglobin increase from baseline between the two groups (P=0.11). Adverse events were similar between both treatment groups.
Treatment with FCM resulted in a rapid increase in hemoglobin levels in patients with anemia due to AUB, with similar increases in hemoglobin over a 12-week period. Clinical Trial Registration (www.ctri.nic.in):CTRI/2015/09/006224.
比较静脉注射羧基麦芽糖铁(FCM)与静脉注射蔗糖铁(ISC)治疗异常子宫出血(AUB)所致贫血的疗效和安全性。
2013年4月至2014年5月,在印度新德里一家医院对年龄大于18岁的AUB所致贫血患者进行了一项随机对照试验。患者按1:1比例随机分组,接受静脉注射FCM或ISC治疗。在12周内监测主要结局指标,即血红蛋白较基线水平的升高情况。纳入完成全部治疗和随访方案的患者进行分析。参与者和研究者未对治疗分配情况设盲。
总体上,每组分配30例患者。FCM组在6周时血红蛋白水平较基线的平均升高幅度显著更高(P = 0.005)。在12周时,两组血红蛋白较基线的升高幅度无显著差异(P = 0.11)。两个治疗组的不良事件相似。
FCM治疗使AUB所致贫血患者的血红蛋白水平迅速升高,在12周内血红蛋白升高幅度相似。临床试验注册(www.ctri.nic.in):CTRI/2015/09/006224。