Treatment with ferric carboxymaltose in stable patients with severe iron deficiency anemia in the emergency department

被引:16
作者
Motta, Irene [1 ,2 ]
Mantovan, Giulia [3 ]
Consonni, Dario [4 ]
Brambilla, Anna Maria [5 ]
Materia, Maria [6 ]
Porzio, Marianna [6 ]
Migone De Amicis, Margherita [2 ]
Montano, Nicola [1 ]
Cappellini, Maria Domenica [1 ,2 ]
机构
[1] Univ Milan, Dept Clin Sci & Community Hlth, Milan, Italy
[2] Osped Maggiore Policlin, Fdn IRCCS Ca Granda, UOC Med Gen, Dept Internal Med, Via F Sforza 35, I-20122 Milan, Italy
[3] Univ Milan, Sch Med, Milan, Italy
[4] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Epidemiol Unit, Milan, Italy
[5] L Sacco Hosp Vialba, ASST FBF Sacco, Emergency Med, Dept Internal Med, Milan, Italy
[6] Osped Maggiore Policlin, Fdn IRCCS Ca Granda, Emergency Dept, Milan, Italy
关键词
Severe anemia; Iron deficiency; Ferric carboxymaltose; Transfusion; Choosing wisely; BLOOD-CELL TRANSFUSION; FAST-TRACK ANEMIA; EFFICACY; TRIAL;
D O I
10.1007/s11739-019-02223-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The AABB Choosing Wisely Campaign recommends "don't transfuse for iron deficiency without hemodynamic instability". However, the management of iron deficiency anemia (IDA) in the emergency department (ED) is heterogeneous and patients are often over-transfused. Intravenous iron is effective in correcting anemia and new formulations, including ferric carboxymaltose (FCM), allow the administration of high doses with low immunogenicity. The aim of this retrospective study was to analyze the management of hemodynamically stable patients aged 18-55 years with severe IDA (hemoglobin < 8 g/dL), who presented to the ED from January 2014 to July 2018. Patients who received FCM (FCM1) and those who did not receive FCM (FCM0) were compared. Efficacy and safety of FCM at follow-up were evaluated. Seventy-one subjects fulfilled the inclusion criteria (FCM0 n = 48; FCM1 n = 23). The mean Hb at admission was 6.6 g/dL. 40% in the FCM0 and 13% in FCM1 were transfused (p = 0.02). 21% of FCM0 patients were admitted to the ward, while all FCM1 were discharged (p = 0.02). Within 2 weeks, the Hb increase was 2.8 +/- 1 g/dL in the FCM1 group. Sixteen FCM1 patients were evaluated at 52 +/- 28 days (median 42, range 27-122): the average Hb increase was 5.3 +/- 1.4 g/dL. In summary, we showed that FCM administration in the ED in hemodynamically stable patients was associated with fewer transfusions and hospital admissions compared to the FCM0 group; moreover, it succeeded in safely, effectively and rapidly increasing Hb levels after discharge from the ED. Further studies are needed to develop recommendations for IDA in the ED and to identify transfusion thresholds for non-hospitalized patients.
引用
收藏
页码:629 / 634
页数:6
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