Overview

Comparing Intravenous and Oral Iron in Postoperative Anemia

Status:
Completed
Trial end date:
2013-01-01
Target enrollment:
0
Participant gender:
All
Summary
Postoperative anaemia are common in patients undergoing major orthopaedic surgery. The main consequence of perioperative anaemia is an increased risk of red blood cell (RBC) transfusions. Allogeneic RBC transfusion and anaemia are associated with higher postoperative mortality and morbidity. The aim of this study was to compare the efficacy of postoperative i.v. ferric carboxymaltose (FCM) and oral ferrous glycine sulphate (FS) for early improvement of postoperative anaemia after total knee arthroplasty and whether iron treatment could facilitate recovery from surgery.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Parc de Salut Mar
Collaborator:
Vifor Pharma
Treatments:
Ferric Compounds
Glycine
Iron
Criteria
Inclusion Criteria:

- Adult patients (≥18 years of age) were recruited at the scheduled preoperative visit
(21 to 30 days prior surgery knee replacement). Anaemia (Hb <12 g/dL) and/or iron
deficiency (TSAT <20%) the day after surgery

Exclusion Criteria:

- Patients with known hypersensitivity or contraindications to iron, liver insufficiency
(aspartate aminotransferase or alanine aminotransferase >60 IU/L), bronchial asthma,
presence of acute or chronic infection, severe heart disease, significant history of
allergies (rash, etc.) or anti-anaemia treatment within 15 days prior to surgery were
excluded from participation. Also pregnant or nursing women were excluded (negative
pregnancy urine test within 7 days prior first study treatment or amenorrhoea for at
least 12 months).