Comparing Intravenous and Oral Iron in Postoperative Anemia

NCT01913808 — Phase 4, Completed, 122 participants, Parc de Salut Mar

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Efficacy of Intravenous Ferric Carboxymaltose in the Improvement of Anemia in Patients With Postoperative Knee Prosthesis

RegistryNCT01913808
StatusCompleted
PhasePhase 4
Study typeInterventional; randomized, parallel, masking: single, treatment
Enrollment122 (Actual)
SponsorParc de Salut Mar (Other); collaborators: Vifor Pharma
ConditionsPostoperative Anemia, Osteoarthritis, Knee
InterventionsFerric carboxymaltose, ferrous glycine sulphate (Drug)
Datesstart 2011-01-01, primary completion 2012-02-01, completion 2013-01-01, first posted 2013-08-01, last updated 2016-04-06
Locations1 site in Spain

Related Papers Related Patents Related Grants Related Experts
All trials for Postoperative Anemia All trials for Osteoarthritis, Knee All trials of Ferric carboxymaltose All trials of ferrous glycine sulphate

-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.

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+Detailed description

Both pre- and 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. Since blood transfusions increase Hb levels only transiently but come at the price of higher mortality and morbidity (e.g. postoperative infections), the three-pillar concept of patient blood management (PBM) has been developed to reduce the risk of blood transfusions and improve patient outcomes. Among its three pillars, the treatment or prevention of preoperative anaemia is the mainstay of PBM. Also the second pillar, minimisation of intraoperative blood loss,15 targets at least indirectly the patient's haemoglobin (Hb) levels.

The third PBM pillar, use of low Hb cut-off levels triggering transfusion, means that a certain degree of postoperative anaemia is taken into account. However, it remains unclear whether a lowered transfusion threshold allows optimal functional recovery and quality of life. Since patients undergoing total knee arthroplasty (TKA) are often elderly and have several comorbidities, prolonged exposure to low Hb levels is not a good option for this population. Furthermore, TKA patients should be mobilised as soon as possible after surgery which increases the metabolic demand.

Although, depending on the timescale before surgery, oral iron is suggested for preoperatively anaemic patients with absolute iron deficiency, oral iron showed no benefit over placebo in anaemic patients after lower limb arthroplasty. In patients at risk of functional iron deficiency due to chronic inflammation of different aetiologies, intravenous (i.v.) iron administration has proven its superiority over oral iron. Even in iron-deficient patients without established anaemia, i.v. iron improved physical performance and cardiac functional class. Thus, postoperative anaemia treatment with i.v. iron might not only reduce RBC requirements but also improve performance, rehabilitation and outcomes.

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.

+Arms and interventions

ArmTypeInterventionsDescription
Ferric carboxymaltoseExperimentalDrug: Ferric carboxymaltoseFerric carboxymaltose (Ferinject®, Vifor-France) was given as a single i.v. dose to correct the total iron deficit calculated by the Ganzoni formula (total iron deficit \[mg\] = 2.4 x patient's weight \[kg\] x (target Hb \[13 g/dL\] - current Hb \[g/dL\]) + 500 \[mg iron stores\]
Ferrous glycine sulphateActive comparatorDrug: ferrous glycine sulphateFerrous glycine sulphate (Ferbisol-Bial Industrial Farmacéutica, Spain) was given as a once daily oral dose of 100 mg iron from the day of discharge (Day 7) to the rehabilitation visit 30 days after surgery
  • Ferric carboxymaltose (Drug), also known as intravenous iron: Single intravenous dose ferric carboxymaltose
  • ferrous glycine sulphate (Drug), also known as Oral iron: Daily oral dose of 100 mg iron (ferrous glycine sulphate)

+Outcome measures

Primary outcomes

  • Change in hemoglobin concentration [30 days]: Change in hemoglobin concentrations from baseline to 30 days

Secondary outcomes

  • Anemia [30 days]: Number of subjects without anemia (hemoglobin > 12g/dL)
  • Hemoglobin concentration [30 days]: Concentration of hemoglobin at day 30
  • Quality of life [30 days]: Quality of life measured by European Quality of Life-5 Dimensions (EQ-5D)(before and 30 days)
  • Independence in daily activities [30 days]: Independence in daily activities measured by the Barthel questionnaire (before and 30 days)
  • Walk test [30 days]: 6 minutes walking test (before and 30 days)
  • Adverse events [30 days]: Adverse event (clinical and analytical, before to 30 days)

+Eligibility

Sex: All, ages: 18 Years to any

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).

+Locations (1)

FacilityCityCountryStatus
Hospital de la Esperanza (Parc de Salut MAR)Barcelona, BarcelonaSpain

+Publications

  • Results publication: Bisbe E, Molto L, Arroyo R, Muniesa JM, Tejero M. Randomized trial comparing ferric carboxymaltose vs oral ferrous glycine sulphate for postoperative anaemia after total knee arthroplasty. Br J Anaesth. 2014 Sep;113(3):402-9. doi: 10.1093/bja/aeu092. Epub 2014 Apr 29. PMID 24780615

+Investigators