Perioperative medicine & outcomes

IRON NOF trial: IV iron for anaemic patients with femoral fracture

BJA OpenPublished Randomised controlled trial

Primary result · Incidence of blood transfusionResult — go to the resultOdds ratio 1.70 95% CI 0.83–3.47
  • terminated early
  • Terminated early because of jurisdictional changes to more restrictive transfusion practices and changes in consent requirements

Authors' conclusion

In anaemic patients undergoing surgery for hip fracture, i.v. iron did not reduce the overall proportion of patients receiving blood transfusion.

Study context

Population
Patients >60 yr with preoperative anaemia undergoing surgery for femoral neck or subtrochanteric fracture, seven Australian hospitals
Participants
143 patients
Comparison
IV iron carboxymaltose 1000 mg vs placebo at operation
  • i.v. ironn = 70
  • Placebon = 73reference
Primary endpoint
Blood transfusion use
Methodological detailsphase III, double-blind, placebo-controlled, multicentre
  • Phase III
  • Double-blind
  • Placebo-controlled
  • Multicentre

Primary result

Incidence of blood transfusion

Odds ratio

1.70

95% CI 0.83–3.47

P = 0.15

Events by treatment group

Placebo vs IV iron
OR 1.70 (95% CI 0.83–3.47); P = 0.15

As reported in the abstract

Secondary outcomes

OutcomeEstimateP value
Number of blood units transfusedPlacebo vs IV iron · no overall difference in median unitsOR 1.52 (95% CI 0.77–3.00)P = 0.22
Units of blood transfused, younger patients without major bleeding (subgroup)Placebo vs IV ironIRR 3.88 (95% CI 1.16–13.0)P = 0.03
OutcomePlaceboP value
Hb · 6 weeksIV iron vs Placebo108 g L-1P = 0.01
  • Hb: IV iron 116 g L-1

Hospital LOS, rehabilitation duration to discharge, 6-month mortality

No difference observed

Original publication

IRON NOF trial: IV iron for anaemic patients with femoral fracture. BJA Open. Published 12 August 2023. doi:10.1016/j.bjao.2023.100222

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