Anaemia is a common problem in patients undergoing surgery. About half of patients undergoing a major operation have anaemia, often a consequence of the disease requiring surgery. Anaemia causes patients to feel tired and unwell. Anaemia at the time of surgery increases the requirement for blood transfusion (50% if anaemic compared to only 15% without anaemia). Both anaemia and blood transfusions are associated with increased complications from surgery, delayed recovery and prolonged hospital stay. The investigators propose that giving intravenous iron before operation can be used to correct anaemia in these patients. Consequently if patients are not anaemic they are less likely to need blood transfusion. Also patients feel better and their health is improved before their operation they are more likely to tolerate the surgery, recover faster, be less likely to have complications from surgery and return home sooner. This will have benefits to the individual patient and also to the NHS by reducing costs. Oral Iron tablets are not effective as they take 3-6 months to increase blood levels, the tablets are often not tolerated as cause constipation or stomach pain, overall only 30-50% of people continue taking oral iron. A full treatment dose of intravenous iron can be given in 15 minutes with minimal side effects. The effect is to rapidly increase blood counts in 2-4 weeks. The investigators propose that this treatment can be incorporated to patient preparation pathways for surgery as an outpatient without the need for additional visits to hospital. Small studies have suggested a benefit of iron therapy in orthopaedic and gynaecological surgery. This study will look at 500 patients undergoing major surgery at 20 hospitals in the UK. The investigators anticipate half of patients treated will have their anaemia corrected before operation. Patients with anaemia will be identified as part of the routine blood tests taken preoperatively and invited to take part in the study. Following informed consent, they will be randomly allocated to receive either intravenous iron or a placebo infusion of saline. Intravenous iron is a dark liquid given continuously into a vein over 15 minutes. To ensure neither doctor nor patient knows which treatment is being given both infusions will be prepared and administered by an unblinded authorised person via a black bag through black tubing. There will be no other changes to the patient's normal treatment. The main aim of this study is to assess if intravenous iron will reduce the need for blood transfusion in the time period around the operation. Further outcome measures will include; patient-reported quality of life, complications, length of hospital stay, and cost. Outcomes will be assessed both during hospital stay and after the patient has been discharged. The trial will be run through a Clinical Trials Unit with considerable experience in conducting large trials. The team has a large range of experience in anaemia management and assessment of complications, quality of life and the cost of health care. The main aim of this study is to assess if intravenous iron will reduce the need for blood transfusion in the time period around the operation. Further outcome measures will include; patient-reported quality of life, complications, length of hospital stay, and cost. Outcomes will be assessed both during hospital stay and after the patient has been discharged. The trial will be run through a Clinical Trials Unit with considerable experience in conducting large trials. The team has a large range of experience in anaemia management and assessment of complications, quality of life and the cost of health care.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
487
1000mg of ferric carboxymaltose will be administered as an i.v. infusion (100ml normal saline)
Normal saline will be administered as an i.v. infusion (100ml normal saline)
Basildon University Hospital
Basildon, United Kingdom
Blackpool Teaching Hospitals
Blackpool, United Kingdom
Southmead Hospital
Bristol, United Kingdom
Broomfield Hospital
Broomfield, United Kingdom
Countess of Chester Hospital
Chester, United Kingdom
Russells Hall Hospital
Dudley, United Kingdom
Royal Infirmary of Edinburgh
Edinburgh, United Kingdom
Queen Elizabeth Hospital
Gateshead, United Kingdom
Hereford County Hospital
Hereford, United Kingdom
Hillingdon Hospital
Hillingdon, United Kingdom
...and 18 more locations
Risk of blood transfusion or death
Co-primary outcome
Time frame: From randomisation until 30-days following the index operation
Blood transfusion rate (including repeat transfusions)
Co-primary outcome
Time frame: From randomisation until 30-days following the index operation
Change in haemoglobin levels
Time frame: From randomisation to (i) day of index operation, (ii) 8-weeks post index operation and (iii) 6 months post index operation
Total number of units of blood or blood products cross matched, total number of packed red cells and any blood products transfused
Time frame: From randomisation to 30 days post index operation
Post operative morbidity survey (POMS) outcomes (outcomes will be presence of morbidity defined by the domains of the POMS e.g. gastrointestinal, cardiovascular)
Time frame: At days 3, 5, 7 and 14 following the index operation
Health-related quality of life: Change in The Multidimensional Fatigue Inventory (MFI) questionnaire total score
Time frame: From baseline to the 10 day assessment and at 8 weeks and 6 months post operatively
Health-related quality of life: Change in European Quality of Life: 5 Dimensions-5 Levels (EQ-5D-5L) questionnaire total score
Time frame: From baseline to the 10 day assessment and at 8 weeks and six months post operatively
Health-related quality of life: Change in Single Question Outcome Measure (SQOM)
Time frame: From baseline to the 10 day assessment and at 8 weeks and six months post operatively
Health resource utilisation
Time frame: Pre-admission, during admission for index operation, 8 weeks post index operation, and 6 months post index operation
Calculated direct, indirect and total costs for the NHS from two perspectives (payer's and societal perspective)
Time frame: From baseline to 6 months post-surgery
Cost effectiveness of treatment options using relevant effectiveness parameters
Time frame: From baseline to 6 months post-surgery
Any reaction or side effect from trial therapy
Any reaction or side effect from whole blood or blood product, transfusion reaction
Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs)
Length of hospital stay
Mortality
Time frame: 8 weeks and 6 months post-operatively
Readmission
Time frame: Within 8 weeks and within 6 months of the index operation
Blood transfusion
Time frame: From randomisation to 8 weeks and 6 months post-operatively
Change in e-GFR
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