Fractures of the upper end of the femur, called commonly "Hip fractures" are very common, with an incidence of approximately 1.6 million cases per year worldwide. This high incidence is anticipated to grow rapidly in the next decades, driven by population aging. Anemia is very frequent on admission for hip fracture, concerning up to 45% of the patients, with a mean hemoglobin level of 12.5±0.2 g/dl. This high prevalence of anemia together with blood losses, secondary to the fracture itself and surgery are responsible for a high rate of blood transfusion (approximately 40-50% of the patients). However, both anemia and blood transfusion are associated with poor outcome, including increased mortality, length of stay, infection rate etc. In addition, blood is a scarce and expensive resource and its use should be limited as much as possible. There is therefore a need to treat this anemia and/or to prevent the decrease in hemoglobin. For this purpose, intravenous iron has been proposed. Some non-randomized, mainly retrospective, studies have shown that perioperative intravenous iron was able to reduce blood transfusion (i.e. the number of patients transfused and the number of units per patient). Another way to reduce blood transfusion would be to reduce perioperative bleeding. Tranexamic acid has proven to be efficient for this purpose both in trauma patients and in elective surgery patients.The interest for perioperative blood management has recently increased thanks to better recognition of the adverse effects of blood transfusion, better understanding of iron metabolism, new intravenous iron drugs and a renewed interest in former medications (i.e. tranexamic acid). HiFIT study therefore propose a 2X2 factorial design for this study in order to answer questions vis-à-vis the interest of iron and tranexamic acid to reduce blood transfusion in hip fracture patients.
Fractures of the upper end of the femur, called commonly "Hip fractures"are very common, with an incidence of approximately 1.6 million cases per year worldwide. This high incidence is anticipated to grow rapidly in the next decades, driven by population aging. Anemia is very frequent on admission for hip fracture, concerning up to 45% of the patients, with a mean hemoglobin level of 12.5±0.2 g/dl. This high prevalence of anemia together with blood losses, secondary to the fracture itself and surgery are responsible for a high rate of blood transfusion (approximately 40-50% of the patients). However, both anemia and blood transfusion are associated with poor outcome, including increased mortality, length of stay, infection rate etc. In addition, blood is a scarce and expensive resource and its use should be limited as much as possible. There is therefore a need to treat this anemia and/or to prevent the decrease in hemoglobin. For this purpose, intravenous iron has been proposed. Some non-randomized, mainly retrospective, studies have shown that perioperative intravenous iron was able to reduce blood transfusion (i.e. the number of patients transfused and the number of units per patient). Indeed, a pooled analysis of 5 studies including 1,361 patients suggests that intravenous iron could reduce perioperative transfusion in hip fracture patients. However, there is no definitive data. Another way to reduce blood transfusion would be to reduce perioperative bleeding. Tranexamic acid has proven to be efficient for this purpose both in trauma patients and in elective surgery patients. However, there are only two randomized studies investigating the interest of tranexamic acid in hip fractures, and they are not conclusive probably owing to a lack of power. In addition, use of intravenous tranexamic acid could be limited in this population of frail patients and topical use of tranexamic acid, notably to prevent the intraoperative bleeding, appear to be an accurate and sure alternative. Although hip fracture is a very frequent pathology, with a high burden of care, few data are available that focus on the management of perioperative anemia in this context. The interest for perioperative blood management has recently increased thanks to better recognition of the adverse effects of blood transfusion, better understanding of iron metabolism, new intravenous iron drugs and a renewed interest in former medications (i.e. tranexamic acid). hiFIT study therefore propose a 2X2 factorial design for this study in order to answer questions vis-à-vis the interest of iron and tranexamic acid to reduce blood transfusion in hip fracture patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
419
Iron Isomaltoside 1000 will be use. Blinding procedure will be put in place for the administration of the treatment
Tranexamic acid will be use.
placebo of Iron Isomaltoside 1000 correspond to a saline solution. Blinding procedure will be put in place for the administration of this treatment
placebo of tranexamic acid correspond to a saline solution.
CHU Angers - DEPARTEMENT D'ANESTHESIE REANIMATION
Angers, France
Clinique de L'Anjou- Anesthesie Reanimation
Angers, France
HIA Clermont-Tonnerre
Brest, France
Chu Grenoble - Departement D'Anesthesie Reanimation
Grenoble, France
CHD Vendée
La Roche-sur-Yon, France
CHU Lille
Lille, France
Hospices Civils Lyon
Lyon, France
Ramsay Santé, Clinique de la Sauvegarde
Lyon, France
Chu Montpellier - Departement D'Anesthesie Reanimation
Montpellier, France
Chu Nantes- Service de Reanimation Chirurgicale
Nantes, France
...and 3 more locations
Proportion of patients who received a blood transfusion during their hospital stay following surgery
Proportion of patients who received a blood transfusion during their hospital stay following surgery
Time frame: From the day of surgery until hospital discharge (or until day 30 if patient is still hospitalized).
Proportion of patients who received a blood transfusion after surgery
Proportion of patients who received a blood transfusion during the month following surgery (including fresh frozen plasma and platelets)
Time frame: From the day of surgery until Day 3, Day 7 and Day 30 post surgery.
Number of packed red blood cell units transfused per patient, as well as number of fresh frozen plasma and platelets units
Number of packed red blood cell units transfused per patient, as well as number of fresh frozen plasma and platelets units
Time frame: Till postoperative Day3, first week posteratively,and till hospital discharge (or one month if patients still hospitalised)
Hemoglobin concentration
Hemoglobin concentration
Time frame: At inclusion and on days 3, 7 (or hospital discharge if it happens first) and 30.
Proportion of patients with anemia (hemoglobin <12 g/dL in women and <13 g/dL in men)
Proportion of patients with anemia (hemoglobin \<12 g/dL in women and \<13 g/dL in men)
Time frame: At inclusion and on days 3, 7, hospital discharge (if it happens before Day 30) and 30.
Reticulocytes count
Reticulocytes count
Time frame: On days 3, 7 (or hospital discharge if it happens first) and 30 post surgery
Perioperative blood loss (estimated according to a formula based on hematocrit variation).
Perioperative blood loss (estimated according to a formula based on hematocrit variation): (HtD0 - HtD3)\*TBV + number of RPBC transfused unit x 200 ml. Ht = Haematocrit, TBV = total blood volume (70 mL/kg in men and 65 mL/kg in women)
Time frame: During surgery
Post operative Iron deficiency rate
Proportion of patients with Iron deficiency (defined as a ferritin \< 100 ng/ml or \< 300 ng/ml together with transferrin saturation \<20%), measurement of ferritin and transferrin saturation
Time frame: On Day 7 (or hospital discharge if it happens first) and Day 30.
Number of hospitalization days
Number of hospitalization days
Time frame: On Day 30 and Day 90 following surgery.
Proportion of patients at home
Proportion of patients returned at home (or at their previous place of living)
Time frame: On Day 30 and Day 90.
Proportion of patients able to walk a distance of ten feet without assistance
Proportion of patients able to walk a distance of ten feet without assistance
Time frame: On Day 30 and Day 90
Variation of quality of life
Variation of EQ-5D score
Time frame: From inclusion to Day 30 and Day 90
Variation of perceived quality of life
Variation of perceived quality of life with a single overall item from PQOL scale
Time frame: From inclusion to Day 7 (or hospital discharge if it happens first) and Day 90.
Variation of IADL test
Variation of IADL test
Time frame: From inclusion to Day 90.
Death rate from all causes
Death rate from all causes
Time frame: From inclusion to Day 90
Rate of adverse events including the following clinical complications: Vascular events, Heart failure; Renal failure; Infectious complications; Anaphylactic reaction; Transfusion-related complications
Rate of adverse events including the following clinical complications: Vascular events, Heart failure; Renal failure; Infectious complications; Anaphylactic reaction; Transfusion-related complications
Time frame: From inclusion to Day 90
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