Abstract:Aims: The primary objective of this review was to determine whether tranexamic acid (TXA) reduces transfusion rates in patients undergoing surgery for hip fractures. The secondary objective was to assess the effects of TXA on mortality and thromboembolic events in the same cohort. Methods: A systematic review of electronic databases was performed in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. We included randomized controlled trials comparing perioperative TXA… Show more
“…It possesses great potential in reducing blood loss and allogeneic blood transfusion safely in patients with hip fractures undergoing surgery. Five meta-analyses [ 116 , 117 , 118 , 119 , 120 ] of RCTs comparing intraoperative administration of TXA with placebo in patients undergoing hip fracture surgery showed significant differences between groups regarding transfusion rates of allogeneic blood, total blood loss, intraoperative blood loss, postoperative blood loss and postoperative haemoglobin, without affecting the rates of thromboembolic events, deep venous thrombosis, acute coronary syndrome, cerebrovascular events, wound complications or mortality.…”
Hip fractures are an important socio-economic problem in western countries. Over the past 60 years orthogeriatric care has improved the management of older patients admitted to hospital after suffering hip fractures. Quality of care in orthogeriatric co-management units has increased, reducing adverse events during acute admission, length of stay, both in-hospital and mid-term mortality, as well as healthcare and social costs. Nevertheless, a large number of areas of controversy regarding the clinical management of older adults admitted due to hip fracture remain to be clarified. This narrative review, centered in the last 5 years, combined the search terms “hip fracture”, “geriatric assessment”, “second hip fracture”, “surgery”, “perioperative management” and “orthogeriatric care”, in order to summarise the state of the art of some questions such as the optimum analgesic protocol, the best approach for treating anemia, the surgical options recommendable for each type of fracture and the efficiency of orthogeriatric co-management and functional recovery.
“…It possesses great potential in reducing blood loss and allogeneic blood transfusion safely in patients with hip fractures undergoing surgery. Five meta-analyses [ 116 , 117 , 118 , 119 , 120 ] of RCTs comparing intraoperative administration of TXA with placebo in patients undergoing hip fracture surgery showed significant differences between groups regarding transfusion rates of allogeneic blood, total blood loss, intraoperative blood loss, postoperative blood loss and postoperative haemoglobin, without affecting the rates of thromboembolic events, deep venous thrombosis, acute coronary syndrome, cerebrovascular events, wound complications or mortality.…”
Hip fractures are an important socio-economic problem in western countries. Over the past 60 years orthogeriatric care has improved the management of older patients admitted to hospital after suffering hip fractures. Quality of care in orthogeriatric co-management units has increased, reducing adverse events during acute admission, length of stay, both in-hospital and mid-term mortality, as well as healthcare and social costs. Nevertheless, a large number of areas of controversy regarding the clinical management of older adults admitted due to hip fracture remain to be clarified. This narrative review, centered in the last 5 years, combined the search terms “hip fracture”, “geriatric assessment”, “second hip fracture”, “surgery”, “perioperative management” and “orthogeriatric care”, in order to summarise the state of the art of some questions such as the optimum analgesic protocol, the best approach for treating anemia, the surgical options recommendable for each type of fracture and the efficiency of orthogeriatric co-management and functional recovery.
“…It possesses great potential in reducing blood loss and allogeneic blood transfusion safely in patients with hip fractures undergoing surgery. 5 meta-analyses [115][116][117][118][119] of RCTs comparing intraoperative administration of TXA with placebo in patients undergoing hip fracture surgery showed significant differences between groups regarding transfusion rates of allogeneic blood, total blood loss, intraoperative blood loss, postoperative blood loss and postoperative haemoglobin, without affecting the rates of thromboembolic events, deep venous thrombosis, acute coronary syndrome, cerebrovascular events, wound complications or mortality.…”
Section: Anemia and Patients Blood Managementmentioning
Hip fractures are an important socio-economic problem in western countries. Over the past 60 years orthogeriatric care has improved the management of older patients admitted to hospital after suffering hip fractures. Orthogeriatric co-management units have increased quality of care, reducing adverse events during acute admission, length of stay, both in-hospital and mid-term mortality, as well as healthcare and social costs. Nevertheless, a large number of areas of controversy regarding the clinical management of older adults admitted due to hip fracture remain to be clarified. This narrative review, centered in the last 5 years, combined the search terms “hip fracture”, “geriatric assessment”, “second hip fracture”, “surgery”, “perioperative management” and “orthogeriatric care”, in order to summarise the state of the art of some questions such as the optimum analgesic protocol, the best approach for treating anemia, the surgical options recommendable for each type of fracture and the efficiency of orthogeriatric co-management and functional recovery.
“… 27 Two recent meta-analyses report a significant reduction in blood transfusion using intravenous TXA in patients with HF; however, the heterogeneity is important (I 2 =60%) and the sample size is too small to evaluate the tolerance of this treatment. 28 29 In addition, use of intravenous TXA could be limited in this population of frail patients and topical use of TXA appears to be an effective and safe alternative, at least in major orthopaedic surgery patients. 30–32 It has also been reported that the combined use of intravenous and topical TXA may be superior to intravenous alone in orthopaedic surgery patients.…”
IntroductionBlood transfusion and anaemia are frequent and are associated with poor outcomes in patients with hip fracture (HF). We hypothesised that preoperative intravenous iron and tranexamic acid (TXA) may reduce the transfusion rate in these patients.Methods and analysisThe HiFIT study is a multicentre, 2×2 factorial, randomised, double-blinded, controlled trial evaluating the effect of iron isomaltoside (IIM) (20 mg/kg) vs placebo and of TXA (intravenously at inclusion and topically during surgery) versus placebo on transfusion rate during hospitalisation, in patients undergoing emergency surgery for HF and having a preoperative haemoglobin between 95 and 130 g/L. 780 patients are expected. The primary endpoint is the proportion of patients receiving an allogenic blood transfusion of packed red blood cells from the day of surgery until hospital discharge (or until D30 if patient is still hospitalised). Enrolment started on March 2017 in 11 French hospitals. The study was stopped between July 2017 and August 2018 (because of investigation of serious AEs with IIM in Spain) and slowed down since March 2020 (COVID-19 crisis). The expected date of final follow-up is May 2022. Analyses of the intent-to-treat and per-protocol populations are planned.Ethics and disseminationThe HiFIT trial protocol has been approved by the Ethics Committee of Comité de Protection des Personnes Ouest II and the French authorities (ANSM). It will be carried out according to the principles of the Declaration of Helsinki and the Good Clinical Practice guidelines. The results will be disseminated through presentation at scientific conferences and publication in peer-reviewed journals. The HiFIT trial will be the largest study evaluating iron and TXA in patients with HF.Trial registration numberclinicalTrials.gov identifier: NCT02972294; EudraCT Number 2016-003087-40.
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