Abstract
This review provides the clinician with a summary of the causes, implications and potential treatments for the management of anaemia in the older surgical patient. The prevalence of anaemia increases with age and is frequently identified in older surgical patients. Anaemia is associated with increased postoperative morbidity and mortality. Allogenic blood transfusion is commonly used to treat anaemia but involves inherent risks and may worsen outcomes. Various strategies for the correction of pre- and postoperative anaemia have evolved. These include correction of nutritional deficiencies and the use of intravenous iron and erythropoesis stimulating therapy. Clear differences exist between the elective and emergency surgical populations and the translation of research findings into these individual clinical settings requires more work. This should lead to a standardized approach to the management of this frequently encountered clinical scenario.
Introduction
The common issue of anaemia in the older surgical population has a significant impact on postoperative morbidity and mortality. Anaemic patients frequently proceed to surgery without considered assessment and management of this risk factor for adverse outcome. The current mainstay of management for anaemia in the older surgical patient, allogenic blood transfusion, can contribute to negative outcomes and is increasingly avoided where possible. Physicians are often asked to advise on optimizing anaemic patients preoperatively. The advice provided varies widely between physicians and anaesthetists or surgeons managing the same patient group. All those involved in preoperative optimization and postoperative management of older surgical patients should ensure that a considered and consistent approach to anaemia is part of routine management.
To date, there is a lack of a narrative synthesis review comprehensively drawing on literature from both elective and emergency surgical populations. This review aims to provide the clinician with a summary of the causes, implications and potential treatments for the management of anaemia in the older surgical population. A literature search was conducted in PubMed using search terms ‘preoperative anaemia’, ‘postoperative anaemia’ and ‘surgery’ combined with ‘blood transfusion’, ‘intravenous iron’ and ‘erythropoietin’.
Definition and prevalence of anaemia
Anaemia is defined by the World Health Organization (WHO) as a haemoglobin (Hb) level of <13 g/dL in men and <12 g/dL in women.1 The prevalence of anaemia increases with age but varies with subpopulation.2 While < 10% of community dwelling over-65-year-olds are anaemic,3 the older frailer nursing home population has a prevalence of anaemia of 48%.4,5 Estimates of the prevalence of anaemia in the surgical population vary widely from 5% to 75%.6–8 This variation is due to different definitions, types of surgical procedure, presence of malignancy, and emergency or elective presentation. Within octogenarians undergoing elective cardiac surgery, 40.4% of men were anaemic at presentation for surgery.9 A similar prevalence (46%) was observed in emergency surgical patients with hip fracture.10
Aetiology of anaemia in older surgical patients
The causes of anaemia in older surgical patients are varied and relate to physiological ageing, the effect of co-morbidities and the surgical procedure itself.
Anaemia and ageing
Ageing is associated with dysregulation of proinflammatory cytokines, which negatively influence haemopoesis either through the inhibition of erythropoietin production or impaired erythropoietin receptor function.11
Anaemia secondary to iron or nutritional deficiency
Anaemia related to iron deficiency is common.11,12 NHANES III data suggest that 35% of anaemia in over-65-year-olds in the United States is caused by deficiencies in iron, folate and vitamin B12.13 In the developed world, iron deficiency anaemia is most commonly related to gastrointestinal blood loss from ulceration or malignancy.13,14 Vitamin B12 and folate deficiency result from inadequate intake or reduced absorption.15,16
Anaemia of chronic disease
The older population commonly display multimorbidity, so it is unsurprising that they frequently develop the ‘anaemia of chronic disease or chronic inflammation’. The pathophysiology of this condition is multifactorial and likely mediated by proinflammatory cytokines (interleukin-1 [IL-1], IL-6, tumour necrosis factor-α [TNF-α]).11,17 These cytokines influence the secretion and action of erythropoietin, median red blood cell survival, progenitor apoptosis and iron processing.11,18,19
Haemoglobin and renal function progressively decline with advancing age.11 Chronic kidney disease is an important cause of anaemia in the elderly20 and primarily occurs primarily due to a decline in erythropoietin. As the glomerular filtration rate decreases, the prevalence of anaemia increases.20 There is also emerging evidence describing the influence of cytokines in anaemia related to chronic kidney disease.20
Unexplained anaemia
Epidemiological work has shown that unexplained anaemia accounts for about one-third of anaemia in older people.11–13,21–23 In confirmation of this epidemiological finding, a study using bone marrow analysis in an older anaemic population also found a lack of apparent cause for anaemia in a similar proportion of patients.21
Postoperative anaemia
Postoperative anaemia has multiple causes. It can result from pre-existing preoperative anaemia or occur secondary to traumatic or operative blood loss often worsened by haemodilution. Inflammatory cytokine release (IL-1, interferon-γ, TNF-α) after surgery can cause reduced gastrointestinal iron uptake, iron sequestration in macrophages, decreased erythroid response to erythropoietin and diminished erythropoietin production.18,24,25 This results in less available iron for erythropoesis despite normal iron stores in the bone marrow macrophages.25,26 All these factors can exacerbate postoperative anaemia.
Implications of anaemia on the older surgical patient
Within the older surgical population, anaemia has been shown to increase mortality, postoperative complication rates, length of hospital stay and worsen functional outcomes.27–30
Mortality
Preoperative anaemia (defined either by preoperative haemoglobin or haematocrit) is independently associated with an increased 30- and 90-day mortality after various types of non-emergency non-cardiac surgery.31–35 Using preoperative haematocrit from the NSQUIP database and based on clinical reasoning and existing literature,8 anaemia was categorized as severe (21–25%), moderate (26–29%), mild (30–37%) or not anaemic (≥38%).33 The adverse composite outcome of myocardial infarction, stroke, progressive renal insufficiency or death within 30 days of operation was more likely to occur in those with severe (odds ratio [OR] 1.83; 95% confidence interval [CI] 1.05–3.19), moderate (OR 2.19; 95% CI 1.63–2.94) and mild anaemia (OR 1.49; 95% CI 1.20–1.86) when compared to non-anaemic patients.33 Unsurprisingly, this increased mortality was more significant in those with pre-existing cardiovascular disease.31 Furthermore, this finding of increased mortality persisted even after patients with severe anaemia (Hb < 9.5 g/dL) and patients who received red cell transfusions were excluded from the analysis.32
Postoperative complications
Anaemia has a negative impact on medical postoperative outcomes, functional status and quality of life (QOL) in both elective and emergency surgical populations. Within elective cardiac and non-cardiac surgical populations preoperative anaemia is associated with increased risk of perioperative cardiac events, infective complications, respiratory failure, and renal and central nervous system adverse outcomes.30,31,35 Furthermore, and particularly relevant to older surgical patients, a postoperative haematocrit of <30% in patients aged over 50 undergoing major elective non-cardiac surgery is an independent predictor of postoperative delirium.36 This is important as delirium itself carries a risk of increased mortality, morbidity, longer length of hospital stay and higher chance of institutionalization.37–39 In elective patients undergoing joint replacement, the effects of anaemia on QOL are mixed. Initial studies suggested that perioperative anaemia adversely affected QOL,40–42 but this finding was not confirmed by two larger and more recent studies which showed no association between postoperative haemoglobin and QOL.43,44
In emergency patients following hip fracture, anaemia on admission confers a negative impact on postoperative functional recovery, length of hospital stay and readmission rate.10,45,46 In the first three days following hip fracture surgery, a significant linear association is shown between higher haemoglobin level and improved functional status29 (measured using the validated cumulated ambulation score47). Within this study, anaemia was an independent risk factor for inability to walk on the third postoperative day.29
While not universally observed,48 the majority of the evidence suggests an association between preoperative anaemia and adverse postoperative outcome. This raises the question of whether treatment of the condition may contribute to poor outcome.
Red cell transfusion
Preoperative anaemia, postoperative anaemia and red cell transfusion are closely linked, so accurately identifying the independent effects of each issue can be problematic. Preoperative anaemia in surgical patients increases the chance of requiring allogenic red cell transfusion49–52 which is itself associated with adverse effects.49,52,53 Furthermore, red cell transfusion occurs more commonly in unwell patients, who are more likely to develop complications and die.54,55
Our understanding of red blood cell storage effects and the immunomodulatory effects of allogenic transfusion is improving. This has led to the exploration of the risk–benefit ratio of transfusion.56,57 The results from observational studies are mixed. Studies from the adult intensive care, trauma and surgical populations assert that red cell transfusion is associated with increased morbidity and mortality and recommend conservative transfusion triggers.58,59
In contrast, two large retrospective studies report that while transfusion is associated with increased mortality if the preoperative haematocrit is between 30% and 35.9% with less than 500 mL blood loss, conversely in patients with over 500 mL blood loss or a preoperative haematocrit of less than 24%, transfusion may actually reduce mortality risk.60 More recently, the same group concluded that, at an institutional level, hospitals with higher transfusion rates for significant perioperative blood loss (more than 500 mL) report reduced 30-day mortality rates.61
To address this controversy, three recent randomized controlled trials (RCT) have examined the impact of restrictive versus liberal transfusion strategies in patients undergoing cardiac62 and hip fracture surgery.63,64 Restrictive transfusion triggers are defined as haemoglobin of 8 g/dL or haematocrit of ≥24% and liberal transfusion triggers as haemoglobin of 10 g/dL or haematocrit of ≥30%. These studies reported no difference in mortality between the restrictive and liberal groups suggesting that arbitrarily maintaining a higher haemoglobin level may not be beneficial.
In terms of morbidity, blood transfusion has been associated with increased rates of postoperative infection in both emergency hip fracture patients65 and a mixed cohort of emergency and elective patients undergoing non-cardiac surgery.66 Following hip fracture surgery, no difference was seen in functional status at 60-day follow-up (defined as inability to walk unaided across a room) in patients transfused using either the restrictive or liberal trigger.63
This may seem counter to the clinical experience of numerous physicians involved in the rehabilitation of older postoperative patients who often report the benefits of transfusion in enabling rehabilitation. Nevertheless, while results are mixed, given these data our usage of allogenic blood transfusion should be cautious instead focusing efforts on transfusion sparing approaches to managing anaemia in the older surgical patient.
Elective versus emergency surgery
A recent meta-analysis included randomized studies in both elective and emergency orthopaedic surgery to assess the impact of iron administration on morbidity and mortality. This analysis acknowledged concerns regarding randomization, concealed allocation, blinding, acceptable levels of compliance and use of intention to treat analysis. The paper concluded that while administration of iron conclusively raised haemoglobin level in comparison with placebo, overall there was no significant difference observed in postoperative morbidity, mortality, rate of volume of allogenic blood transfusion or length of hospital stay.67 Treatment durations in the trials ranged from one to six weeks with follow-up periods lasting from 21 days to one year.
Elective surgery
Elective surgery offers the potential for preoperative optimization of haemoglobin levels before undergoing surgery. Treatment options include iron (orally or intravenously), vitamin supplementation, erythropoiesis stimulating therapy and autologous blood donation or cell salvage technology.
In elective orthopaedic patients, recommendations from an expert consensus panel (Network for Advancement of Transfusion Alternatives, NATA) suggest measuring haemoglobin at least 28 days prior to scheduled surgery to allow adequate corrective methods.68 If anaemic (using WHO criteria), NATA suggest evaluation of iron status, renal function, and vitamin B12 and folate levels. Guidelines then advise gastroenterology or nephrology assessment, iron replacement therapy (oral or intravenous depending on intolerances and timeline before surgery) and vitamin B12 and folate replacement. When anaemia is related to chronic disease without other nutritional replacement possible, erythropoietic stimulating therapy is advised.68 A small study of intra- and postoperative intravenous iron and erythropoietin administration in patients undergoing elective bilateral total knee replacement also showed favourable results on reducing postoperative transfusions in the six weeks following surgery.69
In elective colorectal70 and gynaecological71 surgical populations, contradictory results exist regarding the impact of intravenous iron in improving postoperative haemoglobin. The timing of iron administration in these studies differed (iron administered two weeks earlier in the hysterectomy study) which may account for the discrepancy in results with no benefit on postoperative haemoglobin seen in the colorectal group.
Furthermore, the use of oral iron after elective orthopaedic surgery appears to be ineffective at increasing postoperative haemoglobin without causing adverse side-effects.72,73 This finding supports the assertion by NATA that assessment for anaemia should occur early in the preoperative pathway so that prompt treatment occurs.68
Other studies advocate the use of preoperative autologous blood donation with or without erythropoietin stimulating therapy in elective surgical groups. In general, autologous blood donation reduces rates of allogenic blood transfusion although the effects on other clinical outcomes have not been examined. This approach is labour intensive, expensive and inefficient, and is not routinely used within the UK.51,74–80 Cell salvage is the process of collecting and then reinfusing blood shed from wound drainage peri- and postoperatively. Following initial safety concerns, more recent literature suggests that this may represent a safe and cost-effective mechanism to reduce allogenic red cell transfusion.81–83
Emergency surgery
Most data on anaemia in emergency surgery comes from the hip fracture population. In contrast to elective surgery, these patients do not have a clear window for optimization particularly in light of current guidance advocating prompt surgical fixation of fractured neck of femur.84
While individual regimens for administration of intravenous iron and erythropoietin vary between studies, in general the initial dose of iron sucrose is administered preoperatively on the day of admission, with one or two subsequent doses given on consecutive postoperative days.
Two observational studies have prospectively examined the effect of intravenous iron in hip fracture patients. Both show a significantly lower rate of postoperative allogenic blood transfusion in the intervention groups.85,86 Furthermore, one study showed a reduction in length of stay and 30-day mortality85 and the other a reduction in postoperative infections in the intervention group.86
Two further observational studies prospectively examined the effect of combining intravenous iron with erythropoietin versus intravenous iron alone. Again there was a significant reduction in postoperative blood transfusion in the intervention groups.26,87 The first, and smaller, of these studies also found a reduction in postoperative infections in the intervention arm,26 yet this finding was not confirmed by a larger study which found no difference in postoperative cardiovascular complications, thromboembolic events, postoperative infections, length of stay, discharge destination or 30-day mortality between the two groups.87
In contrast to this observational work, a more recent RCT failed to show a difference in the primary outcome of postoperative transfusion in hip fracture patients given intravenous iron versus standard care (no intravenous iron). Although subgroup analysis suggested intervention in those with intracapsular fractures reduced postoperative transfusion rate, the small numbers mean that this finding warrants replication.88 This discrepancy in the results between observational and randomized studies strengthens the case for definitive research.
More conclusively, the use of oral iron following hip fracture surgery appears ineffective.72,89–91 A recent RCT assessing the effect of a six-week course of oral iron following hip fracture surgery concluded that there was no significant difference in length of hospital stay or one-year mortality rates between the iron and placebo groups.92
In summary, despite mixed results, the current evidence broadly supports the use of intravenous iron or intravenous iron and erythropoietin in reducing transfusion rates following hip fracture surgery. The acceptable safety profiles reported in these studies and the ability to administer iron or erythropoietin without delaying surgery suggests that such treatments should be employed clinically.
Patient blood management
Given the heterogeneity of approaches to improve haemoglobin levels and reduce use of red cell transfusion, coupled with the differing demands of elective and emergency surgical populations, the use of a set of guidelines or a standardized approach to management is appropriate. Patient blood management (PBM) is a programme or collection of approaches tailored to the individual patient aimed at minimizing the need for red cell transfusion and thus improving postoperative outcomes.80,93–98 It centres on three ‘pillars’ (first, optimization of haemopoesis; second, minimizing blood loss and bleeding; and third, optimizing tolerance of anaemia) all of which have a preoperative, intraoperative and postoperative component. This approach is established in Australia and several centres in the USA but has been inconsistently adopted in Europe.98 Recent work shows how this systematic approach to optimizing haemoglobin in surgical patients has been effectively and pragmatically implemented and appraised with improved 90-day postoperative outcomes within a UK centre.99
Conclusions
Proactively assessing and managing anaemia presents different challenges in the elective and emergency surgical groups. Despite these challenges, evidence is emerging for methods of ‘transfusion sparing’ intervention in order to optimize patients in the perioperative period. Given the current literature, we recommend employing patient blood management programmes incorporating the NATA guidelines when assessing patients prior to elective surgery and the use of intravenous iron possibly with the addition of erythropoietin in the management of anaemic emergency surgical patients. Such interventions could be employed using guidance from the PBM approach. More research is required into the timing and methods of optimization in the anaemic surgical patient, particularly with respect to emergency surgery in order to provide definitive answers. A large RCT powered to robustly examine the effect of iron and erythropoietin on clinical outcomes after emergency surgery in anaemic subjects would help the formulation of a standardized approach to this common clinical scenario. Such work should weigh the benefit of optimizing anaemia against the need to expedite surgery within defined patient groups, in addition to evaluating cost-effectiveness.
Learning points
Anaemia is common in the elderly surgical population.
The commonest causes of anaemia in older people are iron deficiency anaemia and anaemia of chronic disease or inflammation. One-third of older anaemic patients have ‘unexplained’ anaemia.
Anaemia is an independent risk factor for mortality, postoperative complication rates, length of hospital stay and poor functional outcomes in various elective and emergency surgical populations.
Even ‘mild’ anaemia has a negative impact on mortality.
Within the elective anaemic surgical population, prompt assessment for underlying cause, timely investigations and optimization using intravenous iron, nutritional supplementation, erythropoesis stimulating therapy and transfusion where necessary should be employed.
Conservative or restrictive transfusion triggers are now recommended with evidence suggesting that such practice does not affect mortality or functional status postoperatively.
Patient blood management programmes can be successfully implemented in the UK with benefits shown for surgical patients.
Further work should evaluate the use and timing of iron and erythropoietin in large adequately powered RCTs on outcomes meaningful to older surgical patients.
DECLARATIONS
Competing interests
None declared
Funding
None declared
Ethical approval
Not applicable
Guarantor
JD
Contributorship
JP/JD reviewed the literature and drafted the manuscript. DH and JG provided editorial input
Acknowledgements
None
Provenance
Submitted; peer reviewed by Simon Green
References
- 1. World Health Organization. Nutritional Anemia: Report of a WHO Scientific Group. Geneva: WHO, 1968.
- 2.Ershler WB, Sheng S, McKelvey J, et al. Serum erythropoietin and aging: a longitudinal analysis. J Am Geriatr Soc 2005; 53: 1360–9 [DOI] [PubMed] [Google Scholar]
- 3.Inelmen EM, D'Alessio M, Gatto MR, et al. Descriptive analysis of the prevalence of anemia in a randomly selected sample of elderly people living at home: some results of an Italian multicentric study. Aging (Milano) 1994; 6: 81–9 [DOI] [PubMed] [Google Scholar]
- 4.Artz AS, Fergusson D, Drinka PJ, et al. Mechanisms of unexplained anemia in the nursing home. J Am Geriatr Soc 2004; 52: 423–7 [DOI] [PubMed] [Google Scholar]
- 5.Artz AS, Fergusson D, Drinka PJ, et al. Prevalence of anemia in skilled-nursing home residents. Arch Gerontol Geriatr 2004; 39: 201–6 [DOI] [PubMed] [Google Scholar]
- 6.Haljamae H, Stefansson T, Wickstrom I. Preanesthetic evaluation of the female geriatric patient with hip fracture. Acta Anaesthesiol Scand 1982; 26: 393–402 [DOI] [PubMed] [Google Scholar]
- 7.Cappell MS, Goldberg ES. The relationship between the clinical presentation and spread of colon cancer in 315 consecutive patients. A significant trend of earlier cancer detection from 1982 through 1988 at a university hospital. J Clin Gastroenterol 1992; 14: 227–35 [DOI] [PubMed] [Google Scholar]
- 8.Shander A, Knight K, Thurer R, Adamson J, Spence R. Prevalence and outcomes of anemia in surgery: a systematic review of the literature. Am J Med 2004; 116: 58S–69S [DOI] [PubMed] [Google Scholar]
- 9.Carrascal Y, Maroto L, Rey J, et al. Impact of preoperative anemia on cardiac surgery in octogenarians. Interact Cardiovasc Thorac Surg 2013; 10: 249–55 [DOI] [PubMed] [Google Scholar]
- 10.Gruson KI, Aharonoff GB, Egol KA, Zuckerman JD, Koval KJ. The relationship between admission hemoglobin level and outcome after hip fracture. J Orthop Trauma 2002; 16: 39–44 [DOI] [PubMed] [Google Scholar]
- 11.Eisenstaedt R, Penninx BW, Woodman RC. Anemia in the elderly: current understanding and emerging concepts. Blood Rev 2006; 20: 213–26 [DOI] [PubMed] [Google Scholar]
- 12.Beghe C, Wilson A, Ershler WB. Prevalence and outcomes of anemia in geriatrics: a systematic review of the literature. Am J Med 2004; 116: 3S–10S [DOI] [PubMed] [Google Scholar]
- 13.Guralnik JM, Eisenstaedt RS, Ferrucci L, Klein HG, Woodman RC. Prevalence of anemia in persons 65 years and older in the United States: evidence for a high rate of unexplained anemia. Blood 2004; 104: 2263–8 [DOI] [PubMed] [Google Scholar]
- 14.Rockey DC, Cello JP. Evaluation of the gastrointestinal tract in patients with iron deficiency anaemia. N Engl J Med 1993; 328: 1691–5 [DOI] [PubMed] [Google Scholar]
- 15.Smith DL. Anemia in the elderly. Am Fam Physician 2000; 62: 1565–72 [PubMed] [Google Scholar]
- 16.Carmel R. Anemia and aging: an overview of clinical, diagnostic and biological issues. Blood Rev 2001; 15: 9–18 [DOI] [PubMed] [Google Scholar]
- 17.Papadaki HA, Kritikos HD, Valatas V, Boumpas DT, Eliopoulos GD. Anemia of chronic disease in rheumatoid arthritis is associated with increased apoptosis of bone marrow erythroid cells: improvement following anti-tumor necrosis factor-alpha antibody therapy. Blood 2002; 100: 474–82 [DOI] [PubMed] [Google Scholar]
- 18.Weiss G, Goodnough LT. Anemia of chronic disease. N Engl J Med 2005; 352: 1011–23 [DOI] [PubMed] [Google Scholar]
- 19.Tilg H, Ulmer H, Kaser A, Weiss G. Role of IL-10 for induction of anemia during inflammation. J Immunol 2002; 169: 2204–9 [DOI] [PubMed] [Google Scholar]
- 20.McClellan W, Aronoff SL, Bolton WK, et al. The prevalence of anemia in patients with chronic kidney disease. Curr Med Res Opin 2004; 20: 1501–10 [DOI] [PubMed] [Google Scholar]
- 21.Nilsson-Ehle H, Jagenburg R, Landahl S, Svanborg A, Westin J. Haematological abnormalities and reference intervals in the elderly. A cross-sectional comparative study of three urban Swedish population samples aged 70, 75 and 81 years. Acta Med Scand 1988; 224: 595–604 [PubMed] [Google Scholar]
- 22.Joosten E, Pelemans W, Hiele M, Noyen J, Verhaeghe R, Boogaerts MA. Prevalence and causes of anaemia in a geriatric hospitalized population. Gerontology 1992; 38: 111–7 [DOI] [PubMed] [Google Scholar]
- 23.Ania BJ, Suman VJ, Fairbanks VF, Rademacher DM, Melton LJ., 3rd Incidence of anemia in older people: an epidemiologic study in a well defined population. J Am Geriatr Soc 1997; 45: 825–31 [DOI] [PubMed] [Google Scholar]
- 24.Clemens J, Spivak JL. Serum immunoreactive erythropoietin during the perioperative period. Surgery 1994; 115: 510–15 [PubMed] [Google Scholar]
- 25.Andrews NC. Disorders of iron metabolism. N Engl J Med 1999; 341: 1986–95 [DOI] [PubMed] [Google Scholar]
- 26.Garcia-Erce JA, Cuenca J, Munoz M, et al. Perioperative stimulation of erythropoiesis with intravenous iron and erythropoietin reduces transfusion requirements in patients with hip fracture. A prospective observational study. Vox Sang 2005; 88: 235–43 [DOI] [PubMed] [Google Scholar]
- 27.Dunne JR, Malone D, Tracy JK, Gannon C, Napolitano LM. Perioperative anemia: an independent risk factor for infection, mortality, and resource utilization in surgery. J Surg Res 2002; 102: 237–44 [DOI] [PubMed] [Google Scholar]
- 28.Hagino T, Ochiai S, Sato E, et al. The relationship between anemia at admission and outcome in patients older than 60 years with hip fracture. J Orthop Traumatol 2009; 10: 119–22 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Foss NB, Kristensen MT, Kehlet H. Anaemia impedes functional mobility after hip fracture surgery. Age Ageing 2008; 37: 173–8 [DOI] [PubMed] [Google Scholar]
- 30.Kulier A, Levin J, Moser R, et al. Impact of preoperative anemia on outcome in patients undergoing coronary artery bypass graft surgery. Circulation 2007; 116: 471–9 [DOI] [PubMed] [Google Scholar]
- 31.Carson JL, Duff A, Poses RM, et al. Effect of anaemia and cardiovascular disease on surgical mortality and morbidity. Lancet 1996; 348: 1055–60 [DOI] [PubMed] [Google Scholar]
- 32.Beattie WS, Karkouti K, Wijeysundera DN, Tait G. Risk associated with preoperative anemia in noncardiac surgery: a single-center cohort study. Anesthesiology 2009; 110: 574–81 [DOI] [PubMed] [Google Scholar]
- 33.Leichtle SW, Mouawad NJ, Lampman R, Singal B, Cleary RK. Does preoperative anemia adversely affect colon and rectal surgery outcomes? J Am Coll Surg 2011; 212: 187–94 [DOI] [PubMed] [Google Scholar]
- 34.Wu WC, Schifftner TL, Henderson WG, et al. Preoperative hematocrit levels and postoperative outcomes in older patients undergoing noncardiac surgery. JAMA 2007; 297: 2481–8 [DOI] [PubMed] [Google Scholar]
- 35.Musallam KM, Tamim HM, Richards T, et al. Preoperative anaemia and postoperative outcomes in non-cardiac surgery: a retrospective cohort study. Lancet 2011; 378: 1396–407 [DOI] [PubMed] [Google Scholar]
- 36.Marcantonio ER, Goldman L, Orav EJ, Cook EF, Lee TH. The association of intraoperative factors with the development of postoperative delirium. Am J Med 1998; 105: 380–4 [DOI] [PubMed] [Google Scholar]
- 37.Robinson TN, Raeburn CD, Tran ZV, Angles EM, Brenner LA, Moss M. Postoperative delirium in the elderly: risk factors and outcomes. Ann Surg 2009; 249: 173–8 [DOI] [PubMed] [Google Scholar]
- 38.McCusker J, Cole M, Abrahamowicz M, Primeau F, Belzile E. Delirium predicts 12-month mortality. Arch Intern Med 2002; 162: 457–63 [DOI] [PubMed] [Google Scholar]
- 39.Minden SL, Carbone LA, Barsky A, et al. Predictors and outcomes of delirium. Gen Hosp Psychiatry 2005; 27: 209–14 [DOI] [PubMed] [Google Scholar]
- 40.Conlon NP, Bale EP, Herbison GP, McCarroll M. Postoperative anemia and quality of life after primary hip arthroplasty in patients over 65 years old. Anesth Analg 2008; 106: 1056–61 [DOI] [PubMed] [Google Scholar]
- 41.Wallis JP. Disentangling anemia and transfusion. Transfusion 2011; 51: 8–10 [DOI] [PubMed] [Google Scholar]
- 42.Wallis J, Wells AW, Whitehead S, Brewster N. Recovery from post-operative anaemia. Trans Med 2005; 15: 413–18 [DOI] [PubMed] [Google Scholar]
- 43.So-Osman C, Nelissen R, Brand R, Brand A, Stiggelbout AM. Postoperative anemia after joint replacement surgery is not related to quality of life during the first two weeks postoperatively. Transfusion 2011; 51: 71–81 [DOI] [PubMed] [Google Scholar]
- 44.Vuille-Lessard E, Bourdreault D, Girard F, Ruel M, Chagnon M, Hardy JF. Postoperative anemia does not impede functional outcome and quality of life after hip and knee arthroplasties. Transfusion 2012; 52: 261–70 [DOI] [PubMed] [Google Scholar]
- 45.Halm EA, Wang JJ, Boockvar K, et al. The effect of perioperative anemia on clinical and functional outcomes in patients with hip fracture. J Orthop Trauma 2004; 18: 369–74 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Lawrence VA, Silverstein JH, Cornell JE, Pederson T, Noveck H, Carson JL. Higher Hb level is associated with better early functional recovery after hip fracture repair. Transfusion 2003; 43: 1717–22 [DOI] [PubMed] [Google Scholar]
- 47.Foss NB, Kristensen MT, Kehlet H. Prediction of postoperative morbidity, mortality and rehabilitation in hip fracture patients: the cumulated ambulation score. Clin Rehabil 2006; 20: 701–8 [DOI] [PubMed] [Google Scholar]
- 48.Mantilla CB, Wass CT, Goodrich KA, et al. Risk for perioperative myocardial infarction and mortality in patients undergoing hip or knee arthroplasty: the role of anemia. Transfusion 2011; 51: 82–91 [DOI] [PubMed] [Google Scholar]
- 49.Melis M, McLoughlin JM, Dean EM, et al. Correlations between neoadjuvant treatment, anemia, and perioperative complications in patients undergoing esophagectomy for cancer. J Surg Res 2009; 153: 114–20 [DOI] [PubMed] [Google Scholar]
- 50.Gombotz H, Rehak PH, Shander A, Hofmann A. Blood use in elective surgery: the Austrian benchmark study. Transfusion 2007; 47: 1468–80 [DOI] [PubMed] [Google Scholar]
- 51.Spahn DR. Anemia and patient blood management in hip and knee surgery: a systematic review of the literature. Anesthesiology 2010; 113: 482–95 [DOI] [PubMed] [Google Scholar]
- 52.Bursi F, Barbieri A, Politi L, et al. Perioperative red blood cell transfusion and outcome in stable patients after elective major vascular surgery. Eur J Vasc Endovasc Surg 2009; 37: 311–18 [DOI] [PubMed] [Google Scholar]
- 53.Glance LG, Dick AW, Mukamel DB, et al. Association between intraoperative blood transfusion and mortality and morbidity in patients undergoing noncardiac surgery. Anesthesiology 2011; 114: 283–92 [DOI] [PubMed] [Google Scholar]
- 54.Carson JL, Kim S. Intraoperative transfusion in older patients with low preoperative haematocrit levels and substantial blood loss during major non-cardiac surgery is associated with lower 30-day postoperative mortality. Evid Based Med 2010; 15: 185–6 [DOI] [PubMed] [Google Scholar]
- 55.Carson JL, Reynolds RC, Klein HG. Bad bad blood? Crit Care Med 2008; 36: 2707–8 [DOI] [PubMed] [Google Scholar]
- 56.Raghavan M, Marik PE. Anemia, allogenic blood transfusion, and immunomodulation in the critically ill. Chest 2005; 127: 295–307 [DOI] [PubMed] [Google Scholar]
- 57.Toy P, Popovsky MA, Abraham E, et al. Transfusion-related acute lung injury: definition and review. Crit Care Med 2005; 33: 721–6 [DOI] [PubMed] [Google Scholar]
- 58.Marik PE, Corwin HL. Efficacy of red blood cell transfusion in the critically ill: a systematic review of the literature. Crit Care Med 2008; 36: 2667–74 [DOI] [PubMed] [Google Scholar]
- 59.Hebert PC, Wells G, Tweeddale M, et al. Does transfusion practice affect mortality in critically ill patients? Transfusion Requirements in Critical Care (TRICC) Investigators and the Canadian Critical Care Trials Group. Am J Respir Crit Care Med 1997; 155: 1618–23 [DOI] [PubMed] [Google Scholar]
- 60.Wu WC, Smith TS, Henderson WG, et al. Operative blood loss, blood transfusion, and 30-day mortality in older patients after major noncardiac surgery. Ann Surg 2010; 252: 11–17 [DOI] [PubMed] [Google Scholar]
- 61.Wu WC, Trivedi A, Friedmann PD, et al. Association between hospital intraoperative blood transfusion practices for surgical blood loss and hospital surgical mortality rates. Ann Surg 2012; 255: 708–14 [DOI] [PubMed] [Google Scholar]
- 62.Hajjar LA, Vincent JL, Galas FR, et al. Transfusion requirements after cardiac surgery: the TRACS randomized controlled trial. JAMA 2010; 304: 1559–67 [DOI] [PubMed] [Google Scholar]
- 63.Carson JL, Terrin ML, Noveck H, et al. Liberal or restrictive transfusion in high-risk patients after hip surgery. N Engl J Med 2011; 365: 2453–62 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Foss NB, Kristensen MT, Jensen PS, Palm H, Krasheninnikoff M, Kehlet H. The effects of liberal versus restrictive transfusion thresholds on ambulation after hip fracture surgery. Transfusion 2009; 49: 227–34 [DOI] [PubMed] [Google Scholar]
- 65.Shokoohi A, Stanworth S, Mistry D, Lamb S, Staves J, Murphy MF. The risks of red cell transfusion for hip fracture surgery in the elderly. Vox Sang 2012; 103: 223–30 [DOI] [PubMed] [Google Scholar]
- 66.Weber WP, Zwahlen M, Reck S, et al. The association of preoperative anemia and perioperative allogeneic blood transfusion with the risk of surgical site infection. Transfusion 2009; 49: 1964–70 [DOI] [PubMed] [Google Scholar]
- 67.Yang Y, Li H, Li B, Wang Y, Jiang S, Jiang L. Efficacy and safety of iron supplementation for the elderly patients undergoing hip or knee surgery: a meta-analysis of randomized controlled trials. J Surg Res 2011; 171: e201–7 [DOI] [PubMed] [Google Scholar]
- 68.Goodnough LT, Maniatis A, Earnshaw P, et al. Detection, evaluation, and management of preoperative anaemia in the elective orthopaedic surgical patient: NATA guidelines. Br J Anaesth 2011; 106: 13–22 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 69.Na HS, Shin SY, Hwang JY, Jeon YT, Kim CS, Do SH. Effects of intravenous iron combined with low-dose recombinant human erythropoietin on transfusion requirements in iron-deficient patients undergoing bilateral total knee replacement arthroplasty. Transfusion 2011; 51: 118–24 [DOI] [PubMed] [Google Scholar]
- 70.Edwards TJ, Noble EJ, Durran A, et al. Randomized clinical trial of preoperative intravenous iron sucrose to reduce blood transfusion in anaemic patients after colorectal cancer surgery. Br J Surg 2009; 96: 1122–8 [DOI] [PubMed] [Google Scholar]
- 71.Diez-Lobo AI, Fisac-Martin MP, Bermejo-Aycar I, et al. Preoperative intravenous iron administration corrects anemia and reduces transfusion requirement in women undergoing abdominal hysterectomy. Trans Alternatives Trans Med 2007; 9: 114–19 [Google Scholar]
- 72.Mundy GM, Birtwistle SJ, Power RA. The effect of iron supplementation on the level of haemoglobin after lower limb arthroplasty. J Bone Joint Surg Br 2005; 87: 213–17 [DOI] [PubMed] [Google Scholar]
- 73.Weatherall M, Maling TJ. Oral iron therapy for anaemia after orthopaedic surgery: randomized clinical trial. ANZ J Surg 2004; 74: 1049–51 [DOI] [PubMed] [Google Scholar]
- 74.Cushner FD, Scott WN, Scuderi G, et al. Blood loss and transfusion rates in bilateral total knee arthroscopy. J Knee Surg 2005; 18: 102–7 [DOI] [PubMed] [Google Scholar]
- 75.Sinclair KC, Clarke HD, Noble BN. Blood management in total knee arthroscopy: a comparison of techniques. Orthopedics 2009; 32: 19–19 [DOI] [PubMed] [Google Scholar]
- 76.Colomina MJ, Bago J, Pellise F, Godet C, Villanueva C. Preoperative erythropoietin in spine surgery. Eur Spine J 2004; 13: S40–9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 77.Gandini G, Franchini M, Bertuzzo D, et al. Preoperative autologous blood donation by 1073 elderly patients undergoing elective surgery: a safe and effective practice. Transfusion 1999; 39: 174–8 [DOI] [PubMed] [Google Scholar]
- 78.Gandini G, Franchini M, de Gironcoli M, et al. Preoperative autologous blood donation by elderly patients undergoing orthopaedic surgery. Vox Sang 2001; 80: 95–100 [DOI] [PubMed] [Google Scholar]
- 79.Shander A, Puzio T, Javidroozi M. Variability in transfusion practice and effectiveness of strategies to improve it. J Cardiothorac Vasc Anesth 2012; 26: 541–4 [DOI] [PubMed] [Google Scholar]
- 80.Shander A, Javidroozi M. Strategies to reduce the use of blood products: a US perspective. Curr Opin Anaesthesiol 2012; 25: 50–8 [DOI] [PubMed] [Google Scholar]
- 81.Walsh TS, Palmer J, Watson D, et al. Multicentre cohort study of red blood cell use for revision hip arthroplasty and factors associated with greater risk of allogeneic blood transfusion. Br J Anaesth 2012; 108: 63–71 [DOI] [PubMed] [Google Scholar]
- 82. Weltert L, Nardella S, Rondinelli MB, Pierelli L, De Paulis R. Reduction of allogeneic red blood cell usage during cardiac surgery by an integrated intra- and postoperative blood salvage strategy: results of a randomized comparison. Transfusion. Epub ahead of print 6 August 2012. DOI: 10.1111/j.1537-2995.2012.03836.x. [DOI] [PubMed]
- 83.Rao VK, Dyga R, Bartels C, Waters JH. A cost study of postoperative cell salvage in the setting of elective primary hip and knee arthroplasty. Transfusion 2012; 52: 1750–60 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 84.Simunovic N, Devereaux PJ, Spraque S, et al. Effect of early surgery after hip fracture on mortality and complications: systematic review and meta-analysis. CMAJ 2010; 182: 1609–16 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Cuenca J, Garcia-Erce JA, Martinez AA, Solano VM, Molina J, Munoz M. Role of parenteral iron in the management of anaemia in the elderly patient undergoing displaced subcapital hip fracture repair: preliminary data. Arch Orthop Trauma Surg 2005; 125: 342–7 [DOI] [PubMed] [Google Scholar]
- 86.Cuenca J, Garcia-Erce JA, Munoz M, Izuel M, Martinez AA, Herrera A. Patients with pertrochanteric hip fracture may benefit from preoperative intravenous iron therapy: a pilot study. Transfusion 2004; 44: 1447–52 [DOI] [PubMed] [Google Scholar]
- 87.Garcia-Erce JA, Cuenca J, Haman-Alcober S, Martinez AA, Herrera A, Munoz M. Efficacy of preoperative recombinant human erythropoietin administration for reducing transfusion requirements in patients undergoing surgery for hip fracture repair. An observational cohort study. Vox Sang 2009; 97: 260–7 [DOI] [PubMed] [Google Scholar]
- 88.Serrano-Trenas JA, Ugalde PF, Cabello LM, Chofles LC, Lazaro PS, Benitez PC. Role of perioperative intravenous iron therapy in elderly hip fracture patients: a single-center randomized controlled trial. Transfusion 2011; 51: 97–104 [DOI] [PubMed] [Google Scholar]
- 89.Zauber NP, Zauber AG, Gordon FJ, et al. Iron supplementation after femoral head replacement for patients with normal iron stores. JAMA 1992; 267: 525–7 [PubMed] [Google Scholar]
- 90.Prasad N, Rajamani V, Hullin D, Murray JM. Post-operative anaemia in femoral neck fracture patients: does it need treatment? A single blinded prospective randomised controlled trial. Injury 2009; 40: 1073–6 [DOI] [PubMed] [Google Scholar]
- 91.Sutton PM, Cresswell T, Livesey JP, Speed K, Bagga T. Treatment of anaemia after joint replacement. A double-blind, randomised, controlled trial of ferrous sulphate versus placebo. J Bone Joint Surg Br 2004; 86: 31–3 [PubMed] [Google Scholar]
- 92.Parker MJ. Iron supplementation for anemia after hip fracture surgery: a randomized trial of 300 patients. J Bone Joint Surg Am 2010; 92: 265–9 [DOI] [PubMed] [Google Scholar]
- 93.Gonzalez-Porras JR, Colado E, Conde MP, Lopez T, Nieto MJ, Corral M. An individualized pre-operative blood saving protocol can increase pre-operative haemoglobin levels and reduce the need for transfusion in elective total hip or knee arthroplasty. Transfus Med 2009; 19: 35–42 [DOI] [PubMed] [Google Scholar]
- 94.Goodnough LT, Shander A. Patient blood management. Anesthesiology 2012; 116: 1367–76 [DOI] [PubMed] [Google Scholar]
- 95.Spahn DR, Moch H, Hofmann A, Isbister JP. Patient blood management: the pragmatic solution for the problems with blood transfusions. Anesthesiology 2008; 109: 951–3 [DOI] [PubMed] [Google Scholar]
- 96.Spahn DR, Theusinger OM, Hofmann A. Patient blood management is a win-win: a wake-up call. Br J Anaesth 2012; 108: 889–92 [DOI] [PubMed] [Google Scholar]
- 97. Shander A, Aregbeyen O, Caylan M. Sacrificing quality for quantity? RE: Clinical benefits and cost-effectiveness of allogeneic red blood cell transfusion in severe symptomatic anemia A. M. Beliaev, R. J. Marshall, M. Gordon, W. Smith & J. A. Windsor. Vox Sang 2012;103:360–1. [DOI] [PubMed]
- 98.Shander A, Van Aken H, Colomina MJ, et al. Patient blood management in Europe. Br J Anaesth 2012; 109: 55–68 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 99.Kotze A, Carter LA, Scally AJ. Effect of a patient blood management programme on preoperative anaemia, transfusion rate, and outcome after primary hip or knee arthroplasty: a quality improvement cycle. Br J Anaesth 2012; 108: 943–52 [DOI] [PubMed] [Google Scholar]