1. Top of page
  2. Abstract
  3. Introduction
  4. Assessing the impact of disease and treatment
  5. Assessing the patient
  6. Optimization
  7. Improving functional reserve
  8. Attenuating the challenge to the patient
  9. Disclosure
  10. References


Although surgical resection remains the central element in curative treatment of gastrointestinal cancer, increasing emphasis and resource has been focused on neoadjuvant or adjuvant therapy. Developments in these modalities have improved outcomes, but far less attention has been paid to improving oncological outcomes through optimization of perioperative care.


A narrative review is presented based on available and updated literature in English and the authors' experience with enhanced recovery research.


A range of perioperative factors (such as lifestyle, co-morbidity, anaemia, sarcopenia, medications, regional analgesia and minimal access surgery) are modifiable, and can be optimized to reduce short- and long-term morbidity and mortality, improve functional capacity and quality of life, and possibly improve oncological outcome. The effect on cancer-free and overall survival may be of equal magnitude to that achieved by many adjuvant oncological regimens. Modulation of core factors, such as nutritional status, systemic inflammation, and surgical and disease-mediated stress, probably influences the host's immune surveillance and defence status both directly and through reduced postoperative morbidity.


A wider view on long-term effects of expanded or targeted enhanced recovery protocols is warranted. Copyright © 2012 British Journal of Surgery Society Ltd. Published by John Wiley & Sons, Ltd.


  1. Top of page
  2. Abstract
  3. Introduction
  4. Assessing the impact of disease and treatment
  5. Assessing the patient
  6. Optimization
  7. Improving functional reserve
  8. Attenuating the challenge to the patient
  9. Disclosure
  10. References

Resection of the primary tumour remains the principal element of treatment and potential cure for the majority of solid epithelial malignancies. However, surgery itself is only one component of a complex series of assessments and interventions that make up the patient's cancer journey. Beyond a histological diagnosis and radiological staging, patients may undergo neoadjuvant chemotherapy, resection of the primary lesion, adjuvant chemotherapy, surgical metastasectomy, palliative chemotherapy, palliative surgery and then be entered into phase I drug trials. Not all will pass down this complex route, particularly those with early-stage disease for whom surgical cure is readily achieved. For those with significant co-morbidity or advanced disease, the complexities and toxicities of their treatments mean that at various critical time points, without due attention to optimizing overall physiology, the opportunity to achieve the best oncological outcome may be compromised.

Most patients with cancer are managed by multiprofessional and multidisciplinary teams (MDTs) involving surgeons, pathologists, radiologists, medical and clinical oncologists, cancer nurse specialists and audit support. Despite this, treatment plans will sometimes be agreed before a patient is assessed fully and discussions do not always consider the patient's specific co-morbidities, nutritional status or cardiopulmonary reserve. A pragmatic view might be that the cancer treatment is necessary and that, beyond gross impairment, patients will survive. On the other hand, variation in outcomes suggests that variables outside routine MDT decision-making may be important and worthy of consideration. For example, there are surgeon and institution league tables that show considerable variation in 30-day morbidity and mortality for standard cancer surgery1, and international comparisons of long-term cancer outcomes show considerable variation between countries2. The main discussion at a MDT meeting may focus on the small but significant benefit of adjuvant or neoadjuvant chemotherapy or radiotherapy. However, it is relevant to consider that effects of the same magnitude on long-term cancer recurrence and survival may result from postoperative morbidity, for example an anastomotic leak3, 4 or a complication that delays significantly the start of adjuvant chemotherapy5. Equally, being elderly and undergoing an oesophagectomy is associated with reduced use of adjuvant therapy, increased 30-day mortality, reduced overall 5-year survival and reduced 5-year cancer-free survival6. It is against this background that the issue of patient optimization for cancer surgery needs to be considered.

The likelihood of metastatic spread depends on the balance between the metastatic potential of the tumour and host defences, of which cell-mediated immunity and natural killer cell function are particularly influential. These components provide immune surveillance, and are influenced by factors including nutritional status and systemic inflammation. This has led to a focus on modifiable perioperative factors that may tip the balance in favour of reduced cancer spread and recurrence.

Over the past 10 years there has been a revolution in the nature of perioperative care with the introduction of enhanced recovery after surgery (ERAS) protocols. These place particular emphasis on diminishing the stress response while maintaining homeostasis. Although it is clear that ERAS is safe and reduces complications7, there has been no systematic review that identifies specific elements of an ERAS pathway that positively and independently influence long-term cancer outcomes.

Short-term issues such as 30-day morbidity and mortality and the longer-term cancer-specific outcomes (local and systemic recurrence, disease-free survival) are important to both clinicians and patients. The purpose of this review is to explore how these two domains interact during the perioperative period, to determine when the surgeon and anaesthetist should influence one to improve the other, and suggest methods whereby this might be achieved.

Assessing the impact of disease and treatment

  1. Top of page
  2. Abstract
  3. Introduction
  4. Assessing the impact of disease and treatment
  5. Assessing the patient
  6. Optimization
  7. Improving functional reserve
  8. Attenuating the challenge to the patient
  9. Disclosure
  10. References

The disease

The spectrum of clinical presentation of malignant disease can range from small tumours that produce neither symptoms nor physiological dysfunction to disseminated disease precipitating anaemia, malnutrition and cachexia and the need for palliative surgical intervention. As such, disseminated cancer constitutes a risk factor for morbidity and mortality following surgery8.

Some tumours, even when still at a curable stage, may cause physiological derangements and malnutrition, increasing risk of complications and death. Usually, these are tumours obstructing the upper gastrointestinal (GI) or biliary tracts. Conversely, the effects of obstruction on local tissues that influence healing and the risk of anastomotic leak can be quite different. Grossly dilated large bowel caused by a obstructing tumour is a risk factor for anastomotic leak9, whereas an obstructed and dilated duct in an atrophic and chronically inflamed pancreatic gland is favourable in terms of risk of fistula formation or anastomotic breakdown10.

Neoadjuvant treatments

In some GI cancers, at a locoregional level, neoadjuvant chemotherapy (and/or radiotherapy) affects outcome by reducing tumour size, improving ease of resection and the likelihood of positive margins. Still, preoperative oncological therapy per se, or the choice of agent or radiation doses, may increase short-term morbidity or even mortality and in generating morbidity may adversely alter long-term outcome. These risks must be considered carefully for each patient. Apart from the consequences following bone marrow depression or gut mucosal sloughing, some organ-specific side-effects are well described. Rectal resections are associated with a higher risk of short-term morbidity following preoperative radiation therapy11, and oesophageal radiation induces local tissue healing problems12, as well as being toxic to the heart and lungs13. Preoperative chemotherapy for colorectal liver metastasis, mainly with irinotecan and oxaliplatin, may cause damage to the liver parenchyma, increasing both complication rates and critical volume for the future liver remnant14. Neoadjuvant chemotherapy for oesophageal cancer is associated with significant loss of skeletal muscle mass15, a reduction in quality of life and impaired physical activity levels16. Trials evaluating perioperative chemotherapy for resectable gastric adenocarcinomas have not identified an increase in postoperative complications17.

Surgical treatment

The nature and extent of surgery is often determined by the perceived stage of disease and frequently follows a standardized approach. However, it is important to recognize situations in which modifications are needed owing to deranged physiology that cannot be corrected promptly or because of unexpectedly severe side-effects following preoperative oncological treatments. Based on large databases, various case-mix or prognostic tools rank abdominal operations according to the magnitude of surgical trauma and hence complication risks18–20. For abdominal cancer surgery, the risks are highest in oesophageal resection, major pancreatic and hepatic resection, and abdominoperineal resection18, 20.

Tools have been developed to take into account the factors above and the state of the patient's resilience to trauma (see below). These tools, such as the Portsmouth modification of the Physiological and Operative Severity Score for the enUmeration of Mortality and morbidity (P-POSSUM) and the modified form of Estimation of Physiologic Ability and Surgical Stress (mE-PASS)19, 20, attempt to encompass the disease, the planned oncological and surgical treatment, as well as patient factors. Although validated repeatedly against large outcome registries, such tools have yet to gain wide adoption for individuals. They are useful as case-mix calculators to allow comparison between larger groups treated differently or by different centres, to ensure comparable baseline risk.

Assessing the patient

  1. Top of page
  2. Abstract
  3. Introduction
  4. Assessing the impact of disease and treatment
  5. Assessing the patient
  6. Optimization
  7. Improving functional reserve
  8. Attenuating the challenge to the patient
  9. Disclosure
  10. References


Socioeconomic status, health literacy and ethnicity are associated with significant disparities in cancer-related outcome21, 22, and age is probably an independent risk factor23. Daily smokers and abusers of alcohol have an increased risk of postoperative complications24, 25, and in both situations outcome has been improved following preoperative abstinence26–29. Obesity is linked to ethnicity and socioeconomic status30, 31, but its role as an independent risk factor for surgical morbidity is not clear32–36. Obesity is associated with increased conversion rate, operating time and postoperative morbidity in some laparoscopic colorectal surgery series, but does not affect surgical safety or oncological margins37.


Ageing is characterized by changes in pulmonary and cardiovascular systems, metabolic disorders and reduced muscle mass. Co-morbidities associated with ageing include hypertension, hypercholesterolaemia, chronic obstructive airway disease and diabetes. Age per se is not an exclusion criterion for cancer surgery. The presence of coexisting diseases has a greater impact on postoperative morbidity and mortality than age alone.

In the context of traditional perioperative care, reduced total body protein mass (mainly skeletal muscle) has been linked to adverse surgical outcome38. In an ERAS setting, when the stress of surgery is minimized, low body mass index (BMI) does not appear to be an independent risk factor for complications or prolonged length of stay, suggesting that baseline nutritional status may not be as critical in this setting as in more traditional perioperative care39. The epidemic of obesity in Western societies means that the average BMI of patients is often in the overweight or obese range and this may hide underlying muscle wasting. A recent study has demonstrated that the presence of low muscle mass is predictive of complications and length of stay following colorectal surgery40. Whether such muscle wasting relates to pre-existing co-morbidity or cancer-associated muscle loss is not known. Obesity is often present in patients with cancer, and the associated metabolic syndrome with insulin resistance leads to a constellation of pathological changes that in turn can impair recovery.

Pulmonary dysfunction such as chronic obstructive pulmonary disease has been associated with postoperative pulmonary complications in oesophageal cancer resection41. Similarly, cardiac diseases and abnormalities of cardiac rhythm can influence the course of postoperative events42. Anxiety and depression are common features in patients with cancer, and result in poorer postoperative healing and recovery43.


  1. Top of page
  2. Abstract
  3. Introduction
  4. Assessing the impact of disease and treatment
  5. Assessing the patient
  6. Optimization
  7. Improving functional reserve
  8. Attenuating the challenge to the patient
  9. Disclosure
  10. References

Patient information and counselling

Personal counselling addressing core items of the perioperative pathway may reduce discomfort and anxiety and improve recovery44, 45, and is generally recommended in ERAS protocols46, 47.

Obstructive jaundice

Jaundice is associated with immunosuppression and gut mucosal dysfunction. A high bilirubin level in combination with low albumin and raised creatinine concentrations is strongly predictive of adverse outcome following major biliary tract surgery48. Although researched extensively49–53, the effects of preoperative biliary drainage on outcome have been inconsistent, suggesting neither harm nor benefit. The most recent of the large randomized trials concluded that patients with serum bilirubin concentrations below 250 µmol/l should not undergo routine preoperative biliary drainage54.


Anaemia is generally considered a risk factor for surgery55, associated with more advanced disease stage, higher mortality and morbidity rates, and longer hospital stay56. Although extensive blood loss during surgery must be replaced, transfusion of allogeneic red blood cells is associated with earlier cancer recurrence and poorer long-term survival57–60. Establishing a causal relationship is impossible from observational studies alone61, as intraoperative difficulties and postoperative complications are confounders. The concept of an immunosuppressive effect (such as a reduction in T helper cell and natural killer cell count, and a reduction in cytokine production including interferon γ) from blood transfusion affecting the host's immunological surveillance is well accepted61. Interestingly, transfusions may have a greater adverse effect when given after surgery than when given during the operation58, 61, and neither autologous transfusion (self-donation) nor leucocyte reduction of transfused blood changes recurrence rates or survival62, 63.

The consequence of preoperative correction of malignant or iron-deficiency anaemia is uncertain. For patients with colorectal cancer, preoperative oral iron therapy has been submitted to randomized study, reducing transfusion requirements and increasing haemoglobin and ferritin levels64. More evidence is needed to establish a role for intravenous iron therapy and/or erythropoietin in the preoperative and perioperative setting65, 66.

Cardiovascular and respiratory insufficiency

Cardiac complications are a major source of intraoperative and postoperative morbidity and mortality67. The literature on cardiac adverse events has evolved from prediction to optimization through intervention. Careful risk stratification is fundamental67, 68. In general, risk factors include age, congestive cardiac failure, BMI greater than 30 kg/m2, cardiovascular disease, hypertension, emergency surgery, duration of surgery and units of blood transfused. More specific clinical risk indices exist that have high capability for discriminating patients at risk of major cardiac events69 and assist in decision-making with preoperative optimization.

Pre-emptive beta-blockade has received much attention70. Although repeatedly shown to reduce the risk of perioperative cardiac complications70, the risk of serious stroke was increased significantly in some trials71, 72. Well regulated preoperative beta-blockade has been advocated to be safer than perioperative initiation73. Careful selection and dosage is crucial to achieve a net reduction in postoperative complications68. Beta-blockers should not be used routinely for perioperative treatment of patients undergoing non-cardiac surgery unless they are being taken for clinically indicated reasons, such as heart failure, coronary artery disease or previous myocardial infarction74.

Statin use has been associated with a decreased mortality rate after non-cardiac surgery75, probably owing to anti-inflammatory and plaque-stabilizing effects.

Aspirin therapy for the purposes of primary and secondary prevention of cardiovascular disease should be continued during the perioperative period in all patients with coronary artery, cerebrovascular or peripheral vascular disease76.

Assessment of pulmonary function is a valid indicator of postoperative pulmonary complications. A forced expiratory volume in 1 s of less than 70 per cent of predicted value requires assessment and treatment. Preoperative respiratory muscle training in patients undergoing thoracic surgery has been shown to prevent postoperative pulmonary complications by increasing inspiratory and expiratory muscle strength77.

Renal failure

Chronic kidney disease, even in relatively early stages, is associated with an increased rate of postoperative infection78, 79. Patients should be kept adequately hydrated, and further hazards to renal function (such as antibiotics or analgesics) assessed and modified78.

Cirrhosis and liver failure

The liver hosts the largest resident macrophage population (Kupffer cells) in the body and liver failure is associated with systemic immunosuppression. Cirrhosis in non-hepatic surgery is associated with increased complications and mortality80. This risk increases significantly in both major surgery and emergency surgery, and in the presence of portal hypertension80. Morbidity and mortality rates correlate with the degree of cirrhosis as measured by standard models, including the preoperative Model for End-stage Liver Disease (MELD) and Child–Turcotte–Pugh (CTP) grade80. On the other hand, the majority of minor and intermediate procedures can be undertaken relatively safely in patients with low MELD score or CTP grade A80. The overall benefit of preoperative transjugular intrahepatic portosystemic shunt in patients with portal hypertension remains unclear80.


Pre-existing diabetes mellitus confers an increased risk of postoperative morbidity and mortality in colorectal surgery81, 82. Although anastomotic leak rates are not increased, mortality rates after a leak are substantially increased in diabetics81. There appears to be an association between morbidity and preoperative hyperglycaemia81, indicating that these patients require careful assessment. The effect of rigid glycaemic control before surgery is, however, less clear81, 82.

Malnutrition and cachexia/sarcopenia

Poor nutritional status is associated with worse outcome after major surgery. Traditionally, patients with gross cancer cachexia requiring surgery have received 10–14 days of preoperative parenteral or enteral nutrition83. It is relevant to consider that patients with gross cachexia may have more advanced disease than previously assumed and should be restaged carefully as heroic attempts at resection of their primary disease may be unsuccessful. A more conservative approach (such as luminal stenting) may provide a better overall outcome.



Recent epidemiological studies have examined the impact of perioperative anaesthetic or analgesic agents on long-term survival after surgery for various types of malignancy including rectal84 and prostate85 cancer. Some studies suggest a reduced recurrence with regional anaesthesia/reduced use of opioids84, 85, whereas others do not86. Potential mechanisms include reduced stress response–immunosuppression with regional anaesthesia or a direct effect of opioids on tumour growth and metastasis. The effect of morphine on tumour growth is controversial, with both growth-promoting and growth-inhibiting effects being observed. Evidence suggests that morphine can affect proliferation and migration of tumour cells as well as angiogenesis. Various signalling pathways are implicated, including co-activation of the epidermal growth factor receptor by the µ-opioid receptor87 and overexpression of the µ-opioid receptor in lung cancer promoting Akt and mTOR activation, tumour growth and metastasis88. The potential for suppression of the immune system by morphine is an additional issue.


A number of basic science and clinical studies have suggested that oral anticoagulants may improve the survival of patients with cancer through an antitumour effect in addition to their antithrombotic effect. Existing evidence does not, however, support a mortality benefit from oral anticoagulation in patients with cancer. There is an increased risk of bleeding89.

Non-steroidal anti-inflammatory drugs

Prostanoids have long been recognized as potential tumour autocrine growth factors. There is increasing epidemiological evidence that aspirin can reduce cancer prevalence and recurrence90. There is evidence from animal models that a single perioperative dose of the cyclo-oxygenase 2 inhibitor celecoxib can inhibit chronic morphine-induced promotion of angiogenesis, tumour growth, metastasis and mortality91. The influence of perioperative use of non-steroidal anti-inflammatory drugs on long-term outcomes of patients with cancer is not known.

Improving functional reserve

  1. Top of page
  2. Abstract
  3. Introduction
  4. Assessing the impact of disease and treatment
  5. Assessing the patient
  6. Optimization
  7. Improving functional reserve
  8. Attenuating the challenge to the patient
  9. Disclosure
  10. References

Physical prehabilitation

Subpopulations of patients with cancer with pre-existing dementia, low preoperative albumin level, poor exercise tolerance and frailty remain especially vulnerable to postoperative complications. Cognitive impairment delays return to baseline performance. A decline in physical activity as a result of ageing and cancer represents a significant risk that can be attenuated by physical exercise as a preventive intervention. Poor preoperative fitness scores are associated with increased mortality, longer postoperative hospital stay and increased complications92, 93. Most physiotherapy and dietary interventions aimed to promote recovery are carried out after surgery (rehabilitation) when patients are fatigued and emotionally vulnerable, and thus unable to comply with intense recovery programmes. It seems plausible that optimal physical functioning before surgery (prehabilitation) might result in better postoperative outcome.

Aerobic and muscular strength training in elderly patients has been shown to increase endurance capacity, reduce weight gain, and improve muscle strength and range of motion in a number of joints94. Although constraints to proceeding with surgery limit the time for initiation of preoperative physical activity, 3 weeks may be sufficient to obtain a moderate gain in aerobic and muscle strength reserve. Studies on prehabilitation before thoracic and GI cancer surgery showed an increase in postoperative functional exercise capacity, decreased postoperative complications and shorter hospital stay95, 96. It appears that patients who are deconditioned require only moderate physical training to obtain an increase in functional capacity97, 98. The addition of nutritional supplements to physical training has been shown to enhance further physiological reserve and impacts positively on postoperative functional exercise capacity99.

Whether such preoperative regimens produce long-term benefits is untested. However, in the post-treatment phase, an increase in physical activity has been associated with improved disease-specific and overall survival, regardless of prediagnosis activity levels100–102.

Nutritional therapy

For adequately nourished patients submitted to routine surgery within an ERAS programme there should be no requirement for artificial nutritional support as return of GI function is a key priority, and the patient should be able to eat and drink within 24 h of (non-oesophageal) surgery with a low risk of prolonged gut dysfunction. It has been shown that combining preoperative oral carbohydrate treatment, epidural analgesia and early enteral nutrition balances nitrogen equilibrium with almost complete abrogation of the metabolic response to injury103. For patients who are at significant risk of malnutrition (for example those undergoing oesophagectomy), the use of cancer-specific enteral feeds may be justified to maintain lean body mass104.


Different combinations of diets containing components aimed to enhance immune function in surgical patients have been studied. These diets, often termed ‘immunonutrition’, usually contain combinations of arginine, glutamine, omega-3 fatty acids and nucleotides. Several meta-analyses have been published on their clinical effectiveness. Most studies have shown clinical benefit by reducing complications and shortening length of stay in the context of traditional perioperative care, but the results are heterogeneous105. There is evidence to suggest that such treatment is most effective in malnourished patients, but there are no trials in an ERAS setting when stress is minimized.

Carbohydrate loading

To avoid patients undergoing surgery in an unfed state, complex carbohydrates can safely be administered orally 2–3 h before induction of anaesthesia. Carbohydrate treatment like this has been shown to attenuate protein and nitrogen loss, and decrease postoperative insulin resistance. It reduces the sense of hunger, thirst and anxiety106–108. Gut function immediately after colorectal surgery may be improved109, as well as preservation of skeletal muscle mass110. Results are not uniform111, 112, however, and further data are needed, especially in diabetic patients113, 114.

Modifying the immunological effects of cancer and surgery

Abnormal postoperative immune function increases risks of postoperative infection and metastasis of tumour cells115, 116. Therefore, maintaining normal immune function, particularly cell-mediated immunity, in the perioperative period may affect long-term oncological results. Compared with traditional open surgery, laparoscopic operations have been shown to decrease the stress response, to result in lower levels of interleukin (IL) 6 and C-reactive protein, and to be associated with better preservation of immune competence as measured by human leucocyte antigen expression on monocytes117. Whether minimizing the effect on cell-mediated immunity produces true oncological advantage has yet to be proven, although extrapolations have been made from studies in which a survival advantage was identified in stage III colorectal cancer treated in the laparoscopic arm118. No other randomized trials have identified a similar survival advantage with laparoscopy and critics have raised concerns that a disparity in adjuvant therapy use may have produced apparent advantage in the laparoscopic arm. However, others suggest that the transition to adjuvant chemotherapy was facilitated by more prompt recovery in the laparoscopic arm. There are no additional data that provide a clear explanation.

It is also relevant to consider the effect of postoperative morbidity on immune function and outcome, and the potential systemic immunosuppressive effect of sepsis and inflammation. Infectious complications are associated with an excessive and persisting synthesis and release of proinflammatory cytokines. Persisting high levels of IL-6 may decrease the number, maturation and activity of cytotoxic T lymphocytes, natural killer and other immunocompetent circulating cells, such as dendritic antigen-presenting cells. Low plasma levels of these cells and high levels of IL-6 in the late postoperative period are correlated with poor prognosis in colorectal cancer119, 120.

It is clear that all efforts should be made to reduce morbidity to an absolute minimum, and a combination of protocol-driven perioperative care and minimally invasive surgery may permit this. Further studies are needed to determine the relative contributions of both minor (such as wound infection) and major (for example reoperation, anastomotic leak and unplanned admission to the intensive care unit) morbidities on cancer-specific, disease-free and overall survival.

Attenuating the challenge to the patient

  1. Top of page
  2. Abstract
  3. Introduction
  4. Assessing the impact of disease and treatment
  5. Assessing the patient
  6. Optimization
  7. Improving functional reserve
  8. Attenuating the challenge to the patient
  9. Disclosure
  10. References

Surgical access

Laparoscopy attenuates the stress response, causes less tissue damage and fewer adhesions, reduces pain and produces a shorter time to functional recovery, compared with open surgery. The role of laparoscopy has been scrutinized most closely in colorectal cancer surgery, although its application for other GI malignancies is evolving.

The safety and advantages of laparoscopic colectomy for cancer have been much debated and several randomized clinical trials have clarified these issues. When performed by surgeons with adequate experience and training, it is clear that laparoscopic colorectal surgery dramatically improves functional outcome following bowel resection. However, open abdominal surgery with modern enhanced recovery protocols46, 47, 121 has also produced remarkable reductions in time to functional recovery and length of stay121, 122. Nevertheless, there is still a significant difference between open and laparoscopic surgery, and this is evident in both observational series and more recent randomized trials. Failure to identify differences within ERAS care between open and laparoscopic colorectal resection in earlier comparative studies is likely to relate to the steep learning curve associated with laparoscopic resection and a broad variation in what has been regarded as ‘laparoscopic’123–125.

The recent LAparoscopy and/or FAst track multimodal management versus standard care (LAFA) trial included 400 patients from nine hospitals126. The study randomized patients between laparoscopic or open surgery, and also between ERAS and ‘standard’ care. It demonstrated that laparoscopy was the only predictive factor with an effect on hospital stay and morbidity. Within the non-ERAS group six of the predefined 15 ERAS elements were applied routinely, as it was felt unethical to leave these out.

The role of laparoscopy in the management of rectal cancer has been assessed in the COlorectal cancer Laparoscopic or Open Resection (CoLOR) II trial, with 2 : 1 randomization to laparoscopy or open surgery143. Although operating times were longer, blood loss, hospital stay and time to first bowel movement were significantly improved in the laparoscopic group, with no difference in the anastomotic leak rate, overall morbidity or mortality. Similar studies are being conducted in the US (American College of Surgeons Oncology Group (ACOSOG) Z6051) and in Japan (Japan Clinical Oncology Group (JCOG) 0404 trial). Trials that include thousands of patients are likely to be required to determine the long-term oncological effects of laparoscopy–ERAS.

Enhanced recovery pathways

ERAS protocols designate a multimodal and evidence-based protocol-driven approach to perioperative care that aims to attenuate the surgical stress response and in consequence reduce rates of complications, enhance recovery and reduce length of stay. As a by-product, cost savings from successful protocols are substantial. A number of such protocols have been published46, 47, 121, 127–137, varying in comprehensiveness, numbers of elements employed routinely and the degree of validation138. Until recently, the surgical community largely ignored this evidence, although ERAS protocols are being used increasingly.

The benefits of introducing ERAS programmes have been demonstrated consistently, particularly in colorectal surgery7, 138–140, but the impact on outcomes other than time to recovery has been modest. It should be noted than measuring direct improvements after successful protocol implementation is notoriously difficult. For observational cohort series, bias is introduced from the Hawthorne effect (patients in trials do better)141, 142. For experimentation, finding a truly ‘pure’ control group, which has received no part of an enhanced recovery protocol as standard care, is practically impossible. It is likely that, if such a group existed, ethical concerns would preclude their inclusion in an experimental design. The true effect of these comprehensive protocols must be shown as benefits from each and every protocol item (where feasible) or from large, multi-institutional and consecutive registries where compliance and outcome are carefully recorded.

Although conventional ERAS–laparoscopic pathways have focused on optimizing short-term recovery, it is now evident that current elements of ERAS may need to be modified and expanded to take account of the growing literature that identifies the many factors that may influence long-term oncological outcomes. The challenge will be to design and conduct trials with sufficient sample size to prove the value of each intervention.


  1. Top of page
  2. Abstract
  3. Introduction
  4. Assessing the impact of disease and treatment
  5. Assessing the patient
  6. Optimization
  7. Improving functional reserve
  8. Attenuating the challenge to the patient
  9. Disclosure
  10. References
  • 1
    van Gijn W, Gooiker GA, Wouters MW, Post PN, Tollenaar RA, van de Velde CJ. Volume and outcome in colorectal cancer surgery. Eur J Surg Oncol 2010; 36(Suppl 1): S55S63.
  • 2
    Baili P, Micheli A, De AR, Weir HK, Francisci S, Santaquilani M et al.; CONCORD Working Group. Life tables for world-wide comparison of relative survival for cancer (CONCORD study). Tumori 2008; 94: 658668.
  • 3
    Akyol AM, McGregor JR, Galloway DJ, Murray GD, George WD. Anastomotic leaks in colorectal cancer surgery: a risk factor for recurrence? Int J Colorectal Dis 1991; 6: 179183.
  • 4
    Mirnezami A, Mirnezami R, Chandrakumaran K, Sasapu K, Sagar P, Finan P. Increased local recurrence and reduced survival from colorectal cancer following anastomotic leak: systematic review and meta-analysis. Ann Surg 2011; 253: 890899.
  • 5
    Des GG, Nicolas P, Perret GY, Morere JF, Uzzan B. Does delaying adjuvant chemotherapy after curative surgery for colorectal cancer impair survival? A meta-analysis. Eur J Cancer 2010; 46: 10491055.
  • 6
    Markar SR, Karthikesalingam A, Thrumurthy S, Ho A, Muallem G, Low DE. Systematic review and pooled analysis assessing the association between elderly age and outcome following surgical resection of esophageal malignancy. Dis Esophagus 2012; [Epub ahead of print].
  • 7
    Varadhan KK, Neal KR, Dejong CH, Fearon KC, Ljungqvist O, Lobo DN. The enhanced recovery after surgery (ERAS) pathway for patients undergoing major elective open colorectal surgery: a meta-analysis of randomized controlled trials. Clin Nutr 2010; 29: 434440.
  • 8
    Tseng WH, Yang X, Wang H, Martinez SR, Chen SL, Meyers FJ et al. Nomogram to predict risk of 30-day morbidity and mortality for patients with disseminated malignancy undergoing surgical intervention. Ann Surg 2011; 254: 333338.
  • 9
    Kingham TP, Pachter HL. Colonic anastomotic leak: risk factors, diagnosis, and treatment. J Am Coll Surg 2009; 208: 269278.
  • 10
    Ansorge C, Strommer L, Andrén-Sandberg A, Lundell L, Herrington MK, Segersvard R. Structured intraoperative assessment of pancreatic gland characteristics in predicting complications after pancreaticoduodenectomy. Br J Surg 2012; 99: 10761082.
  • 11
    Fleming FJ, Pahlman L, Monson JR. Neoadjuvant therapy in rectal cancer. Dis Colon Rectum 2011; 54: 901912.
  • 12
    Vande WC, Ceelen WP, Boterberg T, Vande PD, Van NY, Varin O et al. Anastomotic complications after Ivor Lewis esophagectomy in patients treated with neoadjuvant chemoradiation are related to radiation dose to the gastric fundus. Int J Radiat Oncol Biol Phys 2012; 82: e513e519.
  • 13
    Mukherjee S, Aston D, Minett M, Brewster AE, Crosby TD. The significance of cardiac doses received during chemoradiation of oesophageal and gastro-oesophageal junctional cancers. Clin Oncol (R Coll Radiol) 2003; 15: 115120.
  • 14
    Lehmann K, Rickenbacher A, Weber A, Pestalozzi BC, Clavien PA. Chemotherapy before liver resection of colorectal metastases: friend or foe? Ann Surg 2012; 255: 237247.
  • 15
    Awad S, Tan BH, Cui H, Bhalla A, Fearon KC, Parsons SL et al. Marked changes in body composition following neoadjuvant chemotherapy for oesophagogastric cancer. Clin Nutr 2012; 31: 7477.
  • 16
    Ferriolli E, Skipworth RJ, Hendry P, Scott A, Stensteth J, Dahele M et al. Physical activity monitoring: a responsive and meaningful patient-centered outcome for surgery, chemotherapy, or radiotherapy? J Pain Symptom Manage 2012; 43: 10251035.
  • 17
    Ott K, Lordick F, Blank S, Buchler M. Gastric cancer: surgery in 2011. Langenbecks Arch Surg 2011; 396: 743758.
  • 18
    Copeland GP, Jones D, Walters M. POSSUM: a scoring system for surgical audit. Br J Surg 1991; 78: 355360.
  • 19
    Prytherch DR, Whiteley MS, Higgins B, Weaver PC, Prout WG, Powell SJ. POSSUM and Portsmouth POSSUM for predicting mortality. Physiological and Operative Severity Score for the enUmeration of Mortality and morbidity. Br J Surg 1998; 85: 12171220.
  • 20
    Haga Y, Ikejiri K, Wada Y, Takahashi T, Ikenaga M, Akiyama N et al. A multicenter prospective study of surgical audit systems. Ann Surg 2011; 253: 194201.
  • 21
    Murphy MM, Tseng JF, Shah SA. Disparities in cancer care: an operative perspective. Surgery 2010; 147: 733737.
  • 22
    Murphy MM, Simons JP, Hill JS, McDade TP, Chau NS, Whalen GF et al. Pancreatic resection: a key component to reducing racial disparities in pancreatic adenocarcinoma. Cancer 2009; 115: 39793990.
  • 23
    Bettelli G. Preoperative evaluation in geriatric surgery: comorbidity, functional status and pharmacological history. Minerva Anestesiol 2011; 77: 637646.
  • 24
    Bluman LG, Mosca L, Newman N, Simon DG. Preoperative smoking habits and postoperative pulmonary complications. Chest 1998; 113: 883889.
  • 25
    Tonnesen H, Kehlet H. Preoperative alcoholism and postoperative morbidity. Br J Surg 1999; 86: 869874.
  • 26
    Tonnesen H, Rosenberg J, Nielsen HJ, Rasmussen V, Hauge C, Pedersen IK et al. Effect of preoperative abstinence on poor postoperative outcome in alcohol misusers: randomised controlled trial. BMJ 1999; 318: 13111316.
  • 27
    Sorensen LT, Karlsmark T, Gottrup F. Abstinence from smoking reduces incisional wound infection: a randomized controlled trial. Ann Surg 2003; 238: 15.
  • 28
    Lindstrom D, Sadr AO, Wladis A, Tonnesen H, Linder S, Nasell H et al. Effects of a perioperative smoking cessation intervention on postoperative complications: a randomized trial. Ann Surg 2008; 248: 739745.
  • 29
    Sørensen LT. Wound healing and infection in surgery: the pathophysiological impact of smoking, smoking cessation, and nicotine replacement therapy: a systematic review. Ann Surg 2012; 255: 10691079.
  • 30
    Deboer MD. Ethnicity, obesity and the metabolic syndrome: implications on assessing risk and targeting intervention. Expert Rev Endocrinol Metab 2011; 6: 279289.
  • 31
    Olsen NJ, Mortensen EL, Heitmann BL. Predisposition to obesity: should we target those most susceptible? Curr Obes Rep 2012; 1: 3541.
  • 32
    Gaujoux S, Torres J, Olson S, Winston C, Gonen M, Brennan MF et al. Impact of obesity and body fat distribution on survival after pancreaticoduodenectomy for pancreatic adenocarcinoma. Ann Surg Oncol 2012; 19: 29082916.
  • 33
    Makino T, Shukla PJ, Rubino F, Milsom JW. The impact of obesity on perioperative outcomes after laparoscopic colorectal resection. Ann Surg 2012; 255: 228236.
  • 34
    Nobuoka D, Gotohda N, Kato Y, Takahashi S, Konishi M, Kinoshita T. Influence of excess body weight on the surgical outcomes of total gastrectomy. Surg Today 2011; 41: 928934.
  • 35
    Greenblatt DY, Kelly KJ, Rajamanickam V, Wan Y, Hanson T, Rettammel R et al. Preoperative factors predict perioperative morbidity and mortality after pancreaticoduodenectomy. Ann Surg Oncol 2011; 18: 21262135.
  • 36
    Tsai S, Choti MA, Assumpcao L, Cameron JL, Gleisner AL, Herman JM et al. Impact of obesity on perioperative outcomes and survival following pancreaticoduodenectomy for pancreatic cancer: a large single-institution study. J Gastrointest Surg 2010; 14: 11431150.
  • 37
    Zhou Y, Wu L, Li X, Wu X, Li B. Outcome of laparoscopic colorectal surgery in obese and nonobese patients: a meta-analysis. Surg Endosc 2012; 26: 783789.
  • 38
    Windsor JA, Hill GL. Protein depletion and surgical risk. Aust N Z J Surg 1988; 58: 711715.
  • 39
    Hendry PO, Hausel J, Nygren J, Lassen K, Dejong CH, Ljungqvist O et al.; Enhanced Recovery After Surgery Study Group. Determinants of outcome after colorectal resection within an enhanced recovery programme. Br J Surg 2009; 96: 197205.
  • 40
    Lieffers JR, Bathe OF, Fassbender K, Winget M, Baracos VE. Sarcopenia is associated with postoperative infection and delayed recovery from colorectal cancer resection surgery. Br J Cancer 2012; 107: 931936.
  • 41
    Ferguson MK, Durkin AE. Preoperative prediction of the risk of pulmonary complications after esophagectomy for cancer. J Thorac Cardiovasc Surg 2002; 123: 661669.
  • 42
    Lee TH, Marcantonio ER, Mangione CM, Thomas EJ, Polanczyk CA, Cook EF et al. Derivation and prospective validation of a simple index for prediction of cardiac risk of major noncardiac surgery. Circulation 1999; 100: 10431049.
  • 43
    Gouin JP, Kiecolt-Glaser JK. The impact of psychological stress on wound healing: methods and mechanisms. Immunol Allergy Clin North Am 2011; 31: 8193.
  • 44
    Carli F, Charlebois P, Baldini G, Cachero O, Stein B. An integrated multidisciplinary approach to implementation of a fast-track program for laparoscopic colorectal surgery. Can J Anaesth 2009; 56: 837842.
  • 45
    Stergiopoulou A, Birbas K, Katostaras T, Mantas J. The effect of interactive multimedia on preoperative knowledge and postoperative recovery of patients undergoing laparoscopic cholecystectomy. Methods Inf Med 2007; 46: 406409.
  • 46
    Fearon KC, Ljungqvist O, Von Meyenfeldt M, Revhaug A, Dejong CH, Lassen K et al. Enhanced recovery after surgery: a consensus review of clinical care for patients undergoing colonic resection. Clin Nutr 2005; 24: 466477.
  • 47
    Lassen K, Soop M, Nygren J, Cox PBW, Hendry PO, Spies C et al.; Enhanced Recovery After Surgery (ERAS) Group. Consensus review of optimal perioperative care in colorectal surgery: Enhanced Recovery After Surgery (ERAS) Group recommendations. Arch Surg 2009; 144: 961969.
  • 48
    Blamey SL, Fearon KC, Gilmour WH, Osborne DH, Carter DC. Prediction of risk in biliary surgery. Br J Surg 1983; 70: 535538.
  • 49
    Sewnath ME, Karsten TM, Prins MH, Rauws EJ, Obertop H, Gouma DJ. A meta-analysis on the efficacy of preoperative biliary drainage for tumors causing obstructive jaundice. Ann Surg 2002; 236: 1727.
  • 50
    Saleh MM, Norregaard P, Jorgensen HL, Andersen PK, Matzen P. Preoperative endoscopic stent placement before pancreaticoduodenectomy: a meta-analysis of the effect on morbidity and mortality. Gastrointest Endosc 2002; 56: 529534.
  • 51
    Wang Q, Gurusamy KS, Lin H, Xie X, Wang C. Preoperative biliary drainage for obstructive jaundice. Cochrane Database Syst Rev 2008; (3)CD005444.
  • 52
    Qiu YD, Bai JL, Xu FG, Ding YT. Effect of preoperative biliary drainage on malignant obstructive jaundice: a meta-analysis. World J Gastroenterol 2011; 17: 391396.
  • 53
    Garcea G, Chee W, Ong SL, Maddern GJ. Preoperative biliary drainage for distal obstruction: the case against revisited. Pancreas 2010; 39: 119126.
  • 54
    van der Gaag NA, Rauws EA, van Eijck CH, Bruno MJ, van der HE, Kubben FJ et al. Preoperative biliary drainage for cancer of the head of the pancreas. N Engl J Med 2010; 362: 129137.
  • 55
    Chamogeorgakis T, Anagnostopoulos C, Kostopanagiotou G, Bhora F, Toumpoulis I, Georgiannakis E et al. Does anemia affect outcome after lobectomy or pneumonectomy in early stage lung cancer patients who have not received neo-adjuvant treatment? Thorac Cardiovasc Surg 2008; 56: 148153.
  • 56
    Goodnough LT, Shander A, Spivak JL, Waters JH, Friedman AJ, Carson JL et al. Detection, evaluation, and management of anemia in the elective surgical patient. Anesth Analg 2005; 101: 18581861.
  • 57
    Dionigi G, Rovera F, Boni L, Carrafiello G, Recaldini C, Mangini M et al. The impact of perioperative blood transfusion on clinical outcomes in colorectal surgery. Surg Oncol 2007; 16(Suppl 1): S177S182.
  • 58
    Yeh JJ, Gonen M, Tomlinson JS, Idrees K, Brennan MF, Fong Y. Effect of blood transfusion on outcome after pancreaticoduodenectomy for exocrine tumour of the pancreas. Br J Surg 2007; 94: 466472.
  • 59
    Clark E, Connor S, Taylor MA, Hendry CL, Madhavan KK, Garden OJ et al. Perioperative transfusion for pancreaticoduodenectomy and its impact on prognosis in resected pancreatic ductal adenocarcinoma. HPB (Oxford) 2007; 9: 472477.
  • 60
    Kwon AH, Matsui Y, Kamiyama Y. Perioperative blood transfusion in hepatocellular carcinomas: influence of immunologic profile and recurrence free survival. Cancer 2001; 91: 771778.
  • 61
    Kneuertz PJ, Patel SH, Chu CK, Maithel SK, Sarmiento JM, Delman KA et al. Effects of perioperative red blood cell transfusion on disease recurrence and survival after pancreaticoduodenectomy for ductal adenocarcinoma. Ann Surg Oncol 2011; 18: 13271334.
  • 62
    Amato A, Pescatori M. Perioperative blood transfusions for the recurrence of colorectal cancer. Cochrane Database Syst Rev 2006; (1)CD005033.
  • 63
    Busch OR, Hop WC, Marquet RL, Jeekel J. The effect of blood transfusions on survival after surgery for colorectal cancer. Eur J Cancer 1995; 31A: 12261228.
  • 64
    Lidder PG, Sanders G, Whitehead E, Douie WJ, Mellor N, Lewis SJ et al. Pre-operative oral iron supplementation reduces blood transfusion in colorectal surgery—a prospective, randomised, controlled trial. Ann R Coll Surg Engl 2007; 89: 418421.
  • 65
    Beris P, Muñoz M, García-Erce JA, Thomas D, Maniatis A, Van der Linden P. Perioperative anaemia management: consensus statement on the role of intravenous iron. Br J Anaesth 2008; 100: 599604.
  • 66
    Devon KM, McLeod RS. Pre and peri-operative erythropoietin for reducing allogeneic blood transfusions in colorectal cancer surgery. Cochrane Database Syst Rev 2009; (1)CD007148.
  • 67
    Arora V, Velanovich V, Alarcon W. Preoperative assessment of cardiac risk and perioperative cardiac management in noncardiac surgery. Int J Surg 2011; 9: 2328.
  • 68
    Bakker EJ, Ravensbergen NJ, Poldermans D. Perioperative cardiac evaluation, monitoring, and risk reduction strategies in noncardiac surgery patients. Curr Opin Crit Care 2011; 17: 409415.
  • 69
    Poldermans D, Bax JJ, Boersma E, De HS, Eeckhout E, Fowkes G et al. Guidelines for pre-operative cardiac risk assessment and perioperative cardiac management in non-cardiac surgery: the Task Force for Preoperative Cardiac Risk Assessment and Perioperative Cardiac Management in Non-cardiac Surgery of the European Society of Cardiology (ESC) and endorsed by the European Society of Anaesthesiology (ESA). Eur J Anaesthesiol 2010; 27: 92137.
  • 70
    Mason KE, Davis LL. Perioperative beta blockade in noncardiac surgery: a review of the literature. AANA J 2006; 74: 113117.
  • 71
    Talati R, Reinhart KM, White CM, Phung OJ, Sedrakyan A, Kluger J et al. Outcomes of perioperative beta-blockade in patients undergoing noncardiac surgery: a meta-analysis. Ann Pharmacother 2009; 43: 11811188.
  • 72
    White CM, Talati R, Phung OJ, Baker WL, Reinhart K, Sedrakyan A et al. Benefits and risks associated with beta-blocker prophylaxis in noncardiac surgery. Am J Health Syst Pharm 2010; 67: 523530.
  • 73
    Ellenberger C, Tait G, Beattie WS. Chronic beta blockade is associated with a better outcome after elective noncardiac surgery than acute beta blockade: a single-center propensity-matched cohort study. Anesthesiology 2011; 114: 817823.
  • 74
    López-Sendón J, Swedberg K, McMurray J, Tamargo J, Maggioni AP, Dargie H et al.; Task Force On Beta-Blockers of the European Society of Cardiology. Expert consensus document on beta-adrenergic receptor blockers. Eur Heart J 2004; 25: 13411362.
  • 75
    Lindenauer PK, Pekow P, Wang K, Gutierrez B, Benjamin EM. Lipid-lowering therapy and in-hospital mortality following major noncardiac surgery. JAMA 2004; 291: 20922099.
  • 76
    Gerstein NS, Schulman PM, Gerstein WH, Petersen TR, Tawil I. Should more patients continue aspirin therapy perioperatively?: clinical impact of aspirin withdrawal syndrome. Ann Surg 2012; 255: 811819.
  • 77
    Hulzebos EH, Helders PJ, Favié NJ, De Bie RA, Brutel de la Riviere A, Van Meeteren NL. Preoperative intensive inspiratory muscle training to prevent postoperative pulmonary complications in high-risk patients undergoing CABG surgery: a randomized clinical trial. JAMA 2006; 296: 18511857.
  • 78
    Canedo J, Ricciardi K, Dasilva G, Rosen L, Weiss EG, Wexner SD. Are postoperative complications more common following colon and rectal surgery in patients with chronic kidney disease? Colorectal Dis 2012; [Epub ahead of print].
  • 79
    Ackland GL, Moran N, Cone S, Grocott MP, Mythen MG. Chronic kidney disease and postoperative morbidity after elective orthopedic surgery. Anesth Analg 2011; 112: 13751381.
  • 80
    de Goede B, Klitsie PJ, Lange JF, Metselaar HJ, Kazemier G. Morbidity and mortality related to non-hepatic surgery in patients with liver cirrhosis: a systematic review. Best Pract Res Clin Gastroenterol 2012; 26: 4759.
  • 81
    Ziegler MA, Catto JA, Riggs TW, Gates ER, Grodsky MB, Wasvary HJ. Risk factors for anastomotic leak and mortality in diabetic patients undergoing colectomy: analysis from a statewide surgical quality collaborative. Arch Surg 2012; 147: 600605.
  • 82
    Stein KB, Snyder CF, Barone BB, Yeh HC, Peairs KS, Derr RL et al. Colorectal cancer outcomes, recurrence, and complications in persons with and without diabetes mellitus: a systematic review and meta-analysis. Dig Dis Sci 2010; 55: 18391851.
  • 83
    Braga M, Ljungqvist O, Soeters P, Fearon K, Weimann A, Bozzetti F; ESPEN. ESPEN Guidelines on Parenteral Nutrition: surgery. Clin Nutr 2009; 28: 378386.
  • 84
    Gupta A, Björnsson A, Fredriksson M, Hallböök O, Eintrei C. Reduction in mortality after epidural anaesthesia and analgesia in patients undergoing rectal but not colonic cancer surgery: a retrospective analysis of data from 655 patients in central Sweden. Br J Anaesth 2011; 107: 164170.
  • 85
    Biki B, Mascha E, Moriarty DC, Fitzpatrick JM, Sessler DI, Buggy DJ. Anesthetic technique for radical prostatectomy surgery affects cancer recurrence: a retrospective analysis. Anesthesiology 2008; 109: 180187.
  • 86
    Tsui BC, Rashiq S, Schopflocher D, Murtha A, Broemling S, Pillay J et al. Epidural anesthesia and cancer recurrence rates after radical prostatectomy. Can J Anaesth 2010; 57: 107112.
  • 87
    Fujioka N, Nguyen J, Chen C, Li Y, Pasrija T, Niehans G et al. Morphine-induced epidermal growth factor pathway activation in non-small cell lung cancer. Anesth Analg 2011; 113: 13531364.
  • 88
    Lennon FE, Mirzapoiazova T, Mambetsariev B, Salgia R, Moss J, Singleton PA. Overexpression of the mu-opioid receptor in human non-small cell lung cancer promotes Akt and mTOR activation, tumor growth, and metastasis. Anesthesiology 2012; 116: 857867.
  • 89
    Akl EA, Vasireddi SR, Gunukula S, Yosuico VE, Barba M, Terrenato I et al. Oral anticoagulation in patients with cancer who have no therapeutic or prophylactic indication for anticoagulation. Cochrane Database Syst Rev 2011; (6)CD006466.
  • 90
    Thun MJ, Jacobs EJ, Patrono C. The role of aspirin in cancer prevention. Nat Rev Clin Oncol 2012; 9: 259267.
  • 91
    Farooqui M, Li Y, Rogers T, Poonawala T, Griffin RJ, Song CW et al. COX-2 inhibitor celecoxib prevents chronic morphine-induced promotion of angiogenesis, tumour growth, metastasis and mortality, without compromising analgesia. Br J Cancer 2007; 97: 15231531.
  • 92
    Cook JW, Pierson LM, Herbert WG, Norton HJ, Fedor JM, Kiebzak GM et al. The influence of patient strength, aerobic capacity and body composition upon outcomes after coronary artery bypass grafting. Thorac Cardiovasc Surg 2001; 49: 8993.
  • 93
    Biccard BM. Relationship between the inability to climb two flights of stairs and outcome after major non-cardiac surgery: implications for the pre-operative assessment of functional capacity. Anaesthesia 2005; 60: 588593.
  • 94
    Carli F, Zavorsky GS. Optimizing functional exercise capacity in the elderly surgical population. Curr Opin Clin Nutr Metab Care 2005; 8: 2332.
  • 95
    Valkenet K, van de Port IG, Dronkers JJ, de Vries WR, Lindeman E, Backx FJ. The effects of preoperative exercise therapy on postoperative outcome: a systematic review. Clin Rehabil 2011; 25: 99111.
  • 96
    Mayo NE, Feldman L, Scott S, Zavorsky G, Kim do J, Charlebois P et al. Impact of preoperative change in physical function on postoperative recovery: argument supporting prehabilitation for colorectal surgery. Surgery 2011; 150: 505514.
  • 97
    Carli F, Charlebois P, Stein B, Feldman L, Zavorsky G, Kim DJ et al. Randomized clinical trial of prehabilitation in colorectal surgery. Br J Surg 2010; 97: 11871197.
  • 98
    Carli F, Brown R, Kennepohl S. Prehabilitation to enhance postoperative recovery for an octogenarian following robotic-assisted hysterectomy with endometrial cancer. Can J Anaesth 2012; 59: 779784.
  • 99
    Li C, Carli F, Lee L, Charlebois P, Stein B, Liberman AS et al. Impact of a trimodal prehabilitation program on functional recovery after colorectal cancer surgery: a pilot study. Surg Endosc 2012; [Epub ahead of print].
  • 100
    Meyerhardt JA, Giovannucci EL, Holmes MD, Chan AT, Chan JA, Colditz GA et al. Physical activity and survival after colorectal cancer diagnosis. J Clin Oncol 2006; 24: 35273534.
  • 101
    Meyerhardt JA, Giovannucci EL, Ogino S, Kirkner GJ, Chan AT, Willett W et al. Physical activity and male colorectal cancer survival. Arch Intern Med 2009; 169: 21022108.
  • 102
    Meyerhardt JA, Heseltine D, Niedzwiecki D, Hollis D, Saltz LB, Mayer RJ et al. Impact of physical activity on cancer recurrence and survival in patients with stage III colon cancer: findings from CALGB 89803. J Clin Oncol 2006; 24: 35353541.
  • 103
    Soop M, Carlson GL, Hopkinson J, Clarke S, Thorell A, Nygren J et al. Randomized clinical trial of the effects of immediate enteral nutrition on metabolic responses to major colorectal surgery in an enhanced recovery protocol. Br J Surg 2004; 91: 11381145.
  • 104
    Ryan AM, Reynolds JV, Healy L, Byrne M, Moore J, Brannelly N et al. Enteral nutrition enriched with eicosapentaenoic acid (EPA) preserves lean body mass following esophageal cancer surgery: results of a double-blinded randomized controlled trial. Ann Surg 2009; 249: 355363.
  • 105
    Zhang Y, Gu Y, Guo T, Li Y, Cai H. Perioperative immunonutrition for gastrointestinal cancer: a systematic review of randomized controlled trials. Surg Oncol 2012; 21: e87e95.
  • 106
    Ljungqvist O, Nygren J, Thorell A. Modulation of post-operative insulin resistance by pre-operative carbohydrate loading. Proc Nutr Soc 2002; 61: 329336.
  • 107
    Hausel J, Nygren J, Lagerkranser M, Hellstrom PM, Hammarqvist F, Almstrom C et al. A carbohydrate-rich drink reduces preoperative discomfort in elective surgery patients. Anesth Analg 2001; 93: 13441350.
  • 108
    Helminen H, Viitanen H, Sajanti J. Effect of preoperative intravenous carbohydrate loading on preoperative discomfort in elective surgery patients. Eur J Anaesthesiol 2009; 26: 123127.
  • 109
    Noblett SE, Watson DS, Huong H, Davison B, Hainsworth PJ, Horgan AF. Pre-operative oral carbohydrate loading in colorectal surgery: a randomized controlled trial. Colorectal Dis 2006; 8: 563569.
  • 110
    Yuill KA, Richardson RA, Davidson HI, Garden OJ, Parks RW. The administration of an oral carbohydrate-containing fluid prior to major elective upper-gastrointestinal surgery preserves skeletal muscle mass postoperatively—a randomised clinical trial. Clin Nutr 2005; 24: 3237.
  • 111
    Bisgaard T, Kristiansen VB, Hjortsø NC, Jacobsen LS, Rosenberg J, Kehlet H. Randomized clinical trial comparing an oral carbohydrate beverage with placebo before laparoscopic cholecystectomy. Br J Surg 2004; 91: 151158.
  • 112
    Li L, Wang Z, Ying X, Tian J, Sun T, Yi K et al. Preoperative carbohydrate loading for elective surgery: a systematic review and meta-analysis. Surg Today 2012; 42: 613624.
  • 113
    Gustafsson UO, Nygren J, Thorell A, Soop M, Hellstrom PM, Ljungqvist O et al. Pre-operative carbohydrate loading may be used in type 2 diabetes patients. Acta Anaesthesiol Scand 2008; 52: 946951.
  • 114
    Breuer JP, von Dossow V, von Heymann C, Griesbach M, von Schickfus M, Mackh E et al. Preoperative oral carbohydrate administration to ASA III–IV patients undergoing elective cardiac surgery. Anesth Analg 2006; 103: 10991108.
  • 115
    Salo M. Effects of anaesthesia and surgery on the immune response. Acta Anaesthesiol Scand 1992; 36: 201220.
  • 116
    Shigemitsu Y, Saito T, Kinoshita T, Kobayashi M. Influence of surgical stress on bactericidal activity of neutrophils and complications of infection in patients with esophageal cancer. J Surg Oncol 1992; 50: 9097.
  • 117
    Veenhof AA, Vlug MS, van der Pas MH, Sietses C, van der Peet DL, de Lange-de Klerk ES et al. Surgical stress response and postoperative immune function after laparoscopy or open surgery with fast track or standard perioperative care: a randomized trial. Ann Surg 2012; 255: 216221.
  • 118
    Lacy AM, García-Valdecasas JC, Delgado S, Castells A, Taurá P, Piqué JM et al. Laparoscopy-assisted colectomy versus open colectomy for treatment of non-metastatic colon cancer: a randomised trial. Lancet 2002; 359: 22242229.
  • 119
    Brivio F, Lissoni P, Perego MS, Lissoni A, Fumagalli L. Abrogation of surgery-induced IL-6 hypersecretion by presurgical immunotherapy with IL-2 and its importance in the prevention of postoperative complications. J Biol Regul Homeost Agents 2001; 15: 370374.
  • 120
    Brivio F, Lissoni P, Tisi E, Erba L, Barni S, Tancini G et al. Effects of a preoperative therapy with interleukin-2 on surgery-induced lymphocytopenia in cancer patients. Oncology 1992; 49: 215218.
  • 121
    van Dam RM, Hendry PO, Coolsen MM, Bemelmans MH, Lassen K, Revhaug A et al.; Enhanced Recovery After Surgery (ERAS) Group. Initial experience with a multimodal enhanced recovery programme in patients undergoing liver resection. Br J Surg 2008; 95: 969975.
  • 122
    Basse L, Hjort Jakobsen D, Billesbolle P, Werner M, Kehlet H. A clinical pathway to accelerate recovery after colonic resection. Ann Surg 2000; 232: 5157.
  • 123
    Basse L, Jakobsen DH, Bardram L, Billesbolle P, Lund C, Mogensen T et al. Functional recovery after open versus laparoscopic colonic resection: a randomized, blinded study. Ann Surg 2005; 241: 416423.
  • 124
    Majeed AW, Troy G, Nicholl JP, Smythe A, Reed MW, Stoddard CJ et al. Randomised, prospective, single-blind comparison of laparoscopic versus small-incision cholecystectomy. Lancet 1996; 347: 989994.
  • 125
    Lassen K, Høye A, Myrmel T. Randomised trials in surgery: the burden of evidence. Rev Recent Clin Trials 2012; 7: 244248.
  • 126
    Vlug MS, Wind J, Hollmann MW, Ubbink DT, Cense HA, Engel AF et al.; LAFA study group. Laparoscopy in combination with fast track multimodal management is the best perioperative strategy in patients undergoing colonic surgery: a randomized clinical trial (LAFA-study). Ann Surg 2011; 254: 868875.
  • 127
    Maffezzini M, Campodonico F, Capponi G, Manuputty E, Gerbi G. Fast-track surgery and technical nuances to reduce complications after radical cystectomy and intestinal urinary diversion with the modified Indiana pouch. Surg Oncol 2012; 21: 191195.
  • 128
    Yamada T, Hayashi T, Cho H, Yoshikawa T, Taniguchi H, Fukushima R et al. Usefulness of enhanced recovery after surgery protocol as compared with conventional perioperative care in gastric surgery. Gastric Cancer 2012; 15: 3441.
  • 129
    Cascales Campos PA, Gil Martínez J, Galindo Fernández PJ, Gil Gómez E, Martínez Frutos IM, Parrilla Paricio P. Perioperative fast track program in intraoperative hyperthermic intraperitoneal chemotherapy (HIPEC) after cytoreductive surgery in advanced ovarian cancer. Eur J Surg Oncol 2011; 37: 543548.
  • 130
    Quality of life and clinical trials. Lancet 1995; 346: 12.
  • 131
    di Sebastiano P, Festa L, De Bonis A, Ciuffreda A, Valvano MR, Andriulli A et al. A modified fast-track program for pancreatic surgery: a prospective single-center experience. Langenbecks Arch Surg 2011; 396: 345351.
  • 132
    Munitiz V, Martinez-de-Haro LF, Ortiz A, Ruiz-de-Angulo D, Pastor P, Parrilla P. Effectiveness of a written clinical pathway for enhanced recovery after transthoracic (Ivor Lewis) oesophagectomy. Br J Surg 2010; 97: 714718.
  • 133
    Balzano G, Zerbi A, Braga M, Rocchetti S, Beneduce AA, Di Carlo V. Fast-track recovery programme after pancreatico-duodenectomy reduces delayed gastric emptying. Br J Surg 2008; 95: 13871393.
  • 134
    Chughtai B, Abraham C, Finn D, Rosenberg S, Yarlagadda B, Perrotti M. Fast track open partial nephrectomy: reduced postoperative length of stay with a goal-directed pathway does not compromise outcome. Adv Urol 2008; 507543.
  • 135
    Löhr G, Keller H, Kütscher J, Huber R. [Fast-track rehabilitation after open aorto-iliac vascular procedures.] Zentralbl Chir 2008; 133: 344348.
  • 136
    Mukherjee D. ‘Fast-track’ abdominal aortic aneurysm repair. Vasc Endovascular Surg 2003; 37: 329334.
  • 137
    Mukherjee D, Becker TE. An update on the ‘fast-track’ abdominal aortic aneurysm repair. Int J Angiol 2008; 17: 9397.
  • 138
    Spanjersberg WR, Reurings J, Keus F, van Laarhoven CJ. Fast track surgery versus conventional recovery strategies for colorectal surgery. Cochrane Database Syst Rev 2011; (2)CD007635.
  • 139
    Eskicioglu C, Forbes SS, Aarts MA, Okrainec A, McLeod RS. Enhanced recovery after surgery (ERAS) programs for patients having colorectal surgery: a meta-analysis of randomized trials. J Gastrointest Surg 2009; 13: 23212329.
  • 140
    Gouvas N, Tan E, Windsor A, Xynos E, Tekkis PP. Fast-track vs standard care in colorectal surgery: a meta-analysis update. Int J Colorectal Dis 2009; 24: 11191131.
  • 141
    Franke RH, Kaul JD. The Hawthorne experiments: first statistical interpretation. Am Soc Rev 1978; 43: 623643.
  • 142
    McCarney R, Warner J, Iliffe S, van Haselen R, Griffin M, Fisher P. The Hawthorne effect: a randomised, controlled trial. BMC Med Res Methodol 2007; 7: 30.
  • 143