Abstract
Aim
Enhanced recovery after surgery (ERAS) programmes aim to standardise perioperative care leading to optimal patient outcomes. Despite these programmes, variation in outcomes still persists. This study aimed to assess the influence of lifestyle factors on short-term outcomes after colorectal surgery within this optimal recovery programme.
Methods
Consecutive patients enrolled on an ERAS pathway who underwent elective colorectal surgery (June 2013 to July 2014) at one site were included. We used data routinely collected by ERAS nurse specialists and during preassessment to analyse association between patient and lifestyle factors and likelihood of developing postoperative complications or having an increased length of stay.
Results
A total of 199 patients were included: mean age 61.8 years (range 17–90 years) and 53.8% male. Age, sex, deprivation, smoking status, alcohol intake, body mass index or level of comorbidity were not associated with postoperative complications. Patients reporting limited preoperative physical capacity (unable to climb two flights of stairs) were more than four times as likely to have a postoperative complication on univariate analysis and were found to still have increased risk of postoperative complications on multivariate analysis. Patients reporting limited preoperative physical capacity were shown to have significantly longer hospital stay on univariate analysis. In the multivariate analysis, limited physical capacity was not associated with prolonged length of stay due to confounding factors of age and deprivation.
Conclusions
Limited physical capacity was the only patient and lifestyle factor associated with poorer postoperative complications and prolonged hospital stay after elective colorectal surgery within an ERAS programme. Consideration should be given to individualised prehabilitation that aims to increase physical capacity pre-operatively to improve patient outcomes.
Keywords: General surgery, Outcomes, Colorectal surgery, Lifestyle
Introduction
Since being first described by Kehlet and Mogensen,1 there has been widespread adoption by colorectal surgeons of enhanced recovery after surgery (ERAS) programmes.1–4 ERAS consists of multimodal components including shorter fasting times, carbohydrate preloading, preoperative counselling, appropriate fluid therapy, early initiation of oral diet and early mobilisation, which aimed to standardise and subsequently optimise postoperative care.5,6 The latter has been achieved with several meta-analyses confirming that ERAS programmes result in reduced length of hospital stay, without accompanying increases in readmissions, and significant reductions in postoperative complication rates.7,8 However, despite this standardisation of perioperative care, there remains significant published variation in outcomes in patients undergoing elective colorectal surgery, suggesting other influencing factors that need to be identified for further improved surgical outcomes.9
Before widespread integration of ERAS programmes, patient-related factors and lifestyle factors were proven to strongly influence perioperative outcomes. Patient-related factors included increasing age, presence of increasing number of comorbidities and socioeconomic deprivation.10–15 It can be seen that most of these are non-modifiable except for the presence of comorbidities, which is assessed preoperatively with onward referrals and investigations made to ensure optimisation prior to surgery. In contrast, lifestyle factors are modifiable and include smoking, excess alcohol, excess weight/obesity and physical inactivity. Prior to the integration of ERAS programmes, all these lifestyle factors had individually or collectively been shown to increase the risk of postoperative complications, including wound infection/dehiscence; cardiorespiratory deterioration/critical care admission; conversion from laparoscopic to open surgery, delirium and, in some circumstances, postoperative death.16–18
In the era of ERAS being considered the optimal perioperative care pathway, not only do these modifiable lifestyle factors still persist, but several have now become major public health issues.19–22 In relation to diet and obesity, the Health Survey for England reported in 2016 that 58% of women and 68% of men in England were at least overweight, with 26% obese.23 The next generation are following, with National Child Measurement Programme England reporting over one-third of children are overweight or obese by the time they leave primary school.24 After smoking, which is reducing in incidence with the smoking ban and e-cigarettes,25 excess weight and obesity are the most important known avoidable causes of several cancers, including colorectal cancer.26 Alcohol has also been found to cause 3% of cancer cases in the UK.27 In 2017, the Office for National Statistics found that 27% of people in the UK who had drunk alcohol the week before interview were classed as binge drinkers (men drinking more than 8 units of alcohol in one sitting and women drinking over 6 units).28 The recommended physical activity is only 150 minutes of moderate level of activity over one week but only 61% of UK adults were achieving this in 2017.29,30
The continuing presence of these modifiable lifestyle factors could potentially explain the variation in documented perioperative outcomes despite patients undergoing optimal perioperative care in the form of an ERAS programme. This study therefore had two aims: first, to document the prevalence of lifestyle factors in a colorectal patient population undergoing elective surgery, and second to analyse any influence that lifestyle factors might have on perioperative outcomes within an established ERAS programme.
Methods
A dedicated ERAS nurse in a single-centre colorectal department prospectively collected details of consecutive patients undergoing elective colorectal surgery within an established ERAS programme over a 12-month period (June 2013 to July 2014). All patients admitted for elective colorectal surgery (benign or malignant pathology; resectional or non-resectional) were included in the ERAS programme. Any patient undergoing emergency or expedited colorectal surgery was excluded.
All data were entered into a clinical database that was established early 2013 and is part of the Whole System Patient Flow Improvement Programme initiated and led by the Scottish Government,31 Briefly, this programme has Caldicott approval and requires monthly data submission from all elective colorectal surgery departments across Scotland with central and individual interpretation of key ERAS performance indicators, allowing departmental feedback and maintenance of standards. Details of the multimodal ERAS programme are detailed in Appendix 1.
Appendix 1.
Summary of enhanced recovery after surgery programme
| Before surgery: |
| • Attend preoperative assessment, given information, counselling and supply of carbohydrate drinks. |
| • Should drink four cartons over the course of the evening prior to surgery. |
| Day of surgery (Day 0): |
| • Eat until 2am, drink two further carbohydrate drinks and fluids prior to 6am. |
| • Minimally invasive surgery where possible, adequate pain management in the perioperative period. |
| • TED stockings to be worn, enoxaparin prophylactically post-surgery. |
| • Encourage eating and drinking once out of surgery. |
| Day 1: |
| • Sit in chair for two hours in morning and two hours in evening. |
| • Assisted to walk the length of the ward and back. |
| • Eat light diet and drink two litres of fluid. |
| • Staff to encourage drinking two to three high protein drinks. |
| • Regular analgesia and antiemetics in addition to epidural or patient-controlled analgesia. |
| Day 2: |
| • Catheter and/or drip and/or epidural removed. |
| • Sit in chair for six hours. |
| • Assisted walk the length of the ward four times. |
| • Eat normal diet and drink two litres of fluid. |
| • Further three protein drinks (will take from fridge themselves). |
| Day 3 and onwards: |
| • Continue to eat and drink normally. |
| • Three high protein drinks per day. |
| • Continue to sit out of bed for six hours. |
| • Walk the length of the ward four times (or more) unassisted. |
| • Thinking about discharge (around day 5). |
| Discharge when: |
| • Pain is under control. |
| • Mobile. |
| • Eating and drinking normally. |
| • Patient feels reassured about going home. |
From this database, age, gender, laparoscopic versus open procedure and comorbidity were analysed using the Charlson comorbidity score.32 Additional data regarding socioeconomic circumstances were calculated using patients’ postcode of residence linked to the Scottish Index of Multiple Deprivation (SIMD): an area-based measure of deprivation.33 Lifestyle factors were routinely recorded at each patient’s surgical preassessment visit as part of hospital standard care. These were smoking status (defined as current, ex-smoker, non-smoker), alcohol intake (excess: over 14 units/week; within guidelines: equal to or less than 14 units/week or none);34 body mass index (BMI: underweight < 20: healthy 20–24.9; overweight 25–29.9; obese 30 and above) and physical capacity. Physical capacity was divided into two groups: moderate and limited, according to whether the patient self-reported that they could (moderate) or could not complete (limited) two flights of stairs without stopping.
Postoperative complications, including mortality, were defined as any complication or death occurring within 30 days of surgery. For the purposes of binary analysis, all grades of complications were included and compared with patients without complications.35
Statistical analysis
To determine the influence of modifiable lifestyle factors on postoperative complications (any Clavien–Dindo grading) and increased length of stay (greater than median cohort length of stay), univariate and multivariate logistic regression models were developed. Odds ratios (OR) are presented with 95% confidence intervals (CI); P-value less than 0.05 was considered statistically significant. Analysis was performed using STATA software package version 11(IC).
Results
A total of 199 consecutive patients were included: 46% female (n = 92); mean age 61.8 years (range, 17–90 years) and 63.8% (n = 127) scoring at least 3 on the Charlson Index. Of these patients, 43% (n = 85) were classified as deprived (SIMD 1 and 2; Table 1).
Table 1.
Demographics and characteristics of patients undergoing elective colorectal surgery.
| Demographic | Patients (N = )199 |
| Sex: | |
| Male | 107 (53.8) |
| Female | 92 (46.2) |
| Age, mean years (SD) | 61.8 (14.4) |
| Deprivation (SIMD 2012): | |
| 1 (most deprived) | 50 (25.1) |
| 2 | 35 (17.6) |
| 3 | 47 (23.6) |
| 4 | 31 (15.6) |
| 5 (least deprived) | 36 (18.1) |
| Smoking status: | |
| Current | 33 (16.6) |
| Ex-smoker | 56 (28.1) |
| Non-smoker | 74 (37.2) |
| Unknown | 36 (18.1) |
| Alcohol intake: | |
| < Recommended limit | 140 (70.4) |
| > Recommended limit | 21 (10.6) |
| Unknown | 38 (19.1) |
| Body mass index: | |
| Normal (18–25) | 50 (25.1) |
| Overweight (25–30) | 60 (30.2) |
| Obese (30–40) | 51 (25.6) |
| Unknown (> 40) | 38 (19.1) |
| Physical capacity: | |
| < 2 flights of stairs | 12 (6.0) |
| ≥ 2 flights of stairs | 152 (76.4) |
| Unknown | 35 (17.6) |
| Charlson comorbidity score: | |
| 0 | 30 (15.1) |
| 1 | 17 (8.5) |
| 2 | 25 (12.6) |
| ≥ 3 | 127 (63.8) |
| Length of stay, mean days (SD) | 8.4 (4.5) |
| Postoperative complications (Clavien–Dindo): | |
| 0 | 134 (67.3) |
| 1 | 31 (15.6) |
| 2 | 21 (10.6) |
| 3 | 11 (5.5) |
| 4 | 2 (1.0) |
| Surgery: | |
| Open | 112 (56.3) |
| Laparoscopic | 87 (43.7) |
SD, standard deviation from the mean; SIMD, Scottish Index of Multiple Deprivation.
In relation to modifiable lifestyle factors, 44.7% (n = 89) of patients were current or former smokers, 10.6% (n = 21) reported excess alcohol consumption, 55.8% (n = 111) were overweight or obese and 6% (n = 12) reported limited physical capacity.
There were 112 open procedures cases (56.3%) with the rest recorded as laparoscopic. Overall, 65 patients (32.7%) developed any grade of postoperative complication and the mean length of postoperative hospital stay was 8.4 days (range, 3–32 days). There was no recorded 30-day mortality.
Lifestyle factors associated with postoperative complications (any Clavien–Dindo score) are shown in Table 2. On univariate analysis, the only patient or modifiable lifestyle factor associated with the development of a postoperative complication was limited physical capacity. Patients who were unable to climb two flights of stairs were more than four times more likely to develop a postoperative complication than patients who could climb two flights of stairs (OR 4.2; 95% CI 1.21, 14.6; P = 0.024). Limited physical capacity remained independently associated with postoperative complication on multivariable analysis (OR 6.64; 95% CI 1.51, 29.13; P = 0.012].
Table 2.
Univariate and multivariate logistic regression model examining patient and modifiable lifestyle factors associated with postoperative complications.
| Patient/lifestyle factor | Univariate | Multivariate | ||
| OR (95% CI) | P-value | OR (95% CI) | P-value | |
| Sex: | ||||
| Male | 1.00 | 1.00 | ||
| Female | 0.99 (0.55, 1.80) | 0.988 | 1.10 (0.55, 2.23) | 0.784 |
| Age (years): | ||||
| < 60 | 1.00 | 1.00 | ||
| 60–74 | 0.91 (0.47, 1.76) | 0.781 | 0.92 (0.34, 2.45) | 0.861 |
| ≥ 75 | 0.85 (0.37, 1.96) | 0.710 | 0.48 (0.14, 1.68) | 0.249 |
| Deprivation (SIMD 2012): | ||||
| 1 (most deprived) | 1.00 | 1.00 | ||
| 2 | 0.85 (0.35, 2.10) | 0.726 | 0.81 (0.29, 2.24) | 0.681 |
| 3 | 0.50 (0.21, 1.21) | 0.123 | 0.40 (0.15, 1.07) | 0.068 |
| 4 | 0.57 (0.21, 1.52) | 0.260 | 0.69 (0.23, 2.02) | 0.498 |
| 5 (least deprived) | 1.17 (0.49, 2.79) | 0.732 | 1.34 (0.51, 3.55) | 0.558 |
| Smoking status: | ||||
| Non-smoker | 1.00 | 1.00 | ||
| Ex-smoker | 1.45 (0.71, 2.99) | 0.311 | 1.50 (0.65, 3.46) | 0.348 |
| Smoker | 0.91 (0.37, 2.20) | 0.827 | 0.83 (0.29, 2.34) | 0.722 |
| Unknown | 0.60 (0.24, 1.50) | 0.271 | 1.51 (0.11, 20.50) | 0.756 |
| Alcohol intake: | ||||
| < Recommended limit | 1.00 | 1.00 | ||
| > Recommended limit | 1.44 (0.57, 3.65) | 0.445 | 1.65 (0.55, 5.00) | 0.373 |
| Unknown | 0.51 (0.22, 1.20) | 0.124 | 0.62 (0.04, 8.70) | 0.721 |
| Body mass index: | ||||
| Normal | 1.00 | 1.00 | ||
| Overweight | 0.96 (0.44, 2.10) | 0.913 | 0.88 (0.37, 2.11) | 0.772 |
| Obese | 0.97 (0.43, 2.19) | 0.941 | 0.63 (0.24, 1.68) | 0.356 |
| Unknown | 0.47 (0.18, 1.25) | 0.132 | 0..56 (0.11, 2.75) | 0.475 |
| Physical capacity: | ||||
| 2 flights stairs | 1.00 | 1.00 | ||
| < 2 flights stairs | 4.20 (1.21, 14.64) | 0.024 | 6.64 (1.51, 29.13) | 0.012 |
| Unknown | 0.62 (0.26, 1.47) | 0.280 | 1.37 (0.30, 6.20) | 0.686 |
| Charlson comorbidity score: | ||||
| 0 | 1.00 | 1.00 | ||
| 1 | 2.07 (0.61, 7.11) | 0.246 | 2.36 (0.60, 9.21) | 0.217 |
| 2 | 0.58 (0.17, 2.04) | 0.399 | 0.47 (0.09, 2.31) | 0.350 |
| ≥ 3 | 1.19 (0.50, 2.83) | 0.687 | 1.41 (0.40, 4.93) | 0.590 |
| Surgery: | ||||
| Laparoscopic | 1.00 | 1.00 | ||
| Open | 2.03 (1.09, 3.78) | 0.025 | 2.21 (1.09, 4.48) | 0.028 |
CI, confidence interval; OR, odds ratio; SIMD, Scottish Index of Multiple Deprivation.
Lifestyle factors associated with prolonged postoperative length of stay (length of stay more than the cohort mean) are shown in Table 3. Both limited physical capacity and the development of a postoperative complication were associated with a prolonged inpatient stay on univariate analysis. Patients who were unable to climb two flights of stairs were more than four times more likely to have a prolonged postoperative inpatient stay than patients who could climb two flights of stairs (OR 4.47; 95% CI 1.28, 15.57; P = 0.019). In the multivariate analysis, limited physical capacity was no longer associated with prolonged length of stay due to an interaction between age (patients over 75 years more likely to stay in hospital longer (OR 5.69; 95% CI 1.04, 31.18; P = 0.045] and deprivation (least deprived patients less likely to stay in hospital longer (OR 0.24; 95% CI 0.06, 0.92; P = 0.038]. Postoperative complications remained associated with increased length of stay (OR 20.95; 95% CI 7.99, 54.95; P < 0.001].
Table 3.
Univariate and multivariate logistic regression model examining patient and modifiable lifestyle factors associated with prolonged postoperative length of staya
| Patient/lifestyle factor | OR (95% CI) | P-value | OR (95% CI) | P-value | |
| Sex: | |||||
| Male | 1.00 | 1.00 | |||
| Female | 0.62 (0.33, 1.13) | 0.118 | 0.61 (0.25, 1.53) | 0.296 | |
| Age (years): | |||||
| < 60 | 1.00 | ||||
| 60–74 | 0.77 (0.39, 1.53) | 0.453 | 1.00 | ||
| ≥ 75 | 1.67 (0.75, 3.71) | 0.205 | 1.63 (0.40, 6.60) | 0.495 | |
| Deprivation (SIMD 2012): | |||||
| 1 (most deprived) | 1.00 | 5.69 (1.04, 31.18) | 0.045 | ||
| 2 | 0.32 (0.12, 0.86) | 0.025 | 0.25 (0.06, 1.08) | 0.062 | |
| 3 | 0.44 (0.18, 1.03) | 0.059 | 0.67 (0.20, 2.23) | 0.510 | |
| 4 | 0.83 (0.32, 2.00) | 0.639 | 1.74 (0.44, 6.77) | 0.428 | |
| 5 (least deprived) | 0.49 (0.20, 1.23) | 0.127 | 0.24 (0.06, 0.92) | 0.038 | |
| Smoking status: | |||||
| Non-smoker | 1.00 | 1.00 | |||
| Ex-smoker | 1.09 (0.53, 2.26) | 0.819 | 0.96 (0.34, 2.73) | 0.936 | |
| Smoker | 0.85 (0.35, 2.06) | 0.723 | 1.40 (0.36, 5.40) | 0.624 | |
| Unknown | 0.56 (0.22, 1.41) | 0.218 | 3.08 (0.17, 57.46) | 0.451 | |
| Alcohol intake: | |||||
| < Recommended limit | 1.00 | 1.00 | |||
| > Recommended limit | 0.74 (0.27, 2.04) | 0.563 | 0.25 (0.06, 1.09) | 0.064 | |
| Unknown | 0.50 (0.21, 1.16) | 0.107 | 0.20 (0.01, 4.09) | 0.293 | |
| Body mass index: | |||||
| Normal | 1.00 | 1.00 | |||
| Overweight | 0.83 (0.37, 1.86) | 0.654 | 0.36 (0.11, 1.19) | 0.094 | |
| Obese | 1.25 (0.56, 2.82) | 0.587 | 1.17 (0.33, 4.13) | 0.810 | |
| Unknown | 0.52 (0.20, 1.37) | 0.186 | 0.41 (0.06, 3.01) | 0.383 | |
| Physical capacity: | |||||
| 2 flights stairs | 1.00 | 1.00 | |||
| < 2 flights stairs | 4.47 (1.28, 15.57) | 0.019 | 1.65 (0.27, 10.08) | 0.586 | |
| Unknown | 0.66 (0.28, 1.57) | 0.347 | 1.23 (0.21, 7.24) | 0.818 | |
| Charlson comorbidity score: | |||||
| 0 | 1.00 | 1.00 | |||
| 1 | 2.07 (0.61, 7.11) | 0.246 | 2.46 (0.46, 13.25) | 0.296 | |
| 2 | 0.44 (0.12, 1.67) | 0.230 | 0.41 (0.05, 3.34) | 0.408 | |
| ≥ 3 | 1.15 (0.49, 2.74) | 0.747 | 0.58 (0.12, 2.91) | 0.508 | |
| Surgery: | |||||
| Laparoscopic | 1.00 | 1.00 | |||
| Open | 3.21 (1.66, 6.21) | 0.001 | 4.05 (1.60, 10.25) | 0.003 | |
| Post-operative complication: | |||||
| No | 1.00 | 1.00 | |||
| Yes | 12.68 (6.23, 25.83) | <0.001 | 20.95 (7.99, 54.95) | <0.001 |
a Prolonged = length of stay more than the cohort mean.
CI, confidence interval; OR, odds ratio; SIMD, Scottish Index of Multiple Deprivation.
Patients who underwent open surgery were more than twice as likely to develop a postoperative complication than those who underwent laparoscopic surgery (OR 2.03; 95% CI 1.09, 3.78; P = 0.025). In the multivariate analysis, open surgery remained associated with an increased risk of postoperative complications compared with laparoscopic surgery (OR 2.21; 95% CI 1.09, 4.48; P = 0.028). Likewise, patients undergoing open procedures were three times as likely to have prolonged hospital stay when compared with those who underwent laparoscopic surgery (OR 3.21; 95% CI 1.66, 6.21; P = 0.001). In the multivariate analysis this also remained significant (OR 4.05; 95% CI 1.60, 10.25; P = 0.003).
Discussion
This study has shown that lifestyle factors are prevalent in elective colorectal surgical patients. In addition, limited physical capacity resulted in poorer perioperative outcomes despite patients undergoing optimal perioperative care within an ERAS programme. The inability of a patient to climb two flights of stairs was associated with an increase in postoperative complications that resulted in a longer length of hospital stay. These results support a potential role for physical capacity prehabilitation in surgical patients prior to undergoing elective surgery within an ERAS programme, especially in those undergoing an open approach, which carry a higher risk of poorer postoperative complications.36–39
Prehabilitation, or pretreatment intervention, is currently an area of research interest which, like ERAS programmes, can be multimodal, including physical activity/exercise, lifestyle reduction advice including diet and weight, pharmacy rationalising or optimising and patient counselling, both about pathology and perioperative pathways. With many components to choose from, published prehabilitation programmes vary, making comparisons between the small number of studies difficult. However, a 2016 systematic review found that prehabilitation decreased the incidence of postoperative complications, especially pulmonary, after major abdominal surgery (OR 0.59; 95% CI 0.38–0.91).40
In addition, in one of the first randomised controlled studies including only high-risk patients (age over 70 years and/or American Society of Anesthesiologists score III or IV) undergoing major abdominal surgery, a significant reduction in postoperative complications was recorded: 31% in prehabilitation group compared with 62% in standard care group (P = 0.001).41 With these potential improvements in perioperative outcomes reported after a mean intervention time of only six weeks, it can be seen that treatment targets would not need to be significantly altered to potentially reduce complications in this vulnerable patient group.
Although the evidence for prehabilitation is in evolution and has focused, like this study, on short-term outcomes, all members of the perioperative care team should be aware of the growing evidence that preoperative limited physical capacity influences long-term survival outcome in a range of different cancers, including colorectal cancers.42–46 The CHALLENGE study from Canada is currently underway both in Northern America and Europe and is the first trial to try to provide level one evidence in this area.49
Strengths
One of the strengths of this work is the use of a prospective cohort that allowed us to measure multiple patient-related variables and outcomes contemporaneously. Analysing this prospectively collected dataset retrospectively also reduced the potential for collection bias during data collection. The cohort nature of this study also led to all patients being included for analysis leading to a representative dataset of typical colorectal patients within our ERAS programme. This is evident from the wide range of patient factors and lifestyle factors documented.
Limitations
The main limitation of the study design was that it relied on patient self-reporting of lifestyle factors. Although this is easy to apply and a non-invasive approach, unlike cardiopulmonary exercise testing for exercise capacity or serum cotinine to establish smoking status, patients may under- or overestimate their consumption and physical capacity.48,49 Further work is needed to focus on a direct comparison between self-reported physical capacity and an objective measurement of such. A further limitation is that, although all data were collected prospectively, the authors acknowledge that some are missing, reflecting the pragmatic nature of this study.
Conclusion
In conclusion, the present study has shown that despite undergoing an elective colorectal ERAS programme, a patient with limited preoperative physical capacity remains at higher risk of poorer short-term outcomes. Identifying this high-risk patient group preoperatively could lead to targeted prehabilitation strategies aimed at optimising patient outcomes within an ERAS programme.
Acknowledgements
We would like to acknowledge Claire McCutcheon and Jane Porteous for their work as ERAS nurse specialists during the study period.
References
- 1.Kehlet H, Mogensen T. Hospital stay of 2 days after open sigmoidectomy with a multimodal rehabilitation programme. Br J Surg 1999; : 227–230. [DOI] [PubMed] [Google Scholar]
- 2.Kehlet H, Wilmore DW. Evidence-based surgical care and the evolution of fast-track surgery. Ann Surg 2008; (2): 189–198. [DOI] [PubMed] [Google Scholar]
- 3.Gouvas N, Tan E, Windsor A. Fast-track vs. standard care in colorectal surgery: a meta-analysis update. Int J Colorectal Dis 2009; : 1119–1131. [DOI] [PubMed] [Google Scholar]
- 4.Adamina M, Kehlet H, Tomlinson GA et al. Enhanced recovery pathways optimize health outcomes and resource utilization: a meta-analysis of randomized controlled trials in colorectal surgery. Surgery 2011; (6): 830–840. [DOI] [PubMed] [Google Scholar]
- 5.Gustafsson UO, Scott MJ, Schwenk W et al. Guidelines for perioperative care in elective colonic surgery: Enhanced Recovery After Surgery (ERAS )Society Recommendations. Clin Nutr 2012; (6): 783–800. [DOI] [PubMed] [Google Scholar]
- 6.Nygren J, Thacker J, Carli F et al. Guidelines for perioperative care in elective rectal/ pelvic surgery: Enhanced Recovery After Surgery (ERAS) Society Recommendations. Clin Nutr 2012; (6): 801–816. [DOI] [PubMed] [Google Scholar]
- 7.Greco M, Capretti G, Beretta L et al. Enhanced recovery program in colorectal surgery: a metaanalysis of randomized controlled trials. World J Surg 2013; : 1531–1541. [DOI] [PubMed] [Google Scholar]
- 8.Zhuang C-L, Ye X-Z, Zhang X-D et al. Enhanced recovery after surgery programs versus traditional care for colorectal surgery: a meta-analysis of randomized controlled trials. Dis Colon Rectum 2013; : 667–678. [DOI] [PubMed] [Google Scholar]
- 9.National Bowel Cancer Audit Annual Report 2017 Version 2. www.nboca.org.uk/content/uploads/2017/12/NBOCA-annual-report-2017-v2.pdf (cited December 2018).
- 10.Beckmann K, Moore J, Wattchow D et al. Short-term outcomes after surgical resection for colorectal cancer in South Australia. J Eval Clin Pract 2017; (2): 316–324. [DOI] [PubMed] [Google Scholar]
- 11.Margadant CC, Bruns ER, Sloothaak DA et al. Lower muscle density is associated with major postoperative complications in older patients after surgery for colorectal cancer. Eur J Surg Oncol 2016; (11): 1654–1659. [DOI] [PubMed] [Google Scholar]
- 12.Bai Z, Wang Z, Wang J et al. Clinicopathologic parameters associated with postoperative complications and risk factors for tumor recurrence and mortality after tumor resection of patients with colorectal cancer. Clin Transl Oncol 2017; (2): 176–192. [DOI] [PubMed] [Google Scholar]
- 13.Champagne BJ, Nishtala M, Brady JT et al. Laparoscopic colectomy in the obese, morbidly obese, and super morbidly obese: when does weight matter? Int J Colorectal Dis 2017; (10): 1447–1451. [DOI] [PubMed] [Google Scholar]
- 14.Bircan HY, Koc B, Ozcelik U et al. Are there any differences between age groups regarding colorectal surgery in elderly patients? BMC Surg 2014; : 44. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Oliphant R, Nicholson GA, Horgan PG et al. ; West of Scotland Colorectal Cancer Managed Clinical Network . Deprivation and colorectal cancer surgery: longer-term survival inequalities are due to differential postoperative mortality between socioeconomic groups. Ann Surg Oncol 2013; (7): 2132–2139. [DOI] [PubMed] [Google Scholar]
- 16.Robinson TN, Wu DS, Sauaia A et al. Slower walking speed forecasts increased postoperative morbidity and one-year mortality across surgical specialties. Ann Surg 2013; (4): 582–590. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Cakir H, Heus C, van der Ploeg TJ, Houdijk AP. Visceral obesity determined by CT scan and outcomes after colorectal surgery; a systematic review and meta-analysis. Int J Colorectal Dis 2015; (7): 875–882. [DOI] [PubMed] [Google Scholar]
- 18.Tønnesen H, Nielsen PR, Lauritzen JB, Møller AM. Smoking and alcohol intervention before surgery: evidence for best practice. Br J Anaesth 2009; : 297–306. [DOI] [PubMed] [Google Scholar]
- 19.Health and Social Care information Centre Statistics on Obesity, Physical Activity and Diet. England 2016. http://content.digital.nhs.uk/catalogue/PUB20562/obes-phys-acti-diet-eng-2016-rep.pdf (cited December 2018).
- 20.National Statistics Scottish Health Survey 2015 edition Summary. Edinburgh: Scottish Government; 2016. [Google Scholar]
- 21.National Assembly for Wales National Survey for Wales: Population Health 2017–18. https://gov.wales/statistics-and-research/national-survey/?tab=el_home&topic=population_health&lang=en (cited December 2018).
- 22.Lee IM, Shiroma EJ, Lobelo F et al. Impact of physical inactivity on the world’s major non-communicable diseases. Lancet 2012; (9838): 219–229. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.National Statistics Health Survey for England 2016: Summary of Key Findings. Leeds: NHS Digital; 2017. [Google Scholar]
- 24.National Statistics National Child Measurement Programme England, 2016/17 School Year. Leeds: NHS Digital; 2017. [Google Scholar]
- 25.Office for National Statistics Adult Smoking Habits for Adults in the UK: 2016. London: ONS; 2017. [Google Scholar]
- 26.World Health Organization Diet, Nutrition and the Prevention of Chronic Diseases: Report of a Joint WHO/FAO Expert Consultation. WHO Technical Report Series 916 Geneva: WHO; 2003. [Google Scholar]
- 27.Brown K, Rumgay H, Dunlop C et al. The fraction of cancer attributable to modifiable risk factors in England, Wales, Scotland, Northern Ireland and the United Kingdom in 2015. Br J Cancer 2018; : 1130–1141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Office of National Statistics Adult Drinking Habits in Great Britain: 2017. London: ONS; 2018. [Google Scholar]
- 29.British Heart Foundation Physical Inactivity and Sedentary Behaviour Report 2017. London: British Heart Foundation; March 2017. [Google Scholar]
- 30.Bull FC; British Heart Foundation Expert Working Groups . Physical activity Guidelines in the UK: Review and Recommendations. Technical Report Loughborough: School of Sport, Exercise and Health Sciences, Loughborough University; 2010. [Google Scholar]
- 31.NHS Scotland Annual Report 2014 Reporting on the Quality and Efficiency Support Team. Edinburgh: Scottish Government; 2015. [Google Scholar]
- 32.Charlson M, Szatrowski TP, Peterson J et al. Validation of a combined comorbidity index. J Clin Epidemiol 1994; : 1245–1251. [DOI] [PubMed] [Google Scholar]
- 33.Scottish Government Scottish Index of Multiple Deprivation SMID16. www.gov.scot/Topics/Statistics/SIMD (cited December 2018).
- 34.Department of Health UK Chief Medical Officers’ Low Risk Drinking Guidelines. London: DoH; 2018. [Google Scholar]
- 35.Clavien PA, Barkun J, de Oloveria ML et al. The Clavien-Dindo classification of surgical complications: five-year experience. Ann Surg 2009; (2): 187–196. [DOI] [PubMed] [Google Scholar]
- 36.Carli F, Charlebois P, Stein B et al. Randomized clinical trial of prehabilitation in colorectal surgery. Br J Surg 2010; : 1187–1197. [DOI] [PubMed] [Google Scholar]
- 37.West MA, Loughney L, Lythgoe D et al. Effect of prehabilitation on objectively measured physical fitness after neoadjuvant treatment in preoperative rectal cancer patients: a blinded interventional pilot study. Br J Anaesth 2015; : 244–251. [DOI] [PubMed] [Google Scholar]
- 38.Mayo NE, Feldman L, Scott S et al. Impact of perioperative change in physical function on postoperative recovery: argument supporting prehabilitation for colorectal surgery. Surgery 2011; (3): 505–514. [DOI] [PubMed] [Google Scholar]
- 39.Morielli AR, Usmani N, Boule NG et al. A Phase 1 study examining the feasibility and safety of an aerobic exercise intervention in patients with rectal cancer during and after neoadjuvant chemoradiotherapy. Oncol Nurs Forum 2016; (3): 352–362. [DOI] [PubMed] [Google Scholar]
- 40.Moran J, Wilson F, Guinan E et al. Role of cardiopulmonary exercise testing as a risk-assessment method in patients undergoing intra-abdominal surgery: a systematic review. Br J Anaesth 2016; : 177–191. [DOI] [PubMed] [Google Scholar]
- 41.Barberan-Garcia A, Ubre M, Roca J et al. Personalised prehabilitation in high-risk patients undergoing elective major abdominal surgery. Ann Surg 2018; : 50–56. [DOI] [PubMed] [Google Scholar]
- 42.Campbell PT, Patel AV, Newton CC et al. Associations of recreational physical activity and leisure time spent sitting with colorectal cancer survival. J Clin Oncol 2013; : 876–885. [DOI] [PubMed] [Google Scholar]
- 43.Meyerhardt JA, Giovannucci EL, Holmes MD et al. Physical activity and survival after colorectal cancer diagnosis. J Clin Oncol 2006; : 3527–3534. [DOI] [PubMed] [Google Scholar]
- 44.Holmes MD, Chen WY, Feskanich D et al. Physical activity and survival after breast cancer diagnosis. JAMA 2005; : 2479–2486. [DOI] [PubMed] [Google Scholar]
- 45.Wolin KY, Yan Y, Colditz GA, Lee IM. Physical activity and colon cancer prevention: a meta-analysis. Br J Cancer 2009; (4): 611–616. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Alexander D, Allardice GM, Moug SJ, Morrison DS. A retrospective cohort study of the influence of lifestyle factors on survival of patients undergoing surgery for colorectal cancer. Colorectal Dis 2017; (6): 544–550. [DOI] [PubMed] [Google Scholar]
- 47.Courneya KS, Booth CM, Gill S et al. The colon health and life-long exercise change trial: a randomized trial of the National Cancer Institute of Canada Clinical Trials Group. Curr Oncol 2008; : 279–285. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Vartiainen E, Seppala T, Lillsunde P, Puska P. Validation of self reported smoking by serum cotinine measurement in a community-based study. J Epidemiol Community Health 2002; : 167–170. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Gorber SC, Schofield-Hurwitz S, Hardt J et al. The accuracy of self-reported smoking: a systematic review of the relationship between self-reported and cotinine-assessed smoking status. Nicotine Tob Res 2009; (1): 12–24. [DOI] [PubMed] [Google Scholar]
