Objective To systematically review the effects of preoperative and postoperative resistance exercise training on the recovery of physical function in patients undergoing abdominal surgery for cancer.
Data sources A systematic review of English articles using Medline, Physiotherapy Evidence Database, CINAHL and the Cochrane Library electronic databases was undertaken.
Eligibility criteria for selecting studies Studies were included if they used a randomised, quasi-randomised or controlled trial study design and compared the effects of a muscle-strengthening exercise intervention (±other therapy) with a comparative non-exercise group; involved adult participants (≥18 years) who had elected to undergo abdominal surgery for cancer; and used muscle strength, physical function, self-reported functional ability, range of motion and/or a performance-based test as an outcome measure.
Results Following screening of titles and abstracts of the 588 publications retrieved from the initial search, 24 studies met the inclusion criteria and were accessed for review of the full-text version of the article, and 2 eligible studies met the inclusion criteria and were included in the review. One exercise programme was undertaken preoperatively and the other postoperatively, until discharge from hospital. The exercise interventions of the included studies were performed for five and eight sessions, respectively. There were no differences between groups in either study.
Conclusion The only two studies designed to determine whether preoperative or postoperative resistance muscle-strengthening exercise programmes improved or negatively affected physical function outcomes in patients undergoing abdominal surgery for cancer provide inconclusive results.
- exercise training
- physical fitness
This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
What is already known?
Abdominal and thoracic cancers cause debilitating illness, and surgery is associated with significant decline in physical function.
Exercise initiated after completion of active cancer treatment has a beneficial effect on health-related quality of life.
What are the new findings?
There is insufficient evidence that preoperative or postoperative resistance muscle-strengthening exercise improves or negatively affects functional outcomes in patients undergoing abdominal surgery for cancer.
Large-scale, well-designed clinical trials are required to determine whether resistance muscle-strengthening exercise is beneficial for patients undergoing abdominal surgery for cancer.
Abdominal and thoracic cancers affect about 12 000 people annually in the UK. Many of these patients will undergo surgery, after which there is a high risk of postoperative complications and significant decline in physical function. A systematic review of exercise for people with cancer by Stevinson et al 1 found some evidence that those who exercised had better physical function compared with those who did not exercise, but there was insufficient evidence to demonstrate improvement in quality of life. In addition, they were not able to determine which type of exercise intervention was best or if any had long-term benefit. A more recent Cochrane review of exercise for people with cancer by Mishra et al 2 found that exercise initiated after completion of active cancer treatment (ie, surgery, chemotherapy, radiation therapy or hormone therapy) has a beneficial effect on health-related quality of life, although no parallel improvement in self-reported physical function was found. The exercise interventions included in this review varied greatly and included strength training, yoga, walking, cycling, tai chi and qi gong. However, due to the small number of studies available, these authors were not able to evaluate the effect of different modes and intensities of exercise. Furthermore, studies of exercise in the preoperative and early postoperative stages were not included in the review. Therefore, it is not known whether exercise, when commenced before the end of active cancer treatment, would have additional benefit on physical function for those undergoing surgery.
While there is growing evidence on the beneficial effects of aerobic exercise, resistance exercise training has received much less attention.3–6 It is thought that resistance exercise training could act to aid recovery of muscle function.7 It has long been established that resistance exercise training is effective in stimulating muscle anabolic processes and increasing muscle strength.8 It may even counteract some of the metabolic pathophysiology associated with cachexia.9 Furthermore, it can be performed with very little equipment and space and while patients are bed-bound in hospital or at home. Although there have been previous systematic reviews of the effects of exercise training, there have not been any that have specifically focused on resistance training.
Previous reviews, relating to exercise training for patients with cancer, have mostly focused on specific outcomes such as fatigue and quality of life,4 5 and most have centred on specific types of cancer.10–17 Galvão and Newton18 published a review of exercise intervention studies for all cancers and a meta-analysis of exercise training interventions. However, their review included a heterogeneous group of studies including some that were not randomised or had no control group. Quality systematic reviews require critical appraisal of the quality of the reviewed studies and share accurate descriptions of the design, delivery and interpretation of what was done in the study. In some instances detailed description of these aspects is not available.19
One of the main challenges in studying the effects of a resistance exercise programme on physical function in cancer surgery patients is in identifying an appropriate outcome measure. The review by Mishra and colleagues found no significant improvement in physical function as evaluated using self-report questionnaires, but they did not measure any index of physical performance.2 Therefore, our aim was to undertake a systematic review of the literature on interventional studies investigating the effects of preoperative and postoperative resistance exercise training on recovery of physical function in patients undergoing abdominal surgery for cancer. The findings will provide clinicians and investigators a basis to choose exercise interventions for use in clinical practice or for future research.
The Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines on systematic reviews were followed for this review.20 Figure 1 summarises the review process.
The Cochrane Library, EBSCO (SPORTDiscus and Cumulative Index to Nursing and Allied Health Literature (CINAHL)), PLOS, PubMed (Medline) and Elsevier (Scopus) electronic databases were searched up to and including December 2014. The search strategy used was exercise OR training OR isometric OR static OR isotonic OR concentric OR eccentric OR resistance OR strengthening exercise OR exercise therapy OR circuit training OR rehabilitation OR physiotherapy; AND neoplasm OR abdominal cancer OR stomach cancer OR gastric cancer OR bowel cancer OR pancreatic cancer OR colorectal cancer OR colon cancer OR rectal cancer OR gastrointestinal cancer OR ovarian cancer OR endometrial cancer OR cervical cancer OR renal cancer OR kidney cancer OR bladder cancer OR uterine cancer OR gynaecological cancer OR urological cancer; AND abdominal surgery OR laparotomy OR laparoscopy OR laparoscopic OR anterior resection OR colectomy OR hemicolectomy; AND clinical trial OR random controlled trial OR quasi-randomised controlled trial OR controlled trial OR comparative trial.
All titles and abstracts generated by the search were independently screened for inclusion by three authors (DS, FH and KC). Disagreement between authors was discussed and consensus was reached. The search was restricted to English language and were included if the following criteria were met: (1) randomised, quasi-randomised or controlled trial study design comparing a muscle-strengthening exercise intervention (ie, exercise using resistance to induce muscular contraction) ± other therapy with a comparative group; (2) included adult participants (≥18 years) who underwent abdominal surgery (ie, surgery pertaining to the contents of the abdominal cavity, its walls and orifices) for cancer; and (3) included muscle strength, physical function, self-reported functional ability, range of motion and/or performance-based test as an outcome measure.
Participants’ age, gender, diagnosis, surgical procedure and sample size were extracted from the included studies, along with a description of the exercise intervention, including muscle group or groups exercised, contraction effort, number of repetitions and frequency, length of programme, length of follow-up, group or individual exercise programme, home or supervised exercise programme, and timing of programme (presurgery and/or postsurgery).
Data synthesis and analysis
The aim of this review was to evaluate the effect of resistance muscle strengthening on physical function in people undergoing abdominal surgery for cancer. For each study, means and SD of outcomes focused on physical function were extracted. Outcomes relating directly to surgery, length of stay, infection and other postsurgical complications were not considered in this review.
Assessment was made of the outcome measures for physical function that were used in different studies, before progression to pooling of data for analysis of the most common outcome measure. Treatment effect of individual studies is reported as mean difference and 95% CIs, and the data summarised.
Risk of bias was assessed with the Physiotherapy Evidence Database (PEDro) scale.21 Items assessed included exclusion criteria, procedures for group allocation and missing data, participant, therapist and assessor blinding, and reporting of results. Studies were then graded using the Cochrane Reviews Grading of Recommendations Assessment, Development and Evaluation criteria.21 22
Search strategy and selection of articles
The initial search strategy resulted in 588 publications. Following screening of titles and abstracts, 24 studies met the inclusion criteria and were accessed for review of the full text, of which 2 eligible studies23 24 were included in the review (see table 1 and figure 1). Full-text studies were excluded for a number of reasons: (1) the study lacked a well-defined muscle-strengthening intervention (n=18); (2) the study did not include patients undergoing abdominal surgery for cancer (n=4); and (3) the study did not use a physical function outcome measure (muscle strength, self-report questionnaires or physical performance measures).
Description of included studies
Characteristics of the participants and intervention of the two included studies are presented in table 1. Both were small (n=42 and 31) single-centre studies investigating participants undergoing abdominal surgery for excision of cancer of the colon. Dronkers et al 23 investigated the effect of a preoperative exercise programme on preoperative outcomes, and Ahn et al 24 investigated the effect of a postoperative exercise programme on short-term outcomes at discharge from hospital. The participants in the preoperative study were aged 10–15 years older than those in the postoperative study. In terms of gender, a higher proportion of men participated in both studies.
The preoperative intervention of Dronkers et al 23 included a twice-weekly supervised exercise programme and a home-based programme of walking or cycling for a minimum of 30 min per day for 2–4 weeks before admission for surgery. In addition to a single set of resistance strengthening exercises of the leg (8–15 repetitions at 60%–80% of the one repetition maximum), the programme included inspiratory muscle training, aerobic training at 55%–75% max heart rate (HR) or perceived exertion of 11–13 Borg Scale for 20–30 min, and functional activities. A full description of the resistance exercise was not published. Three of the intervention groups (13.6%) did not complete the study with their data analysed as intention to treat.
The postoperative intervention of Ahn et al 24 comprised a twice-daily 15 min supervised exercise programme performed by the participant until discharge from hospital (mean 8.87±2.28 days). In addition to resistance strengthening exercises of the chest, shoulder, arm, thigh and calf leg, the programme included stretching exercises for the neck, shoulder, wrist, ankle and pelvis, core trunk exercises and ambulation. In terms of the strengthening exercises, resistance was applied manually by the therapist initially and then using 1 lb free weights. During phase 2, one set of 10 repetitions was performed, and in phase 3, three sets of 12 repetitions were performed. Because these studies used different outcome measures, it was not possible to pool the data in order to analyse mean changes in physical function outcomes.
Risk of bias of included studies
The methodological quality of the two included studies was rated as moderate according to the GRADE criteria, that is, randomised studies with unclear bias or well-designed observational studies with large, consistent and precise estimates of the magnitude of an intervention effect. Difficulty in blinding trial participants and therapists to the intervention meant studies were not rated as high. Both studies scored 8 out of 11 on the PEDro scale. Block randomisation using prepared envelopes, stratified by age (60–70 and >70) by someone independent of the study, was used in the preoperative study. Randomisation, at a 1-to-1 ratio, into study groups via minimisation to balance prognostic factors between groups (age and gender) was used in the postoperative study. In the preoperative study the gender distribution was similar in the control and intervention groups; however, in the postoperative study, twice as many men were randomised to the exercise group than the control group despite the minimisation procedures to balance gender between groups. In relation to the description of the intervention, some information was lacking in terms of equipment and methodology with regard to the aerobic and functional activity components of the preoperative intervention.
Effect of strengthening exercise
Preoperative muscle strengthening
The mean difference and upper and lower 95% CI between the control and intervention group in the study by Dronkers et al 23 are shown in table 2. The five-session preoperative exercise programme had no significant effect on preoperative Timed Up and Go, chair rise time test, self-reported physical activity, quality of life and fatigue. Statistical power for six out of the seven measures was unacceptably low. Effect on postsurgery outcomes was not evaluated.
Postoperative muscle strengthening
The mean difference and upper and lower 95% CI between the control and intervention groups in the study by Ahn et al 24 are also shown in table 2. The inpatient postoperative exercise programme had no significant effect at time of discharge from hospital on ability to balance on one leg, number of sit-to-stands in 30 s or aerobic capacity (estimated from performance of the Tecumseh step test). Statistical power was not sufficient to allow any conclusion for or against the preferential use of any of the outcome measures that were used in this trial. Effect on functional recovery postdischarge from hospital was not evaluated.
Our aim was to systematically review the evidence on the effectiveness of preoperative and postoperative strengthening exercises on short-term and long-term recovery of physical function in patients undergoing abdominal surgery for cancer. Two studies were included, which represented 73 patients (48 men and 25 women) undergoing abdominal surgery for cancer. One exercise programme was undertaken preoperatively and the other postoperatively until discharge from hospital. This represents insufficient evidence to determine whether this type of preoperative or postoperative resistance muscle-strengthening exercise programme improves or negatively affects functional outcomes in patients undergoing abdominal surgery for cancer.
The study by Dronkers et al,23 which investigated a preoperative exercise programme, was statistically underpowered with the exception of the functional measure derived from the quality of life scale. The programme included resistance strengthening of the lower limb muscle extensors and was performed for a mean of five sessions. This may not be sufficient to provide an adequate training stimulus to significantly increase muscle strength. Indeed, guidelines published by the American College of Sports Medicine recommend resistance exercise 2–3 times per week with 2–4 sets of 10–15 repetitions to improve strength in middle-aged and older persons.25
In contrast, the study by Ahn et al 24 investigated a postoperative exercise programme, but this was also statistically underpowered and provides inconclusive evidence in support of the intervention and the use of particular outcome measures. The intervention was different from that of Dronkers et al 23 in that it used a progressive resistance programme involving the upper and lower limbs, together with stretching, functional balance strengthening and walking. Also, isometric strengthening exercises were commenced early postoperatively while the patient was still in bed and then progressed to ‘resistance-through-range’ strengthening as well as balance strengthening exercises, until discharge from hospital. The mean hospital length of stay, for the study of Dronkers et al 23 was 7 days for the control group, and in the exercise group it was 8 days. Similarly, for the study by Ahn et al,24 it was 8 days of exercise, and it is likely that this will not provide an adequate training stimulus to significantly increase muscle strength and function.
There are some limitations to our review. We limited our inclusion by study design, only including randomised or quasi-randomised studies where there was a clear resistance muscle strengthening component as part of an exercise programme. It is possible that other studies have included muscle-strengthening exercises or functional exercises that will have an effect on muscle strength that have not been included in this review due to our inclusion criteria, and we advocate the Consensus on Exercise Reporting Template guidelines for reporting exercise intervention studies.26 The two studies included in the review recruited almost twice as many men as women, and the results may not reflect the general population. Future studies should focus on detailed descriptions of the exercise intervention, consistent outcome measures and longer intervention and follow-up times.27
Our systematic review suggests that the use of resistance exercise interventions for recovery of physical function in patients undergoing abdominal surgery for cancer must be considered with caution. The small number of included underpowered studies and the inability to pool the results due to the heterogeneity of outcome measures mean that there is a lack of evidence for or against the use of this type of resistance muscle-strengthening exercise programmes to improve functional outcomes in these patients. While the studies give encouraging preliminary evidence that muscle-strengthening programmes may be feasible for abdominal cancer surgery patients, further large-scale, well-designed clinical trials are required to determine whether this type of exercise intervention is beneficial for this group of patients.
Contributors DS, FH, KC performed the systematic review. DS, FH, KC, AB, MG, RPH, MH, IH, DPL, TPH, CS, IS, LT, WH and HA contributed to study design, data analysis and interpretation and preparation of the manuscript.
Funding The study was funded by an NIHR Research for Patient Benefit grant (PB-PG-0613–31107).
Competing interests None declared.
Patient consent Not required.
Provenance and peer review Not commissioned; externally peer reviewed.