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The Canadian Bandaging Trial: Evidence-informed leg ulcer care and the effectiveness of two compression technologies



Objective: To determine the relative effectiveness of evidence-informed practice using two high compression systems: four-layer (4LB) and short-stretch bandaging (SSB) in community care of venous leg ulcers. Design and Setting: Pragmatic, multi-centre, parallel-group, open-label, randomized controlled trial conducted in 10 centres. Cognitively intact adults (≥18 years) referred for community care (home or clinic) with a venous ulceration measuring ≥0.7cm and present for ≥1 week, with an ankle brachial pressure index (ABPI) ≥0.8, without medication-controlled Diabetes Mellitus or a previous failure to improve with either system, were eligible to participate.


Consenting individuals were randomly allocated (computer-generated blocked randomization schedule) to receive either 4LB or SSB following an evidence-informed protocol. Primary endpoint: time-to- healing of the reference ulcer. Secondary outcomes: recurrence rates, health-related quality of life (HRQL), pain, and expenditures.


424 individuals were randomized (4LB n = 215; SSB n = 209) and followed until their reference ulcer was healed (or maximum 30 months). An intent-to-treat analysis was conducted on all participants. Median time to ulcer healing in the 4LB group was 62 days [95% confidence interval (CI) 51 to 73], compared with 77 days (95% CI 63 to 91) in the SSB group. The unadjusted Kaplan-Meier curves revealed the difference in the distribution of cumulative healing times was not significantly different between group (log rank χ2 = 0.001, P = 0.98) nor ulcers recurrence (4LB, 10.1%; SSB, 13.3%; p = 0.345). Multivariable Cox Proportional Hazard Modeling also showed no significant between-bandage differences in healing time after controlling for significant covariates (p = 0.77). At 3-months post-baseline there were no differences in pain (no pain: 4LB, 22.7%; SSB, 26.7%; p = 0.335), or HRQL (SF-12 Mental Component Score: 4LB, 55.1; SSB, 55.8; p = 0.615; SF-12 Physical Component Score: 4LB, 39.0; SSB, 39.6; p = 0.675). The most common adverse events experienced by both groups included infection, skin breakdown and ulcer deterioration.


The Canadian Bandaging Trial revealed that in the practice context of trained RNs using an evidence-informed protocol, the choice of bandage system (4LB and SSB) does not materially affect healing times, recurrence rates, HRQL, or pain. From a community practice perspective, this is positive news for patient-centred care allowing individual/family and practitioner choice in selecting compression technologies based on circumstances and context.

Trial registration Identifier: NCT00202267

Peer Review reports


Community care of individuals with chronic wounds has become an important issue for home care authorities as they deal with a growing demand for wound care in the community. In Canada, the impact of caring for individuals with leg ulcers is only now being recognized due to the increased pressure on the home care environment caused by nursing shortages and tightening of healthcare budgets [1]. In the UK, Luker and Kenrick estimated that up to 13% of community nurses' time was spent in leg ulcer care [2], and more recently NHS leg ulcer treatments (bandages and dressings) were reported to cost £300-600 million per annum in England [3]. Our previous work in one Ontario region demonstrated that 192 people with leg ulcers received on average 12 homecare visits per month, and expenditures for supplies and nursing visits were estimated at $1.3 million per annum [4]. While there are no national data, it is reasonable to believe that leg ulcer care in Canada consumes hundreds of millions of dollars annually.

For individuals with leg ulcers, the condition has a profound impact on quality of life [57]. It is chronic, may take years to heal, 66% of individuals experience recurring ulceration and 45% have a history dating back ten years [8]. Studies using the Short Form (36) Health Survey (SF-36®) instrument to measure health-related quality of life (HRQL) have demonstrated that individuals with leg ulcers have lower mean scores than Canadian population norms [911]. Multiple studies document the discomfort with venous leg ulcers, with the prevalence of pain estimated to be between 48-96 percent [1223].

Best practice recommendations, supported by high level evidence, indicate that the most effective treatment for venous leg ulcers is high compression bandaging [2436] applied by well-trained healthcare professionals [3740]. However the initial Cochrane review had little evidence about the comparative effectiveness of the available types of high compression [41, 42]. This is an issue given there are substantive clinical, practical and economic differences in the classes of compression technology. Early trials of bandaging systems were methodologically weak due to factors such as being underpowered [25]. By 2000 the VenUS I trial [43] was underway in the UK to determine the relative effectiveness of two of the most popular high compression systems, 'four-layer' (4LB: strictly speaking a four-component bandage system) and short-stretch bandaging (SSB). As the effectiveness and costs of the compression systems are likely related to service delivery and bandaging skills, we realized that the UK trial would not be able to completely answer the question for the Canadian healthcare system. In 2002, a Canadian team, working with the leads of VenUS I (Drs. E.A. Nelson and N. Cullum), set out to conduct a concurrent trial to provide more data about clinical and cost-effectiveness of the high compression technologies since the results of available published trials (Duby, Scriven, Partsch: n = 226 participants) were equivocal [4446]. The Canadian trial, funded by the Canadian Institutes of Health Research (CIHR), was launched in 2004. Canadian homecare authorities were interested in a comparison of these commonly available bandaging systems based on a health services outcome, i.e. a 4-week difference in healing based on known costs of delivering the technologies in Canada. Thus, the purpose of this Canadian trial was to compare healing rates between two bandaging technologies, specifically: 1) determine if healing occurred at least 4 weeks earlier with SSB vs. 4LB; 2) assess related outcomes such recurrence rates, HRQL, pain, and adverse events over a one-year follow-up; and 3) identify potential baseline factors that predict healing.


The Canadian Bandaging Trial (CBT) was a multi-centre parallel-group, randomized controlled trial conducted in 10 centres in three provinces. Recruitment involved all individuals referred for community wound care services (homecare or nurse clinic) with new, existing or recurrent venous ulceration. Ethics approval for the trial was received from Queen's University Research Ethics Board, Kingston Canada (REB# NURS-140-03).

Study population

Individuals in community care were eligible for inclusion based on the following: adult (≥18 years), English-speaking or with access to translation, able to provide written informed consent, clinical presentation of venous insufficiency with an ankle brachial pressure index (ABPI) ≥0.8, and a leg ulcer with minimum duration of one week that measured at least 0.7 cm in any one dimension. After conducting a small pilot study, the eligibility criterion was changed from having an ulcer of at least 1 cm in any one dimension to 0.7 cm since it was found that too many individuals were being excluded that would have normally been treated with compression. Exclusion criteria were: medication-controlled diabetes mellitus, failure to improve over a 3-month period with either bandaging system prior to the trial, previous enrollment in the trial, and cognitive impairment.


All participating study sites were supported to develop their evidence-informed protocols for venous leg ulcer management during the preliminary and pilot phase of this enquiry [47]. Protocol development is described elsewhere [10, 48] but in brief, the local protocol was developed from guideline recommendations using a systematic 10-step adaptation process [49, 50]. Training was provided on the use of both SSB and 4LB technologies and site investigators conducted random audits of protocol delivery to ensure ongoing compliance.

Upon referral for leg ulcer care, individuals received a comprehensive, standardized clinical assessment by specially trained registered nurses (RNs). Individuals were informed of the study and invited to participate. Consenting individuals were randomly allocated by research staff, available 7 days/week over day and evening hours via a remote telephone service, to receive one of two high compression technologies; 4LB or SSB. A computer-generated blocked randomization schedule was used to allocate participants. Allocation was sealed in opaque, serially numbered envelopes. Randomization was controlled centrally from the university research office and stratified by centre, ulcer size (≤ 5 or > 5 cm2), ulcer duration (≤ 6 or > 6 months), and whether they had a previous ulcer, as these factors may influence healing rates [51, 52]

Intervention: High Compression Bandages

The 4LB system (control arm) was originally developed in the UK (Charing Cross Hospital) [53]. The commercial product widely used in Canada is Profore® (Smith & Nephew Medical Ltd.). Precise components of the 4LB depend on the ankle circumference [54]. Bandages can remain in situ for up to one week (e.g. if minimal wound exudate) with bandages being changed when required. Bandages were discarded after each use.

Cotton short-stretch bandages (SSB) Comprilan® (Beiersdorf-Jobst, Inc.) were applied using the modified Putter technique [55]. Varying widths of bandage, e.g., 8 cm, 10 cm and 12 cm, were used according to the width of the limb. A layer of orthopedic wool padding was applied beneath the bandage to distribute the compression evenly. Bandages were changed when required, as determined by the attending nurse. Participants washed and reused the short stretch wherever possible. For both 4LB and SSB, bandaging continued until the affected limb completely healed.

Data Collection and Management

Baseline data collection began at the time of initial assessment through interview, clinical assessment and chart review. Socio-demographic and clinical assessment, and measurements of primary and secondary outcomes were completed at baseline. Monthly, the participant's reference ulcer (defined as the largest ulcer at randomization) was traced onto acetate to measure the wound surface. Adverse events and referrals to specialists were recorded. A Participant Satisfaction Survey was administered one month post-baseline or at healing (whichever came first) to capture patients' perspectives of their allocated bandage treatment and health services received. Economic data were also recorded and a report is in preparation. Study participants were followed until their reference leg ulcer was healed or for a maximum of 30 months until March 31, 2009. After healing, follow-up continued for one year to assess durability of healing.

Quality assurance procedures [5658], included a detailed protocol manual for the site study teams and a log record to track the status of participants throughout the duration of the trial. Participants were assigned a unique identifying number used on study documentation to ensure confidentiality. Withdrawals from either arm of the study were monitored and reasons documented. Case records (10%) were randomly selected to assess data entry accuracy every 3 months.

Primary and secondary outcomes

The primary endpoint was time (weeks) to complete healing of the reference ulcer. A healed ulcer was defined as fully epithelialized; no scab remaining, and no drainage. The point of healing was confirmed by: 1) serial tracing of the leg ulcer and 2) photographing the ulcer at the time of healing which was verified by a remote researcher, masked to allocation (EAN). Secondary outcomes included recurrence rates, HRQL, pain, and expenditures over a one-year follow-up. Adverse events related to the bandages were tracked.

Sample size calculation

Our trial was adequately powered to detect whether the median healing time of SSBs is 4-weeks shorter than that of 4LBs. Sample size calculation was based on time-to-healing. Using local research on leg ulcer healing and service delivery [10, 48], and the largest available trial at the time comparing 4LB and SSB (Partsch 2001, n = 112) [45] it was postulated that the median time to healing with 4LB would be 16 weeks. To determine the minimally important difference (MID) that would warrant changing from 4LB to SSB as first-line therapy, practitioners and homecare administrators were consulted. The consensus was that to opt for SSB over 4LB would be justified if no additional nursing visits were required. Local experience showed that during the first month of treatment with 4LB, on average 2.5 visits/week were required, followed by ~1.5 visits/week until healing occurred. For SSB, on average 3 visits/week were required for the first month, then 2 visits/week thereafter until healing. Assuming a median time-to-healing with 4LB of 16 weeks, an average 28 nursing visits would be required. Given the higher frequency of nursing visits with SSB, 28 nursing visits would occur over 12 weeks of care. Therefore, for SSB to be considered an attractive option for Canadian homecare regions, it would have to demonstrate a median time-to-healing of 12 weeks or less, thus a 4-week difference in healing was identified as the MID in time-to-healing.

With a median difference of 4-weeks in healing time (baseline, 16 weeks), 80% power, and a 5% level of significance, it was determined that 207 participants would be required in each arm (414 total) allowing a 5% loss to follow-up. A review of our previous studies' recruitment and activity status data revealed that the lost to follow-up rate was slightly higher than 5% therefore the sample size was increased to 424 participants.


The primary analysis was based on 'intention-to-treat'. Index scores were generated for the Short Form McGill Pain Questionnaire (SF-MPQ), and SF-12® Physical Component (PCS) and Mental Component Summaries (MCS) were derived using the Quality Metric SF Health Outcomes™ Scoring algorithm [59, 60]. Individual missing items for the SF-12® were imputed using assignment of mean score (AMS) [61, 62]. Following a descriptive analysis, the baseline and clinical characteristics of the 4LB and SSB groups were compared. The primary outcome, time-to-healing of the reference ulcer, was compared between individuals randomized into the two groups. Kaplan-Meier survival curves were constructed for the two groups. The statistical significance of the difference between the two bandaging groups was tested using log rank tests. Cox proportional hazards modeling was used to identify baseline demographic and prognostic indicators of time to healing, in addition to assessing the effect of treatment group. Indicators included geographic location, sex, age, living situation, co-morbidities, pain, mobility, ankle flexion, edema, ABPI, ulcer episode, ulcer duration, and ulcer size [51, 6367]. Factors that predicted healing in bivariable analyses (p ≤ 0.15) were included in the multivariable analysis. The assumption of proportionality of hazards was tested for all factors using log-minus-log plots. The chi-square test was used to compare the proportion of ulcers that recurred in the two groups. Adverse events and participants' perceptions of the bandaging systems were compared using chi-square tests. All analyses were completed using IBM© SPSS© Statistics software (Version 19 for Windows).


Over a 50 month recruitment period (January 2004 - March 2008), 2820 individuals referred for community leg ulcer care were screened (see Figure 1). Many of those referred for care did not have purely venous leg ulcers, thus the trial procedures required a major screening effort. For example more than half screened had diabetic or arterial issues (hence mixed ulcer aetiology) but there was no way of knowing this prior to examination by the nurse and it was vital to maintain an evidence-informed clinical assessment consistently. Consequently only 520 were assessed as eligible with 82% of those (n = 424) agreeing to participate.

Figure 1
figure 1

CBT Recruitment and Randomization.

Of the 424 trial participants, 215 were randomized to receive 4LB, and 209 to receive SSB. There were no differences on admission between the participants randomized to either bandage on their socio-demographic, circumstance of living, HRQL or clinical characteristics (Table 1).

Table 1 Baseline and clinical characteristics of the study population by intervention group

Mean age of the participants was 65 years with slightly more women (54%) than men and the majority being English-speaking (91%). Most participants were fully mobile and lived with others. For more than half (55%), this was their first episode of ulceration and the median ulcer duration at baseline was nearly 12 weeks. PCS baseline scores were much lower than the age- and sex-adjusted Canadian norms (39.1 vs. 51.7); indicating that those with venous leg ulcer had much poorer physically oriented HRQL. However, mental HRQL was better, with MCS scores comparable to Canadian norms (51.4 vs. 50.5) [68]. There were no differences in key aspects of the clinical care received by the two groups (Table 2).

Table 2 Adherence to the Evidence-Informed Protocol


The median time to reference ulcer healing in the 4LB group was 62 days [95% confidence interval (CI) 51 to 73], compared with 77 days (95% CI 63 to 91) in the SSB group. Figure 2 shows the unadjusted Kaplan-Meier curves. The difference in the distribution of cumulative healing times between the two groups was not significantly different (log rank χ2 = 0.001, P = 0.98).

Figure 2
figure 2

Kaplan-Meier curves showing proportion of ulcers healed by treatment with four-layer and short-stretch bandages.

Factors affecting time-to-healing

Several factors were associated with time-to-healing in bivariable analysis, however in multivariable analysis, only age, ulcer size at baseline and geographic location, predicted time-to-healing (Table 3).

Table 3 Treatment effect on time to healing adjusted for explanatory co-variates

Secondary Outcomes

The proportion of people who experienced a recurrence of their reference ulcer after healing during the one year follow-up was relatively small (10% for 4LB, 13% for SSB; no statistically significant difference). At 3-months post-baseline there were no differences in pain (no pain: 4LB, 22.7%; SSB, 26.7%; p = 0.335) or HRQL outcomes (SF-12 MCS: 4LB, 55.1; SSB, 55.8; p = 0.615; SF-12 PCS: 4LB, 39.0; SSB, 39.6; p = 0.675) and little improvement from the group's low baseline values on the PCS.

Adverse Events

Adverse events were tracked up to 30 months. In both groups the most common adverse events were infection, skin breakdown and ulcer deterioration with 29% of the 4LB group and 33% of the SSB group experiencing an adverse event (not significant, Table 4). The SSB group took 2 weeks longer to heal thus, were 'at risk' of adverse event occurrence for a longer period of time.

Table 4 Adverse events potentially related to compression bandages (max. 30 months)

Participant Satisfaction Survey

Analysis of participants' perceptions revealed 41% of the 4LB group reported experiencing a problem with their bandaging compared to 28% of those allocated SSB (p = 0.01). In particular, there was significantly greater discomfort with the 4LB (p = 0.05), and participants felt it was often applied to tight (p < 0.01). The majority in both groups reported being very satisfied with the nurses' skills in applying the bandage, and reported that the nurses provided verbal and written information regarding ulcer care and prevention (Table 5).

Table 5 Participant's perceptions at 1-month post-baseline of compression bandages and care received


The Canadian Bandaging Trial was adequately powered to detect a minimally important difference of 4-weeks in median healing time between 4LBs and SSBs. We put much emphasis on testing the compression technologies within an evidence-informed approach to care i.e. a protocol for venous leg ulcer assessment and management, well developed training procedures, and well prepared RNs. With these elements in place, results from our trial suggest that the two compression bandaging technologies tested are not different in terms of time-to-healing, recurrence rates, HRQL, or pain. However, individuals were less satisfied with 4LB, with more reporting problems with the bandaging system.

These healing results should be viewed in the context of all the trials making this comparison. O'Meara et al. [33] conducted a meta-analysis of individual patient data to evaluate the intervention effect of 4LBs relative to SSBs. They concluded that venous leg ulcers in patients treated with 4LBs heal faster, on average, than those treated with SSBs; and the benefits were consistent across patients with differing prognostic profiles. In contrast, our trial (the largest to date), put much emphasis on other aspects of venous leg ulcer care, namely an evidence-informed protocol of care and well-prepared RNs in administering these bandaging systems. With these elements of care in place, there were no differences between the technologies except that individuals may have more problems with 4LBs.

In the O'Meara meta-analysis, the intervention effect estimate from the UK VenUS I was weighted heavily towards the pooled effect estimate (i.e. 63% from this trial among five others). As the only other large scale trial comparable to this Canadian RCT, the UK VenUS I showed that with 4LBs there was a shorter healing time. We were unable to replicate this finding despite comparable sample sizes. Several factors may be contributing to this difference. Nurse wound-care teams in Canada have more training and experience in both technologies. The SSB was newly introduced to UK primary care just prior to their trial and there was a higher withdrawal rate in the SSB arm of the VenUS I trial. The UK authors [43] state they "investigated the introduction (their emphasis) of a high-level compression bandage system into a setting where an acceptable mode of compression was already in use" and a reasonable conclusion is that short stretch is "a useful alternative" (pg. 1298). Based on the experience from the UK trial, our Canadian sites had initial and ongoing training including quality checks to ensure adherence to the evidence-informed assessment and management protocol for either bandage. In the Canadian trial, the nurses may have been more confident and competent in delivery of both bandage systems thus reducing operator experience/preference as a source of bias. Another context factor may be important. Canadian site teams actively participated in the development of the protocol in their local settings to make it as seamless as possible within their normal delivery of care. Based on best practice recommendations, they carefully constructed an approach to adhere to key aspects of leg ulcer assessment and management. For example, the initial comprehensive assessment may have been carried out by specially trained nurses in the home with portable equipment whereas at some sites, it was more feasible at a designated clinic location where a wound expert and equipment were centralized.

In considering the site differences our team thought there were factors that should be further explored in a future study. Although we tracked key elements of the evidence-informed protocol (comprehensive assessment and use of compression), and all sites delivered these recommendations, there may be subtle differences contributing to healing rates. For example, some sites were newer and less experienced and may have been less supported regionally in the delivery of care. As well, because the trial was conducted in a large number of jurisdictions the referral and wait-times may have varied influencing the time to assessment which may have affected outcomes. Unfortunately we did not have data to drill down and explore these issues in this trial.

Lastly, healing in the Canadian trial for 4LB was 62 days compared to 77 days with SSB - both much shorter than the UK study population. This may be partly explained by their healing outcome being complete healing of all ulcers not just a reference ulcer. Nevertheless in examining healing over time compared to previous trials (Table 6), the Canadian group had higher proportions healed at 12, 16, 24 and 52 week time-points for both SSB and 4LB except SSB at 16 weeks in the Partsch study [45].

Table 6 Healing Rates at 12, 16, 24, and 52 weeks in trials comparing four-layer and short-stretch bandages

From this large Canadian trial the key message regarding healing is 'when delivered in the practice context of trained RNs and an evidence-informed protocol choice of bandage system (4LB and SSB) does not materially affect healing times, recurrence rates, HRQL, or pain'. Expenditures and resource use should be another consideration. According to results from the UK VenUS I trial on average, 4LB was associated with greater health benefits and lower costs than SSB. In a separate cost-effectiveness analysis, we are addressing whether this finding holds in the community care setting in Canada.

Limitations of the Study

This trial has some limitations that should be considered when interpreting the results. It might be considered a limitation that nurses providing care were involved in collection of outcomes data. Blinding the nurse to the compression technology was not feasible and once bandages were applied it would have been excessively intrusive (and monumentally expensive) to remove them solely for the purpose of an outcome assessment. However, our small team of dedicated specially trained nurses, ensured expert, quality outcome assessments by measuring healing in a rigorous and consistent manner and this was validated by photo assessment by an expert remote from the site of care and who was blinded to allocation group. The results may not be generalizable beyond the study population but since the trial took place in multiple sites in three provinces (Ontario, Manitoba and Saskatchewan) that included both urban and rural locations, and culturally mixed populations this should increase the likelihood of generalizability.


This RCT is the largest community wound trial conducted in Canada and the largest trial evaluating these two compression technologies internationally. The trial's pragmatic approach emulated the usual delivery of assessment and care with healing outcomes confirmed by an individual blinded to study arm. The comparative effectiveness of SSB and 4LB systems in healing ulcers will be more precisely addressed when the Canadian trial is added to the meta-analysis from the Cochrane Wounds Group [33] recognizing that context is important and contributing to the sub-groups analysis of trial result by country of study.


Internationally this is the largest reported trial on bandaging systems and should immediately contribute to body of evidence at the Cochrane Library and elsewhere. We were unable to replicate the results of the largest UK trial, VenUS I. Within the Canadian context, the implications are that homecare authorities and community providers can expect similar healing, quality of life, pain and recurrence results from 4LB and SSB compression technologies. It is vital to note that these results are dependent on compression bandages being delivered within an overall approach of evidence-informed care by well-prepared providers - this cannot be overstated. From a community practice perspective, these results are positive news as it allows individual/family and practitioner choice in selecting a technology class based on the circumstances and context. This means being better able to deliver patient-centred care. Given either bandage is effective, the choice can be made with individuals and practitioners based on bandage preference. The bandage systems require different self-care ability and supports, levels of nursing time, variation in individual comfort, and preparation and teaching. From a policy perspective, the organization of care can be adjusted to account for the different requirements with either bandaging technology. If delivery of only one, or the other, is possible because of local factors and resources, it is important to know that the expectation of healing would not be compromised whichever is selected. Several next steps to advance leg ulcer care emerge from this Canadian study, including:

  • Conducting a meta-analysis to include this large Canadian trial to the existing reports on SSBs and 4LBs to increase power and add another country's experience

  • Analyzing the economic implications of the Canadian trial for SSB and 4LB in order to position the effectiveness results for planners and policy makers.

  • Addressing the deficit in evidence for people with diabetes who have leg ulcers. Although typically excluded from compression trials, in practice compression is used with this group. Healing rates and other outcomes are unknown (people with diabetes comprised ~24% of those excluded in this trial). We suggest the conduct of a pragmatic trial using a similar approach (qualified team, evidence-informed protocol).

  • Research to integrate the multiple possible wound outcomes into administrative databases is needed to reduce the need for primary data collection for costly follow-up in large scale studies. In particular recurrence rates are clinically and administratively important but add enormously to trial costs. Issues include the organization, accessibility and quality of data currently collected in the community and home care environment. Chronic wounds e.g. leg ulcers (arterial and venous), diabetic and pressure ulcers, are increasingly being cared for in the community. Future wound studies would all be aided by improved administrative tracking of outcomes.

  • Given the self-management aspects with compression bandages, research into the supportive care needed for self-management is an important area for enquiry.

In conclusion the Canadian bandaging trial adds new information to the international literature focused on the management of leg ulcers in the community. Two commonly available technologies, short-stretch and four-layer bandages, are viable options that result in similar healing, recurrence, HRQL and pain outcomes when delivered by trained nurses using an evidence-informed protocol.

Other information


This trial is registered at, identified by number NCT00202267.


The full trial protocol is not publicly available at this time.


  1. Shannon RJ: A cost utility evaluation of best practice implementation of leg and foot ulcer care in the Ontario Community. Wound Care Can. 2007, 5: S53-S56.

    Google Scholar 

  2. Luker KA, Nurs B, Kenrick M: Towards knowledge-based practice; an evaluation of a method of dissemination. Int J Nurs Stud. 1995, 32: 59-67. 10.1016/0020-7489(94)00023-D.

    Article  CAS  PubMed  Google Scholar 

  3. National Health Service (NHS): Prescription Cost Analysis: England 2006. 2007

    Google Scholar 

  4. Friedberg EH, Harrison MB, Graham ID: Current home care expenditures for persons with leg ulcers. J Wound Ostomy Continence Nurs. 2002, 29: 186-192.

    PubMed  Google Scholar 

  5. Lindholm C, Bjellerup M, Christensen OB, Zederfeldt B: Quality of life in chronic leg ulcer patients. An assessment according to the Nottingham Health Profile. Acta Derm Venereol. 1993, 73: 440-443.

    CAS  PubMed  Google Scholar 

  6. Price P, Harding K: Measuring health-related quality of life in patients with chronic leg ulcers. Wounds: A Compendium of Clinical Research and Practice. 1996, 8: 91-93.

    Google Scholar 

  7. Persoon A, Heinen MM, van d, de Rooij MJ, van de Kerkhof PC, van AT: Leg ulcers: a review of their impact on daily life. J Clin Nurs. 2004, 13: 341-354. 10.1046/j.1365-2702.2003.00859.x.

    Article  PubMed  Google Scholar 

  8. Callam MJ, Harper DR, Dale JJ, Ruckley CV: Chronic ulcer of the leg: clinical history. Br Med J (Clin Res Ed). 1987, 294: 1389-1391. 10.1136/bmj.294.6584.1389.

    Article  CAS  Google Scholar 

  9. Franks PJ, McCullagh L, Moffatt CJ: Assessing quality of life in patients with chronic leg ulceration using the Medical Outcomes Short Form-36 questionnaire. Ostomy Wound Manage. 2003, 49: 26-37.

    PubMed  Google Scholar 

  10. Harrison MB, Graham ID, Lorimer K, Friedberg E, Pierscianowski T, Brandys T: Leg-ulcer care in the community, before and after implementation of an evidence-based service. Canadian Medical Association Journal. 2005, 172: 1447-1452. 10.1503/cmaj.1041441.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Jull A, Walker A, Hackett M: Leg Ulceration and perceived health: A population base case-control study. Age Aging. 2004, 33: 236-241. 10.1093/ageing/afh087.

    Article  Google Scholar 

  12. Flaherty E: The views of patients living with healed venous leg ulcers. Nurs Stand. 2005, 19: 78, 80, 82-78, 80, 83.

    Article  Google Scholar 

  13. Hareendran A, Bradbury A, Budd J, Geroulakos G, Hobbs R, Kenkre J, Symonds T: Measuring the impact of venous leg ulcers on quality of life. J Wound Care. 2005, 14: 53-57.

    Article  CAS  PubMed  Google Scholar 

  14. Charles H: Venous leg ulcer pain and its characteristics. J Tissue Viability. 2002, 12: 154-158.

    Article  PubMed  Google Scholar 

  15. Hofman D, Ryan TJ, Arnold F, Cherry GW, Lindholm C, Bjellerup M, Glynn C: Pain in venous leg ulcers. J Wound Care. 1997, 6: 222-224.

    CAS  PubMed  Google Scholar 

  16. Nemeth KA, Harrison MB, Graham ID, Burke S: Pain in pure and mixed aetiology venous leg ulcers: a three-phase point prevalence study. Journal of Wound Care. 2003, 12: 336-340.

    Article  CAS  PubMed  Google Scholar 

  17. Nemeth KA, Harrison MB, Graham ID, Burke S: Understanding venous leg ulcer pain: results of a longitudinal study. Ostomy Wound Manage. 2004, 50: 34-46.

    PubMed  Google Scholar 

  18. Ryan S, Eager C, Sibbald RG: Venous leg ulcer pain. Ostomy Wound Manage. 2003, 49: 16-23.

    PubMed  Google Scholar 

  19. Walshe C: Living with a venous leg ulcer: a descriptive study of patients' experiences. J Adv Nurs. 1995, 22: 1092-1100.

    Article  CAS  PubMed  Google Scholar 

  20. McMullen M: The relationship between pain and leg ulcers: a critical review. Br J Nurs. 2004, 13: S30-S36.

    Article  PubMed  Google Scholar 

  21. Briggs M, Closs SJ, Ellis FR: Painful Leg Ulcers: Prevalence, Characteristics and the Impact of Treatment [abstract]. Wounds uk. 2003

    Google Scholar 

  22. Cooper SM, Hofman D, Burge SM: Leg ulcers and pain: a review. Int J Low Extrem Wounds. 2003, 2: 189-197. 10.1177/1534734603260556.

    Article  PubMed  Google Scholar 

  23. Noonan L, Burge SM: Venous leg ulcer: is pain a problem?. Plebology. 1998, 13: 14-19.

    Google Scholar 

  24. CREST: Guidelines for the assessment and management of leg ulceration. Recommendations for practice. Clinical Resource Efficiency Support Team. 1998

    Google Scholar 

  25. Fletcher A, Cullum N, Sheldon TA: A systematic review of compression treatment for venous leg ulcers. BMJ. 1997, 315: 576-580.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Kunimoto B, Cooling M, Gulliver W, Houghton P, Orsted H, Sibbald RG: Best practices for the prevention and treatment of venous leg ulcers. Ostomy Wound Manage. 2001, 47: 34-50.

    CAS  PubMed  Google Scholar 

  27. Moffatt CJ, O'Hare L: Venous leg ulceration: treatment by high compression bandaging. Ostomy Wound Manage. 1995, 41: 16-5.

    CAS  PubMed  Google Scholar 

  28. NHS Centre for Reviews and Dissemination: Compression Therapy for Venous Leg Ulcers. Effective Health Care Bulletin. 1997, 3: 1-12.

    Google Scholar 

  29. NZGG: Care of People with Chronic Leg Ulcers. New Zealand Guidelines Group. 1999, 1-46.

    Google Scholar 

  30. O'Brien JF, Grace PA, Perry IJ, Hannigan A, Clarke MM, Burke PE: Randomized clinical trial and economic analysis of four-layer compression bandaging for venous ulcers. Br J Surg. 2003, 90: 794-798. 10.1002/bjs.4167.

    Article  PubMed  Google Scholar 

  31. Scanlon E, McGinnis P: Effective Wound Health Care. JCN Online. 1998, 12: [Cited 2004 Aug 26]

    Google Scholar 

  32. Turner-Boutle M, Fletcher A, Sheldon T, Cullum N: Compression therapy for venous ulcers: a systematic review. Nurs Times. 1997, 93: 52-53.

    CAS  PubMed  Google Scholar 

  33. O'Meara S, Cullum NA, Nelson EA: Compression for venous leg ulcers. Cochrane Database Syst Rev. 2009, CD000265-

    Google Scholar 

  34. RCN Institute: Clinical Practice Guideline. The nursing management of patients with venous leg ulcers. Recommendations for assessment, compression therapy, cleansing, debridement, dressings, skin grafts and skin replacements, contact sensitivity, therapeutic ultrasound, laser, electrotherapy, topical negative pressure and pharmacological agents, training/education and quality assurance. 2006, Royal College of Nursing Institute

    Google Scholar 

  35. SIGN: Management of chronic venous leg ulcers: A National Clinical Guideline. Scottish Intercollegiate Guidelines Network. 2010, 26: 1-29.

    Google Scholar 

  36. RNAO Nursing Best Practice Guideline: Assessment and Management of Venous Leg Ulcers. 2004, Registered Nursing Association of Ontario

    Google Scholar 

  37. Nelson EA, Ruckley CV, Barbenel JC: Improvements in bandaging technique following training. J Wound Care. 1995, 4: 181-184.

    CAS  PubMed  Google Scholar 

  38. Logan RA, Thomas S, Harding EF, Collyer GJ: A comparison of sub-bandage pressure produced by experienced and inexperienced bandagers. J Wound Care. 1992, 1: 23-26.

    Google Scholar 

  39. Stockport JC, Groarke L, Ellison DA, McCollum C: Single-layer and multilayer bandaging in the treatment of venous leg ulcers. J Wound Care. 1997, 6: 485-488.

    CAS  PubMed  Google Scholar 

  40. Reynolds S: The impact of a bandage training programme. J Wound Care. 1999, 8: 55-60.

    Article  CAS  PubMed  Google Scholar 

  41. Cullum N, Nelson EA, Fletcher AW, Sheldon TA: Compression for venous leg ulcers. Cochrane Database Syst Rev. 2000, CD000265-

    Google Scholar 

  42. Cullum N: Compression for Venous Leg Ulcers. Medscape today. 2007

    Google Scholar 

  43. Nelson EA, Iglesias CP, Cullum N, Torgerson DJ: Randomized clinical trial of four-layer and short-stretch compression bandages for venous leg ulcers (VenUS I). Br J Surg. 2004, 91: 1292-1299. 10.1002/bjs.4754.

    Article  CAS  PubMed  Google Scholar 

  44. Duby T, Hofman J, Cameron D, Doblhoff-Brown D, Cherry G, Ryan T: A randomized trial in the treatment of venous leg ulcers comparing short stretch bandages, four layer bandage system, and a long stretch-paste bandage system. Wounds: A Compendium of Clinical Research and Practice. 1993, 6: 276-279.

    Google Scholar 

  45. Partsch H, Damstra RJ, Tazelaar DJ, Schuller-Petrovic S, Velders AJ, de Rooij MJ, Sang RR, Quinlan D: Multicentre, randomised controlled trial of four-layer bandaging versus short-stretch bandaging in the treatment of venous leg ulcers. Vasa. 2001, 30: 108-113. 10.1024/0301-1526.30.2.108.

    Article  CAS  PubMed  Google Scholar 

  46. Scriven JM, Taylor LE, Wood AJ, Bell PR, Naylor AR, London NJ: A prospective randomised trial of four-layer versus short stretch compression bandages for the treatment of venous leg ulcers. Ann R Coll Surg Engl. 1998, 80: 215-220.

    CAS  PubMed  PubMed Central  Google Scholar 

  47. Smith LJ, Harrison MB, Graham ID, Lamb M: Community leg ulcer bandaging study: lessons learned in a pilot, randomized controlled trial. Ostomy Wound Manage. 2010, 56: 32-42.

    PubMed  Google Scholar 

  48. Harrison MB, Graham ID, Lorimer K, VanDenKerkhof E, Buchanan M, Wells P, Brandys T, Pierscianowski T: Nurse clinic versus home delivery of evidence-based community leg ulcer care: A randomized health services trial. BMC Health Services Research. 2008, 8: 243-10.1186/1472-6963-8-243.

    Article  PubMed  PubMed Central  Google Scholar 

  49. Graham ID, Harrison MB, Lorimer K: Adapting National and International leg ulcer practice guidelines for local use: The Ontario Leg Ulcer Community Care Protocol. Advances in Skin & Wound Care. 2005, 18: 307-318. 10.1097/00129334-200507000-00011.

    Article  Google Scholar 

  50. Graham ID, Lorimer K, Harrison MB, Pierscianowski T: Evaluating the quality of international clinical practice guidelines for leg ulcers: Preparing for a Canadian adaptation. Canadian Association of Enterostomal Therapy Journal. 2000, 19: 15-31.

    Google Scholar 

  51. Margolis DJ, Berlin JA, Strom BL: Which venous leg ulcers will heal with limb compression bandages?. Am J Med. 2000, 109: 15-19. 10.1016/S0002-9343(00)00379-X.

    Article  CAS  PubMed  Google Scholar 

  52. Chaby G, Viseux V, Ramelet AA, Ganry O, Billet A, Lok C: Refractory venous leg ulcers: a study of risk factors. Dermatol Surg. 2006, 32: 512-519. 10.1111/j.1524-4725.2006.32104.x.

    CAS  PubMed  Google Scholar 

  53. Blair SD, Wright DD, Backhouse CM, Riddle E, McCollum CN: Sustained compression and healing of chronic venous ulcers. BMJ. 1988, 297: 1159-1161. 10.1136/bmj.297.6657.1159.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Moffatt CJ, Franks PJ, Oldroyd M, Bosanquet N, Brown P, Greenhalgh RM, McCollum CN: Community clinics for leg ulcers and impact on healing. BMJ. 1992, 305: 1389-1392. 10.1136/bmj.305.6866.1389.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Finnie A: Bandages and bandaging techniques for compression therapy. Br J Community Nurs. 2002, 7: 134-142.

    Article  PubMed  Google Scholar 

  56. Gilliss CL, Kulkin IL: Monitoring nursing interventions and data collection in a randomized clinical trial. West J Nurs Res. 1991, 13: 416-422. 10.1177/019394599101300312.

    Article  CAS  PubMed  Google Scholar 

  57. Kirchhoff KT, Dille CA: Issues in intervention research: maintaining integrity. Appl Nurs Res. 1994, 7: 32-38. 10.1016/0897-1897(94)90018-3.

    Article  CAS  PubMed  Google Scholar 

  58. Rabeneck L, Viscoli CM, Horwitz RI: Problems in the conduct and analysis of randomized clinical trials. Are we getting the right answers to the wrong questions?. Arch Intern Med. 1992, 152: 507-512. 10.1001/archinte.152.3.507.

    Article  CAS  PubMed  Google Scholar 

  59. Ware JE, Snow KK, Kosinski M, Gandek B: SF-36® Health Survey Manual and Interpretation Guide. 1993, Boston, MA: New England Medical Center, The Health Institute

    Google Scholar 

  60. Ware JE, Kosinski M, Keller SD: SF-36 Physical and mental health summary scales: A user manual and interpretation guide. 1994, Boston, Massachusetts: The Health Institute, New England Medical Center

    Google Scholar 

  61. Perneger TV, Burnand B: A simple imputation algorithm reduced missing data in SF-12 health surveys. J Clin Epidemiol. 2005, 58: 142-149. 10.1016/j.jclinepi.2004.06.005.

    Article  PubMed  Google Scholar 

  62. Hopman WM, Harrison MB, Carley M, VanDenKerkhof E: Additional support for simple imputation of missing quality of life data in nursing research. ISRN Nursing.

  63. Skene AI, Smith JM, Dore CJ, Charlett A, Lewis JD: Venous leg ulcers: a prognostic index to predict time to healing. BMJ. 1992, 305: 1119-1121. 10.1136/bmj.305.6862.1119.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Margolis DJ, len-Taylor L, Hoffstad O, Berlin JA: The accuracy of venous leg ulcer prognostic models in a wound care system. Wound Repair Regen. 2004, 12: 163-168. 10.1111/j.1067-1927.2004.012207.x.

    Article  PubMed  Google Scholar 

  65. Myers MB, Rightor M, Cherry G: Relationship between edema and the healing rate of stasis ulcers of the leg. Am J Surg. 1972, 124: 666-668. 10.1016/0002-9610(72)90108-0.

    Article  CAS  PubMed  Google Scholar 

  66. Gaylarde PM, Dodd HJ, Sarkany I: Venous leg ulcers and arthropathy. Br J Rheumatol. 1990, 29: 142-144. 10.1093/rheumatology/29.2.142.

    Article  CAS  PubMed  Google Scholar 

  67. Castineira F, Fisher H, Coleman D, Grace PA, Burke P: The Limerick Leg-Ulcer Project: early results. Ir J Med Sci. 1999, 168: 17-20. 10.1007/BF02939574.

    Article  CAS  PubMed  Google Scholar 

  68. Hopman WM, Towheed T, Anastassiades T, Tenenhouse A, Poliquin S, Berger C, Joseph L, Brown JP, Murray TM, Adachi JD: Canadian normative data for the SF-36 health survey. Canadian Medical Association Journal. 2000, 163: 265-271.

    CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgements and funding

The Canadian Bandaging Trial Group made this large scale enquiry possible: Arleene Arnold, Maureen Buchanan, Donna Flahr, Connie Harris, Theresa Hurd, Karen Lorimer, Estrella Mercurio, Susan Mills-Zorzes, Mary Catherine Rilett, Laura Teague, and Michelle Todoruk-Orchard. Their commitment in producing and using evidence for best practice is inspiring. The research team is indebted to the many individuals with leg ulcers who gave generously of their time to participate in this trial. We gratefully acknowledge Elaine Friedberg and Val Angus for trial coordination and logistical support, and Monica Prince for data management support. Lastly we would like to acknowledge the beneficial feedback received from Ba' Pham, University of Toronto, on an earlier version of this manuscript

The study was funded by a grant from the Canadian Institutes of Health Research (CIHR #63175, CIHR funded trials ISRCTN37782978). During the time of this study M.B. Harrison and I.D. Graham held research personnel awards from the Canadian Institutes of Health Research.

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The authors declare that they have no competing interests.

Authors' contributions

MBH was principal investigator on the trial and responsible for conceptualization, ethical approval, the conduct and management of the RCT, analysis and interpretation of the data. IDG, EAN, and EGV were trial co-investigators and contributed to the conceptualization, analysis and interpretation of the data.

WMH was responsible for the HRQL analysis and contributed to interpretation of the trial data. MEC was responsible for data management and contributed to the analysis.

The 'Canadian Bandaging Trial Group' members served as site investigators and contributed to the feasibility and conduct of the trial protocol.

All primary authors have read and approved the final manuscript.

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Harrison, M.B., VanDenKerkhof, E.G., Hopman, W.M. et al. The Canadian Bandaging Trial: Evidence-informed leg ulcer care and the effectiveness of two compression technologies. BMC Nurs 10, 20 (2011).

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