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Atrial fibrillation (AF) patients with a high risk of stroke are recommended anticoagulation with warfarin. However, the benefit of warfarin is dependent upon time spent within the target therapeutic range (TTR) of their international normalised ratio (INR) (2.0 to 3.0). AF patients possess limited knowledge of their disease and warfarin treatment and this can impact on INR control. Education can improve patients' understanding of warfarin therapy and factors which affect INR control.
Randomised controlled trial of an intensive educational intervention will consist of group sessions (between 2-8 patients) containing standardised information about the risks and benefits associated with OAC therapy, lifestyle interactions and the importance of monitoring and control of their International Normalised Ratio (INR). Information will be presented within an 'expert-patient' focussed DVD, revised educational booklet and patient worksheets. 200 warfarin-naïve patients who are eligible for warfarin will be randomised to either the intervention or usual care groups. All patients must have ECG-documented AF and be eligible for warfarin (according to the NICE AF guidelines). Exclusion criteria include: aged < 18 years old, contraindication(s) to warfarin, history of warfarin USE, valvular heart disease, cognitive impairment, are unable to speak/read English and disease likely to cause death within 12 months. Primary endpoint is time spent in TTR. Secondary endpoints include measures of quality of life (AF-QoL-18), anxiety and depression (HADS), knowledge of AF and anticoagulation, beliefs about medication (BMQ) and illness representations (IPQ-R). Clinical outcomes, including bleeding, stroke and interruption to anticoagulation will be recorded. All outcome measures will be assessed at baseline and 1, 2, 6 and 12 months post-intervention.
More data is needed on the clinical benefit of educational intervention with AF patients receiving warfarin.
Atrial fibrillation (AF) is the most common arrhythmia in clinical practice, for people aged 40 years and older the lifetime risk of developing AF is approximately 25% . AF is an independent risk factor for stroke, conferring a five-fold excess risk in AF patients compared to those in sinus rhythm  and accounts for almost 10-15% of all ischaemic strokes and approximately one in four strokes in those aged over 80 years . Furthermore, when a stroke occurs in association with AF, patients have substantially greater mortality, morbidity, disability and longer hospital stays .
Despite the overwhelming evidence that thromboprophylaxis with warfarin substantially reduces the incidence of stroke and mortality compared to placebo  and is associated with a marked reduction in all strokes when compared to aspirin , it remains under-utilised . Dose-adjusted warfarin does not confer a significant increased risk of bleeding , however, poor anticoagulation control, evidenced by a 10% rise in time out of INR range (2.0 to 3.0), was significantly associated with an increased risk of death (OR, 1.29 [95% CI, 1.23 to 1.36]), ischaemic stroke (OR, 1.10 [1.03 to 1.18]), and thromboembolic events (OR, 1.12 [1.06 to 1.19]) . Recent analyses have demonstrated that the minimum threshold of time spent in the therapeutic INR range for warfarin to be efficacious is ≥ 58%, although a TTR >65% is associated with a 2.29% (95% CI 1.57-3.35; p < 0.0001) reduction in stroke risk . Analyses from an observational UK cohort of AF patients  found that 51% of patients at high risk of stroke (CHADS2 score ≥ 2) were outside the therapeutic range for 50% or more of the time for the duration of their warfarin treatment  and that TTR needed to be >71% for warfarin to be efficacious .
Patients' illness representations and their beliefs about their health are crucial determinants of whether anticoagulant treatment, particularly with warfarin, is successful [10-12]. Patients need to clearly understand the causes and consequences of their AF, as well as the risks and benefits of warfarin therapy, and incorporate this complex medical information into their own belief system. Studies suggest where patients have a greater knowledge of warfarin therapy, INR values are more often within target range (p = 0.024) . However, patients often exhibit limited knowledge of their condition and their anticoagulant therapy [13-16]. It is important that interventions specifically target this group of patients to increase TTR and maximise clinical outcomes with warfarin.
Behavioural and educational interventions that targeted patients receiving oral anticoagulant (OAC) therapy, the majority for AF (other indications included deep vein thrombosis, prosthetic heart valves etc), found reduced incidence of major bleeding and mortality and increased TTR (e.g. Khan et al  found TTR 61.1% prior to intervention vs. 70.4% post intervention; mean difference 8.8; 95% CI: -0.2-17.8; p = 0.054), when compared to usual care [17,18]. Our earlier pilot study exclusively with AF patients  demonstrated a significant improvement in the awareness of target therapeutic INR (p < 0.0001) and factors which may affect INR levels (p = 0.005), with a trend towards improvement in the awareness of the benefits of anticoagulants and bleeding risks, six weeks after a brief educational intervention. Patients need key information about their condition and treatment to actively participate in their treatment management.
TREAT is a 'TRial of an Educational intervention on patients' knowledge of Atrial fibrillation and anticoagulant therapy, INR control, and outcome of Treatment with warfarin'. It is a randomised controlled trial (RCT [ISRCTN93952605]) of an educational intervention versus usual care in a population of AF patients that have been newly prescribed anticoagulation treatment with warfarin. The project is funded by an investigator-initiated grant from Bayer Healthcare. The primary research question will examine the effects of an intensive educational intervention on patients' International Normalised Ratio (INR) control within the therapeutic range (INR 2.0 to 3.0) compared to patients receiving usual care. The secondary endpoints will determine the effects of the educational intervention on patients' knowledge of, and perceptions of AF and their beliefs about anticoagulant therapy. In addition, the relationship between INR control and the incidence of major and minor bleeding, stroke and thromboembolic events compared to patients receiving usual care will be explored.
To explore these endpoints TREAT will determine whether there are differences between the intervention group and the usual care group at baseline, 1, 2, 6 and 12 months post-intervention. Subgroup analysis of patient groups (using age, gender and socio-demographic data) will determine whether data outcomes relate to other factors such as the age or gender of the participants. Finally, a health-care utilisation assessment will be undertaken to determine the costs of the intensive educational intervention compared to usual care. This will determine whether the intervention would be cost effective if used on a larger scale as part of standard 'usual care'.
AF patients newly referred for warfarin therapy, with ECG-documented AF, will be eligible for inclusion. Patients will be excluded from participation if they are aged < 18 years old, have any contraindication to warfarin, have previously received warfarin, have valvular heart disease, are cognitively impaired, are unable to speak or read English and have any disease likely to cause their death within 12 months. Patients will be recruited from the outpatient AF clinics at City Hospital, Sandwell District General Hospital (part of SWBH NHS Trust) and Good Hope Hospital which collectively receive approximately 600 referrals for AF patients requiring anticoagulant prophylaxis per annum (see figure figure1.1. for CONSORT recruitment flow diagram). Sandwell and West Birmingham NHS Trust serves a multi-ethnic inner-city population of approximately 600,000 people, while Good Hope Hospital serves North Birmingham, Sutton Coldfield, and a large part of South-East Staffordshire, with a catchment of 450,000.
Demographic and clinical information will be recorded at baseline from the patient's hospital records. Individualised annual risk of stroke will be determined based on risk stratification proposed by the NICE guidelines (low/moderate/high risk)  and the CHADS2 scheme . Patients who are eligible for OAC therapy will receive a standard explanation of the need for OAC therapy, and the risks/benefits of such treatment. Those who are accepting of anticoagulant therapy will be approached to participate in this intervention study. Patients accepting of warfarin therapy and who consent to participate will be randomised to receive 'usual care' or the intensive intervention.
Ethics approval for the TREAT study has been granted by the Black Country Research Ethics Committee. All participants will provide written informed consent.
At the stage of randomisation the primary researcher will check to ensure the patient meets the eligibility criteria and does not meet any of the exclusion criteria. If the patient is willing to take part consent, will be obtained prior to randomisation. A computer generated list will randomise patients in blocks of four and on an individual basis with stratification by (a) age [< 70 and 70+]/sex and (b) specialist AF clinic versus 'general' cardiology clinic. There is one specialist AF clinic vs. two general cardiology clinics involved in the trial. The specialist clinic is a large clinic receiving AF referrals from the entire SWBH Trust, therefore providing patient numbers equal to those provided by the general cardiology clinics. Patients will receive either 'usual care' (minimum of n = 78) or the intensive educational intervention (minimum of n = 78), in addition to 'usual care'. The randomisation schedule was designed by an independent trials unit and the random allocation will be obtained by the researcher telephoning an associate researcher (who is not involved in the data collection or data entry). The primary researcher will be blinded to patient identification to ensure allocation concealment. A third researcher will match patient identification numbers (generated by the primary researcher) with randomisation codes (generated by the associate researcher). Once the random allocation has been obtained baseline data will be collected and an intervention session will be arranged. Patients who refuse to be randomised will be offered their respective hospitals 'usual care' package.
Patients randomised to usual care will be informed about their condition and the need for anticoagulant therapy only. All patients will also receive the standard information booklet which contains basic lifestyle recommendations pertaining to OAC therapy. When patients are first prescribed OAC, dosing officers and anticoagulation nurses use an educational checklist to ensure they have discussed all of the key information with the patients. This information includes the purpose of their treatment, future INR monitoring and factors which affect INR. This yellow patient information booklet contains some basic information pertaining to OAC therapy and their INR record book.
Those in the intensive educational intervention arm will attend one group session (between 2-8 patients) for one hour, where they will be shown a DVD of information about the need for warfarin, the risks and benefits associated with OAC therapy, potential interactions with food, drugs, and alcohol, and the importance of monitoring, and control of their INR. The information on the DVD will be communicated in a variety of ways [i.e. by expert patients, a cardiology consultant and examples of food/alcohol dietary components with educational information as a voiceover script].
The intervention session will be interactive, where the patients will be encouraged to ask questions following each 10 minute DVD section. Patients will also be asked to complete a worksheet-based exercise which will serve to reinforce the information presented. The chapters will focus on AF and treatment recommendations, INR and lifestyle recommendations and patient concerns about OAC [including frequently asked questions answered by the consultant cardiologist]. The content and format of the information presented was finalised after consultation with a focus group of AF patients currently taking OAC, and was based on the NICE guidelines for patients  to ensure that it is suitable for a wide-range of patients. In addition to the interactive group sessions, patients will also be given the revised educational booklet, which was originally developed for and employed in our pilot study . The complete intervention pack contains a treatment diary whereby patients can self-monitor the factors which affect the stability of their INR, an alert card and their session worksheet. The content of the educational booklet will be covered in the group session and will serve to reinforce the information and enable the patient to refer to it in the future.
The primary endpoint is the proportion of time spent in the therapeutic INR range, 2.0 to 3.0. All patients (intervention and usual care groups) will attend the anticoagulant outpatient clinic to have their INR checked using a capillary blood sample. The frequency of the INR visits will be at the discretion of the OAC clinic. The OAC clinic staff will be blinded to the intervention arm the patient is randomised to, to enable as 'naturalistic' as possible follow-up and monitoring). Every INR result from baseline to the end of the study (12-months) will be recorded. The proportion of time each patient spends in the therapeutic INR range (2.0 to 3.0) will be calculated by the method of linear interpolation  using data from months 1 to 12 (to allow attainment of the correct dose of warfarin during the first four weeks).
Secondary endpoints include (1) patients' knowledge [an increase/decrease/or no change in knowledge will be measured by a change in score +/-/no change], (2) beliefs about medication  (3) anxiety and depression  and (4) illness representations ( see table table1).1). Ancillary analyses will explore the relationship between INR control and incidence of minor and major bleeding, stroke, thromboembolic events (given that the trial is not powered to detect these differences) and frequency of INR checks. The number of strokes, bleeding and thromboembolic events will be determined from the computerised clinical information system at the hospital. Patients in both arms of the trial will receive the follow-up questionnaires by post 1, 2, 6 and 12 months after commencing OAC therapy. If returned questionnaires are not fully completed, an independent researcher will contact the patient by telephone to facilitate 100% completion of the questionnaires.
Power for the primary endpoint was calculated based on data from a secondary analysis of the time within therapeutic range (TTR) from the ACTIVE-W cohort by Connolly et al . The power calculation assumes that usual care patients would have mean TTR of 58% with a standard deviation [SD] of 7.5. We hypothesise a 6% improvement in mean TTR in the intervention group (i.e. to 64%) with a similar SD (i.e. 7.5). In order for this improvement to be statistically significant with a 1-beta power of 0.99 and alpha = 0.01 we need a sample size of 154 subjects in two equal groups of 77 each. However, to ensure confidence and to allow for attrition, we intend to recruit in excess of this figure.
For the secondary endpoint of improvement in knowledge following the intervention, sample size was calculated based a study by Khan et al . A sample size of 100 patients (allowing for a 20% attrition rate in completion of the questionnaires) will have at least 80% power to detect an 18.5% increase in knowledge about the condition and factors affecting INR control between baseline and follow-up.
All data will be analysed by intention to treat. All analyses will be stratified by centre. Comparisons with the primary and secondary outcome measures will be made at all time points to determine short and long term effects of the intervention. For continuous variables (e.g., changes in illness perception questionnaire or changes in time spent within INR therapeutic range), the weighted mean difference would be used. As the sample is randomised we would not expect baseline differences between groups.
In addition to the cost of the intervention delivery (production, staffing and resource costs) and anticoagulation management, all patients will complete a questionnaire (previously employed by Jowett et al ) to evaluate their costs for two separate visits to the OAC clinic. Patient costs incurred when travelling to the clinic, including travel costs, other out of pocket expenses, loss of leisure time and net wage deduction associated with patients' clinic visits during working time will be collected. Additional societal costs also include the value of a companion's time.
The TREAT trial seeks to recruit warfarin-naïve patients from cardiology clinics who are recommended for and accepting of OAC with warfarin. Providing an intensive educational intervention will determine whether increasing the information available to patients yields both clinical benefit and cost effectiveness. This is a pragmatic trial, thus limitations of the design are necessary for the initial trial of the intervention. For example, patients are not blinded to which arm of the trial they receive and results will not be generalisable to patients with cognitive impairment or limited English ability. However, if the trial is successful the intervention will be available for carers of patients with cognitive deficits and could potentially be translated and piloted in a range of other languages. Whilst the TREAT trial is powered for a surrogate outcome marker, TTR, clinical outcomes will be observed. TTR is an important outcome as INR control substantially reduces the risk of adverse events. Thus the TREAT study outcomes have implications for the management of all patients receiving OAC, as the intervention aims to improve knowledge on the key lifestyle factors which affect INR control and medication adherence. If the results are positive the educational intervention has potential for online dissemination and the materials are such that they can be delivered by a range of health-care professionals, with suitable training. The final results of this study will not be available before late 2011.
The TREAT study is funded by an Investigator-Initiated Educational Grant from Bayer Healthcare.
DES, GYHL, and DAL conceived the idea for the trial, DES and DAL drafted the manuscript. HP, CBX and GYHL read and revised the manuscript. All authors contributed to the development of the intervention.
The pre-publication history for this paper can be accessed here: