- Robert Peveler, clinical reader in psychological medicine ()a,
- Charles George, professor of clinical pharmacologyb,
- Ann-Louise Kinmonth, professor of general practicec,
- Michael Campbell, professor of medical statisticsd,
- Chris Thompson, professor of psychiatrya
- a Mental Health Group, University of Southampton, Royal South Hants Hospital, Southampton SO14 0YG
- b Clinical Pharmacology Group, Biomedical Sciences Building, Southampton SO16 7PX
- c General Practice and Primary Care Unit, Institute of Public Health Medicine, University of Cambridge, Cambridge CB2 2SR
- d School of Health and Related Research, University of Sheffield, Northern General Hospital, Sheffield S5 7AU
- Correspondence to: R Peveler
- Accepted 20 May 1999
Objectives: To evaluate two different methods of improving adherence to antidepressant drugs.
Design: Factorial randomised controlled single blind trial of treatment leaflet, drug counselling, both, or treatment as usual.
Setting: Primary care in Wessex
Participants: 250 patients starting treatment with tricyclic antidepressants.
Main outcome measures: Adherence to drug treatment (by confidential self report and electronic monitor); depressive symptoms and health status.
Results: 66 (63%) patients continued with drugs to 12 weeks in the counselled group compared with 42 (39%) of those who did not receiving counselling (odds ratio 2.7, 95% confidence interval 1.6 to 4.8; number needed to treat=4) Treatment leaflets had no significant effect on adherence. No differences in depressive symptoms were found between treatment groups overall, although a significant improvement was found in patients with major depressive disorder receiving drug doses of at least 75 mg (depression score 4 (SD 3.7) counselling v 5.9 (SD 5.0) no counselling, P=0.038).
Conclusions: Counselling about drug treatment significantly improved adherence, but clinical benefit was seen only in patients with major depressive disorder receiving doses ≥75 mg. Further research is required to evaluate the effect of this approach in combination with appropriate targeting of treatment and advice about dosage.
Non-adherence is a serious problem in the treatment of depression by general practitioners
In this study a brief psychosocial intervention delivered by a nurse greatly improved adherence
Clinical benefit was apparent only in patients with major depressive episodes on higher doses of drugs
Counselling should be targeted at patients with symptoms of at least moderate severity and combined with therapeutic drug doses
Depressive illness is an important public health problem.1–2 In Britain most patients are managed in primary care, with depression accounting for about 10% of consultations for new illness episodes.3 Antidepressants account for 7% of primary care pharmaceutical expenditure (N Hardy, personal communication). Although antidepressants are effective in patients with “major depression,”4 effectiveness is reduced by non-adherence. Estimates of discontinuation at one month range from 30% to 68%.5–9 Non-adherence is difficult to measure10: methods such as self reporting or counting pills have serious limitations. The development of electromechanical medication monitors represents an important advance.
A systematic review of interventions to improve adherence called for further research in clinical populations with appropriate designs, incorporating assessment of both adherence and outcomes.11 “Compliance therapy” is effective in improving adherence and outcome for patients with schizophrenia.12 The feasibility of using practice nurses to improve care of depressed patients has also been shown.13 We therefore developed a brief intervention for patients receiving antidepressants (antidepressant drug counselling) for administration by practice nurses. We conducted a randomised trial in primary care to compare the counselling programme with a prescription information leaflet14 and treatment as usual.
Participants and methods
General practitioners in Wessex were asked to notify the research team of patients aged 18 or over who were starting new courses of treatment with dothiepin or amitriptyline. Forty three practices agreed; 28 entered patients. Inclusion was based on clinical diagnosis of depressive illness; research diagnostic criteria for major depressive disorder were applied only to permit subgroup analysis. Patients were excluded if they had received either drug within 3 months, had a contraindication (allergy, heart disease, glaucoma, or pregnancy), or were receiving other incompatible drugs. The research interviewer assessed suicide risk, and any patient at high risk was excluded.
We sent general practitioners a questionnaire after the end of recruitment to assess referral bias. Two steps were taken to minimise bias. Firstly, the study was explained as an evaluation of treatment satisfaction: the principal purpose of assessing adherence was concealed. Secondly, we recruited an “attention control” group, which received only a 12 week interview, to assess the effect of closer monitoring by the research team on adherence.
Assignment and blinding
Immediately after referral, patients were individually randomised in blocks of eight to one of four treatment groups (treatment as usual, leaflet, drug counselling, or both interventions) by prearranged random number sequence, stratified by drug type, in a factorial design. To maintain blinding the randomisation key was concealed from interviewers. Leaflets were included in an opaque sealed envelope with study information. Patients were unaware of their allocation at first interview and asked not to reveal drug counselling sessions to the interviewer subsequently. A formal test of blindness was not conducted. All local research ethics committees granted ethical approval.
The information leaflet was developed according to published principles and European Union directives.15 16 It contained information about the drug, unwanted effects, and what to do in the event of missing a dose. Patients were given drug counselling by a nurse at weeks 2 and 8, according to a written protocol. Four nurses acted as therapists: all had general nursing qualifications, had worked for at least 10 years since qualification, and had primary care experience; none had specialist mental health experience or training. Training for antidepressant drug counselling (conducted by RP) took 4 hours. Sessions included assessment of daily routine and lifestyle, attitudes to treatment, and understanding of the reasons for treatment. Education was given about depressive illness and related problems, self help, and local resources. The importance of drug treatment was emphasised, and side effects and their management discussed. Advice was given about the use of reminders and cues, the need to continue treatment for up to 6 months, and what to do in the event of forgetting a dose. The feasibility of involving family or friends with medicine taking was explored.
At entry we obtained demographic information and medical and psychiatric history from patients and applied diagnostic criteria for major depressive disorder (DSM-IIIR).17 Depressive symptoms were measured by the hospital anxiety and depression scale,18 and functional status was measured by the SF-36 health survey.19 Interviews were conducted at baseline, 6 weeks, and when drugs were discontinued or at 12 weeks, whichever was sooner. A postal questionnaire was sent at 12 weeks to all those who discontinued. At 6 weeks, self reported adherence, depressive symptoms, and unwanted effects of treatment were assessed. At the final visit, reported adherence, satisfaction with treatment, and unwanted effects were reassessed and the depression scale and SF-36 repeated.
To check reliability of self reported adherence we monitored adherence in a subgroup using an electromechanical monitor (MEMS, Ardex). Patients were seen at 3 weeks to resupply drugs and pills were surreptitiously counted. At 6 weeks, the container was collected and the cap data downloaded.
The principal outcome variable was self reported adherence at 6 and 12 weeks, and the trial was analysed on an intention to treat basis. We investigated time to stopping drugs using survival analysis. Assuming that the intervention would increase the proportion of patients continuing drugs at 6 weeks from 35% to 50%, a proportional odds power calculation dictated a sample size of 376 for a power of 90% to detect an effect at 5% (two sided) significance.20
Participant flow and follow up
Of 266 patients referred, eight were excluded (three glaucoma, one recent myocardial infarction, one recent dothiepin treatment, one too confused to consent, two left area immediately after referral) and eight declined to participate, leaving 250 eligible subjects (94%). Thirty seven were allocated to the attention control group, and 213 were randomised (table 1). Eighty eight patients had their adherence monitored; 84 container lids were evaluable.
The response rate to the bias questionnaire was 77%: six general practitioners (13%) had retired or left the area, and five (10%) did not respond. The commonest reason given for not entering patients was that the general practitioner was “too busy” or “forgot about the study.” General practitioners reported entering fewer patients with chronic depression (54%), comorbid physical illness (51%), postnatal depression (39%), and older patients (25%).
Table 2 shows the characteristics of patients. Half met criteria for major depressive episode within the past month. Almost two thirds had had previous treatment for depression, usually drugs from their general practitioner.
Delivery of interventions
Of 105 patients allocated to drug counselling, 89 (85%) received a first visit, and 73 (70%) received both (table 1). Visits were cancelled if drug treatment had been discontinued. At 2 weeks, 11 patients (10%) had discontinued drugs and five patients (5%) refused the visit. At 8 weeks, 20 patients (19%) had stopped drugs and eight (8%) refused. The mean durations of the two visits were 45 (SD 15) min and 33 (SD 13) min.
Patients allocated to receive a leaflet were asked whether they recalled receiving it: 82 (78%) did. Ten patients received more than one leaflet, and 18 not allocated to receive a leaflet reported receiving one from elsewhere (doctor or pharmacist).
Table 3 shows self reported adherence to drug treatment. The proportion of controls continuing treatment at week 12 was 19/37 (51%). In logistic regression, allocation to counselling was a significant predictor of self reported adherence (6 weeks: odds ratio 2.1, 95% confidence interval 1.1 to 4.0; 12 weeks: 2.7, 1.6 to 4.8; number needed to treat =4) but allocation to receive a leaflet was not (6 weeks: 1.0, 0.55 to 1.9; 12 weeks: 1.1, 0.64 to 2.0). There was no significant interaction between treatments. Sex, previous treatment, initial depression severity, and drug dose did not materially influence the findings. Subgroup analysis of patients meeting criteria for major depressive episode showed that drug counselling had a significant effect on adherence (χ2= 6.33, df =1, P=0.012) but the leaflet did not.
The figure shows the survival analysis. The analysis confirmed that allocation to counselling had a significant effect compared with usual treatment (mean treatment duration 87 (SE 4) v 63 (4) days, log rank test 10.83, df=1, P=0.001; hazard ratio=2.1, 95% confidence interval 1.3 to 3.2); allocation to leaflet had no effect (hazard ratio=1.1, 0.72 to 1.6).
Adherence was monitored in a subgroup of patients to check the validity of self reported adherence. There was no difference in self reported adherence between monitored patients and other patients. Self reported and monitored adherence were significantly related (mean duration of monitored treatment 41.7 (SD 5.8) days in patients reporting continuation compared with 26.1 (SD 15.9) days in those reporting cessation, t=6.6, df=82, P<0.001). In the monitored group there was a trend towards higher adherence among those who had drug counselling (Mann-Whitney z =1.72, P=0.08).
Although counselling increased both self reported and monitored adherence, we found no overall effect on outcome of depression. All patients showed considerable improvement at 12 weeks (depression score 4.6 (SD 4.5) in counselled patients v 5.5 (SD 3.6) in those with no intervention, t=1.55, df=199, P=0.124). However, change in depression score and number of days of treatment were significantly correlated (ρ=0.264, P<0.0001), and patients who had met criteria for major depression at the outset and received doses above the median value of 75 mg had a significant difference in depression score (4.0 (SD 3.7) v 5.9 (SD 5.0), t=2.18, P=0.032).
No overall differences in SF-36 subscales were found, but among patients receiving doses of at least 75 mg drug counselling had a significant effect on scores on the mental health subscale (68.4 (SD 15.8) v 60.8 (SD 22.6), t=1.98, df =97, P=0.05). In subjects who had major depression and received doses of 75 mg or more this difference reached significance (64.9 (SD 14.5) v 54.0 (SD 23.5), t=2.1, df=53, P=0.038). Counselling had no significant effect on the number of general practitioner visits, hospital admissions, or time off work.
We assessed adherence to drug treatment in a large representative primary care sample of depressed patients and validated reported adherence by electromechanical monitoring. The overall pattern of adherence was consistent with that reported in previous studies,5 8 9 with 40-50% of patients continuing treatment at 12 weeks. It was practicable for nurses to administer an educational and behavioural intervention in primary care, and this was acceptable to most patients. The nurse intervention raised the proportion of patients continuing treatment at 12 weeks to two thirds.
Leaflets had no effect on adherence, either on their own or in combination with counselling. Although recruitment was slower than demanded by the power calculation, the result was significant because the effect on adherence was greater than predicted. Nurse training took 4 hours but could be reduced with the help of a training manual for private study. No special therapeutic or psychological skills were required.
The methods used reflect the fact that the study was designed to be as naturalistic as possible, yielding background rates of non-adherence in usual clinical practice against which to assess the interventions The main weakness of this design is that it is impossible to know whether there was significant bias in patient selection by general practitioners. Our attempt to evaluate bias retrospectively suggests that patients with chronic depression, concurrent physical illness, or postnatal depression may have been under-represented. Inclusion of the control group showed that the extra attention given to patients in the main study did not itself improve adherence.
The improvement in adherence produced by counselling was not matched by a significant improvement in clinical outcome or use of service for all patients, but there was evidence that symptoms and health did improve in patients with more severe symptoms receiving higher doses of drugs. Only half the sample met the criteria for major depressive disorder, and over half were receiving drug doses which are believed to be of doubtful efficacy. Further studies are therefore needed to test whether drug counselling would be more beneficial if it included advice about dose of antidepressants and when targeted at patients with at least moderately severe symptoms.
We thank all the general practitioners who referred patients to the trial. The research nurses were Sabine Heiliger, Cathy Douglas-Wallis, Sandy Staff, and Lynn Timms. Professor Renwick helped with blood level analyses. The study administrators were Jackie Threapleton and Lorna Campbell. Pharmacy assistance was provided by Elizabeth Bere.
Contributors: RP designed the protocol with help from A-LK, CG, and CT. RP supervised data collection and analysis. MC assisted with the power calculation and with data analysis. The manuscript was prepared by RP and commented on by all authors. RP is the study guarantor.
Funding Medical Research Council (grant G9322875). Dothiepin for electromechanically monitored patients was donated by Knoll pharmaceuticals.
Competing interests None declared.