Objective To identify and prioritise uncertainties regarding epilepsy treatment from people with epilepsy, their carers and epilepsy clinicians.
Background Failure to acknowledge and address genuine treatment uncertainties has caused unnecessary iatrogenic harm. The authors define an uncertainty as a question that cannot be sufficiently answered by a systematic review of the literature. The database of the uncertainties of the effects of treatment (DUETs) is a collection of ‘known unknowns’ that enables patient-prioritised research.
Design and participants The authors organised five separate focus groups (two consisting of clinicians, three of patients and carers) to garner questions on epilepsy treatment uncertainties; these yielded 398 potential research questions. Participants were asked to rank the questions in terms of importance. The authors then performed a thematic analysis.
Results Patients rated questions concerning cognitive drug side effects, managing the consequences of side effects and improving public awareness about the treatment of epilepsy through improved services as most important. For clinicians, the most important themes were treatment programmes for non-epileptic attack disorder (NEAD), concerns about side effects in utero and uncertainties regarding prescribing in pregnancy.
Conclusions Patient uncertainties were often focussed on very practical considerations—how to take prescribed medication, access to services and how to minimise drug side effects. Clinicians' questions were also practical but clustered around ‘the challenging consultation’—for example, NEAD, sudden unexplained death in epilepsy and prescribing in pregnancy. The authors have published the research questions on NHS Evidence and are working with them to identify those questions which represent genuine uncertainties. The authors encourage other clinicians to seek patient and carers' priorities in order to shape their research agenda.
Statistics from Altmetric.com
It is often unclear how research topics are chosen and prioritised. Industry-sponsored projects may be selected to display their product to advantage,1 2 and the availability of time, money and personnel may determine topics chosen for independent investigation.3 Grant committees rightly ask applicants to consider patients' views when submitting an application, but this is difficult without knowledge of exactly what is uncertain and which topics are patient priorities. Do funded research questions address the priorities of people with epilepsy?4 Do they even reflect the uncertainties prioritised by clinicians?
When prescribing for certain groups, for example, people with epilepsy and learning disability, we often work in an evidence vacuum, extrapolating from relevant studies of related patient groups. Our comfort with uncertainty and our acceptance of this ‘grey area’ have unwittingly promoted a climate where immeasurable harm is perpetrated through labelling situations as ‘uncertain’ where there is already sufficient evidence to make them certain—for example, corticosteroids in head injury,5 caffeine for neonates6 or prophylactic antiarrhythmics after myocardial infarction.7 The James Lind Initiative aims to promote ‘identification of the most important gaps in knowledge about the effects of treatments’ through developing a database of uncertainties of treatments (DUETs), published online at NHS Evidence.8 As part of this project, we enabled people affected by epilepsy and its treatment (patients, carers, clinicians and scientists) to create and prioritise treatment uncertainties.
Using qualitative methodology based upon the consultations in rheumatoid arthritis,9 we arranged five separate focus groups: three with patients and carers, and two with clinicians and health professionals. The sequence of meetings was Cardiff professionals, Cardiff patients, Swansea professionals, Swansea patients and Cardiff patients; beyond geographical convenience there was no attempt to place people in specific focus groups for balance. Patients were invited from several sources: clinic appointments, previous involvement in local projects with the Wales Epilepsy Research Network (WERN), and membership of local charity groups. Involvement was voluntary and unpaid; meetings lasted 90–120 min. We did not discourage anyone from attending who expressed an interest in doing so. Participants were invited to try to ensure a balance of adult and paediatric, oligoepilepsy and refractory epilepsy, pre- and postsurgical candidates, people with learning disability, parents and children, carers and support workers (see table 1).
Each meeting had the same agenda, and two of us were present to write the questions onto an overhead projector and to chair the discussion. The focus groups were asked to identify questions addressing treatment uncertainties; therefore, we excluded questions exclusively addressing diagnosis, service complaints or the natural history of epilepsy. When facilitating the meetings, we encouraged each participant to consider all patient-groups and possible treatments, and offer questions on the topic. So as to maintain participation, we did not attempt (during the consultation) to answer any of the questions posed, or suggest that the answers may already be known. Each participant then ranked the questions created in their meeting only, enabling us to identify the most important potential research questions.
Using an interpretive phenomenological approach to analysis, we used not only the text of the question produced but also our knowledge of who asked the question and the context in which it was created to better understand what was being asked. Blinded to the ranking, CH and RT grouped the questions into themes to allow us to compare professionals' and patients' questions in content, number and relative ranking. Some subcategories involving special groups (eg, people with learning disability or children) were teased out from the main themes for comparison (box 1). The themes were developed both individually and in group work until it was agreed that the identified themes were all-encompassing and useful. We did not limit the number of questions that could be posed over the course of a meeting, and so to compare the relative rank, we must adjust for the number of questions. We standardised each prioritised question as a value on a scale between 1 and 100; the lower the standardised rank score, the more important its rating. In order to test the significance of the differences between focus groups or themes, we examined the most highly ranked questions. We identified, for every participant, the number of questions from each theme ranked in the top quartile. We performed the Mann–Whitney U test, using asymptotic significance, to identify differences between the focus groups, or between the themes, with statistical significance taken as p<0.05. We identified both differences between the two groups and the similarities: the shared priorities. Finally, a database of unique uncertainties was produced for publication in the UK DUETs database.6
Box 1 Thematic groupings
Who should be treating epilepsy?
Special groups—children, older people and pregnant women
Ongoing therapeutic monitoring
Uncertainties about drug action (such as drug interactions)
Drug side effects
Recognition and acknowledgement of side effects
Management of drug side effects
Specific side effects—mood, fertility, bone health, cognitive side effects and side effects in utero
Oxygen and midazolam
Status and non-convulsive status epilepticus
Including withdrawal in non-epileptic attack disorder
How best to take prescribed medications
Adherence with prescribed medications
Choice and presurgical considerations
Uncertainties following surgery
Non-drug treatments of epilepsy that are supervised by a professional
Considering the patient as an individual
Special groups—Pregnancy, older people, learning disability
Non-epileptic attack disorder
Effect of lifestyle on seizures
Drugs, alcohol and diet
Complementary therapies and stress management
Depression, cognitive problems and sudden unexplained death in epilepsy
Information based epilepsy management
Public awareness of seizure management
The meetings produced 188 questions from 25 patients and carers, and 210 questions from 17 professionals. Despite the repetition of research themes, patients and clinicians posed only 11 identical questions. Box 2 shows the top two prioritised questions from each group.
Box 2 Highest-ranked research questions
Both groups prioritised practical uncertainties affecting the greatest number of people ahead of esoteric questions or single issue, minority group uncertainties.
Patients and carers
‘Should you take a forgotten dose as soon as you remember or skip a dose and take your next dose as normal?’
‘What training should teachers and school nurses have about epilepsy and treatment of seizures?’
‘What are the neurodevelopmental effects of exposure to each of the antiepileptic drugs in pregnancy?’
‘How is the choice of second monotherapy influenced by the seizure type/syndrome?’
Patients and carers
Patients' and carers' highest-ranked themes were: cognitive drug side effects (mean standardised rank 13.3, n=5); managing the consequences of any side effect from an antiepileptic drug (AED) (25.7, n=5); improving public awareness about the treatment of epilepsy and seizures through services (26.2, n=8) and non-medical treatment of cognitive problems (28.1, n=2). Patients rated information-based management (such as improving public awareness) a consistently higher priority than did clinicians (p=0.001).
The highest-ranked uncertainties concerned the following themes: individual differences in the treatment of non-epileptic attack disorder (mean rank 10.2, number of questions=3); AED side effects; AEDs exposure in utero (11.5, n=3); prescribing in pregnancy (14.2, n=50; treatment of depression in epilepsy (17.8, n=3) and AED mood side effects (19.1, n=5). Box 3 illustrates key questions from the themes. Clinicians rated prescribing uncertainties (including for older people, children and pregnant women) as more important than patients did (p<0.0001). In contrast, AED side effects were more important to patients and carers (p<0.0001).
Box 3 Example questions from key themes
Patients and carers
Managing the consequences of any antiepileptic drug side effect
‘How frequently should we test or look for side effects of antiepileptic drugs?’
Improving public awareness about the treatment of epilepsy and seizures through services
‘Would rapid access to epilepsy specialists improve treatment for people with epilepsy?’
Considering individual differences in the treatment of non-epileptic attack disorder
‘What is the best treatment programme for non-epileptic attacks?’
Individual differences in the treatment of depression in epilepsy
‘What is the optimal support for those with depression and epilepsy?’
Cognitive drug side effects
Patients—‘Do different epilepsy medications affect people differently? Are the problems reversible?’
Clinicians—‘Are certain people more likely to develop cognitive side effects, and can they be predicted?’
Improving epilepsy control by improving public awareness of epilepsy
Patients—‘What advice should be given to all schools about epilepsy, and how would this improve epilepsy control for schoolchildren?’
Clinicians—‘Can better education about epilepsy improve quality of life for people with epilepsy by reducing stigma?’
There was a great deal of consensus between the groups concerning the themes that were important to both. The most important shared priority was research into the cognitive side effects of AEDs (table 2). Five of the top 12 shared priorities concerned AED side effects, two pregnancy priorities and two mood disorders uncertainties. Themes that dealt with starting AEDs were more of a priority than AED withdrawal (p<0.001).
This study demonstrates that patients and clinicians have different agendas when asked independently to produce and prioritise lists of treatment uncertainties. We recognise some limitations including that the presence of a doctor at the three patient meetings may have introduced an observer bias and that there were no newly diagnosed patients in those groups. The uncertainties generated by our participants are certainly not exhaustive, in part because we concentrated on treatment rather than natural history, causation and investigation. Our list of epilepsy therapeutic uncertainties needs to be supplemented by ‘fresh’ prospectively gleaned uncertainties by scouring recent Cochrane and other systematic reviews, and clinical guidelines. Furthermore, the database, no matter how dynamic, is redundant if we do not attempt to confirm whether the questions posed (by both clinicians and patients) are genuine uncertainties, that is, ‘known unknowns.’ The first 60 questions have been scrutinised via systematic review and the outcomes published on the DUETs website of NHS Evidence: the majority have remained uncertainties following review.8 This project provides the framework and content which can be used by professionals in targeting genuinely patient-focussed research, and we welcome validation of these results from other cohorts and geographical areas.
We might have expected patients to focus more on their individual needs regarding epilepsy treatment; however, the qualitative and statistical analysis does not generally support this. Not only did epilepsy professionals produce an equal number of questions under the theme of ‘considering the patient as an individual’ (n=14), but they ranked these uncertainties as more important than patients did. Both groups prioritised practical considerations that were specific to them.
Fifteen questions were produced exclusively by patients and carers focused on how to take prescribed medication (theme ‘How best to take AEDS;’ box 1). Four questions were raised about the general practitioner's role in epilepsy: all came from patients and carers, including two questions about repeat prescription access. Strikingly, not only did patients and carers generate eight of the nine questions regarding public awareness of epilepsy and seizures, but three of these questions were in the patients' and carers' top quartile.
Clinicians also prioritised practical considerations from their viewpoint, all of which clustered around ‘the challenging consultation.’ Clinicians posed all the questions about treatment of non-epileptic attack disorder (n=6, 2 were highly rated). Clinicians also accorded side effects in utero and prescribing issues in pregnancy greater importance than patients and carers did. However, half of the patients were 45 years or older and as a result may not have rated prescribing in pregnancy as a priority. Patients and carers did not volunteer any of the questions about prevention of sudden unexpected death in epilepsy (n=3); clinicians produced all 10 questions focussing on older people's needs (six regarding prescribing AEDs, four focussing on more general therapeutic needs); clinicians asked most of questions on the considerations before starting treatment (8/9), medication adherence (10/11) and nutritional support (11/12).
When discussing uncertainties about epilepsy treatment, we expected to receive questions about ‘curing epilepsy’ and achieving lifelong seizure freedom: such questions were conspicuous by their absence. Patients asked two questions, and epilepsy professionals 11, regarding how best to manage seizure freedom—most of these questions were about safe drug withdrawal. Does this mirror pragmatism (as opposed to idealism) represented in the important priorities? Epilepsy is not necessarily lifelong—several participants had achieved seizure freedom, both with surgery and with medication.
We are still at an early stage in promoting an environment that engenders genuine patient involvement in posing questions and developing outcomes that matter,10 and in mapping mismatches between researchers' and patients' priorities. For patients with rheumatoid arthritis, the priority treatment outcome is not pain reduction, but control of fatigue and sleep quality.1 9 11 12 The James Lind Alliance has identified patient research uncertainties in several other conditions including schizophrenia13 and urinary incontinence.14 A key theme from their priority setting partnership for incontinence mirrors the practical considerations of people with epilepsy: people with continence difficulties want more public toilets.
We encourage researchers in other disciplines to engage with patients and carers to help people with a personal experience of a condition to express their research priorities and condition-specific uncertainties. We would welcome any group keen to address an epilepsy uncertainty or to undertake a systematic review to consult DUETs. We will need the help of the epilepsy community in both continuously updating the uncertainty database and answering the questions that are raised. ‘Uncertainties’ is an occasional BMJ feature15 16 that is supported by editors of BMJ Knowledge, BMJ Clinical Evidence and BMJ Point of Care. We would like to encourage authors and editors to consider explicitly the uncertainties apparent in a body of work, in addition to the areas that they directly address. This study involves patients and professionals as partners in a consultancy about research, and as such no one is considered a participant in research.17
We are grateful to the members of the WERN health-clinicians' and patients' research and development groups for giving up their time to assist in this project. We also want to thank I Chalmers, M Fenton and N Thomas for their editorial assistance in the production of this paper.
Funding This was made possible by a grant, ‘The Database of Uncertainties about the Effects of treatment (DUETs) for schizophrenia and epilepsy,‘ received from the Wales Office of Research and Development (WORD).
Competing interests None.
Provenance and peer review Not commissioned; externally peer reviewed.
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.