Countrygirl
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Here's some heart-sink nonsense.
A friend has just introduced me to this web site.The Nottingham Toolkit: bad news for people with ME. Here is the driving force behind the implementation of MUS, with CFS quoted as an example. Nurses are to be given four months training to cure us of our 'mental' health condition. Just look at the cost of it! Think of the research that could have funded!
http://impact.ref.ac.uk/casestudies2/refservice.svc/GetCaseStudyPDF/28021
A friend has just introduced me to this web site.The Nottingham Toolkit: bad news for people with ME. Here is the driving force behind the implementation of MUS, with CFS quoted as an example. Nurses are to be given four months training to cure us of our 'mental' health condition. Just look at the cost of it! Think of the research that could have funded!
http://impact.ref.ac.uk/casestudies2/refservice.svc/GetCaseStudyPDF/28021
Institution: University of Nottingham Unit of Assessment: UoA4 - Psychology, Psychiatry and Neuroscience
Title of case study: The development of psychological treatment pathways and better identification of Medically Unexplained Symptoms (MUS) in primary care
1. Summary of the impact Work on better management and identification of Medically Unexplained Symptoms (MUS) has led to the introduction of new treatments in primary care in England through the Improving Access to Psychological Treatment (IAPT) programme as well as having an impact on service planning and commissioning.
These approaches have also been implemented into the routine training and practice of General Practitioners (GPs) in parts of Europe. A clinical and economic evaluation of a psychosocial approach to chronic fatigue syndrome using general nurses and development of a cognitive behaviour therapy approach has changed general practice and enhanced the patient experience for those with MUS.
Effectiveness of reattribution training In order to provide a framework for GPs to tackle these issues through the use of a structured approach to increase confidence, a psychosocial approach called reattribution was adapted for a broader group of patients with MUS. Reattribution refers to an intensive structured consultation delivered by a GP, which aims to provide a psychological explanation to patients with somatised mental disorder.
To explore the potential advantages of reattribution within a clinical setting, a randomised controlled trial (‘Training family practitioners in reattribution to manage patients with Medically Unexplained Symptoms: MUST- see section 3 for details) was conducted2 .
The trial compared reattribution with treatment as usual in 16 GP practices with 74 GPs and 141 MUS patients to explore feasibility. A six hour training package was developed and adapted for use by GPs to deliver reattribution to patients with MUS.
Morriss and colleagues developed training materials and practice-based delivery of such training by mental health facilitators to improve both the recognition and management of such patients.
Findings showed that such practice-based training improved doctor-patient communication and highlighted a number of attitudinal, practical and organisational issues that needed to be addressed e.g. that patients needed GPs to demonstrate to them that they would take any new symptoms seriously in terms of physical disease rather than assume them to be psychologically created.
Challenges in the implementation of reattribution in a clinical setting were explored through qualitative methods and results showed that barriers included the complexity of patients' problems and patients' judgements about how to manage their presentation of this complexity. Many patients reported not trusting doctors with discussion of emotional aspects of their problems and therefore chose not to present them.
Therefore it was concluded that simply improving GP explanation of unexplained symptoms is insufficient to reduce patients' concerns. Rather, GPs need to help patients to make sense of the complex nature of their presenting problems, communicate that attention to psychosocial factors will not preclude vigilance to physical disease and ensure a quality of doctor-patient relationship in which patients can perceive psychosocial enquiry as appropriate3 .
In light of this, more recent research funded by the Medical Research Council showed that with training and ongoing supervision, psychological treatment for some MUS patients with specific syndromes such as Chronic Fatigue Syndrome could be delivered by adult specialty general nurses who had received four months’ training, including supervised practice, in each of the supportive listening and rehabilitation interventions4 .
This streamlined the process and reduced barriers to delivery such as patients not disclosing psychological problems to GPs. Better identification of patients with MUS Previous research highlighted the need for a streamlined process of identification of MUS within general practice. Therefore,
Morriss and colleagues conducted Department of Health (Care Services Improvement Partnership, CSIP) funded research investigating streamlined diagnosis of MUS by developing methods for estimating the number of patients suffering with MUS using electronic patient records held by practices5 . With additional support of CSIP, Morriss developed a search tool ‘The Nottingham Tool’.
This searches a GP Practice Database, to identify a cohort of patients that fulfil the criteria for MUS. This cohort provides an overview to the commissioners, or the practice, about the number of people likely to have a MUS.
The tool is designed to generate a list for GPs of patients with possible MUS. The GP can then refine the list to exclude or include patients known to have the condition. Morriss noted that whilst identifying the individual patient is important, it is also important for commissioners of services to have a better understanding of the numbers of people who are likely to have a MU symptom. It is important so that appropriate services can be planned and commissioned6 .
As a result of such work on both the organisation of care and the development of The Nottingham Tool to help GPs estimate the care needs of patients in their practice, the National Health Service (NHS) in England extended the provision of specialist psychological care as part of the IAPT programme for such patients.
Therefore, in summary, taken as a whole, Morriss’s body of research about MUS has shown how GPs can be taught to deliver better doctor-patient communication, organise care for such patients, estimate the numbers needing care, better identify patients and develop strategies to engage patients in psychological treatment at a time when the NHS in England will be spending nearly £200 million over a 3 year period on such treatment.
Introduction of a national streamlined pathway for psychological treatment (IAPT) In April 2008, the Government announced that they would invest approximately £33 million in 2008/09, a further £70 million in 2009/10 and an additional £70 million in 2010/11 (totalling £173 million) to introduce IAPT treatment for MUS and long-term conditionsa . This document was prepared in collaboration with the Care Services Improvement Partnership (CSIP) and the NHS commissioning team for MUS/long-term conditions (LTC).
Later, in October 2008, the Positive Practice Guide published by IAPTb outined changes in clinical practice proposed by Morriss and colleagues, discussing barriers to treatment, identification, the impact of psychological problems and gaps in GP training. Morriss is a key member of the MUS/LTC special interest group for IAPT who also aim to improve access to psychological therapies for the whole community by removing barriers to treatment and increased understanding of patient needs, thus translating the work directly to local communitiesc . Work conducted by Morriss through this group has had impact on patients by raising awareness of MUS as a long-term debilitating condition and a disabilityd .
This formed a major part of the need for increased government funding to address the issue. Based upon more recent work by Morriss6 , the government have decided to introduce nurse-delivered and CBT psychological interventions for MUS in primary care. This has resulted in a major training programme to be developed to expand the psychological therapist workforce in order to respond more effectively to the needs to patients with MUS/LTC and co-morbid anxiety and depressionc . In 2009, Morriss’s work on reattribution training (cited in research from 2007)1,2 informed the Royal College of Psychiatrists Practical Management Guide for Patients with Physical and Psychological Problems in Primary Caree as well as the practical guidance document for GPs to help manage MUS by encouraging reattribution and reducing GP anxieties about tackling psychological problems with the patientf .
More recently, in 2012, a NHS Emotional Wellbeing and Physical Health Care Case for Change described Morriss’s findings on symptom reattribution as a successful technique as part of a wider package of care for people with MUSg thus further improving the patient experience.
Looking forward, and as evidence of government acknowledgment of its importance, in 2010 the government decided to increase the funding of IAPT services to £400 million over the next 4 years to fund the expansion of work into further areas including medically unexplained symptomsh .
Increased recognition of MUS in general practice through The Nottingham Tool For further impact on GPs and patients, Morriss’s work has increased recognition of MUS cases in primary care through the development of The Nottingham Tool. This tool has helped estimate the need for psychosocial treatment through better identification of patients with MUS within the general practice community. In 2009, NHS Commissioning Support for London recommended
The Nottingham Tool for general practitioners to increase recognition of MUS within the local community by scanning medical records to generate a list of patients with MUSk . The Tool has its impact primarily on commissioners, raising awareness of numbers of individuals within local communities with MUS so that funding can be distributed appropriately. The Tool has been praised by practitioners, including the chair of Sainsbury Centre for Mental Health and IAPT MUS/LTC special interest group.
Finally, Morriss’s continued work on this topic continues to be cited as important in informing the thinking of health-care decisions, in particular in the domain of mental health. Publications are on-going with new advances being made in 2012 (e.g. Morriss: Role of mental health professionals in the management of functional somatic symptoms in primary care).
The chair of Sainsbury Centre for Mental Health commented on these on-going contributions. ‘I have no doubt that your work has advanced national and international knowledge and practice, and continues to do so; I am currently a CCG Governing Body Member, leading on mental health - but I am still asked regularly for advice on this subject, part of my reply usually references your work’l . 5. Sources to corroborate the impact a. Improving Access to Psychological Therapies, Commissioning Toolkit.
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