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Community Health Sheffield NHS Trust
Academic Department of Psychiatry, The Longley Centre, Norwood Grange Drive, Sheffield S57JT; Honorary Specialist Registrar, Community Health Sheffield NHS Trust
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Abstract |
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We aimed to determine, using clinical audit, the effect of implementing national guidelines on the quality of responsible medical officers' (RMOs') reports to the mental health review tribunal (MHRT). We blindly assessed the quality of 50 consecutive reports concerning patients detained under Sections 3 and 37. Twenty-five reports were written before guidelines were circulated; a further 25 were written following the distribution of guidelines and a checklist with every request for a report.
RESULTS
The quality of reports, as measured by our checklist, significantly improved following the circulation of guidelines.
CLINICAL IMPLICATIONS
Increasing the awareness of guidelines by widespread circulation and the audit process is an effective way of improving the quality of RMOs' reports to the MHRT.
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Introduction |
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Previous literature regarding the quality of reports has, for the most part, offered expert opinion as to which points should specifically be included by RMO authors (Woolf, 1991; Langley, 1993). Audit has demonstrated that the majority of reports do not address the basic criteria for detention required by the MHA (Ismail et al, 1998) but that improvement might follow the formulation of local guidelines (Davison & Perez de Albeniz, 1997). The previous studies have been limited by the absence of agreed national criteria, on which to base standards, and by unblinded research methodologies that may have allowed the introduction of bias during appraisal of report quality.
Recently, and for the first time, comprehensive report-writing guidelines have been circulated by the MHRT (Regional Chairmen of the MHRT for England and Wales, 2000) after consultation with the Royal College of Psychiatrists. These provide guidance as to what the MHRT finds useful in RMOs' reports. We aimed to determine, using clinical audit, the effect of implementing the national guidelines on the quality of RMOs' reports to the MHRT. We hypothesised that the introduction and circulation of guidelines in our NHS trust would be associated with an improvement in the quality of reports.
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Method |
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The Study
The audit took place between July 2000 and February 2001. At the outset, we
derived a checklist of 18 criteria from the MHRT guidelines. Criteria were
chosen following discussion with RMOs at the trust's medical audit meeting. We
chose criteria that could be applied to any report, regardless of the
individual clinical circumstances. Reports were included in the audit if they
related to a patient detained under Section 3 or 37. Patients detained on
Section 2 and other Sections were excluded (because the short notice for these
tribunals can lead to the MHRT accepting an oral report from the RMO).
During a pilot phase, interrater reliability was checked. Two raters (P.E. and M.D.H.) independently assessed five randomly selected reports using the checklist. Then the pre-guidelines sample of 25 (22 Section 3; three Section 37) consecutive RMOs' reports between 1 June 2000 and 31 October 2000 was collected.
The intervention stage commenced on 1 November 2000. MHRT guidelines were circulated with every request for a report. Our checklist (effectively a simplified version of the guidelines) was also circulated with report requests. A post-guidelines sample of 25 (22 Section 3; three Section 37) consecutive reports was collected between 1 December 2000 and 27 February 2001.
Each of the 50 reports were then randomly allocated to one of the two assessors. Assessors were blind to the date of the report (the date was concealed in such a way that it was not possible to tell from which sample each report was drawn, but it was possible to check that the author had dated the report). Reports were assessed with the checklist of 18 criteria, and each awarded an overall quality score out of 18.
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Results |
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The 25 pre-guideline reports were compared with the 25 post-guideline reports. Since the data were normally distributed, we used an independent sample t-test to test the null hypothesis that there would be no significant improvement in the mean quality score following the circulation of guidelines. The mean quality score (out of a possible total of 18) was 11.32 pre-guidelines compared with 14.00 post-guidelines (mean difference 2.68; 95% Cl 0.87-4.49; t=2.97; d.f.=48; P<0.005).
The number of reports satisfying each of the individual criteria, before and after the circulation of guidelines, is shown in Table 1. We used Fisher's exact test to test the null hypothesis that the number of reports satisfying each criterion would not increase following the distribution of guidelines.
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Discussion |
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The increased frequency with which RMOs' names appeared in reports resulted from an improvement on the part of junior doctor authors, who had previously tended to state their own name without explicitly identifying the responsible consultant. The other main areas of improvement may reflect increased awareness of the Care Programme Approach (inclusion of keyworker's name), themes related to risk management (effect of immediate discharge and reason why informal treatment not possible) and the benefits of diagnostic precision (use of the ICD10 system; World Health Organization, 1992).
The overall change in quality score was significant but not large (2.68 out of 18; 15% improvement) and it is therefore important to identify those areas where there was room for further improvement. RMOs rarely stated the category of mental disorder under which patients were detained. We propose that this occurred because the classification was not perceived as having clinical significance. It does, however, have considerable legal significance especially with regard to the issue of whether treatment will bring benefit or prevent deterioration.
Drug treatments were well-reported, but non-pharmacological therapies were not. This may have been because RMOs saw pharmacotherapy as the primary treatment modality or because patients were not receiving non-pharmacological treatments. We think that the latter is unlikely; non-drug treatment is invariably a part of the overall management plan (e.g. occupational therapy) but might not always be conceptualised, by doctors, as treatment per se.
The accurate dating of the Section (we accepted date of detention or expiry) also failed to improve following the circulation of guidelines. RMOs might have assumed that the tribunal would be familiar with such details, and hence omit them.
Our method was designed to maximise the reliability and validity of the results. However, we report the findings of an audit cycle, not a controlled trial of an intervention. We cannot prove that the intervention was responsible for the improvement seen, although it is unlikely that it was not. Any confounding factors, such as differences in the populations of authors or differences in the clinical characteristics of detained patients seeking appeal, would tend to be evenly distributed between the before and after phases. It is noteworthy that each of our sampling periods included the junior doctors' rotational date.
Junior doctors wrote a significant proportion of the reports (under RMO supervision and with counter-signature). It is possible that, as the guidelines were circulated to RMOs, they may not always have been passed on to juniors. This means that the effects of the intervention may have been underestimated and would have been larger had RMOs directly compiled all the reports.
Accepting that the improvement seen was significant, but not universal, we consider that, in our NHS trust, the publication of guidelines by the MHRT has been a success. Feedback from RMOs has indicated a secondary benefit writing reports is quicker and easier when authors know what is expected of them. The local challenge is now to continue the audit process with a specific focus on those areas that did not improve following the first cycle. This is of particular importance because the preparation of an adequate report for the MHRT is not only a legal requirement but also an ethical duty of the doctor to his/her detained patient.
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Acknowledgments |
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References |
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DAVISON, P. & PEREZ DE ALBENIZ, A. (1997) Reports
prepared for mental health review tribunals and managers' reviews.
Psychiatric Bulletin,
21,
364
-366.
ISMAIL, K., SMITH, S. & MADEN, T. (1998) Mental health review tribunal medical reports. Psychiatric Bulletin, 22, 615 -618.
LANGLEY, G. E. (1993) Mental health review tribunals in practice. Psychiatric Bulletin, 17, 331 -336.
REGIONAL CHAIRMEN OF THE MENTAL HEALTH REVIEW TRIBUNAL FOR ENGLAND AND WALES (2000) Guidance for the Preparation of Medical Reports for the MHRT. London: Mental Health Review Tribunal Secretariat.
WOOLF, P. G. (1991) The role of the doctor in the
mental health review tribunal. Psychiatric Bulletin,
15,
407
-409.
WORLD HEALTH ORGANIZATION (1992) The ICD-10 classification of Mental and Behavioural Disorders. Geneva: WHO.
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