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Queen Margaret Hospital, Majors Loan, Dunfermline, Fife KY12 OJU
The State Hospital, Carstairs, Lanarkshire
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Abstract |
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This paper is based on two audits carried out in 1996 and 1998 at The State Hospital, Carstairs. Each audit looked at anti-muscarinic drug use within the hospital, in relation to approved prescribing standards issued in 1996. All patients within the hospital on anti-muscarinic drugs were identified at the time of each audit. These prescriptions were compared with the approved prescribing standards. In the 1998 audit additional information was obtained from the case notes and the consultants, when the approved standards were not met.
RESULTS
The percentage of patients on regular anti-muscarinic drugs, falling outwith the prescribing standards, reduced between the two audits. However, in 1998 a small number of patients were still outwith the approved prescribing standards set in 1996.
CONCLUSIONS
An improvement in the prescribing practice of anti-muscarinics occurred following the introduction of prescribing guidelines. However, the guidelines were not fully met in the 1998 audit. This demonstrates the need for further audit and continued monitoring of anti-muscarinic prescription at the State Hospital.
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Introduction |
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Two audits of anti-muscarinic use were carried out at the State Hospital, Carstairs - the sole provider of psychiatric care, in conditions of special security, in Scotland and Northern Ireland (Snowdon, 1995). The audit in 1996 indicated that some patients were prescribed these drugs for extended periods without clear indication. Approved standards for the correct usage of these drugs was circulated in 1996. The audit was repeated in 1998 and compared with these standards.
Although patients are reviewed regularly at the State Hospital, there is a system for a more comprehensive multi-disciplinary review of the whole treatment/care package of each patient, at three monthly intervals. For this reason the standards that relate to anti-muscarinic prescribing focus on their continued prescription beyond three months.
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Approved standards |
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Objectives |
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The study |
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Findings |
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Standard 3
No patients exceeded the recommended British National Formulary
dosage guides in either the 1996 or 1998 audits.
Standard 4
All patients on clozapine alone and on an anti-muscarinic had had problems
of continuing hypersalivation in both the 1996 and 1998 audits (see
Table 2).
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Standard 5
The preferred anti-muscarinic drug was procyclidine in both the 1996 and
1998 audits (see Table 3).
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Assessing if the extended use of anti-muscarinic drugs occurs and the
reasons for it
A review of the last case conference on each of the 70 patients on
anti-mucarinics in 1998 was made. Out of the 70 patients, three did not have a
case conference as they had not been in the hospital long enough. For the
remaining 67 patients the medication the patient was on, including
anti-muscarinics, was documented clearly in the case conference notes.
Medication changes made at the time of the case conference and proposed future
changes were also documented. However, out of the 67 cases, specific reference
to neuroleptic induced side-effects and continued prescription of
anti-muscarinics was made in only three cases. Reasons for continued
anti-muscarinic prescriptions outwith Standard 1 were sought from the relevant
consultant (see Table 4).
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Complex reasons given for prescribing outwith the standards at the State Hospital included:
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Comment |
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A direct comparison of patients outwith the anti-muscarinic prescribing Standard 1 in the 1996 and 1998 audits cannot be made other than to compare the initial number. This is because the 1996 audit did not look at case notes or seek medical staff opinion. In the 1998 audit it would seem that 10 out of the 23 patients outwith the Standard 1, have no clear clinical reason to continue their anti-muscarinic at its present dose without review. The remaining 13 have reasons given for the extended continuation of the anti-muscarinic at its present dose. Reasons such as continuing extrapyramidal side-effects or hypersalivation (clozapine only) would seem pharmacologically valid. Other reasons given, relate to other aspects of the treatment package as a whole and their validity would be a matter for debate.
In terms of medical documentation at the State Hospital, it is the case that the three monthly reviews document all medications prescribed. They also record changes to medication at the time of the review, and for the short-term after the review. As stated before specific reference to anti-muscarinic prescription is rarely made. This is a problem which could easily be addressed, and doing so would aid prescribing practice.
Referring back to the objectives, it would seem there was an improvement in the practice of prescribing anti-muscarinics since the 1996 audit, and the introduction of the prescribing standards at this time. In both audits Standards 2-5 were adhered to rigorously. However, extended use of anti-muscarinics still occurred in 1998, although to a lesser degree than in 1996. This problem, which relates to Standard 1, involves a small but nevertheless, important, number of patients. In the 1998 audit reasons for the extended prescription of anti-muscarinics are given in over 50% of these cases. However, 10 patients are left requiring immediate review. The introduction of standards in 1996 may be responsible for this improvement although it is well recognised that despite publication of prescribing surveys/audits there is a general inertia of change to prescribing habits (Clarke & Holden, 1987).
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Recommendations |
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Acknowledgments |
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References |
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