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Psychiatric Bulletin (2006) 30: 286-288. doi: 10.1192/pb.30.8.286
© 2006 The Royal College of Psychiatrists
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Psychiatric Bulletin (2006) 30: 286-288
© 2006 The Royal College of Psychiatrists

Blood glucose testing for adults prescribed atypical antipsychotics in primary and secondary care

Catharine Jane Tarrant, Consultant Psychiatrist

Sutton Health Centre, New Street, Sutton in Ashfield, Nottinghamshire NG17 1BW, e-mail: jane.tarrant{at}nottshc.nhs.uk

Declaration of interest

None.


   Abstract
 Top
 Abstract
 Introduction
 Method
 Results
 Discussion
 References
 
AIMS AND METHOD

The routine monitoring of blood glucose indices for all patients on atypical antipsychotics in 2004 in a rural adult psychiatric sector was examined. Pragmatic and practical standards were based on consensus expert opinion, National Institute for Clinical Excellence and prescribing guidelines.

RESULTS

The audit was completed on 60 atypical antipsychotic prescriptions. Testing of blood glucose prior to the initiation or change of an atypical antipsychotic was largely followed, with an overall adherence rate of 82%. However, there were large differences in testing between in-patient and community settings. Routine yearly monitoring in the community was inadequate, with an adherence rate of 63%.

CLINICAL IMPLICATIONS

There is a welcome emphasis on the physical health of those with severe and enduring mental illness. New initiatives, including prescribing guidelines, the care programme approach and primary care registers, offer the opportunity to develop consistency and coordination between primary and secondary care in the routine monitoring of psychiatric treatments and physical health in these patients.


   Introduction
 Top
 Abstract
 Introduction
 Method
 Results
 Discussion
 References
 
It has been estimated that the prevalence of type 2 diabetes in people with schizophrenia is around 2-4 times higher than in the general population (Bushe & Holt, 2004). The complications of type 2 diabetes can lead to significant physical morbidity but these may be limited by effective monitoring and good early management of the disease (National Institute for Clinical Excellence, 2002a).

Evidence suggests that treatment with antipsychotic medication increases the risk of developing diabetes. Although most studies are retrospective they generally report a higher rate of diabetes in those on atypical preparations compared with typical antipsychotics (Haddad, 2004). It remains uncertain whether any particular atypical preparation is more likely to cause type 2 diabetes than another and it is therefore prudent to consider the changes in glucose metabolism as a class effect for these drugs (Koro et al, 2002; Newcomer et al, 2002; Howes et al, 2004).

Since a diagnosis of schizophrenia and its treatment with an antipsychotic both increase the risk of impaired glucose tolerance and diabetes, patients should expect routine, standardised monitoring and screening (Haupt & Newcomer, 2001; Boilson & Hamilton, 2003; Expert Group, 2004). In-patient surveys of blood glucose monitoring and testing for diabetes in those on antipsychotics indicate that this is neither routine nor systematic and little is known about the screening practices in primary care/community populations prescribed these medications (Boilson & Hamilton, 2003; Taylor et al, 2004).


   Method
 Top
 Abstract
 Introduction
 Method
 Results
 Discussion
 References
 
The sample comprised all adult patients in a sector of rural Derbyshire who were prescribed atypical antipsychotics in 2004. Standards were developed based on the proposed pragmatic pathway for managing diabetes risks in those prescribed atypical antipsychotics from the consensus summary of the Expert Group (2004), the Maudsley Prescribing Guidelines (Taylor et al, 2003), the National Institute for Clinical Excellence (NICE) guidelines (NICE, 2002b), clinicians' best practice and local service expectations. The standards are shown in Table 1.


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Table 1. Adherence to audit standards
 

Patients were identified using psychiatric case notes, trust pharmacy records and general practitioner (GP) prescribing records. Information was gathered from multiple sources, including pathology and pharmacy records and psychiatric and GP case notes. Blood monitoring took place at Derby City Hospital. All information was recorded using an audit sheet designed to investigate the standards. A pilot study of five patients was initially undertaken. Diagnoses were recorded according to ICD-10 (World Health Organization, 1993) from the trust register and using information in medical notes. Basic descriptive statistics have been used to collate results.


   Results
 Top
 Abstract
 Introduction
 Method
 Results
 Discussion
 References
 
Population, diagnosis and prescriptions
The sector covers a total population of approximately 40 000. There were a total of 55 patients on atypical antipsychotic medications (30 men and 25 women); 41 had a primary diagnosis of functional psychosis (ICD-10 codes F20-29), 12 an affective psychosis (F30-39) and 2 other diagnoses of organic mania (F06.3) and emotionally unstable personality (F60.3) respectively. The audit was completed on the total number of atypical prescription scripts (60) over the year January to December 2004. This accounted for some patients who within the year had both started and changed atypical antipsychotic medication.

There were 10 patients who had a definitive diagnosis of type 2 diabetes. Their average age at the time of audit was 53 years and their median duration of treatment 40 months. There were 7 that had been diagnosed with diabetes after prescription of an atypical antipsychotic; 3 had been diagnosed within the year of the audit by their GP following a routine random blood glucose and subsequent glucose tolerance test.

Table 2 gives details of the drugs prescribed, the mean age of the patients and the median duration of treatment for each medication.


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Table 2. Atypical antipsychotics according to number of prescriptions, patient age and duration of treatment
 

Standards
Adherence to each of the standards is shown in Table 1. The overall number of instances of initiation or change of atypical antipsychotics was 24. In 13 instances this occurred during an in-patient stay with a random or fasting blood glucose test in accordance with the first standard. In 11 instances the initiation or change took place in an out-patient setting; in only 2 was a blood glucose test recorded. Fifteen of those initiated or changed also reached 4 months' duration of treatment within the audit year. All of those who were in-patients at 4 months had a random blood glucose test. None of those reaching 4 months' duration of treatment as out-patients had such a test.

There was a noticeable difference in the rates of testing for different medications. Those stable on olanzapine and clozapine were more likely to have had tests performed.

All patients who were known to have diabetes were receiving appropriate care for this. However, adherence to the last standard was only 51%, as patients who had not had a blood test and had missing data were considered potentially to have diabetes.


   Discussion
 Top
 Abstract
 Introduction
 Method
 Results
 Discussion
 References
 
This medical audit compared our practices with emerging, growing and more definitive evidence about the longer-term side-effects of antipsychotic treatment. It has been conducted with an awakening awareness of the lifestyle and physical health needs of those with severe and enduring mental illnesses (Connolly & Kelly, 2005). Differences in the surveillance practice for each atypical antipsychotic are in accordance with previous research (Citrome et al, 2004; Taylor et al, 2004). This might reflect the current lack of a clear consensus from multiple and differing guidelines on the necessary monitoring for both primary and secondary care. It is noteworthy that the most common reference used for prescribing, the British National Formulary (http://bnf.org/bnf), suggests that olanzapine and clozapine are more liable to cause hyperglycaemia or diabetes as side-effects.

There were large differences between the routine monitoring of blood glucose in in-patient and out-patient settings. In-patients benefited from a physical examination with routine physical tests at the time of admission to the ward. However, a random blood glucose test was not necessarily a standard and routine minimum requested by the admitting doctor. This concurs with the findings of Boilson & Hamilton (2003) that for psychiatric admission physical tests are often performed on an ad hoc basis.

Blood glucose testing for out-patients was markedly different and poor. The main barrier to both the initiation and routine monitoring of blood glucose as an out-patient was effective communication between services and consistency of information. The standard form of communication between the psychiatrist and GP remains a letter and/or telephone conversation. Requests for testing of out-patients in letters to the GP may be and were easily missed. There have been no previous studies investigating the physical monitoring of psychiatric out-patients. However, the need for improved communication and coordination of services between primary and secondary care is well recognised and emphasised by this audit.

Any assumption by psychiatrists that all physical care is the territory of the GP can hinder the monitoring of psychiatric treatment. The roles and responsibilities of primary and secondary care can seem unclear. Emphasis has been placed on the importance of psychiatrists arranging appropriate monitoring of medications that they are prescribing. Furthermore, advice and information given to the patient about their treatment is essential for good clinical practice (NICE, 2002b) and aids adherence to treatment and monitoring. Psychiatrists therefore need to work closely with GPs and their patients to ensure this happens (Connolly & Kelly, 2005).

There is a new emphasis on the need to attend to the long-overlooked physical health of those with severe and enduring mental illness. The new GP contract, the development of registers in primary care, guidance on clinical indicators (British Medical Association, 2004) and the care programme approach have already given impetus for consistency and routine monitoring in these areas. Opportunities exist to take advantage of this locally by developing a standard and coordinated approach across primary care and mental health trusts. With some limited and preliminary evidence that lifestyle changes can reduce the random blood glucose level in those on clozapine (Smith & White, 2004), there could also be potential practical preventive interventions for patients on these treatments.


   References
 Top
 Abstract
 Introduction
 Method
 Results
 Discussion
 References
 
BOILSON, M. & HAMILTON, B. J. (2003) A survey of monitoring of weight and blood glucose in in-patients. Psychiatric Bulletin, 27, 424 -426.[Abstract/Free Full Text]

BRITISH MEDICAL ASSOCIATION (2004) Quality and Outcomes Framework Guidance. Section 2: Clinical Indicators. Mental Health. London: BMA. http://www.bma.org.uk/ap.nsf/Content/QualityOutcomes~clinical~mh

BUSHE, C. & HOLT, R. (2004) Prevalence of diabetes and impaired glucose tolerance in patients with schizophrenia. British Journal of Psychiatry, 84 (suppl. 47), s67 -s71.

CITROME, L., JAFFE, A., LEVINE, J., et al (2004) Relationship between antipsychotic medication treatment and new cases of diabetes among psychiatric in-patients. Psychiatric Services, 55, 1006 -1013.[Abstract/Free Full Text]

CONNOLLY, M. & KELLY, C. (2005) Lifestyle and physical health in schizophrenia. Advances in Psychiatric Treatment, 11, 125 -132.[Abstract/Free Full Text]

EXPERT GROUP (2004) ‘Schizophrenia and Diabetes 2003’ Expert Consensus Meeting, Dublin 3-4 October 2003: consensus summary. British Journal of Psychiatry, 184 (suppl. 47), s112 -s114.[Free Full Text]

HADDAD, P. M. (2004) Antipsychotics and diabetes: review of nonprospective data. British Journal of Psychiatry, 184 (suppl.74), s80 -s86.[Abstract/Free Full Text]

HAUPT, D. W. & NEWCOMER, J. W. (2001) Hyperglycaemia and antipsychotic medications. Journal of Clinical Psychiatry, 62 (suppl. 27), 15 -26.

HOWES, O. D., BHATNAGAR, A., GAUGHRAN, E. P., et al (2004) A prospective study of impairment in glucose control caused by clozapine without changes in insulin resistance. American Journal of Psychiatry, 161, 361 -363.[Abstract/Free Full Text]

KORO, C. E., FEDDER, D. O., L'ITALIEN, G. J., et al (2002) Assessment of independent effect of olanzapine and risperidone on risk of diabetes among patients with schizophrenia: population based nested case-control study. BMJ, 325, 243 -248.[Abstract/Free Full Text]

NATIONAL INSTITUTE FOR CLINICAL EXCELLENCE (2002a) Management of Type 2 Diabetes - Managing Blood Glucose Levels (Guideline G). http://www.nice.org.uk/page.aspx?o=36737

NATIONAL INSTITUTE FOR CLINICAL EXCELLENCE (2002b) The Clinical Effectiveness and Cost Effectiveness of Newer Atypical Antipsychotic Drugs for Schizophrenia (Technology Appraisal 43). http://www.nice.org.uk/page.aspx?o=ta043

NEWCOMER, J. W., HAUPT, D. W., FUCETOLA, R., et al (2002) Abnormalities in glucose regulation during antipsychotic treatment of schizophrenia. Archives of General Psychiatry, 59, 337 -345.[Abstract/Free Full Text]

SMITH, H. & WHITE,T. (2004) Low glycaemic index diet in patients prescribed clozapine: pilot study. Psychiatric Bulletin, 28, 292 -294.[Abstract/Free Full Text]

TAYLOR, D., PATTON, C. & KERWIN, R. (2003) The Maudsley 2003 Prescribing Guidelines. (7th edn) . London: Martin Dunitz.

TAYLOR, D., YOUNG, C., ESOP, R., et al (2004) Testing for diabetes in hospitalised patients prescribed antipsychotic drugs. British Journal of Psychiatry, 185, 152 -156.[Abstract/Free Full Text]

WORLD HEALTH ORGANIZATION (1993) The ICD-10 Classification of Mental and Behavioural Disorders: Clinical Descriptions and Diagnostic Guidelines. Geneva: WHO.


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This Article
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British Journal of Psychiatry Advances in Psychiatric Treatment All RCPsych Journals