Department of Health Services Research, University of Limerick, and Department of Adult Psychiatry, Midwestern Regional Hospital, Limerick, Republic of Ireland, email: davidjmeagher{at}gmail.com
Midwestern Regional Hospital, Limerick
Limerick Mental Health Services, Limerick, Republic of Ireland
D.M. has received an unrestricted educational grant from AstraZeneca Pharmaceuticals.
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We studied the impact of an evidence-based multidisciplinary intervention to reduce six sub-optimal aspects of psychotropic prescribing, combined as a Prescribing Practice Quality (PPQ) score over a 5-year follow-upperiodinacommunity mental health service.
RESULTS
Sub-optimal prescribing practices were significantly reduced after 1 year and these improvements were sustained at 5-year follow-up. The PPQ scores were significantly reduced (P<0.001) in both the overall population attending at each follow-up point as well as in the ever-present population (n=163). Use of high-dose antipsychotics and thioridazine ceased entirely; use of sedative hypnotic agents was less amenable to reduction.
CLINICAL IMPLICATIONS
Multifaceted interventions can achieve sustained improvements in prescribing practices in real-world settings.
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Although information on the use of psychotropic agents is readily available, prescribing in real-world settings frequently deviates from suggested guidelines and licensing arrangements (Harrington et al, 2002; Hodgson & Belgamwar, 2006; Spinewine et al, 2007). A recent review by the Royal College of Psychiatrists (2007) highlighted the lack of data regarding the frequency of unlicensed prescribing in UK services, but European studies indicate that up to 66% of out-patient antipsychotic prescriptions are for unlicensed indications. In part, this reflects the complexities of real-world clinical practice where patient profiles often differ considerably from those of efficacy studies. Combination strategies, for example, benefit many patients with difficult-to-treat illness but remain insufficiently studied and not included within licensed indications (Karow & Lambert, 2003). However, other practices are discouraged because of concerns over safety such as increased risk of accidents (Department of Health and Children, 2002) or cardiotoxicity (Reilly et al, 2000).
We have previously investigated factors associated with six aspects of psychotropic prescribing (Meagher & Moran, 2003) and studied the impact of a multidisciplinary intervention on practices at 1-year (Moran et al, 2006) and 2-year (Raju & Meagher, 2005) follow-up. This work indicated that sub-optimal prescribing practices (e.g. polypharmacy and use of maintenance benzodiazepines) was substantially reduced by an intervention involving clear guidelines for discontinuation, education, provision of alternative non-pharmacological supports (e.g. anxiety management interventions) and regular monitoring of prescribing patterns. We further studied prescribing practices as part of an annual prescribing audit 5 years after the initial intervention to identify the extent to which improvements in prescribing were sustained at 5-year follow-up, the success in reducing individual sub-optimal practices, and factors associated with sustained improvement.
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In the period since the original intervention there has been continued emphasis on the agreed prescribing protocols, with a brief educational session for each new doctor as part of service induction. In addition, an annual audit allows monitoring of service contacts, ICD-10 diagnoses and prescribing practices within the service, and allows feedback as to prescribing patterns as part of ongoing service review. Two specific aspects of practice were not considered sub-optimal for the purposes of this study because they reflected specific agreed practices in the service: the first was targeted polypharmacy with the combination of a serotonin – noradrenaline reuptake inhibitor (either venlafaxine or duloxetine) with mirtazapine for treatment-resistant depressive illness (Meagher et al, 2006; Hannon et al, 2007), and the second was short-term use of quetiapine in low doses (25 - 100 mg) as a hypnotic agent.
| Box 1. Prescribing Practice Quality (PPQ) items and scoring
Scoring: 1 point per item present; range 0-6; higher scores indicate less optimal prescribing.
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Statistical analysis was conducted using SPSS version 14 for Windows. The PPQ scores for total populations at each point were compared with Wilcoxon signed ranks testing. Independent t-tests were used to compare age and duration of service attendance. Chi-squared tests were used to compare the frequency of severe mental illness, depot antipsychotic treatment and individual PPQ items between those ever-present in the service and those not.
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View this table: [in a new window] | Table 1. Demographic and clinical characteristics (2001–2006) |
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View this table: [in a new window] | Table 2. Sub-optimal prescribing practices (2001–2006) |
Two aspects of prescribing - use of thioridazine, and high-dose antipsychotic treatment - ceased entirely over the course of the study. In contrast, the use of anticholinergic agents and benzodiazepines declined during the initial phase of the study (2001-2) but remained relatively stable between 2002 and 2006, indicating that the initial reduction in use was sustained over the longer period of follow-up. The specific hypnotic agents prescribed did alter, with relatively greater use of zopiclone over time: n=24 (23% of total hypnotic use) in 2001, n=24 (30%) in 2002 and n=30 (49%) in 2006.
A total of 163 patients were clients of the service at all three evaluation points. These ever-present patients were older than the general population attending in 2006 (P<0.001), and were more likely to have severe mental illness (66% v. 26%, P<0.001) and to be in receipt of depot antipsychotic treatment (18% v. 3%, P<0.001). The mean PPQ scores for these patients are shown in Table 3. The percentage of patients from this population who had at least one aspect of prescribing that was sub-optimal (i.e. a PPQ score of 1 or more) diminished over time from 46% in 2001 to 38% in 2002 and 33% in 2006. Mean PPQ scores were significantly reduced at 2002 v. 2001 (P<0.001) and at 2006 v. both 2001 (P<0.001) and 2002 (P<0.001).
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View this table: [in a new window] | Table 3. Prescribing Practice Quality scores for ever-present patients (n=163) |
The ever-present population was further subdivided into those who had maintained improved prescribing (n=58) and those who had not (n=105) at 5-year follow-up. A greater likelihood of being in the improved group was associated with higher baseline PPQ score: 0.2 (s.d.=0.5) v. 2.1 (s.d.=0.9), P<0.001. There were trends towards greater likelihood of having improved PPQ scores in those with severe mental illness (P=0.09) and older age (P=0.06). Improved PPQ score was not related to gender, duration of service attendance, treatment with depot antipsychotic medication, frequency of attendance at services within the previous year or receipt of multidisciplinary shared care (i.e. attending at least two members of the multidisciplinary team).
Thirty-nine patients were receiving depot antipsychotic agents at the 2006 review. These patients were significantly older (mean age 55.9 years, s.d.=12.4; P<0.001), had attended the service for longer (mean 15.9 years, s.d.=10.3; P<0.001) and had significantly higher PPQ scores (mean score 0.85, s.d.=0.78; P<0.001) than those not receiving depot antipsychotic medication. This reflected a high rate of anticholinergic use (52%) and concomitant oral antipsychotic use (38%) in this population.
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Measuring the longer-term impact of interventions and identifying predictors of change is complicated by factors illustrated in this study. The only identified positive predictor of improved prescribing practice at 5-year follow-up was baseline PPQ score. We previously identified exposure to adjunctive supportive inputs (e.g. anxiety management) and chronicity of sub-optimal prescribing practice as predictors of improved prescribing at 1-year follow-up, but these factors were difficult to measure over more prolonged periods. It is interesting that patients receiving depot antipsychotic medications continued to have less than optimal prescribing despite being previously highlighted for particular attention (Meagher & Moran, 2003), reflecting the tendency for use of anticholinergic agents and antipsychotic polypharmacy in this group. In addition, the PPQ was affected by changing practices, with some of the original measures (e.g. use of thioridazine) now extremely uncommon and less useful indicators of prescribing quality. Moreover, even though some aspects of prescribing are enduring indicators (polypharmacy, benzodiazepine use), the specific agents involved changed over time.
Where polypharmacy is driven by emerging evidence of efficacy, or as a means to reduce side-effects (e.g. clozapine augmentation with atypical antipsychotics), it can reflect optimal practice. Moreover, polypharmacy may be driven by demonstrated benefits for individual patients even if efficacy studies are lacking. It may be that optimal patient outcomes require a low frequency of practices that are generally considered sub-optimal but have demonstrable benefits for individual patients. Moreover, clinical practice is sometimes more advanced than standards identified by randomised controlled trials or that use specifically licensed by regulatory bodies. However, it is often the case that in reality much sub-optimal prescribing reflects educational deficits or other constraints such as a lack of access to alternate interventions for disabling problems (Stone et al, 2002) and often occurs by default rather than design. This spectrum of prescribing is highlighted in a recent report (Royal College of Psychiatrists, 2007) and ranges from near-label prescribing to practices that have little foundation in evidence.
Benzodiazepine use is associated with risk of dependence, daytime sedation, cognitive impairment and falls (American Psychiatric Association, 1990). Although use of this class of drugs is discouraged in prescribing guidelines, it is common in real-world settings and is often resistant to change (Oude Voshaar et al, 2003; Caswell et al, 2006). It is interesting that reduction in use does not necessarily equate with lower subsequent incidence of associated adverse events such as falls (Wagner et al, 2007), emphasising the gap that can exist between clinical activities and presumed benefits in patient outcomes. In our population we noted a gradual increase in use of zopiclone, in keeping with a perception of better tolerability and reduced dependency potential compared with benzodiazepines, but gathering evidence of misuse and dependence potential needs to be noted (Mahomed et al, 2002). Other work suggests low-dose antipsychotics as a relatively benign substitute for benzodiazepines (Hamann et al, 2003), but emerging evidence of metabolic and cerebrovascular effects is a cause for considerable concern (Lieberman, 2004; Schneider et al, 2005) and emphasises the need for careful monitoring where these agents are used off licence.
Some aspects of prescribing are more difficult to reduce owing to factors such as patient reluctance (Oude Voshaar et al, 2003; Raju & Meagher, 2005) as well as perceived clinical benefit. Some have justified long-term benzodiazepine treatment for patients with disabling and treatment-refractory anxiety disorders where benzodiazepine use is associated with enhanced quality of life (Williams & McBride, 1999), but the characteristics of these patients remain unclear and evidence points to over- rather than under-utilisation in current practice. In the case of anticholinergic use, current opinion (World Health Organization, 1990) suggests that approximately 5% of patients receiving typical antipsychotic treatment require maintenance anticholinergic treatment. Consequently, a low level of use is consistent with optimal management of extrapyramidal symptoms. It remains unclear to what extent further reduction in these practices is consistent with optimal outcomes for patients. The need for evidence linking greater guideline adherence with improved patient outcomes is highlighted by Simpson et al (2005), who linked strict enforcement of National Institute for Health and Clinical Excellence (NICE) guidelines around cholinesterase inhibitor use to poorer patient outcomes. Other work (e.g. Mortimer et al, 2005), using similar parameters of sub-optimal prescribing to those used in our study, has linked greater side-effect burden to less-optimal prescribing that reduced as these practices diminished.
Ultimately a balanced approach to managing prescribing is required. Although some practices are clearly undesirable, others are acceptable for a minority of patients. The desire for greater evidence-based practice needs to recognise the limited capacity of available knowledge to guide many aspects of treatment (especially augmentation and combination therapy) as well as respecting the autonomy and judgement of clinicians and patients in identifying optimal individualised therapeutic plans. As a basic principle, where prescribing deviates from suggested norms, this should reflect targeted pharmacological management, the benefits of which are carefully monitored over time.
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