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BMJ 2004;329:431 (21 August), doi:10.1136/bmj.38182.591238.EB (published 5 August 2004)
Ineke Welschen, junior researcher1, Marijke M Kuyvenhoven, associate professor1, Arno W Hoes, professor of clinical epidemiology1, Theo J M Verheij, professor of general practice1
1 University Medical Center Utrecht, Julius Center for Health Sciences and Primary Care, PO Box 85060, 3508 AB Utrecht, Netherlands
Correspondence to: I. Welschen i.welschen{at}med.uu.nl
Design Randomised controlled trial.
Subjects Twelve peer review groups including 100 general practitioners with their collaborating pharmacists in the region of Utrecht, Netherlands.
Intervention The intervention consisted of group education meetings, with a consensus procedure on indication for and type of antibiotics and with training in communication skills; monitoring and feedback on prescribing behaviour; group education for assistants of general practitioners and pharmacists; and educational material for patients. The control group did not receive any of these elements.
Main outcome measures Antibiotic prescription rates for acute symptoms of the respiratory tract and patients' satisfaction.
Results 89 general practitioners completed the study (89%). At baseline, prescription rates for antibiotics for respiratory tract symptoms did not differ between intervention and control group (27% v 29%, respectively). After nine months, the prescription rates in the intervention group fell to 23%, whereas the control group's rose to 37% (mean difference in change -12%, 95% confidence interval -18.9% to -4.0%). Multilevel analysis confirmed the results of the unadjusted analysis (intervention effect -10.7%, -20.3% to -1.0%). Patients' satisfaction was high and did not differ in the two groups at baseline or after the intervention.
Conclusions A multiple intervention reduced prescribing rates of antibiotics for respiratory tract symptoms while maintaining a high degree of satisfaction among patients. Further research should focus on the sustainability and cost effectiveness of this intervention.
In a randomised controlled trial we evaluated the effectiveness of a multiple intervention aimed at reducing antibiotic prescription rates for respiratory tract symptoms in primary care.
Randomisation
We thought that it was essential to achieve comparability between the intervention and control arms with regard to the volume of antibiotic prescribing (above or below the median), working in a rural or urban area, and the number of general practitioners per group (above or below median). On the basis of the above variables we therefore allocated the 12 peer review groups who agreed to participate to groups A or B, to achieve comparability. MMK, who was blinded to the composition of the groups, flipped a coin to determine whether group A became the intervention or control group.
Intervention
The intervention consisted of a group education meeting with a consensus procedure on, firstly, the indication for and first choice of antibiotics for acute otitis media, sinusitis, tonsillitis, and acute cough, combined with communication skills training. The second component was monitoring and feedback on prescribing behaviour six months after the intervention; the third, group education for assistants of general practitioners and pharmacists; and the fourth, educational material for patients (see bmj.com for details).
The control group did not receive any part of the intervention.
Outcome measures
General practitioners registered all patients presenting with acute symptoms of the respiratory tract during three weeks in the autumn and winter of 2000 and 2001. Doctors noted diagnosis and management in patients' records as usual. Research assistants, who were blinded to the intervention status of the practices, extracted information on age, sex, diagnoses, antibiotic prescriptions, and referrals to hospital doctors.
After the consultation, general practitioners asked patients to fill in a questionnaire to rate their satisfaction with the consultation on a scale ranging from 1 (very dissatisfied) to 5 (very satisfied). Turkish and Arabic translations of this questionnaire were available.
Main outcome variables were the proportion of practice encounters for acute symptoms of the respiratory tract for which antibiotics were prescribed and the degree of patients' satisfaction with the encounter. Secondary outcome variables were insurance claims data over the period 2000-2, to assess differences in volumes of antibiotic prescribing before and after the intervention, independent from general practitioners' registrations and referral rates to hospital doctors, because we assumed that reduced antibiotic prescribing in primary care might increase hospital referral rates.
Analysis
We used t tests for unpaired samples. We performed a multilevel analysis to assess effectiveness, adjusted for clustering of general practitioners in practices and peer review groups and calculated intra-class correlation coefficients to rate the degree of clustering in practices and peer review groups.
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At baseline, mean antibiotic prescription rates for registered encounters for respiratory tract symptoms did not differ significantly between the two groups (27% v 29%, 95% confidence interval -9.1 to 5.0). In 2001, antibiotic prescription rates in the intervention group fell by 4% and those in the control group rose by 8% (table 2). Multilevel analysis confirmed the results of the unadjusted analysis (intervention effect -11%, -20% to -1%), while intra-class correlation coefficients showed that variation could be attributed to practice and group levels 0.17 and 0.09, respectively).
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The multiple intervention did not change patients' degree of satisfaction; they remained very satisfied with the consultation (table 2). These results were also confirmed by multilevel analysis (intervention effect on patients' satisfaction -0.03, -0.2 to 0.1).
Claims data over 2000 and 2001 were in line with our results: no significant differences occurred in the number of antibiotic prescriptions between intervention and control group in 2000. In 2001, however, the mean number of antibiotic prescriptions had decreased by 9.7 prescriptions per 1000 patients (P = 0.05 in the intervention group), whereas in the control group it had increased (P = 0.60). This increase was also seen in the non-participating general practitioners in the same region (mean difference in change between intervention and control group -11.6 prescriptions/1000 patients, -23.2 to -0.03) and confirmed by multilevel analysis. After 15 months, the number of antibiotic prescriptions in the intervention group was still lower than in the pre-intervention period (data not shown). Referral rates (about 2%) remained stable over time and did not differ between intervention and control groups (mean difference in change -0.1, -2.0 to 1.8).
About half of the patients received and returned the patients' questionnaire. Non-response can at least partly be explained by the fact that not all patients were given a questionnaire by doctors, probably because of time constraints during the encounter; this can be considered as a more or less random phenomenon in both groups. Nevertheless, satisfied patients may be over-represented in our sample because general practitioners may tend to give out questionnaires to patients in whom they expected a high level of satisfaction. Importantly, however, this will not bias the results if satisfied patients are over-represented in both groups, as is most likely. Bias would occur only if general practitioners in one of the two groups were more inclined to administer questionnaires to satisfied patients than the doctors in the other group. We think this is highly unlikely.
Although our study was not powered to assess an intervention effect on individual diagnoses, the percentage of antibiotics prescribed decreased for all diagnoses in the intervention group compared with the control group except for pneumonia (data not shown). This was expected since antibiotic treatment is strongly recommended in cases of pneumonia.
Comparison with other trials
A randomised controlled trial of Zwar et al, which evaluated the effectiveness of an intervention consisting of prescribing feedback, educational material, patient educational materials, and face to face instruction for high or wrong prescribers, showed the same effect size,16 whereas a more passively delivered complex intervention had little effect in changing practice.17
Outlook
Uncertainty remains about the sustainability of intervention effects.18 However, claims data over the first trimester of 2002 provided a rough indication about the longer term effectiveness of this intervention. After 15 months, the number of antibiotic prescriptions in the intervention group was still lower than in the period before the intervention. It is possible that the peer review group structure reinforces the changed behaviour. Further research should focus on structural sustainability and cost effectiveness of these interventions.
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This is the abridged version of an article that was posted on bmj.com on 5 August 2004: http://bmj.com/cgi/doi/10.1136/bmj.38182.591238.EB We thank the general practitioners and their patients who participated in this study and our data managers, P Zuithoff and F Verheij, for their help with data processing and analyses. We also want to thank the Municipal Health Service of Utrecht and the Dutch Institute for Rational Drug Use (DGV Nederlands Instituut voor Verantwoord Medicijngebruik) for their cooperation with the development of the intervention. We thank the regional health insurance company (Agis) for supply of the claims data.
Funding: Netherlands Organisation for Health Research and Development (Zorg Onderzoek Nederland) project number 2200.0057 and Foundation for the Advancement of Appropriate Prescription Drug Usage in the Central Region of the Netherlands (Stichting Doelmatig Geneesmiddelengebruik Midden Nederland).
Competing interests: None declared.
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