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Does home based medication review keep older people out of hospital? T
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     1 School of Medicine, Health Policy and Practice, University of East Anglia, Norwich NR4 7TJ, 2 Great Yarmouth Teaching Primary Care Trust, Astley Cooper House, Estcourt Road, Great Yarmouth, Norfolk NR14 8AB, 3 Academic Pharmacy Practice Unit, University of East Anglia, Norwich NR4 7TJ, 4 Suffolk Public Health Network, Suffolk House, St Clement's, Foxhall Road, Ipswich IP3 8LS

    Correspondence to: R Holland r.holland@uea.ac.uk

    Abstract

    Twenty eight per cent of all prescribed drugs in the United Kingdom are consumed by the 7% of the population aged over 751 2; 6.5% of hospital admissions have recently been shown to be related to adverse drug reactions, and these are significantly more likely to occur in older patients.3 This may be due to a combination of factors, including polypharmacy and age related physiological changes. Older patients can also have considerable problems with adhering to their drug regimens—up to 50% of prescribed drugs are estimated to be not taken as prescribed.4 5

    The national service framework for older people and the NHS plan recommend regular medication reviews for older patients to maximise therapeutic benefit and minimise potential harm.6 7 Historically, UK studies of medication review have focused on prescribing outcomes rather than effects on hospital admissions.8-10 An Australian study of a home based medication review-type intervention showed a 25% reduction in admissions and a reduction in deaths outside hospital.11 We sought to investigate the effectiveness of home based medication review in terms of its impact on hospital admissions in the United Kingdom. We chose home visits to ensure that the intervention could reach all very elderly participants. We also considered that home visits would allow pharmacists to gain greater insight into patients' methods of managing their drugs. The trial involved a large number of pharmacists delivering the intervention to ensure its generalisability.

    Methods

    Participant flow and follow up

    We invited 1399 patients to participate after screening them for eligibility between October 2000 and December 2002; 872 (62%) patients agreed and were randomised (fig 1). We excluded 17 recruited patients after randomisation. Reasons for exclusion were elective baseline admission (n = 5), discharge to nursing or residential home (5), death before discharge (4), previously recruited (2), and taking fewer than two drugs (1). Table 1 shows that the two groups were very similar at baseline. Twenty patients withdrew from the trial, and six moved from the study area. Primary outcome data were thus available for 829 (97%) patients.

    Fig 1 Flowchart showing progress of patients through the HOMER trial

    Table 1 Baseline comparison of intervention and control group patients. Values are numbers (percentages) unless stated otherwise

    Review pharmacists and intervention visits

    We recruited 22 review pharmacists. Of 429 patients in the intervention group, 362 received first visits. Reasons for not visiting were visit not wanted (46 patients), pharmacist unavailable (11 patients), and patient unavailable due to death or early readmission (10 patients). Review pharmacists carried out a mean of 17 (range 1-37) first visits. More than 90% of first visits occurred within two weeks of recruitment (mean 7.2 days), and visits lasted a mean (SD) of 61 (23) minutes. Second visits were conducted for 297 patients and took a mean (SD) of 42 (19) minutes. Visits generated a total of 933 recommendations or comments to general practitioners (2.58/visited patient); 120 of these referred to possible drug reactions or interactions in 81 patients (22% of visited patients).

    Compliance aids and pharmacists' view of intervention

    Review pharmacists recommended compliance aids in 39 patients (11% of those receiving first visits). Pharmacists were asked after their second visit to record whether they believed the visits had been useful. For 216 (73%) patients, pharmacists felt the visits were definitely or probably useful; for 81 (27%) patients, pharmacists felt the visits were unlikely to be useful or not at all useful, generally when patients were found to be coping very well.

    Number of hospital readmissions

    A total of 178 emergency readmissions occurred in the control group and 234 in the intervention group (table 2). The Poisson model indicated a 30% greater rate of readmission in the intervention group (rate ratio = 1.30, 95% confidence interval 1.07 to 1.58; P = 0.009).

    Table 2 Number of emergency hospital readmissions by group during six month trial follow up

    Secondary outcomes

    Mortality data were available for 829 (97%) patients. Fewer deaths occurred in the intervention group (49 v 63). Figure 2 shows the Kaplan-Meier survival graph. The hazard ratio for the intervention group compared with the control group was 0.75 (0.52 to 1.10; P = 0.14). Data on residential or nursing home admissions were available on fewer patients, as these were collected by telephone (585, 68%). Table 3 shows that fewer control patients than intervention patients were admitted to residential or nursing homes, but again these differences were not statistically significant.

    Fig 2 Survival analysis over six month follow up period for patients in the HOMER trial

    Table 3 Number of admissions to residential or nursing homes by group during six month trial follow up

    Quality of life data

    Change in utility scores could be calculated for 308/380 (81%) surviving intervention patients and 284/362 (78%) surviving control patients. Both groups' scores decreased over the six month follow up period, but the changes were not significantly different between the groups (table 4). Scores on the visual analogue health scale also fell; the difference of 4.1 (95% confidence interval 0.15 to 8.09) units in favour of the control group was statistically significant (P = 0.042).

    Table 4 Mean EQ-5D scores and visual analogue health scale scores for groups at baseline, three months, and six months follow up

    Primary care data

    We included 165 patients from 12 practices in this analysis (84 intervention, 81 control). General practitioners carried out 204 home visits in the intervention group and 125 in the control group, a difference of 43% (rate ratio = 1.43, 1.14 to 1.80; P = 0.002). No statistically significant differences occurred between the groups in attendance at general practices or prescription items received.

    Discussion

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