Table 3.
Primary and secondary outcomes at last follow-up
Outcomes | Decision support group | Control group | Adjusted comparison estimate (95% CI) | P value (sensitivities) | |||
---|---|---|---|---|---|---|---|
No | Estimate* | No | Estimate* | ||||
Primary outcome | |||||||
First unplanned hospital admission or death† | 1953 | 997 (51.0%) | 1951 | 1055 (54.1%) | OR: 0.88 (0.73 to 1.07) | 0.19 (MI‡ 0.114) | |
Sensitivity: time to first unplanned hospital admission or death | 1953 | 0.46 (0.01)§ | 1951 | 0.50 (0.01)§ | HR: 0.93 (0.82 to 1.05) | 0.24 | |
Key secondary outcome | |||||||
Last recorded No of drugs | 1953 | 10.12 (3.01) | 1951 | 10.52 (2.94) | Coefficient¶: 0.95 (0.94 to 0.97) | <0.001 (MI<0.001) (BS<0.001) | |
Sensitivity: change in No of drugs from baseline | 1953 | −0.42 (2.16) | 1951 | 0.06 (2.04) | MD: −0.45 (−0.63 to -0.26) | <0.001 (MI<0.001) (BS<0.001) | |
Other secondary outcomes | |||||||
Death† | 1953 | 380 (19.5%) | 1951 | 366 (18.8%) | OR: 1.01 (0.73 to 1.38) | 0.96 | |
Sensitivity: time to death | 1953 | 0.11 (0.01)§ | 1951 | 0.12 (0.01) § | HR: 0.90 (0.71 to 1.13) | 0.35 | |
First unplanned hospital admission† | 1953 | 945 (48.4%) | 1951 | 990 (50.7%) | OR: 0.92 (0.76 to 1.10) | 0.36 | |
Sensitivity: time to hospital admission | 1953 | 0.49 (0.01)§ | 1951 | 0.52 (0.01)§ | HR: 0.95 (0.83 to 1.07) | 0.38 | |
No of unplanned hospital admission | 1953 | 0.76 (1.24) | 1951 | 0.87 (1.34) | IRR: 0.91(0.69 to 1.20) | 0.51 (BS 0.351) | |
Duration of unplanned hospital admission (days) | 1949 | 7.89 (17.43) | 1948 | 8.47 (18.18) | IRR: 0.95 (0.67 to 1.35) | 0.79 (BS 0.707) | |
No of falls over trial period | 1798 | 0.50 (1.26) | 1785 | 0.51 (1.24) | IRR: 1.08 (0.88 to 1.34) | 0.44 (BS 0.287) | |
≥1 fractures during trial period | 1953 | 59 (3.0%) | 1951 | 45 (2.3%) | OR: 1.37 (0.87 to 2.16) | 0.17 | |
SF-12: | |||||||
Physical component score (0-100) | 1223 | 36.73 (9.44) | 1146 | 36.32 (9.11) | MD: 0.07 (-0.69 to 0.83) | 0.85 | |
Mental component score (0-100) | 1224 | 46.66 (11.09) | 1145 | 46.27 (11.18) | MD: 0.34 (-0.69 to 1.37) | 0.52 |
OR=odds ratio; MI=multiple imputation; HR=hazard ratio; BS=bootstrap; MD=mean difference; IRR=incidence rate ratio.
Mean (standard deviation) or number (%) unless otherwise indicated.
Participants who dropped out were analysed as having reached the endpoint.
Participants who dropped out were analysed using multiple imputation.
Estimated proportion (standard error) reaching endpoint by 24 months, from survivor function.
Coefficient represents the adjusted ratio of the number of prescribed drugs in participants assigned to electronic decision support versus those assigned to treatment as usual (control group).