Table 2.
Prediction plus phone reminders compared to usual scheduling for managing appointment attendance | |||||
---|---|---|---|---|---|
Patient or population: outpatients | |||||
Setting: outpatient clinics | |||||
Intervention: prediction plus phone reminders | |||||
Comparison: usual scheduling | |||||
Outcomes | Anticipated absolute effectsa (95% CI) |
Relative effect (95% CI) | No. participants (studies) | Certainty of the evidence (GRADE) | |
Risk with usual scheduling | Risk with prediction plus phone reminders | ||||
|
226 per 1000 | 0 per 1000 (111–169)b | RR ranged from 0.49 to 0.75 | 4959 (3 RCTs)b |
|
Prediction plus text message reminders compared to usual scheduling for managing appointment attendance | |||||
---|---|---|---|---|---|
Patient or population: outpatients | |||||
Setting: outpatient clinics | |||||
Intervention: prediction plus text message reminders | |||||
Comparison: usual scheduling | |||||
Outcomes | Anticipated absolute effectsa (95% CI) |
Relative effect (95% CI) | No. participants (studies) | Certainty of the evidence (GRADE) | |
Risk with usual scheduling | Risk with prediction plus text message reminders | ||||
|
114 per 1000 | 0 per 1000 (102–106) | RR ranged from 0.89 to 0.93c | 158669 (1 RCT) |
|
Prediction plus patient navigator compared to usual scheduling for managing appointment attendance | |||||
---|---|---|---|---|---|
Patient or population: outpatients | |||||
Setting: outpatient clinics | |||||
Intervention: prediction plus patient navigator | |||||
Comparison: usual scheduling | |||||
Outcomes | Anticipated absolute effectsa (95% CI) |
Relative effect (95% CI) | No. participants (studies) | Certainty of the evidence (GRADE) | |
Risk with usual scheduling | Risk with prediction plus patient navigator | ||||
|
131 per 1000 | 72 per 1000 (60–88) | RR 0.55 (0.46–0.67) | 4425 (1 RCT) |
|
Abbreviations: CI: confidence interval; RCTs: randomized controlled trials; RR: risk ratio.
The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
Participant numbers and risk ratios were unavailable for Lee et al42 for all outcomes. Lee et al42 reported a statistically significant decrease of −18.7% (P < .001) in no-show rate.
Results were reported separately for mental health and primary care patients.
Two of 3 studies were at high risk of bias; this included high risk of bias for randomization in the largest study.
Single study at high risk of bias for randomization.