Study information | Patient characteristics | ED visits | Other outcomes | |
---|---|---|---|---|
Follow-up telephone call | ||||
 Biese et al. (2014) [20], USA  Trial no.: NCT01207180  Funder: Duke Endowment and the Community Connection for Seniors  Industry sponsored: no | Study design: RCT Intervention type: follow-up telephone call Comparator: TAU and placebo | N: intervention = 39; control = 46; placebo = 35 Age (mean): 75 years % female: intervention = 59%; control = 61%; placebo = 60% | 22% of intervention patients revisited ED compared to 33% of placebo and 27% of control (p = 0.41) | Costs: intervention had a 70% chance of being cost saving and a 3% chance of being cost-effective and 27% chance of resulting in more return visits at higher total costs |
 Biese et al. (2018) [21], USA  Trial no.: NCT01893931z  Funder: Duke Endowment, the Kenan Family Foundation, and Mr. John A. McNeill, Jr  Industry sponsored: no | Study design: RCT Intervention type: follow-up telephone call Comparator: control group | N: intervention = 974; control = 975 Age (mean): intervention = 74.2 years; control = 73.9 years % female: intervention = 59.1%; control = 61.1% | Rate of return to ED, hospitalization, or death: 15.5% (95% CI: 13.2–17.8) in intervention; 15.2% (95% CI: 12.9–17.5) in control, p = 0.86 Return to ED: 12.2% (95% CI: 10.1–14.3) in intervention; 12.5% (95% CI: 10.4–14.6) in control | Hospitalization within 30 days: 9% (95% CI: 7.2–10.8) in intervention; 7.4% (95% CI: 5.8–9.0) in control Outpatient use, seeing a PCP within 30 days: 80.8% in both groups Stratifying by age did not find a benefit |
 van Loon-van Gaalen et al. (2021) [11, 33], Netherlands  Trial no.: trial NL6598  Funder: Jacobus Foundation  Industry sponsored: no | Study design: RCT Intervention type: follow-up telephone call Comparator: control group | N: intervention = 1516; control = 1659 Age (median): intervention = median 78 years; control = median 78 years % female: intervention = 58%; control = 58% | Unplanned hospital admission and/or ED revisit within 30 days: 16% of intervention; 14% of control, OR 1.16, 95% CI: 0.96–1.42; separate rates were not significant | Stratifying by age: patients aged < 78 years: intervention patients had more unplanned hospital admissions and/or ED revisits than control pts. (18% vs 14%, OR 1.33, 95% CI: 1.01–1.75) |
Comprehensive geriatric assessment + other | ||||
 Foo et al. (2014) [31], Singapore  Trial no.: National Healthcare Group (NHG) Domain-Specific Review Board (DSRB) C/09/023  Funder: Ministry of Health’s Healthcare Quality Improvement and Innovation (HQI2) Fund  Industry sponsored: no | Study design: RCT Intervention type: geriatric assessment, referral Comparator: TAU | N: intervention = 234; control = 425 Age (median): intervention = 77 years; control = 77 years % female: intervention = 53.6%; control = 56.2% | ED reattendance, 3 months: 37.2% in control; 36.8% in intervention, p = 0.97, adjusted OR = 0.91, 95% CI: 0.67–1.24 ED reattendance, 6 months: 50.8% in control; 47.9% in intervention, p = 0.84, OR: 0.82, 95% CI: 0.61–1.11 ED reattendance, 9 months: 59.8% in control; 54.6% in intervention, p = 0.19, OR: 0.74, 95% CI: 0.55–1.01 ED reattendance, 12 months: 66.0% in control; 61.1% in intervention, p = 0.19, OR: 0.75, 95% CI: 0.55–1.03 | Hospitalization, 3 months: 28.8% of control; 27.9% of intervention, p = 0.84, adjusted OR: 0.88, 95% CI: 0.63–1.22 Hospitalization, 6 months: 40.4% in control; 38.2% in intervention, p = 0.60, OR: 0.84, 95% CI: 0.62–1.14 Hospitalization, 9 months: 48.2% in control; 43.9% in intervention; p = 0.28, OR: 0.76, 95% CI: 0.56–1.03 Hospitalization, 12 months: 53.8% in control; 49.6% in intervention, p = 0.30, OR: 0.77, 95% CI: 0.57–1.04 |
 Heeren et al. (2019) [29], Belgium  Trial no.: ISRCTN91449949  Funder: the Flemish government agency for Innovation by Science and Technology  Industry sponsored: no | Study design: observational study Intervention type: geriatric assessment tool, care plan, case-manager follow-up, referral to geriatric clinic Comparator: cohort collected prior to intervention period | N: intervention = 886; control = 794 Age (Q2): intervention = 81 years; control = 80 years % female: intervention = 52.9%; control = 54.9% | Unplanned ED readmission, 30 days: 12.1% in control; 13.1% in intervention, p = 0.21 Unplanned ED readmission, 90 days: 22.1% in control; 23.9% in intervention, p = 0.11 Median time to unplanned ED readmission within 90 days: 25.1 days (min 0.3, max 88.3) for control; 27.6 (min 0.2, max 88.0) days in intervention, p = 0.66 | Median ED LOS: 19.1 h in control; 12.7 h in intervention, p < 0.001 Hospitalization: 70.0% in intervention; 67.0% in control, p = 0.003 Median hospital LOS: 8.7 days in control; 8.6 days in intervention, p = 0.15 |
 Lin et al. (2021) [34], Taiwan  Trial no.: IRB no. CE18256  Funder: Veterans Affairs Council, Taiwan  Industry sponsored: no | Study design: observational study Intervention type: comprehensive geriatric assessment, case management Comparator: TAU | N: intervention = 236; control = 122 Age (median): intervention = 82 years; control = 82 years % female: intervention = 50.4%; control = 69.7% | ED revisits within three months: 35.3% pre-intervention; 28.4% post-intervention Not statistically significant | Hospitalization: decreased by 27% (50.8% pre-intervention, 23.1% post-intervention) Male gender associated with decreased ORs of admission following index ED visit |
 Pedersen et al. (2016) [30], Denmark  Trial no.: none reported  Funder: none reported  Industry sponsored: not reported | Study design: RCT Intervention type: geriatric assessment, home visit by geriatrician and nurse Comparator: TAU | N: intervention = 693; control = 637 Age (mean): intervention = 86.4 years; control = 86.4 years % female: intervention = 60%; control = 64% | None reported | Discharges: 56% of intervention patients were discharged directly from the ED compared to 46% of control, p = 0.01 Hospitalization: 12% in intervention; 23% in control, p < 0.001 Of those admitted, LOS for intervention patients (median = 2 days) was significantly shorter than for control (median = 3 days), p = 0.03 |
Pharmacist-lead intervention | ||||
 Santolaya-Perrin et al. (2019) [32], Spain  Trial no.: none reported  Funder: RED-FASTER of SEFH (Sociedad Española de Farmacia Hospitalaria)  Industry sponsored: no | Study design: RCT Intervention type: medication review programme Comparator: TAU | N: intervention = 323; control = 342 Age (mean): intervention = 78.99 years; control = 78.2 years % female: intervention = 51.6%; control = 53.5% | Emergency visits and hospital admissions: no significant differences between groups RR, 95% CI: 0.857, 0.652–1.126 for 3 months RR, 95% CI: 0.917, 0.715–1.176 for 6 months RR, 95% CI: 0.954, 0.766–1.187 for 12 months | None reported |
 Shaw et al. (2016) [26], USA  Trial name: EMBRACE ED  Funder: Kaiser Permanente Colorado  Industry sponsored: yes | Study design: observational study Intervention type: pharmacist intervention Comparator: non-clinical pharmacist + elder ED, and non-elder ED + clinical pharmacist | N: intervention = 4103 patients in total; 342 treated by EMBRACE clinical pharmacy specialist; control = 530 treated with non-clinical pharmacy specialist but in EMBRACE; 3231 non-EMBRACE Age (mean): 77 years overall % female: 58% overall | Patients in CPS + EMBRACE group more likely to experience a 30-day return visit than those in non-EMBRACE group (unadjusted OR 1.42, 95% CI: 1.09–1.85), and a 90-day return visit than those in the non-EMBRACE group (unadjusted OR 1.34, 95% CI: 1.06–1.69) 30-day ED return visit: 24% in intervention, 18.2% in non-EMBRACE, 18.9% in non-CPS 90-day ED return visit: 36.3% in intervention, 29.8% in non-EMBRACE, 30.6% in non-CPS | Admitted from index ED visit: 42.4% in intervention, 42.1% in non-EMBRACE, 42.5% in non-CPS; no differences |
Care transition intervention | ||||
 Schumacher et al. (2021) [35], USA  Trial no.: NCT02079987  Funder: Patient-Centered Outcomes Research Institute award  Industry sponsored: no | Study design: RCT Intervention type: care transition intervention Comparator: TAU | Definition of frequent user: 3 or more visits in prior year N: intervention = 557; control = 544 Age (mean): intervention = 72.4 years; control = 72.8 years % female: intervention = 60%; control = 63% | Post-intervention: 627 return ED visits made within 60 days ED visit: OR 1.08 (95% CI: 0.83–1.39), not statistically significant | Intervention did not significantly affect hospital-based acute care, but ED return visits were less likely to result in hospitalization Hospital admission at index ED visit: intervention participants had 36% lower odds of hospitalization upon ED return (OR 0.64, 95% CI: 0.45–0.91) Outpatient visit: OR 1.13 (95% CI: 0.77–1.67), not statistically significant Reasons for ED return visits: patients were confident they would get needed care in the ED, PCP often encourage patients to seek emergency care Reasons for not visiting outpatient clinics: barriers to timely outpatient care, difficulty scheduling appointments, office-based outpatient visits discouraged if diagnostic tests were required Physician perspective on hospital admissions: ED physicians often hospitalize patients if outpatient follow-up or social support are in question |
Early assessment and intervention | ||||
 Cassarino et al. (2021) [22], USA  Trial no.: NCT03739515  Funder: Health Research Board of Ireland through the Research Collaborative for Quality and Patient Safety  Industry sponsored: no | Study design: RCT Intervention type: early assessment and intervention Comparator: TAU | N: intervention = 176; control = 177 Age (mean): intervention = 78.6 years; control = 80.6 years % female: intervention = 61.4%; control = 57.1% | 30-day ED revisit: 18.8% for intervention; 13.6% for control, OR 1.42 (95% CI: 0.79–2.55), p = 0.23 6-month ED revisit: 31.4% for intervention; 43.3% for control, OR = 0.65 (95% CI: 0.42–1.02), p = 0.06 | Time spent in ED, index visit, median (IQR), hours: 6.43 (4.05–14.87) for intervention; 12.1 (6.18–22.14) for control, p < 0.001 Hospitalization at index visit: 19.3% for intervention; 55.9% for control, p < 0.001 Unscheduled hospital admission at 30 days: 11.9% for intervention; 12.4% for control, OR 0.96 (95% CI: 0.51–1.84), p = 0.92 Unscheduled hospital admission at 6 months: 19.4% for intervention; 33.3% for control, OR = 0.52 (95% CI: 0.32–0.88), p = 0.02 Hospital LOS at index visit, median (IQR), days: 9 (3–13) for intervention; 9 (5–24) for control, p = 0.32 Satisfaction at index visit, mean (SD): 25.8 (3.03) for intervention; 24.8 (3.74) for control, p = 0.008 |
Physical therapy | ||||
 Lesser et al. (2018) [24], USA  Trial no.: none reported  Funder: none reported  Industry sponsored: not reported | Study design: observational study Intervention type: physical therapy services Comparator: TAU | N: intervention = 17,791; control = 173,651 Age (mean): intervention = 82.4 years; control = 80.6 years % female: intervention = 70.4%; control = 66.2% | 30-day follow-up, all-cause ED: 20.4% in intervention; 21.7% in control Fall-related ED revisits at 30 days: 1.7% in intervention; 2.6% for control Fall-related ED revisits at 60 days: 2.5% in intervention; 3.6% in control p < 0.01 for both 30 and 60 days | None reported |
Multi-faceted interventions | ||||
 Arendts et al. (2018) [27], Australia  Trial no.: ACTRN12612000798864  Funder: State Health Research Advisory Council of Western Australia  Industry sponsored: no | Study design: RCT Intervention type: education, follow-up telephone call, referral Comparator: TAU | N: intervention = 81; control = 80 Age (mean): intervention = 78 years; control = 78 years % female: intervention = 39%; control = 37% | 8% absolute (95% CI: 7–20) and 20% relative risk reduction for an intervention patient making an unplanned ED reattendance within 28 days | Hospitalization: no significant difference in 28-day hospitalization rates or hospital bed day usage |
 Goldberg et al. (2020) [23], USA  Trial no.: NCT03360305  Funder: National Institute on Aging and Society for Academic Emergency Medicine Foundation/Emergency Medicine Foundation GEMSSTAR for Emergency Medicine Supplemental Funding  Industry sponsored: no | Study design: RCT Intervention type: pharmacist-led medication review; physical therapy consultation Comparator: TAU | N: intervention = 55; control = 55 Age (median): intervention = 81.9 years; control = 80.1 years % female: intervention = 67%; control = 67% | Total visits: control = 66; intervention = 30 Adjusted rate of all ED visits: control = 1.54 (95% CI: 1.04–2.30); intervention = 0.73 (95% CI: 0.45–1.17), IRR: 0.47 (95% CI: 0.29–0.74) | ED LOS: control = 5.3 h; intervention = 5 h, p < 0.94 Hospitalization: control = 34; intervention = 19; adjusted rate: control = 0.77 (95% CI: 0.46–1.31); intervention = 0.44 (95% CI: 0.24–0.82); IRR: 0.57 (95% CI: 0.31–1.04) |
 Liberman et al. (2020) [25], USA  Trial name: the GAP-ED project (Geriatric and Palliative Emergency Department)  Funder: Fan Fox and Leslie R. Samuels Foundation  Industry sponsored: no | Study design: observational study Intervention type: care plan, education, referral Comparator: historical usual-care group | N: intervention = 283; control = 283 Age: intervention = 11% 65–75 years, 40% 76–85 years, 44% 86–94 years, 5% 95 + ; control = 11% 65–75 years, 40% 76–85 years, 44% 86–94 years, 5% 95 +  % female: intervention = 78%; control = 78% | Average revisits within 30 days: 0.22 in control, 0.20 in intervention, p = 0.34 In both groups, over 80% of patients had no revisits | Hospitalization: of those who revisited within 30 days, 40% of intervention were admitted, and 57% of control were admitted, p = 0.001 |
 Shrapnel et al. (2019) [28], Australia  Trial no.: none reported  Funder: the Mater Hospital Brisbane funded one full-time nursing position to implement the MACIAE study; co-author ED is funded by an Australian National Health and Medical Research Council Early Career Fellowship  Industry sponsored: no | Study design: observational study Intervention type: care coordination, support Comparator: TAU | N: intervention = 391; control = 730 Age (not specified): intervention = 83.1 years; control = 84.8 years % female: not reported | Revisit within 28 days: 4.6% for intervention; 17.8% for control, p < 0.001 | Admission after ED presentation: 40.6% for intervention; 71.9% for control, p < 0.001 LOS, days, mean (SD): 1.0 (3.5) for intervention; 2.0 (3.5) for control, p = 0.840 |