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Can a Rapid 2 Day Followup After Discharge From the ED Reduce Readmissions and Death for Patients 75 Years and Older?

University of North Carolina (UNC) logo

University of North Carolina (UNC)

Status

Completed

Conditions

Emergencies

Treatments

Other: 2-3 day return appointment

Study type

Interventional

Funder types

Other

Identifiers

NCT01769495
DE 6366-SP

Details and patient eligibility

About

Our hypothesis is that a rapid follow up for elderly patients in a Geriatric Clinic discharged from the Emergency Department (ED) will have fewer unplanned return ED visits and fewer unplanned hospital admissions with no attendant increase in mortality.

Patients 75 years of age and older will be randomized following discharge from the ED into two groups. The first will receive standard post ED care. The second will receive an appointment to our Geriatric Clinic within 2-3 days for stabilization, further treatment and contact with the patient's primary physician to communicate the course of the patient's illness and to schedule subsequent follow-up with the patients regular medical provider.

There will be two primary outcomes: The first will be a composite of morality and/or return to the ED at 30 days, and the secondary primary outcome will be mortality. Economic data regarding resource utilization by patients will also be analyzed.

Enrollment

26 patients

Sex

All

Ages

75+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients 75 years of age and older discharged from the ED

Exclusion criteria

  • Younger than 75.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

26 participants in 2 patient groups

Control
No Intervention group
Description:
Standard post ED care
2-3 day return appointment
Experimental group
Description:
Patients will receive further treatment in Geriatric Clinic 2-3 days post ED discharge.
Treatment:
Other: 2-3 day return appointment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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