- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03256734
Does a Complex Care Discharge Planning Initiative Reduce Unplanned Hospital Readmissions? (G78717-Readmits)
Does a Complex Care Discharge Planning Initiative Reduce Unplanned Hospital Readmissions?
Unplanned hospital readmissions are associated with increases in morbidity, mortality, cost and patient dissatisfaction,. Policymakers continue to seek effective policy solutions to avoid readmissions in order to improve quality of care and reduce unnecessary expenditures,. One attempt to reduce readmissions was implemented on June 1 2012, when the Specialist Services Committee of British Columbia (a partnership of Doctors of BC and the Ministry of Health) introduced the new "G78717" fee code for physicians. The objective of the fee code was to create a financial incentive for physicians to provide a point-of-care supplemental discharge summary to patients and their primary care providers prior to discharge from hospital. Initially, only urgent hospital admissions were eligible for this incentive payment but on Nov 1 2015 the incentive was extended to include elective admissions as well. The other eligibility criteria remained unchanged.
The effectiveness and cost-effectiveness of the fee code intervention is unknown. This study will address important questions relevant to this policy intervention using rigorous methods and empirical data.
This study will employ two methods for measuring changes in readmission risk. First, we will use interrupted (multivariate) time series to measure whether there was a temporal change in provincial readmission risk associated with the implementation of the new fee code.
We will complement the above analyses with a stronger design, comparing hospitalizations for which the fee code was charged (intervention group) with a cohort of clinically similar hospitalizations for which the fee code was not charged (control group). For this approach, multivariate logistic regression will be the primary statistical method. Using this analytic strategy, 30-day readmission risk between the intervention and control group will be measured over time, adjusted for patient-, provider-, and hospitalization-level covariates.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: John A Staples, MD
- Phone Number: 604-682-2344
- Email: john.a.staples@gmail.com
Study Contact Backup
- Name: Jason M Sutherland, PhD
- Phone Number: 604-822-6812
- Email: jsutherland@chspr.ubc.ca
Study Locations
-
-
British Columbia
-
Vancouver, British Columbia, Canada, V6T 1Z3
- Recruiting
- Population Data BC
-
Contact:
- Tim Choi
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Our study population will be representative of medical and surgical hospital admissions in BC.
The Interrupted time series (ITS) cohort will be comprised of hospital separations eligible for submission of fee code G78717. We will include all urgent admissions to BC hospitals with discharge dates between 1 Jan 2002 and 30 June 2017 that had a length of stay (LOS) of >4 days and are associated with a specialist Most Responsible Physician (MRP).
The regression analysis cohort study will be identical to the ITS cohort but will be restricted to index hospitalization discharge dates between 1 Jun 2012 and 31 Jul 2017 (ie. the post-G78717 period).
The unit of analysis is the index hospital admission (ie. the initial hospital admission of interest). Individual patients can contribute multiple hospital admissions to the cohort over time (although only hospital admissions occurring >30 days after a prior discharge are eligible as index hospital admissions).
Description
Inclusion Criteria:
The study population will be comprised of all hospital discharges in British Columbia between 1 Jan 2002 and 30 June 2017.
Exclusion Criteria:
We will exclude separations with the following International Statistical Classification of Diseases and Related Health Problems, 10th Revision, Canada (ICD-10-CA) codes as the Most Responsible Diagnosis:
- Codes O00 - O99 [Pregnancy, childbirth and the puerperium]
- Codes P00 - P96 [Certain conditions originating in the perinatal period]
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Unplanned hospital readmission within 30 days
Time Frame: 30 days
|
Unplanned hospital readmission within 30 days
|
30 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Unplanned (urgent) hospital readmission within 1 year of index hospital discharge
Time Frame: 1 year
|
Unplanned (urgent) hospital readmission within 1 year of index hospital discharge
|
1 year
|
Primary care visits within 30 days and 1 year of index hospital discharge
Time Frame: 30 days and 1 year
|
Primary care visits within 30 days and 1 year of index hospital discharge
|
30 days and 1 year
|
Emergency department visit
Time Frame: 30 days and 1 year
|
Emergency department visit within 30 days and 1 year of index hospital discharge
|
30 days and 1 year
|
Death
Time Frame: 30 days and 1 year
|
Death within 30 days and 1 year of index hospital discharge
|
30 days and 1 year
|
Use of transitional or stepdown care
Time Frame: 30 days and 1 year
|
Use of transitional or stepdown care (eg.
rehabilitation, extended care, intermediate /personal care) after discharge from acute care but prior to return home
|
30 days and 1 year
|
Improvements in appropriate population-level post-discharge prescription prevalence of an indicated medication
Time Frame: 60 days
|
Using health services records, we will identify a sub-cohort of patients with an index admission for acute coronary syndrome, heart failure, or chronic ischemic heart disease.
Within this subcohort, we will determine the proportion of patients who filled at least one prescription for beta-blockers within 60 days of index hospital discharge date.
|
60 days
|
Improvements in appropriate population-level post-discharge prescription prevalence of a contraindicated medication
Time Frame: 60 days
|
Using health services records, we will identify a sub-cohort of older adults (aged >/=65 years at date of index hospital discharge date).
Within this subcohort, we will determine the proportion of patients who filled at least one prescription for a "potentially inappropriate medication" within 60 days of index hospital discharge date.
Our list of "potentially inappropriate medications" has been adapted from those listed in the American Geriatrics Society 2015 Updated Beers Criteria.
|
60 days
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- H17-01039
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Patient Readmission
-
Northwestern UniversityNorthwestern Memorial HospitalCompletedPatient ReadmissionUnited States
-
AltaMed Health Services CorporationNational Institute on Aging (NIA); University of Southern CaliforniaRecruitingPatient ReadmissionUnited States
-
University Hospital Inselspital, BerneBrigham and Women's Hospital; Swiss National Science Foundation; University of...CompletedPatient ReadmissionSwitzerland
-
NYU Langone HealthThe New York Community Trust; United Hospital FundCompletedHospitalization | Patient ReadmissionUnited States
-
Cedars-Sinai Medical CenterNational Institute on Aging (NIA)Active, not recruitingPolypharmacy | Readmission | Nonadherence, PatientUnited States
-
Stony Brook UniversityUnknown
-
Lille Catholic UniversityCompletedElderly | Medication Reconciliation | Patient ReadmissionFrance
-
Singapore General HospitalWithdrawnPatient ReadmissionSingapore
-
Brigham and Women's HospitalAgency for Healthcare Research and Quality (AHRQ); CricoCompletedAdverse Event | Readmission | Patient Portals | Transitions of Care | General Medicine | Discharge Checklist | Patient-provider CommunicationUnited States
-
The Guthrie ClinicNot yet recruitingHeart Failure | Patient Readmission
Clinical Trials on Policy intervention
-
Shanghai Stroke Service SystemChanghai Hospital; Shanghai Zhongshan Hospital; RenJi Hospital; Huashan Hospital; Ruijin Hospital and other collaboratorsUnknown
-
National Institute of Environmental Health Sciences...Completed
-
Klein Buendel, Inc.National Institute on Alcohol Abuse and Alcoholism (NIAAA); Pacific Institute... and other collaboratorsEnrolling by invitationCannabis | Alcoholic Intoxication | Automobile AccidentUnited States
-
Forman Christian College, PakistanUNICEFRecruitingMaternal Health | Maternal Health LiteracyPakistan
-
Johns Hopkins Bloomberg School of Public HealthEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompleted
-
Penn State UniversityLondon School of Hygiene and Tropical Medicine; William T. Grant Foundation; Child... and other collaboratorsCompletedChild Abuse | Family and Household | Legislation | PolicyUnited States, United Kingdom
-
University of MinnesotaNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Centers...Completed
-
Queen Mary University of LondonUniversity College London HospitalsRecruiting
-
Karolinska InstitutetStockholm County Council (Center of Epidemiology and Community Medicine)Active, not recruitingPhysical Activity | Sedentary BehaviorSweden