NCT Number: NCT02677272
Factors Predisposing to Inappropriate Transfers of Nursing Home Residents to Emergency Departments
According to the data of our nursing homes (NH) research network (REHPA - Gérontopôle Toulouse, 345 nursing home in France), 13.5% of NH residents are hospitalized every 3 months or about 50% per year. These hospitalizations concern for half, transfers to emergency department (ED). Data from the literature and the PLEIAD study, conducted with 300 NH in France, confirm that intense flows between NH and ED. These studies also support the idea that these transfers to ED potentially expose some NH residents to iatrogenic complications, a risk of functional decline, an increased risk of mortality, and generate additional health costs. To transfer to ED residents who will benefit from emergency care and not to transfer to ED residents for whom this transfer generates a higher risk than the expected benefit is the goal to reach to guarantee the better quality of care for NH residents.
Inappropriate transfer to ED may be defined by the absence of somatic emergency and / or palliative care known before transferring to ED and / or the presence of advance directives of non-hospitalization in the resident's file. This is a clinical situation that could be managed by other means that the transfer to ED without loss of opportunity for the patient.
The primary objective of our study is to determine the factors predisposing NH residents to inappropriate transfer to ED.
Our hypothesis is that inappropriate transfers to the ED of NH residents are conditioned by factors accessible to interventions such as the organization of the NH care system or by improving the management of some diseases in NH. Investigators also hypothesize that the cost of inappropriate transfers to the ED is considerable. Acknowledgement of costs generated by inappropriate transfers to ED would allow policy makers to make strategic decisions to improve care system.
Looking for future studies?
Notify MeKey information
Conditions
Sex eligibility
All sexes
Study type
Observational
Primary location
CH d'Albi, Albi, France
About this study
This is a retroprospective study conducted in sixteen hospitals in south-west of France. Inclusion will last one year, including 4 periods (one per season) of 7 days (24h / 24, including necessarily each day of the week). All the NH residents admitted in ED will be included. For each resident included, medical and non-medical data will be collected in 4 times: retrospectively before transfer to ED (=T0); and prospectively : at ED (= T1), in hospital services in case the patient is hospitalized (=T2) and at the patient's return to NH (=T3).
At T0 data collected will concern the NH and resident basis medical state, resident's medical state the week before transfer and resident medical state before transfer to ED.
At T3 data collected will concern the resident's return modality and his/her autonomy 7 days after his/her return
Time frame:
between T1 and T3 : mean expected duration will variate from few hours if the resident isn't hospitalized (ED visit) to an average 12.4 days, which is the average length of hospital stay of NH resident hospitalized after a transfer to ED (cf Pleiad study, Rolland 2012) plus 7 days as Investigators will collect T3's data 7 days after the NH resident's return to NH
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- to live in a Nursing Home
- to be directly transferred from the NH to ED
- to have not previously been included in FINE study
Exclusion criteria
- to live in structures other than Nursing Home (i.e. sheltered housing, seniors' residences, housing homes, retirement homes, long-term care units)
- to live in the community
- to be transferred to ED from elsewhere than the NH
- to have previously been included in FINE study
Treatment and study plan
Primary outcomes
-
Inappropriate transfer to ED of NH residents
Time frame: Baseline (T1 = inclusion at ED): retro-prospectively by the group of experts
Inappropriateness of the NH residents' transfers to ED : the inappropriateness of ED transfers will be determined by the opinion of a group of experts composed of geriatricians, emergency physicians, general practitioners and pharmacists. Inappropriate transfer to ED is defined by the absence of somatic emergency and / or palliative care known before decision to transfer and / or the presence of advance directives of non-hospitalization in the resident's file. This is a clinical situation that could be managed by other means that the transition to ED without loss of opportunity for the resident. To judge the inappropriateness of the transfer to ED, the group of experts will use a rating scale of usual emergencies. Individual and independent rating divergences will lead to a concerted evaluation of the clinical situation by the group.
Analyse retro-prospectively by the group of experts.
Secondary outcomes
-
Cost of the NH resident transfer to ED
Time frame: 6 months before to 6 months after the transfer
The cost of ED transfers (i.e. appropriate and inappropriate transfers) and the direct medical costs of residents 6 months before and 6 months after the first transfer will be calculated.This work will be lead in partnership with the Regional Direction of the Medical Service of the region and the medico-economic cell of the Medical Information Department of Toulouse University Hospital
-
Avoidability of the NH resident transfer to ED
Time frame: Baseline (T1 = inclusion at ED)
Potentially avoidable transfers to ED: When a transfer is considered appropriate it also can be considered as potentially avoidable if adequate preventive measures were implemented. The Ambulatory Care Sensitive Diagnosis usually used in the literature will be used to characterize the transfers as potentially avoidable. When a transfer is considered inappropriate it is always considered as potentially avoidable. Analyse retro-prospectively by the group of experts.
-
NH resident's autonomy using Katz'ADL
Time frame: Change at different time points: T0, T2 (up to 12 days,if concerned) and T3 (7 days after return to NH)
- Residents' autonomy will be assessed using Katz'ADL at the NH before transfer (T0); at the end of the hospitalization if the resident is concerned (T2), and at the resident's return to ED (T3)
-
Analysis of Medical prescription, with a focus on psychotropic drug
Time frame: Change at different time points: T1 (baseline), T2 (up to 12 days,if concerned) and T3 (7 days after return to NH)
- Medical prescriptions will be collected at inclusion (T1), at the end of the hospitalization if the resident is concerned (T2), and at the resident's return to ED (T3)
Sponsors and collaborators
Lead sponsor
University Hospital, Toulouse
Other
Collaborators
- Agence Régionale de la Santé - Midi Pyrénées
- Ministry of Health, France
Registry information
Acronym: FINE
Important dates
- Study start
- 2016
- Primary completion
- 2018
- Study completion
- 2018
- First posted
- Feb 9, 2016
- Registry last updated
- Feb 23, 2024
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Fine-tuned Physical Training to Improve Quality of Life in Older Individuals
NCT07546734
Aging, Aging Frailty
Rome, Italy
View Trial DetailsCognitive Function and Prevalence of Amyloid Marker in Frail Older Adults
NCT03129269
Alzheimer Disease, Brain Diseases
Toulouse, France
View Trial DetailsSynergizing Home Health Rehabilitation Therapy
NCT05411393
Activities of Daily Living, Frail Elderly
Gainesville, Florida, United States
View Trial DetailsProject to Improve Communication About Serious Illness - Pilot Study
NCT03746392
Brain Diseases, Cardiovascular Diseases
Seattle, Washington, United States
View Trial Details