With the Cardiac Care Bridge trial, we hypothesize a 12.5% absolute risk reduction on the composite endpoint of first all-cause unplanned hospital readmission or mortality within six months after randomization.
ID
Bron
Verkorte titel
Aandoening
Elderly, aged, older, geriatric, functional decline, functional loss, cadiovascular disease, heart failure, acute myocardial infarction, transitional care, disease management, case management, home-based cardiac rehabilitation, readmission, rehospitalization, mortality
Ouderen, geriatrie, functionele achteruitgang, functieverlies, cardiovasculaire aandoeiningen, hartfalen, acuut myocardinfarct, transmurale zorg, diseasemanagement, casemanagement, hartrevalidatie, heropname, overlijden
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The incidence of the composite end-point of first all-cause unplanned hospital readmission or mortality.
Achtergrond van het onderzoek
After a hospital admission for heart disease, older patients are at high risk of adverse outcomes such as readmission and death. The current treatment in older cardiac patients is focused on disease management while less attention is paid to general healthcare needs. In the Cardiac Care Bridge (CCB) program we aim to examine the effectiveness of a nurse-coordinated transitional intervention including case management, cardiovascular risk management and home-based rehabilitation for older cardiac patients at high risk of functional loss.
Doel van het onderzoek
With the Cardiac Care Bridge trial, we hypothesize a 12.5% absolute risk reduction on the composite endpoint of first all-cause unplanned hospital readmission or mortality within six months after randomization.
Onderzoeksopzet
The primary outcome will be measured at six months. Secondary outcomes will be measured at three months (phone), six months (home visit) and twelve months (phone)
Onderzoeksproduct en/of interventie
Patients admitted to the department of cardiology or cardiac surgery of > 70 years, at high risk of functional loss and admitted > 48 hours are eligible for inclusion. The program combines case management, disease management and home-based cardiac rehabilitation. All participants will receive a comprehensive geriatric assessment (CGA), performed by a cardiac nuse. Participants in the intervention group will receive care based on identified problems from the CGA in three phases.
1.In the clinical phase, an integrated care plan will be established for all participants. The department of geriatrics will be consulted in case of at least 1 identified problem on the psychological domain or minimal 5 identified geriatric problems in general.
2. In the transitional phase, before discharge, a coordinating community care registered nurse (CCRN) visits the participant in the hospital to receive a face-to-face handover from the cardiac nurse.
3. The post-clinical phase consists of four home visits by the CCRN to continue care based on the integrated care plan, including cardiovascular risk management and evaluation of participants' health status. The CCRN works in close collaboration with the physiotherapist, who will perform nine home-based cardiac rehabilitation sessions to improve participants' functional status.
Algemeen / deelnemers
Bianca Buurman
AMC, Kamer F4-108
Amsterdam 1100 DD
The Netherlands
+31 (0)20 5665991
b.m.vanes@amc.nl
Wetenschappers
Bianca Buurman
AMC, Kamer F4-108
Amsterdam 1100 DD
The Netherlands
+31 (0)20 5665991
b.m.vanes@amc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- 70 years and older
- Admitted patients to the departments of cardiology or cardiac surgery
- Admission > 48 hours
- High risk of functional decline according to the VMS screening-tool for frailty of the Dutch Safety Management Program (screening on ADL-functioning, fall risk, malnutrition and delirium): score >=2 in patients aged 70-79 years and score >= 1 in patients aged 80 years and older
- Mini-Mental State Examination Score (MMSE) >= 15
- Per 28 February 2018, patients with an unplanned hospital admission in the previous six months are also eligible for inclusion (independent of the score on the VMS screening tool for frailty)
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Congenital heart disease
- Terminal illness: defined as a life expectancy of less than three months, for example because of cancer or serious heart failure.
- Transferred from or planned discharge to a nursing home
- Planned discharge to another hospital not participating in this study
- Unable to communicate in Dutch
- Delirium as confirmed by the treating physician
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
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Andere (mogelijk minder actuele) registraties in dit register
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In overige registers
Register | ID |
---|---|
NTR-new | NL6169 |
NTR-old | NTR6316 |
Ander register | NL55636.018.16 (CCMO) : METC2016_024 (AMC) |