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Regional integration between a cardiac centre and a referring hospital

Enhancing regional integration between a cardiac centre and a referring hospital by focusing on clinical outcomes, patient satisfaction, and process and structure measures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11311830
Enrollment
12000
Registered
2018-10-01
Start date
2017-05-01
Completion date
Unknown
Last updated
2020-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary artery disease (CAD) Circulatory System Heart patients diagnosed with coronary artery disease and treated by coronary artery bypass graft (CABG) or percutaneous coronary intervention (PCI)

Interventions

In 2014, different interventions were implemented in both hospitals included in the study (Catharina Cardiac Centre and SJG Weert), such as modification of patient brochures, implementation of a new p

Sponsors

Catharina Ziekenhuis
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18 years and older 2. Diagnosed with coronary artery disease 3. Referred from other hospitals to Catharina Cardiac Centre and back for coronary artery bypass graft (CABG) or percutaneous coronary intervention (PCI) between 2011 and 2016 AND/OR referred from the hospital SJG Weert to Catharina Cardiac Centre in the year 2013 and in the period January until September 2015

Exclusion criteria

Exclusion criteria: 1. Treated with combined treatments, such as aortic valve replacement in combination with CABG 2. Not referred from another hospital

Design outcomes

Primary

MeasureTime frame
Primary outcome measures 1-4 were assessed from electronic health records and cardiac databases of both hospitals within 30 days after the interventions: 1. Mortality 2. Deep sternal wound infection (DSWI) 3. Surgical re-exploration 4. Myocardial infarction 5. 120 day mortality, assessed from electronic health records and cardiac databases of both hospitals 120 days after the interventions 6. Urgent coronary artery bypass graft (CABG) within 24 hours, assessed from the electronic health records of the Catharina Cardiac Centre 7. Cerebrovascular accidents (CVA) within 72 hours, assessed from the electronic health records of the Catharina Cardiac Centre

Secondary

MeasureTime frame
1. Degree of patient satisfaction, assessed several months after patients were treated in the heart centre (this differs between each patient, ranging from 14 days to 5 months after treatment) using self-administered questionnaires, consisting of 28 items regarding: 1.1. Communication with the hospital (2 items) 1.2. Communication between the hospitals and the patient's general practitioner (2 items) 1.3. Education and education material (4 items) 1.4. Consistency and compatibility between the two hospitals (2 items) 1.5. Access time (2 items) 1.6. Quality of care (4 items) 1.7. Unexpected events and complications (3 items) 1.8. Hospital stay (4 items) 1.9. Personal contact with physician in both hospitals (2 items) 1.10. An overall grade from 1-10 2. Process and structure, regarding the following, assessed using indicators commonly used in quality inspections by the Dutch Association of Cardiologists (NVVC) and European Society of Cardiology (ESC) (such as the KISZ survey of the Dutch Association of Internists and standard operating procedures), before (in 2013) and after (in 2015) the implementation of the interventions: 2.1. Organisation 2.2. Cooperation 2.3. Outpatient clinic 2.4. Echo and ergometry 2.5. Coronary care unit 2.6. Cardiac catheterisation lab

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 27, 2026