Improving the Quality of Coronary Artery Bypass Grafting
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Interventions for healthcare professionals in hospitals with low usage rates, Interventions for healthcare professionals in hospitals with high usage rates.
- Who it may be relevant to
- Registry conditions: Coronary Artery Bypass Grafting (CABG). Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Quality Improvement Intervention on Utilization of Arterial Grafts for Coronary Artery Bypass Grafting
Overview
This is a healthcare quality improvement study focused on increasing the utilization of arterial grafts in isolated coronary artery bypass grafting (CABG). Evidence indicates that arterial grafts, compared with venous grafts, provide superior long-term patency, which are recommended to use by the clinical practice guidelines. In hospitals where the use of the internal mammary artery as a graft is relatively low(\<90%) among CABG patients, multiple interventions will be implemented to improve its adoption rate. In hospitals where internal mammary artery graft utilization is already high(≥90%), various interventions will be introduced to promote the use of multiple arterial grafts (defined as the use of two or more arterial conduits). The study targets healthcare professionals as the primary subjects of intervention, with no direct interventions applied to patients during the study period. Changes in the internal mammary artery graft utilization rate and the multiple arterial graft utilization rate before and after the intervention will serve as the primary endpoints for evaluating intervention effectiveness in the two types of hospitals, respectively.
Interventions
- Behavioral Interventions for healthcare professionals in hospitals with low usage rates
Hospitals with low usage rates aim to improve internal mammary artery graft utilization through interventions including education, theoretical training, technical training, conference exchanges, and regular feedback on quality monitoring results. - Behavioral Interventions for healthcare professionals in hospitals with high usage rates
Hospitals with already high usage rates focus on increasing multi-arterial graft usage rates through similar intervention methods such as education, theoretical training, technical training, conference exchanges focus on multi-arterial graft use. The usage rates of multi-arterial graft for each hospital will be regular feed backed.
Primary outcome measures
- Hospitals with low usage rates of internal mammary artery: internal mammary artery graft utilization rate [Time frame: Duration of hospital stay(from date of admission to date of discharge)]
- Hospitals with high usage rates of internal mammary artery: multiple arterial graft utilization rate [Time frame: Duration of hospital stay(from date of admission to date of discharge)]
Secondary outcome measures (1)
- In-hospital all-cause mortality rate [Time frame: Duration of hospital stay(from date of admission to date of discharge)]
Eligibility criteria
Patients whose data used to monitor the quality
Inclusion criteria
Aged ≥ 18 years old; Indicated for CABG and undergoing CABG.
Exclusion criteria
History of prior CABG; Concurrent other cardiac surgeries on the day of CABG; Malignant tumor or life expectancy < 1 year;
- 50% stenosis of left subclavian artery; Pregnant women; Individuals diagnosed with mental illness or cognitive impairment (International Classification of Diseases-10 codes F01-F99); Patients considered by the investigator to have other factors unsuitable for inclusion.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Health services research
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07377149 · 2025-2849 · 2025ZD0546704