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China PEACE II: Quality Improvement for Acute Myocardial Infarction

China Patient-centered Evaluative Assessment of Cardiac Events II: Quality Improvement for Acute Myocardial Infarction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02322944
Acronym
PEACE-QI-AMI
Enrollment
8000
Registered
2014-12-23
Start date
2014-12-31
Completion date
2016-07-31
Last updated
2016-10-24

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

Conditions

Acute Myocardial Infarction

Keywords

acute myocardial infarction, quality improvement, reperfusion therapy

Brief summary

This study aims to develop quality improvement strategies and relevant tools focusing on reperfusion therapy in patients with STEMI, and to evaluate their effectiveness via a hospital-level cluster randomized clinical trial, based on the nationally representative collaborative network of over 100 hospitals established in China PEACE retrospective study. In a baseline survey period, through consecutively recruiting all eligible inpatients and collecting relevant medical information, the performance of all participating hospitals before the implementation of the intervention will be assessed. During the following intervention period, 6-10 hospitals that show the strong willingness and ability to collaborate will be selected as process optimization group. Their clinical pathways and team building will be re-organized for the purpose of quality improvement, and develop individualized treatment strategies and process. Meanwhile, other participating hospitals will be divided into intervention and control groups in a 1:1 ratio, in which the intervention group will take the treatment improvement strategy into implementation, while the control group will maintain the routine practice pattern. All hospitals will consecutively recruit qualified patients in the same method adopted in baseline period. Then the reperfusion rates and other performance measures will be compared among different groups (process optimization, intervention and control).

Detailed description

This study aims to develop quality improvement strategies and relevant tools focusing on reperfusion therapy in patients with STEMI, and to evaluate their effectiveness via a hospital-level cluster randomized clinical trial, based on the nationally representative collaborative network of over 100 hospitals established in China PEACE retrospective study. The primary outcome measure is reperfusion rate among eligible patients with STEMI, and secondary ones include timeliness of primary PCI (D2B) and fibrinolytic therapy (D2N). the assessment is based on consecutively recruiting all eligible inpatients, as well as collecting relevant medical information via a case report form finished by local doctors and central medical record abstraction. During the first study period, the baseline performance of all 100 participating hospitals before the implementation of the intervention will be assessed. During the following period, 3-5 PCI-capable and 3-5 non-PCI capable hospitals that show the strong willingness and ability to collaborate will be selected as process optimization group. Their clinical pathways and team building will be re-organized for the purpose of quality improvement, and develop individualized treatment strategies and process, including examining local hospitals' workflow to determine the key link affecting the rate of reperfusion therapy and its timeliness (such as pre-paid policy for fibrinolytic or PPCI, thrombolytic drug preparation, cardiac catheterization laboratory preparation, transferring from the ER to the Cath lab, interventional medical team gathering, etc.). Also, QI strategies and tools developed in the current study will be provided to these hospital, including training in standardized treatment pattern; building quality management team and determining improvement goals; periodical quality feedback report and regular quality meeting; tools like a wristband in order to remind all medical staff involved in the treatment process, workflow posters and cards, a CRF including a flowchart to inform the management steps, study website serving as the communication platform. Meanwhile, other participating hospitals will be divided into intervention and control groups in a 1:1 ratio using minimization allocation, in which the intervention group will take the QI strategies and tools developed in the current study as mentioned above, while the control group will maintain the routine practice pattern. Then the outcome measures and other performance indicators will be compared among different groups (process optimization, intervention and control).

Interventions

Training in standardized treatment pattern; building quality management team and determining improvement goals; tools (a wristband in order to remind all medical staff involved in the treatment process; workflow posters and cards; a CRF including a flowchart to inform the management steps); periodical quality feedback report and regular quality meeting; study website serving as the communication platform.

BEHAVIORALProcess optimization

Examining local hospitals' workflow to determine the key link affecting the rate of reperfusion therapy and its timeliness (such as thrombolytic drug preparation, cardiac catheterization laboratory preparation, transferring from the ER to the cath lab, interventional medical team gathering, etc.) and systems (such as pre-paid policy for thrombolysis or PPCI)

Sponsors

China National Center for Cardiovascular Diseases
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients with STEMI who arrive at the hospital within 12 hours from the symptoms onset.

Exclusion criteria

* Received reperfusionthrombolytic therapy before the index hospitalization; * AMI occurring during hospitalization; * Chest trauma resulting in secondary acute myocardial infarction.

Design outcomes

Primary

MeasureTime frameDescription
Reperfusion therapy rate24 hours after admissionReperfusion therapy rate is defined as utilization rate of thrombolytic therapy or primary PCI treatment among patients indicated with the reperfusion therapy.

Secondary

MeasureTime frameDescription
Timeliness of primary PCI24 hours after admissionThe proportion of door to balloon (D2B) within 90 minutes among all patients receiving PPCI.
Timeliness of thrombolytic therapy24 hours after admissionThe proportion of door to needle time (D2N) within 30 minutes among all patients receiving fibrinolytic therapy.

Other

MeasureTime frameDescription
Evaluation of left ventricular function24 hours after admissionProportion of left ventricular function evaluation within 24 hours of admission among all patients.
β-blockers use during hospitalization10 days on average (during hospitalization)Proportion of β-blockers use during hospitalization among eligible patients.
Statins use during hospitalization10 days on average (during hospitalization)Proportion of statins use during hospitalization among eligible patients.
ACEI/ARB use during hospitalization10 days on average (during hospitalization)Proportion of ACEI/ARB use during hospitalization among eligible patients.
In-hospital mortality10 days on average (during hospitalization)Proportion of in-hospital mortality or withdraw treatment due to a terminal status at discharge.
Clopidogrel (or ticagrelor) use at discharge10 days on average (during hospitalization)Proportion of Clopidogrel (or ticagrelor) use at discharge among eligible patients.
β-blockers use at discharge10 days on average (during hospitalization)Proportion of β-blockers use at discharge among eligible patients.
ACEI/ARB use at discharge10 days on average (during hospitalization)Proportion of ACEI/ARB use at discharge among eligible patients.
Statins use at discharge10 days on average (during hospitalization)Proportion of statins use at discharge among eligible patients.
Aspirin use at discharge10 days on average (during hospitalization)Proportion of aspirin use at discharge among eligible patients.
Aspirin use within 24 hours24 hours after admissionProportion of aspirin use within 24 hours of admission among eligible patients
Heparin use within 24 hours24 hours after admissionProportion of heparin use within 24 hours of admission among eligible patients

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026