Intensive Education on Lipid Management
Acute Coronary Syndrome
About this trial
This is an interventional treatment trial for Acute Coronary Syndrome focused on measuring acute coronary syndrome, statins, LDL-C, intensive education
Eligibility Criteria
Inclusion Criteria:
- The patients admitted to the hospital with a diagnosis of ACS including those for first consulting or with recurrence. The patient was prescribed atorvastatin (Lipitor®) by physicians in hospital;
- The age of patient enrolled will be ≥18 years old;
- The patient is able to understand and complete questionnaire.
- The patients agree to accept follow-up visits, and willing to participate in patient education courses and sign informed consent form.
Exclusion Criteria:
- The patient has contraindications to statins, such as active hepatic disease, patient has a history of intolerance or hypersensitivity to statins or has a history of prior rhabdomyolysis on a statin.
- The patient who uses other statins except Lipitor® when discharged from the hospital;
- Cardiac function class of the patient is class IV(NYHA);
- The patient has a malignant tumor;
- The patient has a severe arrhythmia.
Sites / Locations
- Fujian Medical University Union Hospital
- The 2nd affiliated hospital of harbin medical university
- Xi'an Jiaotong University College of Medicine
- The Luhe Teaching Hospital of the Capital Medical University
- Shanghai Zhongshan Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
Intensive Educational Group
Control Group
The Intensive Educational Group will receive 5 visits, including 2 visits via phone contacts. The expected dates for each visit will be stamped on the follow-up brochure for convenience. Patient education in this group includes routine education at discharge; 4 educational brochures, a calendar with health tips, and follow-up brochure with medical expert letter sent to patients at the day for discharge (baseline); and educational short messages through message platform once a week. Dosage and adjustment of statins, and concomitant medications in all the treated patients will be recorded.
The Control Group will receive 3 visits and receive care as per usual practice by the treating doctor and a follow-up brochure without medical expert letter. Dosage and adjustment of statins, and concomitant medications in all the treated patients will be recorded. Blood lipid panel (4 items), hepato-renal functions, and creatine kinase will be examined; while, Morisky 8-item questionnaire will be used to evaluate medication compliance at outpatient visits. In addition, the occurrence of major cardiovascular events and AE/SAE will be collected during the study.