acute myocardium infarction
Conditions
Interventions
Study group:Furosemide
Control group:None
Sponsors
Xuzhou Central Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patients with acute myocardial infarction within 72 hours of onset with B-line score of 2 or greater and without dyspnea on bedside pulmonary ultrasonography. 2) Age 18-80 3) Sign the informed consent
Exclusion criteria
Exclusion criteria: 1) Severe pulmonary fibrosis, pulmonary infection, pneumonia, acute respiratory distress syndrome (ARDS) and other lung diseases 2) Moderate to severe renal insufficiency patients with creatinine greater than 120umol/L 3) Acute myocardial infarction with severe mechanical complications 4) Cardiogenic shock 5) Severe hypotension (systolic blood pressure less than 90mmHg or 40mmHg decrease from the original systolic blood pressure) 6) Severe valvular disease and congenital heart disease without surgical treatment 7) Any known allergic reaction, hypersensitivity reaction and other contraindications to furosemide 8) Pregnant and lactating women 9) Cancer patients with a predicted survival of less than 1 year 10) Severe mental disorder, unable to express wishes 11) The presence of obvious other abnormal signs, laboratory tests and clinical diseases is not suitable for investigator participation in the judgment of the investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occurrence of symptomatic heart failure (dyspnea); | — |
Secondary
| Measure | Time frame |
|---|---|
| Cardiac arrhythmias during hospitalization;Comorbid pulmonary infection during hospitalization;Changes in blood markers, renal function, creatinine values during hospitalization (at the time of admission and before discharge).; | — |
Countries
China
Contacts
Public ContactLILI
Xuzhou Central Hospital
Outcome results
None listed