Condition 1: Angina pectoris. Condition 2: acute myocardial infarction. Condition 3: Subsequent myocardial infarction. Condition 4: Certain current complications following acute myocardial infarction. Condition 5: Acute ischemic heart disease, unspecified. Angina pectoris ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction Subsequent ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction Certain current complications following ST elevation (STEMI) and n
Conditions
Interventions
Intervention 1: Intervention group: This group will receive care according to the comprehensive care plan, in which a new method of triage will be used for patients and they'll receive supportive care
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: patients older than 18 years old and younger than 65 years old patients with signs and symptoms related to myocardial ischemia that have lasted more than 10 minutes and less than 12 hours. e.g. chest pain; referred pain to arms, neck, jaw, shoulders, and back; dyspnea; diaphoresis; nausea and vomiting and lightheadedness patients without any known cognitive and perceptual impairments patients who can read and write
Exclusion criteria
Exclusion criteria: withdrawal from the study or death of the participant not cooperating during the study patients that has been transferred from another facility to the facility of the study patients that their chief complaint is not acute coronary syndrome
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| DTE (Door to ECG) time. Timepoint: Patient arrival to the emergency department. Method of measurement: Time (minutes).;DTB (Door to Balloon) time. Timepoint: Patient arrival to the emergency department. Method of measurement: Time (minutes).;Satisfaction with nursing care. Timepoint: after the intervention. Method of measurement: PSNCQQ questionnaire.;Pain scale. Timepoint: after the intervention. Method of measurement: VAS (Visual Analogue Scale).;Readmission rate. Timepoint: until two month after the discharge. Method of measurement: statistics.;Mortality rate. Timepoint: until one month after the discharge. Method of measurement: Statistics. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShayan Mahmoudi
Tehran University of Medical Sciences
Outcome results
None listed