The Prognostic Value of Anion Gap in Predicting Major Adverse Cardiovascular Events Among Patients With ST-Segment Elevation Myocardial Infarction
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: Anion gap.
- Who it may be relevant to
- Registry conditions: ST-segment Elevation Myocardial Infarction (STEMI). Basic parameters: 18 years — 70 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
- Indonesia
- 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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Overview
This study aims to evaluate the prognostic value of the anion gap in predicting major adverse cardiovascular events among patients with ST-segment elevation myocardial infarction. Researchers will collect information based on hospital registry as secondary data of in patient who had diagnosed as ST-segment elevation myocardial infarction and underwent primary percutaneous coronary intervention. The data consist of demographic data, clinical presentation, laboratory, and angiography result were collected from hospital registry by reviewing medical record. Then, the data was analyzed by using IBM SPSS Statistics v26.
Interventions
- Diagnostic test Anion gap
Patient was taken blood examination before PPCI
Primary outcome measures
- Major Adverse Cardiovascular Events (MACE) [Time frame: During hospitalization, up to 1 weeks]
Secondary outcome measures (6)
- Incidence of mortality [Time frame: During hospitalization, up to 1 weeks]
- Incidence of reinfarction [Time frame: During hospitalization, up to 1 weeks]
- Incidence of stroke [Time frame: During hospitalization, up to 1 weeks]
- Incidence of lethal arrhythmia [Time frame: During hospitalization, up to 1 weeks]
- Incidence of acute lung oedema [Time frame: During hospitalization, up to 1 weeks]
- Incidence of cardiogenic shock [Time frame: During hospitalization, up to 1 weeks]
Eligibility criteria
Inclusion criteria
- Adults with 18 - 70 years old with diagnosis of STEMI who underwent PPCI
Exclusion criteria
- History of heart failure due to any causes
- Cardiogenic shock before PPCI
- Any infection at the time of presentation
- Pregnant woman
- Other causes of high anion gap levels such as chronic kidney disease, metabolic acidosis, etc
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-control
Study locations
Indonesia · 1 center
- Dr. Kariadi Central General Hospital — Semarang
Identifiers
NCT: NCT06586424 · Undip_Kardio 2