25% of AMI in patients >17 and
ID
Bron
Verkorte titel
Aandoening
Acute myocardial infarction
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
To investigate the incidence of DOA use in patients between 18 and 45 years old presenting at the emergency department (ED or coronary care unit (CCU) at the participating hospitals with AMI.
Achtergrond van het onderzoek
Rationale: Little is known about the risk for manifestations of cardiac ischemia due to Drugs Of Abuse (DOA). The strong correlation between cocaine and Acute Myocardial Infarction (AMI) at a young age is well studied. However, the relation between cardiac ischemia and other DOA remains unclear.
Objective: The aim of this study is to evaluate the incidence of DOA use in young adults aged 18-45 years old, diagnosed with an Acute Myocardial Infarction.
Study design: Multicenter exploratory cohort study
Study population: Adults aged18 till 45 years old diagnosed with AMI (all subtypes) in the Emergency Department (ED) or Coronary Care Unit (CCU) of the OLVG hospital and the Amsterdam UMC in Amsterdam, the Netherlands.
Intervention: No interventions are performed
Main study parameters/endpoints: The main endpoint is the number of patients and type of DOA that patients with AMI test positive for using the Toxtyper test.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: There is no risk or burden for participants as no extra interventions are performed. An extra blood sample is collected for Toxtyper testing during routine blood tests that are taken within common practice for treating AMI.
Doel van het onderzoek
25% of AMI in patients >17 and <45 years old have a positive toxtyper screening for recreational drug use
Onderzoeksopzet
Start 1 march 2020
Onderzoeksproduct en/of interventie
none
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
• Age >17 and <46 years old
• Diagnosed with AMI according to ESC protocol
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
• Start of symptoms of ACS >48hr prior to inclusion
• No informed consent obtained
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
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In overige registers
Register | ID |
---|---|
NTR-new | NL8112 |
Ander register | MECU : R19.076 |