The PreHEART score supports EMS staff in their decision to convey a patient with undifferentiated chest pain and increases the non-conveyance up to 20%, which leads to fewer presentations to an ED.
ID
Bron
Verkorte titel
Aandoening
Acute coronary syndrome
Non-st segment Elevated Myocardial Infarction
Undifferentiated chest pain
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Unexpected Serious Adverse Events (USAE) at 3 and 30 days from the index contact.
Achtergrond van het onderzoek
Decisions on (non-)conveyance of patients are challenging for the ambulance personnel (emergency medical services [EMS]). The majority (>75%) of patients presenting with undifferentiated chest pain (or discomfort) is conveyed to the nearest hospital. Improving pre-hospital assessment of patients with undifferentiated chest pain may improve safety, optimize the efficacy of care, and reduce health-related costs.
Observational data in patients conveyed to the hospital suggests that our recently developed pre-hospital HEART (preHEART) risk score represents a reliable tool to identify individuals at very low risk (±38% of patients), low-intermediate (±5%) and very high risk (±7%) of severe cardiovascular pathology requiring urgent care. Whether adding this decision support tool in clinical practice to support the decision-making process on (non-)conveyance by the ambulance personnel is safe and more.
Doel van het onderzoek
The PreHEART score supports EMS staff in their decision to convey a patient with undifferentiated chest pain and increases the non-conveyance up to 20%, which leads to fewer presentations to an ED.
Onderzoeksopzet
3 days, 3 and 12 month
Onderzoeksproduct en/of interventie
The PreHEART is available to a randomized patient whose risk of an ACS has been assessed. The decision to convey can be guided by the preHEART score which suggestion to non-convey for patients with a very low risk of ACS, or convey patients with intermediate risk to the nearest hospital, or convey a patient to a hospital with PCI facilities.
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Adults with undifferentiated chest pain.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Communication barrier (e.g. language, understanding)
ST-segment elevation (electrocardiogram on scene is standard workup)
Any obvious etiology for the symptoms requiring direct treatment (e.g. trauma)
Being previously evaluated by ambulance personnel for the same complaint (already considered for participation)
High clinical suspicion of a life-threating condition (e.g. sudden death survivor, hypothermia, shock, aortic dissection, hypoxia or intoxication)
Cognitive impairment
End-stage renal disease
Pregnancy
Inability or unwillingness to provide informed consent
Not registered with a GP (huisarts)
COVID suspicion
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Toelichting
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL7866 |
Ander register | METC UMCG : METC approval pending |