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Early Diagnosis of Acute Myocardial Infarction: Impact of an Educational and Organizational Intervention

Early Diagnosis of Acute Myocardial Infarction: Impact of an Educational and Organizational Intervention

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04333381
Enrollment
450
Registered
2020-04-03
Start date
2019-07-01
Completion date
2022-12-31
Last updated
2020-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Education, Emergency Room, Myocardial Infarction, Nurses, STEMI

Brief summary

The hypothesis is that an educational program aimed at emergency nurses and the implementation of measures at the organizational level reduce the time between arrival at the emergency room and the opening of the artery or balloon by 40% in patients attending for acute myocardial infarction.

Detailed description

The time between arrival in the emergency room (ER) and balloon time (D2B) in ST segment elevation myocardial infarction (STEMI) is one of the best indicators of quality care in patients with STEMI. Hospitals with more strategies to improve this quality of care have a shorter door-to-balloon time. The aim is to evaluate the effectiveness, in the time between the arrival in the ER and the balloon time, of an educational and organizational intervention for the early diagnosis of myocardial infarction for emergency nurses. The aim of this study is to improve the time between arrival to ER and balloon time. The study consists of two phases: Phase I (PRE): in this phase, the aim is to describe the attendance times and to evaluate the causes of delay in attendance in STEMI patients. With the findings, a plan will be drawn up that includes the integration of an educational program for emergency nurses and organizational measures; oriented to improve the early diagnosis and delays in STEMI. Phase II (POST): in this phase, the aim is to evaluate the effectiveness in improving delays in the care of patients with STEMI after the implementation of the educational and organizational intervention developed in phase 1. On the other hand, will evaluate the satisfaction of the emergency nurses with the training they received through educational and organizational intervention.

Interventions

OTHEREducational and organizational intervention

Patients included after a systematic educational and organizational intervention for early diagnosis and care in myocardial infarction, aimed at emergency nurses of a tertiary Hospital capable in primary PCI. 1. The educational intervention will consist: Systematized educational intervention on acute myocardial infarction for emergency triage nurses will consist of theoretical and practical training through case presentations and clinical simulation. 2. The organizational intervention will consist: * Development and dissemination of an early diagnostic tool for acute myocardial infarction: STEMI infographics. It will be provided to all emergency nurses and emergency triage boxes * Update the STEMI hospital protocol and adapt it to the current clinical guidelines of the European Society of Cardiology (ESC) * Review organizational strategies and definition of new improvement measures * Audit the delays in STEMI * Periodic multi-disciplinary update sessions

Common practice is based on care by emergency nurses who did not receive any systematized education of acute myocardial infarction led by interventional cardiology nurses. On the other hand, emergency management is based on Plan-Do-Study-Act methodology and in the historical sample some organizational improvement strategies did not exist or were beginning to be implemented

Sponsors

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Quasi-experimental design study, pre-post intervention type

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients ≥18 years * Admitted to the emergency room of the same center

Exclusion criteria

* Pregnant women * Patients who did not receive coronariography were excluded

Design outcomes

Primary

MeasureTime frameDescription
Door-to-balloon time (D2B)up to 30 days; From the arrival at the emergency room to the balloon time up to dischargeThe time between arrival at the emergency room (ER) and balloon time (D2B) in STEMI

Secondary

MeasureTime frameDescription
ER arrival-ECG timeup to 30 days; from the arrival at the emergency department to the ECG realization up to dischargeThe time between the arrival at the emergency department and the ECG.

Countries

Spain

Contacts

Primary ContactGemma Berga Congost, RN, MSc, PhD student
gberga@santpau.cat932919000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026