Transient ischaemic attack (TIA) Circulatory System
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients will be eligible for the study if they are: 1. Attended by a trial paramedic during the recruitment period 2. Coded as low-risk suspected TIA by the attending paramedic using the standard tool 3. Attended in the catchment area of the two hospitals taking part in the trial All paramedics working in within the study area are eligible
Exclusion criteria
Exclusion criteria: There are no exclusion criteria for paramedics. Patient exclusion criteria: 1. Unable to give informed consent (lacks capacity) 2. Apparent or known cognitive impairment (such as a diagnosis of dementia), due to the potential for inaccuracies in the reporting of symptoms 3. Patients with crescendo TIAs (i.e. patient has had similar symptoms within the last week) 4. Patients with ongoing symptoms (i.e. cannot definitely be classified as a TIA)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Time to subsequent emergency contact (999 call or ED attendance) or death 2. Time to specialist assessment by a stroke consultant or TIA specialist nurse | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Outcome of contact: whether patient is taken to hospital or left at home and referred or left at home but not referred, together with time from onset to additional therapy; and attendance at TIA clinic (who and when) 2. Health care utilisation in one month and three months following contact 3. Patient-reported outcomes: satisfaction with care received (Quality of Care Monitor); health status (SF-12) at one month and three months 4. Costs of implementation, and costs of care and consequences per patient 5. Appropriateness of clinical management | — |
Countries
United Kingdom, Wales