Transient Ischemic Attack
Conditions
Keywords
Biomarkers, TIA, Diagnosis
Brief summary
MIND-TIA is primarily an observational diagnostic study that aims to evaluate the role of novel biomarkers in the diagnosis of Transient Ischemic Attack (TIA)in primary care. Rapid and adequate diagnosis of TIA is of great importance to enable a rapid start of treatment, and thereby decrease the risk of subsequent ischemic stroke.
Detailed description
Rationale: A Transient Ischaemic Attack (TIA) does not cause permanent damage of brain tissue, but the risk of a subsequent ischemic stroke in the short term is high. Timely recognition of TIA would result in early treatment and reduce the risk of ischaemic stroke, and other adverse cardiovascular events. To improve the management of TIA adequate diagnosis is of imminent importance. However the diagnosis is notoriously difficult, for both GP and neurologist. Adequate biomarkers for brain ischaemia could improve the early diagnosis and thus the subsequent management of TIA. Objectives: 1. To assess the added diagnostic value of biomarkers beyond the clinical assessment (medical history, signs and symptoms) in patients suspected of TIA. Secondary objectives 2. To assess the prognostic value of biomarkers in patients with an established diagnosis of TIA. 3. To assess the time delay and factors related to delay in patients suspected of TIA. Study population: 350 adult persons suspected of TIA from primary care. Methods: Recruitment of patients will be performed at the general practices of 200 GPs in the vicinity of 4 to 5 participating hospitals. During a home visit a research nurse collects a blood sample, and takes two health-related questionnaires. Participants will be referred by their GP to the regional TIA outpatient clinic for additional investigations, including brain imaging. The diagnostic accuracy of a set of biomarkers will be assessed with the 'definite' diagnosis of TIA by a panel of neurologists as the reference standard.
Interventions
None listed
Sponsors
Saltro, diagnostic center for primary care.
UMC Utrecht
Study design
Observational model
COHORT
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Being adult (18 years and older) * Presenting to the GP with a new episode of symptoms suspected of TIA and the GP considering further investigations to confirm or exclude TIA at the TIA outpatient clinic. * A blood sample can be collected within 72 hours after onset of symptoms.
Exclusion criteria
* The patient still has active symptoms or signs suspected of an ongoing ischemic stroke and immediate referral to the neurologist seems indicated. * Valid history taking is impossible because of severe cognitive impairment or insufficient knowledge of the Dutch language. * Patient with a life expectancy of \< 6 months. * Patient is not willing or able to give written informed consent
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 'Definite' Diagnosis of TIA | After 6 months of follow-up | Determined by expert panel consisting of 3 neurologists |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Ischemic stroke and other cardiovascular events | During 6 months of follow-up | Assessed in the medical records of the GPs |
| Time delay to GP consultation and start of treatment | 1 day of home visit | — |
Countries
Netherlands
Contacts
Primary ContactLouis Servaas Dolmans, MD
Outcome results
None listed