Randomised controlled trials (RCTs), quasi-RCTs, cohort studies, case-control studies and hospital- and emergency-based registers where pre-hospital stroke code procedures were administered in the field were eligible for inclusion. Studies where patients were transferred from another hospital or where evaluation data were not reported were excluded.
Most studies compared use of a pre-hospital stroke code procedure to standard procedures on the delivery of patients with acute stroke to hospital care. Pre-hospital stroke assessment instruments differed across studies; nearly 50% did not report the use of a standardised screening instrument. Time limits to activate pre-hospital stroke screening procedures ranged from within two to six hours from symptom onset. Approximately half of the studies were conducted in Spain; all studies were in urban areas.
Titles and abstracts were screened by two reviewers; it was unclear whether inclusion criteria were applied to full papers by independent reviewers.