Kim 2017.
Study characteristics | |||
Patient sampling | Study conducted in Busan, Republic of Korea Sampling: people with suspected stroke transported to a single hospital by EMS paramedics and people with true stroke without stroke recognition by EMS for 12 months; data extracted from emergency care records including CPSS documented by EMS paramedics and hospital medical records. |
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Patient characteristics and setting |
Inclusion and exclusion criteria: people with suspected stroke referred by paramedics and people with true stroke admitted during the same period (no further details). Participant characteristics: not reported |
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Index tests |
Index test: CPSS Test administrator: paramedics Training: not reported |
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Target condition and reference standard(s) |
Target condition: stroke/TIA Reference standard: hospital medical records (no further details) |
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Flow and timing | 268 people with suspected stroke referred, of whom 152 had confirmed stroke/TIA; time between CPSS and final diagnosis not reported. | ||
Comparative | |||
Diagnostic test accuracy data |
Prevalence: 152/268 (56.7%) participants had stroke/TIA CPSS: TP = 142, FP = 31, FN = 10, TN = 85 |
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Notes |
Proportion of stroke/TIA: stroke = 149, TIA = 3 Alternative diagnoses: not reported Additional information: people with ischemic stroke with stroke recognition by EMS using CPSS had a higher NIHSS score (10 with CPSS vs 6 with negative or no documented CPSS; P = 0.001) and shorter on‐scene to door time (22 with CPSS vs 25 minutes with negative or no documented CPSS; P = 0.009) and were more likely to be treated with tissue plasminogen activator (49.7% with CPSS vs 32.2% with negative or no documented CPSS; P = 0.007) than these with negative or no documented CPSS. |
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Methodological quality | |||
Item | Authors' judgement | Risk of bias | Applicability concerns |
DOMAIN 1: Patient Selection | |||
Was a consecutive or random sample of patients enrolled? | No | ||
Was a case‐control design avoided? | Yes | ||
Did the study avoid inappropriate exclusions? | Unclear | ||
Prospective design | No | ||
High | Low | ||
DOMAIN 2: Index Test Index tests | |||
Were the index test results interpreted without knowledge of the results of the reference standard? | Yes | ||
If a threshold was used, was it pre‐specified? | Yes | ||
Low | Low | ||
DOMAIN 3: Reference Standard | |||
Is the reference standards likely to correctly classify the target condition? | Unclear | ||
Were the reference standard results interpreted without knowledge of the results of the index tests? | Unclear | ||
Unclear | Low | ||
DOMAIN 4: Flow and Timing | |||
Was there an appropriate interval between index test and reference standard? | Unclear | ||
Did all patients receive the same reference standard? | Unclear | ||
Were all patients included in the analysis? | Unclear | ||
Did all patients receive a reference standard? | Unclear | ||
Unclear |