Table 1.
References | Study design | Patient selection | Threshold | Blinded index test results | Valid reference test | Disease progression | Verification | Withdrawal | Risk of bias | Representative patient sample | Extractable data | Applicability | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
I-FABP | Block et al. [37] | Cohort | ● | ○ | ● | ● | ● | ○ | ● | Low | ● | ◐ | Moderate |
Cronk et al. [40] | Cohort | ● | ◐ | ● | ● | ● | ◐ | ● | Low | ● | ● | High | |
Güzel et al. [41] | Case–control | ◐ | ● | ● | ● | ○ | ● | ● | Moderate | ● | ● | High | |
Kanda et al. [15]a | Case–control | ◐ | ● | ● | ● | ○ | ○ | ● | Moderate | ● | ● | High | |
Kanda et al. [42] | Cohort | ● | ● | ● | ● | ○ | ◐ | ● | Low | ● | ● | High | |
Kittaka et al. [43] | Cohort | ● | ● | ● | ● | ● | ◐ | ● | Low | ● | ● | High | |
Matsumoto et al. [44] | Cohort | ● | ● | ● | ● | ● | ◐ | ● | Low | ● | ● | High | |
Matsumoto et al. [45] | Cohort | ● | ● | ● | ● | ○ | ● | ● | Low | ● | ● | High | |
Shi et al. [38] | Cohort | ● | ● | ● | ● | ● | ◐ | ● | Low | ● | ● | High | |
Thuijls et al. [46] | Cohort | ● | ● | ● | ● | ● | ◐ | ● | Low | ● | ● | High | |
Uzun et al. [47] | Case–control | ◐ | ● | ● | ◐ | ○ | ○ | ● | High | ● | ● | High | |
Vermeulen et al. [48] | Cohort | ● | ● | ● | ● | ● | ◐ | ● | Low | ● | ● | High | |
Voort et al. [39]a | Cohort | ● | ○ | ● | ● | ● | ◐ | ● | Low | ● | ◐ | Moderate | |
Camkiran et al. [49] | Cohort | ● | ○ | ● | ○ | ● | ○ | ● | High | ● | ○ | Low | |
Lieberman et al. [50]a | Case–control | ◐ | ○ | ● | ○ | ○ | ○ | ● | High | ◐ | ◐ | Low | |
d-Lactate | Assadian et al. [51] | Cohort | ● | ○ | ● | ● | ● | ● | ● | Low | ● | ◐ | High |
Block et al. [37] | Cohort | ● | ◐ | ● | ● | ● | ◐ | ● | Low | ● | ● | High | |
Collange et al. [52] | Cohort | ● | ◐ | ● | ● | ● | ● | ● | Low | ● | ○ | Low | |
Murray et al. [53] | Case–control | ◐ | ◐ | ○ | ● | ○ | ● | ● | Moderate | ● | ● | High | |
Poeze et al. [21] | Case–control | ◐ | ◐ | ● | ◐ | ○ | ◐ | ● | High | ● | ● | High | |
Shi et al. [38] | Cohort | ● | ● | ● | ● | ● | ● | ● | Low | ● | ● | High | |
Voort et al. [39]a | Cohort | ● | ○ | ● | ● | ● | ◐ | ● | Low | ● | ◐ | Moderate | |
α-GST | Block et al. [37] | Cohort | ● | ◐ | ● | ● | ● | ◐ | ● | Low | ● | ● | High |
Delaney et al. [54] | Case–control | ◐ | ● | ● | ● | ● | ● | ● | Low | ● | ● | High | |
Gearhart et al. [55] | Cohort | ● | ◐ | ● | ● | ● | ◐ | ◐ | Low | ● | ● | High | |
IMA | Gunduz et al. [56] | Case–control | ◐ | ● | ● | ● | ● | ● | ● | Low | ● | ● | High |
Polk et al. [57] | Cohort | ● | ● | ● | ● | ● | ● | ● | Low | ● | ● | High | |
C | Kulu et al. [58] | Case–control | ○ | ● | ● | ● | ○ | ● | ● | Low | ● | ● | High |
Patient selection: ● consecutive order, well described in- and exclusion criteria ◐ case–control with consecutive case selection ○ inappropriate exclusions. Threshold: ● based on ROC-analysis ◐ pre-specified ○ not reported. |Blinded index test results: ● yes ○ no/not reported. Valid reference standard: ● surgery, endoscopy, autopsy, full clinical recovery ◐ CT scanning, lab findings ○ none/not reported. Disease progression: ● < 12 h ○ ≥ 12 h/not reported. Verification: ●all patients received both index and reference test. Reference test was the same for all patients ◐ selected patients received equal reference tests ○ selected patients received different reference tests. Withdrawal: ● no loss to follow up ◐loss to follow up, reasons given ○ loss to follow up without reasons given/not reported. Representative patient sample: ● patients with suspected AMI ◐ healthy control group ○ non-matching domain. Extractable data: ● 2 × 2 table data extractable ◐ levels of biomarkers reported, no 2 × 2 data extractable ○ only correlation, no data on AMI
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