Zeboulon 2020b.
Study characteristics | |||
Patient Sampling | Retrospective, machine‐learning, experimental study. 22,066 Orbscan (Bausch&Lomb, USA) examinations were randomly extracted from the Orbscan database using the batch export functionality. The last examination of the first visit for each eye of each person was selected. This process reduced the number of examinations to 13,705. The cases were divided into the following groups: normal, keratoconus, history of myopic refractive surgery, Fuchs' corneal dystrophy, and other. |
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Patient characteristics and setting |
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Index tests | The efficiency of unsupervised algorithms was tested to extract and sort usable examinations from a large unlabelled corneal topography database into different diagnostic clusters, with little human intervention, data cleaning or feature selection. Convolutional neural network (CNN) was used. |
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Target condition and reference standard(s) | All 13,705 examinations were manually labelled and checked by 2 corneal topography experts (with at least 5 years of practice in a corneal and refractive surgery department) in a random order. The cases were diagnosed before the convolutional neural network analysis. |
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Flow and timing | All participants were diagnosed by 2 cornea specialists. All cases were included in the analysis. | ||
Comparative | Not applicable | ||
Notes | No funding source mentioned. | ||
Methodological quality | |||
Item | Authors' judgement | Risk of bias | Applicability concerns |
DOMAIN 1: Patient selection | |||
Was a consecutive or random sample of patients enrolled? | Yes | ||
Was a case‐control design avoided? | No | ||
Did the study avoid inappropriate exclusions? | No | ||
Could the selection of patients have introduced bias? | High risk | ||
Are there concerns that the included patients and setting do not match the review question? | High | ||
DOMAIN 2: Index test (All 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? | Unclear | ||
Was the model designed in an appropriate manner? | Yes | ||
Could the conduct or interpretation of the index test have introduced bias? | Low risk | ||
Are there concerns that the index test, its conduct, or interpretation differ from the review question? | Low concern | ||
DOMAIN 3: Reference standard | |||
Is the reference standard likely to correctly classify the target condition? | Yes | ||
Were the reference standard results interpreted without knowledge of the results of the index tests? | Yes | ||
Could the reference standard, its conduct, or its interpretation have introduced bias? | Low risk | ||
Are there concerns that the target condition as defined by the reference standard does not match the question? | Low concern | ||
DOMAIN 4: Flow and timing | |||
Did all patients receive the same reference standard? | Yes | ||
Were all patients included in the analysis? | Yes | ||
Could the patient flow have introduced bias? | Low risk | ||
DOMAIN 5: Comparative |
AI: artificial intelligence; AS‐OCT: anterior segment optical coherence tomography; AST: astigmatism index; BAD‐D: Belin‐Ambrósio Enhanced Ectasia Display total deviation; D: dioptre; I‐S: inferior‐superior; KISA% index: keratoconus percentage index, derived from central keratometry, the inferior‐superior value, the astigmatism index, and the SRAX index, an expression of irregular astigmatism occurring in keratoconus; LASIK: laser‐assisted in situ keratomileusis; OCT: optical coherence tomography; PPK: percent probability of keratoconus; SD: standard deviation; TMS: Topographic Modeling System.