Maeda 1995b.
Study characteristics | |||
Patient Sampling | Single‐centre, case‐control study. Corneal topographic maps of the TMS‐1 were drawn from the Louisiana State University Eye Center patient population. | ||
Patient characteristics and setting | Participants were divided into the following 7 categories.
The study excluded maps in which focusing or alignment were not properly achieved or that contained atypical topographic appearances. For this project, 183 eyes were selected. The maps were randomly divided into a training set (108 maps) and a test set (75 maps). |
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Index tests | Neural network constructed in 3 layers. The input layer consisted of 11 neurons equal to 11 topographic indices. There was 1 hidden layer of 18 neurons. The output layer consisted of 7 neurons, 1 for each topographic category. | ||
Target condition and reference standard(s) | Topography images were made with the TMS‐1. All eyes were diagnosed by the 3 study authors and classified according to the topographic image and clinical records. The diagnosis was made before the images were analysed by the algorithm. | ||
Flow and timing | All eyes received the same reference standard, and all data were included in a 2 × 2 table. | ||
Comparative | Not applicable | ||
Notes | Supported in part by US Public Health Service grant EY03311 and EY01377 from the National Eye Institute, National Institutes of Health (Bethesda, MD); Computed Anatomy (New York, NY); Menicon Co. Ltd. (Nagoya, Japan). | ||
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? | No | ||
Did the study avoid inappropriate exclusions? | Unclear | ||
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? | Unclear | ||
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? | Unclear risk | ||
Are there concerns that the target condition as defined by the reference standard does not match the question? | Unclear | ||
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 |