Grewal 2011.
Study characteristics | |||
Patient Sampling | Cohort study. Participants aged 40 years and older were recruited from an ophthalmology clinic. Data from the right eye were included in the analysis. | ||
Patient characteristics and setting | Sample size: 265 eyes (28 narrow angle and 237 open angle). Age: mean (SD), 55.3 ± 5.1 years, (narrow angle 56.2 ± 6.5; controls 58.3 ± 5.7). Sex: 136 (51.3%) female. Setting: secondary care. Country: India. Ethnicity: Indian. Exclusions: history of glaucoma, intraocular surgery, laser treatment, penetrating trauma, and corneal disorders that precluded imaging. |
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Index tests |
AS‐OCT: spectral domain, RTVue 100 (Optovue Inc., Fremont, CA, USA, software version 4.0). Anterior segment morphology was assessed with the corneal adaptor module long (CAM‐L), using the angle scan protocol, which captured 1 x 1024 A‐scans in the nasal and temporal quadrants. Optimal cut‐off values were derived from the study data at AOD500 and TISA 500. Scheimpflug photography: Pentacam (Oculus, software version 1.11). Optimal cut‐off values were derived from the study data using ACD and ACV. |
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Target condition and reference standard(s) | Static gonioscopy, Shaffer grading system was used and an occludable angle was defined as Shaffer grade 1 or less in all four quadrants (360 degrees). | ||
Flow and timing | 300 participants were recruited; 35 participants were excluded because of an undetectable scleral spur on AS‐OCT. Data from 265 eyes were included in the final analysis. The index test and reference standard were conducted on the same occasion. | ||
Comparative | |||
Notes | Conflict of interest: the authors declare no conflict of interest. | ||
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? | Yes | ||
Did the study avoid inappropriate exclusions? | Yes | ||
Could the selection of patients have introduced bias? | Low risk | ||
Are there concerns that the included patients and setting do not match the review question? | Low concern | ||
DOMAIN 2: Index Test (LACD) | |||
DOMAIN 2: Index Test (Scheimpflug photography) | |||
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? | No | ||
Could the conduct or interpretation of the index test have introduced bias? | High risk | ||
Are there concerns that the index test, its conduct, or interpretation differ from the review question? | Low concern | ||
DOMAIN 2: Index Test (AS‐OCT) | |||
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? | No | ||
Could the conduct or interpretation of the index test have introduced bias? | High risk | ||
Are there concerns that the index test, its conduct, or interpretation differ from the review question? | Low concern | ||
DOMAIN 2: Index Test (SPAC) | |||
DOMAIN 2: Index Test (Flashlight) | |||
DOMAIN 3: Reference Standard | |||
Is the reference standards 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 | |||
Was there an appropriate interval between index test and reference standard? | Yes | ||
Were all patients included in the analysis? | Yes | ||
Did all patients receive a reference standard | Yes | ||
Could the patient flow have introduced bias? | Low risk |