Methods
The present research was an associated study of the imaging in PIC described elsewhere.15 In brief, it was a cross-sectional study of the performance of AS-OCT in detection of PIC based on standardised UBM criteria, undertaken at a tertiary eye care centre in Rajavithi Hospital. All investigations were carried out in accordance with the Declaration of Helsinki, and neither patients nor the public were involved in the design, conduct, reporting or dissemination plans of our research.
We enrolled phakic patients with PACD for UBM and AS-OCT investigation. PACD, including primary angle-closure suspect (PACS), PAC, and PAC glaucoma (PACG), were defined in accordance with the International Society of Geographical and Epidemiological Ophthalmology (ISGEO) classification by Foster et al.16 Exclusion criteria were individuals who could not be evaluated with both devices, such as patients with corneal opacity. Subjects with pseudophakia, secondary angle-closure, postglaucoma surgery and post argon laser peripheral iridoplasty (ALPI) were excluded.
Complete ocular examinations including visual acuity, slit lamp evaluation of anterior eye segment, Goldmann applanation tonometry, dynamic gonioscopy and fundus ophthalmoscopy were performed by glaucoma specialists and clinical fellows, and diagnosis was made by a senior glaucoma specialist. Since our objective was focused on PIC detection, we performed laser peripheral iridotomy (LPI) to break PB in all patients at least 1 month before scanning with the two imaging systems. PACD patients who had residual angle closure in which the trabecular meshwork could not be seen by gonioscopy for at least 180° were included for UBM and AS-OCT examination.
AS-OCT (Visante, V.3.0.1.8, Carl Zeiss Meditec, Dublin, California, USA) was first performed by an experienced operator in the sitting position for horizontal and vertical axes in a standard room light (230 lux). During vertical scanning, upper and lower lids were held gently, avoiding inadvertent ocular compression. The patient was placed in the supine position and UBM, Paradigm 60 or VuMAX HD (Sonomed Escalon, Lake Success, NY) scanning was performed by a trained research fellow (WP) who had 2 years’ experience of using this device. Immersion with water eyecup was gently performed to avoid unintentional ocular compression, followed by scanning in the superior, inferior, nasal and temporal quadrants. All images were deidentified and transferred to a personal computer.
UBM-PIC was defined as anteriorly-positioned ciliary process, absence of ciliary sulcus and peripheral iris root angulation with flat iris centrally, whereas non-PIC was assumed when these criteria were not fulfilled. UBM quadrant-wise images were classified by a senior glaucoma specialist (BW) as either PIC or non-PIC. Intraobserver agreement was assessed for reproducibility of the classification on 30 images, kappa=0.79. Interobserver agreements were tested by two glaucoma specialists (KS and NP), with kappa=0.71 and 0.73, respectively.15 At eye level, UBM-PIC in at least two quadrants was defined as diagnosis of PIC (DxPIC).
AS-OCT images were separately classified by three glaucoma specialists, graders 1–3 (BW, KS and NP, respectively). Four mechanisms of PACD are shown in figure 1: PB-like (figure 1A), PIC (figure 1B), TPIR (figure 1C) and ELV (figure 1D). AS-OCT-PIC was defined as peripheral iris root angulation with flat iris centrally and normal ACD. If the two quadrants of axis images did not show the same mechanism, forced classification of the dominant mechanism was performed.
Statistics
We tested sensitivity, specificity and accuracy of AS-OCT for prediction of DxPIC. Positive predictive values (PPV) and negative predictive values (NPV) were also tested, with an estimated disease prevalence of PIC of 30%.17 18 Statistical analysis was performed with SPSS V.20 (SPSS) and Medcalc (https://www.medcalc.org/calc/diagnostic_test.php, accessed 22 March 2021).
Kappa (k) represents agreement between the classifications of the two devices, defined as: 0–0.2 slight agreement; 0.21–0.4, fair agreement; 0.41–0.6, moderate agreement; 0.61–0.8, substantial agreement; greater than 0.81, highest agreement.19