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Table 1.  

Study Description Major exclusions Participants Sensitivity/Specificity
Bagchi et al. 2019[26] Retrospective audit of patients who presented to a retinal clinic in the United Kingdom with high myopia (<−6D or AL > 26 mm) and new onset visual disturbance who received FA, OCTA and SD-OCT imaging. Excluded patients who did not receive all three imaging modalities. Excluded patients with poor quality images. Excluded patients with other co- existing major ocular conditions. 27 eyes of 26 patients (18 female, 6 male) Mean age 47.7 ± 19.7 years OCTA vs FA: Sensitivity 19/23, specificity 3/4 SD-OCT vs FA: Sensitivity 23/23, specificity 0/4
Milani et al.[24] Retrospective audit of patients seen at a research hospital in Italy with recent vision deterioration, pathologic myopia (<−6D and staphyloma) and suspected mCNV who received near infrared, autofluorescence, FA and SD-OCT imaging at first presentation. Excluded patients who did not receive all four imaging modalities. Excluded patients with poor quality images. Excluded patients who had previous vitreoretinal surgery, diabetes, signs of age-related macular degeneration, or vitreoretinal interface-related pathologies. 65 eyes of 62 patients (44 female, 21 male) Mean age 66.72 years, range 18–89 Mean refraction −9.72D, range −6 to −22 SD-OCT vs FA: Sensitivity 48/49, specificity 16/16
Miyata et al. 2016[25] Prospective study of consecutive patients who presented to a university ophthalmology clinic in Japan with pathologic myopia (<−6D or AL > 26 mm, plus chorioretinal abnormalities) and treatment naïve exudative lesions. Patients with OCTA images of insufficient quality were excluded from analysis. 28 eyes of 26 patients (22 female, 4 male) Included in analysis: 21 eyes of 20 patients (17 female, 3 male) Mean age 63.0 ± 13.6 years OCTA vs FA: Sensitivity 16/17, specificity 4/4
Querques et al. 2017[28] Retrospective audit of patients who presented to a university hospital’s retinal clinic in Italy with pathologic myopia (<−8D or AL > 26.5 mm, plus characteristic degenerative changes of the sclera/ choroid/retina) who were diagnosed with mCNV using FA.a An additional cohort of patients with pathologic myopia and no evidence of mCNV were enrolled as a negative control group. Excluded patients with co-existing retinal conditions, history of ocular inflammation in the study eye, significant media opacities, or large haemorrhage. Patients with OCTA images of insufficient quality or who did not have FA performed on the same day as OCTA were excluded from analysis. Negative control group: Excluded patients with co- existing retinal conditions, or previous ocular treatments in the study eye. 36 eyes of 28 patients (23 female, 5 male) Included in analysis: 21 eyes of 17 patients (14 female, 3 male) Mean age 57.8 ± 14.5 years= Negative control group: 32 eyes of 32 patients (27 female, 5 male) Mean age 56.2 ± 14.4 years, range 26–84 OCTA vs FAa: Sensitivity 19/21, specificity 30/32
Su et al. 2014[27] Prospective study of patients who presented to a macular service centre in China with high myopia (< −6D and AL > 26.5 mm) and myopic maculopathy. Excluded patients with other retinal or choroidal diseases, or dense cataracts. 69 eyes of 42 patients (23 female, 19 male) Mean age 47.3 ± 17.3 years, range 20–79 SD-OCT vs FA: Sensitivity 16/16, specificity 53/53

Table 1. Key details of included studies.

D Dioptres, AL Axial length, FA Fluorescein angiography, OCTA Optical coherence tomography angiography, SD-OCT Spectral domain optical coherence tomography, mCNV Myopic choroidal neovascularisation.
aUse of FA as reference standard was clarified by direct communication with the corresponding author.

Table 2.  

  Outcome (95% CI) Outcome (95% CI)
OCTA compared to FA
Individual studiesa TP FP FN TN Sensitivity Specificity
Bagchi 2019 19 1 4 3 0.83 (0.61–0.95) 0.75 (0.19–0.99)
Miyata 2016 16 0 1 4 0.94 (0.71–1.00) 1.00 (0.40–1.00)
Querques 2017 19 2 2 30 0.90 (0.70–0.99) 0.94 (0.79–0.99)
Pooled results from meta-analysisb Sensitivity Specificity
  0.89 (0.78–0.94) 0.93 (0.79–0.98)
  LR of a positive test LR of a negative test
  11.8 (3.96–35.25) 0.12 (0.061–0.25)
  Positive PV Negative PV
  0.95 (0.79–0.99) 0.85 (0.61–0.94)
SD-OCT compared to FA
Individual studiesa TP FP FN TN Sensitivity Specificity
Bagchi 2019 23 4 0 0 1.00 (0.85–1.00) 0.00 (0.00–0.60)
Milani 2016 48 0 1 16 0.98 (0.89–1.00) 1.00 (0.79–1.00)
Su 2014 16 0 0 53 1.00 (0.79–1.00) 1.00 (0.93–1.00)
Pooled results from meta-analysisb Sensitivity Specificity
  0.99 (0.91–1.00) unestimatable
  LR of a positive test LR of a negative test
  unestimatable 0.01 (0.001–0.095)
  Positive PV Negative PV
  unestimatable unestimatable

Table 2. Test accuracy of individual studies and pooled results from meta-analysis.

CI confidence interval, OCTA optical coherence tomography angiography, FA fluorescein angiography, TP true positive, FP false positive, FN false negative, TN true negative, LR likelihood ratio, PV predictive value, SD-OCT spectral domain optical coherence tomography.
aCalculated using RevMan Ver 5.4.1.
bCalculated using SAS macro MetaDAS v1.3.

Table 3.  

Test

Recommendation

OCTA

Conditionally recommend the use of OCTA to achieve a diagnosis when mCNV is clinically suspected. Statement was conditional because all studies excluded patients from analysis due to image quality issues.

  • •  Recommend OCTA as an initial screening study to rule out mCNV.
  • •  Recommend OCTA to rule in the presence of mCNV. However, due to a possible high false positive rate, a positive diagnosis should be confirmed by FA.

SD-OCT

Conditionally suggest clinicians may consider the use of SD-OCT to achieve a diagnosis when mCNV is clinically suspected. Statement was conditional because of the inability to estimate a pooled specificity for SD-OCT resulting in an unknown false positive rate.

  • •  Recommend SD-OCT as an initial screening study to rule out mCNV.
  • •  Do not recommend reliance on SD-OCT alone to rule in the presence of mCNV because the false positive rate of SD-OCT is unknown. A positive diagnosis must be confirmed by FA.

OCTA + SD-OCT

Clinicians may consider using SD-OCT if an OCTA image of sufficient quality cannot be acquired.

  • •  If either OCTA or SD-OCT return a negative result, clinicians may be fairly confident in ruling out mCNV.
  • •  If either OCTA or SD-OCT return a positive result, FA should be performed to rule out false positives and confirm the diagnosis.

Table 3. Key recommendations.

OCTA Optical coherence tomography angiography, mCNV Myopic choroidal neovascularisation, FA Fluorescein angiography, SD-OCT Spectral domain optical coherence tomography.

CME

Diagnostic Accuracy of OCTA and OCT for Myopic Choroidal Neovascularisation: A Systematic Review and Meta-Analysis

  • Authors: Sharon Ho, BOptom; Angelica Ly, BOptom, PhD; Kyoko Ohno-Matsui, MD, PhD; Michael Kalloniatis, BSci (Optom), PhD; Gordon S. Doig, DVM, PhD
  • CME Released: 12/2/2022
  • Valid for credit through: 12/2/2023, 11:59 PM EST
Start Activity

  • Credits Available

    Physicians - maximum of 1.00 AMA PRA Category 1 Credit(s)™

    You Are Eligible For

    • Letter of Completion

Target Audience and Goal Statement

This activity is intended for ophthalmologists and other clinicians caring for patients with myopic choroidal neovascularization (mCNV).

The goal of this activity is for learners to be better able to describe the test accuracy of optical coherence tomography angiography (OCTA) and spectral domain (SD)-OCT in diagnosing mCNV compared with the reference standard, fluorescein angiography, according to a meta-analysis with primary outcome of pooled sensitivity and specificity and additional outcomes of pooled likelihood ratios and patient-oriented outcomes.

Upon completion of this activity, participants will:

  • Describe test accuracy, pooled sensitivity and pooled specificity of optical coherence tomography angiography (OCTA) and spectral domain (SD)-OCT in diagnosing myopic choroidal neovascularization (mCNV) compared with fluorescein angiography (FA) as the reference standard, according to a meta-analysis
  • Determine clinical recommendations for using OCTA and SD-OCT in diagnosing mCNV, according to a meta-analysis
  • Identify other clinical and research implications of test accuracy, pooled sensitivity and pooled specificity of OCTA and SD-OCT in diagnosing mCNV compared with FA as the reference standard, according to a meta-analysis


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Faculty

  • Sharon Ho, BOptom

    Centre for Eye Health
    University of New South Wales (UNSW) Medicine and Health
    School of Optometry and Vision Science
    UNSW Medicine and Health
    New South Wales, Australia

  • Angelica Ly, BOptom, PhD

    Centre for Eye Health
    University of New South Wales (UNSW) Medicine and Health
    School of Optometry and Vision Science
    UNSW Medicine and Health
    Brien Holden Vision Institute
    New South Wales, Australia

  • Kyoko Ohno-Matsui, MD, PhD

    Department of Ophthalmology and Visual Science
    Tokyo Medical and Dental University
    Tokyo, Japan

  • Michael Kalloniatis, BSci (Optom), PhD

    Centre for Eye Health
    School of Optometry and Vision Science
    University of New South Wales (UNSW) Medicine and Health
    New South Wales, Australia

  • Gordon S. Doig, DVM, PhD

    Centre for Eye Health
    School of Optometry and Vision Science
    University of New South Wales (UNSW) Medicine and Health
    New South Wales, Australia

CME Author

  • Laurie Barclay, MD

    Freelance writer and reviewer
    Medscape, LLC

    Disclosures

    Laurie Barclay, MD, has the following relevant financial relationships:
    Formerly owned stocks in: AbbVie

Editor

  • Sobha Sivaprasad, MD

    Editor, Eye

Compliance Reviewer

  • Leigh Schmidt, MSN, RN, CNE, CHCP

    Associate Director, Accreditation and Compliance, Medscape, LLC

    Disclosures

    Leigh Schmidt, MSN, RN, CNE, CHCP, has no relevant financial relationships.


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From Eye
CME

Diagnostic Accuracy of OCTA and OCT for Myopic Choroidal Neovascularisation: A Systematic Review and Meta-Analysis

Authors: Sharon Ho, BOptom; Angelica Ly, BOptom, PhD; Kyoko Ohno-Matsui, MD, PhD; Michael Kalloniatis, BSci (Optom), PhD; Gordon S. Doig, DVM, PhDFaculty and Disclosures

CME Released: 12/2/2022

Valid for credit through: 12/2/2023, 11:59 PM EST

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