Differentiating stages of functional vision loss from glaucoma using the Disc Damage Likelihood Scale and cup:disc ratio.

Diagnostic tests/Investigation Glaucoma

Journal

The British journal of ophthalmology
ISSN: 1468-2079
Titre abrégé: Br J Ophthalmol
Pays: England
ID NLM: 0421041

Informations de publication

Date de publication:
18 Jan 2023
Historique:
received: 11 04 2022
accepted: 07 01 2023
entrez: 18 1 2023
pubmed: 19 1 2023
medline: 19 1 2023
Statut: aheadofprint

Résumé

Glaucoma staging is critical for treatment planning but has rarely been tested in severe/end-stage disease. We compared the performance of the Disc Damage Likelihood Scale (DDLS) and cup:disc ratio (CDR) using a functional glaucoma staging system (GSS) as the reference standard. Post hoc analysis of a randomised controlled trial at the Eye Department of Kilimanjaro Christian Medical Centre, Tanzania. Eligible participants (aged ≥18 years) with open-angle glaucoma, intraocular pressure (IOP) of >21 mm Hg, were randomised to timolol 0.5% eye drops or selective laser trabeculoplasty. Fundoscopy established vertical and horizontal CDRs and DDLS. Visual acuity and static visual fields were graded (GSS). The study used area under the receiver operating characteristic (AROC) curves and Spearman's rank correlation coefficients to compare staging systems. Logistic regression with generalised estimating equations determined risk factors of functional severe/end-stage glaucoma. 382 eyes (201 participants) were evaluated; 195 (51%) had severe or end-stage glaucoma; mean IOP was 26.7 (SD 6.9) mm Hg. DDLS yielded an AROC of 0.90 (95% CI 0.87 to 0.93), vertical cup:disc ratio (vCDR) of 0.88 (95% CI 0.85 to 0.91, p=0.048) for identifying severe/end-stage disease. Correlation coefficients comparing GSS to DDLS and vCDRs were 0.73 and 0.71, respectively. Advanced structural stages, vision impairment, higher IOP and less financial resources were risk factors of functional severe/end-stage glaucoma. This study indicates that both structural staging systems can differentiate severe/end-stage glaucoma from less severe disease, with a moderate advantage of DDLS over CDR. Clinical examination of the optic disc plays an important role in addition to functional assessment when managing severe/end-stage glaucoma.

Sections du résumé

BACKGROUND BACKGROUND
Glaucoma staging is critical for treatment planning but has rarely been tested in severe/end-stage disease. We compared the performance of the Disc Damage Likelihood Scale (DDLS) and cup:disc ratio (CDR) using a functional glaucoma staging system (GSS) as the reference standard.
METHODS METHODS
Post hoc analysis of a randomised controlled trial at the Eye Department of Kilimanjaro Christian Medical Centre, Tanzania. Eligible participants (aged ≥18 years) with open-angle glaucoma, intraocular pressure (IOP) of >21 mm Hg, were randomised to timolol 0.5% eye drops or selective laser trabeculoplasty. Fundoscopy established vertical and horizontal CDRs and DDLS. Visual acuity and static visual fields were graded (GSS). The study used area under the receiver operating characteristic (AROC) curves and Spearman's rank correlation coefficients to compare staging systems. Logistic regression with generalised estimating equations determined risk factors of functional severe/end-stage glaucoma.
RESULTS RESULTS
382 eyes (201 participants) were evaluated; 195 (51%) had severe or end-stage glaucoma; mean IOP was 26.7 (SD 6.9) mm Hg. DDLS yielded an AROC of 0.90 (95% CI 0.87 to 0.93), vertical cup:disc ratio (vCDR) of 0.88 (95% CI 0.85 to 0.91, p=0.048) for identifying severe/end-stage disease. Correlation coefficients comparing GSS to DDLS and vCDRs were 0.73 and 0.71, respectively. Advanced structural stages, vision impairment, higher IOP and less financial resources were risk factors of functional severe/end-stage glaucoma.
CONCLUSION CONCLUSIONS
This study indicates that both structural staging systems can differentiate severe/end-stage glaucoma from less severe disease, with a moderate advantage of DDLS over CDR. Clinical examination of the optic disc plays an important role in addition to functional assessment when managing severe/end-stage glaucoma.

Identifiants

pubmed: 36653163
pii: bjo-2022-321643
doi: 10.1136/bjo-2022-321643
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Wellcome Trust
ID : 207472/Z/17/Z
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: GG reports personal fees from Alcon, Allergan, Belkin, Equinox, Genentech–Roche, Glaukos, Ivantis, Reichert, Sight Sciences, and Thea; grants from Belkin, Santen and Thea; and non-financial involvement with the patient advocacy group GlaucomaUK, outside the submitted work; he is also a coinvestigator on three other major SLT trials (LIGHT, COAST and Belkin laser). All other authors declare no competing interests.

Auteurs

Heiko Philippin (H)

International Centre for Eye Health, London School of Hygiene and Tropical Medicine Department of Clinical Research, London, UK Heiko.Philippin@lshtm.ac.uk.
Eye Centre, Medical Centre, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.

Einoti Naino Matayan (EN)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.
Kilimanjaro Christian Medical University College, Moshi, Tanzania, United Republic of.

Karin Marianne Knoll (KM)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.

Edith Macha (E)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.

Sia Mbishi (S)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.

Andrew Makupa (A)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.
Kilimanjaro Christian Medical University College, Moshi, Tanzania, United Republic of.

Cristóvão Daniel Matsinhe (CD)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.
Provincial Hospital of Pemba, Pemba, Mozambique.

Isac Vasco da Gama (IV)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.
Hospital Central de Quelimane, Quelimane, Mozambique.

Mário Jorge Monjane (MJ)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.

Joyce Awum Ncheda (JA)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.
Presbyterian Eye Hospital, Bafoussam, Cameroon.

Francisco Alcides Francisco Mulobuana (FAF)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.

Elisante Muna (E)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.

Nelly Fopoussi Guylene (NF)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.
Eye Department, Cameroon Baptist Convention Health Services, Douala, Cameroon.

Gus Gazzard (G)

National Institute for Health Research (NIHR) Biomedical Research Centre (BRC) for Ophthalmology at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, UK.
Institute of Ophthalmology, University College London, London, UK.

Ana Patricia Marques (AP)

International Centre for Eye Health, London School of Hygiene and Tropical Medicine Department of Clinical Research, London, UK.

Peter Shah (P)

Institute of Ophthalmology, University College London, London, UK.
Ophthalmology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

David Macleod (D)

MRC International Statistics & Epidemiology Group, London School of Hygiene & Tropical Medicine, London, UK.

William Makupa (W)

Eye Department, Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United Republic of.
Kilimanjaro Christian Medical University College, Moshi, Tanzania, United Republic of.

Matthew J Burton (MJ)

International Centre for Eye Health, London School of Hygiene and Tropical Medicine Department of Clinical Research, London, UK.
National Institute for Health Research (NIHR) Biomedical Research Centre (BRC) for Ophthalmology at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, UK.

Classifications MeSH