Personalized Management of Dry Eye Disease: Beyond Artificial Tears.

aqueous deficient customized dry eye disease evaporative individualized inflammation

Journal

Clinical ophthalmology (Auckland, N.Z.)
ISSN: 1177-5467
Titre abrégé: Clin Ophthalmol
Pays: New Zealand
ID NLM: 101321512

Informations de publication

Date de publication:
2022
Historique:
received: 03 08 2022
accepted: 01 11 2022
entrez: 1 12 2022
pubmed: 2 12 2022
medline: 2 12 2022
Statut: epublish

Résumé

Dry eye disease (DED) is a multifactorial disease of the ocular surface that may be accompanied by discomfort and visual disturbances to a level that reduces quality of life. Artificial tears are a common first-line therapy for DED that aim to supplement the tear film but do not address the underlying causes of DED. Because of the complexity and variability of the disease, personalized treatment beyond artificial tears is important for successful management. This review describes artificial tears and the current knowledge in the personalized approach to the management of DED. There is evidence that artificial tears can reduce symptoms and signs of DED; however, a proportion of patients have been found to show limited or no improvement with artificial tears. Furthermore, the effectiveness of artificial tears may depend on patient compliance and type of artificial tear product used. Personalized management of DED with other treatments involves identifying features of the disease, including the subtype of DED, the presence of inflammation, and the coexistence of external and behavioral contributing factors. Various measures exist to characterize DED, including assessments of the tear film lipid layer, the meibomian glands, tear volume, tear osmolarity, and matrix metalloproteinase 9 levels. Because individuals can show variable features, the most prominent clinical findings, comorbidities, triggering events, and treatment history should be considered to determine the best treatment choices for patients.

Identifiants

pubmed: 36452043
doi: 10.2147/OPTH.S384819
pii: 384819
pmc: PMC9704006
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

3911-3918

Informations de copyright

© 2022 Matossian et al.

Déclaration de conflit d'intérêts

Cynthia Matossian is a speaker and consultant for Novartis. Micaela Crowley reports relationships with CooperVision, Kala Pharmaceuticals, Novartis, NovaBay Pharmaceuticals, Oyster Point. Laura Periman is an advisor for Allergan, Avellino, NuSight Medical, ScienceBased Health, Sun, ThermaMEDx; consultant for Allergan, Alcon, Bruder, Eyedetec, Eyevance, Horizon, Kala, Mallinkrodt, Novartis, NuSight Medical, Olympic Ophthalmics, Omera, ScienceBased Health, Sun, TearLab, ThermaMEDx, Wellness 26; a speaker for Allergan, Alcon, Eyevance, Johnson & Johnson, Lumenis, Mallinkrodt, Novartis, NuSight Medical, Optase, ScienceBased Health, Sun; independent contractor for Bausch and Lomb, Kala, Lumenis, Novartis, Olympic Ophthalmics, Tarsus, Novaliq, Oyster Point; and holds individual stocks of Eyedetec, Visant, Omera, Wellness 26. Steven Sorkin reports relationships with B+L SVP, Blanchard, BostonSight, Eyevance, Kala, Oyster Point, Sight Sciences, and Synergeyes. The authors report no other conflicts of interest in this work.

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Auteurs

Cynthia Matossian (C)

Matossian Eye Associates, Pennington, NJ, USA.
Matossian Eye Associates, Doylestown, PA, USA.

Micaela Crowley (M)

Lexington Eye Associates, Lexington, MA, USA.

Laura Periman (L)

Periman Eye Institute, Seattle, WA, USA.

Steven Sorkin (S)

Corneal Associates of New Jersey, Fairfield, NJ, USA.

Classifications MeSH