Real-Life Management of Central and Branch Retinal Vein Occlusion: A Seven-Year Follow-Up Study.


Journal

Thrombosis and haemostasis
ISSN: 2567-689X
Titre abrégé: Thromb Haemost
Pays: Germany
ID NLM: 7608063

Informations de publication

Date de publication:
Oct 2021
Historique:
pubmed: 12 3 2021
medline: 11 2 2022
entrez: 11 3 2021
Statut: ppublish

Résumé

Retinal vein occlusion is the second most common retinal vascular pathology after diabetic retinopathy and a major cause of vision impairment. Nowadays, both central retinal vein occlusion (CRVO) and branch retinal vein occlusion (BRVO) can be well-managed by intravitreal treatments. However, considering the long-life expectance of the patients, few data are present in the literature about the very long-term outcome of CRVO and BRVO. The present study was an interventional, retrospective analysis of the morphological and functional long-term outcome of CRVO and BRVO patients, followed in an Italian referral center. We collected data from 313 eyes (178 CRVO eyes and 135 BRVO eyes). Mean follow-up was 45 ± 25 months (range 12-84 months). Both CRVO and BRVO eyes experience a significant visual acuity improvement secondary to anti-vascular endothelial growth factor/dexamethasone treatments (from 0.57 ± 0.25 to 0.41 ± 0.24 LogMAR in CRVO and from 0.53 ± 0.42 to 0.30 ± 0.41 LogMAR in BRVO, respectively) (

Identifiants

pubmed: 33706397
doi: 10.1055/s-0041-1725197
doi:

Substances chimiques

Angiogenesis Inhibitors 0
Drug Implants 0
Glucocorticoids 0
VEGFA protein, human 0
Vascular Endothelial Growth Factor A 0
Dexamethasone 7S5I7G3JQL

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1361-1366

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

F.B. consultant for: Alcon (Fort Worth, Texas, USA), Alimera Sciences (Alpharetta, Georgia, USA), Allergan Inc (Irvine, California, USA), Farmila-Thea (Clermont-Ferrand, France), Bayer Shering-Pharma (Berlin, Germany), Bausch And Lomb (Rochester, New York, USA), Genentech (San Francisco, California, USA), Hoffmann-La-Roche (Basel, Switzerland), NovagaliPharma (Évry, France), Novartis (Basel, Switzerland), Sanofi-Aventis (Paris, France), Thrombogenics (Heverlee, Belgium), and Zeiss (Dublin, USA). All other authors have no disclosures to declare.

Auteurs

Alessandro Arrigo (A)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Anna Crepaldi (A)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Chiara Viganò (C)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Emanuela Aragona (E)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Rosangela Lattanzio (R)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Giovanni Scalia (G)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Antonio Giordano Resti (AG)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Francesca Calcagno (F)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Adelaide Pina (A)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Hassan Farah Rashid (HF)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Francesco Bandello (F)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

Maurizio Battaglia Parodi (M)

Department of Ophthalmology, IRCCS San Raffaele Hospital, University Vita-Salute, Milan, Italy.

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Classifications MeSH