Reducing the clinical burden of ranibizumab treatment for neovascular age-related macular degeneration using an individually planned regimen.

Détails

Ressource 1Télécharger: BIB_6DDD88E26EF8.P001.pdf (867.10 [Ko])
Etat: Public
Version: Final published version
ID Serval
serval:BIB_6DDD88E26EF8
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Reducing the clinical burden of ranibizumab treatment for neovascular age-related macular degeneration using an individually planned regimen.
Périodique
British Journal of Ophthalmology
Auteur⸱e⸱s
Mantel I., Niderprim S.A., Gianniou C., Deli A., Ambresin A.
ISSN
1468-2079 (Electronic)
ISSN-L
0007-1161
Statut éditorial
Publié
Date de publication
2014
Peer-reviewed
Oui
Volume
98
Numéro
9
Pages
1192-1196
Langue
anglais
Notes
Publication types: JOURNAL ARTICLE
Résumé
AIMS: The purpose of this study was to clinically validate an individually planned treatment regimen for neovascular age-related macular degeneration (nAMD), termed, observe and plan. This regimen was based on the predictability of an individual's need for retreatment and aimed to reduce the clinical burden, while obtaining good functional results.
METHODS: This was a prospective case series that included 104 patients (115 eyes) with treatment-naive nAMD. Following three loading doses of ranibizumab, monthly observation visits allowed the disease recurrence interval to be determined. The recurrence interval was reduced by 2 weeks to give the retreatment interval for the next three injections. Periodical control visits (at least every 6 months) allowed the effectiveness of the treatment to be assessed and individual intervals adjusted.
RESULTS: Mean visual acuity (VA) improved by 8.7 and 9.8 letters in months 3 and 12, respectively. The mean number of injections during the 12-month study was 7.8, while the mean number of ophthalmic examinations between months 3 and 12 was 3.97. The mean treatment interval after the loading doses was 1.97 months.
CONCLUSIONS: The observe-and-plan regimen significantly improved VA. This was obtained with fewer clinic visits compared with other regimens, which could ease the burden of nAMD treatment.
TRIAL REGISTRATION NUMBER: Commission cantonale (VD) d'éthique de la recherché Clinique, Université de Lausanne, Protocole 351/11.
Pubmed
Web of science
Open Access
Oui
Création de la notice
05/05/2014 15:20
Dernière modification de la notice
20/08/2019 15:27
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