Purpose: To assess the effect of patient baseline characteristics on the efficacy of ocriplasmin treatment for symptomatic vitreomacular adhesion (VMA) with full-thickness macular hole (FTMH) from phase 3/4 studies.
Methods: Patients with symptomatic VMA and FTMH at baseline and receiving ocriplasmin treatment 125 g were pooled from the MIVI-TRUST, OASIS, and ORBIT studies. Multivariable logistic regression analysis was used to evaluate whether patient baseline characteristics were predictors of having VMA resolution by Day 28 and FTMH closure by Month 6.
Results: Two hundred and seventy-four patients receiving ocriplasmin treatment were assessed. Overall, 22.6% (62/274) of the patients experienced both VMA resolution by Day 28 and non-surgical FTMH closure by Month 6. Patients with FTMH 250 µm at baseline had a significantly higher success rate compared to those with FTMH 400 µm (29.9% [41/137] vs 2.2% [1/48]; = 0.009). In patients with VMA resolution by Day 28, both small FTMH size ( = 0.001) and FTMH width at RPE ( = 0.012) were significantly associated with a higher FTMH closure rate. Patients with VMA resolution had higher rates of FTMH closure. Previously identified baseline predictive factors, including age, lens status, or presence of epiretinal membrane (ERM) were not found to be predictive of both VMA release and FTMH closure.
Conclusion: The analysis revealed that FMTH 250 µm was the only factor predictive for achieving both pharmacological VMA resolution by Day 28 and nonsurgical FTMH closure by Month 6; neither lens status or presence of ERM, previously identified baseline characteristics favoring VMA resolution, showed statistically significant predictive power for both outcomes.
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http://dx.doi.org/10.18502/jovr.v16i1.8250 | DOI Listing |
Phys Chem Chem Phys
May 2024
Department of Physics, University of Kerala, Kariavattom, Thiruvananthapuram, Kerala, 695581, India.
In this study, we have synthesized nanostructured titanium dioxide (TiO) photocatalysts under different configurations, , anatase, rutile and anatase/rutile heterophase ( = 3.14-2.96 eV) through a sol-gel route.
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February 2024
Clical Centre Zemun, Belgrade, Serbia; School of Medicine University of Belgrade, Belgrade, Serbia.
Eye (Lond)
February 2024
Ophthalmology Services, Eye and ENT Clinic, Royal Victoria Hospital, Grosvenor Road, Belfast, BT12 6BA, UK.
Graefes Arch Clin Exp Ophthalmol
July 2023
Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, 54 Shogoin-Kawahara-Cho, Sakyo-Ku, Kyoto City, Kyoto Prefecture, 606-8507, Japan.
Nat Commun
October 2022
The Vaccine and Immunotherapy Center, The Wistar Institute of Anatomy and Biology, Philadelphia, PA, 19104, USA.
Monoclonal antibody therapy has played an important role against SARS-CoV-2. Strategies to deliver functional, antibody-based therapeutics with improved in vivo durability are needed to supplement current efforts and reach underserved populations. Here, we compare recombinant mAbs COV2-2196 and COV2-2130, which compromise clinical cocktail Tixagevimab/Cilgavimab, with optimized nucleic acid-launched forms.
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