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1.
J Fr Ophtalmol ; 42(2): 109-117, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30679130

ABSTRACT

PURPOSE: To evaluate the outcomes of bimanual intraocular foreign body (IOFB) removal with vitrectomy and describe the techniques of "active aspiration to forceps" and "forceps to forceps handshake" for IOFB removal. METHODS: Retrospective, interventional, single surgeon case series. The patients who had an IOFB and underwent vitrectomy with bimanual IOFB removal techniques and had a minimum follow-up period of 12 months were included. The main outcome measure was the functional and anatomical results of the bimanual surgical techniques. RESULTS: Twenty eyes were included. The mean follow-up time after surgery was 16.5±3.6 months (range 12-24 months). The baseline best corrected visual acuity (BCVA) was light perception in 8 eyes (40%), hand motions in one eye (5%), and≥1.0LogMAR in 11 eyes (55%). BCVA improved in 14 eyes (70%); was stable in 3 eyes (15%), and decreased in 3 eyes (15%). CONCLUSIONS: Both bimanual handshake techniques were safe and effective methods in the surgical treatment of IOFBs<5mm in size. The "active aspiration to forceps handshake" technique might be a gentle technique for the removal of IOFBs that are located on the surface of or trapped within the retina.


Subject(s)
Endophthalmitis/surgery , Eye Foreign Bodies/surgery , Eye Injuries, Penetrating/surgery , Vitrectomy/statistics & numerical data , Adolescent , Adult , Cohort Studies , Endophthalmitis/epidemiology , Eye Foreign Bodies/epidemiology , Eye Injuries, Penetrating/epidemiology , Follow-Up Studies , Hand , Humans , Male , Middle Aged , Posterior Eye Segment/surgery , Retrospective Studies , Suction , Surgeons , Surgical Instruments , Treatment Outcome , Vitrectomy/instrumentation , Vitrectomy/methods , Young Adult
2.
J Fr Ophtalmol ; 42(1): 22-31, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30578008

ABSTRACT

PURPOSE: To evaluate baseline predictive markers of early and late anatomical response to anti-vascular endothelial growth factor (anti-VEGF) treatment in patients with neovascular age-related macular degeneration (nAMD). METHODS: The records of the nAMD patients who underwent intravitreal ranibizumab or aflibercept treatment, received the 3 monthly loading doses, and completed a follow-up period of 12 months were included retrospectively. The anatomical treatment response at month 3 (early) and between month 3 and 12 (late) was classified as good, intermediate or poor. Baseline demographic, fluorescein angiography, and optical coherence tomography findings were compared among the three groups. RESULTS: One hundred and ten eyes (74.3%) showed good, 18 (12.2%) showed intermediate and 20 (13.5%) showed poor anatomical response at month 3, and 114 eyes (77.0%) showed good, 27 (18.2%) showed intermediate and 7 (4.7%) showed poor anatomical response between month 3 and month 12. Of the evaluated parameters, drug type (better in aflibercept), showed a statistically significant difference in regards to anatomical outcomes at both the early and late periods (P=0.02 and P=0.03). The greatest linear dimension of choroidal neovascularization (CNV) and presence of peaked pigment epithelial detachment (PED) were important factors for early anatomical anti-VEGF treatment response. CONCLUSION: Larger CNV and the presence of a peaked PED appeared to be associated with a good early response, and the drug type seemed to be associated with both early and late poor anatomical response of anti-VEGF treatment in nAMD patients. Aflibercept appears to be more effective than ranibizumab in regards to the percentage of patients with better anatomical response in both the early and late treatment periods.


Subject(s)
Angiogenesis Inhibitors/therapeutic use , Biomarkers, Pharmacological/analysis , Choroidal Neovascularization/drug therapy , Macular Degeneration/drug therapy , Multimodal Imaging/methods , Aged , Aged, 80 and over , Case-Control Studies , Choroidal Neovascularization/complications , Choroidal Neovascularization/diagnosis , Female , Fluorescein Angiography , Follow-Up Studies , Humans , Intravitreal Injections , Macular Degeneration/complications , Macular Degeneration/diagnosis , Male , Prognosis , Ranibizumab/administration & dosage , Ranibizumab/adverse effects , Receptors, Vascular Endothelial Growth Factor/administration & dosage , Recombinant Fusion Proteins/administration & dosage , Recombinant Fusion Proteins/adverse effects , Retrospective Studies , Time Factors , Tomography, Optical Coherence , Treatment Outcome , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Vascular Endothelial Growth Factor A/immunology
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