Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 8 de 8
Filter
1.
BMC Ophthalmol ; 14: 138, 2014 Nov 22.
Article in English | MEDLINE | ID: mdl-25416399

ABSTRACT

BACKGROUND: The study aims to survey longstanding funduscopic and functional outcomes of age-related macular degeneration (AMD) after ranibizumab treatment and verify the accuracy of a new method to compare the retinal thickness measured with different optical coherence tomography (OCT) tools. METHODS: Case series included 314 eyes with 2-4 years of follow-up. Main Outcome Measures were visual acuity (VA), number of injections, retinal thickness, OCT morphology, and final macular funduscopic status. RESULTS: One hundred twenty-two men and 177 women (mean age, 78.3 years) were included. The mean time to the first injection was 17.3 ± 14.6 days. Initial VA was O.8(20/125) ± 0.5; 0.7(20/100) ± 0.5 at 3 months; 0.8(20/125) ± 0.5 at a year; 1(20/200) ± 0.6 at year 2; 1(20/200) ± 0.6 at year 3 and 1.1(20/250) ± 0.6 at year 4. Number of visits at 3 months was 2.7 ± 0.8; 7.3 ± 2.1 at a year; 5.2 ± 2.7 along the 2nd year; 3.9 ± 2.3 at year 3 and 3.6 ± 2.2 at year 4. Number of injections at 3 months was 2.6 ± 0.5; 3.9 ± 1.5 at a year; 1.1 ± 1.5 along the 2nd year; 1.5 ± 2.4 at year 3 and 1.8 ± 3.1 at year 4. Patients with worse VA outcomes received more injections and were older. The formula to calculate changes in retinal thickness showed a 30% reduction in thickness, which correlated well with the OCT morphology. Patients with polypoidal choroidal vasculopathy (PCV) had a worse final outcome. The final disciform macular status (37%) was related to fewer injections and a greater decrease in thickness. Final well-preserved maculas (12.%) needed more injections and treatment changes; those that were atrophic at the final visit (30.8%) had a worse initial VA and greater decrease in thickness at the 3-month visit. CONCLUSIONS: Younger patients had better final outcomes. Our method to compare retinal thickness using different OCT tools worked well. The final visual outcome after a long follow-up was poor, which may be related to advanced age, poor initial VA, and the high incidence of final fibrosis or atrophy.


Subject(s)
Angiogenesis Inhibitors/therapeutic use , Antibodies, Monoclonal, Humanized/therapeutic use , Wet Macular Degeneration/drug therapy , Aged , Aged, 80 and over , Female , Fluorescein Angiography , Follow-Up Studies , Humans , Intravitreal Injections , Male , Middle Aged , Ophthalmoscopy , Organ Size , Ranibizumab , Retina/pathology , Retrospective Studies , Spain , Tomography, Optical Coherence , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Visual Acuity/physiology , Wet Macular Degeneration/physiopathology
2.
Curr Eye Res ; 38(2): 278-82, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23330822

ABSTRACT

PURPOSE: To evaluate the efficacy of different anesthetics and topical anti-inflammatory treatment in patients undergoing intravitreal injections (IVI). METHODS: Prospective, randomized, double masked, comparative study. Patients undergoing 0.05 mL IVI were randomized to two different preoperative anesthetic regimes (regime A [0.5% tetracaine + naphazoline] versus regime B [5% lidocaine]) and two different post-injection topical protocols (protocol 1 [tobramycin qid] versus protocol 2 [tobramycin qid + diclofenac qid]). Patients were trained to score pain using a numerical rating pain scale from 0 (no pain) to 10 (excruciating pain) immediately after the injection, 30 min and 24 h later. Patients were instructed to take oral paracetamol (650-1000 mg, adjusted to the patient's weight) every six hours ad lib if necessary. RESULTS: A total of 156 patients were enrolled; 86 patients were randomized to regime A and 70 to regime B; 78 patients were assigned to each of the post-injection topical protocols. The average pain score immediately after the IVI was 2.77 (SD 2.12) for the whole group (2.85, SD 2.23 with tetracaine and 2.67, SD 2.00 with lidocaine; p = 0.73, Mann-Whitney U-test). Twenty-four hours later, the average pain score was 1.84, SD 2.45 (topical diclofenac + tobramycin) versus 1.75, SD 1.83 (topical tobramycin; p = 0.46, Mann-Whitney U-test). Forty-seven patients (30%) required oral paracetamol (average 3.3 and range 1-5 tablets). Conjunctival hemorrhage 30 min after the injection was less frequent and severe in eyes treated with topical naphazoline (p = 0.055, Mann-Whitney U-test). CONCLUSIONS: Topical tetracaine and lidocaine provide similar anesthesia before IVI. Topical diclofenac does not seem to reduce pain scores after IVI.


Subject(s)
Antibodies, Monoclonal, Humanized/administration & dosage , Eye Pain/prevention & control , Intravitreal Injections/adverse effects , Lidocaine/administration & dosage , Retinal Diseases/drug therapy , Tetracaine/administration & dosage , Aged , Aged, 80 and over , Anesthetics, Local/administration & dosage , Angiogenesis Inhibitors/administration & dosage , Anti-Bacterial Agents/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Bevacizumab , Diclofenac/administration & dosage , Double-Blind Method , Drug Therapy, Combination , Eye Pain/drug therapy , Female , Humans , Male , Middle Aged , Naphazoline/administration & dosage , Nasal Decongestants/administration & dosage , Prospective Studies , Ranibizumab , Tobramycin/administration & dosage
3.
Ophthalmologica ; 228(2): 78-83, 2012.
Article in English | MEDLINE | ID: mdl-22710369

ABSTRACT

PURPOSE: To study whether anti-vascular endothelial growth factor (VEGF) therapy improves visual acuity (VA) in patients with exudative age-related macular degeneration (AMD) complicated with retinal pigment epithelium (RPE) tears. METHODS: Retrospective case-control series. Group I (control group) included 9 patients with RPE tears that received no treatment, and group II (intervention group) incorporated 12 patients treated with anti-VEGF. RESULTS: A statistically significant difference was found in VA between the groups from the 3rd month to the final follow-up (p = 0.034). Final VA improved in the treatment group (p = 0.015). No differences were found in central macular thickness between the groups either before or after treatment. Mean number of injections in group II was 5.75 (SD = 1.19). Most patients presented a grade 3 rip. All lesions were inactive at the end of follow-up in group II and 1 remained active in group I. The number of final atrophic/disciform scars was 6/8 in group I and 7/5 in group II. CONCLUSIONS: RPE tears treated with antiangiogenic drugs experienced functional benefit. To the authors' knowledge, this is the first controlled series reporting effectiveness of suppression of neovascular activity with antiangiogenic treatment after RPE rip in AMD.


Subject(s)
Angiogenesis Inhibitors/administration & dosage , Macular Degeneration/drug therapy , Retinal Perforations/drug therapy , Aged , Aged, 80 and over , Antibodies, Monoclonal, Humanized/administration & dosage , Aptamers, Nucleotide/administration & dosage , Bevacizumab , Case-Control Studies , Female , Fluorescein Angiography , Follow-Up Studies , Humans , Intravitreal Injections , Macular Degeneration/physiopathology , Male , Middle Aged , Ranibizumab , Retinal Perforations/physiopathology , Retinal Pigment Epithelium , Retrospective Studies , Tomography, Optical Coherence , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Visual Acuity/physiology
4.
Eur J Ophthalmol ; 21(4): 503-5, 2011.
Article in English | MEDLINE | ID: mdl-21279982

ABSTRACT

PURPOSE: To report the anatomic and functional outcome of intravitreal bevacizumab (IVB) to treat choroidal neovascularization (CNV) following photodynamic therapy (PDT) to treat recurrent central serous choroidopathy (CSC). METHODS: This was an interventional case report in which verteporfin PDT was performed in a case of recurrent CSC. RESULTS: Following PDT, the patient developed juxtafoveal CNV that was later treated by IVB, achieving CNV closure and recovery of visual acuity. CONCLUSIONS: Photodynamic therapy is a useful therapy to treat recurrent CSC, though it may be associated with potentially severe complications such as CNV. Intravitreal bevacizumab seems a good alternative treatment in the management of this condition.


Subject(s)
Angiogenesis Inhibitors/administration & dosage , Antibodies, Monoclonal, Humanized/administration & dosage , Central Serous Chorioretinopathy/drug therapy , Choroidal Neovascularization/drug therapy , Photochemotherapy/adverse effects , Adult , Bevacizumab , Central Serous Chorioretinopathy/physiopathology , Choroidal Neovascularization/etiology , Choroidal Neovascularization/physiopathology , Combined Modality Therapy , Fluorescein Angiography , Humans , Intravitreal Injections , Male , Photosensitizing Agents/therapeutic use , Porphyrins/therapeutic use , Recurrence , Tomography, Optical Coherence , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Verteporfin , Visual Acuity/physiology
5.
Ocul Immunol Inflamm ; 19(1): 48-50, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21250924

ABSTRACT

PURPOSE: To report spectral domain optical coherence tomography (SD OCT) findings in acute posterior multifocal placoid pigment epitheliopathy (APMPPE). DESIGN: Prospective, observational case report. METHODS: Complete ophthalmologic examination, including fluorescein angiography and SD OCT. RESULTS: A 31-year-old female with APMPPE presented with large intraretinal cysts in the outer nuclear layer consistent with intraretinal edema on SD OCT. Spontaneous normalization of the gross anatomy of the fovea with disruption of the inner/outer photoreceptor segment junction was observed in both eyes. CONCLUSION: The findings show that massive intraretinal edema may occur in the early stages of APMPPE.


Subject(s)
Cysts/diagnosis , Papilledema/diagnosis , Retinal Detachment/diagnosis , Retinal Diseases/diagnosis , Tomography, Optical Coherence/methods , Acute Disease , Adult , Female , Fluorescein Angiography , Humans , Visual Acuity
7.
J Neuroophthalmol ; 27(1): 36-40, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17414871

ABSTRACT

A 34-year-old woman in whom multiple sclerosis (MS) had been diagnosed 2 years earlier developed progressive bilateral visual loss associated with peripapillary exudative retinal detachment and other features of Vogt-Koyanagi-Harada (VKH) syndrome. She was treated with corticosteroid pulses and interferon beta-1A with visual acuity improvement and resolution of the retinal detachment. This is the first reported case of VKH syndrome in a patient with MS. The combination of VKH syndrome and MS suggests a common autoimmune pathogenesis.


Subject(s)
Multiple Sclerosis/complications , Uveomeningoencephalitic Syndrome/etiology , Adjuvants, Immunologic/administration & dosage , Adjuvants, Immunologic/therapeutic use , Adult , Diagnosis, Differential , Disease Progression , Drug Administration Routes , Drug Therapy, Combination , Female , Fluorescein Angiography , Fundus Oculi , Glucocorticoids/administration & dosage , Glucocorticoids/therapeutic use , Humans , Interferon beta-1a , Interferon-beta/administration & dosage , Interferon-beta/therapeutic use , Magnetic Resonance Imaging , Multiple Sclerosis/diagnosis , Tomography, Optical Coherence , Uveomeningoencephalitic Syndrome/diagnosis , Uveomeningoencephalitic Syndrome/drug therapy , Visual Acuity
8.
International Eye Science ; (12): 1255-1257, 2006.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-641721

ABSTRACT

· AIM: To determine the influence of topical anaesthetic drops, age and central corneal thickness (CCT) in the determination of intraocular pressure (IOP) by non contact tonometry (NCT). · METHODS: Ninety-three eyes from 47 patients were examined for CCT and lOP by NCT before and after the instillation of topical anaesthetic drops.· RESULTS: Average age was 66.4 (SD 16, range 34 to 88years-of-age). Thirty one patients were female and 16 were male. Average basal IOP was 16.0 mmHg (SD 4.0, range 8.5to 26.1). IOP pressure one minute after topical anesthesia instillation was 15.0 mmHg (SD 3.8, range 7.7 to 26.7), and 14.9 mm Hg (SD 3.9, range 7.6 to 26.3) five minutes after the instillation. The differences were statistically significant for the 0 to 1 minute lapse (P=0.0007) and for the 0 to 5minute lapse (P=0.0003), but not for the 1 to 5 minute lapse (P=0.27) (Student's t test for paired data). Average CCT before topical anaesthetic drops was 565.4 microns. Simple linear regression analysis demonstrated absence of significant variation between age and IOP changes and between CCT and IOP changes,· CONCLUSION: Our study confirms that the instillation of topical anaesthetics causes a reduction in IOP, which is progressive during the first 5 minutes after instillation. This IOP reduction does not seem to be associated with basal CCT or age.

SELECTION OF CITATIONS
SEARCH DETAIL
...