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1.
BMC Ophthalmol ; 18(1): 62, 2018 Feb 27.
Article in English | MEDLINE | ID: mdl-29486754

ABSTRACT

BACKGROUND: To compare visual function and structural improvements in pseudophakic eyes with diabetic macular oedema (DMO) treated with the 0.19mg Fluocinolone Acetonide (FAc) intravitreal implant (IluvienTM) in a 'real world' setting. METHODS: A single centre retrospective evaluation of patients with DMO unresponsive to conventional treatment treated with the FAc implant according to UK guidelines. Primary efficacy endpoint was best corrected visual acuity (BCVA); secondary endpoints included optical coherence tomography evaluations of the macula (a) central retinal and (b) peak macular thickness collected at annual time points. Primary safety endpoint was new rise in IOP >27mmHg or glaucoma surgery. Patients with <1 year follow-up were excluded. RESULTS: Twenty-nine eyes were included, with mean(SD) follow up of 792(270) days. Improvement in BCVA and reduction in macular oedema was noted at all timepoints. Mean improvement in BCVA from baseline was 6 ETDRS letters at year 1(n=29), 6.5L at year 2(n=22) and 11L at year 3(n=6). Mean central retinal thickness at baseline was 451 microns, 337 microns at year 1, 342 microns at year 2 and 314 microns at year 3. Two eyes required IOP-lowering drops post implant. Supplementary treatment for persistence or recurrence of DMO was necessary in 18 eyes over the total study period of 3 years with mean time to supplementary treatment being 12 months. CONCLUSIONS: Our evaluation of the 0.19mg FAc implant delivered in a real-world setting, provides additional evidence that it is effective and safe in the treatment of patients with DMO, and can provide sustained benefit for patients with previously refractory disease.


Subject(s)
Diabetic Retinopathy/drug therapy , Fluocinolone Acetonide/administration & dosage , Glucocorticoids/administration & dosage , Macular Edema/drug therapy , Adult , Aged , Aged, 80 and over , Diabetic Retinopathy/pathology , Diabetic Retinopathy/physiopathology , Drug Implants , Female , Humans , Intravitreal Injections , Macular Edema/pathology , Macular Edema/physiopathology , Male , Middle Aged , Retina/pathology , Retrospective Studies , United Kingdom , Visual Acuity/physiology
2.
Br J Ophthalmol ; 101(12): 1673-1678, 2017 12.
Article in English | MEDLINE | ID: mdl-28487377

ABSTRACT

AIM: To assess the rate of 'treatment-requiring diabetic macular oedema (DMO)' in eyes for the two years before and after cataract surgery. METHODS: Multicentre national diabetic retinopathy (DR) database study with anonymised data extraction across 19 centres from an electronic medical record system. INCLUSION CRITERIA: eyes undergoing cataract surgery in patients with diabetes with no history of DMO prior to study start. The minimum dataset included: age, visual acuity (all time-points), injection episodes, timing of cataract surgery and ETDRS grading of retinopathy and maculopathy. MAIN OUTCOME MEASURE: rate of developing first episode of treatment-requiring DMO in relation to timing of cataract surgery in the same eye. RESULTS: 4850 eyes met the inclusion criteria. The rate of developing treatment-requiring DMO in this cohort was 2.9% in the year prior to surgery versus 5.3% in the year after surgery (p<0.01). The risk of 'treatment-requiring DMO' increased sharply after surgery, peaking in the 3-6 months' period (annualised rates of 5.2%, 6.8%, 5.6% and 4.0% for the 0-3, 3-6, 6-9 and 9-12 months' post-operative time periods respectively). Risk was associated with pre-operative grade of retinopathy: risk of DMO in the first year post-operatively being 1.0% (no DR pre-operatively), 5.4% (mild non-proliferative diabetic retinopathy; NPDR), 10.0% (moderate NPDR), 13.1% (severe NPDR) and 4.9% (PDR) (p<0.01). CONCLUSIONS: This large real-world study demonstrates that the rate of developing treatment-requiring DMO increases sharply in the year after cataract surgery for all grades of retinopathy, peaking in the 3-6 months' postoperative period. Patients with moderate and severe NPDR are at particularly high risk.


Subject(s)
Cataract Extraction , Cataract/complications , Diabetic Retinopathy/complications , Electronic Health Records , Macular Edema/etiology , Outcome Assessment, Health Care , Visual Acuity , Aged , Diabetic Retinopathy/diagnosis , Diabetic Retinopathy/therapy , Female , Follow-Up Studies , Humans , Macular Edema/diagnosis , Macular Edema/therapy , Male , Middle Aged , Postoperative Period , Time Factors , Tomography, Optical Coherence , United Kingdom
3.
Surv Ophthalmol ; 62(2): 113-126, 2017.
Article in English | MEDLINE | ID: mdl-27751823

ABSTRACT

Punctate inner choroidopathy (PIC), an idiopathic inflammatory multifocal chorioretinopathy that predominantly affects young myopic women, appears to be relatively rare, but there are limited data to support accurate estimates of prevalence, and it is likely that the condition is underdiagnosed. The etiological relationship between PIC and other conditions within the "white dot syndromes" group remains uncertain. We, like others, would suggest that PIC and multifocal choroiditis with panuveitis represent a single disease process that is modified by host factors (including host immunoregulation) to cause the range of clinical phenotypes seen. The impact of PIC on the patient is highly variable, with outcome ranging from complete spontaneous recovery to bilateral severe sight loss. Detection and monitoring have been greatly facilitated by modern scanning techniques, especially optical coherence tomography and autofluorescence imaging and may be enhanced by coregistration of sequential images to detect change over time. Depending on the course of disease and nature of complications, appropriate treatment may range from observation to systemic immunosuppression and antiangiogenic therapies. PIC is a challenging condition where treatment has to be tailored to the patient's individual circumstances, the extent of disease, and the risk of progression.


Subject(s)
Choroid/diagnostic imaging , Choroiditis/diagnosis , Fluorescein Angiography/methods , Tomography, Optical Coherence/methods , Diagnosis, Differential , Fundus Oculi , Humans , Multifocal Choroiditis , Visual Acuity
4.
Ophthalmology ; 123(6): 1252-6, 2016 06.
Article in English | MEDLINE | ID: mdl-26996340

ABSTRACT

PURPOSE: To investigate if previous intravitreal therapy is a predictor of posterior capsule rupture (PCR) during cataract surgery. DESIGN: Multicenter, national electronic medical record (EMR) database study with univariate and multivariate regression modeling. PARTICIPANTS: A total of 65 836 eyes of 44 635 patients undergoing cataract surgery. METHODS: Anonymized data were extracted for eyes undergoing cataract surgery from 20 hospitals using the same EMR for cases performed between 2004 and 2014. Variables included as possible risk indicators for PCR were age, sex, number of previous intravitreal injections, indication for intravitreal therapy, grade of healthcare professional administering intravitreal therapy, advanced cataract, and cataract surgeon grade. MAIN OUTCOME MEASURES: Presence or absence of posterior capsular rupture during cataract surgery. RESULTS: Data were available on 65 836 cataract operations, of which 1935 had undergone previous intravitreal therapy (2.9%). In univariate regression analyses, patient age, advanced cataract, junior cataract surgeon grade, and number of previous intravitreal injections were significant predictors of PCR. By considering the number of previous intravitreal injections as a continuous variable, the odds ratio for PCR per intravitreal injection was 1.04 (P = 0.016) after adjusting for age, advanced cataract, and cataract surgeon grade. Repeat analysis considering intravitreal injections as a categoric variable showed 10 or more previous injections were associated with a 2.59 times higher likelihood of PCR (P = 0.003) after again adjusting for other significant independent predictors. CONCLUSIONS: Previous intravitreal therapy is associated with a higher likelihood of PCR during cataract surgery. This study provides data to help inform surgeons and patients about the risk of complications when undergoing cataract surgery after multiple prior intravitreal injections. Further investigation is required to determine the cause behind the increased PCR risk.


Subject(s)
Angiogenesis Inhibitors/administration & dosage , Glucocorticoids/administration & dosage , Lens Capsule, Crystalline/injuries , Phacoemulsification/adverse effects , Posterior Capsular Rupture, Ocular/etiology , Vitreous Body/drug effects , Aged , Aged, 80 and over , Electronic Health Records , Female , Humans , Intravitreal Injections , Male , Middle Aged , Multivariate Analysis , Retinal Diseases/drug therapy , Risk Factors , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Visual Acuity
5.
Clin Ophthalmol ; 9: 347-52, 2015.
Article in English | MEDLINE | ID: mdl-25733801

ABSTRACT

PURPOSE: The aim of this study was to determine whether social deprivation is a risk factor for late presentation of patients with proliferative diabetic retinopathy and whether it affects their access to urgent laser treatment. METHODS: Using a 2:1 case: control design, 102 patients referred to a UK teaching hospital as part of the UK Diabetic Retinopathy National Screening Programme were identified for the period between 1 June 2010 to 1 June 2013. Social deprivation was scored using the Index of Multiple Deprivation 2010. Additional variables considered included age, duration of disease, ethnicity, and HbA1c at time of referral. RESULTS: The cases comprised 34 patients referred with proliferative (grade R3) retinopathy with a control group of 68 patients with lower retinopathy grades; two control patients were excluded due to incomplete data. On univariate analysis, R3 retinopathy was associated with higher social deprivation (P<0.001, Mann-Whitney U-test), and with higher HbA1c (11.5% vs 8.4%; P<0.001, Mann-Whitney U-test). Forward stepwise multivariable analysis showed that the association of R3 retinopathy with deprivation was significant even after adjusting for HbA1c (P=0.016). On univariate analysis South Asian ethnicity was also identified as being a risk factor for presentation with R3 retinopathy, but this was no longer significant when HbA1c was adjusted for in a forward stepwise logistic regression analysis. CONCLUSION: In our cohort social deprivation appears to be associated with late presentation of proliferative diabetic retinopathy. Our study supports the need to target these groups to reduce preventable blindness and to identify strategies which overcome barriers to care.

6.
Retina ; 34(11): 2282-9, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25170860

ABSTRACT

PURPOSE: To assess the visual needs of the adult population with Bardet-Biedl syndrome (BBS) and to ensure that this is addressed by a national Bardet-Biedl Service. METHODS: A cross-sectional analysis of all adults under a national BBS Clinic (Birmingham, United Kingdom) was performed using the BBS Ophthalmic Assessment Tool, a novel tool designed to capture the key elements of visual function, impact on lifestyle, and clinical findings relevant to BBS. RESULTS: Sixty-two adult patients were confirmed to have BBS. Bardet-Biedl syndrome mutations were identified in 51, most commonly BBS1 (n = 35), BBS2 (n = 6), and BBS10 (n = 5). In 11 patients (18%), BBS had not been diagnosed until adulthood. Median visual acuity was hand motion (range, 0.0 logMAR-no perception of light). More advanced retinopathy was associated with increasing age, worsening visual acuity, and the presence of nystagmus. Forty patients (65%) had undertaken mainstream education with 29 (47%) achieving higher education; 7 patients (11%) had moderate or severe learning difficulties. Most (90%) were registered sight-impaired or severely sight-impaired patients. CONCLUSION: The BBS Ophthalmic Assessment Tool provides a wide-ranging assessment of ophthalmic status and vision-related needs of the BBS population. This evaluation demonstrates the spectrum of visual disability in this population and its correlation with worsening retinopathy over time.


Subject(s)
Bardet-Biedl Syndrome/physiopathology , Visual Acuity/physiology , Adult , Age Factors , Bardet-Biedl Syndrome/diagnosis , Cross-Sectional Studies , Educational Status , Female , Health Services Needs and Demand , Humans , Life Style , Male , Middle Aged , Needs Assessment , Phenotype , United Kingdom , Young Adult
7.
Br J Ophthalmol ; 98(12): 1625-8, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24997180

ABSTRACT

BACKGROUND/AIMS: Advances in therapy have improved outcomes for patients with neovascular age-related macular degeneration (nAMD). Prompt access to treatment is a priority and may be used as a key performance indicator. In this study, we investigate how social deprivation may impact on access to services, treatment and visual impairment registration. METHODS: Patients were identified retrospectively through the Certificate of Visual Impairment system for the University Hospitals Birmingham Medical Retina service. The Index of Multiple Deprivation (IMD) 2007 score was calculated for each patient. The impact of deprivation, age, gender and ethnicity on key stages in the care pathway was assessed. RESULTS: 120 patients were identified. Patients with greater social deprivation were under-represented, had worse visual acuity at first presentation (correlation of the better-seeing eye with IMD 0.225 (p=0.013)) and had sight-impairment registration earlier (correlation -0.246; p=0.007). Deprivation did not affect time to first appointment, and was not associated with a higher rate of non-attendance. CONCLUSIONS: The late presentation and under-representation of patients with greater social deprivation is a serious concern. Our study strongly suggests that this vulnerable group is encountering barriers in accessing treatment in nAMD, and that these occur prior to entry into the Hospital Eye Service.


Subject(s)
Choroidal Neovascularization/psychology , Health Services Accessibility , Quality of Health Care , Social Isolation/psychology , Wet Macular Degeneration/psychology , Aged , Aged, 80 and over , Female , Humans , Male , Registries , Retrospective Studies , United Kingdom , Visually Impaired Persons/psychology
9.
J Neurol Sci ; 263(1-2): 184-6, 2007 Dec 15.
Article in English | MEDLINE | ID: mdl-17588608

ABSTRACT

Charles Bonnet syndrome is characterised by the occurrence of complex visual hallucinations in the presence of normal cognition in elderly individuals. It commonly happens following conditions where there has been a profound loss of vision or interruption of visual input into the occipital cortex. It is important to distinguish this largely innocuous condition from psychiatric conditions that exist in the same age group. This article describes a rare variant of this condition where such hallucinations occur in the hemianopic visual field of a patient with an occipital infarct whose visual acuity is largely unimpaired. The article details the various conditions where this phenomenon has been experienced; the theories that have been postulated for its aetiology and the treatment options. The variations of this case from the commonly observed scenarios are highlighted questioning previously held convictions as well as providing an insight into the widening spectrum of the phenomenon as more cases are described. The article hopes to raise awareness of this condition, which is much commoner than perceived by healthcare practitioners, as most patients in that age group are reluctant to be forthcoming with their symptoms for fear of being diagnosed with a psychiatric disorder.


Subject(s)
Cerebral Infarction/complications , Cerebral Infarction/pathology , Hallucinations/etiology , Occipital Lobe/pathology , Vision Disorders/etiology , Visual Fields/physiology , Aged , Humans , Magnetic Resonance Imaging/methods , Male
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