Literature DB >> 23060022

Post-intravitreal anti-VEGF endophthalmitis in the United Kingdom: incidence, features, risk factors, and outcomes.

D A M Lyall1, A Tey, B Foot, S T D Roxburgh, M Virdi, C Robertson, C J MacEwen.   

Abstract

PURPOSE: To describe the incidence, features, management, and risk factors of post-intravitreal anti-VEGF endophthalmitis (PIAE) in patients undergoing treatment for exudative age-related macular degeneration in the United Kingdom.
METHODS: Prospective observational case control study. Forty-seven cases of PIAE were identified through the British Ophthalmological Surveillance Unit from January 2009 to March 2010. Data collected at diagnosis and at 6 months follow-up included patient demographics, intravitreal injection details, pre- and post-injection management, visual acuity, clinical features and management of PIAE, causative organisms, and clinical outcomes. Details were compared with 200 control cases from 10 control centres to identify potential risk factors.
RESULTS: Estimated PIAE was 0.025%. Culture-positive PIAE incidence was 0.015%. Mean age of presentation was 78 years. Mean number of intravitreal injections before PIAE was 5. Mean days to presentation was 5 (range 1-39). Positive microbiology culture was found in 59.6%. The majority of causative organisms were Gram positive (92.8%). Significant risk factors were failure to administer topical antibiotics immediately after the injection (P=0.001), blepharitis (P=0.006), subconjunctival anaesthesia (P=0.021), patient squeezing during the injection (P=0.021), and failure to administer topical antibiotics before anti-VEGF injection (P=0.05). DISCUSSION: The incidence of PIAE in the United Kingdom is comparable to other studies at a rate of 0.025%. The most common causative organisms were Gram positive. Measures to minimise the risk of PIAE include treatment of blepharitis before injection, avoidance of subconjunctival anaesthesia, topical antibiotic administration immediately after injection with consideration to administering topical antibiotics before injection.

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Year:  2012        PMID: 23060022      PMCID: PMC3522835          DOI: 10.1038/eye.2012.199

Source DB:  PubMed          Journal:  Eye (Lond)        ISSN: 0950-222X            Impact factor:   3.775


  45 in total

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2.  Ranibizumab versus verteporfin for neovascular age-related macular degeneration.

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3.  Ranibizumab for neovascular age-related macular degeneration.

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4.  Toxic anterior segment syndrome and possible association with ointment in the anterior chamber following cataract surgery.

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5.  Prevalence of age-related maculopathy in older Europeans: the European Eye Study (EUREYE).

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6.  Endophthalmitis after cataract surgery: a nationwide prospective study evaluating incidence in relation to incision type and location.

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  45 in total

1.  Predictive factors for recurrence of macular edema after successful intravitreal bevacizumab therapy in branch retinal vein occlusion.

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2.  Reply to Alexander et al (Subconjunctival anaesthesia for intravitreal injections).

Authors:  D A M Lyall; A Tey; B Foot; S T D Roxburgh; M Virdi; C Robertson; C J MacEwen
Journal:  Eye (Lond)       Date:  2013-06-28       Impact factor: 3.775

3.  Subconjunctival anaesthesia for intravitreal injections.

Authors:  P Alexander; D Sahu; A J Lotery
Journal:  Eye (Lond)       Date:  2013-06-28       Impact factor: 3.775

4.  Reply to Bhavsar et al.

Authors:  D A M Lyall; A Tey; B Foot; S T D Roxburgh; M Virdi; C Robertson; C J MacEwen
Journal:  Eye (Lond)       Date:  2013-10-18       Impact factor: 3.775

5.  Intravitreal injections, antibiotics and endophthalmitis.

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Journal:  Eye (Lond)       Date:  2013-10-18       Impact factor: 3.775

6.  Predictors of Endophthalmitis after Intravitreal Injection: A Multivariable Analysis Based on Injection Protocol and Povidone Iodine Strength.

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7.  Culture-Proven Endophthalmitis After Intravitreal Injection: A 10-Year Analysis.

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10.  Endophthalmitis Associated with Intravitreal Anti-Vascular Endothelial Growth Factor Injections.

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Journal:  Curr Ophthalmol Rep       Date:  2014-03-01
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