4.6 Article

Acanthamoeba keratitis in 194 patients: risk factors for bad outcomes and severe inflammatory complications

期刊

BRITISH JOURNAL OF OPHTHALMOLOGY
卷 102, 期 10, 页码 1431-1435

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/bjophthalmol-2017-310806

关键词

cornea; epidemiology; contact lens; infection; inflammation

资金

  1. Moorfields Eye Hospital Special Trustees Reference MEC [1307A]
  2. National Institute for Health Research (NIHR) Biomedical Research Centre, based at Moorfields Eye Hospital NHS Foundation Trust
  3. UCL Institute of Ophthalmology
  4. NHMRC [APP1036728]
  5. University of NSW Scientia Fellowship

向作者/读者索取更多资源

Background/aims To determine demographic and clinical features of patients with Acanthamoeba keratitis (AK) that are independent risk factors both for bad outcomes and for severe inflammatory complications (SIC). Methods A retrospective audit of medical records of AK cases at Moorfields Eye Hospital from July 2000 to April 2012, including 12 earlier surgical cases. Cases with a bad outcome were defined as those having one or more of the following: corneal perforation, keratoplasty, other surgery (except biopsy), duration of antiamoebic therapy (AAT) >= 10.5 months (the 75th percentile of the whole cohort) and final visual acuity <= 20/80. SICs were defined as having scleritis and/or a stromal ring infiltrate. Multivariable analysis was used to identify independent risk factors for both bad outcomes and SICs. Results Records of 194 eyes (194 patients) were included, having bad outcomes in 93 (48%). Bad outcomes were associated with the presence of SIC, aged >34 years, corticosteroids used before giving AAT and symptom duration >37 days before AAT. The development of SIC was independently associated with aged >34 years, corticosteroids used before giving AAT and herpes simplex virus (HSV) keratitis treatment before AAT. Conclusions The prompt diagnosis of AK, avoidance of a misdiagnosis of HSV keratitis and corticosteroid use before the exclusion of AK as a potential cause of keratitis are essential to the provision of a good outcome for patients and for the avoidance of SIC. Older age is an unmodifiable risk factor that may reflect differences in the immune response to AK in this patient subset.

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