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Clinical effectiveness of the Manchester Glaucoma Enhanced Referral Scheme

机译:曼彻斯特青光眼增强转诊计划的临床效果

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Background Glaucoma referral filtering schemes have operated in the UK for many years. However, there is a paucity of data on the false-negative (FN) rate. This study evaluated the clinical effectiveness of the Manchester Glaucoma Enhanced Referral Scheme (GERS), estimating both the false-positive (FP) and FN rates. Method Outcome data were collected for patients newly referred through GERS and assessed in 'usual-care' clinics to determine the FP rate (referred patients subsequently discharged at their first visit). For the FN rate, glaucoma suspects deemed not requiring referral following GERS assessment were invited to attend for a 'reference standard' examination including all elements of assessment recommended by National Institute for Health and Care Excellence (NICE) by a glaucoma specialist optometrist. A separate 33 cases comprising randomly selected referred and non-referred cases were reviewed independently by two glaucoma specialist consultant ophthalmologists to validate the reference standard assessment. Results 1404 patients were evaluated in GERS during the study period; 651 (46.3%) were referred to the Hospital Eye Service (HES) and 753 (53.6%) were discharged. The FP rate in 307 assessable patients referred to the HES was 15.5%. This study reviewed 131 (17.4%) of those patients not referred to the HES through the GERS scheme; 117 (89.3%) were confirmed as not requiring hospital follow-up; 14 (10.7%) required follow-up, including 5 (3.8%) offered treatment. Only one patient (0.8%) in this sample met the GERS referral criteria and was not referred (true FN). There were no cases of missed glaucoma or non-glaucomatous pathology identified within our sample. Conclusion The Manchester GERS is an effective glaucoma filtering scheme with a low FP and FN rate.
机译:背景技术青光眼推荐过滤方案多年来在英国运营。但是,假阴性(FN)速率存在缺乏数据。本研究评估了曼彻斯特青光眼增强型转诊计划(GERS)的临床效果,估计假阳性(FP)和FN率。对新闻组织的患者收集了方法结果数据,并在“通常保理”诊所评估以确定FP率(提到患者随后在第一次访问时出院)。对于FN率,被邀请被视为GERS评估后不需要转介的青光眼嫌疑人参加“参考标准”审查,包括国家健康和护理学院(漂亮的卓越奖项所建议的评估内容(漂亮)的全部评估。通过两个青光眼专科顾问眼科医生独立审查包括随机选择的提到和未提到的病例的单独33例,以验证参考标准评估。结果在研究期间在GERS中评估了1404名患者; 651(46.3%)被提交给医院的眼睛服务(HES),753(53.6%)排出。 307名评估患者的FP率为11患者为15.5%。本研究通过GERS计划审查了131名(17.4%)的患者,这些患者没有提到他; 117(89.3%)确认不需要医院的随访; 14(10.7%)所需随访,包括5(3.8%)提供的治疗。该样本中只有一个患者(0.8%)达到GERS推荐标准,并未参考(真实FN)。在我们的样本中没有发现错过的青光眼或非青光瘤病理学的病例。结论曼彻斯特GER是一种有效的青光眼滤波方案,具有低FP和FN率。

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  • 来源
    《British journal of ophthalmology》 |2019年第8期|共6页
  • 作者单位

    Manchester Univ NHS Fdn Trust Manchester Manchester Royal Eye Hosp Manchester M13 9WL Lancs;

    Manchester Univ NHS Fdn Trust Manchester Manchester Royal Eye Hosp Manchester M13 9WL Lancs;

    Univ London Ctr Appl Vis Res Div Optometry &

    Visual Sci London England;

    Univ London Ctr Appl Vis Res Div Optometry &

    Visual Sci London England;

    Univ London Ctr Appl Vis Res Div Optometry &

    Visual Sci London England;

    Univ Manchester Sch Hlth Sci Ctr Biostat Manchester Lancs England;

    Manchester Univ NHS Fdn Trust Manchester Manchester Royal Eye Hosp Manchester M13 9WL Lancs;

    Manchester Univ NHS Fdn Trust Manchester Manchester Royal Eye Hosp Manchester M13 9WL Lancs;

    Manchester Univ NHS Fdn Trust Manchester Manchester Royal Eye Hosp Manchester M13 9WL Lancs;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 眼科学;
  • 关键词

    glaucoma;

    机译:青光眼;

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