The North East, North Central London and Essex Health Innovation & Education Cluster.
BMJ Open. 2013 Jul 21;3(7). doi: 10.1136/bmjopen-2013-002715. Print 2013.
A comparison of glaucoma referral refinement schemes (GRRS) in the UK during a time period of considerable change in national policy and guidance.
Retrospective multisite review.
The outcomes of clinical examinations by optometrists with a specialist interest in glaucoma (OSIs) were compared with optometrists with no specialist interest in glaucoma (non-OSIs). Data from Huntingdon and Nottingham assessed non-OSI findings, while Manchester and Gloucestershire reviewed OSI findings.
1086 patients. 434 patients were from Huntingdon, 179 from Manchester, 204 from Gloucestershire and 269 from Nottingham.
The first-visit discharge rate (FVDR) for all time periods for OSIs was 14.1% compared with 36.1% from non-OSIs (difference 22%, CI 16.9% to 26.7%; p<0.001). The FVDR increased after the April 2009 National Institute for Health and Clinical Excellence (NICE) glaucoma guidelines compared with pre-NICE, which was particularly evident when pre-NICE was compared with the current practice time period (OSIs 6.2-17.2%, difference 11%, CI -24.7% to 4.3%; p=0.18, non-OSIs 29.2-43.9%, difference 14.7%, CI -27.8% to -0.30%; p=0.03). Elevated intraocular pressure (IOP) was the commonest reason for referral for OSIs and non-OSIs, 28.7% and 36.1%, respectively, of total referrals. The proportion of referrals for elevated IOP increased from 10.9% pre-NICE to 28.0% post-NICE for OSIs, and from 19% to 45.1% for non-OSIs.
In terms of 'demand management', OSIs can reduce FVDR of patients reviewed in secondary care; however, in terms of 'patient safety' this study also shows that overemphasis on IOP as a criterion for referral is having an adverse effect on both the non-OSIs and indeed the OSIs ability to detect glaucomatous optic nerve features. It is recommended that referral letters from non-OSIs be stratified for risk, directing high-risk patients straight to secondary care, and low-risk patients to OSIs.
在国家政策和指导发生重大变化的时期,比较英国的青光眼转诊细化方案(GRRS)。
回顾性多地点研究。
具有青光眼专业兴趣的验光师(OSI)进行的临床检查结果与没有青光眼专业兴趣的验光师(非 OSI)进行了比较。亨廷顿和诺丁汉的数据评估了非 OSI 的发现,而曼彻斯特和格洛斯特郡则评估了 OSI 的发现。
1086 名患者。434 名患者来自亨廷顿,179 名来自曼彻斯特,204 名来自格洛斯特郡,269 名来自诺丁汉。
所有时间段 OSI 的首次就诊出院率(FVDR)为 14.1%,而非 OSI 为 36.1%(差异 22%,CI 16.9%至 26.7%;p<0.001)。与 NICE 青光眼指南发布前的情况相比,2009 年 4 月国家健康与临床卓越研究所(NICE)发布指南后,FVDR 增加,尤其是在将 NICE 前与当前实践时间段进行比较时更为明显(OSI 为 6.2%至 17.2%,差异 11%,CI-24.7%至 4.3%;p=0.18,非 OSI 为 29.2%至 43.9%,差异 14.7%,CI-27.8%至-0.30%;p=0.03)。升高的眼内压(IOP)是 OSI 和非 OSI 转诊的最常见原因,分别占总转诊的 28.7%和 36.1%。NICE 前,OSI 因升高的 IOP 而转诊的比例从 10.9%上升至 NICE 后的 28.0%,而非 OSI 的比例从 19%上升至 45.1%。
就“需求管理”而言,OSI 可以降低二级保健中接受检查的患者的 FVDR;然而,就“患者安全”而言,本研究还表明,过分强调 IOP 作为转诊标准,对非 OSI 乃至 OSI 检测青光眼视神经特征的能力都产生了不利影响。建议对非 OSI 的转诊信进行风险分层,将高危患者直接转诊至二级保健,将低危患者转诊至 OSI。