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20至64岁人群的常规眼部检查:一项基于证据的分析。

Routine eye examinations for persons 20-64 years of age: an evidence-based analysis.

出版信息

Ont Health Technol Assess Ser. 2006;6(15):1-81. Epub 2006 Jul 1.

Abstract

OBJECTIVE

The objective of this analysis was to determine the strength of association between age, gender, ethnicity, family history of disease and refractive error and the risk of developing glaucoma or ARM?

CLINICAL NEED

A routine eye exam serves a primary, secondary, and tertiary care role. In a primary care role, it allows contact with a doctor who can provide advice about eye care, which may reduce the incidence of eye disease and injury. In a secondary care role, it can via a case finding approach, diagnose persons with degenerative eye diseases such as glaucoma and or AMD, and lead to earlier treatment to slow the progression of the disease. Finally in a tertiary care role, it provides ongoing monitoring and treatment to those with diseases associated with vision loss. Glaucoma is a progressive degenerative disease of the optic nerve, which causes gradual loss of peripheral (side) vision, and in advanced disease states loss of central vision. Blindness may results if glaucoma is not diagnosed and managed. The prevalence of primary open angle glaucoma (POAG) ranges from 1.1% to 3.0% in Western populations, and from 4.2% to 8.8% in populations of African descent. It is estimated up to 50% of people with glaucoma are aware that they have the disease. In Canada, glaucoma disease is the second leading cause of blindness in people aged 50 years and older. Tonometry, inspection of the optic disc and perimetry are used concurrently by physicians and optometrists to make the diagnosis of glaucoma. In general, the evidence shows that treating people with increased IOP only, increased IOP and clinical signs of early glaucoma or with normal-tension glaucoma can reduce the progression of disease. Age-related maculopathy (ARM) is a degenerative disease of the macula, which is a part of the retina. Damage to the macula causes loss of central vision affecting the ability to read, recognize faces and to move about freely. ARM can be divided into an early- stage (early ARM) and a late-stage (AMD). AMD is the leading cause of blindness in developed countries. The prevalence of AMD increases with increasing age. It is estimated that 1% of people 55 years of age, 5% aged 75 to 84 years and 15% 80 years of age and older have AMD. ARM can be diagnosed during fundoscopy (ophthalmoscopy) which is a visual inspection of the retina by a physician or optometrist, or from a photograph of the retina. There is no cure or prevention for ARM. Likewise, there is currently no treatment to restore vision lost due to AMD. However, there are treatments to delay the progression of the disease and further loss of vision.

THE TECHNOLOGY

A periodic oculo-visual assessment is defined "as an examination of the eye and vision system rendered primarily to determine if a patient has a simple refractive error (visual acuity assessment) including myopia, hypermetropia, presbyopia, anisometropia or astigmatism." This service includes a history of the presenting complaint, past medical history, visual acuity examination, ocular mobility examination, slit lamp examination of the anterior segment, ophthalmoscopy, and tonometry (measurement of IOP) and is completed by either a physician or an optometrist.

REVIEW STRATEGY

THE MEDICAL ADVISORY SECRETARIAT CONDUCTED A COMPUTERIZED SEARCH OF THE LITERATURE IN THE FOLLOWING DATABASES: OVID MEDLINE, MEDLINE, In-Process & Other Non-Indexed Citations, EMBASE, INAHTA and the Cochrane Library. The search was limited to English-language articles with human subjects, published from January 2000 to March 2006. In addition, a search was conducted for published guidelines, health technology assessments, and policy decisions. Bibliographies of references of relevant papers were searched for additional references that may have been missed in the computerized database search. Studies including participants 20 years and older, population-based prospective cohort studies, population-based cross-sectional studies when prospective cohort studies were unavailable or insufficient and studies determining and reporting the strength of association or risk- specific prevalence or incidence rates of either age, gender, ethnicity, refractive error or family history of disease and the risk of developing glaucoma or AMD were included in the review. The Grading of Recommendations Assessment, Development and Evaluation (GRADE) system was used to summarize the overall quality of the body of evidence.

SUMMARY OF FINDINGS

A total of 498 citations for the period January 2000 through February 2006 were retrieved and an additional 313 were identified when the search was expanded to include articles published between 1990 and 1999. An additional 6 articles were obtained from bibliographies of relevant articles. Of these, 36 articles were retrieved for further evaluation. Upon review, 1 meta-analysis and 15 population-based epidemiological studies were accepted for this review PRIMARY OPEN ANGLE GLAUCOMA: Age Six cross-sectional studies and 1 prospective cohort study contributed data on the association between age and PAOG. From the data it can be concluded that the prevalence and 4-year incidence of POAG increases with increasing age. The odds of having POAG are statistically significantly greater for people 50 years of age and older relative to those 40 to 49 years of age. There is an estimated 7% per year incremental odds of having POAG in persons 40 years of age and older, and 10% per year in persons 49 years of age and older. POAG is undiagnosed in up to 50% of the population. The quality of the evidence is moderate. Gender Five cross-sectional studies evaluated the association between gender and POAG. Consistency in estimates is lacking among studies and because of this the association between gender and prevalent POAG is inconclusive. The quality of the evidence is very low. Ethnicity Only 1 cross-sectional study compared the prevalence rates of POAG between black and white participants. These data suggest that prevalent glaucoma is statistically significantly greater in a black population 50 years of age and older compared with a white population of similar age. There is an overall 4-fold increase in prevalent POAG in a black population compared with a white population. This increase may be due to a confounding variable not accounted for in the analysis. The quality of the evidence is low. Refractive Error Four cross-sectional studies assessed the association of myopia and POAG. These data suggest an association between myopia defined as a spherical equivalent of -1.00D or worse and prevalent POAG. However, there is inconsistency in results regarding the statistical significance of the association between myopia when defined as a spherical equivalent of -0.5D. The quality of the evidence is very low. Family History of POAG Three cross-sectional studies investigated the association between family history of glaucoma and prevalent POAG. These data suggest a 2.5 to 3.0 fold increase in the odds having POAG in persons with a family history (any first-degree relative) of POAG. The quality of the evidence is moderate. AGE-RELATED MACULOPATHY: Age Four cohort studies evaluated the association between age and early ARM and AMD. After 55 years of age, the incidence of both early ARM and AMD increases with increasing age. Progression to AMD occurs in up to 12% of persons with early ARM. The quality of the evidence is low Gender Four cohort studies evaluated the association between gender and early ARM and AMD. Gender differences in incident early ARM and incident AMD are not supported from these data. The quality of the evidence is lows. Ethnicity One meta-analysis and 2 cross-sectional studies reported the ethnic-specific prevalence rates of ARM. The data suggests that the prevalence of early ARM is higher in a white population compared with a black population. The data suggest that the ethnic-specific differences in the prevalence of AMD remain inconclusive. Refractive Error Two cohort studies investigated the association between refractive error and the development of incident early ARM and AMD. The quality of the evidence is very low. Family History Two cross-sectional studies evaluated the association of family history and early ARM and AMD. Data from one study supports an association between a positive family history of AMD and having AMD. The results of the study indicate an almost 4-fold increase in the odds of any AMD in a person with a family history of AMD. The quality of the evidence, as based on the GRADE criteria is moderate.

ECONOMIC ANALYSIS

The prevalence of glaucoma is estimated at 1 to 3% for a Caucasian population and 4.2 to 8.8% for a black population. The incidence of glaucoma is estimated at 0.5 to 2.5% per year in the literature. The percentage of people who go blind per year as a result of glaucoma is approximately 0.55%. The total population of Ontarians aged 50 to 64 years is estimated at 2.6 million based on the April 2006 Ontario Ministry of Finance population estimates. The range of utilization for a major eye examination in 2006/07 for this age group is estimated at 567,690 to 669,125, were coverage for major eye exams extended to this age group. This would represent a net increase in utilization of approximately 440,116 to 541,551. The percentage of Ontario population categorized as black and/or those with a family history of glaucoma was approximately 20%. Therefore, the estimated range of utilization for a major eye examination in 2006/07 for this sub-population is estimated at 113,538 - 138,727 (20% of the estimated range of utilization in total population of 50-64 year olds in Ontario), were coverage for major eye exams extended to this sub-group. This would represent a net increase in utilization of approximately 88,023 to 108,310 within this sub-group.

COSTS

The total cost of a major eye examination by a physician is $42. (ABSTRACT TRUNCATED)

摘要

目的

本分析的目的是确定年龄、性别、种族、疾病家族史和屈光不正与患青光眼或年龄相关性黄斑变性(ARM)风险之间的关联强度。

临床需求

常规眼科检查具有一级、二级和三级护理作用。作为一级护理,它能让患者接触到可以提供眼部护理建议的医生,这可能会降低眼部疾病和损伤的发生率。作为二级护理,它可以通过病例发现方法,诊断患有青光眼和/或年龄相关性黄斑变性等退行性眼病的患者,并促使早期治疗以减缓疾病进展。最后作为三级护理,它为那些患有与视力丧失相关疾病的患者提供持续监测和治疗。青光眼是一种视神经的进行性退行性疾病,会导致周边(侧面)视力逐渐丧失,在疾病晚期会导致中心视力丧失。如果青光眼未得到诊断和治疗,可能会导致失明。原发性开角型青光眼(POAG)在西方人群中的患病率为1.1%至3.0%,在非洲裔人群中为4.2%至8.8%。据估计,高达50%的青光眼患者知道自己患有该病。在加拿大,青光眼是50岁及以上人群失明的第二大主要原因。医生和验光师同时使用眼压测量、视盘检查和视野检查来诊断青光眼。一般来说,证据表明仅治疗眼压升高的患者、眼压升高且有早期青光眼临床体征的患者或正常眼压性青光眼患者,可以减缓疾病进展。年龄相关性黄斑病变(ARM)是黄斑的一种退行性疾病,黄斑是视网膜的一部分。黄斑受损会导致中心视力丧失,影响阅读、识别面部和自由活动的能力。ARM可分为早期(早期ARM)和晚期(年龄相关性黄斑变性,AMD)。AMD是发达国家失明的主要原因。AMD的患病率随年龄增长而增加。据估计,55岁人群中有1%、75至84岁人群中有5%以及80岁及以上人群中有15%患有AMD。ARM可在眼底镜检查(检眼镜检查)期间由医生或验光师对视网膜进行目视检查时诊断,也可从视网膜照片中诊断。目前尚无治愈或预防ARM的方法。同样,目前也没有治疗方法可以恢复因AMD而丧失的视力。然而,有一些治疗方法可以延缓疾病进展和进一步的视力丧失。

技术

定期眼视觉评估被定义为“主要为确定患者是否有单纯屈光不正(视力评估),包括近视、远视、老花眼、屈光参差或散光而对眼睛和视觉系统进行的检查”。这项服务包括现病史、既往病史、视力检查、眼球运动检查、前段裂隙灯检查、检眼镜检查和眼压测量(眼压测量),由医生或验光师完成。

综述策略

医学咨询秘书处对以下数据库进行了计算机文献检索:OVID MEDLINE、MEDLINE、在研及其他未索引引文、EMBASE、INAHTA和Cochrane图书馆。检索限于2000年1月至2006年3月发表的涉及人类受试者的英文文章。此外,还检索了已发表的指南、卫生技术评估和政策决策。对相关论文参考文献的书目进行了搜索,以查找在计算机数据库搜索中可能遗漏的其他参考文献。纳入综述的研究包括20岁及以上的参与者、基于人群的前瞻性队列研究、在前瞻性队列研究不可用或不足时基于人群的横断面研究,以及确定并报告年龄、性别、种族、屈光不正或疾病家族史与患青光眼或AMD风险之间关联强度或风险特异性患病率或发病率的研究。使用推荐分级评估、制定和评价(GRADE)系统来总结证据总体质量。

研究结果总结

检索到2000年1月至2006年2月期间的498篇引文,当搜索范围扩大到包括1990年至1999年发表的文章时,又识别出313篇。从相关文章的参考文献中又获得6篇文章。其中,36篇文章被检索出来进行进一步评估。经审查,1篇荟萃分析和15项基于人群的流行病学研究被纳入本综述。原发性开角型青光眼:年龄 六项横断面研究和一项前瞻性队列研究提供了关于年龄与POAG之间关联的数据。从这些数据可以得出结论,POAG的患病率和4年发病率随年龄增长而增加。50岁及以上人群患POAG的几率相对于40至49岁人群在统计学上显著更高。估计40岁及以上人群每年患POAG的几率增加7%,49岁及以上人群每年增加10%。高达50%的POAG患者未被诊断出来。证据质量为中等。性别 五项横断面研究评估了性别与POAG之间的关联。各研究之间的估计缺乏一致性,因此性别与POAG患病率之间的关联尚无定论。证据质量非常低。种族 仅有一项横断面研究比较了黑人和白人参与者中POAG的患病率。这些数据表明,50岁及以上的黑人人群中青光眼患病率在统计学上显著高于同年龄的白人人群。黑人人群中POAG的患病率总体比白人人群高4倍。这种增加可能是由于分析中未考虑的混杂变量导致的。证据质量低。屈光不正 四项横断面研究评估了近视与POAG的关联。这些数据表明,等效球镜度数为-1.00D或更差的近视与POAG患病率之间存在关联。然而,对于等效球镜度数为-0.5D时近视与POAG关联的统计学显著性,结果存在不一致性。证据质量非常低。POAG家族史 三项横断面研究调查了青光眼家族史与POAG患病率之间的关联。这些数据表明,有POAG家族史(任何一级亲属)的人患POAG的几率增加2.5至3.0倍。证据质量为中等。年龄相关性黄斑病变:年龄 四项队列研究评估了年龄与早期ARM和AMD之间的关联。55岁以后,早期ARM和AMD的发病率均随年龄增长而增加。高达12%的早期ARM患者会进展为AMD。证据质量低。性别 四项队列研究评估了性别与早期ARM和AMD之间的关联。这些数据不支持早期ARM和AMD发病存在性别差异。证据质量低。种族 一项荟萃分析和两项横断面研究报告了特定种族的ARM患病率。数据表明,白人人群中早期ARM的患病率高于黑人人群。关于AMD患病率的种族特异性差异的数据尚无定论。屈光不正 两项队列研究调查了屈光不正与早期ARM和AMD发病之间的关联。证据质量非常低。家族史 两项横断面研究评估了家族史与早期ARM和AMD之间的关联。一项研究的数据支持AMD家族史阳性与患AMD之间存在关联。该研究结果表明,有AMD家族史的人患任何AMD的几率几乎增加4倍。根据GRADE标准,证据质量为中等。

经济分析

据估计,白种人群中青光眼的患病率为1%至3%,黑种人群中为4.2%至8.8%。文献中估计青光眼的发病率为每年0.5%至2.5%。每年因青光眼失明的人数比例约为0.55%。根据2006年4月安大略省财政部的人口估计,50至64岁的安大略省总人口估计为260万。如果将主要眼科检查的覆盖范围扩大到该年龄组,2006/07年度该年龄组主要眼科检查的使用范围估计为567,690至669,125人次。这将代表使用量净增加约440,116至541,551人次。被归类为黑人或有青光眼家族史的安大略省人口比例约为20%。因此,如果将主要眼科检查的覆盖范围扩大到该亚组,2006/07年度该亚组主要眼科检查的使用范围估计为113,538 - 138,727人次(安大略省50 - 64岁总人口估计使用范围的20%)。这将代表该亚组内使用量净增加约88,023至108,310人次。

成本

医生进行一次主要眼科检查的总成本为42美元。(摘要截断)

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本文引用的文献

1
Ranibizumab versus verteporfin for neovascular age-related macular degeneration.
N Engl J Med. 2006 Oct 5;355(14):1432-44. doi: 10.1056/NEJMoa062655.
2
Ranibizumab for neovascular age-related macular degeneration.
N Engl J Med. 2006 Oct 5;355(14):1419-31. doi: 10.1056/NEJMoa054481.
3
The price of sight--ranibizumab, bevacizumab, and the treatment of macular degeneration.
N Engl J Med. 2006 Oct 5;355(14):1409-12. doi: 10.1056/NEJMp068185.
4
JAMA patient page. Age-related macular degeneration.
JAMA. 2006 May 24;295(20):2438. doi: 10.1001/jama.295.20.2438.
5
A 76-year-old man with macular degeneration.
JAMA. 2006 May 24;295(20):2394-406. doi: 10.1001/jama.295.20.2394.
7
Prevalence of open-angle glaucoma in a rural south Indian population.
Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4461-7. doi: 10.1167/iovs.04-1529.
8
Nine-year incidence of age-related macular degeneration in the Barbados Eye Studies.
Ophthalmology. 2006 Jan;113(1):29-35. doi: 10.1016/j.ophtha.2005.08.012. Epub 2005 Nov 10.
9
Photodynamic therapy for neovascular age-related macular degeneration.
Cochrane Database Syst Rev. 2005 Oct 19(4):CD002030. doi: 10.1002/14651858.CD002030.pub2.
10
Screening for glaucoma: recommendation statement.
Ann Fam Med. 2005 Mar-Apr;3(2):171-2. doi: 10.1370/afm.294.

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