Streamlined Ophthalmologist-Led Pathway to Diagnosis and Accessibility of Genetics Testing for Patients with Inherited Retinal Dystrophies in Canada

IF 4.4 Q1 OPHTHALMOLOGY Ophthalmology. Retina Pub Date : 2025-02-01 DOI:10.1016/j.oret.2024.08.007
Grace S. Yin MD, MPhil , Zhuo Shao MDCM, PhD , Hanna Faghfoury MDCM, FRCPC , Brian G. Ballios MD, PhD
{"title":"Streamlined Ophthalmologist-Led Pathway to Diagnosis and Accessibility of Genetics Testing for Patients with Inherited Retinal Dystrophies in Canada","authors":"Grace S. Yin MD, MPhil ,&nbsp;Zhuo Shao MDCM, PhD ,&nbsp;Hanna Faghfoury MDCM, FRCPC ,&nbsp;Brian G. Ballios MD, PhD","doi":"10.1016/j.oret.2024.08.007","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>To investigate the ability of a new clinical model to improve accessibility and expedite the pathway to molecular diagnosis for patients with suspected inherited retinal diseases (IRDs).</div></div><div><h3>Design</h3><div>Retrospective cohort study of electronic patient records.</div></div><div><h3>Participants</h3><div>All patients referred to general medical genetic clinic between September 2017 and September 2019 and an ophthalmologist-led IRD clinic between October 2021 and July 2023 for suspected IRD were included.</div></div><div><h3>Methods</h3><div>The difference in timeliness and accessibility to diagnosis and genetics testing for patients referred for suspected IRDs were compared based on whether they were referred to a general medical genetics clinic or an ophthalmologist-led IRD clinic.</div></div><div><h3>Main Outcome Measures</h3><div>The primary outcomes were time to consult from referral; time from initial consult to molecular diagnosis; and the time from initial consult to genetics result disclosure and counseling. Secondary outcomes included number of prior providers investigating the chief complaint, the proportion of patients undergoing genetics testing, and the range of diagnostic investigations undertaken.</div></div><div><h3>Results</h3><div>Four hundred seventy-three patients were included, with 212 cases from a general medical genetics clinic and 261 from a medical retina clinic. The mean time from referral to initial consult was 14 months (±3.33 months) and 4 months (±3.4 months) for the general medical genetics and the ophthalmologist-led IRD clinics, respectively. The mean time from initial consult to genetics disclosure and counseling was 6 months (±3.6 months) and 3.5 months (±1.8 months) for the medical genetics and the ophthalmologist-led models, respectively. The total time from initial referral to genetics disclosure and counseling for the medical geneticist-led clinic model was 20 to 24 months. The total time from initial referral to genetics disclosure and counseling for the ophthalmologist-led retinal clinic was 5 to 8 months. The average number of prior providers seen before presenting to the ophthalmologist-led retina clinic was 2.05 (range, 1–10).</div></div><div><h3>Conclusions</h3><div>Shifting from the traditional medical genetics model to the new ophthalmologist-led IRD clinical model may improve accessibility and expedite the pathway to molecular diagnosis and subsequent gene therapy trials for patients with suspected IRDs.</div></div><div><h3>Financial Disclosure(s)</h3><div>Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.</div></div>","PeriodicalId":19501,"journal":{"name":"Ophthalmology. Retina","volume":"9 2","pages":"Pages 180-186"},"PeriodicalIF":4.4000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ophthalmology. Retina","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468653024003671","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective

To investigate the ability of a new clinical model to improve accessibility and expedite the pathway to molecular diagnosis for patients with suspected inherited retinal diseases (IRDs).

Design

Retrospective cohort study of electronic patient records.

Participants

All patients referred to general medical genetic clinic between September 2017 and September 2019 and an ophthalmologist-led IRD clinic between October 2021 and July 2023 for suspected IRD were included.

Methods

The difference in timeliness and accessibility to diagnosis and genetics testing for patients referred for suspected IRDs were compared based on whether they were referred to a general medical genetics clinic or an ophthalmologist-led IRD clinic.

Main Outcome Measures

The primary outcomes were time to consult from referral; time from initial consult to molecular diagnosis; and the time from initial consult to genetics result disclosure and counseling. Secondary outcomes included number of prior providers investigating the chief complaint, the proportion of patients undergoing genetics testing, and the range of diagnostic investigations undertaken.

Results

Four hundred seventy-three patients were included, with 212 cases from a general medical genetics clinic and 261 from a medical retina clinic. The mean time from referral to initial consult was 14 months (±3.33 months) and 4 months (±3.4 months) for the general medical genetics and the ophthalmologist-led IRD clinics, respectively. The mean time from initial consult to genetics disclosure and counseling was 6 months (±3.6 months) and 3.5 months (±1.8 months) for the medical genetics and the ophthalmologist-led models, respectively. The total time from initial referral to genetics disclosure and counseling for the medical geneticist-led clinic model was 20 to 24 months. The total time from initial referral to genetics disclosure and counseling for the ophthalmologist-led retinal clinic was 5 to 8 months. The average number of prior providers seen before presenting to the ophthalmologist-led retina clinic was 2.05 (range, 1–10).

Conclusions

Shifting from the traditional medical genetics model to the new ophthalmologist-led IRD clinical model may improve accessibility and expedite the pathway to molecular diagnosis and subsequent gene therapy trials for patients with suspected IRDs.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
在加拿大,简化眼科医生主导的诊断途径,为遗传性视网膜营养不良症患者提供遗传学检测。
目的研究一种新的临床模式能否提高疑似遗传性视网膜疾病(IRD)患者的可及性并加快分子诊断的进程:对电子病历进行回顾性队列研究:纳入2017年9月至2019年9月期间转诊至普通医学遗传诊所和2021年10月至2023年7月期间转诊至眼科医生主导的IRD诊所的所有疑似IRD患者:比较疑似IRD患者转诊至普通医学遗传学门诊还是眼科医生主导的IRD门诊在诊断和遗传学检测的及时性和可及性方面的差异:主要结果包括:从转诊到就诊的时间;从初次就诊到分子诊断的时间;以及从初次就诊到遗传学结果披露和咨询的时间。次要结果包括调查主诉的先前医疗服务提供者的数量、接受遗传学检测的患者比例以及所做诊断检查的范围:共纳入 473 名患者,其中 212 例来自普通医学遗传学诊所,261 例来自医学视网膜诊所。普通医学遗传学门诊和眼科医生主导的IRD门诊从转诊到初次就诊的平均时间分别为14个月(±3.33个月)和4个月(±3.4个月)。医学遗传学模式和眼科医生主导的IRD模式从初次咨询到遗传学信息披露和咨询的平均时间分别为6个月(±3.6个月)和3.5个月(±1.8个月)。医学遗传学专家主导的诊所模式从初次转诊到遗传学信息披露和咨询的总时间为20-24个月。眼科医生主导的视网膜诊所从初次转诊到遗传学信息披露和咨询的总时间为 5-8 个月。在到眼科医生主导的视网膜诊所就诊之前,曾就诊过的医疗服务提供者的平均人数为 2.05 人(范围为 1-10 人):结论:从传统的医学遗传学模式转变为眼科医生主导的新型 IRD 临床模式,可提高疑似 IRD 患者的可及性,加快分子诊断和后续基因治疗试验的进程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Ophthalmology. Retina
Ophthalmology. Retina Medicine-Ophthalmology
CiteScore
7.80
自引率
6.70%
发文量
274
审稿时长
33 days
期刊最新文献
Spontaneous Remodeling of Abnormal Choroidal Vasculature. Re: Cai et al.: Similar risk of kidney failure among patients with blinding diseases who receive ranibizumab, aflibercept, and bevacizumab: an observational health data sciences and informatics network study (Ophthalmol Retina. 2024;8:733-743.). Reply. Extensive Myelinated Nerve Fibers in a Case of Straatsma Syndrome. Intravitreal Silicone Oil Bubbles after Perforating Needlestick Open-Globe Injury.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1