Simonelli Francesca, Sodi Andrea, Falsini Benedetto, Bacci Giacomo, Iarossi Giancarlo, Di Iorio Valentina, Giorgio Dario, Placidi Giorgio, Andrao Assia, Reale Luigi, Fiorencis Alessandra, Aoun Manar
Eye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, University of Campania "L. Vanvitelli", Naples, Italy.
Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy.
Clin Ophthalmol. 2021 Dec 2;15:4591-4605. doi: 10.2147/OPTH.S331218. eCollection 2021.
Timely detection and multidisciplinary management of -related inherited retinal disorders (IRDs) can significantly improve both disease management and patient care. Thus, this Narrative Medicine (NM) project aimed to investigate the evolution of the care pathway and the expectations on genetic counseling and gene therapy by patients, caregivers, and healthcare professionals.
This project was conducted between July and December 2020, involving five Italian eye clinics specialized in IRDs, targeted pediatric and adult patients, their caregivers, attending retinologists and multidisciplinary healthcare professionals. Narratives and parallel charts, together with a sociodemographic survey, were collected through the project webpage. In-depth interviews were conducted with Patient Association (PA) members and multidisciplinary healthcare professionals. All data were entered into the Nvivo Software for coding and analysis.
Three pediatric and five adult patients with early-onset -related IRDs as well as eight caregivers were enrolled; 11 retinologists globally wrote 27 parallel charts; in-depth interviews were done with five multidisciplinary healthcare professionals and one PA member. Early diagnosis remains challenging, and patients reported to have changed up to 10 healthcare professionals before accessing their specialized center. Despite the oftentimes lack of awareness of patients and caregivers on the purpose of genetic testing, participants generally consider gene therapy as a therapeutic chance and a historic breakthrough for the management of -related IRDs. Well-organized networks to support the patient's referral to specialized centers - as well as a proper communication of the clinical and genetic diagnosis and the multidisciplinary approach - emerge as crucial aspects in facilitating an early diagnosis and management and a timely initiation of the rehabilitation pathway.
The project investigated the -related IRDs care pathway while integrating the different perspectives involved through NM. The analysis explored the patient's pathway in Italy and confirmed the need for a well-organized network and multidisciplinary care while highlighting several preliminary areas of improvement in the management of -related IRDs.
及时检测和多学科管理与[疾病名称]相关的遗传性视网膜疾病(IRD)可显著改善疾病管理和患者护理。因此,本叙事医学(NM)项目旨在调查护理路径的演变以及患者、护理人员和医疗保健专业人员对遗传咨询和基因治疗的期望。
本项目于2020年7月至12月开展,涉及五家意大利专门诊治IRD的眼科诊所,目标人群为儿科和成年患者、他们的护理人员、主治视网膜专家以及多学科医疗保健专业人员。通过项目网页收集了叙事和平行病历,以及一份社会人口学调查。对患者协会(PA)成员和多学科医疗保健专业人员进行了深入访谈。所有数据都录入Nvivo软件进行编码和分析。
招募了3名患有早发性与[疾病名称]相关IRD的儿科患者、5名成年患者以及8名护理人员;全球11名视网膜专家撰写了27份平行病历;对5名多学科医疗保健专业人员和1名PA成员进行了深入访谈。早期诊断仍然具有挑战性,患者报告称在进入专科中心之前最多更换了10名医疗保健专业人员。尽管患者和护理人员常常对基因检测的目的缺乏认识,但参与者普遍认为基因治疗是与[疾病名称]相关IRD管理的一个治疗机会和历史性突破。建立组织完善的网络以支持患者转诊至专科中心,以及对临床和基因诊断及多学科方法进行恰当沟通,是促进早期诊断和管理以及及时启动康复路径的关键方面。
该项目调查了与[疾病名称]相关IRD的护理路径,同时通过NM整合了所涉及的不同观点。分析探索了意大利患者的就医路径,确认了建立组织完善的网络和多学科护理的必要性,同时突出了与[疾病名称]相关IRD管理中几个初步的改进领域。