Care Pathway of RPE65-Related Inherited Retinal Disorders from Early Symptoms to Genetic Counseling: A Multicenter Narrative Medicine Project in Italy

Abstract

Purpose

Timely detection and multidisciplinary management of RPE65-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.

Patients and Methods

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.

Results

Three pediatric and five adult patients with early-onset RPE65-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 RPE65-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.

Conclusion

The project investigated the RPE65-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 RPE65-related IRDs.

Introduction

Inherited retinal dystrophies (IRDs) are a group of genetically and clinically heterogeneous degenerative conditions¹ affecting approximately 1 in 2–3000 people worldwide.² IRDs related to mutations involving the RPE65 gene are characterized by a progressive loss of photoreceptor cells and visual function impairment, resulting in an irreversible visual decline³ and potential blindness;⁴ retinitis pigmentosa (RP)⁵ and Leber congenital amaurosis (LCA)⁶ are the most common phenotypes.

The deterioration of visual acuity and peripheral vision follows early symptoms: visual impairment in different luminance conditions, night blindness, and nystagmus.^7,8 While IRDs management remains mainly support-oriented with a focus on monitoring, education, and counseling,³ gene therapy represents a novel potential treatment^3,9–11 as no treatments yet could slow or stop the progression of sight loss.¹² Since the age of onset ranges from early childhood to middle age, a timely detection of IRDs^13,14 and an optimal multidisciplinary management¹⁵ can significantly influence the improvement of the patient’s quality of life and offer therapeutic perspectives: an early diagnosis is critical to proper visual rehabilitation, as well as for genetic diagnosis and counseling and gene replacement therapies.^16,17 In particular, referral to highly specialized centers ensures multidisciplinary and personalized care,¹⁸ while a genetic diagnosis is critical to establish eligibility for an optimal gene therapy.¹⁷

Given the lack of data related to care pathways and patient’s quality of life,¹⁹ patient self-reporting has become crucial for the development of a suitable multidisciplinary management strategy.²⁰ Moreover, as affirmed in other studies,²¹ it is crucial to investigate methodologies that can gather patient experience that mere analysis of clinical pathway could not determine.

The World Health Organization (WHO) highlighted the significance of researching the illness experience more broadly²² to inform clinical practice,²³ and recommended the use of narrative research.

As described in other studies,^24,25 Narrative Medicine (NM) deals with illness narratives²⁶ to pursue the integration of the biomedical sphere with the individual and social experience of a condition.²⁷ Within the research, NM helps identify feasible interventions and implement the care pathway, by integrating the perspectives of all the factors involved;^28,29 its findings have been increasingly used to improve the quality of care,^30,31 also in the clinical genetics practice.³²

The NM project “BIRDS – The Beat of IRD Stories” aimed to study the RPE65-related IRDs illness experience through the analysis of narratives (a) to investigate the evolution of the care pathway and the expectations about genetic counseling and gene therapy as experienced by patients, caregivers, and healthcare professional; (b) to reveal the impact of these conditions on the personal and social quality of life; and finally (c) to provide insights for a better knowledge and clinical practice on RPE65-related IRDs. This study focuses on the first purpose of the project; to the best of our knowledge, no other study investigated the RPE65-related IRDs care pathway while considering at the same time the perspectives of underage and adult patients, caregivers, retina specialists and multidisciplinary healthcare professionals.

Methods

Research Design and Setting

The project was conducted between July and December 2020, targeting pediatric and adult patients with an RPE65-related IRD, caregivers, retina specialists, and other healthcare professionals from multidisciplinary teams involved in providing care. Five Italian eye clinics specialized in IRDs – ie, two pediatric hospitals and three university hospitals (Supplementary file 1) – were involved in the enrollment of participants. In July 2020, researchers from “Istituto Studi Direzionali” (ISTUD) Foundation trained the Steering Committee – which involved one Patient Association (PA) member and five retinologists specialized in IRDs – on NM and on the project’s purposes, design, and investigation tools; afterward, researchers invited them to engage patients and caregivers in participating in the research by accessing the project webpage [http://www.medicinanarrativa.eu/birds].

A clinical RPE65-related IRD diagnosis, determined at the reference medical center, or the caregiving of a person with this condition were the eligibility criteria for pediatric and adult patients and caregivers, together with the willingness to share their experience on the care pathway; thus, the ability to communicate in Italian was also critical.

Data Collection

Researchers ensured the survey accessibility by following the Web Content Accessibility Guidelines (WCAG) 2.1;³³ furthermore, patients could share their experience either by writing or recording an audio file, to address their low vision challenges and obtain age-appropriated support in writing, if underage. Narratives were anonymously collected through the Alchemer platform, available on the project webpage; subsequently, raw narratives were downloaded as Microsoft Excel spreadsheets. An illness plot³⁴ – ie, a plot characterized by evocative words to encourage individual expression³⁵ and aimed to retrace the illness experience in order to identify its evolution over time – was formed based on the written narrative for patients and caregivers, together with a sociodemographic survey.

Researchers gathered retina specialists’ care experience through the parallel chart³⁶ – ie, a personal notebook where the retinologists could record their thoughts and feelings in plain language, in addition to the technical reports.³⁷ The patients described in parallel charts could not be the same ones participating in the projects, as well as the patients’ caregivers could not be the same ones sharing their experience.

These investigation tools (Supplementary file 2) were designed for the three groups of participants to address common aspects: (a) the onset of symptoms, the pathway toward the clinical diagnosis, and the clinical encounter; (b) the experience of genetic counseling and the participants’ expectations about gene therapy; and (c) the evolution of the care relationship over time and the target areas to be improved.

Furthermore, researchers performed an in-depth interview³⁸ with five multidisciplinary healthcare professionals involved in IRD management and one PA member, to further help care pathway-related issues to emerge; each participant approved the final transcript before the analysis.

The investigation tools, summarized in Table 1, were designed by two ISTUD researchers with different academic backgrounds and were reviewed within the Steering Committee to reduce any cognitive bias.

Table 1.

Investigation Tools Used in the Project

Category of Participants	Investigation Tools
Underage and adult patients	Sociodemographic survey
	Illness plot, to collect written narratives
	Audio track, to present and promote audio narratives
Caregivers	Sociodemographic survey
	Illness plot, to collect written narratives
Retinologists	Sociodemographic survey
	Parallel chart
Multidisciplinary healthcare professionals and Patient Association member	Sociodemographic survey
	In-depth interview

Ethical Considerations

The project was carried out according to the Declaration of Helsinki and approved by the Ethical Committee of the “Luigi Vanvitelli” University Hospital (Naples, Italy) in September 2020. The retinologists involved obtained a written informed consent to participate from the parents of underage participants during the first project meeting; adult participants provided their web-based informed consent after briefing on the research purposes and confidential data processing procedures according to the General Data Protection Regulation of the European Union 2016/679³⁹ and the Italian Law 196/2003.⁴⁰ All informed consents included the publication of anonymized responses and narratives (Supplementary file 3).

Analysis

Survey data was analyzed through descriptive statistics; answering questions or filling in fields in the illness plots and the parallel charts was not mandatory, thus the varying sample sizes. Researchers entered anonymous narratives into the Nvivo software for coding and analysis;⁴¹ three narratives for each group and one in-depth interview were collectively coded to assess the consistency across team members and then reviewed during weekly peer debriefings, to limit any cognitive bias. Researchers employed open interpretive coding to identify and analyze the emerging topics in the narratives and in-depth interviews.

The Steering Committee examined the results to collectively address any issues emerged and the data interpretation. Researchers followed the Consolidated Criteria for Reporting Qualitative Research (COREQ) reporting guidelines.⁴²

Results

Eight patients with an early RPE65-related IRD onset participated in the project in writing, together with eight caregivers (parental or partner); 11 retinologists specialized in IRDs globally wrote 27 parallel charts. One PA member and five multidisciplinary healthcare professionals – ie, two psychologists, two genetic counselors, and one orientation and mobility instructor – participated in the in-depth interviews.

Tables 2 and 3 summarize the sociodemographic data of participants; non-responders are included as a separate category.

Table 2.

Sociodemographic Data of Patients, Caregivers, and Patients Described in Parallel Charts

	Patients (N=8)	Caregivers (N=8)	Patients in Parallel Charts (N=27)
Gender
Female	6 (75%)	6 (75%)	12 (44%)
Male	2 (25%)	2 (25%)	15 (56%)
Age (yrs)
Median (range)	26 (8–63)	44 (31–70)	17 (5–65)
<18	3 (38%)	–	15 (56%)
>18	5 (62%)	8 (100%)	12 (44%)
Geographic residence
Northern Italy	3 (38%)	2 (24%)	–
Central Italy	4 (50%)	4 (50%)	–
Southern Italy	1 (12%)	1 (13%)	–
Non-responders	–	1 (13%)	-
Education
Elementary school	1 (12%)	–	7 (26%)
Middle school	–	1 (12%)	4 (15%)
High school	1 (12%)	3 (38%)	4 (15%)
Bachelor/Master	3 (38%)	3 (38%)	3 (11%)
Non-responders	3 (38%)	1 (12%)	9 (33%)
Employment status
Student	4 (50%)	–	16 (59%)
Working	3 (38%)	6 (76%)	10 (37%)
Not working	–	–	–
Retired	–	1 (12%)	1 (4%)
Non-responders	1 (12%)	1 (12%)	–
Marital status
Single	6 (75%)	1 (12%)	18 (67%)
Married	2 (25%)	5 (64%)	7 (26%)
Separated	–	1 (12%)	2 (7%)
Non-responders	–	1 (12%)	-

Notes: Data are presented as n (%) or median (range).

Table 3.

Sociodemographic Data of the Retinologists and Multidisciplinary Healthcare Professionals Interviewed

	Retinologists (N=11)	Multidisciplinary Healthcare Professionals (N=6)
Gender
Female	5 (45%)	5 (83%)
Male	6 (55%)	1 (17%)
Age (yrs)
Median (range)	42 (32–64)	54 (49–67)
Geographic residence
Northern Italy	–	2 (33%)
Central Italy	8 (73%)	4 (67%)
Southern Italy	3 (27%)	–
Non-responders	–	-
Professional activity duration (yrs)
Median (range)	16 (6–41)	23 (19–35)
Specialization
Ophthalmologist	8 (73%)	1 (17%)
Pediatric Ophthalmologist	1 (9%)
Orthoptist	2 (18%)
Medical Geneticist		1 (17%)
Rehabilitation technician		1 (17%)
Psychologist		2 (32%)
Patient Association member		1 (17%)
Workplace
Hospital	2 (18%)
University Hospital	9 (82%)	2 (33%)
Other		4 (67%)

Notes: Data are presented as n (%) or median (range).

Figure 1 provides a flowchart to reconstruct the RPE65-related IRDs care pathway from the patients’ and caregivers’ narratives.

Figure 1.

Care pathway flowchart as deduced from patient and caregiver narratives. *Firstly addressed professionals in 57% of patient narratives. **Firstly addressed professionals in 43% of patient narratives.

Abbreviations: HCP, Healthcare professional; ERG, Electroretinogram; VEP, Visually evoked potentials.

Quantitative data are presented as median (range). The following four subsections illustrate the main findings: (a) the onset of the condition, the pathway toward the clinical diagnosis, and the first clinical encounter in a IRDs specialized center; (b) the genetic counseling experience and the personal expectations about gene therapy; (c) the evolution of the care relationship over time and the target areas to be improved; and (d) insights and proposals for the improvement of the care pathway from the in-depth interviews. Figures 2–5 and Tables 4 and 5 report quotes from narratives, parallel charts, and in-depth interviews. Supplementary file 3 provides four narratives from participants (in English). Researchers reduced the re-identification risk by applying different codes from those used to identify participants during data collection.

Figure 2.

First RPE65-related IRDs signals reported by patients and parental caregivers: distribution and quotes from narratives. *Non-responses = 1.

Figure 3.

Genetic test in patients’ and caregivers’ perspectives: distribution and quotes from narratives. *Non-responses = 1.

Figure 4.

Patients and caregivers’ expectations over gene therapy: distribution and quotes from narratives. *Non-responses = 2.

Figure 5.

What patients and caregivers would have wanted thinking the care pathway retrospectively: distribution and quotes from narratives.

Table 4.

The First Diagnostic Visit at a IRDs Specialized Center: Distribution and Quotes from Parallel Charts

Main issues expressed by patients and caregivers
Concern 40%	–They were very concerned about his autonomy and the possibility of leading a normal life in the future. (Parallel chart 024)
Trust 32%	–Parents looked at me as a reference person to confide their fears and thoughts on the evolution of the condition. (Parallel chart 010)
Need for a therapeutic perspective 28%	–They told me that they confided in me to provide a cure soon. (Parallel chart 011)
Retinologists’ communication strategies
Self-identification 18%	–I appealed to my role as a physician and as a parent to fully understand the issues of the child and her family. I tried to integrate the diagnosis by explaining that early-onset retinal dystrophies are the most complex to investigate, because of their confounding and, often, poorly specific clinical features. (Parallel chart 001)
Active listening and empathy 50%	–I listened to him with as much empathy as possible, not having the chance to catch his gaze. I tried to make him feel that I was close to him. (Parallel chart 014)
Correct information 42%	–I tried to convey some concepts that, in my opinion, were critical for her, as well as for all the other patients with these diseases. I tried to explain that a precise diagnosis is fundamental to receive the proper therapy. And I tried to explain that this therapy, in her case, would be applicable in the not-too-distant future. (Parallel chart 015)

Table 5.

Main Topics Emerged from the Patient Association Member and the Multidisciplinary Healthcare Professionals: Quotes from the in-Depth Interviews

Communication of IRDs	–Communication should be evaluated on a case-by-case basis. I believe that communication should be done when both premises and scientific certainties are present; moreover, we should psychologically support the patient. The double possibility of success and failure should always be considered. It is necessary to work on both because “you can die of happiness”: what human beings fear the most is change, and it has been said that we do not react well to change, even if positive, because we can still be afraid of it. (Interviewee 003) –We still have situations in which the communication of the diagnosis is made abruptly. They say, “Unfortunately, there are no cures for the disease, blindness could arrive, although we don’t know when”. Verbal “violence” takes away any hope. […] The main problem after the diagnosis is the psychological aspect. Suppose the diagnosis is communicated together with the possibility of recovery. In that case, you deal with it somehow, but if it is offered without any chance of recovery, people do not even attend control visits anymore; “Why should I even undergo any control?”, they ask. […] This is a significant shortcoming of our system, the absence of a psychologist upon the communication of the diagnosis. (Interviewee 004)
Genetic counseling	–A genetic investigation untrammeled from a multidisciplinary clinical context is unimportant. It represents highly complex information that must be managed by competent professionals, for example when reconstructing a family tree; genetic counseling should give correct and proper information. (Interviewee 005) –The waiting time for genetic testing should be reduced. Surely, we should invest in research. […] I am alone, I can hardly provide answers to everybody. Waiting times are long; we need to increase professional training. (Interviewee 002)
Lack of knowledge of IRDs	–No one knows about retinal dystrophies, because they are rare diseases that you do not encounter often. At first, you do not understand what’s happening to you; these diseases show up in developmental age, we do not always realize that something is wrong. The moment we realize something is wrong, formulating the diagnosis is difficult. The general practitioner is not always able to refer the patient to the specialists who should examine her. Unfortunately, the ophthalmologist is not always able to understand immediately what the problem is. These are diseases that show up early, and they are not always recognized in time. (Interviewee 004)

From the Onset of Symptoms to the Beginning of the Care Pathway

Patients showed the first signs of visual impairment at 2 years and 3 months of age (0,5–6 years). Light gazing and the inability to see objects in luminance change conditions were reported as the critical signs identified during early childhood in 57% of patients’ narratives (Figure 2), followed by balance and coordination issues and night blindness (both 43%). Parental caregivers reported light gazing and lack of eye contact, both present in 83% of the narratives, and night blindness (50%) as the main signs of visual impairment.

Pediatricians and ophthalmologists were the first professionals to be consulted in 57% and 43% of patients’ narratives, respectively. Patients reported to have changed up to 5 (median, 2.5; range, 1–5) medical centers and up to 10 (median, 2; range 0–10) healthcare professionals before accessing the IRDs specialized center; in 75% of patients’ narratives, interregional mobility emerged as highly important in order to access the specialized center in terms of IRDs knowledge and diagnostic capabilities for pediatric patients

My parents started travelling around Italy looking for doctors who could explain what was going on. Pediatricians said that my mother was too anxious […]. The diagnosis came only after many doctors and many trips, Patient 006.

Fifty percent of patients reported communication issues upon the clinical diagnosis, mainly highlighting disorientation

They told my mother that I needed psychological support to cope with the condition, and that the doctor could help me. I cried. I just cried. […] I cannot say who made more mistakes: the doctors I met, so little empathetic, or the school and its bureaucratic procedures, or my family, which raised and treated me as “normal”. Some categories should be included with caution in a child’s life, but it must be done indeed, to avoid worse disorientation, Patient 001.

Or a lack of therapeutic proposals

The trips ended when the lapidary diagnosis arrived: “Retinitis pigmentosa. There is no cure”, Patient 006.

Within the parallel charts, retinologists indicated the need for a therapeutic perspective (28%), the concern for the evolution of the condition (40%), and the trust in the IRDs specialized center (32%) as the main issues expressed by patients and caregivers during the first clinical encounter (Table 4). In addition, they described the communication strategies employed to start an adequate care pathway: active listening and empathy emerged as crucial in 50% of the parallel charts, the effort to provide a proper and correct information in 42% and the self-identification with patients or parental caregivers in 18%.

Genetic Counseling and Expectations About Gene Therapy

All patients reported to have undergone genetic counseling. Nonetheless, 57% accessed the specialized center without knowing the importance of genetics, and without having undergone a genetic test after the clinical diagnosis (Figure 3), while 43% referred to be too young to understand its purpose entirely. Conversely, 25% of caregivers reported having become aware of the aim of genetic test only recently, and 75% considered it a chance to receive definite answers and a complete diagnosis.

Retinologists referred to have proposed the genetic test only in 56% of the parallel charts, highlighting its importance for the prognosis and the therapeutic pathway

An anchor. The genetic test can provide more information on the condition, and potentially on the prognosis and the chances of care, Parallel chart 010.

Gene therapy represented the hope for preventing the progression of sight loss in 83% of patients’ and in 75% of caregivers’ narratives (Figure 4), and a chance for visual improvement in 17% of patients’ and 25% of caregivers’ narratives.

All retinologists considered gene therapy a historic breakthrough for the therapeutic management of RPE65-related IRDs

A turning point for previously incurable conditions, Parallel chart 026.

Thus, in 67% of the parallel charts, retinologists defined the access to gene therapy as still limited to a few patients and requiring to be further clarified and implemented

Gene therapy represents the future of medicine in several areas; access to therapies should be extended to all. However, this is currently a utopian thought. We need more research to make it real, Parallel chart 005.

Also at a communication and professional training level

We have a lot to do in terms of organization, communication and training, Parallel chart 014.

Evolution of Care Relationship and Target Areas to Be Improved

Thirty-three percent of patients stated to hope to access gene therapy; conversely, 67% reported a feeling of self-delusion

I go straight my way with the strategies I have today, and I rarely indulge in fantasies. If I perceive therapy as a fantasy, it remains in its place … But if it were to become a desire, everything would crash down. I cannot afford it, Patient 001.

However, 63% reported to trust the professionals of their specialized center, and 75% expressed a positive evolution of the care relationship

It gives me much confidence. It makes me feel considered – I have never experienced that before, Patient 002.

Retinologists confirmed the positive evolution of the care relationship in 67% of the parallel charts

We monitored the rehabilitation path. The child appeared more confident in his visual potential and increased his self-esteem, Parallel chart 004.

Moreover, they reported the hope for their patients to access gene therapy (19%) and, conversely, their increasing issues in performing everyday tasks due to visual impairment (15%). The provision of an effective support (46%), the improvement of the patients’ autonomy and quality of life (42%) and the promotion of their awareness (12%) emerged as the retinologists’ main goals of care.

With respect to different care pathway experiences (Figure 5), patient preferences were as follows: more involvement (50%) and more support on the part of healthcare professionals (63%), an earlier genetic testing (38%), and an earlier discovery of the gene therapy (38%). Similarly, preferences of caregivers were more support (38%), the possibility to share their caregiving experience with other families experiencing the same situation (13%), earlier genetic testing (50%), and an earlier discovery of the gene therapy (25%).

The survey revealed that patients find information on their condition mainly at the centers specialized in IRDs (71%), while believing that a greater awareness of IRDs clinical manifestations among the general public is highly needed (86%). Furthermore, patients stated that a PA should provide updated and detailed information on the management of IRDs and the therapeutic progress (83%) and suggestions aimed at improving quality of life and autonomy (50%). Patients also suggested that PA members should encourage or organize patients’ self-help groups (50%). Of the caregivers, 83% reported that a PA should provide valuable contacts and information sources about the condition, 33% sought recommendations regarding the lifestyle, and 33% thought that they should connect patient both among themselves and with the specialized centers. According to clinicians, educational programs on IRDs should be highly recommended for patients (64%), as well as for ophthalmologists (55%) and pediatricians (45%).

Insights from in-Depth Interviews

Three main topics transversely emerged from the in-depth interviews done with the PA member and the multidisciplinary healthcare professionals (Table 5):

1. All interviewees emphasized that the information provided to patients and caregivers from the diagnostic suspect onward should be correct and that psychological support should be guaranteed upon the diagnosis and throughout the care pathway. Psychologists suggested that communication should be evaluated on a case-by-case basis. The PA member highlighted that an “abrupt” communication can proactivity impact the patient along her rehabilitation pathway, which is often not timely accessed and properly acknowledged, as outlined by the orientation and mobility instructor.

2. Geneticists stressed that, on the one hand, patients and caregivers often ignore the role of genetic counseling in exploring therapeutic options and that, on the other, such counseling should be integrated within a multidisciplinary approach. Interviewees reported criticalities in accessing genetic testing: the limited number of centers specialized in IRDs and equipped with new generation technologies for genetic testing and challenging waiting times delay both the rehabilitation and the therapeutic pathway.

3. All interviewees highlighted the importance of a continuous work on the awareness of IRDs among both the public opinion and healthcare professionals non-specialized in IRDs, as well as other professionals potentially involved in multidisciplinary care teams – also given the fact that the onset of these conditions occurs during the developmental age.

Furthermore, the interviewees suggested that an effective care pathway should require (a) a well-organized network between centers specialized in IRDs and on a national level and more clinical geneticists specialized in this field; (b) shorter waiting times for genetic testing and rehabilitation; and (c) a multidisciplinary care approach with more training on IRDs for professionals and more room for psychological support.

Discussion

This project represents the first effort to investigate RPE65-related IRDs care pathway in Italy through NM that simultaneously addresses the perspectives of patients, caregivers, and attending physicians and collecting insights from the genetic counselors, psychologists, and orientation and mobility instructors involved in the multidisciplinary teams, as well as from the PA member.

Patients reported to have experienced the first signs of visual impairment during their early childhood. As also shown in other studies,¹⁵ parental caregivers were able to reliably recognize some of the earliest RPE65-related IRDs signs (light gazing, lack of eye contact, night blindness). Since confirming the clinical diagnosis may be challenging in early childhood, parental observation may be crucial for the clinical suspicion, and it may also help pediatricians and ophthalmologists to identify – or suspect – the condition and early refer patients to centers specialized in IRDs.

Patients reported that the communication of their clinical diagnosis was characterized by misleading messages, causing disorientation and sometimes the giving up of visual rehabilitation and follow-up visits; as suggested by the in-depth interviews, a psychological support from the communication of the diagnosis onward may help patients to proactively engage their care pathway. Communication issues can be further investigated and integrated with studies on the making-sense and coping with RPE65-related IRDs.^43,44 Conversely, clinicians from specialized centers reported a strong sense of identification with their patients or caregivers. They were also attentive to the non-clinical aspects of the communication: active listening, empathy, and the effort to give correct and realistic information that may debunk any misleading communication issues also reported by multidisciplinary healthcare professionals and the PA representative during the in-depth interviews, while engaging patients in a positive care relationship, as confirmed in the narratives and the parallel charts.

As for genetic testing, patients reported to have initially been not aware of its importance – due to young age or misleading or inadequate information after the clinical diagnosis. Genetic counselors emerged as critical to correctly support patients and caregivers in understanding the genetic diagnosis and the test result, and genetic counseling should be provided before and after testing; patients and caregivers should also be informed and prepared on the test limitations and the implications of the results.⁴⁵ Conversely, in the narratives and the parallel charts, gene therapy undoubtedly emerged as a historic breakthrough, a chance to maintain or even improving the current visual ability, in line with other studies,⁴⁶ which highlight its emotional impact on patients, caregivers, and even clinicians. However, as stressed in the parallel charts and as emerged in other studies,¹⁷ the eligibility criteria and the possibilities to access gene therapy should be further clarified, to ensure its applicability to as many patients as possible.

The narratives and the in-depth interviews confirmed that RPE65-related IRDs need a specialized approach for a successful evolution of the care pathway and an effective management of these conditions: specialized centers remain well distributed across Italy; thus, a structured network should also be implemented, to efficiently address patients’ and caregivers’ interregional mobility. Moreover, as suggested in other studies,^17,18,47 a multidisciplinary approach is required to understand patients and provide them with support, also focusing on the psychosocial and organizational issues. In this perspective, the present project can provide preliminary suggestions to implement clinical practice:

1. Building a robust and well-organized network, which also includes PAs, to support the patient’s referral to IRDs specialized centers is crucial to facilitate the access to an early diagnosis and management, and to avoid challenging waiting times to initiate the rehabilitation and therapeutic pathway. Genetic counseling, provided by clinical geneticists specialized in IRDs, emerges as critical both before and after genetic testing,⁴⁵ while gene therapy access and eligibility criteria should be further clarified.¹⁷

2. A proper and empathetic communication is central: on the one hand, to effectively provide realistic information about the condition and its management, and, on the other, to engage patients so they could maintain an active perspective on the care pathway and to early access rehabilitation programs.

3. The management of IRDs should be promoted by optimizing a multidisciplinary approach, which is essential to meet the complex care needs of each patient.¹⁸ The psychological support remains critical, from the communication of the clinical diagnosis throughout the care pathway, and dedicated spaces may be provided to patients and their caregivers for them to share and exchange their illness experience. In addition, the role of the orientation and mobility instructor should be further acknowledged, for the purpose of a timely access to the rehabilitation path.

4. The need for an increasing awareness of IRDs emerges as crucial on three levels: educational, for patients, caregivers, and relational networks; informative, for the general public; and professional, for pediatrics, ophthalmologists, and other professionals – from the first signs of the condition onward – to promote an early diagnosis and access to the care pathway.

The low annual incidence of RPE65-related IRDs – approximately 1–2% of all IRD patients referred for genetic testing, with 4–5 new cases identified per year (unpublished data) – in Italy,¹³ where main centers specialized in IRDs and PA are jointly conducting a natural history study on these conditions,⁴⁸ explains the low number of participating patients; nonetheless, the narratives collected suggest a strong dedication to the project, as well as a relationship of trust between patients, caregivers, and the healthcare professionals from the centers involved. Moreover, the data collection phase partially corresponded to the social distancing and local closings measures implemented by the Italian government to contain the Sars-Cov-2 pandemic, with consequences on the clinical follow-up and the participation in the project.

Conclusions

The project investigated RPE65-related IRDs care pathway as experienced by patients, caregivers, and healthcare professionals. Our results provide insights from the PA representatives and multidisciplinary healthcare professionals involved in this pathway. The integration and the analysis of these different perspectives through NM highlighted several preliminary areas of improvement in the management of RPE65-related IRDs, otherwise overlooked by the analysis of the clinical pathway only; finally, the nature of the project may stimulate further investigations on real-life experiences of the care pathway of these conditions.

Funding Statement

This work was funded by Novartis Farma.

Abbreviations

IRDs, inherited retinal disorders; RPE65, retinal pigment epithelium-specific 65 kDa protein; RP, Retinitis Pigmentosa; LCA, Leber congenital amaurosis; WHO, World Health Organization; NM, Narrative Medicine; PA, Patient Association; ISTUD, Istituto Studi Direzionali; WCAG, Web Content Accessibility Guidelines; COREQ, Consolidated Criteria for Reporting Qualitative Research.

Data Sharing Statement

All datasets used and analyzed during the current research are available in Italian from the corresponding author, upon reasonable request.

Ethics Approval

The project was conducted according to the Declaration of Helsinki. The Ethical Committee of the Luigi Vanvitelli University Hospital (Naples, Italy) approved the project rationale, design, investigation questionnaires, and informed consent in September 2020.

Consent to Participate

Participants provided a web-based informed consent before their involvement and after being briefed on the purposes of the research and the procedures for the processing of personal data, according to General Data Protection Regulation of the European Union 2016/679 and the Italian Law 196/2003. The clinicians involved obtained a written informed consent to participate from the parents of underage patients during the first briefing on the project’s methods and purposes. The informed consent included publication of anonymized responses and narratives.

Author Contributions

All authors contributed to the project’s conceptualization, investigation, and data analysis and validation. All authors contributed to data analysis, drafting or revising the article, gave final approval of the version to be published, agreed to the submitted journal, and agree to be accountable for all aspects of the work.

Disclosure

FS received honoraria from Novartis Pharmaceuticals, Italy, for holding webinars and serving advisory boards. AS received honoraria from Novartis Pharmaceuticals, Italy, for serving on advisory boards. BF, received honoraria from Novartis Pharmaceuticals, Italy, for holding webinars and a lecture fee from UVET GBT, Milan, Italy. GB, and GI have received honoraria from Novartis Pharmaceuticals, Italy, for holding webinars; in addition GB received personal fees from Maple Health, personal fees from Kantar health, outside the submitted work. MA is employees of Novartis Pharmaceuticals, Italy, and Region Europe.