Keywords
Kidney Disease, Renal Disorder, Rare Renal Disorders, Transition Care, Transitional Care, Transfer to Adult Care, Young Person
Kidney Disease, Renal Disorder, Rare Renal Disorders, Transition Care, Transitional Care, Transfer to Adult Care, Young Person
The number of young people advancing from paediatric to adult renal care has increased dramatically in recent years due to their improved medical management; patient survival rates have increased by 85–90% (Ferris et al., 2006; Lewis et al., 2009; Watson et al., 2011). Over the past few decades, earlier diagnosis, treatment advancements and the improved management have accelerated patient survival rates and improved the life expectancy of patients (Joly et al., 2015; Stepien et al., 2021). Hence, more patients are required to undergo the healthcare transition, generating an increased need for a structured, well-planned transition from the paediatric to adult healthcare setting (Joly et al., 2015).
Transitional care was first described in the literature approximately 40 years ago and is now considered to be crucial in the context of adolescent health care (Barbero, 1982; Wildes et al., 2023). Transition is defined as ‘the purposeful, planned movement of adolescents and young adults with chronic physical and medical conditions from child-centered to adult healthcare systems’. (Blum et al., 1993, p. 570). Blum et al. (1993), p. 573, further defined how transition ‘attends to the medical, psychosocial, and educational/vocational needs of adolescents’. Transitional care aims to maximise lifelong functioning and potential by providing high-quality, developmentally appropriate healthcare that continues in an uninterrupted fashion when moving between paediatric and adult health services (American Academy of Pediatrics et al., 2002). It is essential that transitional care is carefully differentiated from the “transfer” of care; “Transition” to adult healthcare refers to the process that commences during childhood and ends once the patient is fully integrated within the adult healthcare system, whereas the “transfer” of care is the distinct point in time where the patient moves to the new healthcare setting, provider or both, and is just one aspect of the transition process, which must be an anticipated, co-ordinated process (Marks, 2022).
Transition is particularly challenging for adolescents and young adults (AYAs) living with renal disorders due to the multisystemic complexity of their conditions. For example, patients with renal disorders may receive renal transplantation or other specialist treatments, such as enzyme replacement therapy for Fabry’s disease (Quaglia et al., 2014; Riccio et al., 2020). Furthermore, moving from paediatric to adult care occurs during an emotionally vulnerable phase of the young person’s life (Bell, 2022). The transition process occurs in tandem with the transition from adolescence to adulthood, which is well-recognised as a period of rebellion, engagement in risk-taking and impulsive behaviour, and non-adherence attributed to ongoing brain development and maturation; a period where adolescents often experiment and feel unconquerable (Kreuzer et al., 2019; Tareen & Tareen, 2017; Watson, 2005). It has been recognised that this adolescence/young adulthood period embraces ages 14–24 years, regarding brain development and maturation (Watson et al., 2011). Hence, young people in this age bracket require special consideration, and their life experiences and challenges must be considered during the transition process (Bell, 2007; Watson et al., 2011).
Evidence suggests that most youth and young adults receive inadequate or a total absence of transition preparation, transfer assistance or facilitated care integration (Gabriel et al., 2017). If AYAs transition to adult healthcare in a scenario whereby they are not able to manage their disease adequately, undesirable health outcomes may arise (Ma et al., 2021; Young et al., 2010). This is problematic and adds to the already challenging period that AYAs face at this time; AYAs are navigating their adolescent development transition period, whilst also learning to manage the various aspects of their healthcare, grieve losses experienced in their daily lives, and attend to the practicalities of various treatments, interventions, and appointments that they undergo (Kralik et al., 2010). Young people with kidney disease have specific medical needs, such as steroids, which often alter their appearance and mood, their growth may be stunted, they may be faced with extreme lifestyle modifications such as fluid and diet restrictions, intensive medication regimens with side effects, and AYA’s may have to undergo dialysis, which comes with side-effects such as fatigue, and is time consuming and restrictive (Dallimore et al., 2018).
AYAs must achieve the required competencies to manage such physical and psychosocial aspects of their illness. Hence, efficient self-management is invaluable. Self-management may be defined as ‘the daily activities that individuals undertake to keep the illnesses under control, minimize its impact on physical health status and functioning, and cope with the psychological sequelae of the illness’ (Clark et al., 1991, cited in Gallant, 2003, p.170). AYAs with long term conditions, such as chronic renal conditions, must learn how to manage and live with their condition throughout life. However, they require support to achieve their physical, psychological, and social potential (Nightingale et al., 2019; While et al., 2004). This is particularly important as AYAs move toward adulthood, and health professionals and parents require effective means of supporting AYAs to learn such skills (DOH, 2006; Nightingale et al., 2019).
A favourable health-care transition is one in which AYAs are suitably prepared for the transition and have attained the self-management competencies required both pre and indeed, post the transition (Cooley & Sagerman, 2011; Fredericks et al., 2010; Ma et al., 2021). Based on this, perhaps the re-worded version of Blum et al. (1993) definition for transitional care is more appropriate; Dovey-Pearce and Christie (2013), p.175, reframed transition as ‘the purposeful, planned process that addresses the medical, psychosocial, educational and vocational needs of adolescents and young adults….as they grow up learning to live with their lifelong health condition’. To evaluate such self-management skills and to determine the patients time and mode of transition, transition readiness tools must be utilized, such as the Self-Management and Transition to Adulthood with Rx = Treatment (STARx) (Ferris et al., 2015(a); Ferris et al., 2015(b); Ma et al., 2021).
Failure to transfer adolescents under a well-designed transfer programme, with the required competencies to manage their condition, may lead to reduced attendance at adult renal units (Çiçek & Alpay, 2022). In turn, AYAs are placed at high risk of clinical deterioration, resulting in a cascade of negative health outcomes (Foster & Bell, 2015; Kreuzer et al., 2019; Prüfe et al., 2022; Watson et al., 2011). This may be attributed to multiple factors and not exclusively poor attendance to adult clinics, such as non-adherence to medications or medical treatment and regimens, including non-adherence to life-long immunosuppressive regimens. This, in turn, leads to increased risk of rejection and allograft loss and/or a return to dialysis (Akchurin et al., 2014; Campbell et al., 2016; Crawford et al., 2020; Dobbels et al., 2010; Dobbels et al., 2009; Foster & Bell, 2015; Kreuzer et al., 2019; Mazzucato et al., 2018; Prüfe et al., 2022; Quaglia et al., 2014; Wildes et al., 2023).
Moreover, the transition process must be considered for AYAs living with rare renal disorders. Transition is often challenging for AYAs and families living with rare renal disorders. Over 300 inherited, congenital, and acquired renal disorders meet the criteria to be defined as rare renal disorders (Bassanese et al., 2021). The list of rare disorders with renal involvement is constantly growing. In Europe, renal disorders have an estimated prevalence of approximately 60–80 cases per 100,000, with nearly all children who progress to renal-replacement therapy having an inherited kidney disease (Devuyst et al., 2014). Children born with rare renal disorders, particularly severe congenital nephropathies, often face altered physical, cognitive, and psychosocial development (Aymé et al., 2017). Many children and young people living with such conditions are now surviving into adulthood with conditions that were previously unknown to adult nephrologists (Marks, 2022).
Adult renal services are receiving a growing number of AYAs with rare renal disorders who have transitioned from paediatric services (Watson et al., 2011). The transition from the paediatric to the adult healthcare setting for these patients has been reported to be a challenge to transfer, due to a lack of training and knowledge of adult nephrologists of these rare conditions, amongst several other reasons (Prüfe et al., 2017; Watson et al., 2011). However, this cohort of patients must be carefully considered, as congenital anomalies of the kidney and urinary tract have been cited as the most common causes of end-stage and chronic kidney disease in childhood (Marks, 2022). These patients and their families must be carefully transitioned from paediatric to adult health care, with emphasis placed on the need for these patients and families to have adequate knowledge surrounding how to manage their own health, transfer to adult-centred care with up-to-date medical knowledge, and how to engage in adult health care (Gabriel et al., 2017).
Transition aims to gradually prepare AYAs and families for a successful integration into the adult healthcare system in an uninterrupted manner (Matsuda-Abedini et al., 2022). A positive transition begins in the paediatric health setting and prepares adolescents to become a self-responsible adult patient who manages their condition appropriately and ends with the patient finding their place in the adult healthcare system in a safe and secure manner (Kreuzer et al., 2019; Paone et al., 2006). Transition is considered successful if the patients’ health competence, psychosocial rehabilitation, and self-determination are promoted, including the patient having improved decision-making abilities and the ability to communicate their care effectively (Kreuzer et al., 2019; Prüfe et al., 2022; Watson et al., 2011).
The importance of an effective transition programme, incorporating well-planned interventions and strategies for young people living with renal disorders is apparent. Studies have demonstrated that the highest rate of kidney transplant loss occurs in patients aged between 16–21 years old (Foster & Bell, 2015; Kreuzer et al., 2019; Prüfe et al., 2022; Watson et al., 2011). Therefore, this age group must be carefully managed, as graft failure requires a return to dialysis, which reduces the patient’s quality of life, increases morbidity, shortens life expectancy, and leads to heightened health care expenses (Prüfe et al., 2022). Providing increased knowledge, awareness, and education to AYAs surrounding their condition and the transition process, and providing appropriate, relevant, easily accessible self-management strategies may better support AYAs with the transition process. Psychosocial support, the management of potential extrarenal complications, and genetic and reproductive counselling are other integral components that must be integrated within the transition process (Aymé et al., 2017).
Moreover, it has been established within the literature that the transition process should start early, by at least 12 to 14 years old, providing sufficient time to prepare patients and caregivers for the transition (Aymé et al., 2017; Willis & McDonagh, 2018). Nonetheless, the timing depends upon patient-specific factors, including growth, maturity, and overall readiness (Aymé et al., 2017). An effective transition programme may reduce the risk of declining renal function and acute rejection episodes and may improve long-term graft outcomes in patients (Raina et al., 2018). Due to the complexity of renal diseases, transition support and services must be carefully planned and timed, and focus on empowering a safe transfer of care from the child to the adult healthcare setting for AYAs living with renal diseases, to ensure the risk of negative health outcomes is reduced.
Interventions to support the transition process for AYAs with chronic illness include summer camps, clinics, guidelines, transition readiness scales, online educational and interpersonal communication programmes, e-health i.e., the use of mobile apps, the use of a digital monitoring device, problem solving challenges, role-play, arts-based interventions etc. (Callinan & Coyne, 2020; Catarino et al., 2021; Miller, 2022). The purpose of this scoping review is to map out the interventions that are present to support the transition care of AYAs living with renal disorders, specifically.
A preliminary search of Medline, PROSPERO (PROSPERO, 2022), the Cochrane Database of Systematic Reviews, and Google was conducted on the 1st of October 2022. An ongoing systematic narrative review protocol was located on PROSPERO by Piccoli et al. (2020), which will explore the best approach for the clinical management of young people with chronic kidney disease undergoing transition. However, this scoping review aims to scope the literature and map any intervention to support transitional care for AYAs with renal disorders within healthcare settings, inclusive of rare renal disorders, chronic kidney disease, patients undergoing dialysis, and transplant recipients. For this review, an intervention may be defined as any programme, service, intervention, clinic, scale, model, tool, or activity that aims to support AYAs with renal disorders as they transition from paediatric to adult healthcare services. Interventions will be included if they support AYAs.
The proposed scoping review will be conducted in accordance with the Joanna Briggs Institute (JBI) methodology for scoping reviews (Peters et al., 2015). The methodology for this review employs the five-stage framework, as outlined by Arksey and O’Malley (2005), incorporating more recent methodology refinements as proposed by Levac, Colquhoun and O’Brien (2010) and the JBI (Peters et al., 2020). Arksey and O’Malley (2005) also identified an optional ‘consultation exercise’ to inform and validate findings, as a sixth stage at the end of the review (Arksey & O’Malley, 2005).
This step has been identified as a stage that will improve the study remarkably (Arksey & O’Malley, 2005). Experts in transitional care research, paediatric nephrology, and various relevant stakeholders within the disciplines of psychology, sociology, academia, and research will be invited to be a part of the scoping review, and to appraise and validate the review findings. The Preferred Reporting Items for Systematic reviews and Meta Analyses Scoping Review extension (PRISMA-ScR) checklist will be utilised to increase methodological transparency and ensure consistency when publishing findings (Tricco et al., 2018). The six-stage Scoping Review Framework developed by Arksey and O’Malley (2005) will be employed to guide the scoping review protocol and the preceding scoping review.
The objective of this scoping review is to map the various interventions that are available within the literature to support AYAs and families living with renal disorders as they transition from the paediatric to the adult healthcare system. The following research questions will be addressed:
1. Identify, appraise, and synthesise knowledge surrounding interventions to support the transition process for young people living with renal disorders, including an examination of the theories, models, frameworks, and guidelines that underpin these interventions.
2. Understand what interventions are available to support a successful outcome for AYAs with renal disorders.
3. Ascertain whether the AYAs were involved in the intervention’s development.
4. Determine the study settings, conditions and geographical contexts, and the study types conducted (e.g., qualitative, quantitative or mixed-methods methodology).
5. Ascertain the experiences, barriers and facilitators recognised by young people living with renal disorders, of current transition interventions.
6. Clarify how the concept of “transitional care” has been defined, classified, and understood in the existing literature.
7. Identify research and knowledge gaps in the literature.
The scoping review question guides and directs the development of the review process. In this review, the population, concept, and context (PCC) framework will be utilised, which has been recognised as an effective framework for a scoping review by the JBI (Peters et al., 2020). The preliminary question is:
What is the evidence base for interventions that are available to support the transition of care (Concept) from the paediatric to adult healthcare setting (Context) for adolescents and young adults living with renal disorders (Population)?
A systematic literature review aims to obtain as many relevant studies as possible on a particular topic, using a thorough, objective, and reproducible search of a range of sources (Levay & Craven, 2019). Being systematic minimises bias (Levay & Craven, 2019). The review question has been formulated using the PCC framework. This ensures that appropriate, relevant search terms can be developed, ensuring the retrieval of pertinent results on the interventions available to support the transitional care of young people living with renal conditions, and will ensure that the retrieval of irrelevant results is minimised.
Eligibility criteria
The inclusion and exclusion criteria is developed through the generation of a PCC table (Table 1), as recognised by Boland, Cherry and Dickson (2017) as an effective means of defining criteria. This process remains iterative, and any changes made throughout the review will be recorded and documented to maintain transparency and rigor in reporting.
Population
This scoping review will include AYAs living with any renal condition, encompassing any chronic or rare renal condition, patients who are currently on renal dialysis, and renal transplant recipients. Furthermore, studies that refer to any rare disorder with renal involvement will be included. Studies that focus on AYAs living with renal disorders, or studies that refer to families, caregivers, healthcare providers, programme managers and policymakers involved in the transition process alongside the AYA will also be included.
Age
Studies will be included if they refer to AYAs between the ages of 12–24 years old, who are either (a) preparing for the transition process, (b) currently undergoing the transition process, or (c) having undergone transition from the paediatric to the adult healthcare setting. This age range is deemed appropriate, as 13/14 years old is the recommended age to commence the transition process, and through the inclusion of patients up until the age of 24 years, we can retrieve results from patients who may have completed the process (Willis & McDonagh, 2018). Furthermore, this age group is appropriate, as the International Society of Nephrology and the International Pediatric Nephrology Association have recommended that transition should occur between 14 and 24 years old (Joly et al., 2015). By including 12 and 13 year olds, we can capture patients who are about to commence transition.
Gender
Studies that refer to male, female and non-binary young people with renal disorders will be included in the review. This will avoid gender bias (Upchurch, 2020). Gender is often characterised as female, male or non-binary. This review will include all genders to promote inclusivity and to widen participation.
Concept
This review will examine the concept of transition from a child and family centred healthcare system to the adult centred healthcare system. Transition is defined as the purposeful, planned transition of adolescents with a chronic kidney condition from paediatric, family-centred health services to adult, person-centred health services (Campbell et al., 2016). This review will examine interventions that support the transition process. For this review, interventions encompass any programme, service, intervention, clinic, or activity that aims to support the movement of AYAs and families from paediatric to adult healthcare services.
Context
Setting
This scoping review will consider primary research studies that have been conducted in multiple different settings within secondary and tertiary level health services, including hospitals (including various areas within the hospital such as wards or outpatient departments).
Geographical location
No limits will be placed on the geographical locations included within this study. Furthermore, there will be no language limits placed on our initial search. This ensures that language and publication bias is avoided. As discussed by Boland et al. (2017), language bias may arise if only English-speaking countries are included due to English-language journals being more likely to publish positive results. Due to resource limitations, the literature will be searched in English, with no restrictions placed on language. This ensures maximum retrieval of literature in all potential languages. Efforts will be made to translate study abstracts, where possible, using translation tools such as google translation services. However, literature that is obtained but not in the language of choice (English), and that cannot be readily translated due to resource limitations, will be excluded (Gough et al., 2017).
Nonetheless, by not setting language limitations when searching, all potential literature can be obtained and made readily available for other researchers who may have the resources to translate the articles that are obtained (Gough et al., 2017). Furthermore, publication bias often occurs due to studies with positive results being more likely to be submitted and selected for publication in peer-reviewed journals when compared to studies that report null results (Boland et al., 2017). Therefore, if excluded, the review could potentially miss any negative or null findings and skew the scoping review findings.
Types of sources
This scoping review will consider all study designs and review types that explore interventions to support the transition process amongst young people with renal disorders, including quantitative study designs—both experimental (e.g., randomised control trials, non-randomised trials) and observational (including prospective and retrospective cohort studies, or analytical cross-sectional studies). Qualitative study designs will be included, such as grounded theories, qualitative descriptive, phenomenology, action research or feminist research. In the initial reviewing process, both studies available in full-text and abstract format will be considered for review. This will ensure that the most up-to-date evidence is not missed (Boland et al., 2017). Any literature that does not present data meeting the inclusion criteria will be excluded.
Search strategy
The formulation of a search strategy is invaluable and must be transparent, accountable and replicable, ensuring a systematic process is followed (Gough et al., 2017). A comprehensive search strategy was developed by the primary researcher in consultation with an expert librarian (DS) with experience in undertaking literature searches and using thesaurus tools (Table 2). To develop the search strategy, an initial scoping search was conducted in databases including PubMed, CINAHL, the Cochrane Library and Google Scholar on 14th October 2022. This identified articles relevant to the topic. Free-text words and subject headings/index terms were located from titles, abstracts, and main texts of articles, and were used to further enrich and inform the search strategy (Boland et al., 2017).
The thesaurus tools, subject headings and synonyms were utilised and shared across databases to maximise search results. Furthermore, the use of truncation and ‘proximity’ searching was utilised (Gough et al., 2017). The search strategy encompasses the use of Boolean operators, truncation, subject headings across each database, and free-text headings for each database. The librarian (DS) will provide support and assistance to the primary researcher when carrying out searches of the databases.
Furthermore, the literature search strategy utilised will be reported in the scoping review, within a table in the appendix, to ensure easy replication by others (Tricco et al., 2018). The search strategy is iterative (Gough et al., 2017). Therefore, any modifications or adjustments to the search strategy as the review progresses, will be clearly documented to ensure transparency in searching. Databases will be limited to the year 2000, ensuring that the results portray relevant interventions that consider medical and technological advancements within the realm of healthcare over the past two decades. Furthermore, only peer-reviewed literature will be included in the scoping review.
Quality appraisal
For the scoping review, a quality appraisal will be undertaken, using the Mixed Methods Appraisal Tool (MMAT) (Hong et al., 2018) and the Critical Appraisal Skills Programme (CASP) (Critical Appraisal Skills Programme, 2022). Quality appraisal or critical appraisal is defined as a process whereby research is evaluated carefully and systematically in terms of its trustworthiness, relevance, and value (Burls, 2015). Only peer-reviewed papers that have been published within academic journals will be included in this scoping review.
Case studies, individual case reports, opinion pieces, commentaries, editorials and grey literature will also be excluded from the review, based on resource availability to the primary researcher (MK), including a limited amount of time and funding to undertake the review as part of an academic degree. To ensure a comprehensive mapping of the literature, a broad range of databases will be searched. The databases that will be searched include: (1) Health databases, including PubMed, CINAHL Plus with Full Text and Embase; (2) Social sciences databases, including PsycInfo and ASSIA; and (3) Multidisciplinary databases, including Web of Science.
The rationale for searching more than just one database is justified. The databases selected encompass health and social sciences databases. These databases have been chosen strategically, as Transitional Care requires a multi-disciplinary approach, and must include not only physical support, but also psychosocial support (Aymé et al., 2017). Therefore, it is essential to not only include health databases, but also social sciences and multidisciplinary databases. The author will not undertake complementary search techniques, including bibliographic searching and hand searching, in addition to searching databases due to the time restrictions of the primary author to complete the review in a timely manner as a component of their academic degree.
Each search will be documented systematically, including the date, search terms, results per search string. Following the literature search, all results obtained through the databases will be collated and imported into a bibliographic reference manager EndNote 20. All imported results will be dated and saved to individual libraries, depending upon which database they were collected from. This enables the authors to keep a record and manage their search results. Following the import of the results to EndNote 20, all duplicates will be removed.
The number of articles retrieved following these steps will be added to the PRISMA-ScR flowchart, as recommended by the JBI (Peters et al., 2020) (Figure 1). Furthermore, a PRISMA-ScR flowchart will be completed following the completion of each search to ensure transparency when mapping the number of records identified and to provide a rationale as to why studies were excluded (Page et al., 2021; PRISMA, 2020).
Search results from EndNote will be imported for further screening and reviewing in Covidence systematic review screening and data extraction software tool (Covidence, 2022). Once complete, the screening and data extraction process can commence. This process will be undertaken in three steps: (1) Title and abstract screening; (2) Full-text review; (3) Data extraction in Covidence. Following screening and removal of duplicates, further screening will be performed with the titles and abstracts of all studies obtained being screened against the inclusion and exclusion criteria (Boland et al. 2017). The primary author (MK) and fourth author (SS) will review the title and abstracts independently, before being included or excluded in the review. This reduces bias and makes the review process more robust (Boland et al, 2017).
A pilot testing of literature obtained (n=15) will be undertaken using Covidence software with the inclusion and exclusion criteria inputted to the software tool to ensure consistency of the methodology utilised within the selection process (Peters et al., 2020). This process will be transparent, and document all decisions made surrounding which literature was included or excluded and a rationale for inclusion or exclusion. Covidence will support this process by tracking/logging decisions made throughout the process. Any discrepancies or lack of consensus between authors during the screening process will result in the second author (TK) being consulted and adjudicating. Following this, full-text review will be undertaken by the first and fourth authors (MK & SS).
Once again, if disagreement arises between authors during the screening process, the second independent author (TK) will intervene and further review the literature against the inclusion and exclusion criteria and overcome the differences of opinion. Furthermore, if any missing data is noted within papers, the authors will be contacted by the primary author (MK). This will ensure maximum retrieval of full-text papers when there is no full report available online.
In scoping reviews, data extraction is often referred to as “data charting” (JBI, 2022). Data charting will be undertaken using a version of the JBI data extraction tool, referred to as a charting table, modified by the authors to fit the objectives of the scoping review (Table 3) (Peters et al., 2020). An example of the data extraction tool will be included in the appendix. This charting form will be piloted on two articles, chosen at random by all authors.
This tool may be further refined in the subsequent review during the data extraction process, as the review progresses. Modifications will be detailed in the scoping review for transparency in reporting. The data that will be charted includes details surrounding the population, concept, context, study methodology, quality appraisal, findings that are significant to the review’s objective and questions. We will also extract information on the interventions including their use, whether the intervention was co-designed with AYAs and families, whether a transfer readiness assessment tool was utilised to assess the effectiveness of the intervention on transition outcomes.
The data extraction process will be transparent, and document all decisions made surrounding which literature was included or excluded and a rationale for inclusion or exclusion. An example of the data extraction tool will be included in the appendix. As identified previously, a quality appraisal will be undertaken of all results obtained, using the MMAT (Hong et al., 2018) and the CASP (Critical Appraisal Skills Programme, 2022).
Each data charting form that is completed will be documented within a Microsoft Excel spreadsheet, which will capture information for each study and will be made available for all authors involved in the review via a shared Google Drive. Literature search and screening process results will be presented within a PRIMSA-ScR flow diagram (Peters et al., 2020). Key constructs will be summarised through descriptive content analysis by the authors, in line with the JBI guidance, which advocates that scoping reviews should only incorporate basic descriptive analysis (Peters et al., 2020).
Quantitative studies retrieved will be analysed using basic frequency counts of concepts, populations, and study locations (Peters et al., 2020). Qualitative studies will be summarised through descriptive content analysis by the authors (Peters et al., 2020). Basic data coding data will be undertaken by the authors to categorise data and enable identification and clarification of concepts or definitions within the field (Peters et al., 2020). The results of the review will be discussed between the authors, and with the review team to further enhance and add meaning to the results obtained. The results of the review will be presented in the form of diagrams, tabs and graphics. The authors will be transparent and explicit in their approach to data analysis and will document all decisions made throughout the review.
Consultation for this scoping review will be undertaken in the form of an expert reference panel to support the reviewers throughout all stages of this review. This review will consult with and invite experts from Universities and Healthcare Settings in both the North and South of Ireland to act as an expert panel for this review. It is anticipated that this panel will include individuals with expertise in transitional care, paediatric nephrology multidisciplinary teams, and staff members from the world of academia. Furthermore, and importantly, the review results will be distributed to patient participation involvement (PPI) groups, including AYAs with renal disorders and families. This review is part of a larger PhD study, which is being undertaken by the primary reviewer (MK), and the scoping review will feed into the design of the primary research study.
Various dissemination strategies will be employed post completion of this scoping review. The results of the scoping review will be shared amongst various academic institutions both within Ireland and Northern Ireland. The results will be shared with multi-disciplinary teams within both adult and paediatric clinical settings on a national level that care for AYAs with renal disorders undergoing transition. The authors will engage with these teams to share and discuss the review findings and interpretations and to gather their perspective on the findings obtained from the review. The primary author will also strive to present the findings of this scoping review, through oral and poster presentations, at local, national, and international conferences, as can be facilitated. Finally, post completion of the scoping review, the author will seek publication in peer reviewed journals, such as the Journal of Pediatric Nursing. Publication in a peer-reviewed academic article is an excellent means of reaching academic, clinical and research audiences (Boland et al., 2017).
The scoping review is currently in the preliminary stages of searching the databases.
For AYAs and families living with renal disorders, the transition from paediatric to adult healthcare can be challenging. Transition is often associated with risk, health status deterioration and psychological and social stress. There is an urgent need to better understand the interventions that support AYAs living with renal disorders to obtain the required competencies to support transition to the adult healthcare setting. This scoping review will explore what is known about such interventions to promote patient satisfaction and improve patient outcome measures and experiences.
The results will offer a theoretical and empirical basis for the future development of transitional care interventions for AYAs with renal disorders. This scoping review is part of a larger PhD project examining the current transition care available for AYAs and families living with renal disorders. The results will be invaluable to feed into the research project and gain a better understanding of the interventions utilised during the transition process for this cohort of patients. The findings of this review will seek publication in a peer-reviewed journal, and may be presented at local, national, and international conferences, and shared with nephrologists, the wider multidisciplinary team, researchers, AYAs and families through rare disease and renal organisations.
This scoping review is a phase within a larger PhD degree study that will be undertaken by the first author (MK).
Is the rationale for, and objectives of, the study clearly described?
Yes
Is the study design appropriate for the research question?
Yes
Are sufficient details of the methods provided to allow replication by others?
Partly
Are the datasets clearly presented in a useable and accessible format?
Not applicable
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: I do research in health service delivery with a focus on models of care that support improved care integration. I have done research in the area of transition from paediatric to adult care for children and youth with complex care needs.
Is the rationale for, and objectives of, the study clearly described?
Yes
Is the study design appropriate for the research question?
Yes
Are sufficient details of the methods provided to allow replication by others?
Partly
Are the datasets clearly presented in a useable and accessible format?
Not applicable
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: family, pediatric palliative care, pediatric oncology
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