Health inequities in unscheduled healthcare for children with intellectual disabilities in Ireland: a study protocol

Emma Nicholson; Edel Doherty; Suja Somanadhan; Suzanne Guerin; James Schreiber; Gerard Bury; Thilo Kroll; Meredith Raley; Eilish McAuliffe

doi:10.12688/hrbopenres.12973.1

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Study Protocol

Health inequities in unscheduled healthcare for children with intellectual disabilities in Ireland: a study protocol

[version 1; peer review: 1 approved, 1 approved with reservations]

Emma Nicholson ¹, Edel Doherty², Suja Somanadhan³, [...] Suzanne Guerin⁴, James Schreiber⁵, Gerard Bury⁶, Thilo Kroll¹, Meredith Raley⁷, Eilish McAuliffe¹

Emma Nicholson ¹, Edel Doherty², [...] Suja Somanadhan³, Suzanne Guerin⁴, James Schreiber⁵, Gerard Bury⁶, Thilo Kroll¹, Meredith Raley⁷, Eilish McAuliffe¹

PUBLISHED 23 Jan 2020

Author details Author details

¹ Centre for Interdisciplinary Research, Education and Innovation in Health Systems (IRIS), University College Dublin, Belfield, Dublin 4, Ireland
² J.E. Cairnes School of Business and Economics, National University of Ireland, Galway, University Road, Galway, Ireland
³ UCD School of Nursing, Midwifery & Health Systems, University College Dublin, Belfield, Dublin 4, Ireland
⁴ UCD Centre for Disability Studies, University College Dublin, Belfield, Dublin 4, Ireland
⁵ School of Nursing, Duquesne University, Pittsburgh, PA, USA
⁶ UCD School of Medicine, University College Dublin, Belfield, Dublin 4, Ireland
⁷ Disability Federation of Ireland, Fumbally Court, Dublin 8, Ireland

Emma Nicholson
Roles: Conceptualization, Methodology, Project Administration, Writing – Original Draft Preparation, Writing – Review & Editing

Edel Doherty
Roles: Conceptualization, Methodology, Writing – Review & Editing

Suja Somanadhan
Roles: Conceptualization, Writing – Review & Editing

Suzanne Guerin
Roles: Conceptualization

James Schreiber
Roles: Data Curation, Writing – Review & Editing

Gerard Bury
Roles: Conceptualization, Methodology, Writing – Review & Editing

Thilo Kroll
Roles: Methodology

Meredith Raley
Roles: Writing – Review & Editing

Eilish McAuliffe
Roles: Conceptualization, Methodology, Writing – Review & Editing

OPEN PEER REVIEW

REVIEWER STATUS

This article is included in the Maternal and Child Health collection.

Abstract

Background: Health inequities for children with intellectual disabilities (ID) are prevalent within different health systems, and children with ID have shorter life expectancies than the general population, higher mortality rates before the age of 17 and have a greater risk of potentially preventable hospitalisations. A health systems approach to research in this area provides a useful means through which research can inform policy and practice to ensure people with ID receive equitable healthcare; however, there is a paucity of evidence regarding how to address differences that have been described in the literature to date. The overall aim of this research is to establish the extent of health inequities for children with ID in Ireland compared to children without ID with respect to their utilisation of primary care and rates of hospitalisation, and to gain a better understanding of what influences utilisation of primary care and ED services in this population.
Methods and analysis: The design of this research adopts a mixed-methods approach: statistical analysis of health data to determine the extent of health inequities in relation to healthcare utilisation; discrete choice experiments to explore General Practitioners’ decision making and parental preferences for optimal care; and concept mapping to develop consensus between stakeholders on how to address current healthcare inequities.
Discussion: By applying a systems lens to the issue of health inequities for children with ID, the research hopes to gain a thorough understanding of the varying components that can contribute to the maintenance of such healthcare inequities. A key output from the research will be a set of feasible solutions and interventions that can address health inequities for this population.

Keywords

health inequities, intellectual disability, children, unscheduled healthcare

Corresponding author: Emma Nicholson

Competing interests: No competing interests were disclosed.

Grant information: Health Research Board, Ireland [Applying Research into Policy and Practice Fellowship; ARPP-A-2018-003; to EN).
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Copyright: © 2020 Nicholson E et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to cite: Nicholson E, Doherty E, Somanadhan S et al. Health inequities in unscheduled healthcare for children with intellectual disabilities in Ireland: a study protocol [version 1; peer review: 1 approved, 1 approved with reservations]. HRB Open Res 2020, 3:3 (https://doi.org/10.12688/hrbopenres.12973.1) First published: 23 Jan 2020, 3:3 (https://doi.org/10.12688/hrbopenres.12973.1) Latest published: 16 Jul 2020, 3:3 (https://doi.org/10.12688/hrbopenres.12973.2)

Introduction

The health needs of people with intellectual disabilities (ID) are often complex and this population are known to utilise health services more often than people without ID; an effect that remains generally stable cross-culturally^1,2. Children with ID have poorer reported health status than children without and such health disparities are more marked in children and young people compared to other age groups³. This population has a shorter life expectancy than the general population, with higher mortality rates before the age of 17 in children with disabilities compared to those without⁴. In Ireland, the mortality rate of people with ID under the age of 19 is seven times higher than the general population⁵. Rates of hospitalisation also tend to be higher for this population³ with findings from Australia showing that children with Down syndrome were hospitalised at a rate five times that of the general population⁶ and, in Canada, they have higher ambulatory physician visits and a greater risk of hospitalisation due to injury, respiratory illness and diabetes⁴. A greater risk of further ill-health is exacerbated by an increased risk of socioeconomic disadvantage experienced by children with ID⁷.

Access to healthcare constitutes the fit between the individual and the health system⁸ and is influenced by a myriad of complex factors such as availability, utilisation, effectiveness and equity⁹. Access to quality primary care is associated with improved patient outcomes and reduced hospitalisation rates, however, universal access to primary care is not synonymous with equity of access¹⁰. General practitioners (GPs) experience challenges while treating people with ID related to communication difficulties, deriving incomplete medical histories, lack of knowledge regarding existing supports, and a lack of training^1,11. GPs have also expressed that time restrictions may impact upon the quality of care that they provide for patients with disabilities¹¹. Ambulatory care sensitive conditions are conditions which can be managed with access to timely and appropriate outpatient care¹². Better access to primary care may decrease utilisation of emergency departments and rates of hospitalisation for such conditions^12,13.

There is a significant lack of information related to accessing healthcare services for children with ID in comparison to the general population in an Irish context. Ireland has a national database that records details pertaining to service provision for people with ID, which aims to elucidate the service needs of people with ID in Ireland. While it is a valuable resource, not all people with disabilities are registered with the database, and needs pertaining to access and utilisation of primary care and hospitalisation rates are not recorded. Healthcare provision, planning and coordination tend to be poorer for people within the ID population compared to the wider population³, and such inequities are amenable to change by improvement in quality of healthcare¹⁴. The UN Convention on the Rights of People with Disabilities (UNCRPD) sets out that the guiding principles of the convention will need to be considered in relation to existing policy and practice. Article 25 of the convention states that health professionals are required to provide the same standard of care for people with disabilities and outlines the importance of specialist training and appropriate ethical standards in order to meet the needs of people with disabilities. Moreover, Article 31 recommends that state parties use statistical and research data to support policy planning that will give effect to the Convention and are obliged to identify and address barriers that affect the rights of people with disabilities. While it is important to establish any health disparities that exist for this population, it is also vital that models and strategies for reducing any existing inequalities are also addressed¹. Previous research has suggested that the quality of care GPs can provide people with ID is limited due to factors such as time and lack of knowledge^11,15. However, to the best of our knowledge, no previous research has sought to systematically examine and model the trade-offs that influence GP referral practices when treating children with ID.

While international evidence suggests that people with ID, including children, experience inequality in accessing healthcare¹⁶, there is a paucity of evidence relating to the decision-making by frontline staff and parents in relation to this population. Decision-making is critical within healthcare where limited resources are an ongoing concern and ultimately result in a complex interplay between stakeholder choices and behaviours, which often dictate where competing resources are allocated^17,18. Recognising the complexity of the factors that lead to health disparities for this population, beyond establishing the differences in utilisation, will be critical to identifying avoidable determinants of health disparities and how these can be modified to improve health care provision for this population¹. For instance, continuity of care has been highlighted as a preference for parents of children with developmental disabilities⁴, whereas socioeconomic disadvantages may influence access to care for this population⁸. Moreover, risk factors for emergency department utilisation and hospitalisation may be unique for this population¹⁹. Within health services research, public and patient preferences can inform policy and practice, as ensuring the consideration of all viewpoints will increase the likelihood of demands being adequately met when planning for service provision¹⁷.

There are significant gaps in the evidence base around health inequalities for people with ID whereby, the evidence was generally of low quality and heavily skewed towards psychiatric interventions²⁰. While there is a small evidence base on rates of hospitalisations for physical health conditions for this population³, there is a paucity of evidence related to access to paediatric health care for children with ID and, critically, the decision-making that drives or inhibits this access. One review examined the factors that influenced access to secondary healthcare for people with ID and found that a myriad of issues affected a persons’ experience of care, including poor communication by staff, lack of skills and knowledge about working with people with ID, and poor signage and layout in hospitals²¹. The authors argued for more targeted funding for research that adequately explores the healthcare of people with disabilities. A second systematic review sought to develop a research agenda for primary care research for people with ID and argued that a systems level approach to research would strengthen primary care and improve equitable service¹⁵.

The proposed research herein will provide information about access and utilisation of primary and emergency care of children with ID, particularly in relation to inequalities compared to children without an ID. Modelling the health status and service utilisation of children with ID at a population level is critical to determine their needs and priorities and to build a robust evidence base for policy, planning and service provision⁴. Rigorous mixed-methods research, which adopts a systems approach, will support the identification of targeted strategies and interventions that will strengthen service provision through policy and practice¹⁵. The current research project will aim to examine the utilisation of first-contact healthcare for children with ID in Ireland compared to children without ID, gain greater understanding of parental preferences and GP decision-making that drives this utilisation and finally, devise strategies for improved healthcare for this population during a time of large scale changes within the Irish health system

Methods and analysis

The proposed research will employ a mixed-methods approach over three work packages to address the research objectives. Work package 1 will establish the extent of health inequities between children with and without ID with respect to access to health status, attendance at primary and emergency care, as well as rates of emergency hospitalisations. Work package 2 will examine the decision making and referral practices of GPs and elicit parental preferences for unscheduled healthcare for their children. Finally, work package 3 will seek to utilise the evidence that emerges from the first two work packages to develop strategies for improving access to unscheduled healthcare. The culmination of work packages 1 and 2 will seek to provide a comprehensive picture of the multifaceted issues that impact access and utilisation of healthcare for this population, while work package 3 aims to provide a model of strategies generated by stakeholders in order to foster meaningful impact of the research findings.

Work Package 1. Describing differences in health care utilisation and hospitalisation between children with and without intellectual disabilities

The aim of this work package will be to compare the use of unscheduled health services and emergency hospitalisation of children with ID to children without ID. A similar approach was employed by researchers in Canada who examined 12 years of administrative data to compare health status and use of health services between children with and without developmental disabilities matched by age, gender and place of residence⁴. This method enabled the team to identify significant differences between the health status of the children with developmental disabilities compared to the matched comparison group, with greater risk of mortality before the age of 17 as well as greater risk of respiratory illness, diabetes, injuries and ambulatory care visits, also a risk factor for children with developmental disabilities. The approach and results were deemed crucial to identifying appropriate interventions to meet the service needs for this population⁴.

A cross-sectional population-based study with a matched-group design will be conducted by re-analysing data from an existing database. The databases will contain attendance data for paediatric populations from primary care across Ireland and attendance data from five emergency populations and in-patient data from children admitted to the hospital through the emergency department. Children with ID will be matched 1:3 on specific variables (e.g., age, gender, medical care status, co-morbidities) with children without ID to allow for any differences between the two populations to be established.

The research questions for this work package are as follows:

1. Do children with ID have more attendances at primary care and the emergency department compared to those without in Ireland?
2. Do children with ID have a greater risk of emergency hospitalisations for ambulatory care sensitive conditions compared to those without ID?
3. What is the profile of children with ID who experience unscheduled hospitalisations in Ireland (i.e., age, gender, reasons for emergency hospitalisation [e.g., primary diagnosis], co-morbidities and length of stay)?
4. What is the relative risk of emergency hospitalisations for children with ID compared to those without?

Data analysis plan: Propensity score matching will be used to match the children with ID to those without ID on specific covariates that may influence health outcomes. Descriptive statistics will be used to profile the patients, while chi-square tests and t-tests will allow comparisons to be made between the children with and without ID on the aforementioned factors and test the statistical significance of any variability. Relative risk (RR) will be used to determine if having an intellectual disability is a risk factor for emergency hospitalisations and 95% confidence intervals will be used to establish statistical significance.

Work Package 2. Exploring and modelling the decision-making factors that influence referral practices when treating children with ID and eliciting parental preferences for care

A discrete choice experiment (DCE) is a survey-based methodology that elucidates the relative importance of certain factors or attributes that influence decision-making and preferences. They are increasingly being used in health care research as they provide real-world clinically-relevant scenarios to model decision-making at a more granular level by exploring the trade-offs that typically occur when multiple factors are considered during the decision making processes^17,22. The underlying assumption of this methodology is that services, such as healthcare provision, can be broken into numerous characteristics, with individuals assigning differing values to each²². For example, they have been used to examine preferences for access to primary care which highlighted that waiting time for an appointment was only important to patients when attending a new health concern and, from a parental perspective, if the appointment was for a child⁸. DCEs have adequate external validity and have been shown to accurately mimic real-world decisions for choices within healthcare^22,23. The proposed research will utilise DCEs in order to generate an understanding of the factors that influence GP decision making and referral practices when working with children with ID and to elicit parental preferences for unscheduled healthcare for their children:

1. Exploring decision-making and referral practices of GPs when treating children with ID. The attributes and factors that influence GP decision making and practices regarding referral to the emergency department and wider paediatric services will be examined using the DCE methodology.
2. Eliciting parental preference for primary care for their children. Using the above DCE methodology, the research will seek to model parents’ preferences regarding primary care for children with ID

In keeping with best practice in DCE design, the following four-step approach will be taken to conduct the DCEs:

Step 1. Attribute development: An exploratory step is crucial within a DCE design to establish the attributes that potentially influence decision making and preferences and to define the levels of each attribute^24–27. Attributes may be patient, service or clinician-focused and can have numerous levels within them. For instance, in a DCE examining preferences for access to primary care, one key attribute was waiting time for an appointment with two levels being within 48 hours and in 4 days⁸. An iterative approach is necessary to select attributes and levels that contribute to most variation in decision making²⁶. This will include a systematic review to identify the relevant literature in this area and qualitative inquiry²⁷ to explore factors that influence GP referral practices with this population and parent preferences related to their child’s healthcare.

The qualitative inquiry to develop the attributes will be an iterative two-step process consisting of conceptual development to establish the attributes and then refining the language used to ensure it is meaningful for the intended population²⁶. Interviews and focus groups²⁶ will be utilised with participants including both GPs and parents of children with ID. Purposive sampling will be used to ensure maximum variation of viewpoints are obtained. Topic guides for the qualitative data collection will be developed from the results of the systematic review. The qualitative data will be analysed using the constant comparison approach²⁸, which will allow for questions to be adapted in response to emerging data, which is particularly valuable within DCE²⁶.

Step 2. Structured prioritisation exercise to finalise attributes: Given the large number of possible attributes that may be relevant in the research, it is important to narrow the focus of the DCE to ensure that the included attributes and levels are feasible and meaningful to the wider research question and to safeguard the face validity of the DCE. A structured prioritisation exercise (SPE) will determine the relative importance of the attributes and factors that emerge from the qualitative work. These will be ranked in order of priority for inclusion in the DCE and to ascertain the levels required for each attribute. Considerations for attribute inclusion will comprise of issues relating to sample size calculation, ecological validity and ensuring adequate information is provided in the DCE. A panel made up of researchers, GPs, a health economist, parents and disability advocates will use the evidence from the SPE to decide on final design of the DCE.

Step 3. Pilot study: An experimental design will be used to generate the DCE choice cards that will allow for combinations of attributes and levels to be presented to participants in manageable subsets, presented in either table format or as vignettes. The result will be a series of hypothetical scenarios that each present combinations of attributes and levels to each participant. These will be piloted to test ease of use and to determine the length of time the DCE takes to complete, as well as establishing the plausibility to ensure clinical validity.

Step 4. DCE and analysis: Purposive sampling will be utilised when recruiting participants and sample size will be determined during the design of the DCE as it is contingent on the number of factors that emerge during the exploratory phase²⁴. Recruitment of GPs and parents will target participants to ensure representation based on factors that emerge during the research, e.g., to ensure a geographic spread amongst respondents. The DCE will record relevant participant information such as age, years of experience, training, socio-economic status etc.

Random utility models (including conditional logit models and mixed logit models) will be estimated to establish which factors affect decision making and preferences and the characteristics (e.g., age, level of experience, training, socioeconomic variables) of those making the decisions¹⁸.

Work package 3. A consensus conference to generate evidence-based strategies for improving access to healthcare for children with ID

The final work package will employ a multi-stakeholder concept mapping design within a consensus conference to identify strategies for improving access to healthcare for children with ID based on the results from the two previous work packages and as a means to lessen the gap between policy and practice. Evidence from work package 1 will establish the magnitude of health access disparities for children with ID, particularly relating to a risk of preventable hospitalisations, while the DCEs in work package 2 will explicate GP referral practices and parental preferences for unscheduled healthcare for their children. Work package 3 will build on these findings in order to address areas for improvement by discussing and generating strategies in partnership with patients, parents, healthcare professionals, disability advocates and policy makers. In order to identify workable strategies for improving access to healthcare, it is crucial to engage with stakeholders from all levels of the health system to ensure that the results are aligned with needs and priorities. Concept mapping²⁹ can provide a structured format for key stakeholders, with varying degrees of expertise, and support equal contribution to the development of strategies for improving access to care and discussing the feasibility of these strategies. This methodology has been successfully implemented to address complex issues in primary care where the delivery of primary care was comprehensively explored by stakeholders to provide a practice index for GP integration³⁰. Moreover, a modified version of this approach was used to generate priorities and strategies for improving access to maternity services among women with disabilities who have experienced domestic abuse³¹.

Concept mapping is a methodology that seeks to map ideas or concepts generated by a diverse group of stakeholders through the integration of activities such as brainstorming and unstructured sorting with statistical analyses to map the ideas generated²⁹. The result is a visual map that represents the composite thinking of the group and can provide a framework for planning and programme development that incorporates complex elements perceived to be both important and feasible to stakeholders. A modified version of this approach will be adopted in this work package in the following steps:

1. Sampling and recruitment. Purposive sampling will be employed to ensure adequate representation across gender, disability-type and level of ID (i.e., mild/moderate to severe/profound). Up to 30 participants will be invited to participate and will include people with disabilities, parents of children with disabilities, disability advocates, policy makers, health and social care professionals (e.g., GPs, paediatricians, nursing staff, social care workers) and researchers and academics. Invitations will be sent out to GP surgeries, disability services, and children’s hospitals.
2. Procedure. The findings from work packages 1 and 2 will be presented to the group. Participants will then engage in a brainstorming session to derive strategies to address the issues, challenges and areas for improvement that emerge from the research in the previous work packages. Participants will then be asked to individually rank the strategies in terms of priority on a 5 point Likert scale ranging from 1 (Very High) to 5 (Not a priority) and in terms of feasibility on a 5 point Likert scale ranging from 1 (Very Feasible) to 5 (Impossible). This step is key in the production of data for concept mapping. The participants will then discuss the means through which the results of the can be used as a framework to enhance policy or practice in order to improve access to healthcare for children with ID.
3. Analysis. Findings will be synthesised and mapped to support the development of a set of recommendations for policy and practice to improve access to healthcare for children with ID. Hierarchical cluster-analysis will be used to rank and identify priority areas from the perspective of the different stakeholder groups. A bivariate plot of the two sets of ratings (priority and feasibly) will produce a ‘go zone’ graph to map the stated importance and feasibility of the strategies. The plot is divided into quadrants based on the average priority (x axis) and feasibility (y axis) scores where the top right quadrant will represent the strategies rates as being of highest priority and the most feasible. These ‘go-zones’ will identify the potential courses of action which are highly useful for planning purposes as they provide a detailed outline of the strategies that key stakeholders collectively view as important and feasible.

This procedure will enable the generation of a set of recommendations for policy and practice. Embedding stakeholder involvement throughout this process will provide a valuable mechanism to support meaningful and feasible impact of the research findings.

Ethical considerations

The proposed research has been granted full ethical approval by the University College Dublin Research Ethics Committee (Reference: LS-19-64-Nicholson). All participants will provide written consent on their own behalf for their participation in the study.

Public and patient involvement (PPI)

The project will adopt a disability-centred approach whereby patients, parents and people with disabilities will have input in the design, analysis and dissemination of the research throughout the project. At the outset of the project, a panel of PPI members comprising of parent and patient representatives from the disability community as well as disability advocates will be recruited to the project. This panel will contribute to the governance of the research and will be integral members of each work package sub-committee where they can advise and contribute to the design and analysis of the research. Members of this panel will also facilitate the consensus conference in work package 3.

Study status

Work package 1: Early stages of analysis.

Work package 2A systematic review to inform the qualitative inquiry was recently completed.

Work package 3: Not yet started.

Discussion

The overarching aim of the research is to establish the extent of health inequities for children with ID in Ireland compared to children without ID, with a focus on their utilisation of primary care and rates of hospitalisation, to gain a better understanding of what influences utilisation and avoidable hospitalisations in this population. The focus and timing of this research is of importance given the ratification of the UNCRPD in Ireland. The convention sets out guiding principles that will need to be considered in relation to existing policy and practice; however, there is a paucity of research evidence in Ireland to ascertain health inequities for this population. Applying a systems-approach, whereby the various components of the health systems in which the health inequities and the intricacies of the relationships between these will be considered, can provide evidence towards understating health inequities for this population and seek to identify interventions that can address them^15,32.

While describing the health inequities experienced by people with ID is an important element for study, research must endeavour to establish the causal factors behind inequities, such as increased hospitalisations³, and examine whether they can be considered avoidable and unjust¹ and critically, amenable to improvements in the quality of care¹⁴. The inclusion of the DCE methodology can provide explanatory models that have important applications within policy making in health and, critically, can point to modifiable factors that contribute to any disparities in referral patterns experienced by this population. GPs are required to make highly complex decisions within health systems of scarce resourcing and thus, establishing the trade-offs they dictate, their behaviour is important for planning purposes²⁵. Moreover, preferences for healthcare beyond outcomes alone are important for planning quality care¹⁸ and eliciting parents’ stated preferences for first contact care for children with ID will be key to identifying opportunities for interventions that can support meaningful change. Finally, visits to the emergency department and subsequent emergency hospitalisations are more expensive than primary care¹⁹ and generally, overcrowding can result in poorer health outcomes for children³³.

In keeping with the disability-centred approach of the project, ongoing and continuous knowledge exchange activities will be adopted to support an accessible and wide-reaching dissemination plan. Drawing on an evidence-based model for knowledge transfer of health research³⁴, dissemination will strategically target stakeholders with materials designed specifically for their needs and through avenues chosen to maximise their reach. Four key components will be considered when disseminating the research: messages, stakeholders, processes and contexts. For instance, workshops will be held with health care professionals to outline the results from the studies and receive feedback. A key output from the project will be a set of recommendations developed in collaboration with stakeholders that will be aimed at policymakers. Alongside traditional peer-reviewed publications, accessible materials, such as infographics, will be created to communicate the results from each work package to the disability community. These will outline the results in clear and accessible formats using lay terminology and will be designed with the PPI panel members and developed by a graphic designer to ensure their suitability for dissemination to the general population.

Limitations

Potential inconsistencies in the reporting of ID within the Irish health system may be a limitation for the proposed research, as it may hinder our ability to accurately identify patients with ID from the data administrative systems. For instance, people with mild ID may be significantly underrepresented in the data systems as their care needs will not be considered as great as people with severe and profound ID. Understanding the extent of reporting of ID will be beneficial in and of itself, in order to raise awareness of the differences in health presentations for this population, which may not be widely known among those involved with practice and planning⁵. Monitoring trends and identifying any health disparities for this population is crucial for the development of appropriate interventions that will facilitate good health for people with ID³⁵. The recent ratification of the UNCRPD requires the government to use research and statistical data to develop policies that give effect to the Convention¹⁹ and the availability of appropriate data is key for policy and planning purposes.

Conclusion

The proposed programme of research will apply a systems lens to the issue of health inequities for children with ID, specifically in relation to unscheduled healthcare. Across three work packages, the research will establish the extent of inequities for this population in relation to utilisation of unscheduled health services, elicit parents’ preferences for their children’s healthcare, as well as model the factors that influence GP decision-making. Finally, the study will seek to identify feasible solutions and interventions that can address health inequities for this population.

Data availability

No data are associated with this article.

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References

1. Ouellette-Kuntz H: Understanding Health Disparities and Inequities Faced by Individuals with Intellectual Disabilities. J Appl Res Intellect. 2005; 18(2): 113–21. Publisher Full Text
2. Krahn GL, Fox MH: Health disparities of adults with intellectual disabilities: what do we know? What do we do? J Appl Res Intellect Disabil. 2014; 27(5): 431–46. PubMed Abstract | Publisher Full Text | Free Full Text
3. Dunn K, Hughes-McCormack L, Cooper SA: Hospital admissions for physical health conditions for people with intellectual disabilities: Systematic review. J Appl Res Intellect Disabil. 2018; 31 Suppl 1: 1–10. PubMed Abstract | Publisher Full Text
4. Shooshtari S, Brownell M, Mills RSL, et al.: Comparing Health Status, Health Trajectories and Use of Health and Social Services between Children with and without Developmental Disabilities: A Population-based Longitudinal Study in Manitoba. J Appl Res Intellect Disabil. 2017; 30(4): 584–601. PubMed Abstract | Publisher Full Text
5. McCarron M, Carroll R, Kelly C, et al.: Mortality Rates in the General Irish Population Compared to those with an Intellectual Disability from 2003 to 2012. J Appl Res Intellect Disabil. 2015; 28(5): 406–13. PubMed Abstract | Publisher Full Text
6. Fitzgerald P, Leonard H, Pikora TJ, et al.: Hospital admissions in children with down syndrome: experience of a population-based cohort followed from birth. PLoS One. 2013; 8(8): e70401. PubMed Abstract | Publisher Full Text | Free Full Text
7. Emerson E, Hatton C: Poverty, socio-economic position, social capital and the health of children and adolescents with intellectual disabilities in Britain: a replication. J Intellect Disabil Res. 2007; 51(Pt 11): 866–74. PubMed Abstract | Publisher Full Text
8. Rubin G, Bate A, George A, et al.: Preferences for access to the GP: a discrete choice experiment. Br J Gen Pract. 2006; 56(531): 743–8. PubMed Abstract | Free Full Text
9. Chapman JL, Zechel A, Carter YH, et al.: Systematic review of recent innovations in service provision to improve access to primary care. Br J Gen Pract. 2004; 54(502): 374–81. PubMed Abstract | Free Full Text
10. Cecil E, Bottle A, Cowling TE, et al.: Primary Care Access, Emergency Department Visits, and Unplanned Short Hospitalizations in the UK. Pediatrics. 2016; 137(2): e20151492. PubMed Abstract | Publisher Full Text
11. Lennox NG, Diggens JN, Ugoni AM: The general practice care of people with intellectual disability: barriers and solutions. J Intellect Disabil Res. 1997; 41(Pt 5): 380–90. PubMed Abstract | Publisher Full Text
12. Roos LL, Walld R, Uhanova J, et al.: Physician visits, hospitalizations, and socioeconomic status: ambulatory care sensitive conditions in a canadian setting. Health Serv Res. 2005; 40(4): 1167–85. PubMed Abstract | Publisher Full Text | Free Full Text
13. Balogh R, Brownell M, Ouellette-Kuntz H, et al.: Hospitalisation rates for ambulatory care sensitive conditions for persons with and without an intellectual disability--a population perspective. J Intellect Disabil Res. 2010; 54(9): 820–32. PubMed Abstract | Publisher Full Text
14. Heslop P, Blair PS, Fleming P, et al.: The Confidential Inquiry into premature deaths of people with intellectual disabilities in the UK: a population-based study. Lancet. 2014; 383(9920): 889–95. PubMed Abstract | Publisher Full Text
15. Lennox N, Van Driel ML, van Dooren K: Supporting primary healthcare professionals to care for people with intellectual disability: a research agenda. J Appl Res Intellect Disabil. 2015; 28(1): 33–42. PubMed Abstract | Publisher Full Text
16. Emerson E: The determinants of health inequities experienced by children with learning disabilities. Public Health England. 2015. Reference Source
17. Louviere JJ, Lancsar E: Choice experiments in health: the good, the bad, the ugly and toward a brighter future. Health Econ Policy Law. 2009; 4(Pt 4): 527–46. PubMed Abstract | Publisher Full Text
18. Ryan M: Discrete choice experiments in health care. BMJ. 2004; 328(7436): 360–1. PubMed Abstract | Publisher Full Text | Free Full Text
19. Blaskowitz MG, Hernandez B, Scott PW: Predictors of Emergency Room and Hospital Utilization Among Adults With Intellectual and Developmental Disabilities (IDD). Intellect Dev Disabil. 2019; 57(2): 127–45. PubMed Abstract | Publisher Full Text
20. Robertson J, Hatton C, Baines S, et al.: Systematic Reviews of the Health or Health care of People with Intellectual Disabilities: A Systematic Review to Identify Gaps in the Evidence Base. J Appl Res Intellect Disabil. 2015; 28(6): 455–523. PubMed Abstract | Publisher Full Text
21. Backer C, Chapman M, Mitchell D: Access to Secondary Healthcare for People with Intellectual Disabilities: A Review of the Literature. J Appl Res Intellect Disabil. 2009; 22(6): 514–25. Publisher Full Text
22. Clark MD, Determann D, Petrou S, et al.: Discrete choice experiments in health economics: a review of the literature. Pharmacoeconomics. 2014; 32(9): 883–902. PubMed Abstract | Publisher Full Text
23. de Bekker-Grob EW, Swait JD, Kassahun HT, et al.: Are Healthcare Choices Predictable? The Impact of Discrete Choice Experiment Designs and Models. Value Health. 2019; 22(9): 1050–62. PubMed Abstract | Publisher Full Text
24. De Brún A, Flynn D, Joyce K, et al.: Understanding clinicians' decisions to offer intravenous thrombolytic treatment to patients with acute ischaemic stroke: a protocol for a discrete choice experiment. BMJ Open. 2014; 4(7): e005612. PubMed Abstract | Publisher Full Text | Free Full Text
25. Lancsar E, Louviere J: Conducting discrete choice experiments to inform healthcare decision making: a user's guide. Pharmacoeconomics. 2008; 26(8): 661–77. PubMed Abstract | Publisher Full Text
26. Coast J, Al-Janabi H, Sutton EJ, et al.: Using qualitative methods for attribute development for discrete choice experiments: issues and recommendations. Health Econ. 2012; 21(6): 730–41. PubMed Abstract | Publisher Full Text
27. Kløjgaard ME, Bech M, Søgaard R: Designing a Stated Choice Experiment: The Value of a Qualitative Process. J Choice Model. 2012; 5(2): 1–18. Publisher Full Text
28. Glaser BG, Strauss AL: The discovery of grounded theory: strategies for qualitative research. New York: Aldine de Gruyter; 1999. Publisher Full Text
29. Trochim W, Kane M: Concept mapping: an introduction to structured conceptualization in health care. Int J Qual Health Care. 2005; 17(3): 187–91. PubMed Abstract | Publisher Full Text
30. Southern DM, Young D, Dunt D, et al.: Integration of primary health care services: perceptions of Australian general practitioners, non-general practitioner health service providers and consumers at the general practice–primary care interface. Eval Program Plann. 2002; 25(1): 47–59. Publisher Full Text
31. Bradbury-Jones C, Breckenridge JP, Devaney J, et al.: Disabled women's experiences of accessing and utilising maternity services when they are affected by domestic abuse: a critical incident technique study. BMC Pregnancy Childbirth. 2015; 15(1): 181. PubMed Abstract | Publisher Full Text | Free Full Text
32. Don de Savigny, Adam T, Alliance for Health Policy and Systems Research, et al.: Systems thinking for health systems strengthening. Geneva: World Health Organization (WHO); 2009. Reference Source
33. Chan M, Meckler G, Doan Q: Paediatric emergency department overcrowding and adverse patient outcomes. Paediatr Child Health. 2017; 22(7): 377–81. PubMed Abstract | Publisher Full Text | Free Full Text
34. Payne C, Brown MJ, Guerin S, et al.: EMTReK: An Evidence-based Model for the Transfer & Exchange of Research Knowledge— Five Case Studies in Palliative Care. SAGE Open Nurs. 2019; 5: 2377960819861854. Publisher Full Text
35. Lauer E, McCallion P: Mortality of People with Intellectual and Developmental Disabilities from Select US State Disability Service Systems and Medical Claims Data. J Appl Res Intellect Disabil. 2015; 28(5): 394–405. PubMed Abstract | Publisher Full Text

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Version 2

VERSION 2 PUBLISHED 23 Jan 2020

Author details Author details

Emma Nicholson
Roles: Conceptualization, Methodology, Project Administration, Writing – Original Draft Preparation, Writing – Review & Editing

Edel Doherty
Roles: Conceptualization, Methodology, Writing – Review & Editing

Suja Somanadhan
Roles: Conceptualization, Writing – Review & Editing

Suzanne Guerin
Roles: Conceptualization

James Schreiber
Roles: Data Curation, Writing – Review & Editing

Gerard Bury
Roles: Conceptualization, Methodology, Writing – Review & Editing

Thilo Kroll
Roles: Methodology

Meredith Raley
Roles: Writing – Review & Editing

Eilish McAuliffe
Roles: Conceptualization, Methodology, Writing – Review & Editing

Competing interests

No competing interests were disclosed.

Grant information

Health Research Board, Ireland [Applying Research into Policy and Practice Fellowship; ARPP-A-2018-003; to EN).
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Article Versions (2)

version 2

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Published: 16 Jul 2020, 3:3

https://doi.org/10.12688/hrbopenres.12973.2

version 1

Published: 23 Jan 2020, 3:3

https://doi.org/10.12688/hrbopenres.12973.1

© 2020 Nicholson E et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Nicholson E, Doherty E, Somanadhan S et al. Health inequities in unscheduled healthcare for children with intellectual disabilities in Ireland: a study protocol [version 1; peer review: 1 approved, 1 approved with reservations]. HRB Open Res 2020, 3:3 (https://doi.org/10.12688/hrbopenres.12973.1)

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Reviewer Report 07 May 2020

Reema Harrison, School of Public Health and Community Medicine, University of New South Wales, Sydney, Australia

Approved

https://doi.org/10.21956/hrbopenres.14058.r27298

This protocol presents the proposed study of the utilisation of primary and emergency care amongst children with intellectual disability to understand the influences on this population through a healthcare equity lens.

The project addresses a significant and under-researched area that is of critical importance to health system equity, sustainability, value and quality. The program of work outlined integrates a range of relevant methods to generate the data required to address the proposed questions. The data quality relating to the identification of children with and without intellectual disability is unclear and given the lack of high-quality data identified elsewhere, it may be worth considering the implications of this for the proposed work.

Areas for further consideration:

It is notable that the terminology is a little inconsistent regarding intellectual disability, children and disability and would benefit from clarification. This may be in part due to reliance on literature relating to adult populations or disability more generally to form the development of the study but warrants review across the piece for clarity in some areas.

Whilst a mixed-methods approach is identified, there is insufficient detail as to the process of data synthesis and how these studies collectively address the research questions. Currently, the work packages appear to flow one after the other but it is not clear as to how there will be a higher level synthesis of the knowledge. Overall, whilst the methods are well-described, there is insufficient detail in some of the areas to enable replication based on the protocol alone.

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: Health services research; healthcare quality; patient safety.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

CITE

Report a concern

Author Response 16 Jul 2020

Emma Nicholson, Centre for Interdisciplinary Research, Education and Innovation in Health Systems (IRIS), University College Dublin, Belfield, Ireland

16 Jul 2020

Author Response
This protocol presents the proposed study of the utilisation of primary and emergency care amongst children with intellectual disability to understand the influences on this population through a healthcare equity ... Continue reading
This protocol presents the proposed study of the utilisation of primary and emergency care amongst children with intellectual disability to understand the influences on this population through a healthcare equity lens.

The project addresses a significant and under-researched area that is of critical importance to health system equity, sustainability, value and quality. The program of work outlined integrates a range of relevant methods to generate the data required to address the proposed questions. The data quality relating to the identification of children with and without intellectual disability is unclear and given the lack of high-quality data identified elsewhere, it may be worth considering the implications of this for the proposed work.

The Introduction and Discussion have been amended to address potential international impact

Areas for further consideration:
It is notable that the terminology is a little inconsistent regarding intellectual disability, children and disability and would benefit from clarification. This may be in part due to reliance on literature relating to adult populations or disability more generally to form the development of the study but warrants review across the piece for clarity in some areas.

This has been addressed and intellectual disability has been used throughout

Whilst a mixed-methods approach is identified, there is insufficient detail as to the process of data synthesis and how these studies collectively address the research questions. Currently, the work packages appear to flow one after the other but it is not clear as to how there will be a higher level synthesis of the knowledge. Overall, whilst the methods are well-described, there is insufficient detail in some of the areas to enable replication based on the protocol alone.

Given there is no plan to specifically triangulate data, the term ‘multi-method’ has been used in place of mixed-methods. A figure has also been included to outline the project (see Figure 1). Greater detail has been provided in the method sections.
This protocol presents the proposed study of the utilisation of primary and emergency care amongst children with intellectual disability to understand the influences on this population through a healthcare equity lens.

The project addresses a significant and under-researched area that is of critical importance to health system equity, sustainability, value and quality. The program of work outlined integrates a range of relevant methods to generate the data required to address the proposed questions. The data quality relating to the identification of children with and without intellectual disability is unclear and given the lack of high-quality data identified elsewhere, it may be worth considering the implications of this for the proposed work.

The Introduction and Discussion have been amended to address potential international impact

Areas for further consideration:
It is notable that the terminology is a little inconsistent regarding intellectual disability, children and disability and would benefit from clarification. This may be in part due to reliance on literature relating to adult populations or disability more generally to form the development of the study but warrants review across the piece for clarity in some areas.

This has been addressed and intellectual disability has been used throughout

Whilst a mixed-methods approach is identified, there is insufficient detail as to the process of data synthesis and how these studies collectively address the research questions. Currently, the work packages appear to flow one after the other but it is not clear as to how there will be a higher level synthesis of the knowledge. Overall, whilst the methods are well-described, there is insufficient detail in some of the areas to enable replication based on the protocol alone.

Given there is no plan to specifically triangulate data, the term ‘multi-method’ has been used in place of mixed-methods. A figure has also been included to outline the project (see Figure 1). Greater detail has been provided in the method sections.
Competing Interests: No competing interests were disclosed. Close
Report a concern
Respond or Comment

COMMENTS ON THIS REPORT

Author Response 16 Jul 2020

Emma Nicholson, Centre for Interdisciplinary Research, Education and Innovation in Health Systems (IRIS), University College Dublin, Belfield, Ireland

16 Jul 2020

Author Response
This protocol presents the proposed study of the utilisation of primary and emergency care amongst children with intellectual disability to understand the influences on this population through a healthcare equity ... Continue reading
This protocol presents the proposed study of the utilisation of primary and emergency care amongst children with intellectual disability to understand the influences on this population through a healthcare equity lens.

The project addresses a significant and under-researched area that is of critical importance to health system equity, sustainability, value and quality. The program of work outlined integrates a range of relevant methods to generate the data required to address the proposed questions. The data quality relating to the identification of children with and without intellectual disability is unclear and given the lack of high-quality data identified elsewhere, it may be worth considering the implications of this for the proposed work.

The Introduction and Discussion have been amended to address potential international impact

Areas for further consideration:
It is notable that the terminology is a little inconsistent regarding intellectual disability, children and disability and would benefit from clarification. This may be in part due to reliance on literature relating to adult populations or disability more generally to form the development of the study but warrants review across the piece for clarity in some areas.

This has been addressed and intellectual disability has been used throughout

Whilst a mixed-methods approach is identified, there is insufficient detail as to the process of data synthesis and how these studies collectively address the research questions. Currently, the work packages appear to flow one after the other but it is not clear as to how there will be a higher level synthesis of the knowledge. Overall, whilst the methods are well-described, there is insufficient detail in some of the areas to enable replication based on the protocol alone.

Given there is no plan to specifically triangulate data, the term ‘multi-method’ has been used in place of mixed-methods. A figure has also been included to outline the project (see Figure 1). Greater detail has been provided in the method sections.
This protocol presents the proposed study of the utilisation of primary and emergency care amongst children with intellectual disability to understand the influences on this population through a healthcare equity lens.

The project addresses a significant and under-researched area that is of critical importance to health system equity, sustainability, value and quality. The program of work outlined integrates a range of relevant methods to generate the data required to address the proposed questions. The data quality relating to the identification of children with and without intellectual disability is unclear and given the lack of high-quality data identified elsewhere, it may be worth considering the implications of this for the proposed work.

The Introduction and Discussion have been amended to address potential international impact

Areas for further consideration:
It is notable that the terminology is a little inconsistent regarding intellectual disability, children and disability and would benefit from clarification. This may be in part due to reliance on literature relating to adult populations or disability more generally to form the development of the study but warrants review across the piece for clarity in some areas.

This has been addressed and intellectual disability has been used throughout

Whilst a mixed-methods approach is identified, there is insufficient detail as to the process of data synthesis and how these studies collectively address the research questions. Currently, the work packages appear to flow one after the other but it is not clear as to how there will be a higher level synthesis of the knowledge. Overall, whilst the methods are well-described, there is insufficient detail in some of the areas to enable replication based on the protocol alone.

Given there is no plan to specifically triangulate data, the term ‘multi-method’ has been used in place of mixed-methods. A figure has also been included to outline the project (see Figure 1). Greater detail has been provided in the method sections.
Competing Interests: No competing interests were disclosed. Close
Report a concern

Views

Reviewer Report 12 Feb 2020

Lisa O'Leary, Edinburgh Napier University, Edinburgh, UK

Approved with Reservations

https://doi.org/10.21956/hrbopenres.14058.r27143

This is an important protocol for a potentially valuable study which has the potential to address health inequities experienced by children with ID in Ireland. I recommend this for indexing (subject to a few minor changes which I have specified in the summary below).

A clear rationale has been provided for this study and the objectives of the study have been clearly described. The authors have clearly identified the evidence base for poorer health outcomes in children with ID compared to the general population (with specific reference to higher mortality rates and higher hospital admissions amongst children with ID compared to equivalent general population). They have made reference to studies undertaken both within an Irish and international context, in order to demonstrate this evidence.

The authors have made reference to how inequitable access to health care may contribute to these poorer health outcomes in children with ID. They have also identified a gap in the evidence within an Irish context, wherein there is currently a lack of information related to accessing healthcare services for children with ID. They have referred to UNCRPD principles and gaps in research studies in order to emphasise the rationale for specifically investigating the complexity of factors that lead to health disparities in children with ID. The authors have emphasised the relevance of this within an Irish context (given the ratification of the UNCRPD). However, it would also have been helpful, if the authors could identify how the findings from this prospective study could have international impact on children with ID. This could increase the wider potential impact of the study.

The mixed methods three work package design appears appropriate for the research question. It would have been helpful if a figure was included in order to illustrate how each phase follows on and is integrated to the next, in terms of answering the research question. It would also be helpful to know what specific type of mixed method design is proposed? Do the authors propose to triangulate the results from each of the work packages (phases) of the study in any way?

The authors have identified how they will establish the extent of health inequities between children with and without LD in relation to access to healthcare in the first phase of the study (work package 1). The authors have identified how they will match the cases. They have reported how they will represent the demographic profile of the participants. They have identified the intended statistical tests for drawing comparisons with the general population.

However, I would recommend the following amendment for work package 1 phase, in order to ensure the data analysis plan in described in detail and allows replication by others. More information is required on the following in relation to work package 1. How is the proposed approach similar to the method used in Canada? Were there any adaptions that were made for the current study? How many children with ID are in this database? What specific age groups will the children be subdivided into for the purpose of analysis? What is the gender breakdown of the children in this database? How will missing data be treated? How many matched children are in this database?

The authors have identified how they will use a discrete choice experiment to examine the decision making and referral process of GPs and identify parental preference for unscheduled care for treatment in phase 2 (work package 2). They have specified the four steps of this experiment. In the first attribute development step, they have identified that a systematic review and qualitative inquiry will be undertaken in order to identify the attributes that influence decision making. It would have been helpful if more detail was provided in relation to how the findings from the review will be explored further in the qualitative inquiry. They have specified how the second structured prioritisation exercise to finalise attributes will be undertaken. They have identified that the discrete choice experiment cards will subsequently be piloted in the third phase (specifically looking at length of time/ease of use of completion). It would have been helpful if some information about planned sample of participants in phase 3 could have been included (intended number of participants, age, gender breakdown etc.). The sampling, recruitment and analysis plan for step 4 is clearly identified.

The authors have identified how the concept mapping approach in package 3 builds on findings from step 1 and 2. This is clearly reported and it is identified that the purpose of this is to elicit stakeholders’ recommendations for policy and practice.

Additional comments: the authors used the interchangeable terms of intellectual disability (ID) and disability throughout the transcript. It is suggested that if the focus of this study is just on children with an ID as opposed to children with any type of ‘disability’, then ID should be used instead of disability.

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: Intellectual disabilities, mixed methods, systematic reviews, complex interventions, mortality patterns in people with intellectual disabilities, respiratory health.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.

CITE

Report a concern

Author Response 16 Jul 2020

Emma Nicholson, Centre for Interdisciplinary Research, Education and Innovation in Health Systems (IRIS), University College Dublin, Belfield, Ireland

16 Jul 2020

Author Response
This is an important protocol for a potentially valuable study which has the potential to address health inequities experienced by children with ID in Ireland. I recommend this for indexing ... Continue reading
This is an important protocol for a potentially valuable study which has the potential to address health inequities experienced by children with ID in Ireland. I recommend this for indexing (subject to a few minor changes which I have specified in the summary below).

A clear rationale has been provided for this study and the objectives of the study have been clearly described. The authors have clearly identified the evidence base for poorer health outcomes in children with ID compared to the general population (with specific reference to higher mortality rates and higher hospital admissions amongst children with ID compared to equivalent general population). They have made reference to studies undertaken both within an Irish and international context, in order to demonstrate this evidence.

The authors have made reference to how inequitable access to health care may contribute to these poorer health outcomes in children with ID. They have also identified a gap in the evidence within an Irish context, wherein there is currently a lack of information related to accessing healthcare services for children with ID. They have referred to UNCRPD principles and gaps in research studies in order to emphasise the rationale for specifically investigating the complexity of factors that lead to health disparities in children with ID. The authors have emphasised the relevance of this within an Irish context (given the ratification of the UNCRPD). However, it would also have been helpful, if the authors could identify how the findings from this prospective study could have international impact on children with ID. This could increase the wider potential impact of the study.

The Introduction and Discussion have been amended to address potential international impact

The mixed methods three work package design appears appropriate for the research question. It would have been helpful if a figure was included in order to illustrate how each phase follows on and is integrated to the next, in terms of answering the research question.

A figure has been included to illustrate the project (see Figure 1)

It would also be helpful to know what specific type of mixed method design is proposed? The term mixed methods reflects the variety of methods that will be used. Given there is no aim to triangulate

Multi-method is a more appropriate term to describe the project and this has been amended throughout

Do the authors propose to triangulate the results from each of the work packages (phases) of the study in any way?

No, the data will not be triangulated

The authors have identified how they will establish the extent of health inequities between children with and without LD in relation to access to healthcare in the first phase of the study (work package 1). The authors have identified how they will match the cases. They have reported how they will represent the demographic profile of the participants. They have identified the intended statistical tests for drawing comparisons with the general population.

However, I would recommend the following amendment for work package 1 phase, in order to ensure the data analysis plan in described in detail and allows replication by others. More information is required on the following in relation to work package
1.         How is the proposed approach similar to the method used in Canada?

The reference to this study has been removed

2.         Were there any adaptions that were made for the current study?

See above

3.         How many children with ID are in this database?

It is unclear at this stage how many children with ID are in the databases but it has

4.         What specific age groups will the children be subdivided into for the purpose of analysis?

There is no plan to subdivide the children into age groups.

5.         What is the gender breakdown of the children in this database?

Unknown at this stage, but it is expected that there will be more males than females in keeping with data from the CSO.

6.         How will missing data be treated?

This has been addressed in the section ‘Data Analysis Plan’.

7.         How many matched children are in this database?

Sample sizes have been provided where possible.

The authors have identified how they will use a discrete choice experiment to examine the decision making and referral process of GPs and identify parental preference for unscheduled care for treatment in phase 2 (work package 2). They have specified the four steps of this experiment. In the first attribute development step, they have identified that a systematic review and qualitative inquiry will be undertaken in order to identify the attributes that influence decision making. It would have been helpful if more detail was provided in relation to how the findings from the review will be explored further in the qualitative inquiry. They have specified how the second structured prioritisation exercise to finalise attributes will be undertaken. They have identified that the discrete choice experiment cards will subsequently be piloted in the third phase (specifically looking at length of time/ease of use of completion). It would have been helpful if some information about planned sample of participants in phase 3 could have been included (intended number of participants, age, gender breakdown etc.). The sampling, recruitment and analysis plan for step 4 is clearly identified. The authors have identified how the concept mapping approach in package 3 builds on findings from step 1 and 2. This is clearly reported and it is identified that the purpose of this is to elicit stakeholders’ recommendations for policy and practice.

Additional comments: the authors used the interchangeable terms of intellectual disability (ID) and disability throughout the transcript. It is suggested that if the focus of this study is just on children with an ID as opposed to children with any type of ‘disability’, then ID should be used instead of disability.

The acronym ID has been removed and replaced with intellectual disabilities. Any reference to disability has also been removed and replaced with intellectual disabilities
This is an important protocol for a potentially valuable study which has the potential to address health inequities experienced by children with ID in Ireland. I recommend this for indexing (subject to a few minor changes which I have specified in the summary below).

A clear rationale has been provided for this study and the objectives of the study have been clearly described. The authors have clearly identified the evidence base for poorer health outcomes in children with ID compared to the general population (with specific reference to higher mortality rates and higher hospital admissions amongst children with ID compared to equivalent general population). They have made reference to studies undertaken both within an Irish and international context, in order to demonstrate this evidence.

The authors have made reference to how inequitable access to health care may contribute to these poorer health outcomes in children with ID. They have also identified a gap in the evidence within an Irish context, wherein there is currently a lack of information related to accessing healthcare services for children with ID. They have referred to UNCRPD principles and gaps in research studies in order to emphasise the rationale for specifically investigating the complexity of factors that lead to health disparities in children with ID. The authors have emphasised the relevance of this within an Irish context (given the ratification of the UNCRPD). However, it would also have been helpful, if the authors could identify how the findings from this prospective study could have international impact on children with ID. This could increase the wider potential impact of the study.

The Introduction and Discussion have been amended to address potential international impact

The mixed methods three work package design appears appropriate for the research question. It would have been helpful if a figure was included in order to illustrate how each phase follows on and is integrated to the next, in terms of answering the research question.

A figure has been included to illustrate the project (see Figure 1)

It would also be helpful to know what specific type of mixed method design is proposed? The term mixed methods reflects the variety of methods that will be used. Given there is no aim to triangulate

Multi-method is a more appropriate term to describe the project and this has been amended throughout

Do the authors propose to triangulate the results from each of the work packages (phases) of the study in any way?

No, the data will not be triangulated

The authors have identified how they will establish the extent of health inequities between children with and without LD in relation to access to healthcare in the first phase of the study (work package 1). The authors have identified how they will match the cases. They have reported how they will represent the demographic profile of the participants. They have identified the intended statistical tests for drawing comparisons with the general population.

However, I would recommend the following amendment for work package 1 phase, in order to ensure the data analysis plan in described in detail and allows replication by others. More information is required on the following in relation to work package
1.         How is the proposed approach similar to the method used in Canada?

The reference to this study has been removed

2.         Were there any adaptions that were made for the current study?

See above

3.         How many children with ID are in this database?

It is unclear at this stage how many children with ID are in the databases but it has

4.         What specific age groups will the children be subdivided into for the purpose of analysis?

There is no plan to subdivide the children into age groups.

5.         What is the gender breakdown of the children in this database?

Unknown at this stage, but it is expected that there will be more males than females in keeping with data from the CSO.

6.         How will missing data be treated?

This has been addressed in the section ‘Data Analysis Plan’.

7.         How many matched children are in this database?

Sample sizes have been provided where possible.

The authors have identified how they will use a discrete choice experiment to examine the decision making and referral process of GPs and identify parental preference for unscheduled care for treatment in phase 2 (work package 2). They have specified the four steps of this experiment. In the first attribute development step, they have identified that a systematic review and qualitative inquiry will be undertaken in order to identify the attributes that influence decision making. It would have been helpful if more detail was provided in relation to how the findings from the review will be explored further in the qualitative inquiry. They have specified how the second structured prioritisation exercise to finalise attributes will be undertaken. They have identified that the discrete choice experiment cards will subsequently be piloted in the third phase (specifically looking at length of time/ease of use of completion). It would have been helpful if some information about planned sample of participants in phase 3 could have been included (intended number of participants, age, gender breakdown etc.). The sampling, recruitment and analysis plan for step 4 is clearly identified. The authors have identified how the concept mapping approach in package 3 builds on findings from step 1 and 2. This is clearly reported and it is identified that the purpose of this is to elicit stakeholders’ recommendations for policy and practice.

Additional comments: the authors used the interchangeable terms of intellectual disability (ID) and disability throughout the transcript. It is suggested that if the focus of this study is just on children with an ID as opposed to children with any type of ‘disability’, then ID should be used instead of disability.

The acronym ID has been removed and replaced with intellectual disabilities. Any reference to disability has also been removed and replaced with intellectual disabilities
Competing Interests: No competing interests were disclosed. Close
Report a concern
Respond or Comment

COMMENTS ON THIS REPORT

Author Response 16 Jul 2020

Emma Nicholson, Centre for Interdisciplinary Research, Education and Innovation in Health Systems (IRIS), University College Dublin, Belfield, Ireland

16 Jul 2020

Author Response
This is an important protocol for a potentially valuable study which has the potential to address health inequities experienced by children with ID in Ireland. I recommend this for indexing ... Continue reading
This is an important protocol for a potentially valuable study which has the potential to address health inequities experienced by children with ID in Ireland. I recommend this for indexing (subject to a few minor changes which I have specified in the summary below).

A clear rationale has been provided for this study and the objectives of the study have been clearly described. The authors have clearly identified the evidence base for poorer health outcomes in children with ID compared to the general population (with specific reference to higher mortality rates and higher hospital admissions amongst children with ID compared to equivalent general population). They have made reference to studies undertaken both within an Irish and international context, in order to demonstrate this evidence.

The authors have made reference to how inequitable access to health care may contribute to these poorer health outcomes in children with ID. They have also identified a gap in the evidence within an Irish context, wherein there is currently a lack of information related to accessing healthcare services for children with ID. They have referred to UNCRPD principles and gaps in research studies in order to emphasise the rationale for specifically investigating the complexity of factors that lead to health disparities in children with ID. The authors have emphasised the relevance of this within an Irish context (given the ratification of the UNCRPD). However, it would also have been helpful, if the authors could identify how the findings from this prospective study could have international impact on children with ID. This could increase the wider potential impact of the study.

The Introduction and Discussion have been amended to address potential international impact

The mixed methods three work package design appears appropriate for the research question. It would have been helpful if a figure was included in order to illustrate how each phase follows on and is integrated to the next, in terms of answering the research question.

A figure has been included to illustrate the project (see Figure 1)

It would also be helpful to know what specific type of mixed method design is proposed? The term mixed methods reflects the variety of methods that will be used. Given there is no aim to triangulate

Multi-method is a more appropriate term to describe the project and this has been amended throughout

Do the authors propose to triangulate the results from each of the work packages (phases) of the study in any way?

No, the data will not be triangulated

The authors have identified how they will establish the extent of health inequities between children with and without LD in relation to access to healthcare in the first phase of the study (work package 1). The authors have identified how they will match the cases. They have reported how they will represent the demographic profile of the participants. They have identified the intended statistical tests for drawing comparisons with the general population.

However, I would recommend the following amendment for work package 1 phase, in order to ensure the data analysis plan in described in detail and allows replication by others. More information is required on the following in relation to work package
1.         How is the proposed approach similar to the method used in Canada?

The reference to this study has been removed

2.         Were there any adaptions that were made for the current study?

See above

3.         How many children with ID are in this database?

It is unclear at this stage how many children with ID are in the databases but it has

4.         What specific age groups will the children be subdivided into for the purpose of analysis?

There is no plan to subdivide the children into age groups.

5.         What is the gender breakdown of the children in this database?

Unknown at this stage, but it is expected that there will be more males than females in keeping with data from the CSO.

6.         How will missing data be treated?

This has been addressed in the section ‘Data Analysis Plan’.

7.         How many matched children are in this database?

Sample sizes have been provided where possible.

The authors have identified how they will use a discrete choice experiment to examine the decision making and referral process of GPs and identify parental preference for unscheduled care for treatment in phase 2 (work package 2). They have specified the four steps of this experiment. In the first attribute development step, they have identified that a systematic review and qualitative inquiry will be undertaken in order to identify the attributes that influence decision making. It would have been helpful if more detail was provided in relation to how the findings from the review will be explored further in the qualitative inquiry. They have specified how the second structured prioritisation exercise to finalise attributes will be undertaken. They have identified that the discrete choice experiment cards will subsequently be piloted in the third phase (specifically looking at length of time/ease of use of completion). It would have been helpful if some information about planned sample of participants in phase 3 could have been included (intended number of participants, age, gender breakdown etc.). The sampling, recruitment and analysis plan for step 4 is clearly identified. The authors have identified how the concept mapping approach in package 3 builds on findings from step 1 and 2. This is clearly reported and it is identified that the purpose of this is to elicit stakeholders’ recommendations for policy and practice.

Additional comments: the authors used the interchangeable terms of intellectual disability (ID) and disability throughout the transcript. It is suggested that if the focus of this study is just on children with an ID as opposed to children with any type of ‘disability’, then ID should be used instead of disability.

The acronym ID has been removed and replaced with intellectual disabilities. Any reference to disability has also been removed and replaced with intellectual disabilities
This is an important protocol for a potentially valuable study which has the potential to address health inequities experienced by children with ID in Ireland. I recommend this for indexing (subject to a few minor changes which I have specified in the summary below).

A clear rationale has been provided for this study and the objectives of the study have been clearly described. The authors have clearly identified the evidence base for poorer health outcomes in children with ID compared to the general population (with specific reference to higher mortality rates and higher hospital admissions amongst children with ID compared to equivalent general population). They have made reference to studies undertaken both within an Irish and international context, in order to demonstrate this evidence.

The authors have made reference to how inequitable access to health care may contribute to these poorer health outcomes in children with ID. They have also identified a gap in the evidence within an Irish context, wherein there is currently a lack of information related to accessing healthcare services for children with ID. They have referred to UNCRPD principles and gaps in research studies in order to emphasise the rationale for specifically investigating the complexity of factors that lead to health disparities in children with ID. The authors have emphasised the relevance of this within an Irish context (given the ratification of the UNCRPD). However, it would also have been helpful, if the authors could identify how the findings from this prospective study could have international impact on children with ID. This could increase the wider potential impact of the study.

The Introduction and Discussion have been amended to address potential international impact

The mixed methods three work package design appears appropriate for the research question. It would have been helpful if a figure was included in order to illustrate how each phase follows on and is integrated to the next, in terms of answering the research question.

A figure has been included to illustrate the project (see Figure 1)

It would also be helpful to know what specific type of mixed method design is proposed? The term mixed methods reflects the variety of methods that will be used. Given there is no aim to triangulate

Multi-method is a more appropriate term to describe the project and this has been amended throughout

Do the authors propose to triangulate the results from each of the work packages (phases) of the study in any way?

No, the data will not be triangulated

The authors have identified how they will establish the extent of health inequities between children with and without LD in relation to access to healthcare in the first phase of the study (work package 1). The authors have identified how they will match the cases. They have reported how they will represent the demographic profile of the participants. They have identified the intended statistical tests for drawing comparisons with the general population.

However, I would recommend the following amendment for work package 1 phase, in order to ensure the data analysis plan in described in detail and allows replication by others. More information is required on the following in relation to work package
1.         How is the proposed approach similar to the method used in Canada?

The reference to this study has been removed

2.         Were there any adaptions that were made for the current study?

See above

3.         How many children with ID are in this database?

It is unclear at this stage how many children with ID are in the databases but it has

4.         What specific age groups will the children be subdivided into for the purpose of analysis?

There is no plan to subdivide the children into age groups.

5.         What is the gender breakdown of the children in this database?

Unknown at this stage, but it is expected that there will be more males than females in keeping with data from the CSO.

6.         How will missing data be treated?

This has been addressed in the section ‘Data Analysis Plan’.

7.         How many matched children are in this database?

Sample sizes have been provided where possible.

The authors have identified how they will use a discrete choice experiment to examine the decision making and referral process of GPs and identify parental preference for unscheduled care for treatment in phase 2 (work package 2). They have specified the four steps of this experiment. In the first attribute development step, they have identified that a systematic review and qualitative inquiry will be undertaken in order to identify the attributes that influence decision making. It would have been helpful if more detail was provided in relation to how the findings from the review will be explored further in the qualitative inquiry. They have specified how the second structured prioritisation exercise to finalise attributes will be undertaken. They have identified that the discrete choice experiment cards will subsequently be piloted in the third phase (specifically looking at length of time/ease of use of completion). It would have been helpful if some information about planned sample of participants in phase 3 could have been included (intended number of participants, age, gender breakdown etc.). The sampling, recruitment and analysis plan for step 4 is clearly identified. The authors have identified how the concept mapping approach in package 3 builds on findings from step 1 and 2. This is clearly reported and it is identified that the purpose of this is to elicit stakeholders’ recommendations for policy and practice.

Additional comments: the authors used the interchangeable terms of intellectual disability (ID) and disability throughout the transcript. It is suggested that if the focus of this study is just on children with an ID as opposed to children with any type of ‘disability’, then ID should be used instead of disability.

The acronym ID has been removed and replaced with intellectual disabilities. Any reference to disability has also been removed and replaced with intellectual disabilities
Competing Interests: No competing interests were disclosed. Close
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Lisa O'Leary, Edinburgh Napier University, Edinburgh, UK
Reema Harrison, University of New South Wales, Sydney, Australia

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11 Views

17 Aug 2020 | for Version 2

Lisa O'Leary, Edinburgh Napier University, Edinburgh, UK

11 Views Cite this report Responses(0)

Approved

Thank for addressing all my previous recommendations, I have no further comments to make.

Competing Interests

No competing interests were disclosed.

Reviewer Expertise

Intellectual disabilities, mixed methods, systematic reviews, complex interventions, mortality patterns in people with intellectual disabilities, respiratory health.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

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16 Views

07 May 2020 | for Version 1

Reema Harrison, School of Public Health and Community Medicine, University of New South Wales, Sydney, Australia

16 Views Cite this report Responses(1)

Approved

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

Health services research; healthcare quality; patient safety.

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

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Author Response

16 Jul 2020

Emma Nicholson, Centre for Interdisciplinary Research, Education and Innovation in Health Systems (IRIS), University College Dublin, Belfield, Ireland

The Introduction and Discussion have been amended to address potential international impact

Areas for further consideration:
It is notable that the terminology is a little inconsistent regarding intellectual disability, children and disability and would benefit from clarification. This may be in part due to reliance on literature relating to adult populations or disability more generally to form the development of the study but warrants review across the piece for clarity in some areas.

This has been addressed and intellectual disability has been used throughout

Whilst a mixed-methods approach is identified, there is insufficient detail as to the process of data synthesis and how these studies collectively address the research questions. Currently, the work packages appear to flow one after the other but it is not clear as to how there will be a higher level synthesis of the knowledge. Overall, whilst the methods are well-described, there is insufficient detail in some of the areas to enable replication based on the protocol alone.

Given there is no plan to specifically triangulate data, the term ‘multi-method’ has been used in place of mixed-methods. A figure has also been included to outline the project (see Figure 1). Greater detail has been provided in the method sections.

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Competing Interests

No competing interests were disclosed.

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Reviewer Report

29 Views

12 Feb 2020 | for Version 1

Lisa O'Leary, Edinburgh Napier University, Edinburgh, UK

29 Views Cite this report Responses(1)

Approved With Reservations

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

Intellectual disabilities, mixed methods, systematic reviews, complex interventions, mortality patterns in people with intellectual disabilities, respiratory health.

Respond to this report

Responses (1)

Author Response

16 Jul 2020

Emma Nicholson, Centre for Interdisciplinary Research, Education and Innovation in Health Systems (IRIS), University College Dublin, Belfield, Ireland

The Introduction and Discussion have been amended to address potential international impact

The mixed methods three work package design appears appropriate for the research question. It would have been helpful if a figure was included in order to illustrate how each phase follows on and is integrated to the next, in terms of answering the research question.

A figure has been included to illustrate the project (see Figure 1)

It would also be helpful to know what specific type of mixed method design is proposed? The term mixed methods reflects the variety of methods that will be used. Given there is no aim to triangulate

Multi-method is a more appropriate term to describe the project and this has been amended throughout

Do the authors propose to triangulate the results from each of the work packages (phases) of the study in any way?

No, the data will not be triangulated

The authors have identified how they will establish the extent of health inequities between children with and without LD in relation to access to healthcare in the first phase of the study (work package 1). The authors have identified how they will match the cases. They have reported how they will represent the demographic profile of the participants. They have identified the intended statistical tests for drawing comparisons with the general population.

However, I would recommend the following amendment for work package 1 phase, in order to ensure the data analysis plan in described in detail and allows replication by others. More information is required on the following in relation to work package
1. How is the proposed approach similar to the method used in Canada?

The reference to this study has been removed

2. Were there any adaptions that were made for the current study?

See above

3. How many children with ID are in this database?

It is unclear at this stage how many children with ID are in the databases but it has

4. What specific age groups will the children be subdivided into for the purpose of analysis?

There is no plan to subdivide the children into age groups.

5. What is the gender breakdown of the children in this database?

Unknown at this stage, but it is expected that there will be more males than females in keeping with data from the CSO.

6. How will missing data be treated?

This has been addressed in the section ‘Data Analysis Plan’.

7. How many matched children are in this database?

Sample sizes have been provided where possible.

The authors have identified how they will use a discrete choice experiment to examine the decision making and referral process of GPs and identify parental preference for unscheduled care for treatment in phase 2 (work package 2). They have specified the four steps of this experiment. In the first attribute development step, they have identified that a systematic review and qualitative inquiry will be undertaken in order to identify the attributes that influence decision making. It would have been helpful if more detail was provided in relation to how the findings from the review will be explored further in the qualitative inquiry. They have specified how the second structured prioritisation exercise to finalise attributes will be undertaken. They have identified that the discrete choice experiment cards will subsequently be piloted in the third phase (specifically looking at length of time/ease of use of completion). It would have been helpful if some information about planned sample of participants in phase 3 could have been included (intended number of participants, age, gender breakdown etc.). The sampling, recruitment and analysis plan for step 4 is clearly identified. The authors have identified how the concept mapping approach in package 3 builds on findings from step 1 and 2. This is clearly reported and it is identified that the purpose of this is to elicit stakeholders’ recommendations for policy and practice.

Additional comments: the authors used the interchangeable terms of intellectual disability (ID) and disability throughout the transcript. It is suggested that if the focus of this study is just on children with an ID as opposed to children with any type of ‘disability’, then ID should be used instead of disability.

The acronym ID has been removed and replaced with intellectual disabilities. Any reference to disability has also been removed and replaced with intellectual disabilities

View more View less

Competing Interests

No competing interests were disclosed.

Alongside their report, reviewers assign a status to the article:

Approved - the paper is scientifically sound in its current form and only minor, if any, improvements are suggested

Approved with reservations - A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.

Not approved - fundamental flaws in the paper seriously undermine the findings and conclusions

[1] 1. Ouellette-Kuntz H: Understanding Health Disparities and Inequities Faced by Individuals with Intellectual Disabilities. J Appl Res Intellect. 2005; 18(2): 113–21. Publisher Full Text

[2] 2. Krahn GL, Fox MH: Health disparities of adults with intellectual disabilities: what do we know? What do we do? J Appl Res Intellect Disabil. 2014; 27(5): 431–46. PubMed Abstract | Publisher Full Text | Free Full Text

[3] 3. Dunn K, Hughes-McCormack L, Cooper SA: Hospital admissions for physical health conditions for people with intellectual disabilities: Systematic review. J Appl Res Intellect Disabil. 2018; 31 Suppl 1: 1–10. PubMed Abstract | Publisher Full Text

[4] 4. Shooshtari S, Brownell M, Mills RSL, et al.: Comparing Health Status, Health Trajectories and Use of Health and Social Services between Children with and without Developmental Disabilities: A Population-based Longitudinal Study in Manitoba. J Appl Res Intellect Disabil. 2017; 30(4): 584–601. PubMed Abstract | Publisher Full Text

[5] 5. McCarron M, Carroll R, Kelly C, et al.: Mortality Rates in the General Irish Population Compared to those with an Intellectual Disability from 2003 to 2012. J Appl Res Intellect Disabil. 2015; 28(5): 406–13. PubMed Abstract | Publisher Full Text

[6] 6. Fitzgerald P, Leonard H, Pikora TJ, et al.: Hospital admissions in children with down syndrome: experience of a population-based cohort followed from birth. PLoS One. 2013; 8(8): e70401. PubMed Abstract | Publisher Full Text | Free Full Text

[7] 7. Emerson E, Hatton C: Poverty, socio-economic position, social capital and the health of children and adolescents with intellectual disabilities in Britain: a replication. J Intellect Disabil Res. 2007; 51(Pt 11): 866–74. PubMed Abstract | Publisher Full Text

[8] 8. Rubin G, Bate A, George A, et al.: Preferences for access to the GP: a discrete choice experiment. Br J Gen Pract. 2006; 56(531): 743–8. PubMed Abstract | Free Full Text

[9] 9. Chapman JL, Zechel A, Carter YH, et al.: Systematic review of recent innovations in service provision to improve access to primary care. Br J Gen Pract. 2004; 54(502): 374–81. PubMed Abstract | Free Full Text

[10] 10. Cecil E, Bottle A, Cowling TE, et al.: Primary Care Access, Emergency Department Visits, and Unplanned Short Hospitalizations in the UK. Pediatrics. 2016; 137(2): e20151492. PubMed Abstract | Publisher Full Text

[11] 11. Lennox NG, Diggens JN, Ugoni AM: The general practice care of people with intellectual disability: barriers and solutions. J Intellect Disabil Res. 1997; 41(Pt 5): 380–90. PubMed Abstract | Publisher Full Text

[12] 12. Roos LL, Walld R, Uhanova J, et al.: Physician visits, hospitalizations, and socioeconomic status: ambulatory care sensitive conditions in a canadian setting. Health Serv Res. 2005; 40(4): 1167–85. PubMed Abstract | Publisher Full Text | Free Full Text

[13] 13. Balogh R, Brownell M, Ouellette-Kuntz H, et al.: Hospitalisation rates for ambulatory care sensitive conditions for persons with and without an intellectual disability--a population perspective. J Intellect Disabil Res. 2010; 54(9): 820–32. PubMed Abstract | Publisher Full Text

[14] 14. Heslop P, Blair PS, Fleming P, et al.: The Confidential Inquiry into premature deaths of people with intellectual disabilities in the UK: a population-based study. Lancet. 2014; 383(9920): 889–95. PubMed Abstract | Publisher Full Text

[15] 15. Lennox N, Van Driel ML, van Dooren K: Supporting primary healthcare professionals to care for people with intellectual disability: a research agenda. J Appl Res Intellect Disabil. 2015; 28(1): 33–42. PubMed Abstract | Publisher Full Text

[16] 16. Emerson E: The determinants of health inequities experienced by children with learning disabilities. Public Health England. 2015. Reference Source

[17] 17. Louviere JJ, Lancsar E: Choice experiments in health: the good, the bad, the ugly and toward a brighter future. Health Econ Policy Law. 2009; 4(Pt 4): 527–46. PubMed Abstract | Publisher Full Text

[18] 18. Ryan M: Discrete choice experiments in health care. BMJ. 2004; 328(7436): 360–1. PubMed Abstract | Publisher Full Text | Free Full Text

[19] 19. Blaskowitz MG, Hernandez B, Scott PW: Predictors of Emergency Room and Hospital Utilization Among Adults With Intellectual and Developmental Disabilities (IDD). Intellect Dev Disabil. 2019; 57(2): 127–45. PubMed Abstract | Publisher Full Text

[20] 20. Robertson J, Hatton C, Baines S, et al.: Systematic Reviews of the Health or Health care of People with Intellectual Disabilities: A Systematic Review to Identify Gaps in the Evidence Base. J Appl Res Intellect Disabil. 2015; 28(6): 455–523. PubMed Abstract | Publisher Full Text

[21] 21. Backer C, Chapman M, Mitchell D: Access to Secondary Healthcare for People with Intellectual Disabilities: A Review of the Literature. J Appl Res Intellect Disabil. 2009; 22(6): 514–25. Publisher Full Text

[22] 22. Clark MD, Determann D, Petrou S, et al.: Discrete choice experiments in health economics: a review of the literature. Pharmacoeconomics. 2014; 32(9): 883–902. PubMed Abstract | Publisher Full Text

[23] 23. de Bekker-Grob EW, Swait JD, Kassahun HT, et al.: Are Healthcare Choices Predictable? The Impact of Discrete Choice Experiment Designs and Models. Value Health. 2019; 22(9): 1050–62. PubMed Abstract | Publisher Full Text

[24] 24. De Brún A, Flynn D, Joyce K, et al.: Understanding clinicians' decisions to offer intravenous thrombolytic treatment to patients with acute ischaemic stroke: a protocol for a discrete choice experiment. BMJ Open. 2014; 4(7): e005612. PubMed Abstract | Publisher Full Text | Free Full Text

[25] 25. Lancsar E, Louviere J: Conducting discrete choice experiments to inform healthcare decision making: a user's guide. Pharmacoeconomics. 2008; 26(8): 661–77. PubMed Abstract | Publisher Full Text

[26] 26. Coast J, Al-Janabi H, Sutton EJ, et al.: Using qualitative methods for attribute development for discrete choice experiments: issues and recommendations. Health Econ. 2012; 21(6): 730–41. PubMed Abstract | Publisher Full Text

[27] 27. Kløjgaard ME, Bech M, Søgaard R: Designing a Stated Choice Experiment: The Value of a Qualitative Process. J Choice Model. 2012; 5(2): 1–18. Publisher Full Text

[28] 28. Glaser BG, Strauss AL: The discovery of grounded theory: strategies for qualitative research. New York: Aldine de Gruyter; 1999. Publisher Full Text

[29] 29. Trochim W, Kane M: Concept mapping: an introduction to structured conceptualization in health care. Int J Qual Health Care. 2005; 17(3): 187–91. PubMed Abstract | Publisher Full Text

[30] 30. Southern DM, Young D, Dunt D, et al.: Integration of primary health care services: perceptions of Australian general practitioners, non-general practitioner health service providers and consumers at the general practice–primary care interface. Eval Program Plann. 2002; 25(1): 47–59. Publisher Full Text

[31] 31. Bradbury-Jones C, Breckenridge JP, Devaney J, et al.: Disabled women's experiences of accessing and utilising maternity services when they are affected by domestic abuse: a critical incident technique study. BMC Pregnancy Childbirth. 2015; 15(1): 181. PubMed Abstract | Publisher Full Text | Free Full Text

[32] 32. Don de Savigny, Adam T, Alliance for Health Policy and Systems Research, et al.: Systems thinking for health systems strengthening. Geneva: World Health Organization (WHO); 2009. Reference Source

[33] 33. Chan M, Meckler G, Doan Q: Paediatric emergency department overcrowding and adverse patient outcomes. Paediatr Child Health. 2017; 22(7): 377–81. PubMed Abstract | Publisher Full Text | Free Full Text

[34] 34. Payne C, Brown MJ, Guerin S, et al.: EMTReK: An Evidence-based Model for the Transfer & Exchange of Research Knowledge— Five Case Studies in Palliative Care. SAGE Open Nurs. 2019; 5: 2377960819861854. Publisher Full Text

[35] 35. Lauer E, McCallion P: Mortality of People with Intellectual and Developmental Disabilities from Select US State Disability Service Systems and Medical Claims Data. J Appl Res Intellect Disabil. 2015; 28(5): 394–405. PubMed Abstract | Publisher Full Text

Health inequities in unscheduled healthcare for children with intellectual disabilities in Ireland: a study protocol

Abstract

Keywords

Introduction

Methods and analysis

Work Package 1. Describing differences in health care utilisation and hospitalisation between children with and without intellectual disabilities

Work Package 2. Exploring and modelling the decision-making factors that influence referral practices when treating children with ID and eliciting parental preferences for care

Work package 3. A consensus conference to generate evidence-based strategies for improving access to healthcare for children with ID

Ethical considerations

Public and patient involvement (PPI)

Study status

Discussion

Limitations

Conclusion

Data availability

References

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Health inequities in unscheduled healthcare for children with intellectual disabilities in Ireland: a study protocol

Abstract

Keywords

Introduction

Methods and analysis

Work Package 1. Describing differences in health care utilisation and hospitalisation between children with and without intellectual disabilities

Work Package 2. Exploring and modelling the decision-making factors that influence referral practices when treating children with ID and eliciting parental preferences for care

Work package 3. A consensus conference to generate evidence-based strategies for improving access to healthcare for children with ID

Ethical considerations

Public and patient involvement (PPI)

Study status

Discussion

Limitations

Conclusion

Data availability

References

Comments on this article Comments (0)

Open Peer Review

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Open Peer Review

Reviewer Status

Reviewer Reports

Comments on this article

Competing Interests Policy

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