- Research article
- Open Access
Capturing the complexity of healthcare for people with Down syndrome in quality indicators - a Delphi study involving healthcare professionals and patient organisations
BMC Health Services Research volume 20, Article number: 694 (2020)
Insight into quality of healthcare for people with Down Syndrome (DS) is limited. Quality indicators (QIs) can provide this insight. This study aims to find consensus among participants regarding QIs for healthcare for people with DS.
We conducted a four-round Delphi study, in which 33 healthcare professionals involved in healthcare for people with DS and two patient organisations’ representatives in the Netherlands participated. Median and 75-percentiles were used to determine consensus among the answers on 5-point Likert-scales. In each round, participants received an overview of participants’ answers from the previous round.
Participants agreed (consensus was achieved) that a QI-set should provide insight into available healthcare, enable healthcare improvements, and cover a large diversity of quality domains and healthcare disciplines. However, the number of QIs in the set should be limited in order to prevent registration burden. Participants were concerned that QIs would make quality information about individual healthcare professionals publicly available, which would induce judgement of healthcare professionals and harm quality, instead of improving it.
We unravelled the complexity of capturing healthcare for people with DS in a QI-set. Patients’ rights to relevant information have to be carefully balanced against providers’ entitlement to a safe environment in which they can learn and improve. A QI-set should be tailored to different healthcare disciplines and information systems, and measurement instruments should be suitable for collecting information from people with DS. Results from this study and two preceding studies, will form the basis for the further development of a QI-set.
Down syndrome (DS) is the most prevalent genetic cause of intellectual disability (ID) [1, 2]. People with DS suffer from a large variety of health problems and therefore have complex healthcare needs, with many different healthcare providers involved [2,3,4,5].
It is widely acknowledged that healthcare for people with DS should be of high quality in order to meet their specific healthcare needs [4, 6, 7]. This is supported by the Convention on the Rights of Persons with Disabilities, advocating high-quality healthcare for people with disabilities, and acknowledging the right for obtaining the highest possible level of health . However, little is known about the quality of DS-specialised healthcare [9, 10].
Quality in healthcare is multidimensional. The World Health Organization formulated six dimensions of healthcare quality: 1) effective (evidence-based and based on needs), 2) efficient (maximising resources, avoiding waste), 3) accessible (timely, geographically reasonable, in a suitable setting), 4) acceptable/patient-centred (taking into account preferences, culture of patient), 5) equitable (same level of quality for everyone) and 6) safe (minimising risk and harm) .
Quality indicators (QIs) - also known as quality measures  - are an important tool in healthcare quality, as they can improve clinical decisions, guide organisational reform, and structure the development of multidisciplinary teams . Moreover, QIs can provide patients with information that enables them to choose the best suitable care . However, an authors’ former study revealed that, up to now, QIs measuring quality of healthcare for people with DS, do not appear to exist [9, 10]. The study found that existing QIs concern people with ID in general (not people with DS in particular), or focus, for instance, on care in assisted living facilities (not specifically on healthcare) [9, 10].
According to Donabedian’s (2005) well-known framework for quality in healthcare, a QI-set may include different types of QIs: structure, process, and outcome QIs [13, 15]. Structure refers to the setting in which healthcare is provided (e.g. administrative structure), process to how healthcare is provided (e.g. followed procedures), and outcome to the result of healthcare provided (e.g. recovery, survival) . Generally, QIs are based on quality standards, such as guidelines or protocols [16, 17]. In the Netherlands, a guideline for multidisciplinary healthcare for children with DS  is present and is currently being revised. Until now, such a guideline concerning adults with DS has not been present, but is currently being developed.
The present study aims to find consensus among healthcare professionals and patient organisation representatives regarding QIs for healthcare for people with DS in the Netherlands. This healthcare involves, amongst others: a paediatrician, ID physician (in the Netherlands, there is an ID-specialised training for physicians), general practitioner (GP), physiotherapist, speech therapist, psychiatrist, cardiologist, ophthalmologist, and DS-specialised multidisciplinary outpatient clinics, so-called ‘Down teams’ [3, 5, 7, 19, 20]. There are paediatric and adult ‘Down teams’ in the Netherlands. Paediatric ‘Down teams’ typically include a visit to the paediatrician, physiotherapist, ENT (ear-nose-throat)-specialist and others, all on the same day. Adult ‘Down teams’ are still scarce and have a slightly different composition, due to different needs in adulthood.
The present study is part of a larger project aiming to develop a QI-set for healthcare for people with DS. The project includes a literature review on existing QIs for healthcare for people with DS (indicating the absence of QIs that could serve as a basis for our QI-set) , a qualitative exploration of how people with DS, parents and support staff define quality in healthcare  (see Table 1), and the current study. In the final project step, findings of the three studies will be combined in order to formulate QIs. In the present study, the following research questions are addressed:
According to healthcare professionals and patient organisations’ representatives, how should a QI-set measuring quality in healthcare for people with DS be defined?
Which purposes should it serve?
Which healthcare disciplines, services and quality domains should it cover?
Which type of QIs (structure, process, outcome) should it include and how many?
According to healthcare professionals and patient organisations’ representatives, what factors should be taken into account in the further development and implementation of the QI-set?
A Delphi technique was used in order to achieve consensus among experts in healthcare for people with DS about relevant items for QIs and related practical issues. Our study is an exploratory inquiry concerning personal opinions of professionals on healthcare quality. According to Dutch legislation , ethics approval was deemed unnecessary, since participants in our study were not subject to procedures and were not required to follow rules of behaviour. We obtained a written informed consent statement from all participants prior to the study. This allowed us to use participants’ contact details for sending them the questionnaires, or for contacting them in case of problems with receiving or filling out the questionnaires. In this statement, participants also approved the use of their answers to the Delphi-questionnaires in an anonymous manner for the aims of the study.
We included representatives of all relevant disciplines involved in healthcare for people with DS and patient organisation representatives, all having expertise in healthcare for people with DS. This composition is similar to the composition of the working group developing guidelines for healthcare for people with DS . Recruitment of participants was done by contacting professional organisations from relevant disciplines and two patient organisations (one specific DS organisation and the umbrella organisation of Dutch patient organisations). We explained the purpose of our research and the expected time investment, and asked the organisations to identify members of their organisations with expertise in healthcare for people with DS. When identified members had agreed to participate, contact details were provided to the researchers, who in turn contacted the members. As the Dutch professional organisation of GPs declined to identify eligible GPs because of other priorities, GPs were recruited via the network of the authors and participants, and/or by using publicly available contact details. Table 2 provides an overview of the participant characteristics.
Four-round Delphi procedure
A Delphi study uses a series of questionnaire-rounds in order to establish consensus among a group of experts about a certain topic [12, 23, 24], and is suitable for the selection of QIs . In such an iterative process, each next round is based on the participants’ answers in the previous round. Only items for which no consensus among participants is found, are presented in the next round. Furthermore, participants receive an overview of the overall group response of the previous round, based on which they can reconsider their initial answers [24, 25]. Our study consisted of four consecutive rounds:
Round 1: Introduction to themes, initial inventory of level of consensus;
Round 2: Feedback on Round 1 and revisiting themes on which no consensus existed;
Round 3: Exploration of consensus on sub-domains;
Round 4: Final consensus building
We used online questionnaires, which were composed using QualtricsXM®. Online questionnaires allow participants to fill out the questionnaires wherever they want, allow anonymous participation of experts across various locations, and prevent one (or a few) expert(s) from dominating the consensus process [12, 23].
Questionnaires and consensus
All questionnaires contained questions with a five point Likert-scale, multiple choice questions and open-ended questions.
Using the Likert-scale questions, participants rated items in terms of relevance for the QI-set (1 ‘very important’, 2 ‘important’, 3 ‘neutral’, 4 ‘not that important’, 5 ‘not important at all’), or indicated to what extend they agreed with propositions (1 ‘totally agree’, 2 ‘agree’, 3 ‘neutral’, 4 ‘disagree’, 5 ‘totally disagree’). In round 1 an ‘I don’t know’-option was also included. Consensus was defined in advance, as follows: if at least 75% of the participants rated an item as 1 or 2 and the median was ≤2, consensus was achieved among the participants about including the item in the QI-set, or about agreeing with a proposition. If 75% of the participants rated an item 4 or 5 and the median was ≥4, consensus was achieved among the participants about excluding the item from the QI-set, or about disagreeing with a proposition. In all other situations, it was concluded that consensus was not achieved among participants. Although there is no standard for defining consensus in Delphi studies, using a combination of percentages and median for defining consensus is generally accepted [12, 25]. A 75% cut-off is considered adequate in Delphi studies . We decided to present some items to the participants despite the fact that consensus was obtained for these items in the previous round(s), because some participants had not been able to join the first round, or because we thought the items should be presented as a complete set (e.g. all healthcare disciplines possibly involved in healthcare for people with DS). If we deemed more detailed information was needed, more specialised items/propositions, or differently formulated propositions were presented to the participants (e.g. quality domains were presented in round 1 and sub-domains in round 3).
The multiple choice questions and the open ended questions allowed participants to explain their ‘rated’ answers or add relevant QI-items.
The topics of the questionnaires were largely based on outcomes of the previous study investigating the experiences and opinions of people with DS, parents and support staff regarding quality in healthcare  (see Table 1) and on the multidisciplinary guideline for healthcare for children with DS . Additionally, the questionnaires contained topics related to the development, implementation and use of QIs, informed by literature and expertise of the authors. Topics addressed in the questionnaires and number and type of questions are shown in Table 3. An English translation of the questionnaires can be found in Additional file 1.
Delphi in one day
The first questionnaire was sent out on April 25th 2018, the other three on May 30th 2018. This timeframe was chosen because participants preferred to conduct the study (predominantly) on 1 day. This short study duration would thus prevent participant drop-out related to large time intervals between the rounds. It would also limit time investment of both participants and researchers, as participants do not need re-introduction into the topic at the start of each new round, and data collection proceeds quickly. Although the time intervals between the rounds in our study were much shorter than in classic Delphi studies , literature does not provide any reason to assume that a shorter study duration affects the results . However, in order to allow for such short time intervals, the rounds required thorough preparation, enabling participants to fill out the questionnaires swiftly, and enabling researchers to perform analyses and adapt the questionnaires accordingly. Therefore, the authors composed most questions beforehand, by anticipating the possible responses of the participants and by using preliminary insights resulting from round 1. Because of this, only a few questions needed to be newly composed between round 2, 3 and 4, and most questions only had to be moved, slightly rephrased, or removed. Additionally, used software was set ready to quickly provide the researchers with information needed to assess consensus (median and 75-percentiles) and with an overview of open-ended question answers. Furthermore, roles of the research team (i.e. obtaining medians and 75-percentiles; extracting open-ended question answers, chairing the discussions (see next paragraph “Analysis”), adapting and sending out the questionnaires) were allocated beforehand.
During the study, we used percentages provided by QualtricsXM® and the median calculated using IBM SPSS Statistics 24, to determine whether the answers of the participants on the Likert-scale questions had resulted in consensus. From the multiple choice questions, only frequencies (percentages) were calculated. Analysis of the answers from open-ended questions included reading and discussing the answers by all authors, which resulted in identification and structuring of key issues. All authors were involved in all iterations of the study, in an e-mail conversation (first round) and in a face-to-face meeting (rounds 2–4).
Afterwards, in order to structure the data, a dataset containing data from all rounds was created using IBM SPSS Statistics 24, and median and 75-percentile of the Likert-scale questions were calculated again. The calculations were done with and without the patient organisation representatives’ answers, in order to discover whether their answers differed from the health care professionals’ answers. Differences were indicated together with the concerning findings, in order to interpret the results.
A total of 35 eligible participants was identified. However, one participant could not allocate time for participating in any of the rounds and answered only one question in round two and three. Ten participants could not participate in all rounds. Figure 1 shows a flowchart of the number of participants per round. On average, participants needed 55, 52, 25 and 14 min to complete questionnaires 1, 2, 3 and 4 respectively, with a maximum of 114, 85, 45, and 48 min.
Results Delphi rounds
Distributed across the four rounds, 259 questions were presented to the participants, comprising 20 open-ended questions, 11 closed-ended questions and 228 propositions or items, of which 107 had resulted in consensus among the participants. See Table 4.
Below, the results of the four Delphi rounds are presented in two parts: 1) Defining purposes and identifying QI-topics; and 2) Considerations for further development and implementation of the QI-set. More details about the results can be found in Additional file 2.
Defining purposes and identifying QI-topics
In the first three rounds, participants indicated the purpose(s) to be served by the QI-set. See Table 5, first row (‘Purpose of QIs’).
Related to the purpose “provide healthcare professionals with information on where to find suitable healthcare (providers)”, participants explained that providers could use this information for making referrals. Especially for generalists (such as GPs), who cannot reasonably be expected to have much DS-specialised expertise, QIs could be helpful in identifying specialised healthcare professionals to refer to.
Additional to the purposes “improving healthcare on the national level” and “improve healthcare for people with DS delivered by their organisation (e.g. health centre, hospital, department)”, participants mentioned that QIs could be part of audits, and could be used to improve processes (logistics, management, ICT etc.). Furthermore, participants explained that QIs should enable benchmarking of one’s own functioning as compared to that of colleagues at individual, regional or national level.
About the purpose “using QIs as input for developing guidelines”, consensus was achieved in the first round. However, participants commented that QIs should not be used as input for guidelines, but rather the other way around (guidelines should define indicators). We therefore decided to present this purpose to the participants in round two again, which did not result in consensus.
Although there was consensus concerning “QIs should be used to reduce differences in quality of provided healthcare by different providers”, some participants argued that differences should exist between providers, because if differences would not exist, this may imply that differences between centres of expertise and other healthcare providers - very much needed for healthcare for people with DS – could not exist.
In the first three rounds, participants indicated per quality (sub-)domain how important they considered it to be covered by the QI-set. Table 5, second row (‘Quality domains’) shows the quality domains that, according to consensus among the participants, should be covered by the QI-set.
Although consensus existed regarding including person-centeredness in the QI-set, this was not reflected in participants’ answers regarding sub-domains of person-centeredness, presented to the participants in following rounds. On the one hand, participants explained that QIs should measure whether healthcare is adapted to the needs of the person with DS, which may also increase effectiveness. On the other hand, no consensus existed about: adapting care to the preferences and desires of the person with DS, self-management, considering experienced burden for parents and other caregivers, and organising multidisciplinary appointments on 1 day.
Furthermore, participants argued that concepts such as quality of life and daily functioning should not appear in the QI-set, because they are too complex to be measured by QIs, too little related to quality of delivered care, or more suitable for inclusion in scientific research, than for being part of a QI-set. Others argued that such concepts should appear in the QI-set, because this would result in increased awareness among healthcare professionals about these important concepts.
In round one and two, participants indicated how important they considered each healthcare discipline or service to appear in the QI-set (see Table 5, third row (‘Healthcare disciplines / services’)). Participants unanimously indicated that the set should contain one or more QIs on Down teams for children. It was even argued that a QI for Down teams could function as an indicator for the quality of all other healthcare for a child with DS, because Down teams are expected to have an overview over the total package of care. However, it was also noted that not all children with DS visit Down teams, implying that a ‘Down team QI’ would not be able to indicate quality of healthcare for all children with DS. A QI measuring quality of care provided by a paediatrician would therefore be more important. Similarly, a QI measuring healthcare quality of adult Down teams, would not be representative for all healthcare for adults with DS, since the number of adult Down teams is (too) small, as is the number of ID physicians. Participants explained that GPs sometimes provide the healthcare that is not provided by ID physicians / adult Down teams. Therefore, including a QI on healthcare provided by GPs could be important for adults with DS. However, a reason mentioned for not including GP-care in the QI-set is that GPs were not expected to have DS-expertise, because they have only a small number of patients with DS.
Furthermore, participants did not agree about coverage of visual functioning and dental care. Monitoring visual functioning was mentioned as a candidate indicator, because visual functioning is apt to change over time. However, no consensus was achieved on including visual screening in the set. Participants’ comments about dentistry indicated that some sort of dentistry should be in the QI-set. However, it remains unclear which form of dentistry should be in the QI-set, as some people with DS need a specialised dentist, while for others a general dentist suffices. A mentioned reason for including a QI measuring specialised dental care, was based on the idea that a specialised dentist should always be involved, in order to monitor, recognise and treat DS-specific dental problems.
There was a lot of discussion about including non-medical disciplines/services in the QI-set. For example, consensus about including ‘family support’ was only achieved when the patient organisations’ representatives were included in the analysis, and there was no consensus about including support staff of assisted living facilities in the QI-set. Moreover, the proposition “QIs should also cover non-medical disciplines” did not result in consensus. Some participants argued that including them was especially important because it is too much of a blind spot among healthcare professionals, whereas others explained that non-medical disciplines/services do not belong to a QI-set for quality of healthcare.
Although participants considered adherence to medical guidelines to be an important QI, they also noted that deviation from guidelines may be necessary in order to provide care that answers to the needs of people with DS. Hence, non-adherence to guidelines does not necessarily indicate low quality.
Number and type of QIs
Table 5, fourth row (‘Number of QIs in set’) shows that participants preferred to include all disciplines/services involved in healthcare for people with DS in the QI-set. However, participants also noted that this would result in a QI-set with too many QIs, leading to a too high administrative burden for the users of the QI-set. In round two, participants thought that the total number of QIs in the set should be, or should not exceed, ten. In round three, participants agreed (consensus) that the QI-set should consist of modules: a basic module containing QIs relevant for all people with DS, and additional modules for specific patient groups or healthcare services. In round four, participants thought that each module should contain about ten QIs.
In round two and three, participants indicated that they thought the QI-set should contain structure, process, and outcome QIs (see Table 5, fifth row (‘Type of QIs in set’)). They also argued that the number of outcome indicators should be the highest, followed by process and structure indicators respectively.
Considerations for further development and implementation of the QI-set
Current and future use of indicators
In round one, the majority of the participants indicated that they expected their colleagues (from the same profession) to be willing to register (extra) data for the QI-set. See Table 6, first row (‘Willingness to register’). Participants explained that whether or not healthcare professionals would register data for this QI-set, would be dependent on available time, awareness about the QIs, considered utility of QIs, and frequency of contact with people with DS.
In round one, we also asked participants what kind of quality information they or their organisation currently collected. See Table 6, second row (‘Current collection of data by own organisation’). Most participants (41%) indicated that their organisation did not collect any quality information. If information was being collected, it primarily concerned information about adherence to guidelines, clinical outcomes, and findability of the organisation. Furthermore, most participants indicated that they did not use indicators in their work, and if they did use them, it concerned QIs regarding general (not DS-specific) internal improvement of healthcare or audits (see Table 6 third row (‘Current use of QIs’)). We also asked participants about the guidelines they currently used in their work (see Table 6, fourth row (‘Current use of guidelines’)). The Dutch multidisciplinary medical guideline for children with DS  was the most often mentioned guideline.
Participants were not always in favour of participating in a QI-set that would make quality information publicly available, especially if a QI-set would reveal quality information on the level of individual healthcare professionals. In round one, participants explained that such information would possibly result in long waiting lists for ‘good’ providers or professionals, which may in turn negatively affect quality. Moreover, once a healthcare provider or professional is labelled as ‘not good’, this would possibly affect the choice of patients for this provider or professional for a long period of time. Because of these considerations, clarifying propositions were presented to the participants in rounds three and four (see Table 6, last row (‘Transparency’)). This confirmed the reluctance of participants to publish quality information (provided by the QIs) about individual professionals. It also showed that participants preferred access to this individual information to be limited to healthcare providers, in order to prevent judgement of healthcare professionals by patients or other parties. It should be used for internal improvements instead. Accordingly, participants explained to be reluctant to introduce a quality mark for healthcare providers. However, other participants argued that a QI-set would enable healthcare providers/organisations to profile themselves as ‘good’ healthcare providers, by ‘signing up’ for participating in the QIs, on a voluntary basis. Participation in the QI-set would be an indication of DS-expertise, which would also provide insight into available healthcare for people with DS to caregivers and healthcare professionals.
Data source and development of QIs
Electronic medical records (EMRs) and patient/parent questionnaires were considered the most important information sources for the QI-set. At the same time, participants underlined that both healthcare professionals and people with DS and their caregivers should not be overcharged with registration burden. See Table 7, first row (‘Data source’). Participants suggested to transform (a) patient/parent questionnaire(s) into an easy-to-understand app in order to make it suitable for people with DS. Ideally, such an app should be linked to the information system (EMR) in order to store all information together. However, participants identified the large number of existing information systems, often not mutually communicating, as a potential barrier for implementation of a QI-set.
According to the participants, development of the QIs should be done by researchers (the authors) together with all stakeholders. See Table 7, second row (‘Development of QIs’). Participants mentioned representatives of the same diversity of disciplines as mentioned under ‘healthcare disciplines/services’ to be involved in the development of the QIs. It was also noted that it would be difficult to weigh the different opinions of those involved. The majority of the participants (59%) indicated that whether or not they themselves were willing to participate in development of the QIs depended on the time and effort needed.
In this study we aimed to prefigure quality indicators for healthcare for people with Down syndrome. We used a Delphi technique involving healthcare professionals and patient organisations’ representatives. The findings of this study, together with findings from two previous studies of the authors (a literature review on existing QIs and a qualitative study involving people with DS and their caregivers [10, 21]), will be used to inform the further development and implementation of the QI-set.
According to the participants in the current study, QIs should be suitable to inform healthcare quality improvement, and should be able to provide an overview of available healthcare to people with DS and their caregivers, and to healthcare professionals. Participants stressed that QIs should not be used to judge healthcare professionals. Furthermore, they opted for an evenly distributed mix of structure, process, and outcome QIs, covering the following quality domains: coordination and continuity of healthcare, effectiveness, safety, person-centeredness, and outcomes concerning health and quality of life. Additionally, participants argued that the QIs should cover all healthcare disciplines involved in healthcare for people with DS. However, they urged to keep the number of QIs low, in order to prevent (administrative) burden for healthcare professionals and people with DS and/or caregivers. Furthermore, development of QIs should be done with involvement of all relevant stakeholders.
Quality improvement and well-informed choices
According to the participants in our study, two key purposes of a QI-set for healthcare for people with DS are 1) to improve quality in healthcare and 2) to increase insight into available healthcare, enabling people with DS (and their caregivers) to make well-informed healthcare choices, and supporting healthcare professionals to make well-informed referrals. However, participants in the current study argue that the two purposes may conflict with each other. They explained that if quality information was publicly available, especially when it concerned information on the level of individual providers, a “shaming-and-blaming” situation would emerge. They were concerned that this would hamper quality of care, instead of improve it. A study addressing Parkinson’s disease, showed a similar reticent attitude amongst healthcare professionals towards sharing quality information with patients . On the other hand, current movements in practice and literature have shown the need for encouraging patients to make well-informed healthcare choices, although the influence of QIs on healthcare choices made by patients has been shown to be limited [27,28,29]. Hence, patients’ rights to relevant information, fostering the choice for the best suitable healthcare, have to be carefully balanced against providers’ entitlement to a safe environment in which they can learn and improve.
There was much discussion about defining the coverage of the QI-set. Some participants preferred to include only medical QIs, whereas others were convinced that a QI-set should cover disciplines/services outside healthcare, such as support staff of assisted living facilities, in order to reflect the complexity of healthcare for people with DS [5, 30]. However, based on our results (achieved consensus) we conclude that participants prefer to limit the coverage of the QI-set to the medical domain (including psychological care). This medical focus may be a reflection of the specialised focus of healthcare professionals and their training, or of the fragmented care system in the Netherlands [31, 32]. Another explanation for this medical focus may be found in social psychology [33, 34]: healthcare professionals may consider quality improvement or transparency within the medical domain within their control, while they consider other domains beyond their sphere of influence and therefore less important for a QI-set. The medical focus may however also be a result of the participants’ reluctance to face a high registration burden, which participants repeatedly expressed during the study. This confirms the general understanding that QI-sets should be concise to foster their actual use [35, 36].
However, even if the coverage of the QI-set will be limited to the medical domain, it will, due to the multi-morbidity related to DS [5, 30], include a lot of different disciplines, and many quality domains. Hence, developing a concise QI-set will be challenging, even more so as not all quality domains may be applicable to all disciplines and contexts, and the QI-set will have to be compatible with a large variety of data registration systems used by the different healthcare providers involved. In order to limit registration burden, registration of data for a QI-set should be possible together with other currently registered data in the electronic medical record (EMR). This would also prevent registration of the same data in separate registries , and facilitate data collection (i.e. extraction from information systems) for the QI-set. Literature shows that automated extraction of indicators from EMRs is possible, however, the structure of information systems and the accuracy of registration by professionals is not always sufficient for enabling automated extraction [38, 39]. Nevertheless, most participants in our study thought that their colleagues (of the same profession) would be willing to register extra QI-data, especially if registration efforts would be kept as small as possible.
Patient reported information
Participants also suggested to use patient reported information (for example from questionnaires) as input for the QI-set, which should ideally be stored within the EMR, together with the data registered by healthcare professionals. Such patient information is often obtained using Patient Reported Outcome Measures (PROMs) and/or Patient Reported Experience Measures (PREMs) [40, 41]. PROMs focus on measuring outcomes of treatments related to patient functioning, while PREMs address patient experiences regarding healthcare processes [36, 39]. PREMs/PROMs are considered robust quality measures . However, due to their cognitive abilities , people with DS may not always be able to provide patient reported information, in which case proxies (such as parents) will have to provide this information [42, 43]. Nevertheless, patient involvement in healthcare is considered increasingly important in delivering high quality healthcare in general , and concerning people with ID . It may therefore be worthwhile to explore other ways to obtain information from people with DS that could be used for quality improvements. Examples are using narratives for evaluation  or apps especially designed for people with DS/ID .
Strengths and limitations
The selection of participants reflected the large variety of healthcare providers involved in healthcare for people with DS and included two patient organisations’ representatives. Although this presumably led to heterogeneity in answers, which may complicate the formulation of QIs, it can be considered a strength of the study. Participant heterogeneity enriches the results of a Delphi study, which enhances the credibility and acceptance of resulting QIs .
Another strength of the study is that consensus was defined in advance [12, 24, 25] (median ≤ 2 in combination with a 75% cut-off).
The fact that the members of the research team (i.e. the authors) have been collaborating before, may have led to some advantageous knowledge of each other’s ideas, which may have affected the research team’s discussions, and in turn, the content validity of the Delphi-questionnaires. However, we expect this effect to be small because of the heterogeneity of the research team (see “Authors’ information”) and the limited contact frequency of the team members before the study. Moreover, the fact that consensus was defined in advance, improves reliability of the questionnaire results.
There was variation among the participants regarding the time they had been working in their current position, but they represented ample DS-related experience: 91.4% of the participants had been working in their current position for more than 7 years; 85.7% had at least monthly contact with clients with DS.
Unfortunately, GPs, playing a key role in healthcare for people (especially adults) with DS , were underrepresented. Despite extensive attempts, we were only able to include one GP, who could only participate in round one.
The time intervals between the rounds in our study were much smaller than in classic Delphi studies, which have a total study duration of three to twelve months . The short time-intervals were chosen after consulting the participants about their preferences for taking part in the study, in order to limit participant drop-out. Nevertheless, we could not prevent a drop-out of about 25%. However, a response rate of about 75% is considered quite high in Delphi-studies . This relatively high rate was probably achieved by the personal touch we applied in communication with our participants, which is mentioned to be crucial in limiting drop-out . A possible disadvantage of the short time intervals may be that it entails limited time for analysis and preparation of questions for next rounds. We mitigated this possible effect on data collection and results by preparing a large part of the questions for successive rounds in advance. Another possible disadvantage of short time intervals is related to the fact that participants have less time to reflect on, and adapt, their answers. However, we considered the questionnaires suitable to be completed within short time intervals, as the complexity of the questions presented to the participants was quite low. This is supported by the fact that the participants in our study completed the questionnaires within reasonable time. Moreover, the most complex questions, which may require much reflection time, were placed in the first questionnaire, which participants had to complete within several weeks (instead of within several minutes for the other questionnaires).
Our study showed the complexity of capturing healthcare for people with DS in a QI-set that is relevant for both healthcare providers and people with DS plus their caregivers. We have taken a solid step in unravelling this complexity and its possible impact on developing QIs, thereby making substantial progress in the development of QIs for healthcare for people with DS. Future research can (and will) build further on this foundation.
Since our study involves a large variety of healthcare professionals, with heterogenic view points, our findings may not only be relevant to healthcare for people with DS, but probably to any healthcare discipline. It is even argued that, because of the complexity of healthcare for people with DS, the DS population could be used to assess the quality of the healthcare system in general .
Several important lessons from this study should be taken into account in the further development of a QI-set for healthcare for people with DS. First, our findings indicate that a QI-set for healthcare for people with DS has two main purposes: it should be suitable for 1) identifying possibilities for improvement of healthcare for people with DS; and 2) for supporting patients and providers in choosing appropriate healthcare (providers). However, the two purposes need to be carefully balanced, as extensive information transparency fostering patients’ healthcare choices, may conflict with ensuring safe and supportive working environments for healthcare professionals, and with fair comparison of providers. Second, capturing healthcare for people with DS in a QI-set requires the set to be suitable for use by all different disciplines involved, and to be compatible with different information systems. At the same time, the set has to be as concise and compact as possible, in order to limit administrative burden. Third, measurement instruments providing information for a QI-set should be suitable for collecting information from people with DS and their caregivers.
Availability of data and materials
The datasets used and analysed during the current study are available from the corresponding author on reasonable request. However, most data generated or analysed during this study are included in this published article and its supplementary information files.
Electronic medical record
Ear Nose Throat
Patient reported experience measure
Patient reported outcome measure
Quality of life
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The authors would like to thank all participants in the study for their time and willingness to express their opinions and share their knowledge. Additionally, the authors thank Jessica Maarleveld for her statistical and organisational help.
This work was supported by the Fonds NutsOhra (fund), Amsterdam, the Netherlands [grant number: 1403–029]; and the Jeroen Bosch Hospital, ‘s-Hertogenbosch, the Netherlands.
Both funders did not have a role in the design of the study nor in collection, analysis and interpretation of the data, nor in writing the manuscript.
Ethics approval and consent to participate
According to the Dutch Act on Medical Research Involving Human Subjects (1998), ethics approval was deemed unnecessary.
Written informed consent was obtained from all participants prior to the study. The informed consent concerned the use of participants’ contact details and answers to Delphi-questionnaires for the aims of the study.
Consent for publication
No conflict of interest has been declared.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file 1.
(Questionnaires). English translation of the questionnaires of round 1, 2, 3 and 4. This document contains an English translation of the online questionnaires (in Dutch) that were used in the four Delphi-rounds for data collection.
Additional file 2:
(Supplementary Tables 1–5). Supplementary Tables 1–5: Supplementary Table 1. Extent to which consensus was achieved among participants regarding: Purposes of QIs; Supplementary Table 2. Extent to which consensus was achieved among participants regarding: Quality domains; Supplementary Table 3. Extent to which consensus was achieved among participants regarding: Healthcare services/disciplines; Supplementary Table 4. Preferred number and type of QIs and extent to which consensus was achieved among participants regarding related propositions; Supplementary Table 5. Extent to which consensus was achieved among participants regarding: Information sources and transparency of QIs and practical issues regarding development. Tables indicating the extent to which consensus was achieved among participants regarding different aspects of a QI-set for healthcare for people with DS. Results of the study are largely based on these data.
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van den Driessen Mareeuw, F.A., Coppus, A.M.W., Delnoij, D.M.J. et al. Capturing the complexity of healthcare for people with Down syndrome in quality indicators - a Delphi study involving healthcare professionals and patient organisations. BMC Health Serv Res 20, 694 (2020). https://doi.org/10.1186/s12913-020-05492-z
- Down syndrome
- Quality indicators
- Quality of health care
- Delphi technique