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Van Paul

  • Paul Van Royen, MD, PhD, is Professor Family Medicine within the Department of Primary and Interdisciplinary Care and... moreedit
Over recent decades, the number of available clinical practice guidelines has enormously grown. Guidelines should meet specific quality criteria to ensure good quality. There is a growing need for the developement of a set of criteria to... more
Over recent decades, the number of available clinical practice guidelines has enormously grown. Guidelines should meet specific quality criteria to ensure good quality. There is a growing need for the developement of a set of criteria to ensure that potential biases inherent in guideline development have been properly addressed and that the recommendations for practice are valid and reliable. The AGREE-collaboration is an international network that developed an instrument to critically appraise the methodological quality of guidelines. AGREE promotes a clear strategy to produce, disseminate and evaluate guidelines of high quality. In the first phase of the international project the AGREE-instrument was tested in 11 different countries. Based on this experience the instrument was refined and optimised. In the second phase it was disseminated, promoted and evaluated in 18 participating countries. Belgium was one of them. The Belgian partner in the AGREE-project developed 3 workshops a...
Health promotion is part of GPs' commitments. Some waiting rooms have therefore been implemented with audiovisual aids (posters, pamphlets or screens) for health promotion purposes. Few studies have assessed the effect of audiovisual... more
Health promotion is part of GPs' commitments. Some waiting rooms have therefore been implemented with audiovisual aids (posters, pamphlets or screens) for health promotion purposes. Few studies have assessed the effect of audiovisual aids in primary care. To identify, describe and appraise studies that have investigated the effects of audiovisual aids on health promotion in primary healthcare waiting rooms. To determine which factors influence this impact through literature review. Systematic review. Two independent researchers using predefined keywords searched databases. Additional publications were extracted from the reference lists of the selected articles. The selection of the articles was performed on the title and abstract, followed by complete reading and assessment. Bias and level of evidence were analysed. A total of 909 articles were collected. Most of them were not in primary care settings. Fourteen peer-reviewed articles fully meeting inclusion criteria were include...
The role of gut feelings in diagnostic reasoning is recognized by most GPs throughout Europe, and probably throughout the world. Studies on this topic have emerged from different countries but there is the risk that authors will use... more
The role of gut feelings in diagnostic reasoning is recognized by most GPs throughout Europe, and probably throughout the world. Studies on this topic have emerged from different countries but there is the risk that authors will use different terms for similar concepts. The European Expert Group on Cognitive and Interactive Processes in Diagnosis and Management in General Practice, COGITA for short, was founded in 2008 to conduct cross-border research in the area of non-analytical diagnostic reasoning. Academic GPs, PhD students, psychologists, linguists and students meet once a year to share their experiences, exchange results and initiate new studies on the topic. A milestone in their research is this publication of a short glossary of diagnostic reasoning terms relating to the gut feelings research topic. It was constructed by the COGITA group members following a literature review, which aimed to define salient terms used in their publications. They described the terms, cross-rev...
The Learning Health System (LHS) describes linking routine healthcare systems directly with both research translation and knowledge translation as an extension of the evidence-based medicine paradigm, taking advantage of the ubiquitous... more
The Learning Health System (LHS) describes linking routine healthcare systems directly with both research translation and knowledge translation as an extension of the evidence-based medicine paradigm, taking advantage of the ubiquitous use of electronic health record (EHR) systems. TRANSFoRm is an EU FP7 project that seeks to develop an infrastructure for the LHS in European primary care.Methods. The project is based on three clinical use cases, a genotype-phenotype study in diabetes, a randomised controlled trial with gastroesophageal reflux disease, and a diagnostic decision support system for chest pain, abdominal pain, and shortness of breath.Results. Four models were developed (clinical research, clinical data, provenance, and diagnosis) that form the basis of the projects approach to interoperability. These models are maintained as ontologies with binding of terms to define precise data elements. CDISC ODM and SDM standards are extended using an archetype approach to enable a ...
To support the opinion that doctors should not advise adolescents to abstain from sex a qualitative research study was conducted with focus groups of 17-year-old girls in Antwerp to determine their needs and expectations as well as their... more
To support the opinion that doctors should not advise adolescents to abstain from sex a qualitative research study was conducted with focus groups of 17-year-old girls in Antwerp to determine their needs and expectations as well as their attitudes toward health care providers. Results indicate that although health care providers play an important part in giving certain information to adolescents they should not directly advise them to abstain from sex. They can only encourage the girls to talk to their parents. Findings note that almost 50% of the girls preferred to talk to their mothers about contraceptives and sexual health citing them as the main source of information. Related studies recognized female friends sisters and doctors as other important sources of information. In this perspective an open approach and better communication of health care providers and parents is recommended.
Dyspnoea and chest pain are signs shared with multiple pathologies ranging from the benign to life-threatening diseases. Gut feelings such as the sense of alarm and the sense of reassurance are known to play a substantial role in the... more
Dyspnoea and chest pain are signs shared with multiple pathologies ranging from the benign to life-threatening diseases. Gut feelings such as the sense of alarm and the sense of reassurance are known to play a substantial role in the diagnostic reasoning of general practitioners (GPs). A Gut Feelings Questionnaire (GFQ) has been validated to measure the GP's sense of alarm. A French version of the GFQ is available following a linguistic validation procedure. The aim of the study is to calculate the diagnostic test accuracy of a GP's sense of alarm when confronted with dyspnoea and chest pain. Prospective observational study. Patients aged between 18 and 80 years, consulting their GP for dyspnoea and/or thoracic pain will be considered for enrolment in the study. These GPs will have to complete the questionnaire immediately after the consultation for dyspnoea and/or thoracic pain. The follow-up and the final diagnosis will be collected 4 weeks later by phone contact with the ...
The theme 'patient-centred interprofessional collaboration' of the EGPRN conference in October 2012, captures in just three words important challenges for European primary care and its research agenda. Challenges for future... more
The theme 'patient-centred interprofessional collaboration' of the EGPRN conference in October 2012, captures in just three words important challenges for European primary care and its research agenda. Challenges for future research are formulated, in three domains: clinical, educational and health services research. Transferability of research, based upon advanced computational infrastructure, will facilitate a rapid learning health care system. In educational research, this includes the use of observational and reflexivity methods. Outcomes should be defined in terms of improvement of functional status and social participation rather than in terms of disease-specific outcomes. Partnership with all stakeholders, patients, GPs and their health care colleagues and students, can help in reducing avoidable waste in the production and reporting of research evidence.
The objective of this descriptive study is to investigate the incidence of type 2 diabetes in sentinel general practices in three regions in Belgium and to describe the patient characteristics and the start of the medical management after... more
The objective of this descriptive study is to investigate the incidence of type 2 diabetes in sentinel general practices in three regions in Belgium and to describe the patient characteristics and the start of the medical management after diagnosis. For two successive years all patients who were newly diagnosed with type 2 diabetes were registered. Two weeks after inclusion, the registering physician completed an extensive questionnaire. This questionnaire dealt with risk factors, biochemical parameters, existing complications and treatment. According to this study, the yearly incidence of type 2 diabetes in Belgium is 231 per 100,000 inhabitants. Though the biochemical parameters (BMI, HbA1c, serum cholesterol and triglycerides) do not differ in the three regions of the country being investigated, there are considerable differences in the treatment prescribed for diabetes and its co-morbidity. In Flanders, treatment is usually started with sulphonylurea, in the Walloon provinces with biguanides. Hypolipaemic treatment is also started more frequently in the latter region. In Flanders, hypertension is registered in 51.4% of the newly diagnosed patients with diabetes, which is higher than in the other regions. However, no difference is noted between the different regions in the number of patients with diabetes who are treated for hypertension. A network of sentinel physicians, taking part in voluntary registration, can be helpful in calculating the incidence of a health problem, in particular type 2 diabetes in general practice. The sentinel net can also serve as an instrument for describing patient characteristics and showing how physicians deal with health problems. The regional differences in medical approach that are described require further investigation, mainly with respect to their impact on the patients' outcome.
Diagnostic reasoning is considered to be based on the interaction between analytical and non-analytical cognitive processes. Gut feelings, a specific form of non-analytical reasoning, play a substantial role in diagnostic reasoning by... more
Diagnostic reasoning is considered to be based on the interaction between analytical and non-analytical cognitive processes. Gut feelings, a specific form of non-analytical reasoning, play a substantial role in diagnostic reasoning by general practitioners (GPs) and may activate analytical reasoning. In GP traineeships in the Netherlands, trainees mostly see patients alone but regularly consult with their supervisors to discuss patients and problems, receive feedback, and improve their competencies. In the present study, we examined the discussions of supervisors and their trainees about diagnostic reasoning in these so-called tutorial dialogues and how gut feelings feature in these discussions. 17 tutorial dialogues focussing on diagnostic reasoning were video-recorded and transcribed and the protocols were analysed using a detailed bottom-up and iterative content analysis and coding procedure. The dialogues were segmented into quotes. Each quote received a content code and a parti...
ABSTRACT In chronic diseases such as type 2 diabetes, adherence to treatment is a major public health problem, seriously undercutting the benefits of medical care. Many studies have assessed factors associated with compliance, but the... more
ABSTRACT In chronic diseases such as type 2 diabetes, adherence to treatment is a major public health problem, seriously undercutting the benefits of medical care. Many studies have assessed factors associated with compliance, but the patient perspective is remarkably absent. From these studies, it seems that the patient's role in the process of adhering was to be passive and since the prescriber's view was rational and based on scientific research, it may have been assumed to be superior to the patient's beliefs and wishes. This paper reports on type 2 diabetes patients' health beliefs in relation to their illness, their communication with caregivers and the problems encountered in adhering to treatment regimens.Seven focus groups were held for type 2 diabetes patients recruited by pharmacists in primary care in Flanders, Belgium. These groups focussed on participants' experience of their treatment. Possible explanatory models were generated by qualitative content analysis of the focus group discussions.Forty-six patients recruited from primary care participated in six semi-structured group discussions. The data demonstrate that health beliefs, the quality of doctor/patient communication, and the quality of the information patients receive are important factors for patient adherence to treatment. Possible explanatory models for adherence emerged, relating to knowledge of the illness, body awareness and the doctor/patient relationship.This qualitative research identified explanatory models for adhering to medical treatment from the patient's perspective. Interventions designed to enhance adherence should address the patient perspective using these models in order to maximise effectiveness. Copyright © 2003 John Wiley & Sons, Ltd.
To determine the needs and expectations of adolescent girls concerning contraceptive use as well as their attitude to health care providers, a qualitative research was performed with four focus groups of 17-year-old girls of different... more
To determine the needs and expectations of adolescent girls concerning contraceptive use as well as their attitude to health care providers, a qualitative research was performed with four focus groups of 17-year-old girls of different education levels. All 26 girls except one were of Belgian origin. There was a fixed scenario for each group. The discussions were tape-recorded, transcribed and analysed via content analysis. Knowledge concerning the daily use and side-effects of contraceptives was insufficient. A school physician is not the person they want to talk to. The influence of the peer in the group is very important. The general practitioner is the most frequently consulted health care provider for the first pill prescription, but for a gynaecological examination they thought they had to visit a gynaecologist. The girls expected confidentiality from their general practitioner and wanted sufficient consultation time. Factors inhibiting the visits for obtaining contraceptives were the cost, waiting time and fear of the gynaecological examination. Adolescents intended to visit their general practitioner for contraceptives, but the family practice had to be easily accessible. It is a challenge for general practitioners to provide good contraceptives to adolescents and to promote compliance.
To investigate specific information needs of people who search for information about the human papillomavirus (HPV) on the Internet. We performed a qualitative analysis of the e-mail questions asked by the visitors of a website with... more
To investigate specific information needs of people who search for information about the human papillomavirus (HPV) on the Internet. We performed a qualitative analysis of the e-mail questions asked by the visitors of a website with evidence-based information about HPV. The website, hosted by Antwerp University, provided basic information on epidemiology and natural history of HPV in women and men, diagnostic and treatment options, screening, and vaccination. If visitors did not find an answer to their questions, they could mail their question to an e-mail address associated with the website. We received 713 questions posed by 527 e-mail correspondents. The following themes emerged as most important: transmission of HPV, the HPV vaccine, the natural history of the virus, the vicious circle (re-infection between partners), HPV detection in men and women, treatment of men and women, incubation time, pregnancy/fertility, genital warts (in)fidelity, and symptoms of HPV infection. Both men and women are seeking health information on HPV on the Internet, often after being counseled by a health care provider. Practitioners should be prepared for questions on the themes that concern people most. Practitioners may play a role in guidance towards reliable sources of information.
Vaginal self-sampling may be valuable as an alternative method of cervical cancer screening in areas of poor resources, to enroll women who, otherwise, would not participate in population-based cervical cancer screening and in... more
Vaginal self-sampling may be valuable as an alternative method of cervical cancer screening in areas of poor resources, to enroll women who, otherwise, would not participate in population-based cervical cancer screening and in epidemiological follow-up studies. We assessed the reliability of mailed vaginal samples by evaluating the quantity and quality of genomic DNA in the samples. Mailed swabs (n = 201) were compared with freshly collected samples (n = 200) for DNA concentration (45.1 versus 50.9 ng/microl, respectively) and purity (mean optical density [OD] 260/280 ratio 1.88 versus 1.78, respectively). A small, non-significant, decrease in DNA yield with longer transport time was noted. The DNA yield of mailed samples was significantly lower compared to fresh samples (P < 0.002), but this lower yield had little effect on polymerase chain reaction (PCR) amplification. In conclusion, the large majority of mailed self-sampled vaginal swabs resulted in DNA of adequate purity and concentration for further research.
We describe the use of emergency contraception (EC) and its association with sociodemographic, contraceptive and behavioural characteristics in a sample of family practice attendants in Belgium. The study was part of a large Chlamydia... more
We describe the use of emergency contraception (EC) and its association with sociodemographic, contraceptive and behavioural characteristics in a sample of family practice attendants in Belgium. The study was part of a large Chlamydia trachomatis (CT) prevalence study in general practice. Sexually active women under 40 who consulted their general practitioner for routine gynaecological care were enrolled in the study. Participants completed a questionnaire on sociodemographic variables, urogenital symptoms, sexual history and sexual behaviour, and delivered a sample for CT testing. Logistic regression analysis was performed to identify determinants of a history of EC use in women in this sample. Of 815 questioned women, 23.5% had ever used EC. EC users were a heterogeneous group with respect to educational level, age and ethnicity. The use of emergency contraception was associated with the level of urbanisation, condom use, not having children yet, young age of first sexual intercourse, having had multiple partners in the past year, a history of unintended pregnancy, and current or previous STI. Information on availability and correct use of EC, and on the need for additional testing for STI, are necessary to help primary care attendees to preserve their future reproductive health.
Research Interests:
Problem statement Little is known about how interprofessional healthcare providers in nursing homes work together. We know that interprofessional teamwork evolves from trial and error learning and so interprofessional collaboration has to... more
Problem statement Little is known about how interprofessional healthcare providers in nursing homes work together. We know that interprofessional teamwork evolves from trial and error learning and so interprofessional collaboration has to be actively taught. This study aims to gain insights in the perception of professionals towards interprofessional collaboration in nursing homes and the factors that have an impact on interprofessional collaboration. Approach A qualitative descriptive methodology using focus group interviews and additional semi-structured interviews was performed. In total three focus group sessions with healthcare providers from different disciplines were held and additionally nine semi-structured interviews were executed. A thematic analysis was performed. The transcripts were read to immerse in the data and initial ideas were noted. Both open coding (identification of primary themes) and axial coding (analysis of relationships among themes) were conducted and re...
Physicians' clinical decision-making may be influenced by non-analytical thinking, especially when perceiving uncertainty. Incidental gut feelings in general practice have been described, namely, as "a sense of alarm" and... more
Physicians' clinical decision-making may be influenced by non-analytical thinking, especially when perceiving uncertainty. Incidental gut feelings in general practice have been described, namely, as "a sense of alarm" and "a sense of reassurance". A Dutch Gut Feelings Questionnaire (GFQ) was developed, validated and afterwards translated into English following a linguistic validation procedure. The aims were to translate the GFQ from English into French, German and Polish; to describe uniform elements as well as differences and difficulties in the linguistic validation processes; to propose a procedural scheme for future GFQ translations into other languages. We followed a structured, similar and equivalent procedure. Forward and backward-translations, repeated consensus procedures and cultural validations performed in six steps. Exchanges between the several research teams, the authors of the Dutch GFQ, and the translators involved continued throughout the p...
INTRODUCTION: Multimorbidity is a health issue with growing importance. During the last few decades the populations of most countries in the world have been ageing rapidly. Bulgaria is affected by the issue because of the high prevalence... more
INTRODUCTION: Multimorbidity is a health issue with growing importance. During the last few decades the populations of most countries in the world have been ageing rapidly. Bulgaria is affected by the issue because of the high prevalence of ageing population in the country with multiple chronic conditions. The AIM of the present study was to validate the translated definition of multimorbidity from English into the Bulgarian language. MATERIALS AND METHODS: The present study is part of an international project involving 8 national groups. We performed a forward and backward translation of the original English definition of multimorbidity using a Delphi consensus procedure. RESULTS: The physicians involved accepted the definition with a high percentage of agreement in the first round. The backward translation was accepted by the scientific committee using the Nominal group technique. DISCUSSION: Some of the GPs provided comments on the linguistic expressions which arose in order to i...
In this study the performance of the guidelines produced by the British Chief Medical Officer's expert advisory group for selective screening for Chlamydia trachomatis was evaluated. The guidelines were applied to a sample of 777... more
In this study the performance of the guidelines produced by the British Chief Medical Officer's expert advisory group for selective screening for Chlamydia trachomatis was evaluated. The guidelines were applied to a sample of 777 women in general practice in Antwerp, Belgium. The accuracy of the screening/testing recommendations was suboptimal. The model detected 90% of infections but failed to identify a high-risk population; the population to be screened was reduced by only 21%. The focus on young age as the most important determinant for screening was not appropriate. More attention should be paid to risky sexual behaviour.
The problem of poor compliance/adherence to prescribed treatments is very complex. Health professionals are rarely being asked how they handle the patient's (poor) therapy compliance/adherence. In this study, we examine explicitly the... more
The problem of poor compliance/adherence to prescribed treatments is very complex. Health professionals are rarely being asked how they handle the patient's (poor) therapy compliance/adherence. In this study, we examine explicitly the physicians' expectations of their diabetes patients' compliance/adherence. The objectives of our study were: (1) to elicit problems physicians encounter with type 2 diabetes patients' adherence to treatment recommendations; (2) to search for solutions and (3) to discover escape mechanisms in case of frustration. In a descriptive qualitative study, we explored the thoughts and feelings of general practitioners (GPs) on patients' compliance/adherence. Forty interested GPs could be recruited for focus group participation. Five open ended questions were derived on the one hand from a similar qualitative study on compliance/adherence in patients living with type 2 diabetes and on the other hand from the results of a comprehensive review ...
This paper evaluates the performance of an algorithm developed for opportunistic, selective screening of women for chlamydial infection in general practice in Antwerp, Belgium. Its performance was examined in 2 independent sets of... more
This paper evaluates the performance of an algorithm developed for opportunistic, selective screening of women for chlamydial infection in general practice in Antwerp, Belgium. Its performance was examined in 2 independent sets of patients: A) a cohort of 326 women participating in a pilot screening study, and B) a sample of 25 Chlamydia positive women, identified from the records of a laboratory of clinical microbiology. For group A, positive and negative predictive values were calculated and the accuracy of the algorithm was assessed. For group B, we examined the proportion of patients complying with the algorithm. In group A, the screening algorithm would have detected 73% of the cases in 35.6% of the population. The positive and negative predictive values were 7.7% and 98.4%, respectively. In group B, 84% of patients complied with the algorithm. The screening algorithm worked reasonably well in 2 datasets from a similar population studied 2 y later, but needs further validation.
Aims: People with diabetes have a pivotal role in the management of their illness and should be supported to adopt that role. In amainly curative, symptomdriven health care system, managing a chronic disease with the patient as empowered... more
Aims: People with diabetes have a pivotal role in the management of their illness and should be supported to adopt that role. In amainly curative, symptomdriven health care system, managing a chronic disease with the patient as empowered caretaker is challenging. Recently, the Belgian government commissioned a feasibility study aimed to create and evaluate a regional structured education programme for primary care type 2 diabetes patients within a comprehensive shared care intervention at community level. Methods:Two trained diabetes nurseswere engaged at community level (region of 76.852 inhabitants). An empowerment based education package (individual, group, support in insulin initiation) was developed and offered to all patients in the study area. GP referral was obligatory. A detailed analysis of participants’ characteristics was made. Outcome measures were HbA1c and BMI. Qualitative evaluation (interviews) of GPs’ and patients’ experiences was undertaken. Results: During 32 months 69% (N=55) of all GPs referred 340 patients, representing 20% of the target group. One in three participants was newly diagnosed. Mean age of participants was 65 (±10), 48% were male. Mean duration of diabetes was 6 years (±6), mean Hba1c 7.96% (±1,7) and mean BMI 29.5 (±5) kg/m2. On average people had 4.1 (±3.5) individual sessions per year. First results show an improvement of the mean HbA1c (−0.64%). Patients and GPs feel supported by the programme. Conclusion: The implementation of an empowerment based education programme at community level is feasible in a very liberal, symptom driven health care system. Barriers for nonparticipation.
To determine whether opportunistic screening for Chlamydia trachomatis, based on a selective screening, algorithm, is possible in general practice in Belgium; to assess feasibility of the screening strategy with respect to workload,... more
To determine whether opportunistic screening for Chlamydia trachomatis, based on a selective screening, algorithm, is possible in general practice in Belgium; to assess feasibility of the screening strategy with respect to workload, acceptability, and organisational aspects. Implementation of a pilot screening programme by 37 GPs for a period of 15 weeks. GPs' screening practices were registered and compared with the guidelines they had received. Outcome measures were: the number of patients included in the risk assessment, uptake of screening by eligible patients, prevalence of previously unidentified infection, and uptake of treatment. After the study period GPs evaluated a number of feasibility issues on a scoring form. 326 women underwent the risk assessment and 214 were tested by an amplification assay on a urine sample. Prevalence in woman at risk was 6.4%. Overall effective screening rate was 77.6%; 9 of 11 positives took up treatment. Participating GPs found the strategy feasible and perceived that it was well accepted by their patients. The screening strategy was easily implemented by most GPs but some of them dropped out. The guidelines were followed relatively well and there were no major logistic problems. The uptake of treatment wat suboptimal. Efforts must be made to stimulate and educate more GPs to perform screening; laboratory and storage conditions should be optimised; refunding criteria should be revised; and overscreening must be avoided.

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The European Network for the Joint Evaluation of Connected Health Technologies (ENJECT) is a COST action that brings together an international consortium, including business and revenue modellers, clinicians, technologists, engineers,... more
The European Network for the Joint Evaluation of Connected Health Technologies (ENJECT) is a COST action that brings together an international consortium, including business and revenue modellers, clinicians, technologists, engineers, economists, ethnographers, and health researchers to help society to answer one question – how to connect therapies, patients, and care-givers to deliver optimum health results in an era of stretched resources and increasing demands. This report, which has grown out of an ENJECT survey of 19 European countries, examines the situation of Connected Health in Europe today. It focuses on creating a clear understanding of the current and developing presence of Connected Health throughout European healthcare systems under five headings: The Policy Environment, Education, Business and Health Models, Interoperability, and The Person.

Quality, privacy, and safety, major elements of Connected Health, were evident policy concerns in the Connected Health context. Attention is paid as to how the healthcare systems are evaluated. Evaluation methods and responsibilities range from macro state-level evaluation to more dispersed local evaluation. The constant evolution of European healthcare is reflected in the changing methods of evaluation in countries such as Norway, Greece, Malta, and Serbia.

The vast majority (almost 80%) of respondent countries have eHealth strategies in place or are working on implementing such strategies. In general, e-prescribing and Electronic Health Records are the most common forms of Connected Health activities throughout Europe. There is a clear distinction between patient and consultant usages of these forms of Connected Health. A major issue, especially with the creation of Electronic Health Records, has been ensuring that they are safe and secure and that privacy is attainable. Health Insurance companies also make use of electronic patient records for the storage of and quick access to patient records.

Privacy is recognised as an important factor in the development of accessible patient databases. While two thirds of respondent countries rely on national data protection legislation to protect such databases, others have been more proactive and generated eHealth-specific legislation. Croatia, Germany, Slovenia, the UK, and Macedonia have all begun to recognise the need to draw up legislation which prioritises the protection of patient information recorded through these types of technologies. Public statements and political instruments directly address the topic of Connected Health, helping to protect patients while increasing their awareness of the Connected Health options. Websites and manifestos dedicated to health related activities in various countries are at the centre of this public awareness. Additionally, political parties in some of the respondent countries identify eHealth and Connected Health as an area for improvement in their own manifestos.

Of the nineteen respondents to the survey, fifteen countries contributed specific information on university based programmes that help to ensure that healthcare professionals are aware of and in a position to utilise Connected Health. While few of the programmes focus solely on Connected Health, its inclusion in health and biomedical informatics courses ensures that it will be a part of these future healthcare providers’ understanding of the provision of healthcare. Awareness of Connected Health and the development of health literacy is not solely a concern at third level. Health literacy is a challenge across Europe as a whole. Ad hoc health literacy programmes have been proven to work in some countries, but the public’s infrequent exposure to these forms of literacy, such as television and poster campaigns, means that their benefit is often not fully felt in the long term. The role that Connected Health can play in the improving health literacy does not seem to have been realised, with most countries still relying on leaflets and information booklets to improve patients’ understanding of medical and health related issues. For those countries who actively and regularly promote health literacy, this is done through school systems and specific research communities.

Presenting the business and health models of the healthcare systems in each of the ENJECT respondent’s countries helps to develop an understanding of the level of priority placed upon Connected Health. The majority of European healthcare systems are organised through cooperation between private and public bodies. Their funding and finances primarily come from the public sector, with revenue created through direct and indirect taxes. eHealth models within these healthcare systems’ business models vary significantly across the region and are gradually becoming an accepted part of a healthcare system’s general business models.

To attain an understanding of its healthcare model and patient care pathways, each country has provided a case study of common illnesses. The difference in each country’s method of treatment of the same illness shows how each of the systems operate, with a clear focus on the funding of the treatment in each of the instances.

eHealth Records and digital prescriptions top the list of technically integrated systems at national and
regional levels enabling electronic systems to work across a variety of healthcare contexts. The unification of language and classification systems emerged as a major issue when considering the interoperability of eHealth.

Generally, the level of patient involvement in the design, delivery, and development of health related research programmes is on the increase. With 30% of the respondent countries having a system in place which encourages the inclusion of patients in the design and development of healthcare, this can be seen as a clear starting point for creating even more connected healthcare systems throughout Europe.

In summary, confusion abounds in the area of Connected Health – around wording, application, models, and systems. It involves a complete transformation of the healthcare system in a long-term play that requires dedicated resources and political will. Many of these elements are difficult to capture with data points being largely qualitative and non-comparable. Different countries are at different stages of readiness in terms of Connected Health – both in terms of its research and its implementation. The evaluation criteria employed in different circumstances and different geographies across Europe are neither clear nor standardised. The majority of states and regions are so engaged in the process of ensuring interoperability at a regional or national level that they have little time or attention left to focus on the thorny issue of international interoperability.

We recommend an agenda for future research in Connected Health for Europe that creates a shared language around health records and a database that would facilitate the development of a Connected Health or eHealth scorecard. We would support a common evaluation framework for Connected Health implementations that is multi-faceted, ranging from technology robustness to regulatory compliance, from economic sustainability to user acceptance, and including both qualitative and quantitative measures. There is evident confusion as to the application of existing rights in the context of Connected Health. We recommend an approach specific to eHealth that helps citizens, researchers, companies, and healthcare providers to understand how we live safely and privately in an era of healthcare data. We suggest that studying how some of the ENJECT countries have done this and distilling learnings and best practice from their experience could help to better design future guidelines and interpretations.
Background Multimorbidity, according to the World Health Organization, exists when there are two or more chronic conditions in one patient. This definition seems inaccurate for the holistic approach to Family Medicine (FM) and long-term... more
Background
Multimorbidity, according to the World Health Organization, exists when there are two or
more chronic conditions in one patient. This definition seems inaccurate for the holistic
approach to Family Medicine (FM) and long-term care. To avoid this pitfall the European
General Practitioners Research Network (EGPRN) designed a comprehensive definition of
multimorbidity using a systematic literature review.
Objective
To translate that English definition into European languages and to validate the semantic,
conceptual and cultural homogeneity of the translations for further research.
Method
Forward translation of the EGPRN’s definition of multimorbidity followed by a Delphi consensus
procedure assessment, a backward translation and a cultural check with all teams to ensure the homogeneity of the translations in their national context. Consensus was defined
as 70% of the scores being higher than 6. Delphi rounds were repeated in each country
until a consensus was reached
Results
229 European medical expert FPs participated in the study. Ten consensual translations of
the EGPRN comprehensive definition of multimorbidity were achieved.
Conclusion
A comprehensive definition of multimorbidity is now available in English and ten European
languages for further collaborative research in FM and long-term care.
Research Interests: