Barriers and enablers to providing preventative and early intervention diabetes-related foot care: a qualitative study of primary care healthcare professionals

Author(s):  
Leanne Mullan ◽  
Karen Wynter ◽  
Andrea Driscoll ◽  
Bodil Rasmussen
2019 ◽  
Vol 25 (6) ◽  
pp. 517 ◽  
Author(s):  
Leanne Mullan ◽  
Andrea Driscoll ◽  
Karen Wynter ◽  
Bodil Rasmussen

The aim of this study is to examine barriers and enablers to delivering preventative and early intervention footcare to people with diabetes, from the perspective of healthcare professionals within primary care. MEDLINE, CINAHL and Scopus databases, as well as Google Scholar, were searched in September 2018. Inclusion criteria included: English language, qualitative and quantitative studies, since 1998, reporting on barriers or enablers, as reported by primary care health professionals, to delivering preventative or early intervention footcare to people with diabetes. In total, 339 studies were screened. Eight studies met criteria. Perceived barriers to providing footcare included: geographical, administrative and communication factors; referral and care guideline availability and implementation challenges; limited availability of specialists and high-risk foot services; and limited resources including time and funding. Enablers to footcare were: implementation of footcare programs; education; clear definition of staff roles; development of foot assessment reminder systems; and reminders for people with diabetes to remove their shoes at appointments. Barriers and enablers to footcare are multifaceted. Healthcare professionals are affected by health system and individual factors. By implementing strategies to address barriers to footcare delivery, it is possible to improve outcomes for people with diabetes, thus reducing the effect of diabetes-related foot disease.


BMJ Open ◽  
2018 ◽  
Vol 8 (3) ◽  
pp. e020521 ◽  
Author(s):  
Anne-Marie Burn ◽  
Jane Fleming ◽  
Carol Brayne ◽  
Chris Fox ◽  
Frances Bunn

ObjectivesIn 2012–2013, the English National Health Service mandated hospitals to conduct systematic case-finding of people with dementia among older people with unplanned admissions. The method was not defined. The aim of this study was to understand current approaches to dementia case-finding in acute hospitals in England and explore the views of healthcare professionals on perceived benefits and challenges.DesignQualitative study involving interviews, focus groups and thematic content analysis.SettingPrimary care and secondary care across six counties in the East of England.ParticipantsHospital staff involved in dementia case-finding and primary care staff in the catchment areas of those hospitals.ResultsWe recruited 23 hospital staff and 36 primary care staff, including 30 general practitioners (GPs). Analysis resulted in three themes: (1) lack of consistent approaches in case-finding processes, (2) barriers between primary care and secondary care which impact on case-finding outcomes and (3) perceptions of rationale, aims and impacts of case-finding. The study shows that there were variations in how well hospitals recorded and reported outcomes to GPs. Barriers between primary care and secondary care, including GPs’ lack of access to hospital investigations and lack of clarity about roles and responsibilities, impacted case-finding outcomes. Staff in secondary care were more positive about the initiative than primary care staff, and there were conflicting priorities for primary care and secondary care regarding case-finding.ConclusionsThe study suggests a more evidence-based approach was needed to justify approaches to dementia case-finding. Information communicated to primary care from hospitals needs to be comprehensive, appropriate and consistent before GPs can effectively plan further investigation, treatment or care. Follow-up in primary care further requires access to options for postdiagnostic support. There is a need to evaluate the outcomes for patients and the economic impact on health and care services across settings.


2021 ◽  
Author(s):  
Evalill Nilsson ◽  
Annette Sverker ◽  
Preben Bendtsen ◽  
Ann Catrine Eldh

BACKGROUND Worldwide, the use of e-consultations in healthcare is progressing fast. So far, studies on the advantages and disadvantages of e-consultations in the form of chat services for all enquiries in primary care have focused on the perspective of the healthcare professionals rather than the end-users (patients). OBJECTIVE To explore patients´ experiences of using a chat- and automated medical history-taking service in Swedish regular tax-based not-for-profit primary care. METHODS In this qualitative study, 25 individual interviews were conducted with patients in the catchment areas of five primary care centres (PCCs) in Sweden that tested a chat- and automated medical history-taking service for all kinds of patient enquiries. The semi-structured interviews were transcribed verbatim prior to content analysis, using inductive and deductive strategies, the latter including an unconstrained matrix of Human, Organisation and Technology (HOT) perspectives. RESULTS The service provided an easily managed way for patients to make written contact, which was considered beneficial for some patients and issues, but less suitable for others (like acute or more complex cases). The automated medical history-taking service was perceived as having potential, but still derived from what healthcare professionals need to know and how they address and communicate health and healthcare issues. Technical skills were not considered as necessary for a mobile phone chat as for handling a computer, for example, but patients still expressed concern for people with less digital literacy. The opportunity for patients to take their time and reflect before answering questions from the healthcare professionals was found to be stress reducing and error preventing, and patients speculated that it might be the same for the healthcare professionals on the other end of the system. Patients appreciated the ability to have a conversation from almost anywhere, even from places not suitable for telephone calls. The asynchronicity of the chat service let the patients take more control of the conversation and initiate a chat at any time at their own convenience, but it could also lead to lengthy conversations where a single issue in the worst cases could take days to close. The opportunity to upload photographs made some visits to the PCC redundant which would otherwise have been necessary if a telephone service had been used, saving patients both time and money. CONCLUSIONS Patients generally had a positive attitude towards e-consultations in primary care and were generally pleased with the prospects of the digital tool tested, somewhat more with the actual chat than with the automated history-taking system preceding the chat. While patients expect their PCC to offer a range of different means of communication, the HOT analysis revealed a need for a more extensive (end) user-experience design in the further development of the PCC chat service.


2012 ◽  
Vol 62 (596) ◽  
pp. e183-e190 ◽  
Author(s):  
Helen Lester ◽  
Nagina Khan ◽  
Peter Jones ◽  
Max Marshall ◽  
David Fowler ◽  
...  

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