ArticleBMC medical informatics and decision making2015
Patient and public views about the security and privacy of Electronic Health Records (EHRs) in the UK: results from a mixed methods study.
Article in BMC medical informatics and decision making, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 3 of them syntheses that pooled it.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
48 citing papers in PubMed, 3 syntheses or guidelines pooled it.
- Patient and Public Willingness to Share Personal Health Data for Third-Party or Secondary Uses: Systematic Review.Journal of medical Internet research · 2024Pooled it
- Addressing the Challenges of Electronic Health Records Using Blockchain and IPFS.Sensors (Basel, Switzerland) · 2022Pooled it
- "Giving something back": A systematic review and ethical enquiry into public views on the use of patient data for research in the United Kingdom and the Republic of Ireland.Wellcome open research · 2018Pooled it
- Privacy Fact Sheets for Mitigating Disease-Related Privacy Concerns and Facilitating Equal Access to the Electronic Health Record: Randomized Controlled Trial.JMIR human factors · 2026Trial
- Electronic health records in patient care: strengths, facilitators, challenges, and future directions-a scoping review.BMC health services research · 2026Article
- What are patient perspectives on privacy and trust in digital genomic tools? A qualitative study.Journal of genetic counseling · 2025Article
- Sharing health data for research purposes: results of a population survey in Germany.BMC health services research · 2025Article
- I don't mind my information going to the Moon, but I don't want any letters from Mars: a qualitative exploration of the challenges with secondary use of health data in Ireland.Archives of public health = Archives belges de sante publique · 2025Article
- Qualitative evaluation of the implementation and national roll-out of the NHS App in England.BMC medicine · 2025Article
- Trustworthiness of the electronic health record in Germany: an exploratory, user-centered analysis.Frontiers in digital health · 2025Article
- The perception of facilitators and barriers to the use of e-health solutions in Poland: a qualitative study.BMC medical informatics and decision making · 2024Article
- Perception towards electronic health records & uptake of digital health IDs among the urban residents in northern India: A mixed methods study.The Indian journal of medical research · 2024Article
- Article
- A Call to Reconsider a Nationwide Electronic Health Record System: Correcting the Failures of the National Program for IT.JMIR medical informatics · 2023Article
- Awareness, Attitudes and Willingness to Donate Biological Samples to a Biobank: A Survey of a Representative Sample of Polish Citizens.Healthcare (Basel, Switzerland) · 2023Article
- Extending the Privacy Calculus to the mHealth Domain: Survey Study on the Intention to Use mHealth Apps in Germany.JMIR human factors · 2023Article
- Data-driven research and healthcare: public trust, data governance and the NHS.BMC medical ethics · 2023Review
- Regular measurement is essential but insufficient to improve quality of healthcare.BMJ (Clinical research ed.) · 2023Article
- Genetic Data Governance in Japanese Hospitals.Asian bioethics review · 2023Article
- Attitudes of Covid-19 patients toward sharing their health data: A survey-based study to understand security and privacy concerns.Health science reports · 2023Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
backgroundAlthough policy discourses frame integrated Electronic Health Records (EHRs) as essential for contemporary healthcare systems, increased information sharing often raises concerns among patients and the public. This paper examines patient and public views about the security and privacy of EHRs used for health provision, research and policy in the UK.
methodsSequential mixed methods study with a cross-sectional survey (in 2011) followed by focus group discussions (in 2012-2013). Survey participants (N = 5331) were recruited from primary and secondary care settings in West London (UK). Complete data for 2761 (51.8 %) participants were included in the final analysis for this paper. The survey results were discussed in 13 focus groups with people living with a range of different health conditions, and in 4 mixed focus groups with patients, health professionals and researchers (total N = 120). Qualitative data were analysed thematically.
resultsIn the survey, 79 % of participants reported that they would worry about the security of their record if this was part of a national EHR system and 71 % thought the National Health Service (NHS) was unable to guarantee EHR safety at the time this work was carried out. Almost half (47 %) responded that EHRs would be less secure compared with the way their health record was held at the time of the survey. Of those who reported being worried about EHR security, many would nevertheless support their development (55 %), while 12 % would not support national EHRs and a sizeable proportion (33 %) were undecided. There were also variations by age, ethnicity and education. In focus group discussions participants weighed up perceived benefits against potential security and privacy threats from wider sharing of information, as well as discussing other perceived risks: commercial exploitation, lack of accountability, data inaccuracies, prejudice and inequalities in health provision.
conclusionsPatient and public worries about the security risks associated with integrated EHRs highlight the need for intensive public awareness and engagement initiatives, together with the establishment of trustworthy security and privacy mechanisms for health information sharing.
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.