ArticleBMC medical informatics and decision making2012
Patient access to complex chronic disease records on the Internet.
Article in BMC medical informatics and decision making, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
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
18 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- The impact of different radiology report formats on patient information processing: a systematic review.European radiology · 2025Pooled it
- The Empirical Foundations of Telemedicine Interventions in Primary Care.Telemedicine journal and e-health : the official journal of the American Telemedicine Association · 2016Pooled it
- The Impact of Superfast Broadband, Tailored Booklets for Households, and Discussions With General Practitioners on Personal Electronic Health Readiness: Cluster Factorial Quasi-Randomized Control Trial.Journal of medical Internet research · 2019Trial
- Attitudes towards using electronic health records of patients with psoriasis and dermatologists: a cross-sectional study.BMC medical informatics and decision making · 2020Article
- Patient Use and Experience With Online Access to Electronic Health Records in Norway: Results From an Online Survey.Journal of medical Internet research · 2020Article
- The role of patient portals in enhancing self-care in patients with renal conditions.Clinical kidney journal · 2020Review
- How should electronic health records be designed? A cross-sectional study in patients with psoriasis.BMC medical informatics and decision making · 2019Article
- Identifying How Patient Portals Impact Communication in Oncology.Health communication · 2019Article
- Patient and Health Care Provider Experiences With a Recently Introduced Patient Portal in an Academic Hospital in the Netherlands: Mixed Methods Study.Journal of medical Internet research · 2019Article
- Implications of Patient Portal Transparency in Oncology: Qualitative Interview Study on the Experiences of Patients, Oncologists, and Medical Informaticists.JMIR cancer · 2018Article
- Presentation of laboratory test results in patient portals: influence of interface design on risk interpretation and visual search behaviour.BMC medical informatics and decision making · 2018Article
- Timely Digital Patient-Clinician Communication in Specialist Clinical Services for Young People: A Mixed-Methods Study (The LYNC Study).Journal of medical Internet research · 2017Article
- Using eHealth Technologies: Interests, Preferences, and Concerns of Older Adults.Interactive journal of medical research · 2017Article
- Chinese Internet Searches Provide Inaccurate and Misleading Information to Epilepsy Patients.Chinese medical journal · 2015Article
- Emergency physicians' views of direct notification of laboratory and radiology results to patients using the Internet: a multisite survey.Journal of medical Internet research · 2015Article
- Patients' continuing use of an online health record: a quantitative evaluation of 14,000 patient years of access data.Journal of medical Internet research · 2014Article
- Single-centre experience with Renal PatientView, a web-based system that provides patients with access to their laboratory results.Journal of nephrology · 2014Article
- Patient Access to Online Visit Notes: Perceptions of Doctors and Patients at an Urban HIV/AIDS Clinic.Journal of the International Association of Providers of AIDS CareArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
backgroundAccess to medical records on the Internet has been reported to be acceptable and popular with patients, although most published evaluations have been of primary care or office-based practice. We tested the feasibility and acceptability of making unscreened results and data from a complex chronic disease pathway (renal medicine) available to patients over the Internet in a project involving more than half of renal units in the UK.
methodsContent and presentation of the Renal PatientView (RPV) system was developed with patient groups. It was designed to receive information from multiple local information systems and to require minimal extra work in units. After piloting in 4 centres in 2005 it was made available more widely. Opinions were sought from both patients who enrolled and from those who did not in a paper survey, and from staff in an electronic survey. Anonymous data on enrollment and usage were extracted from the webserver.
resultsBy mid 2011 over 17,000 patients from 47 of the 75 renal units in the UK had registered. Users had a wide age range (<10 to >90 yrs) but were younger and had more years of education than non-users. They were enthusiastic about the concept, found it easy to use, and 80% felt it gave them a better understanding of their disease. The most common reason for not enrolling was being unaware of the system. A minority of patients had security concerns, and these were reduced after enrolling. Staff responses were also strongly positive. They reported that it aided patient concordance and disease management, and increased the quality of consultations with a neutral effect on consultation length. Neither patient nor staff responses suggested that RPV led to an overall increase in patient anxiety or to an increased burden on renal units beyond the time required to enroll each patient.
conclusionsPatient Internet access to secondary care records concerning a complex chronic disease is feasible and popular, providing an increased sense of empowerment and understanding, with no serious identified negative consequences. Security concerns were present but rarely prevented participation. These are powerful reasons to make this type of access more widely available.
Indexed as
Identifiers
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.