Impact of promoting patient access to their Electronic Health Care Record: A Systematic Review (Preprint)

Author(s):  
Archana Tapuria

BACKGROUND A significant cost element of healthcare provision are one-to-one interactions with individuals at clinic visits or by phone. HIT (Health Information technology) (https://www.hit.org.uk) and patient-shared EHRs have the potential to decrease these costs, improve access to healthcare data, self-care, quality of care, and health and patient-centred outcome. OBJECTIVE This systematic literature review is aimed at identifying the benefits and issues around promoting patients access to their own Electronic Healthcare Records (EHRs). The purpose is to outline and summarize study results on the impact of patients’ online access to their own EHRs from the primary healthcare centres and hospitals and access to the patient portals. METHODS Searches were conducted in PubMed, MEDLINE, COCHRANE library, CINHAL and Google scholar. Over 2000 papers were screened, and initially filtered based on duplicates, then by reading the titles and finally based on their abstracts. 54 papers were retained, analysed and summarised, of which 24 were studies involving patient portals. Papers were included if patient access to their own EHRs (including patient portals) was the primary intervention used in the study. The search technique used to identify relevant literature for this paper, involved input from 5 experts. RESULTS While 52% authors agree that access to EHRs would be beneficial to patients and the overall healthcare system, a few (18%) critics have highlighted concerns as well. While the benefits range from re-assurance (8%), reduced anxiety (8%), positive impact on consultations (6%), better doctor-patient relationship (10%) and increased awareness and adherence to medicines (8%), most of the concerns are around security and privacy and confidentiality of personal health information along with anxiety in cases of serious illnesses (18%). Using patient portals was found to improve patient outcomes such as medication compliance, achieving blood pressure control, controlling sugar levels and glycaemic control, improving functional status and reduced high-cost healthcare utilisation in patients with chronic conditions, enhance timely patient centred care. These were noted in a range of study populations. In addition, patient portals were found to improve self-reported levels of engagement or activation related to self-management, enhanced knowledge, and improve recovery scores, and organisational efficiencies in a tertiary level mental health care facility. However, three studies out of 24 did not find statistical effect of patient portals on health outcomes. Along with the overall impact of patients’ access to EHR systems, this review has presented the impact of access to patient portals separately as well. CONCLUSIONS This literature review identified some benefits and harms involved in promoting patients’ access to their own EHRs (including the patient portals). This access is often part of government strategies when developing patient-centric self-management elements of a sustainable healthcare system. The findings of this review could give healthcare providers a framework to analyse the benefits offered by promoting patient access to EHRs and decide on the best approach for their own specialities and clinical set up. A robust cost-benefit evaluation of such initiatives along with its impact on major stakeholders within the healthcare system would be essential in understanding the overall impact of such initiatives. Implementation of patient access to their EHRs could help the government address concerns in developing national standards, whilst taking care of local variations and fulfilling the healthcare needs of the population, e.g. to that goal UK Government is committed to making full GP records available online to every patient by 2018. Ultimately, increasing transparency and promoting personal responsibility are key elements of a sustainable healthcare system for future generations.

2020 ◽  
Author(s):  
Alanna Black ◽  
Cathy Le ◽  
Jeffrey Barnett ◽  
Wan-Yun Tsai ◽  
Shawn Sangha ◽  
...  

BACKGROUND Electronic patient portals in healthcare are quickly becoming the preference of clinicians, patients, and caregivers alike. In times where the demand for all things to be online appears limitless, it is no surprise that portals are requested when updating health information systems worldwide. However, there are barriers to implementing online portals and many countries are lagging behind in updating their systems. With the interest in increasing investment in online portals by the Canadian public healthcare system, decision makers should be considering whether patient access to medical records through portals and mobile devices provides any changes to quality of care. OBJECTIVE This literature review examines available research in Canada and globally on health-related online portals and their impact on quality of care and patient access. Also examined are examples of different health portals, including issues or barriers to full implementation and utilization in the health sphere. METHODS A preliminary search was completed in May 2019 to examine the impact of patient portals on quality of care. The resources utilized in the first stage of the review included the University of British Columbia and the Western University library databases, Google, and Google Scholar. Parameters for the search included search terms such as patient portals, personal health records, effectiveness, quality, and access. Recent articles were prioritized, and included articles were generally published in the last five years. The authors reviewed 52 articles or article abstracts and 29 were included in the current review. Of the mixture of Canadian and international references, five are systematic reviews, and 18 are original research studies. RESULTS This study reviewed the available literature and found that there are some positive trends on patient portals’ impact on quality of care, with overall inconclusive or neutral results. Emerging evidence has showcased some benefits of implementing electronic health and patient portals to improve the quality of patient care and access to pertinent health records. However, general consensus is that there is limited available literature that is not considered to be outdated and as such, further investigation is required to support any previous findings. CONCLUSIONS As health care related technology develops further, better quality, quantity, and larger-scale studies will be available in evidence-based research databases. As such, a future follow-up literature review would be relevant to re-examine this topic.


2020 ◽  
Vol 13 (11) ◽  
pp. 400
Author(s):  
Arnold G. Vulto ◽  
Jackie Vanderpuye-Orgle ◽  
Martin van der Graaff ◽  
Steven R. A. Simoens ◽  
Lorenzo Dagna ◽  
...  

Introduction: Biosimilars have the potential to enhance the sustainability of evolving health care systems. A sustainable biosimilars market requires all stakeholders to balance competition and supply chain security. However, there is significant variation in the policies for pricing, procurement, and use of biosimilars in the European Union. A modified Delphi process was conducted to achieve expert consensus on biosimilar market sustainability in Europe. Methods: The priorities of 11 stakeholders were explored in three stages: a brainstorming stage supported by a systematic literature review (SLR) and key materials identified by the participants; development and review of statements derived during brainstorming; and a facilitated roundtable discussion. Results: Participants argued that a sustainable biosimilar market must deliver tangible and transparent benefits to the health care system, while meeting the needs of all stakeholders. Key drivers of biosimilar market sustainability included: (i) competition is more effective than regulation; (ii) there should be incentives to ensure industry investment in biosimilar development and innovation; (iii) procurement processes must avoid monopolies and minimize market disruption; and (iv) principles for procurement should be defined by all stakeholders. However, findings from the SLR were limited, with significant gaps on the impact of different tender models on supply risks, savings, and sustainability. Conclusions: A sustainable biosimilar market means that all stakeholders benefit from appropriate and reliable access to biological therapies. Failure to care for biosimilar market sustainability may impoverish biosimilar development and offerings, eventually leading to increased cost for health care systems and patients, with fewer resources for innovation.


2018 ◽  
Vol 39 (8) ◽  
pp. 1582-1610 ◽  
Author(s):  
NICK CADDICK ◽  
HELEN CULLEN ◽  
AMANDA CLARKE ◽  
MATT FOSSEY ◽  
MICHAEL HILL ◽  
...  

ABSTRACTThe impact of losing a limb in military service extends well beyond initial recovery and rehabilitation, with long-term consequences and challenges requiring health-care commitments across the lifecourse. This paper presents a systematic review of the current state of knowledge regarding the long-term impact of ageing and limb-loss in military veterans. Key databases were systematically searched including: ASSIA, CINAHL, Cochrane Library, Medline, Web of Science, PsycArticles/PsychInfo, ProQuest Psychology and ProQuest Sociology Journals, and SPORTSDiscus. Empirical studies which focused on the long-term impact of limb-loss and/or health-care requirements in veterans were included. The search process revealed 30 papers relevant for inclusion. These papers focused broadly on four themes: (a) long-term health outcomes, prosthetics use and quality of life; (b) long-term psycho-social adaptation and coping with limb-loss; (c) disability and identity; and (d) estimating the long-term costs of care and prosthetic provision. Findings present a compelling case for ensuring the long-term care needs and costs of rehabilitation for older limbless veterans are met. A dearth of information on the lived experience of limb-loss and the needs of veterans’ families calls for further research to address these important issues.


2018 ◽  
Vol 33 (8) ◽  
pp. 920-927 ◽  
Author(s):  
Hinda Ruton ◽  
Angele Musabyimana ◽  
Erick Gaju ◽  
Atakilt Berhe ◽  
Karen A Grépin ◽  
...  

2020 ◽  
Author(s):  
Shuchih Ernest Chang ◽  
YiChian Chen

BACKGROUND Blockchain technology is leveraging its innovative potential in various sectors and its transformation of business-related processes has drawn much attention. Topics of research interest have focused on medical and health care applications, while research implications have generally concluded in system design, literature reviews, and case studies. However, a general overview and knowledge about the impact on the health care ecosystem is limited. OBJECTIVE This paper explores a potential paradigm shift and ecosystem evolution in health care utilizing blockchain technology. METHODS A literature review with a case study on a pioneering initiative was conducted. With a systematic life cycle analysis, this study sheds light on the evolutionary development of blockchain in health care scenarios and its interactive relationship among stakeholders. RESULTS Four stages—birth, expansion, leadership, and self-renewal or death—in the life cycle of the business ecosystem were explored to elucidate the evolving trajectories of blockchain-based health care implementation. Focused impacts on the traditional health care industry are highlighted within each stage to further support the potential health care paradigm shift in the future. CONCLUSIONS This paper enriches the existing body of literature in this field by illustrating the potential of blockchain in fulfilling stakeholders’ needs and elucidating the phenomenon of coevolution within the health care ecosystem. Blockchain not only catalyzes the interactions among players but also facilitates the formation of the ecosystem life cycle. The collaborative network linked by blockchain may play a critical role on value creation, transfer, and sharing among the health care community. Future efforts may focus on empirical or case studies to validate the proposed evolution of the health care ecosystem.


2017 ◽  
Author(s):  
Leming Zhou ◽  
Bambang Parmanto ◽  
James Joshi

BACKGROUND The widespread application of technologies such as electronic health record systems, mobile health apps, and telemedicine platforms, has made it easy for health care providers to collect relevant data and deliver health care regimens. While efficacious, these new technologies also pose serious security and privacy challenges. OBJECTIVE The training program described here aims at preparing well-informed health information security and privacy professionals with enhanced course materials and various approaches. METHODS A new educational track has been built within a health informatics graduate program. Several existing graduate courses have been enhanced with new security and privacy modules. New labs and seminars have been created, and students are being encouraged to participate in research projects and obtain real-world experience from industry partners. Students in this track receive both theoretical education and hands-on practice. Evaluations have been performed on this new track by conducting multiple surveys on a sample of students. RESULTS We have succeeded in creating a new security track and developing a pertinent curriculum. The newly created security materials have been implemented in multiple courses. Our evaluation indicated that students (N=72) believed that receiving security and privacy training was important for health professionals, the provided security contents were interesting, and having the enhanced security and privacy training in this program was beneficial for their future career. CONCLUSIONS The security and privacy education for health information professionals in this new security track has been significantly enhanced.


Author(s):  
Steven A. Demurjian ◽  
Alberto De la Rosa Algarín ◽  
Jinbo Bi ◽  
Solomon Berhe ◽  
Thomas Agresta ◽  
...  

In health care, patient information of interest to health providers, researchers, public health researchers, insurers, patients, etc., is stored in different locations via electronic media and/or hard-copy formats. All potential users need electronic access to health information technology systems such as: electronic health records, personal health records, patient portals, and ancillary systems such as imaging, laboratory, pharmacy, etc. Controlling access to information from multiple systems requires granularity levels of privileges ranging from one patient to a cohort to an entire population. In this paper, we present a viewpoint of the state of secure digital health care in the United States, focusing on the resources that need to be protected as dictated by legal entities and regulations, the available approaches in the present state-of-the art, and, the potential needs for the future of security for digital health care. By utilizing a real world scenario, the authors explore the limitations of health information exchange in the United States, and present one possible architecture for secure digital health care that builds on existing technology alternatives.


2019 ◽  
Vol 42 (3) ◽  
pp. 194-200
Author(s):  
Leeza A. Struwe ◽  
Myra S. Schmaderer ◽  
Lani Zimmerman

The purpose of this study was to compare results using individual change in level of patient activation measure (PAM) scores, individual point change scores, and group means in an outcome analysis. We evaluated changes in PAM scores (increase in level or increase of ≥5 points) to mean group PAM scores on patients who completed a self-management intervention compared with usual care on health care utilization and health-related quality of life. The sample was a subset of 91 multimorbid patients with complete data at completion of a self-management intervention. Results indicated that using a change in points allowed for more refined analysis of change compared with level changes; however, both individual measures were more reflective of actual change than group means. When tailoring interventions, we should consider using individual change scores. Further research is needed to evaluate how best to use PAM scores to measure the impact on clinical and health care outcomes.


2016 ◽  
Vol 04 (02) ◽  
pp. 102-107
Author(s):  
Neera Gupta ◽  
Tushar Dixit ◽  
Vikram K.

AbstractMake in India is a flagship campaign from the Government of India which is aimed at various sectors. Indian health-care system can take advantages by introducing digital technologies to health care. The possible uses of health information technology as a method to engage with people involving communicable and noncommunicable diseases (NCDs) are wide-ranging. Health information technology can support interventions for prevention, diagnosis, managing surveillance, disease monitoring, and treatment compliance of many conditions. Digital health can offer various technologies such as wearables that are tracked by various mobile or smartphone applications to facilitates patient engagement, self-monitoring, and implementing behavior changes in NCDs such as diabetes. By incorporating the interactive audiovisual items, the digital health tools can create greater interest and engage people from different geographies, age, gender, and culture. Currently, the common digital heath tech issues include hesitancy from doctors to adopt any new product or technology, difficulty in reaching and accessing the needy patients, cultural diversity in population, and inadequate infrastructure. The ethical issues of consent, data security, and privacy of patients need to be addressed as they are highly sensitive in nature.


2015 ◽  
Vol 7 (2) ◽  
pp. 172 ◽  
Author(s):  
Yulong Gu ◽  
Martin Orr ◽  
Jim Warren

Health literacy has been described as the capacity to obtain, process, and understand basic health information and services needed to make appropriate health decisions. Improving health literacy may serve to promote concordance with therapy, engage patients in their own health care, and improve health outcomes. Patient portal technology aims at enabling patients and families to have easy access to key information in their own medical records and to communicate with their health care providers electronically. However, there is a gap in our understanding of how portals will improve patient outcome. The authors believe patient portal technology presents an opportunity to improve patient concordance with prescribed therapy, if adequate support is provided to equip patients (and family/carers) with the knowledge needed to utilise the health information available via the portals. Research is needed to understand what a health consumer will use patient portals for and how to support a user to realise the technology?s potential.


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