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Impact of sharing electronic health records with patients on the quality and safety of care: a systematic review and narrative synthesis protocol.
Neves, Ana Luisa; Carter, Alexander W; Freise, Lisa; Laranjo, Liliana; Darzi, Ara; Mayer, Erik K.
Afiliação
  • Neves AL; Center for Health Policy, Institute of Global Health Innovation, Imperial College London, London, UK.
  • Carter AW; CINTESIS - Center for Health Technology and Services Research, University of Porto, Porto, Portugal.
  • Freise L; Center for Health Policy, Institute of Global Health Innovation, Imperial College London, London, UK.
  • Laranjo L; Center for Health Policy, Institute of Global Health Innovation, Imperial College London, London, UK.
  • Darzi A; Australian Institute of Health Innovation, Centre for Health Informatics, Macquarie University, Macquarie Park, New South Wales, Australia.
  • Mayer EK; Center for Health Policy, Institute of Global Health Innovation, Imperial College London, London, UK.
BMJ Open ; 8(8): e020387, 2018 Aug 13.
Article em En | MEDLINE | ID: mdl-30104310
ABSTRACT

INTRODUCTION:

Providing patients with access to electronic health records (EHRs) has emerged as a promising solution to improve quality of care and safety. As the efforts to develop and implement EHR-based data sharing platforms mature and scale up worldwide, there is a need to evaluate the impact of these interventions and to weigh their relative risks and benefits, in order to inform evidence-based health policies. The aim of this work is to systematically characterise and appraise the demonstrated benefits and risks of sharing EHR with patients, by mapping them across the six domains of quality of care of the Institute of Medicine (IOM) analytical framework (ie, patient-centredness, effectiveness, efficiency, timeliness, equity and safety). METHODS AND

ANALYSIS:

CINAHL, Cochrane, Embase, HMIC, Medline/PubMed and PsycINFO databases will be searched from January 1997 to August 2017. Primary outcomes will include measures related with the six domains of quality of care of the IOM analytical framework. The quality of the studies will be assessed using the Cochrane Risk of Bias Tool, the ROBINS-I Tool and the Drummond's checklist. A narrative synthesis will be conducted for all included studies. Subgroup analysis will be performed by domain of quality of care domain and by time scale (ie, short-term, medium-term or long-term impact). The body of evidence will be summarised in a Summary of Findings table and its strength assessed according to the GRADE criteria. ETHICS AND DISSEMINATION This review does not require ethical approval as it will summarise published studies with non-identifiable data. This protocol complies with the Preferred Reporting Items for Systematic Review and Meta-Analyses Protocols guidelines. Findings will be disseminated widely through peer-reviewed publication and conference presentations, and patient partners will be included in summarising the research findings into lay summaries and reports. PROSPERO REGISTRATION NUMBER CRD42017070092.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Qualidade da Assistência à Saúde / Disseminação de Informação / Registros Eletrônicos de Saúde / Segurança do Paciente Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Aspecto: Equity_inequality / Ethics Limite: Humans Idioma: En Revista: BMJ Open Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Qualidade da Assistência à Saúde / Disseminação de Informação / Registros Eletrônicos de Saúde / Segurança do Paciente Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Aspecto: Equity_inequality / Ethics Limite: Humans Idioma: En Revista: BMJ Open Ano de publicação: 2018 Tipo de documento: Article