2014
DOI: 10.1136/bmjqs-2013-002524
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The experiences of professionals with using information from patient-reported outcome measures to improve the quality of healthcare: a systematic review of qualitative research

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Cited by 398 publications
(449 citation statements)
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“…This approach addresses the PROs, namely valuing, making sense of the data, and using it to make changes to patient care. 8 Implementing decision-support aids was an essential facilitator (local guidelines on referral pathways, online decision tree, quick reference card). The easy access to the decision-aids on the website worked well in the pediatric setting and is an approach recommended for the future.…”
Section: Discussionmentioning
confidence: 99%
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“…This approach addresses the PROs, namely valuing, making sense of the data, and using it to make changes to patient care. 8 Implementing decision-support aids was an essential facilitator (local guidelines on referral pathways, online decision tree, quick reference card). The easy access to the decision-aids on the website worked well in the pediatric setting and is an approach recommended for the future.…”
Section: Discussionmentioning
confidence: 99%
“…As the experience in using these measures increased it became obvious that there is a clinical value in using individual patient PROs profiles in daily practice to give clinicians standardized information on patient problems to identify/monitor symptoms, evaluate treatment outcomes and support shared decisionmaking. [2][3][4][5][6][7][8] Recently, PROs became widely accessible to clinicians via electronic/online reporting with new developments towards integration with Electronic Health Records (EHRs) via patient portals. 2 The integration of PROs with clinical data in EHRs offers innovative opportunities of including patient perspective in Big Dataset for analysis and rapid learning from combined biological, clinical and treatment information.…”
Section: Introductionmentioning
confidence: 99%
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“…On the national level, health care quality improvement has become a focus as health care delivery and reimbursement undergo rapid changes [1], including a shift toward value-based insurance models, which will require evidence-based patient-reported outcomes to help distinguish between high and low value services [2]. Despite the benefits of obtaining patientreported outcome measures, practical barriers with regard to traditional pen and paper data collection are significant, including the time, labor, and resourceintensive nature of this process, all of which may not be conducive to a high-volume practice setting [3].…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5][6][7] Because PROs capture domains that cross conditions and reflect patient-centered priorities, such measures may more accurately reflect the health and well-being of individuals with multiple chronic medical conditions (MCCs) than do common disease-specific quality measures. 8,9 Across populations, higher scores on these and other domains of health-related quality of life (HRQOL) correlate with lower rates of hospitalization, lower overall mortality, lower cardiovascular morbidity, and lower outpatient services utilization in populations of patients with chronic illness.…”
mentioning
confidence: 99%