Patient-reported outcomes in cancer care — hearing the patient voice at greater volume
Key Points The collection of electronic patient-reported outcome (ePRO) data at the point of care is feasible and usually provides more reliable information on the patient's experience than that reported by clinicians ePRO data are of research quality, and are an important element of learning h...
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Veröffentlicht in: | Nature reviews. Clinical oncology 2017-12, Vol.14 (12), p.763-772 |
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description | Key Points
The collection of electronic patient-reported outcome (ePRO) data at the point of care is feasible and usually provides more reliable information on the patient's experience than that reported by clinicians
ePRO data are of research quality, and are an important element of learning health-care systems and 'big-data' initiatives
To maximize the utility of big data in learning health-care systems, they must include the 'patient's voice' via the incorporation of PROs into routine care
To date, big-data initiatives have not adequately included ePROs; this situation can be addressed through data standardization
The routine collection of ePRO data simultaneously improves the quality of care for patients and facilitates big-data initiatives
Evidence obtained over the past few years indicates that the routine collection and inclusion of ePRO data in patient care improves clinical outcomes
In the past decade, the importance of patient-reported outcomes (PROs) as a key measure of the quality of care delivered to patients with cancer has been acknowledged. PROs were used in the context of research studies, but growing evidence indicates that the incorporation of electronic PRO (ePRO) assessments into standard health-care settings can improve the quality of care delivered to patients with cancer. The authors of this Review discuss aspects related to PROs such as measurements, implementation challenges, and outcome improvements associated with their use.
Recording of patient-reported outcomes (PROs) enables direct measurement of the experiences of patients with cancer. In the past decade, the use of PROs has become a prominent topic in health-care innovation; this trend highlights the role of the patient experience as a key measure of health-care quality. Historically, PROs were used solely in the context of research studies, but a growing body of literature supports the feasibility of electronic collection of PROs, yielding reliable data that are sometimes of better quality than clinician-reported data. The incorporation of electronic PRO (ePRO) assessments into standard health-care settings seems to improve the quality of care delivered to patients with cancer. Such efforts, however, have not been widely adopted, owing to the difficulties of integrating PRO-data collection into clinical workflows and electronic medical-record systems. The collection of ePRO data is expected to enhance the quality of care received by patients with cancer; however, for this |
doi_str_mv | 10.1038/nrclinonc.2017.153 |
format | Article |
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The collection of electronic patient-reported outcome (ePRO) data at the point of care is feasible and usually provides more reliable information on the patient's experience than that reported by clinicians
ePRO data are of research quality, and are an important element of learning health-care systems and 'big-data' initiatives
To maximize the utility of big data in learning health-care systems, they must include the 'patient's voice' via the incorporation of PROs into routine care
To date, big-data initiatives have not adequately included ePROs; this situation can be addressed through data standardization
The routine collection of ePRO data simultaneously improves the quality of care for patients and facilitates big-data initiatives
Evidence obtained over the past few years indicates that the routine collection and inclusion of ePRO data in patient care improves clinical outcomes
In the past decade, the importance of patient-reported outcomes (PROs) as a key measure of the quality of care delivered to patients with cancer has been acknowledged. PROs were used in the context of research studies, but growing evidence indicates that the incorporation of electronic PRO (ePRO) assessments into standard health-care settings can improve the quality of care delivered to patients with cancer. The authors of this Review discuss aspects related to PROs such as measurements, implementation challenges, and outcome improvements associated with their use.
Recording of patient-reported outcomes (PROs) enables direct measurement of the experiences of patients with cancer. In the past decade, the use of PROs has become a prominent topic in health-care innovation; this trend highlights the role of the patient experience as a key measure of health-care quality. Historically, PROs were used solely in the context of research studies, but a growing body of literature supports the feasibility of electronic collection of PROs, yielding reliable data that are sometimes of better quality than clinician-reported data. The incorporation of electronic PRO (ePRO) assessments into standard health-care settings seems to improve the quality of care delivered to patients with cancer. Such efforts, however, have not been widely adopted, owing to the difficulties of integrating PRO-data collection into clinical workflows and electronic medical-record systems. The collection of ePRO data is expected to enhance the quality of care received by patients with cancer; however, for this approach to become routine practice, uniquely trained people, and appropriate policies and analytical solutions need to be implemented. In this Review, we discuss considerations regarding measurements of PROs, implementation challenges, as well as evidence of outcome improvements associated with the use of PROs, focusing on the centrality of PROs as part of 'big-data' initiatives in learning health-care systems.</description><identifier>ISSN: 1759-4774</identifier><identifier>EISSN: 1759-4782</identifier><identifier>DOI: 10.1038/nrclinonc.2017.153</identifier><identifier>PMID: 28975931</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/114/1314 ; 692/308/409 ; 692/700/565/2194 ; 692/700/565/415 ; 692/700/784 ; Cancer ; Cancer treatment ; Delivery of Health Care, Integrated ; Electronic medical records ; Evaluation ; Health attitudes ; Humans ; Medicine ; Medicine & Public Health ; Neoplasms - diagnosis ; Neoplasms - therapy ; Oncology ; Patient outcomes ; Patient Reported Outcome Measures ; Patients ; Process Assessment, Health Care ; Quality Improvement ; Quality Indicators, Health Care ; review-article ; Treatment Outcome</subject><ispartof>Nature reviews. Clinical oncology, 2017-12, Vol.14 (12), p.763-772</ispartof><rights>Springer Nature Limited 2017</rights><rights>COPYRIGHT 2017 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Dec 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-bbd28311fe9859f8c8ecfadca5dfe93f64c18cf06b1d0e72b291bccdb0fe7ddc3</citedby><cites>FETCH-LOGICAL-c539t-bbd28311fe9859f8c8ecfadca5dfe93f64c18cf06b1d0e72b291bccdb0fe7ddc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nrclinonc.2017.153$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nrclinonc.2017.153$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28975931$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LeBlanc, Thomas W.</creatorcontrib><creatorcontrib>Abernethy, Amy P.</creatorcontrib><title>Patient-reported outcomes in cancer care — hearing the patient voice at greater volume</title><title>Nature reviews. Clinical oncology</title><addtitle>Nat Rev Clin Oncol</addtitle><addtitle>Nat Rev Clin Oncol</addtitle><description>Key Points
The collection of electronic patient-reported outcome (ePRO) data at the point of care is feasible and usually provides more reliable information on the patient's experience than that reported by clinicians
ePRO data are of research quality, and are an important element of learning health-care systems and 'big-data' initiatives
To maximize the utility of big data in learning health-care systems, they must include the 'patient's voice' via the incorporation of PROs into routine care
To date, big-data initiatives have not adequately included ePROs; this situation can be addressed through data standardization
The routine collection of ePRO data simultaneously improves the quality of care for patients and facilitates big-data initiatives
Evidence obtained over the past few years indicates that the routine collection and inclusion of ePRO data in patient care improves clinical outcomes
In the past decade, the importance of patient-reported outcomes (PROs) as a key measure of the quality of care delivered to patients with cancer has been acknowledged. PROs were used in the context of research studies, but growing evidence indicates that the incorporation of electronic PRO (ePRO) assessments into standard health-care settings can improve the quality of care delivered to patients with cancer. The authors of this Review discuss aspects related to PROs such as measurements, implementation challenges, and outcome improvements associated with their use.
Recording of patient-reported outcomes (PROs) enables direct measurement of the experiences of patients with cancer. In the past decade, the use of PROs has become a prominent topic in health-care innovation; this trend highlights the role of the patient experience as a key measure of health-care quality. Historically, PROs were used solely in the context of research studies, but a growing body of literature supports the feasibility of electronic collection of PROs, yielding reliable data that are sometimes of better quality than clinician-reported data. The incorporation of electronic PRO (ePRO) assessments into standard health-care settings seems to improve the quality of care delivered to patients with cancer. Such efforts, however, have not been widely adopted, owing to the difficulties of integrating PRO-data collection into clinical workflows and electronic medical-record systems. The collection of ePRO data is expected to enhance the quality of care received by patients with cancer; however, for this approach to become routine practice, uniquely trained people, and appropriate policies and analytical solutions need to be implemented. In this Review, we discuss considerations regarding measurements of PROs, implementation challenges, as well as evidence of outcome improvements associated with the use of PROs, focusing on the centrality of PROs as part of 'big-data' initiatives in learning health-care systems.</description><subject>631/114/1314</subject><subject>692/308/409</subject><subject>692/700/565/2194</subject><subject>692/700/565/415</subject><subject>692/700/784</subject><subject>Cancer</subject><subject>Cancer treatment</subject><subject>Delivery of Health Care, Integrated</subject><subject>Electronic medical records</subject><subject>Evaluation</subject><subject>Health attitudes</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neoplasms - diagnosis</subject><subject>Neoplasms - therapy</subject><subject>Oncology</subject><subject>Patient outcomes</subject><subject>Patient Reported Outcome Measures</subject><subject>Patients</subject><subject>Process Assessment, Health Care</subject><subject>Quality Improvement</subject><subject>Quality Indicators, Health Care</subject><subject>review-article</subject><subject>Treatment Outcome</subject><issn>1759-4774</issn><issn>1759-4782</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kc9qFTEUxoNYbL36Ai4kIIibuSaT-ZMsS_EfFNqFgruQSU7uTZlJxiRTcOdD9An7JOZy620rShYnnPy-j5zzIfSKkjUljL_3UY_OB6_XNaH9mrbsCTqhfSuqpuf108O9b47R85SuCOm6pmfP0HHNRXli9AR9v1TZgc9VhDnEDAaHJeswQcLOY628hlhKBHz76wZvQUXnNzhvAc97Ib4OTgNWGW8iqFzo6zAuE7xAR1aNCV7e1RX69vHD17PP1fnFpy9np-eVbpnI1TCYmjNKLQjeCss1B22V0ao1pcVs12jKtSXdQA2Bvh5qQQetzUAs9MZotkLv9r5zDD8WSFlOLmkYR-UhLElS0fRECFHGXaE3f6FXYYm-_K5QXdsQ1nTkntqoEaTzNuSo9M5Unra04YQLwgq1_gdVjoHJ6eDButJ_JHj7QFAWOeZtKpvKLvj0GKz3oI4hpQhWztFNKv6UlMhd7vKQu9zlLkvuRfT6brRlmMAcJH-CLgDbA2neJQjxwez_t_0NBJS9JA</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>LeBlanc, Thomas W.</creator><creator>Abernethy, Amy P.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20171201</creationdate><title>Patient-reported outcomes in cancer care — hearing the patient voice at greater volume</title><author>LeBlanc, Thomas W. ; 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Clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LeBlanc, Thomas W.</au><au>Abernethy, Amy P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Patient-reported outcomes in cancer care — hearing the patient voice at greater volume</atitle><jtitle>Nature reviews. Clinical oncology</jtitle><stitle>Nat Rev Clin Oncol</stitle><addtitle>Nat Rev Clin Oncol</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>14</volume><issue>12</issue><spage>763</spage><epage>772</epage><pages>763-772</pages><issn>1759-4774</issn><eissn>1759-4782</eissn><abstract>Key Points
The collection of electronic patient-reported outcome (ePRO) data at the point of care is feasible and usually provides more reliable information on the patient's experience than that reported by clinicians
ePRO data are of research quality, and are an important element of learning health-care systems and 'big-data' initiatives
To maximize the utility of big data in learning health-care systems, they must include the 'patient's voice' via the incorporation of PROs into routine care
To date, big-data initiatives have not adequately included ePROs; this situation can be addressed through data standardization
The routine collection of ePRO data simultaneously improves the quality of care for patients and facilitates big-data initiatives
Evidence obtained over the past few years indicates that the routine collection and inclusion of ePRO data in patient care improves clinical outcomes
In the past decade, the importance of patient-reported outcomes (PROs) as a key measure of the quality of care delivered to patients with cancer has been acknowledged. PROs were used in the context of research studies, but growing evidence indicates that the incorporation of electronic PRO (ePRO) assessments into standard health-care settings can improve the quality of care delivered to patients with cancer. The authors of this Review discuss aspects related to PROs such as measurements, implementation challenges, and outcome improvements associated with their use.
Recording of patient-reported outcomes (PROs) enables direct measurement of the experiences of patients with cancer. In the past decade, the use of PROs has become a prominent topic in health-care innovation; this trend highlights the role of the patient experience as a key measure of health-care quality. Historically, PROs were used solely in the context of research studies, but a growing body of literature supports the feasibility of electronic collection of PROs, yielding reliable data that are sometimes of better quality than clinician-reported data. The incorporation of electronic PRO (ePRO) assessments into standard health-care settings seems to improve the quality of care delivered to patients with cancer. Such efforts, however, have not been widely adopted, owing to the difficulties of integrating PRO-data collection into clinical workflows and electronic medical-record systems. The collection of ePRO data is expected to enhance the quality of care received by patients with cancer; however, for this approach to become routine practice, uniquely trained people, and appropriate policies and analytical solutions need to be implemented. In this Review, we discuss considerations regarding measurements of PROs, implementation challenges, as well as evidence of outcome improvements associated with the use of PROs, focusing on the centrality of PROs as part of 'big-data' initiatives in learning health-care systems.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>28975931</pmid><doi>10.1038/nrclinonc.2017.153</doi><tpages>10</tpages></addata></record> |
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subjects | 631/114/1314 692/308/409 692/700/565/2194 692/700/565/415 692/700/784 Cancer Cancer treatment Delivery of Health Care, Integrated Electronic medical records Evaluation Health attitudes Humans Medicine Medicine & Public Health Neoplasms - diagnosis Neoplasms - therapy Oncology Patient outcomes Patient Reported Outcome Measures Patients Process Assessment, Health Care Quality Improvement Quality Indicators, Health Care review-article Treatment Outcome |
title | Patient-reported outcomes in cancer care — hearing the patient voice at greater volume |
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