Electronic patient-reported data capture as a foundation of rapid learning cancer care.
about
Comparative effectiveness research in oncologyConsiderations for observational research using large data sets in radiation oncologyPersonalized medicine and opioid analgesic prescribing for chronic pain: opportunities and challengesChallenges and Opportunities for Exploring Patient-Level DataThe value of data collection within a palliative care programIntegrating Patient-Reported Outcomes into Spine Surgical Care through Visual Dashboards: Lessons Learned from Human-Centered DesignA universal decision support system. Addressing the decision-making needs of patients, families, and clinicians in the setting of critical illnessPediatric palliative care and eHealth opportunities for patient-centered careQuality of Life Measurements: Any Value for Clinical Practice?Data for cancer comparative effectiveness research: past, present, and future potential.A systematic review of the impact of routine collection of patient reported outcome measures on patients, providers and health organisations in an oncologic setting.True translational research: bridging the three phases of translation through data and behavior.Missing signposts on the roadmap to quality: a call to improve medication adherence indicators in data collection for population researchLegal and regulatory considerations associated with use of patient-generated health data from social media and mobile health (mHealth) devicesUse of an electronic patient-reported outcome measurement system to improve distress management in oncologyTell Us™: a Web-based tool for improving communication among patients, families, and providers in hospice and palliative care through systematic data specification, collection, and useReview of electronic patient-reported outcomes systems used in cancer clinical care.State-level cancer quality assessment and research: building and sustaining the data infrastructure.Rapid-learning system for cancer care.Structured decision-making: using personalized medicine to improve the value of cancer care.Stakeholder perspectives on implementing the National Cancer Institute's patient-reported outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE).Strategies to use tablet computers for collection of electronic patient-reported outcomes.Bringing PROMIS to practice: brief and precise symptom screening in ambulatory cancer carePalliative care needs of patients with cancer living in the communityIntegrating Patient-Reported Outcome Measures into Routine Cancer Care: Cancer Patients' and Clinicians' Perceptions of Acceptability and Value.Do high symptom scores trigger clinical actions? An audit after implementing electronic symptom screeningQuality of life among long-term survivors of non-Hodgkin lymphoma: a follow-up studyHealth Information Technology: Meaningful Use and Next Steps to Improving Electronic Facilitation of Medication Adherence.Applying Rasch analysis to evaluate measurement equivalence of different administration formats of the Activity Limitation scale of the Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR).An academic-health service partnership in nursing: lessons from the field.Collecting, Integrating, and Disseminating Patient-Reported Outcomes for Research in a Learning Healthcare System.Development and preliminary evaluation of a telephone-based mindfulness training intervention for survivors of critical illness.How Should Remote Clinical Monitoring Be Used to Treat Alcohol Use Disorders?: Initial Findings From an Expert Round Table DiscussionTumor control versus adverse events with targeted anticancer therapies.Improving the management of dyspnea in the community using rapid learning approaches.Setting the vision: applied patient-reported outcomes and smart, connected digital healthcare systems to improve patient-centered outcomes prediction in critical illness.EAPC White Paper on outcome measurement in palliative care: Improving practice, attaining outcomes and delivering quality services - Recommendations from the European Association for Palliative Care (EAPC) Task Force on Outcome Measurement.Clinical pathway for the screening, assessment and management of anxiety and depression in adult cancer patients: Australian guidelines.Feasibility and diagnostic accuracy of the Patient-Reported Outcomes Measurement Information System (PROMIS) item banks for routine surveillance of sleep and fatigue problems in ambulatory cancer care.Symptoms, Quality of Life, and Daily Activities in People With Newly Diagnosed Solid Tumors Presenting to a Medical Oncologist.
P2860
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P2860
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
@ast
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
@en
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
@nl
type
label
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
@ast
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
@en
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
@nl
prefLabel
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
@ast
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
@en
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
@nl
P2093
P1433
P1476
Electronic patient-reported data capture as a foundation of rapid learning cancer care.
@en
P2093
Asif Ahmad
H Kim Lyerly
Jane L Wheeler
Jennifer Barsky Reese
S Yousuf Zafar
P356
10.1097/MLR.0B013E3181DB53A4
P433
P577
2010-06-01T00:00:00Z