The impact of requiring patient authorization for use of data in medical records research.
about
Do published guidelines for evaluation of irritable bowel syndrome reflect practice?Use of a medical records linkage system to enumerate a dynamic population over time: the Rochester epidemiology project.Feasibility of a patient decision aid regarding disclosure of personal health information: qualitative evaluation of the Health Care Information DirectiveThe health care information directive"Let's get the best quality research we can": public awareness and acceptance of consent to use existing data in health research: a systematic review and qualitative study.Development and evaluation of a de-identification procedure for a case register sourced from mental health electronic recordsVariation in recruitment across sites in a consent-based clinical data registry: lessons from the Canadian Stroke NetworkRecord linkage research and informed consent: who consents?Developing a standardized healthcare cost data warehouse.Who doesn't authorize the linking of survey and administrative health data? A general population-based investigationThe privacy paradox: laying Orwell's ghost to rest.Prevalence of multimorbidity in a geographically defined American population: patterns by age, sex, and race/ethnicity.History of the Rochester Epidemiology Project: half a century of medical records linkage in a US population.Patient perspectives of medical confidentiality: a review of the literature.Extra-immunization as a clinical indicator for fragmentation of careRisk of developing multimorbidity across all ages in an historical cohort study: differences by sex and ethnicityChanging Incidence of Serum 25-Hydroxyvitamin D Values Above 50 ng/mL: A 10-Year Population-Based Study.Comparing shingles incidence and complication rates from medical record review and administrative database estimates: how close are they?Risk of herpes zoster in children with asthmaThe use of medical records in research: what do patients want?Risk of Stroke and Myocardial Infarction After Herpes Zoster in Older Adults in a US Community Population.Asthma as a risk factor for zoster in adults: A population-based case-control study.LINKING SURVEY AND ADMINISTRATIVE RECORDS: MECHANISMS OF CONSENT10-year trends in the diagnosis and treatment of hepatitis C and concomitant mental health disorders: 1995 to 2005.Participation bias and its impact on the assembly of a genetic specimen repository for a myocardial infarction cohortRole of individual-housing-based socioeconomic status measure in relation to smoking status among late adolescents with asthmaHerpes zoster eye complications: rates and trendsExacerbations in the pre- and post-COPD diagnosis periods.Health care utilization and cost burden of herpes zoster in a community population.Ethical and practical challenges to studying patients who opt out of large-scale biorepository research.Asthma exacerbations and traffic: examining relationships using link-based traffic metrics and a comprehensive patient database.An Alternative Consent Process for Minimal Risk Research in the ICU.What can large population-based birth cohort study ask about past, present and future of children with disorders of development, learning and behaviour?Application of a Natural Language Processing Algorithm to Asthma Ascertainment. An Automated Chart Review.Parental opinions regarding an opt-out consent process for inpatient pediatric prospective observational research in the US.Asthma and Risk of Appendicitis in Children: A Population-Based Case-Control Study.The effect of privacy legislation on observational research.Heterogeneity of asthma and the risk of celiac disease in children.Automated chart review utilizing natural language processing algorithm for asthma predictive index.Association Between Adiposity and Lean Mass With Long-Term Cardiovascular Events in Patients With Coronary Artery Disease: No Paradox.
P2860
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P2860
The impact of requiring patient authorization for use of data in medical records research.
description
1998 nî lūn-bûn
@nan
1998 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
The impact of requiring patien ...... a in medical records research.
@ast
The impact of requiring patien ...... a in medical records research.
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type
label
The impact of requiring patien ...... a in medical records research.
@ast
The impact of requiring patien ...... a in medical records research.
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prefLabel
The impact of requiring patien ...... a in medical records research.
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The impact of requiring patien ...... a in medical records research.
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P2093
P1476
The impact of requiring patient authorization for use of data in medical records research
@en
P2093
P304
P577
1998-11-01T00:00:00Z