Data Accuracy

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  Subject Areas on Research

  • A Bayesian Approach to Inferring Rates of Selfing and Locus-Specific Mutation. 
  • A Systematic Framework to Rapidly Obtain Data on Patients with Cancer and COVID-19: CCC19 Governance, Protocol, and Quality Assurance. 
  • A hidden Markov model approach to analyze longitudinal ternary outcomes when some observed states are possibly misclassified. 
  • A longitudinal analysis of data quality in a large pediatric data research network. 
  • Accuracy of Self-reported Weight in Hispanic/Latino Adults of the Hispanic Community Health Study/Study of Latinos. 
  • Accuracy of the Liver Imaging Reporting and Data System in Computed Tomography and Magnetic Resonance Image Analysis of Hepatocellular Carcinoma or Overall Malignancy-A Systematic Review. 
  • Accuracy of the medication list in the electronic health record-implications for care, research, and improvement. 
  • Analytical Evaluation of the Abbott RealTime CT/NG Assay for Detection of Chlamydia trachomatis and Neisseria gonorrhoeae in Rectal and Pharyngeal Swabs. 
  • Are three-day voiding diaries feasible and reliable? Results from the Symptoms of Lower Urinary Tract Dysfunction Research Network (LURN) cohort. 
  • Assessing Quality of Surgical Real-World Data from an Automated Electronic Health Record Pipeline. 
  • Bias from Differential Exposure Measurement Error in a Study of Flight Attendants. 
  • Biases introduced by filtering electronic health records for patients with "complete data". 
  • Caveat emptor: the combined effects of multiplicity and selective reporting. 
  • Claims-based cardiovascular outcome identification for clinical research: Results from 7 large randomized cardiovascular clinical trials. 
  • Clinical trial metadata: defining and extracting metadata on the design, conduct, results and costs of 125 randomised clinical trials funded by the National Institute for Health Research Health Technology Assessment programme. 
  • Critical Review of Current Approaches for Echocardiographic Reproducibility and Reliability Assessment in Clinical Research. 
  • Data quality from a longitudinal study of adolescent health at schools near industrial livestock facilities. 
  • Electronic health records to facilitate clinical research. 
  • Enhancing the value of clinical trials: the role of data sharing. 
  • Evaluating fitness-for-use of electronic health records in pragmatic clinical trials: reported practices and recommendations. 
  • Evaluation of identifier field agreement in linked neonatal records. 
  • Evaluation of the Use of Cancer Registry Data for Comparative Effectiveness Research. 
  • Factors Affecting Accuracy of Data Abstracted from Medical Records. 
  • GRADE guidelines: 21 part 1. Study design, risk of bias, and indirectness in rating the certainty across a body of evidence for test accuracy. 
  • GRADE guidelines: 21 part 2. Test accuracy: inconsistency, imprecision, publication bias, and other domains for rating the certainty of evidence and presenting it in evidence profiles and summary of findings tables. 
  • HRS White Paper on interoperability of data from cardiac implantable electronic devices (CIEDs). 
  • Harms are assessed inconsistently and reported inadequately Part 2: nonsystematic adverse events. 
  • Harms are assessed inconsistently and reported inadequately part 1: systematic adverse events. 
  • How to Teach Health IT Evaluation: Recommendations for Health IT Evaluation Courses. 
  • Important considerations for trials for peripheral arterial disease: Lessons learned from the paclitaxel mortality signal: A report on behalf of the registry assessment for peripheral interventional Devices (RAPID) Paclitaxel Pathways Program. 
  • Improving Quality and Safety Through Use of Secondary Data: Methods Case Study. 
  • Individual risk prediction using data beyond the medical clinic. 
  • Laboratory Accuracy Improvement in the UK NEQAS Leucocyte Immunophenotyping Immune Monitoring Program: An Eleven-Year Review via Longitudinal Mixed Effects Modeling. 
  • Level and Prevalence of Spin in Published Cardiovascular Randomized Clinical Trial Reports With Statistically Nonsignificant Primary Outcomes: A Systematic Review. 
  • Medical record bias in documentation of obstetric and neonatal clinical quality of care indicators in Uganda. 
  • Priorities to Overcome Barriers Impacting Data Science Application in Emergency Care Research. 
  • Real-World Data: Policy Issues Regarding their Access and Use. 
  • Recommendations for Reporting Machine Learning Analyses in Clinical Research. 
  • Ten Simple Rules for Effective Statistical Practice. 
  • The Accuracy of the Patient Health Questionnaire-9 Algorithm for Screening to Detect Major Depression: An Individual Participant Data Meta-Analysis. 
  • The Clinical Trials Transformation Initiative: Methodology supporting the mission. 
  • The Complexity of Conducting a Multicenter Clinical Trial: Taking It to the Next Level Stipulated by the Federal Agencies. 
  • The Impact of a Rigorous Quality Program on 3D Echocardiography Data Quality in an International Multisite Randomized Trial. 
  • The challenges of data safety monitoring for a pragmatic study: Lessons from the ADAPTABLE study. 
  • The impact of respiratory gating on improving volume measurement of murine lung tumors in micro-CT imaging. 
  • The use of real-world data/evidence in regulatory submissions. 
  • Under-reporting of TB cases and associated factors: a case study in China. 
  • Using clinical data to effect practice change. 
  • eSource for Standardized Health Information Exchange in Clinical Research: A Systematic Review.