Results 51 to 60 of about 739,459 (302)

Semantic Integration of Cervical Cancer Data Repositories to Facilitate Multicenter Association Studies: The ASSIST Approach [PDF]

, 2009
The current work addresses the unifi cation of Electronic Health Records related to cervical cancer into a single medical knowledge source, in the context of the EU-funded ASSIST research project.
Agorastos, Theodoros, Coorevits, Pascal, Delopoulos, Manolis, Kaufmann, Andreas M., Koutkias, Vassilis, Kurzeja, Roberto, Mitkas, Pericles A., Tantsis, Antonios, Weyers, Steven   +8 more
core   +2 more sources

Quality and Cost Analysis of Nurse Staffing, Discharge Preparation, and Postdischarge Utilization [PDF]

, 2011
Objectives. To determine the impact of unit-level nurse staffing on quality of discharge teaching, patient perception of discharge readiness, and postdischarge readmission and emergency department (ED) visits, and cost-benefit of adjustments to unit ...
Bobay, Kathleen, Weiss, Marianne E., Yakusheva, Olga   +2 more
core   +2 more sources

Evaluating the Utility of Paired Tumor and Germline Targeted DNA Sequencing for Pediatric Oncology Patients: A Single Institution Report

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Objective To evaluate the diagnostic yield and utility of universal paired tumor–normal multigene panel sequencing in newly diagnosed pediatric solid and central nervous system (CNS) tumor patients and to compare the detection of germline pathogenic/likely pathogenic variants (PV/LPVs) against established clinical referral criteria for cancer ...
Natalie Waligorski, Rebecca Ronsley, Shannon M. Stasi, Jeffrey Stevens, Erin R. Rudzinski, Christina M. Lockwood, Sarah E. S. Leary, Bonnie L. Cole, Michelle A. Ting, Vera Paulson   +9 more
wiley   +1 more source

Preferences of Pediatric Patients and Their Caregivers for Chemotherapy‐Induced Nausea and Vomiting Control Endpoints: A Mixed Methods Study

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Purpose Although not always achieved, complete chemotherapy‐induced nausea and vomiting (CINV) control is the conventional goal of CINV prophylaxis. In this two‐center, mixed‐methods study, we sought to understand the preferences of adolescent patients and family caregivers for CINV control endpoints.
Haley Newman, Tadi Hondonga, Alison Berry, Caitlin Elgarten, Jason Freedman, Katelyn Oranges, Sara McDonough, Caroline Diorio, L. Lee Dupuis   +8 more
wiley   +1 more source

Oncology health-care professionals’ perceived effects of patient accessible electronic health records 6 years after launch: A survey study at a major university hospital in Sweden

Health Informatics Journal, 2020
Patient accessible electronic health records have been launched in many countries, and generally, health-care professionals have had strong initial concerns related to the areas patient contact, documentation practices and quality of care.
Jonas Moll, Åsa Cajander
doaj   +1 more source

A meta-narrative review of electronic patient records [PDF]

, 2009
This session comprises four papers that consider how systematic review methods may be developed in order to make the best use of complex evidence in education and health.
Bark, P., Greenhalgh, T., Potts, H.W.W., Swinglehurst, D., Wong, G.   +4 more
core  

Financial Burden Associated With Hospitalisation Among Families of Childhood Brain Tumours in Australia

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Families of children with cancer experience significant financial strain, even with universal healthcare. Indirect costs, such as productivity losses and non‐medical expenses, are rarely included in economic evaluations, and little is known about how effectively financial aid programmes alleviate this burden. Childhood brain tumours
Megumi Lim, Natalie Bradford, David Brain, Sameera Senanayake, Sanjeewa Kularatna, Kate Young, Christine Cashion, Tim Hassall, Susanna Cramb   +8 more
wiley   +1 more source

Patient-Centered Outcomes Measurement: Does It Require Information From Patients?

Journal of Patient-Centered Research and Reviews, 2017
Purpose: Since collecting outcome measure data from patients can be expensive, time-consuming, and subject to memory and nonresponse bias, we sought to learn whether outcomes important to patients can be obtained from data in the electronic health record
Leif I. Solberg, Stephen E. Asche, John Butler, David Carrell, Christine K. Norton, Jeffrey G. Jarvik, Rebecca Smith-Bindman, Juliana O. Tillema, Robin R. Whitebird, Ann M. Werner, Jeanette Y. Ziegenfuss   +10 more
doaj   +1 more source

Evaluating records for free text content [PDF]

, 2010
The PREP team is interested in electronic health records. This project aims to make data in records more usable for researchers. We work on electronic health records with a particular focus on free text (unstructured data) that is not directly amenable ...
Ali, Aishath, Cassell, Jackie
core   +1 more source

Electronic Privacy: Patient Concerns [PDF]

, 2014
This study postulates issues related to electronic privacy and addresses the factors that directly effect personal electronic information. There is no positivist study done to measure patient privacy concerns using Smith et a 1(1996) privacy model and ...
Akram, Anza A.
core   +2 more sources