نتایج جستجو برای: clinical documentation standards
تعداد نتایج: 1292435 فیلتر نتایج به سال:
BACKGROUND The Multiple Sclerosis Outcome Assessments Consortium (MSOAC) was formed by the National MS Society to develop improved measures of multiple sclerosis (MS)-related disability. OBJECTIVES (1) To assess the current literature and available data on functional performance outcome measures (PerfOs) and (2) to determine suitability of using PerfOs to quantify MS disability in MS clinical...
The objective of this work is to provide a formalization of the semantics of SNOMED CT’s refinement rules in Description Logics and to exemplify their usage on a real world wound documentation system. The goal of unambiguous documentation and communication of medical information with explicit semantics can be reached by combining standards and terminologies. Information Models (e.g. the HL7 Cli...
Background: Quality Improvement (QI) is the organised approach to design and apply constant development inperformance. QI in hospitals increase patient satisfaction, staff satisfaction as well quality of care providedby an organisation. In India assessed by different standards which primarily included thoselaid down National Accreditation Board for Hospitals & Healthcare Providers (NABH), w...
Over the last 15 years, a comprehensive range of international standards has been developed to define the general principles of user centred design and good practice in user interface design. Most of the standards specify general principles rather than the precise details of the interface. The paper briefly describes how standards are created and reviews the definitions of usability. HCI and us...
In order to facilitate effective clinical coding and hence the precise financial reimbursement of acute services, in 2005 Western District Health Service (WDHS) (located in regional Victoria, Australia) undertook a provisional coding trial for inpatient medical episodes to determine the magnitude and accuracy of clinical documentation. Utilising clinical coding software installed on a laptop co...
Creating CDISC SDTM domain data sets from existing clinical trial data can be a challenging task, particularly if the database was not designed with the SDTM standards in mind. A key step in the process involves determining which of the STDM domain datasets need to be produced for submission and then determining what conversion process will be necessary to produce them from the existing data. A...
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