Exam 2 Flashcards
ARRA
American Recovery and Reinvestment Act of 2009 - Amended the HIPAA rules. The key goal is to create a national standard for the configuration and content of health records so that health information can be easily shared among providers of different organizations. (the goal is complete EHR)
Source-Oriented Health Record
Documents are grouped according to their point of origin. Labs with labs, imaging with imaging, progress notes with progress notes, etc.
Problem-Oriented Health Record
Is arranged according to a problem list. Each problem is indexed with a unique number, and reports and clinical documentation are keyed to the numbers representing the problems they address. They are arranged in chronological or reverse chronological order.
SOAP
Information in progress notes is organized using this sequence.
S - Subjective Information (such as a patient complaint)
O - Objective data (such as diagnostic test results)
A - Assessment (diagnosis)
P - Plan (treatment)
Integrated Health Record
Is arranged so that the documentation from various sources is intermingled and follows a strict chronological or reverse chronological order. The advantage is that it’s easy for caregivers to follow the course of the patient’s diagnosis, but difficult to compare related information or to even locate specific information. Used in paper charts.
Structured Data
Generally found in checkboxes and drop-down boxes
Unstructured Data
Also called narrative data, can be entered in a free next format
ONC
Office of the National Coordinator for Health Information Technology - Is within the Department of Health and Human Services (HHS). job is to oversee the development of an NHII (National Health Information Infrastructure)
NHII
National Health Information Infrastructure - a framework that will support the appropriate and secure exchange of health information among organizations throughout the nation.
AHRQ
Agency for Healthcare Research and Quality - One of the HHS agencies that provides funding and information for health information technology projects, including grants and state and regional health information exchange (HIE)
Meaningful Use Criteria
A term used by the federal government to describe the requirements healthcare providers must meet to receive incentive payments for implementing different phases of an EHR between 2011 and 2015. There are 3 stages of meaningful use criteria.
Stage 1 - Meaningful Use Criteria
Focuses on electronically capturing health information in an encoded format; using that information for care coordination purposes.
Stage 2 - Meaningful Use Criteria
Encourages the use of health information technology for continuous quality improvement at the point of care and the exchange of information in the most structured format possible, such as the electronic transmission of orders entered.
Stage 3 - Meaningful Use Criteria
Expands on stage 2. Focuses on promoting improvements in quality, safety, and efficiency; using decision support for national high-priority conditions; ensuring patient access to self-management tools; providing access to comprehensive patient date; and improving population health.
What are the 3 National Health Information Network (NHIN) Standards?
- Structure and content standards
- Functionality standards
- Technical standards
Structure and Content Standards
On of the standards of the National Health Information Network - establishes and provides clear and uniform definitions of the data elements to be included in EHR systems. They specify the type of data to be collected in each data field, the length of each data field, and the attributes of each data field, all of which are captured in data dictionaries.
Functionality Standards
One of the standards of the National Health Information Network - Defines the components an EHR needs to support the functions for which it is designed.
Technical Standards
One of the standards of the National Health Information Network - Complement content and structure, and vocabulary standards are also required to make interoperability possible. Technical standards provide the rules for how these data are transmitted from one computer system to another.
CCHIT
Certification Commission for Health Information Technology - is a non-profit organization with the public mission of accelerating the adoption of health IT. The commission established the first comprehensive practical definition of what capabilities were needed in these systems.
ANSI
American National Standards Institute - A private, non-profit organization founded to coordinate the US census systems. Today, ANSI approves official American national standards and includes membership from all sectors, not just healthcare. They are responsible for accrediting healthcare standards development organizations in the U.S.
Data Dictionary
A centralized repository of information about data that includes elements such as meaning, relationships to other data, origin, usage, and format. The purpose is to standardize definitions and ensure consistency of use.
Database
An organized collection of data that have been stored electronically for easy access.
DBMS
Database Management Systems - An integrated set of programs that helps users store and manipulate data easily and efficiently. DBMSs make it possible to create, modify, delete, and view the data in a database.
Clinical Data Repository
A centralized database that captures, sorts, and processes patient data and then returns them to the user.
What are other names for messaging standards?
Interoperability Standards and Data Exchange Standards
CDS
Clinical Decision Support - A clinical system, application, or process that helps health professionals make clinical decisions to enhance patient care. CDS systems help physicians and other clinicians make diagnostic and treatment decisions.
Electronic Signature
A unique personal identifier that is entered by the author of EHR documentation via electronic means.
Digital Signature
A digitized version of a handwritten signature. The author sings his or her name on a pen pad, and the signature is automatically converted into a digital signature that is affixed to the electronic document.
Unique Personal Identifier
A code or password
Biometric Identifier
A fingerprint or retinal scan
Discovery
The formal, pretrial legal process used by parties to a lawsuit to obtain information. Discovery helps ensure that neither party is subjected to surprises at trial.
Health Data Repository
A database that provides immediate national access to local data in the event of primary system failure or system unavailability. The repository is an effort to improve data accessibility and increase disaster preparedness.
Data
Data are the dates, numbers, images, symbols, letters, and words that represent basic facts and observations about people, processes, measurements, and conditions.
Information
Is factual data that have been collected, combined, analyzed, interpreted, and/or converted into a form that can be used for a specific purpose.
Financial Data
Information about patient’s occupation, employer,and insurance coverage.
Implied Consent
Is assumed when a patient voluntarily submits to medical treatment.
Expressed Consent
Is permission that is either spoken or written. (consent to treatment) Patients are usually asked to sign a general consent form during the registration and admissions process.
Informed Consent
A more specific consent required for procedures that involve significant risk.