Chapter 10-11 (Consumer Informatics/Health Information Exchange) Flashcards

1
Q

Blue Button

A

a movement toward an improved healthcare system in which patients and providers use information technology to collaborate and improve health. The Blue Button logo signifies that you—as an individual consumer or patient–can get easy, secure access to your own health information in a format you can use. To “Blue Button” is a verb, meaning, for a consumer, “download my health data so I can use it.”

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2
Q

digital divide

A

the growing gap between the underprivileged members of society, especially the poor, rural, elderly, and handicapped portion of the population who do not have access to computers or the Internet; and the wealthy, middle-class, and young Americans living in urban and suburban areas who have access

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3
Q

Ask Me 3

A

Ask Me 3 is an educational program that encourages patients and families to ask three specific questions of their providers to better understand their health conditions and what they need to do to stay healthy.

What is my main problem?
What do I need to do?
Why is it important for me to do this?

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4
Q

personal health record

A

a health record where health data and other information related to the care of a patient is maintained by the patient

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5
Q

bring your own device (BYOD)

A

a trend involving healthcare practitioners using their personal smartphones or other devices rather than devices provided by the healthcare organization. While acceptable, the personal device must meet specific encryption and other security protocols to protect PHI as required by the healthcare organization.

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6
Q

consent management

A

a system, process, or set of policies that enables patients to choose what health information they are willing to permit their healthcare providers to access and share. Consent management allows patients to affirm their participation in electronic health initiatives such as patient portals, personal health records (PHR), and health information exchange (HIE)

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7
Q

consolidated model (centralized)

A

one of the three models of health information exchange architecture
Many independent healthcare organizations connect with the HIE and aggregate data is stored and shared within a central repository managed by the HIE. This centralized data has a master patient index or a record locator service (RLS).

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8
Q

consumer-mediated exchange

A

a type of health information exchange that is controlled by patients who want to control the use and access of their health information. According to the ONC, “consumer-mediated exchange provides patients with access to their health information, allowing them to manage their health care online in a similar fashion to how they might manage their finances through online banking. When in control of their own health information, patients can actively participate in their care”

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9
Q

directed exchange

A

frequently referred to as a “push exchange” because it pushes authorized and secure information from one healthcare organization to another. For example, if a patient is being transferred from one hospital to another, the patient’s health information would be “pushed” to the receiving hospital in order to provide the background health information to help the transition to continued care

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10
Q

federated model (decentralized)

A

one of the three models of health information exchange architecture
There is no centralized database of patient information. The federated model is more common than the consolidated model because it works much like the Internet. With the advent of cloud computing, the federated model may become the more common HIE model.

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11
Q

health information organization (HIO)

A

a public–private partnership organization that oversees, governs, and facilitates the transmission of health data between different types of healthcare organizations that have various EHR systems, according to nationally recognized standards. Many HIOs started as a local health information organization (LHIO) or regional health information organization (RHIO)

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12
Q

hybrid model

A

combines the advantages of centralized and decentralized models. It has an record locator service, and some data are stored in a central repository while the remainder stays with the other healthcare organizations within the HIE. The hybrid model also has a patient portal to itself, and not to a specific healthcare organization

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13
Q

identity management

A

security measures that ensure that the individual who has been identified in a health information organization system is who they say they are, that they have the authority to do what they want to do, and that their actions are tracked

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14
Q

identity matching

A

(also known as patient matching) the process in which the health information organization identifies the right person within the database to exchange information between healthcare organizations. The process examines different demographic elements from different health information technology (health IT) systems to determine if they refer to the same patient.

From an interoperability perspective, the ability to complete patient matching efficiently, accurately, and at scale has long been identified as a key element of the nation’s health IT infrastructure. Patient matching is almost universally needed to enable the interoperability of health data for all kinds of purposes. Patient matching also requires careful consideration with respect to its effect on patient safety and administrative costs

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15
Q

local health information organization (LHIO)

A

a small-scale, local version of an RHIO

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16
Q

Meaningful Use (MU)

A

a regulation that was issued by the Centers for Medicare and Medicaid (CMS) on July 28, 2010, outlining an incentive program for eligible professionals (EPs), eligible hospitals, and critical access hospitals (CAHs) participating in Medicare and Medicaid programs that adopt and successfully demonstrate meaningful use of certified EHR technology

17
Q

eHealth Exchange

A

formerly called nationwide health information network (NwHIN); it is a set of standards, specifications and policies that enable the secure exchange of health information over the Internet. This program provides a foundation for the exchange of health information across diverse entities, within communities and across the country, helping to achieve the goals of the HITECH Act. The Nationwide Health Information Network Exchange is the first community that implemented these standards, specifications and policies in production

18
Q

opt-in or opt-out consent

A

an option in a health information organization system (HIO) that sets the default for health information of patients to be included in the HIO automatically (opt-in), but the patient can choose not to be included (opt-out)

A variation on this consent is the OPT-OUT WITH EXCEPTIONS model that sets the default for health information for patients to be included, but the patient can opt-out completely or allow only select data to be included

19
Q

query-based exchange

A

a find-and-seek request for information that is sent through the health information organization to find any available health information on a specified individual. It is the opposite of the “push exchange,” so it is thought of as a “pull exchange.” This type of exchange is typically used in urgent and emergency care to seek information that would be relevant for the encounter at hand.

For example, a Medicare patient is brought to the Emergency Department of a local hospital. The Emergency physician requests the patients’ most recent EKG and bloodwork results from her cardiologist. The cardiologist’s EHR is queried and it sends the EKG and labwork to the Emergency Department in response. The Emergency Physician is then able to compare the last EKG and bloodwork with the ones being done currently in order to make an informed decision about the patient’s treatment

20
Q

record locator service (RLS)

A

a software tool that provides the ability to identify where records are located based upon criteria such as a Person ID and/or record data type, as well as providing functionality for the ongoing maintenance of this location information

21
Q

regional health information organization (RHIO)

A

a group of organizations with a business stake in improving the quality, safety and efficiency of healthcare delivery that comes together to exchange information for these purposes. The terms RHIO and Health Information Exchange, or ‘HIE’, are often used interchangeably

22
Q

value-based healthcare

A

an evolving concept focused on three areas:

  1. better care for the individual
  2. better health for the community
  3. lower cost of healthcare through improvement of services and delivery methods
23
Q

vetting

A

the process of critically appraising the abilities of an organization or person to determine if they meet the stated criteria

24
Q

infrastructure

A

the basic physical and organizational structures and facilities (e.g. buildings, roads, power supplies) needed for the operation of a society or enterprise

25
Q

syndromic

A

occurring as a syndrome or part of a syndrome

26
Q

advent

A

the arrival of a notable person, thing, or event