Health care regulations Definitions

  • I

    ICD-10-CM (Clinical Modification)

    The ICD-10-CM (Clinical Modification) is a system used by physicians and other healthcare providers to classify and code all diagnoses, symptoms and procedures recorded in conjunction with hospital care in the United States.

  • ICD-10-PCS

    The International Classification of Diseases, 10th Revision, Procedure Coding System (ICD-10-PCS) is a U.S. cataloging system for procedural codes that track various health interventions taken by medical professionals.

  • ICD-11

    The International Classification of Disease, Eleventh Revision (ICD-11) is a system of medical coding created by the World Health Organization (WHO) for documenting diseases, signs and symptoms, diagnoses and social circumstances.

  • ICD-9-CM (International Classification of Diseases, Ninth Revision, Clinical Modification)

    ICD-9-CM is the current medical coding standard used in hospitals in the United States. It is scheduled to be replaced by ICD-10 by Oct. 1, 2015.

  • J

    Joint Commission

    The Joint Commission is an independent group that presently accredits 20,500 healthcare facilities in the United States by performing onsite evaluations.

  • M

    MACRA (Medicare Access and CHIP Reauthorization Act of 2015)

    MACRA (Medicare Access and CHIP Reauthorization Act of 2015) is U.S. healthcare legislation that provides a new framework for reimbursing clinicians who successfully demonstrate value over volume in patient care.

  • Maintenance Management Information System (MMIS)

    Maintenance Management Information System (MMIS) is a mechanized claims processing and information retrieval system for Medicaid that's required by the federal government.

  • Meaningful Use

    In the context of health IT, meaningful use is a term used to define minimum U.S. government standards for electronic health records (EHR), outlining how clinical patient data should be exchanged between healthcare providers, between providers and insurers and between providers and patients.

  • meaningful use attestation

    Meaningful use attestation, in a health information technology (HIT) context, is a process that documents that an organization or individual has successfully demonstrated meaningful use and is successfully fulfilling the requirements for electronic health records (EHR) and related technology.

  • meaningful use stage 1

    Meaningful use stage 1 is the first phase of the United States federal government's meaningful use incentive program, which details the requirements for the use of electronic health record (EHR) systems by hospitals and eligible health care professionals.

  • meaningful use stage 2

    Meaningful use stage 2 is the second phase of the meaningful use incentive program that details the second phase of requirements for the use of electronic health record (EHR) systems by hospitals and eligible health care providers.

  • meaningful use stage 3

    Meaningful use stage 3 is the third phase of the federal incentive program that details requirements for the use of electronic health record systems by hospitals and eligible healthcare professionals. However, the new MACRA law will change the overall meaningful use program, which may eventually lessen stage 3's influence.

  • medical device class (MDC)

    Medical device class (MDC) is a category that defines the amount of risk involved with a medical device in the United States and the proper procedures that must be followed when manufacturing and using the device.

  • Meditech (Medical Information Technology Inc.)

    Meditech (Medical Information Technology Inc.) is an electronic health record vendor that holds a 19% market share in the hospital industry, but faces intense competition.

  • N

    National Alliance for Health Information Technology (NAHIT)

    The National Alliance for Health Information Technology, or NAHIT, was formed in 2002 in an effort to promote the use of health IT.

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