Test 5 Part 19

Question 1

Restrict the use of restraints and seclusion in all psychiatric facilities that receive federal funds and in non-medical community-based facilities for children and youth

• Use of restraints and seclusion restricted to emergency safety situations only
• Parent or legal guardian must be notified no later than 24 hours after the occurrence

Answer 1

Children’s Health Act of 2000

Question 2

____________ established mandatory quality reporting requirements for long-term care hospitals, inpatient rehabilitation facilities, and hospice programs, went into effect in 2014; may change as new administration works on new healthcare legislation

Answer 2

2010 Affordable Care Act

Question 3

Medicare providers that fail to comply with data reporting requirements are subject to _________ reduction of reimbursement

Answer 3

2 percent

Question 4

__________ Created by Health Care Quality Improvement Act of 1986, information expanded by Medicare and Medicaid Patient and Program Protection Act of 1987

Answer 4

National Practitioner Data Banks (NPDB)

Question 5

The purpose National Practitioner Data Banks (NPDB) is to Identify and discipline those who engage in _________ and restrict ability of incompetent healthcare practitioners to move from State to State without disclosure or discovery of previous medical malpractice payment and adverse action

Answer 5

Unprofessional behavior

Question 6

NPDB merged with _________________ established under Section 1128E of the Social Security Act; operational in 2000 to establish national healthcare fraud and abuse data collection program for reporting of final adverse actions (not including settlements in which no findings of liability have been made) against healthcare providers, suppliers, or practitioners

Answer 6

Healthcare Integrity and Protection Data Bank (HIPDB)

Question 7

Information reported to the data bank is considered confidential and is not disclosed except as specified by regulation
Requirements include:
Who reports
What information is available
Who can query database

Answer 7

NPDB

Question 8

Requires reporting to the FDA and the product manufacturer of medical device occurrences that have or may have contributed to serious illness, serious injury, or death, including occurrences attributed to user error

Answer 8

Safe Medical Devices Act of 1990

Question 9

_________ clarified terms and established a single reporting standard for device users, manufacturers, importers, and distributors

Answer 9

Medical Device Amendments of 1992

Question 10

________ Anything that is used in treatment or diagnosis that is not a drug
X-ray machines, sutures, defibrillators, grafts, syringes, lasers, heating pads, bone screws, pumps, etc.

Answer 10

Medical device