MQSA/EQUIP Flashcards

1
Q

Accreditation with accreditation body is required every

A

3 years

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2
Q

Certification with FDA or state as certifier is required every

A

3 years

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3
Q

MQSA inspection is performed how often

A

Once a year in the same month of the year

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4
Q

When did MQSA become law by congress

A

Oct 27, 1992

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5
Q

All mammography facilities in US were required to be MQSA certified

A

Oct 1, 1994

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6
Q

FDA published Quality Mammography Standards Final Rule

A

Oct 28, 1997

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7
Q

Final Rule went into effect

A

April 28, 1999

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8
Q

More stringent equipment regulations went into effect

A

Oct 28, 2002

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9
Q

MQSA is certified by

A

-FDA or SAC

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10
Q

American College of Radiology

A

Helps with the accreditation portion of the process

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11
Q

Accreditation bodies

A

Help assess clinical images of facility

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12
Q

Minimum of how many mammograms performed in 24 months

A

200

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13
Q

How many CE units every 3 years?

A

15

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14
Q

Mammograms are kept for how many years if they are consecutive mammograms?

A

5 years

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15
Q

Mammograms are kept for how many years is only one mammogram was performed at the facility?

A

10 years

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16
Q

Maintain a record of serious complaints received by the facility for how many years?

A

3 years from the date the complaint was received

17
Q

The eight that matter (image quality attributes)

A

1) positioning
2) compression
3) exposure level
4) contrast
5) sharpness
6) noise
7) artifact
8) exam identification

18
Q

EQUIP

A

enhancing quality using the inspection program

19
Q

when was EQUIP introduced?

A

Oct 27, 2016; implemented Jan 1, 2017

20
Q

Division of Mammography Quality Standards (DMQS)

A

EQUIP

21
Q

how does EQUIP WORK

A

-inspectors check once a year when they come for yearly MQSA inspection and ask three questions and want to see the three q’s answered and documents signed with dates

22
Q

EQUIP initiative places emphasis on what?

A

the significance of clinical image quality, one of the most important determinants of the accuracy of mammography

23
Q

Question one- quality assurance clinical image corrective action

A

1) does the facility have procedures for corrective action (CA) when clinical images are poor quality?
-aimed at making sure facility has a process in place for giving feedback on any poor-quality images presented for interpretation, and for documenting any corrective action taken, such as repeating images
-facility determines its timeframe for completing CA

24
Q

Question 2- clinical image quality

A

2) does the facility have procedures to ensure that clinical images continue to comply with the clinical image quality standards est. by the facility’s accreditation body?

25
Q

Question 3- quality control oversight

A

3) does the facility have a procedure for LIP oversight of QA/QC records and corrective actions?
-inspector will assess for a procedure for LIP oversight of QA/QC records that include overseeing the freq. of performances of all req. test, and determining whether corrective actions were taken when needed