Pt. Care and Safety Flashcards

1
Q

FDA limits for whole body SAR is ___ W/kg
over __ minutes of scanning

A

4W/kg; 15mins

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2
Q

FDA limits for **Head ** SAR is ___ W/kg
over __ minutes of scanning

A

3W/kg; 10mins

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3
Q

Regions of the body that do not quickly dissipate thermal absorption from SAR during MR procedures are the

A

Eyes & Testicles

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4
Q

The primary biological effects of the time varying magnetic fields (TVMF) are

A
  • peripheral nerve stimulation
  • visual light flashes (magnetophosphenes)
  • muscle contractions
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5
Q

The pulse sequence that should be utilized the least in a patient with implanted metallic hardware is a

A

gradient echo sequence

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6
Q

RF heating is more of a concern in____________due to the multiple echo train lengths, leading to potential increases in tissue heating.

A

fast spin echo sequences

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7
Q

Risk factors of MR exposure with regards to SAR include all of the following:

A
  •  Obesity
  •  Hypertension
  •  Cardiovascular disease
  •  Elderly
  •  Sedatives/Diuretics
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8
Q

The general public is limited to a magnetic field of

A

5 Gauss

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9
Q

The percentage of patients reported to have reactions to gadolinium MRI contrast are…

A

less than 1%

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10
Q

During a quench, patients and employees should be evacuated from the scan room to prevent

A
  • frostbite
  • asphyxiation
  • rupture of the tympanic membranes
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11
Q

* Zone 1* signage designates an area intended for

A

the general public

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12
Q

Zone 2 signage designates an area intended for

A

unscreened MRI patients

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13
Q

Zone 3 signage designates an area intended for

A

screened MRI patients/personnel

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14
Q

Zone 4 signage designates an area intended for

A

screened patients under constant direct supervision of trained MR personnel

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15
Q

FDA Regulations for magnetic field strength are__Tesla for the entire population, __ Tesla for those over 1 month of age.

A

4; 8

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16
Q

An implant with this label would require…

A

no restrictions on MR imaging approach, and can safely enter the MR scan room

17
Q

An implant with this label requires….

A

that strict manufacturer guidelines be followed (field strength, scan parameters, duration) to ensure patient safety or entry into the MR scan room

18
Q

An implant with this label….

A

would not be permitted to enter the MR scan room, nor be able to undergo an MR procedure, and alternative imaging methods would need to be considered

19
Q

Cycle of infection:

A

 Pathogen
 Reservoir of infection
 Susceptible host
 Method of transmission

20
Q

In the Cycle of infection a pathogen is

A

cause of the disease

21
Q

In the Cycle of infection the Reservoir of infection is

A

where the pathogen grows

22
Q

In the Cycle of infection Susceptible host means

A

pathogens grow in locations where they are stronger than
the host they occupy

23
Q

In the Cycle of infection Methods of transmission are

A

airborne, droplet, contact

24
Q

Transmission-based precautions are

A

 Contact (isolation) – gloves and gown should be worn
 Droplet – Mask should be worn
 Airborne – Mask should be worn

25
Q

During movement or transfer of patients, a urinary collection bag should be placed

A

below the level of the urinary bladder

26
Q

Non-MR personnel are those with

A

little or no training in MRI safety

27
Q

Level 1 personnel are those with

A

limited training in MRI safety
(education about the magnetic field)

28
Q

Level 2 personnel are those with

A

extensive training in MRI safety, including a vast knowledge of the main magnetic field as well as the RF and gradient fields, and the risks and biological effects of these three magnetic fields.

29
Q

To establish a claim of malpractice, four conditions must be proved
true:

A
  1. The defendant had a duty to provide reasonable care to the patient
  2. The patient has sustained some type of loss or injury
  3. The defendant is the party responsible for the loss
  4. The loss is attributable to negligence or improper practice